-
1
-
-
0029035597
-
Evaluation of cannabinoid receptor binding and in vivo activities for anandamide analogs
-
Adams IB, Ryan W, Singer M, Thomas BF, Compton DR, Razdan RK, Martin BR (1995) Evaluation of cannabinoid receptor binding and in vivo activities for anandamide analogs. J Pharmacol Exp Ther 273:1172-1181
-
(1995)
J Pharmacol Exp Ther
, vol.273
, pp. 1172-1181
-
-
Adams, I.B.1
Ryan, W.2
Singer, M.3
Thomas, B.F.4
Compton, D.R.5
Razdan, R.K.6
Martin, B.R.7
-
2
-
-
73049097844
-
Endocannabinoids and cannabinoid analogues block human cardiac Kv4.3 channels in a receptor-independent manner
-
Amoros I, Barana A, Caballero R, Gomez R, Osuna L, Lillo MP, Tamargo J, Delpon E (2010) Endocannabinoids and cannabinoid analogues block human cardiac Kv4.3 channels in a receptor-independent manner. J Mol Cell Cardiol 48:201-210
-
(2010)
J Mol Cell Cardiol
, vol.48
, pp. 201-210
-
-
Amoros, I.1
Barana, A.2
Caballero, R.3
Gomez, R.4
Osuna, L.5
Lillo, M.P.6
Tamargo, J.7
Delpon, E.8
-
3
-
-
40949151048
-
Influence of dietary fatty acids on endocannabinoid and N-acylethanolamine levels in rat brain, liver and small intestine
-
Artmann A, Petersen G, Hellgren LI, Boberg J, Skonberg C, Nellemann C, Hansen SH, Hansen HS (2008) Influence of dietary fatty acids on endocannabinoid and N-acylethanolamine levels in rat brain, liver and small intestine. Biochim Biophys Acta 1781:200-212
-
(2008)
Biochim Biophys Acta
, vol.1781
, pp. 200-212
-
-
Artmann, A.1
Petersen, G.2
Hellgren, L.I.3
Boberg, J.4
Skonberg, C.5
Nellemann, C.6
Hansen, S.H.7
Hansen, H.S.8
-
4
-
-
72049124048
-
Endocannabinoids and cannabinoid analogues block cardiac hKV1.5 channels in a cannabinoid receptor-independent manner
-
Barana A, Amoros I, Caballero R, Gomez R, Osuna L, Lillo MP, Blázquez C, Guzmán M, Delpon E, Tamargo J (2010) Endocannabinoids and cannabinoid analogues block cardiac hKV1.5 channels in a cannabinoid receptor-independent manner. Cardiovasc Res 85:56-67
-
(2010)
Cardiovasc Res
, vol.85
, pp. 56-67
-
-
Barana, A.1
Amoros, I.2
Caballero, R.3
Gomez, R.4
Osuna, L.5
Lillo, M.P.6
Blázquez, C.7
Guzmán, M.8
Delpon, E.9
Tamargo, J.10
-
5
-
-
0036850272
-
Direct inhibition by cannabinoids of human 5-HT3A receptors: Probable involvement of an allosteric modulatory site
-
Barann M, Molderings G, Bruss M, Bonisch H, Urban BW, Gothert M (2002) Direct inhibition by cannabinoids of human 5-HT3A receptors: probable involvement of an allosteric modulatory site. Br J Pharmacol 137:589-596
-
(2002)
Br J Pharmacol
, vol.137
, pp. 589-596
-
-
Barann, M.1
Molderings, G.2
Bruss, M.3
Bonisch, H.4
Urban, B.W.5
Gothert, M.6
-
6
-
-
0028787448
-
Cannabinomimetic behavioral effects of and adenylate cyclase inhibition by two new endogenous anandamides
-
Barg J, Fride E, Hanus L, Levy R, Matus-Leibovitch N, Heldman E, Bayewitch M, Mechoulam R, Vogel Z (1995) Cannabinomimetic behavioral effects of and adenylate cyclase inhibition by two new endogenous anandamides. Eur J Pharmacol 287:145-152
-
(1995)
Eur J Pharmacol
, vol.287
, pp. 145-152
-
-
Barg, J.1
Fride, E.2
Hanus, L.3
Levy, R.4
Matus-Leibovitch, N.5
Heldman, E.6
Bayewitch, M.7
Mechoulam, R.8
Vogel, Z.9
-
7
-
-
84868237301
-
Identification and quantification of a new family of peptide endocannabinoids (Pepcans) showing negative allosteric modulation at CB1 receptors
-
Bauer M, Chicca A, Tamborrini M, Eisen D, Lerner R, Lutz B, Poetz O, Pluschke G, Gertsch J (2012) Identification and quantification of a new family of peptide endocannabinoids (Pepcans) showing negative allosteric modulation at CB1 receptors. J Biol Chem 287:36944-36967
-
(2012)
J Biol Chem
, vol.287
, pp. 36944-36967
-
-
Bauer, M.1
Chicca, A.2
Tamborrini, M.3
Eisen, D.4
Lerner, R.5
Lutz, B.6
Poetz, O.7
Pluschke, G.8
Gertsch, J.9
-
8
-
-
0031830516
-
An entourage effect: Inactive endogenous fatty acid glycerol esters enhance 2-arachidonoyl-glycerol cannabinoid activity
-
Ben-Shabat S, Fride E, Sheskin T, Tamiri T, Rhee M-H, Vogel Z, Bisogno T, De Petrocellis L, Di Marzo V, Mechoulam R (1998) An entourage effect: inactive endogenous fatty acid glycerol esters enhance 2-arachidonoyl-glycerol cannabinoid activity. Eur J Pharmacol 353:23-31
-
(1998)
Eur J Pharmacol
, vol.353
, pp. 23-31
-
-
Ben-Shabat, S.1
Fride, E.2
Sheskin, T.3
Tamiri, T.4
Rhee, M.-H.5
Vogel, Z.6
Bisogno, T.7
De Petrocellis, L.8
Di Marzo, V.9
Mechoulam, R.10
-
9
-
-
0035952290
-
Synthesis and biological evaluation of novel amides of polyunsaturated fatty acids with dopamine
-
Bezuglov V, Bobrov M, Gretskaya N, Gonchar A, Zinchenko G, Melck D, Bisogno T, Di Marzo V, Kuklev D, Rossi J-C, Vidal J-P, Durand T (2001) Synthesis and biological evaluation of novel amides of polyunsaturated fatty acids with dopamine. Bioorg Med Chem Lett 11:447-449
-
(2001)
Bioorg Med Chem Lett
, vol.11
, pp. 447-449
-
-
Bezuglov, V.1
Bobrov, M.2
Gretskaya, N.3
Gonchar, A.4
Zinchenko, G.5
Melck, D.6
Bisogno, T.7
Di Marzo, V.8
Kuklev, D.9
Rossi, J.-C.10
Vidal, J.-P.11
Durand, T.12
-
10
-
-
0034332637
-
N-acyl-dopamines: Novel synthetic CB1 cannabinoid-receptor ligands and inhibitors of anandamide inactivation with cannabimimetic activity in vitro and in vivo
-
Bisogno T, Melck D, Bobrov MY, Gretskaya NM, Bezuglov VV, De Petrocellis L, Di Marzo V (2000) N-acyl-dopamines: novel synthetic CB1 cannabinoid-receptor ligands and inhibitors of anandamide inactivation with cannabimimetic activity in vitro and in vivo. Biochem J 351:817-824
-
(2000)
Biochem J
, vol.351
, pp. 817-824
-
-
Bisogno, T.1
Melck, D.2
Bobrov, M.Y.3
Gretskaya, N.M.4
Bezuglov, V.V.5
De Petrocellis, L.6
Di Marzo, V.7
-
11
-
-
0032246648
-
Dual activation and inhibition of adenylyl cyclase by cannabinoid receptor agonists: Evidence for agonist-specific trafficking of intracellular responses
-
Bonhaus DW, Chang LK, Kwan J, Martin GR (1998) Dual activation and inhibition of adenylyl cyclase by cannabinoid receptor agonists: evidence for agonist-specific trafficking of intracellular responses. J Pharmacol Exp Ther 287:884-888
-
(1998)
J Pharmacol Exp Ther
, vol.287
, pp. 884-888
-
-
Bonhaus, D.W.1
Chang, L.K.2
Kwan, J.3
Martin, G.R.4
-
12
-
-
0029977961
-
Cerebrodiene, arachidonyl-ethanolamide, and hybrid structures: Potential for interaction with brain cannabinoid receptors
-
Boring DL, Berglund BA, Howlett AC (1996) Cerebrodiene, arachidonyl-ethanolamide, and hybrid structures: potential for interaction with brain cannabinoid receptors. Prostaglandins Leukot Essent Fatty Acids 55:207-210
-
(1996)
Prostaglandins Leukot Essent Fatty Acids
, vol.55
, pp. 207-210
-
-
Boring, D.L.1
Berglund, B.A.2
Howlett, A.C.3
-
13
-
-
22144477527
-
Anandamide induced PPARγ transcriptional activation and 3T3-L1 preadipocyte differentiation
-
Bouaboula M, Hilairet S, Marchand J, Fajas L, Le Fur G, Casellas P (2005) Anandamide induced PPARγ transcriptional activation and 3T3-L1 preadipocyte differentiation. Eur J Pharmacol 517:174-181
-
(2005)
Eur J Pharmacol
, vol.517
, pp. 174-181
-
-
Bouaboula, M.1
Hilairet, S.2
Marchand, J.3
Fajas, L.4
Le Fur, G.5
Casellas, P.6
-
14
-
-
14844282831
-
The expanding field of cannabimimetic and related lipid mediators
-
Bradshaw HB, Walker JM (2005) The expanding field of cannabimimetic and related lipid mediators. Br J Pharmacol 144:459-465
-
(2005)
Br J Pharmacol
, vol.144
, pp. 459-465
-
-
Bradshaw, H.B.1
Walker, J.M.2
-
15
-
-
0032479282
-
Cannabinoid receptor agonist efficacy for stimulating [35S]GTPγS binding to rat cerebellar membranes correlates with agonist-induced decreases in GDP affinity
-
Breivogel CS, Selley DE, Childers SR (1998) Cannabinoid receptor agonist efficacy for stimulating [35S]GTPγS binding to rat cerebellar membranes correlates with agonist-induced decreases in GDP affinity. J Biol Chem 273:16865-16873
-
(1998)
J Biol Chem
, vol.273
, pp. 16865-16873
-
-
Breivogel, C.S.1
Selley, D.E.2
Childers, S.R.3
-
16
-
-
80054011406
-
Characterization of the endocannabinoid system, CB1 receptor signalling and desensitization in human myometrium
-
Brighton PJ, Marczylo TH, Rana S, Konje JC, Willets JM (2011) Characterization of the endocannabinoid system, CB1 receptor signalling and desensitization in human myometrium. Br J Pharmacol 164:1479-1494
-
(2011)
Br J Pharmacol
, vol.164
, pp. 1479-1494
-
-
Brighton, P.J.1
Marczylo, T.H.2
Rana, S.3
Konje, J.C.4
Willets, J.M.5
-
17
-
-
77956278506
-
Cannabinoid receptor-dependent and -independent anti-proliferative effects of omega-3 ethanolamides in androgen receptor-positive and -negative prostate cancer cell lines
-
Brown I, Cascio MG, Wahle KWJ, Smoum R, Mechoulam R, Ross RA, Pertwee RG, Heys SD (2010) Cannabinoid receptor-dependent and -independent anti-proliferative effects of omega-3 ethanolamides in androgen receptor-positive and -negative prostate cancer cell lines. Carcinogenesis 31:1584-1591
-
(2010)
Carcinogenesis
, vol.31
, pp. 1584-1591
-
-
Brown, I.1
Cascio, M.G.2
Wahle, K.3
Smoum, R.4
Mechoulam, R.5
Ross, R.A.6
Pertwee, R.G.7
Heys, S.D.8
-
18
-
-
84869869192
-
Cannabinoids and omega-3/6 endocannabinoids as cell death and anticancer modulators
-
Brown I, Cascio MG, Rotondo D, Pertwee RG, Heys SD, Wahle KWJ (2013) Cannabinoids and omega-3/6 endocannabinoids as cell death and anticancer modulators. Prog Lipid Res 52:80-109
-
(2013)
Prog Lipid Res
, vol.52
, pp. 80-109
-
-
Brown, I.1
Cascio, M.G.2
Rotondo, D.3
Pertwee, R.G.4
Heys, S.D.5
Wahle, K.6
-
19
-
-
0030720938
-
Relative efficacies of cannabinoid CB1 receptor agonists in the mouse brain
-
Burkey TH, Quock RM, Consroe P, Ehlert FJ, Hosohata Y, Roeske WR, Yamamura HI (1997) Relative efficacies of cannabinoid CB1 receptor agonists in the mouse brain. Eur J Pharmacol 336:295-298
-
(1997)
Eur J Pharmacol
, vol.336
, pp. 295-298
-
-
Burkey, T.H.1
Quock, R.M.2
Consroe, P.3
Ehlert, F.J.4
Hosohata, Y.5
Roeske, W.R.6
Yamamura, H.I.7
-
20
-
-
42549088117
-
Endogenous cannabinoid anandamide inhibits nicotinic acetylcholine receptor function in mouse thalamic synaptosomes
-
Butt C, Alptekin A, Shippenberg T, Oz M (2008) Endogenous cannabinoid anandamide inhibits nicotinic acetylcholine receptor function in mouse thalamic synaptosomes. J Neurochem 105:1235-1243
-
(2008)
J Neurochem
, vol.105
, pp. 1235-1243
-
-
Butt, C.1
Alptekin, A.2
Shippenberg, T.3
Oz, M.4
-
21
-
-
84891881348
-
Cross-modulation and molecular interaction at the Cav3.3 protein between the endogenous lipids and the T-type calcium channel antagonist TTA-A2
-
Cazade M, Nuss CE, Bidaud I, Renger JJ, Uebele VN, Lory P, Chemin J (2014) Cross-modulation and molecular interaction at the Cav3.3 protein between the endogenous lipids and the T-type calcium channel antagonist TTA-A2. Mol Pharmacol 85:218-225
-
(2014)
Mol Pharmacol
, vol.85
, pp. 218-225
-
-
Cazade, M.1
Nuss, C.E.2
Bidaud, I.3
Renger, J.J.4
Uebele, V.N.5
Lory, P.6
Chemin, J.7
-
22
-
-
0032586854
-
Modification of 5-HT2 receptor mediated behaviour in the rat by oleamide and the role of cannabinoid receptors
-
Cheer JF, Cadogan A-K, Marsden CA, Fone KCF, Kendall DA (1999) Modification of 5-HT2 receptor mediated behaviour in the rat by oleamide and the role of cannabinoid receptors. Neuropharmacology 38:533-541
-
(1999)
Neuropharmacology
, vol.38
, pp. 533-541
-
-
Cheer, J.F.1
Cadogan, A.-K.2
Marsden, C.A.3
Fone, K.4
Kendall, D.A.5
-
23
-
-
0037126618
-
Direct inhibition of T-type calcium channels by the endogenous cannabinoid anandamide
-
Chemin J, Monteil A, Perez-Reyes E, Nargeot J, Lory P (2001) Direct inhibition of T-type calcium channels by the endogenous cannabinoid anandamide. EMBO J 20:7033-7040
-
(2001)
EMBO J
, vol.20
, pp. 7033-7040
-
-
Chemin, J.1
Monteil, A.2
Perez-Reyes, E.3
Nargeot, J.4
Lory, P.5
-
24
-
-
34047261630
-
Chemical determinants involved in anandamide-induced inhibition of T-type calcium channels
-
Chemin J, Nargeot J, Lory P (2007) Chemical determinants involved in anandamide-induced inhibition of T-type calcium channels. J Biol Chem 282:2314-2323
-
(2007)
J Biol Chem
, vol.282
, pp. 2314-2323
-
-
Chemin, J.1
Nargeot, J.2
Lory, P.3
-
25
-
-
0028265784
-
Effects of anandamide on cannabinoid receptors in rat brain membranes
-
Childers SR, Sexton T, Roy MB (1994) Effects of anandamide on cannabinoid receptors in rat brain membranes. Biochem Pharmacol 47:711-715
-
(1994)
Biochem Pharmacol
, vol.47
, pp. 711-715
-
-
Childers, S.R.1
Sexton, T.2
Roy, M.B.3
-
26
-
-
0038190980
-
N-oleoyldopamine, a novel endogenous capsaicin-like lipid that produces hyperalgesia
-
Chu CJ, Huang SM, De Petrocellis L, Bisogno T, Ewing SA, Miller JD, Zipkin RE, Daddario N, Appendino G, Di Marzo V, Walker JM (2003) N-oleoyldopamine, a novel endogenous capsaicin-like lipid that produces hyperalgesia. J Biol Chem 278:13633-13639
-
(2003)
J Biol Chem
, vol.278
, pp. 13633-13639
-
-
Chu, C.J.1
Huang, S.M.2
De Petrocellis, L.3
Bisogno, T.4
Ewing, S.A.5
Miller, J.D.6
Zipkin, R.E.7
Daddario, N.8
Appendino, G.9
Di Marzo, V.10
Walker, J.M.11
-
27
-
-
73549104997
-
N-oleoyldopamine enhances glucose homeostasis through the activation of GPR119
-
Chu Z-L, Carroll C, Chen R, Alfonso J, Gutierrez V, He H, Lucman A, Xing C, Sebring K, Zhou J, Wagner B, Unett D, Jones RM, Behan DP, Leonard J (2010) N-oleoyldopamine enhances glucose homeostasis through the activation of GPR119. Mol Endocrinol 24:161-170
-
(2010)
Mol Endocrinol
, vol.24
, pp. 161-170
-
-
Chu, Z.-L.1
Carroll, C.2
Chen, R.3
Alfonso, J.4
Gutierrez, V.5
He, H.6
Lucman, A.7
Xing, C.8
Sebring, K.9
Zhou, J.10
Wagner, B.11
Unett, D.12
Jones, R.M.13
Behan, D.P.14
Leonard, J.15
-
28
-
-
0029004101
-
Chemical characterization of a family of brain lipids that induce sleep
-
Cravatt BF, Prospero-Garcia O, Siuzdak G, Gilula NB, Henriksen SJ, Boger DL, Lerner RA (1995) Chemical characterization of a family of brain lipids that induce sleep. Science 268:1506-1509
-
(1995)
Science
, vol.268
, pp. 1506-1509
-
-
Cravatt, B.F.1
Prospero-Garcia, O.2
Siuzdak, G.3
Gilula, N.B.4
Henriksen, S.J.5
Boger, D.L.6
Lerner, R.A.7
-
29
-
-
0034644842
-
Overlap between the ligand recognition properties of the anandamide transporter and the VR1 vanilloid receptor: Inhibitors of anandamide uptake with negligible capsaicin-like activity
-
De Petrocellis L, Bisogno T, Davis JB, Pertwee RG, Di Marzo V (2000) Overlap between the ligand recognition properties of the anandamide transporter and the VR1 vanilloid receptor: inhibitors of anandamide uptake with negligible capsaicin-like activity. FEBS Lett 483:52-56
-
(2000)
FEBS Lett
, vol.483
, pp. 52-56
-
-
De Petrocellis, L.1
Bisogno, T.2
Davis, J.B.3
Pertwee, R.G.4
Di Marzo, V.5
-
30
-
-
0035918311
-
The activity of anandamide at vanilloid VR1 receptors requires facilitated transport across the cell membrane and is limited by intracellular metabolism
-
De Petrocellis L, Bisogno T, Maccarrone M, Davis JB, Finazzi-Agrò A, Di Marzo V (2001) The activity of anandamide at vanilloid VR1 receptors requires facilitated transport across the cell membrane and is limited by intracellular metabolism. J Biol Chem 276:12856-12863
-
(2001)
J Biol Chem
, vol.276
, pp. 12856-12863
-
-
De Petrocellis, L.1
Bisogno, T.2
Maccarrone, M.3
Davis, J.B.4
Finazzi-Agrò, A.5
Di Marzo, V.6
-
31
-
-
34247523747
-
Regulation of transient receptor potential channels of melastatin type 8 (TRPM8): Effect of cAMP, cannabinoid CB1 receptors and endovanilloids
-
De Petrocellis L, Starowicz K, Moriello AS, Vivese M, Orlando P, Di Marzo V (2007) Regulation of transient receptor potential channels of melastatin type 8 (TRPM8): effect of cAMP, cannabinoid CB1 receptors and endovanilloids. Exp Cell Res 313:1911-1920
-
(2007)
Exp Cell Res
, vol.313
, pp. 1911-1920
-
-
De Petrocellis, L.1
Starowicz, K.2
Moriello, A.S.3
Vivese, M.4
Orlando, P.5
Di Marzo, V.6
-
32
-
-
44249117614
-
Plant-derived cannabinoids modulate the activity of transient receptor potential channels of ankyrin type-1 and melastatin type-8
-
De Petrocellis L, Vellani V, Schiano-Moriello A, Marini P, Magherini PC, Orlando P, Di Marzo V (2008) Plant-derived cannabinoids modulate the activity of transient receptor potential channels of ankyrin type-1 and melastatin type-8. J Pharmacol Exp Ther 325:1007-1015
-
(2008)
J Pharmacol Exp Ther
, vol.325
, pp. 1007-1015
-
-
De Petrocellis, L.1
Vellani, V.2
Schiano-Moriello, A.3
Marini, P.4
Magherini, P.C.5
Orlando, P.6
Di Marzo, V.7
-
33
-
-
84870505112
-
A re-evaluation of 9-HODE activity at TRPV1 channels in comparison with anandamide: Enantioselectivity and effects at other TRP channels and in sensory neurons
-
De Petrocellis L, Moriello AS, Imperatore R, Cristino L, Starowicz K, Di Marzo V (2012) A re-evaluation of 9-HODE activity at TRPV1 channels in comparison with anandamide: enantioselectivity and effects at other TRP channels and in sensory neurons. Br J Pharmacol 167:1643-1651
-
(2012)
Br J Pharmacol
, vol.167
, pp. 1643-1651
-
-
De Petrocellis, L.1
Moriello, A.S.2
Imperatore, R.3
Cristino, L.4
Starowicz, K.5
Di Marzo, V.6
-
34
-
-
77954924048
-
RNA editing modulates the binding of drugs and highly unsaturated fatty acids to the open pore of Kv potassium channels
-
Decher N, Streit AK, Rapedius M, Netter MF, Marzian S, Ehling P, Schlichthorl G, Craan T, Renigunta V, Kohler A, Dodel RC, Navarro-Polanco RA, Preisig-Muller R, Klebe G, Budde T, Baukrowitz T, Daut J (2010) RNA editing modulates the binding of drugs and highly unsaturated fatty acids to the open pore of Kv potassium channels. EMBO J 29:2101-2113
-
(2010)
EMBO J
, vol.29
, pp. 2101-2113
-
-
Decher, N.1
Streit, A.K.2
Rapedius, M.3
Netter, M.F.4
Marzian, S.5
Ehling, P.6
Schlichthorl, G.7
Craan, T.8
Renigunta, V.9
Kohler, A.10
Dodel, R.C.11
Navarro-Polanco, R.A.12
Preisig-Muller, R.13
Klebe, G.14
Budde, T.15
Baukrowitz, T.16
Daut, J.17
-
35
-
-
0027078685
-
Isolation and structure of a brain constituent that binds to the cannabinoid receptor
-
Devane WA, Hanuš L, Breuer A, Pertwee RG, Stevenson LA, Griffin G, Gibson D, Mandelbaum A, Etinger A, Mechoulam R (1992) Isolation and structure of a brain constituent that binds to the cannabinoid receptor. Science 258:1946-1949
-
(1992)
Science
, vol.258
, pp. 1946-1949
-
-
Devane, W.A.1
Hanuš, L.2
Breuer, A.3
Pertwee, R.G.4
Stevenson, L.A.5
Griffin, G.6
Gibson, D.7
Mandelbaum, A.8
Etinger, A.9
Mechoulam, R.10
-
36
-
-
0033769188
-
Levels, metabolism, and pharmacological activity of anandamide in CB1 cannabinoid receptor knockout mice: Evidence for non-CB1, non-CB2 receptor-mediated actions of anandamide in mouse brain
-
Di Marzo V, Breivogel CS, Tao Q, Bridgen DT, Razdan RK, Zimmer AM, Zimmer A, Martin BR (2000) Levels, metabolism, and pharmacological activity of anandamide in CB1 cannabinoid receptor knockout mice: evidence for non-CB1, non-CB2 receptor-mediated actions of anandamide in mouse brain. J Neurochem 75:2434-2444
-
(2000)
J Neurochem
, vol.75
, pp. 2434-2444
-
-
Di Marzo, V.1
Breivogel, C.S.2
Tao, Q.3
Bridgen, D.T.4
Razdan, R.K.5
Zimmer, A.M.6
Zimmer, A.7
Martin, B.R.8
-
37
-
-
38049053476
-
Inhibition of [3H]batrachotoxinin A-20α-benzoate binding to sodium channels and sodium channel function by endocannabinoids
-
Duan Y, Zheng J, Nicholson RA (2008) Inhibition of [3H]batrachotoxinin A-20α-benzoate binding to sodium channels and sodium channel function by endocannabinoids. Neurochem Int 52:438-446
-
(2008)
Neurochem Int
, vol.52
, pp. 438-446
-
-
Duan, Y.1
Zheng, J.2
Nicholson, R.A.3
-
38
-
-
0028954055
-
Cannabinoid agonists inhibit the activation of 5-HT3 receptors in rat nodose ganglion neurons
-
Fan P (1995) Cannabinoid agonists inhibit the activation of 5-HT3 receptors in rat nodose ganglion neurons. J Neurophysiol 73:907-910
-
(1995)
J Neurophysiol
, vol.73
, pp. 907-910
-
-
Fan, P.1
-
39
-
-
0027185227
-
Anandamide, an endogenous cannabimimetic eicosanoid, binds to the cloned human cannabinoid receptor and stimulates receptor-mediated signal transduction
-
Felder CC, Briley EM, Axelrod J, Simpson JT, Mackie K, Devane WA (1993) Anandamide, an endogenous cannabimimetic eicosanoid, binds to the cloned human cannabinoid receptor and stimulates receptor-mediated signal transduction. Proc Natl Acad Sci U S A 90:7656-7660
-
(1993)
Proc Natl Acad Sci U S A
, vol.90
, pp. 7656-7660
-
-
Felder, C.C.1
Briley, E.M.2
Axelrod, J.3
Simpson, J.T.4
Mackie, K.5
Devane, W.A.6
-
40
-
-
0029118444
-
Comparison of the pharmacology and signal transduction of the human cannabinoid CB1 and CB2 receptors
-
Felder CC, Joyce KE, Briley EM, Mansouri J, Mackie K, Blond O, Lai Y, Ma AL, Mitchell RL (1995) Comparison of the pharmacology and signal transduction of the human cannabinoid CB1 and CB2 receptors. Mol Pharmacol 48:443-450
-
(1995)
Mol Pharmacol
, vol.48
, pp. 443-450
-
-
Felder, C.C.1
Joyce, K.E.2
Briley, E.M.3
Mansouri, J.4
Mackie, K.5
Blond, O.6
Lai, Y.7
Ma, A.L.8
Mitchell, R.L.9
-
41
-
-
84916613779
-
Modeling, molecular dynamics simulation, and mutation validation for structure of cannabinoid receptor 2 based on known crystal structures of GPCRs
-
Feng Z, Alqarni MH, Yang P, Tong Q, Chowdhury A, Wang L, Xie X-Q (2014) Modeling, molecular dynamics simulation, and mutation validation for structure of cannabinoid receptor 2 based on known crystal structures of GPCRs. J Chem Inf Model 54:2483-2499
-
(2014)
J Chem Inf Model
, vol.54
, pp. 2483-2499
-
-
Feng, Z.1
Alqarni, M.H.2
Yang, P.3
Tong, Q.4
Chowdhury, A.5
Wang, L.6
Xie, X.-Q.7
-
42
-
-
0037181180
-
Noladin ether, a putative novel endocannabinoid: Inactivation mechanisms and a sensitive method for its quantification in rat tissues
-
Fezza F, Bisogno T, Minassi A, Appendino G, Mechoulam R, Di Marzo V (2002) Noladin ether, a putative novel endocannabinoid: inactivation mechanisms and a sensitive method for its quantification in rat tissues. FEBS Lett 513:294-298
-
(2002)
FEBS Lett
, vol.513
, pp. 294-298
-
-
Fezza, F.1
Bisogno, T.2
Minassi, A.3
Appendino, G.4
Mechoulam, R.5
Di Marzo, V.6
-
43
-
-
34548382540
-
COX-2 suppresses tissue factor expression via endocannabinoid-directed PPARδ activation
-
Ghosh M, Wang HB, Ai Y, Romeo E, Luyendyk JP, Peters JM, Mackman N, Dey SK, Hla T (2007) COX-2 suppresses tissue factor expression via endocannabinoid-directed PPARδ activation. J Exp Med 204:2053-2061
-
(2007)
J Exp Med
, vol.204
, pp. 2053-2061
-
-
Ghosh, M.1
Wang, H.B.2
Ai, Y.3
Romeo, E.4
Luyendyk, J.P.5
Peters, J.M.6
Mackman, N.7
Dey, S.K.8
Hla, T.9
-
44
-
-
59149092768
-
The endogenous brain constituent N-arachidonoyl L-serine is an activator of large conductance Ca2þ-activated Kþ channels
-
Godlewski G, Offertáler L, Osei-Hyiaman D, Mo FM, Harvey-White J, Liu J, Davis MI, Zhang L, Razdan RK, Milman G, Pacher P, Mukhopadhyay P, Lovinger DM, Kunos G (2009) The endogenous brain constituent N-arachidonoyl L-serine is an activator of large conductance Ca2þ-activated Kþ channels. J Pharmacol Exp Ther 328:351-361
-
(2009)
J Pharmacol Exp Ther
, vol.328
, pp. 351-361
-
-
Godlewski, G.1
Offertáler, L.2
Osei-Hyiaman, D.3
Mo, F.M.4
Harvey-White, J.5
Liu, J.6
Davis, M.I.7
Zhang, L.8
Razdan, R.K.9
Milman, G.10
Pacher, P.11
Mukhopadhyay, P.12
Lovinger, D.M.13
Kunos, G.14
-
45
-
-
70349339642
-
Novel endogenous peptide agonists of cannabinoid receptors
-
Gomes I, Grushko JS, Golebiewska U, Hoogendoorn S, Gupta A, Heimann AS, Ferro ES, Scarlata S, Fricker LD, Devi LA (2009) Novel endogenous peptide agonists of cannabinoid receptors. FASEB J 23:3020-3029
-
(2009)
FASEB J
, vol.23
, pp. 3020-3029
-
-
Gomes, I.1
Grushko, J.S.2
Golebiewska, U.3
Hoogendoorn, S.4
Gupta, A.5
Heimann, A.S.6
Ferro, E.S.7
Scarlata, S.8
Fricker, L.D.9
Devi, L.A.10
-
46
-
-
0034058250
-
Endocannabinoid 2-arachidonyl glycerol is a full agonist through human type 2 cannabinoid receptor: Antagonism by anandamide
-
Gonsiorek W, Lunn C, Fan X, Narula S, Lundell D, Hipkin RW (2000) Endocannabinoid 2-arachidonyl glycerol is a full agonist through human type 2 cannabinoid receptor: antagonism by anandamide. Mol Pharmacol 57:1045-1050
-
(2000)
Mol Pharmacol
, vol.57
, pp. 1045-1050
-
-
Gonsiorek, W.1
Lunn, C.2
Fan, X.3
Narula, S.4
Lundell, D.5
Hipkin, R.W.6
-
47
-
-
0031914157
-
Dual effects of anandamide on NMDA receptor-mediated responses and neurotransmission
-
Hampson AJ, Bornheim LM, Scanziani M, Yost CS, Gray AT, Hansen BM, Leonoudakis DJ, Bickler PE (1998) Dual effects of anandamide on NMDA receptor-mediated responses and neurotransmission. J Neurochem 70:671-676
-
(1998)
J Neurochem
, vol.70
, pp. 671-676
-
-
Hampson, A.J.1
Bornheim, L.M.2
Scanziani, M.3
Yost, C.S.4
Gray, A.T.5
Hansen, B.M.6
Leonoudakis, D.J.7
Bickler, P.E.8
-
48
-
-
0027489995
-
Two new unsaturated fatty acid ethanolamides in brain that bind to the cannabinoid receptor
-
Hanuš L, Gopher A, Almog S, Mechoulam R (1993) Two new unsaturated fatty acid ethanolamides in brain that bind to the cannabinoid receptor. J Med Chem 36:3032-3034
-
(1993)
J Med Chem
, vol.36
, pp. 3032-3034
-
-
Hanuš, L.1
Gopher, A.2
Almog, S.3
Mechoulam, R.4
-
49
-
-
0035957425
-
2-Arachidonyl glyceryl ether, an endogenous agonist of the cannabinoid CB1 receptor
-
Hanuš L, Abu-Lafi S, Fride E, Breuer A, Vogel Z, Shalev DE, Kustanovich I, Mechoulam R (2001) 2-Arachidonyl glyceryl ether, an endogenous agonist of the cannabinoid CB1 receptor. Proc Natl Acad Sci U S A 98:3662-3665
-
(2001)
Proc Natl Acad Sci U S A
, vol.98
, pp. 3662-3665
-
-
Hanuš, L.1
Abu-Lafi, S.2
Fride, E.3
Breuer, A.4
Vogel, Z.5
Shalev, D.E.6
Kustanovich, I.7
Mechoulam, R.8
-
50
-
-
38049117749
-
Hemopressin is an inverse agonist of CB1 cannabinoid receptors
-
Heimann AS, Gomes L, Dale CS, Pagano RL, Gupta A, de Souza LL, Luchessi AD, Castro LM, Giorgi R, Rioli V, Ferro ES, Devi LA (2007) Hemopressin is an inverse agonist of CB1 cannabinoid receptors. Proc Natl Acad Sci U S A 104:20588-20593
-
(2007)
Proc Natl Acad Sci U S A
, vol.104
, pp. 20588-20593
-
-
Heimann, A.S.1
Gomes, L.2
Dale, C.S.3
Pagano, R.L.4
Gupta, A.5
De Souza, L.L.6
Luchessi, A.D.7
Castro, L.M.8
Giorgi, R.9
Rioli, V.10
Ferro, E.S.11
Devi, L.A.12
-
51
-
-
33644835159
-
Δ9-tetrahydrocannabinol and endogenous cannabinoid anandamide directly potentiate the function of glycine receptors
-
Hejazi N, Zhou C, Oz M, Sun H, Ye JH, Zhang L (2006) Δ9-tetrahydrocannabinol and endogenous cannabinoid anandamide directly potentiate the function of glycine receptors. Mol Pharmacol 69:991-997
-
(2006)
Mol Pharmacol
, vol.69
, pp. 991-997
-
-
Hejazi, N.1
Zhou, C.2
Oz, M.3
Sun, H.4
Ye, J.H.5
Zhang, L.6
-
52
-
-
0033060910
-
Synthesis and characterization of potent and selective agonists of the neuronal cannabinoid receptor (CB1)
-
Hillard CJ, Manna S, Greenberg MJ, Dicamelli R, Ross RA, Stevenson LA, Murphy V, Pertwee RG, Campbell WB (1999) Synthesis and characterization of potent and selective agonists of the neuronal cannabinoid receptor (CB1). J Pharmacol Exp Ther 289:1427-1433
-
(1999)
J Pharmacol Exp Ther
, vol.289
, pp. 1427-1433
-
-
Hillard, C.J.1
Manna, S.2
Greenberg, M.J.3
Dicamelli, R.4
Ross, R.A.5
Stevenson, L.A.6
Murphy, V.7
Pertwee, R.G.8
Campbell, W.B.9
-
53
-
-
0037062411
-
An endogenous capsaicin-like substance with high potency at recombinant and native vanilloid VR1 receptors
-
Huang SM, Bisogno T, Trevisani M, Al-Hayani A, De Petrocellis L, Fezza F, Tognetto M, Petros TJ, Krey JF, Chu CJ, Miller JD, Davies SN, Geppetti P, Walker JM, Di Marzo V (2002) An endogenous capsaicin-like substance with high potency at recombinant and native vanilloid VR1 receptors. Proc Natl Acad Sci U S A 99:8400-8405
-
(2002)
Proc Natl Acad Sci U S A
, vol.99
, pp. 8400-8405
-
-
Huang, S.M.1
Bisogno, T.2
Trevisani, M.3
Al-Hayani, A.4
De Petrocellis, L.5
Fezza, F.6
Tognetto, M.7
Petros, T.J.8
Krey, J.F.9
Chu, C.J.10
Miller, J.D.11
Davies, S.N.12
Geppetti, P.13
Walker, J.M.14
Di Marzo, V.15
-
54
-
-
84860419778
-
A synaptogenic amide N-docosahexaenoylethanolamide promotes hippocampal development
-
Kim H-Y, Spector AA, Xiong Z-M (2011) A synaptogenic amide N-docosahexaenoylethanolamide promotes hippocampal development. Prostaglandins Other Lipid Mediat 96:114-120
-
(2011)
Prostaglandins Other Lipid Mediat
, vol.96
, pp. 114-120
-
-
Kim, H.-Y.1
Spector, A.A.2
Xiong, Z.-M.3
-
55
-
-
0000022561
-
Anandamide, an endogenous cannabinoid receptor ligand, also interacts with 5-hydroxytryptamine (5-HT) receptor
-
Kimura T, Ohta T, Watanabe K, Yoshimura H, Yamamoto I (1998) Anandamide, an endogenous cannabinoid receptor ligand, also interacts with 5-hydroxytryptamine (5-HT) receptor. Biol Pharm Bull 21:224-226
-
(1998)
Biol Pharm Bull
, vol.21
, pp. 224-226
-
-
Kimura, T.1
Ohta, T.2
Watanabe, K.3
Yoshimura, H.4
Yamamoto, I.5
-
56
-
-
0033389724
-
Anandamides inhibit binding to the muscarinic acetylcholine receptor
-
Lagalwar S, Bordayo EZ, Hoffmann KL, Fawcett JR, Frey WH (1999) Anandamides inhibit binding to the muscarinic acetylcholine receptor. J Mol Neurosci 13:55-61
-
(1999)
J Mol Neurosci
, vol.13
, pp. 55-61
-
-
Lagalwar, S.1
Bordayo, E.Z.2
Hoffmann, K.L.3
Fawcett, J.R.4
Frey, W.H.5
-
57
-
-
40649102938
-
GPR55 is a cannabinoid receptor that increases intracellular calcium and inhibits M current
-
Lauckner JE, Jensen JB, Chen H-Y, Lu H-C, Hille B, Mackie K (2008) GPR55 is a cannabinoid receptor that increases intracellular calcium and inhibits M current. Proc Natl Acad Sci U S A 105:2699-2704
-
(2008)
Proc Natl Acad Sci U S A
, vol.105
, pp. 2699-2704
-
-
Lauckner, J.E.1
Jensen, J.B.2
Chen, H.-Y.3
Lu, H.-C.4
Hille, B.5
Mackie, K.6
-
58
-
-
1342343936
-
Oleamide is a selective endogenous agonist of rat and human CB1 cannabinoid receptors
-
Leggett JD, Aspley S, Beckett SRG, D’Antona AM, Kendall DA, Kendall DA (2004) Oleamide is a selective endogenous agonist of rat and human CB1 cannabinoid receptors. Br J Pharmacol 141:253-262
-
(2004)
Br J Pharmacol
, vol.141
, pp. 253-262
-
-
Leggett, J.D.1
Aspley, S.2
Beckett, S.3
D’Antona, A.M.4
Kendall, D.A.5
Kendall, D.A.6
-
59
-
-
84863233685
-
Effects of anandamide on potassium channels in rat ventricular myocytes: A suppression of Ito and augmentation of KATP channels
-
Li Q, Ma H-J, Song S-L, Shi M, Ma H-J, Li D-P, Zhang Y (2012) Effects of anandamide on potassium channels in rat ventricular myocytes: a suppression of Ito and augmentation of KATP channels. Am J Physiol Cell Physiol 302:C924-C930
-
(2012)
Am J Physiol Cell Physiol
, vol.302
, pp. C924-C930
-
-
Li, Q.1
Ma, H.-J.2
Song, S.-L.3
Shi, M.4
Ma, H.-J.5
Li, D.-P.6
Zhang, Y.7
-
60
-
-
0036089489
-
Pharmacological activity of fatty acid amides is regulated, but not mediated, by fatty acid amide hydrolase in vivo
-
Lichtman AH, Hawkins EG, Griffin G, Cravatt BF (2002) Pharmacological activity of fatty acid amides is regulated, but not mediated, by fatty acid amide hydrolase in vivo. J Pharmacol Exp Ther 302:73-79
-
(2002)
J Pharmacol Exp Ther
, vol.302
, pp. 73-79
-
-
Lichtman, A.H.1
Hawkins, E.G.2
Griffin, G.3
Cravatt, B.F.4
-
62
-
-
23844464052
-
Glycine receptors in CNS neurons as a target for nonretrograde action of cannabinoids
-
Lozovaya N, Yatsenko N, Beketov A, Tsintsadze T, Burnashev N (2005) Glycine receptors in CNS neurons as a target for nonretrograde action of cannabinoids. J Neurosci 25:7499-7506
-
(2005)
J Neurosci
, vol.25
, pp. 7499-7506
-
-
Lozovaya, N.1
Yatsenko, N.2
Beketov, A.3
Tsintsadze, T.4
Burnashev, N.5
-
63
-
-
53049105094
-
Characterization of A-425619 at native TRPV1 receptors: A comparison between dorsal root ganglia and trigeminal ganglia
-
McDonald HA, Neelands TR, Kort M, Han P, Vos MH, Faltynek CR, Moreland RB, Puttfarcken PS (2008) Characterization of A-425619 at native TRPV1 receptors: a comparison between dorsal root ganglia and trigeminal ganglia. Eur J Pharmacol 596:62-69
-
(2008)
Eur J Pharmacol
, vol.596
, pp. 62-69
-
-
McDonald, H.A.1
Neelands, T.R.2
Kort, M.3
Han, P.4
Vos, M.H.5
Faltynek, C.R.6
Moreland, R.B.7
Puttfarcken, P.S.8
-
64
-
-
84859046557
-
Δ9-tetrahydrocannabinol and N-arachidonyl glycine are full agonists at GPR18 receptors and induce migration in human endometrial HEC-1B cells
-
McHugh D, Page J, Dunn E, Bradshaw HB (2012) Δ9-tetrahydrocannabinol and N-arachidonyl glycine are full agonists at GPR18 receptors and induce migration in human endometrial HEC-1B cells. Br J Pharmacol 165:2414-2424
-
(2012)
Br J Pharmacol
, vol.165
, pp. 2414-2424
-
-
McHugh, D.1
Page, J.2
Dunn, E.3
Bradshaw, H.B.4
-
65
-
-
0029012014
-
Identification of an endogenous 2-monoglyceride, present in canine gut, that binds to cannabinoid receptors
-
Mechoulam R, Ben-Shabat S, Hanuš L, Ligumsky M, Kaminski NE, Schatz AR, Gopher A, Almog S, Martin BR, Compton DR, Pertwee RG, Griffin G, Bayewitch M, Barg J, Vogel Z (1995) Identification of an endogenous 2-monoglyceride, present in canine gut, that binds to cannabinoid receptors. Biochem Pharmacol 50:83-90
-
(1995)
Biochem Pharmacol
, vol.50
, pp. 83-90
-
-
Mechoulam, R.1
Ben-Shabat, S.2
Hanuš, L.3
Ligumsky, M.4
Kaminski, N.E.5
Schatz, A.R.6
Gopher, A.7
Almog, S.8
Martin, B.R.9
Compton, D.R.10
Pertwee, R.G.11
Griffin, G.12
Bayewitch, M.13
Barg, J.14
Vogel, Z.15
-
66
-
-
0030885267
-
Anandamide may mediate sleep induction
-
Mechoulam R, Fride E, Hanuš L, Sheskin T, Bisogno T, Di Marzo V, Bayewitch M, Vogel Z (1997) Anandamide may mediate sleep induction. Nature 389:25-26
-
(1997)
Nature
, vol.389
, pp. 25-26
-
-
Mechoulam, R.1
Fride, E.2
Hanuš, L.3
Sheskin, T.4
Bisogno, T.5
Di Marzo, V.6
Bayewitch, M.7
Vogel, Z.8
-
67
-
-
77951086898
-
Molecular basis for a high-potency open-channel block of Kv1.5 channel by the endocannabinoid anandamide
-
Moreno-Galindo EG, Barrio-Echavarría GF, Vásquez JC, Decher N, Sachse FB, Tristani-Firouzi- M, Sánchez-Chapula JA, Navarro-Polanco RA (2010) Molecular basis for a high-potency open-channel block of Kv1.5 channel by the endocannabinoid anandamide. Mol Pharmacol 77:751-758
-
(2010)
Mol Pharmacol
, vol.77
, pp. 751-758
-
-
Moreno-Galindo, E.G.1
Barrio-Echavarría, G.F.2
Vásquez, J.C.3
Decher, N.4
Sachse, F.B.5
Tristani-Firouzi-, M.6
Sánchez-Chapula, J.A.7
Navarro-Polanco, R.A.8
-
68
-
-
0038810313
-
Ether-linked analogue of 2-arachidonoylglycerol (Noladin ether) was not detected in the brains of various mammalian species
-
Oka S, Tsuchie A, Tokumura A, Muramatsu M, Suhara Y, Takayama H, Waku K, Sugiura T (2003) Ether-linked analogue of 2-arachidonoylglycerol (noladin ether) was not detected in the brains of various mammalian species. J Neurochem 85:1374-1381
-
(2003)
J Neurochem
, vol.85
, pp. 1374-1381
-
-
Oka, S.1
Tsuchie, A.2
Tokumura, A.3
Muramatsu, M.4
Suhara, Y.5
Takayama, H.6
Waku, K.7
Sugiura, T.8
-
69
-
-
1842534335
-
Functional conversion between A-type and delayed rectifier Kþ channels by membrane lipids
-
Oliver D, Lien C-C, Soom M, Baukrowitz T, Jonas P, Fakler B (2004) Functional conversion between A-type and delayed rectifier Kþ channels by membrane lipids. Science 304:265-270
-
(2004)
Science
, vol.304
, pp. 265-270
-
-
Oliver, D.1
Lien, C.-C.2
Soom, M.3
Baukrowitz, T.4
Jonas, P.5
Fakler, B.6
-
70
-
-
33644627958
-
Deorphanization of a G protein-coupled receptor for oleoylethanolamide and its use in the discovery of small-molecule hypophagic agents
-
Overton HA, Babbs AJ, Doel SM, Fyfe MCT, Gardner LS, Griffin G, Jackson HC, Procter MJ, Rasamison CM, Tang-Christensen M, Widdowson PS, Williams GM, Reynet C (2006) Deorphanization of a G protein-coupled receptor for oleoylethanolamide and its use in the discovery of small-molecule hypophagic agents. Cell Metab 3:167-175
-
(2006)
Cell Metab
, vol.3
, pp. 167-175
-
-
Overton, H.A.1
Babbs, A.J.2
Doel, S.M.3
Fyfe, M.4
Gardner, L.S.5
Griffin, G.6
Jackson, H.C.7
Procter, M.J.8
Rasamison, C.M.9
Tang-Christensen, M.10
Widdowson, P.S.11
Williams, G.M.12
Reynet, C.13
-
71
-
-
0036887679
-
Endogenous cannabinoid, anandamide, acts as a noncompetitive inhibitor on 5-HT3 receptor-mediated responses in Xenopus oocytes
-
Oz M, Zhang L, Morales M (2002) Endogenous cannabinoid, anandamide, acts as a noncompetitive inhibitor on 5-HT3 receptor-mediated responses in Xenopus oocytes. Synapse 46:150-156
-
(2002)
Synapse
, vol.46
, pp. 150-156
-
-
Oz, M.1
Zhang, L.2
Morales, M.3
-
72
-
-
0041932284
-
The endogenous cannabinoid anandamide inhibits α7 nicotinic acetylcholine receptor-mediated responses in Xenopus oocytes
-
Oz M, Ravindran A, Diaz-Ruiz O, Zhang L, Morales M (2003) The endogenous cannabinoid anandamide inhibits α7 nicotinic acetylcholine receptor-mediated responses in Xenopus oocytes. J Pharmacol Exp Ther 306:1003-1010
-
(2003)
J Pharmacol Exp Ther
, vol.306
, pp. 1003-1010
-
-
Oz, M.1
Ravindran, A.2
Diaz-Ruiz, O.3
Zhang, L.4
Morales, M.5
-
73
-
-
4243057253
-
Differential effects of endogenous and synthetic cannabinoids on α7-nicotinic acetylcholine receptor-mediated responses in Xenopus oocytes
-
Oz M, Zhang L, Ravindran A, Morales M, Lupica CR (2004) Differential effects of endogenous and synthetic cannabinoids on α7-nicotinic acetylcholine receptor-mediated responses in Xenopus oocytes. J Pharmacol Exp Ther 310:1152-1160
-
(2004)
J Pharmacol Exp Ther
, vol.310
, pp. 1152-1160
-
-
Oz, M.1
Zhang, L.2
Ravindran, A.3
Morales, M.4
Lupica, C.R.5
-
74
-
-
19444369121
-
Additive effects of endogenous cannabinoid anandamide and ethanol on α7-nicotinic acetylcholine receptor-mediated responses in Xenopus oocytes
-
Oz M, Jackson SN, Woods AS, Morales M, Zhang L (2005) Additive effects of endogenous cannabinoid anandamide and ethanol on α7-nicotinic acetylcholine receptor-mediated responses in Xenopus oocytes. J Pharmacol Exp Ther 313:1272-1280
-
(2005)
J Pharmacol Exp Ther
, vol.313
, pp. 1272-1280
-
-
Oz, M.1
Jackson, S.N.2
Woods, A.S.3
Morales, M.4
Zhang, L.5
-
75
-
-
35548932493
-
The endogenous cannabinoid anandamide inhibits cromakalim-activated Kþ currents in follicle-enclosed Xenopus oocytes
-
Oz M, Yang K-H, Dinc M, Shippenberg TS (2007) The endogenous cannabinoid anandamide inhibits cromakalim-activated Kþ currents in follicle-enclosed Xenopus oocytes. J Pharmacol Exp Ther 323:547-554
-
(2007)
J Pharmacol Exp Ther
, vol.323
, pp. 547-554
-
-
Oz, M.1
Yang, K.-H.2
Dinc, M.3
Shippenberg, T.S.4
-
76
-
-
84899419272
-
Cellular approaches to the interaction between cannabinoid receptor ligands and nicotinic acetylcholine receptors
-
Oz M, Al Kury L, Keun-Hang SY, Mahgoub M, Galadari S (2014) Cellular approaches to the interaction between cannabinoid receptor ligands and nicotinic acetylcholine receptors. Eur J Pharmacol 731:100-105
-
(2014)
Eur J Pharmacol
, vol.731
, pp. 100-105
-
-
Oz, M.1
Al Kury, L.2
Keun-Hang, S.Y.3
Mahgoub, M.4
Galadari, S.5
-
77
-
-
84871380135
-
Anti-inflammatory lipoxin A4 is an endogenous allosteric enhancer of CB1 cannabinoid receptor
-
Pamplona FA, Ferreira J, de Lima OM, Duarte FS, Bento AF, Forner S, Villarinho JG, Bellocchio L, Wotjak CT, Lerner R, Monory K, Lutz B, Canetti C, Matias I, Calixto JB, Marsicano G, Guimarães MZP, Takahashi RN (2012) Anti-inflammatory lipoxin A4 is an endogenous allosteric enhancer of CB1 cannabinoid receptor. Proc Natl Acad Sci U S A 109:21134-21139
-
(2012)
Proc Natl Acad Sci U S A
, vol.109
, pp. 21134-21139
-
-
Pamplona, F.A.1
Ferreira, J.2
De Lima, O.M.3
Duarte, F.S.4
Bento, A.F.5
Forner, S.6
Villarinho, J.G.7
Bellocchio, L.8
Wotjak, C.T.9
Lerner, R.10
Monory, K.11
Lutz, B.12
Canetti, C.13
Matias, I.14
Calixto, J.B.15
Marsicano, G.16
Guimarães, M.17
Takahashi, R.N.18
-
78
-
-
33745255388
-
Sphingo-sine and its analog, the immunosuppressant 2-amino-2-(2-[4-octylphenyl]ethyl)-1,3-propanediol, interact with the CB1 cannabinoid receptor
-
Paugh SW, Cassidy MP, He H, Milstien S, Sim-Selley LJ, Spiegel S, Selley DE (2006) Sphingo-sine and its analog, the immunosuppressant 2-amino-2-(2-[4-octylphenyl]ethyl)-1,3-propanediol, interact with the CB1 cannabinoid receptor. Mol Pharmacol 70:41-50
-
(2006)
Mol Pharmacol
, vol.70
, pp. 41-50
-
-
Paugh, S.W.1
Cassidy, M.P.2
He, H.3
Milstien, S.4
Sim-Selley, L.J.5
Spiegel, S.6
Selley, D.E.7
-
79
-
-
0032802188
-
Pharmacology of cannabinoid receptor ligands
-
Pertwee RG (1999) Pharmacology of cannabinoid receptor ligands. Curr Med Chem 6:635-664
-
(1999)
Curr Med Chem
, vol.6
, pp. 635-664
-
-
Pertwee, R.G.1
-
80
-
-
84884474728
-
Pharmacological actions of cannabinoids
-
Pertwee RG (2005) Pharmacological actions of cannabinoids. Handb Exp Pharmacol 168:1-51
-
(2005)
Handb Exp Pharmacol
, vol.168
, pp. 1-51
-
-
Pertwee, R.G.1
-
81
-
-
84893950824
-
Elevating endocannabinoid levels: Pharmacological strategies and potential therapeutic applications
-
Pertwee RG (2014) Elevating endocannabinoid levels: pharmacological strategies and potential therapeutic applications. Proc Nutr Soc 73:96-105
-
(2014)
Proc Nutr Soc
, vol.73
, pp. 96-105
-
-
Pertwee, R.G.1
-
82
-
-
78650120798
-
International union of basic and clinical pharmacology. LXXIX. Cannabinoid receptors and their ligands: Beyond CB1 and CB2
-
2. Pharmacol Rev 62:588-631
-
(2010)
Pharmacol Rev
, vol.62
, pp. 588-631
-
-
Pertwee, R.G.1
Howlett, A.C.2
Abood, M.E.3
Alexander, S.4
Di Marzo, V.5
Elphick, M.R.6
Greasley, P.J.7
Hansen, H.S.8
Kunos, G.9
Mackie, K.10
Mechoulam, R.11
Ross, R.A.12
-
83
-
-
0030709362
-
Interaction of brain cannabinoid receptors with guanine nucleotide binding protein. A radioligand binding study
-
Petitet F, Jeantaud B, Capet M, Doble A (1997) Interaction of brain cannabinoid receptors with guanine nucleotide binding protein. A radioligand binding study. Biochem Pharmacol 54:1267-1270
-
(1997)
Biochem Pharmacol
, vol.54
, pp. 1267-1270
-
-
Petitet, F.1
Jeantaud, B.2
Capet, M.3
Doble, A.4
-
84
-
-
84955670764
-
Peptide endocannabinoids (Pepcans) are PAMs of CB2 receptors and involved in the innate immune response
-
Research Tri- angle Park, NC, USA
-
2 receptors and involved in the innate immune response. In: 24th annual symposium on the cannabinoids, International Cannabinoid Research Society, Research Tri- angle Park, NC, USA, p 62
-
(2014)
24Th Annual Symposium on the Cannabinoids, International Cannabinoid Research Society
-
-
Petrucci, V.1
Chicca, A.2
Viveros-Paredes, J.M.3
Gertsch, J.4
-
85
-
-
0027932775
-
Cannabinoid receptor binding and agonist activity of amides and esters of arachidonic acid
-
Pinto JC, Potié F, Rice KC, Boring D, Johnson MR, Evans DM, Wilken GH, Cantrell CH, Howlett AC (1994) Cannabinoid receptor binding and agonist activity of amides and esters of arachidonic acid. Mol Pharmacol 46:516-522
-
(1994)
Mol Pharmacol
, vol.46
, pp. 516-522
-
-
Pinto, J.C.1
Potié, F.2
Rice, K.C.3
Boring, D.4
Johnson, M.R.5
Evans, D.M.6
Wilken, G.H.7
Cantrell, C.H.8
Howlett, A.C.9
-
86
-
-
0013662082
-
Anandamide, an endogenous cannabinoid, inhibits Shaker-related voltage-gated Kþ channels
-
Poling JS, Rogawski MA, Salem N, Vicini S (1996) Anandamide, an endogenous cannabinoid, inhibits Shaker-related voltage-gated Kþ channels. Neuropharmacology 35:983-991
-
(1996)
Neuropharmacology
, vol.35
, pp. 983-991
-
-
Poling, J.S.1
Rogawski, M.A.2
Salem, N.3
Vicini, S.4
-
87
-
-
0036260823
-
Characterization of a novel endocannabinoid, virodhamine, with antagonist activity at the CB1 receptor
-
1 receptor. J Pharmacol Exp Ther 301:1020-1024
-
(2002)
J Pharmacol Exp Ther
, vol.301
, pp. 1020-1024
-
-
Porter, A.C.1
Sauer, J.-M.2
Knierman, M.D.3
Becker, G.W.4
Berna, M.J.5
Bao, J.6
Nomikos, G.G.7
Carter, P.8
Bymaster, F.P.9
Leese, A.B.10
Felder, C.C.11
-
88
-
-
24044539957
-
Allosteric modulation of the cannabinoid CB1 receptor
-
Price MR, Baillie GL, Thomas A, Stevenson LA, Easson M, Goodwin R, McLean A, McIntosh L, Goodwin G, Walker G, Westwood P, Marrs J, Thomson F, Cowley P, Christopoulos A, Pertwee RG, Ross RA (2005a) Allosteric modulation of the cannabinoid CB1 receptor. Mol Pharmacol 68:1484-1495
-
(2005)
Mol Pharmacol
, vol.68
, pp. 1484-1495
-
-
Price, M.R.1
Baillie, G.L.2
Thomas, A.3
Stevenson, L.A.4
Easson, M.5
Goodwin, R.6
McLean, A.7
McIntosh, L.8
Goodwin, G.9
Walker, G.10
Westwood, P.11
Marrs, J.12
Thomson, F.13
Cowley, P.14
Christopoulos, A.15
Pertwee, R.G.16
Ross, R.A.17
-
89
-
-
21344452082
-
A role for the anandamide membrane transporter in TRPV1-mediated neurosecretion from trigeminal sensory neurons
-
Price TJ, Patwardhan AM, Flores CM, Hargreaves KM (2005b) A role for the anandamide membrane transporter in TRPV1-mediated neurosecretion from trigeminal sensory neurons. Neuropharmacology 49:25-39
-
(2005)
Neuropharmacology
, vol.49
, pp. 25-39
-
-
Price, T.J.1
Patwardhan, A.M.2
Flores, C.M.3
Hargreaves, K.M.4
-
90
-
-
46749129338
-
TRPV2 is activated by cannabidiol and mediates CGRP release in cultured rat dorsal root ganglion neurons
-
Qin N, Neeper MP, Liu Y, Hutchinson TL, Lubin ML, Flores CM (2008) TRPV2 is activated by cannabidiol and mediates CGRP release in cultured rat dorsal root ganglion neurons. J Neurosci 28:6231-6238
-
(2008)
J Neurosci
, vol.28
, pp. 6231-6238
-
-
Qin, N.1
Neeper, M.P.2
Liu, Y.3
Hutchinson, T.L.4
Lubin, M.L.5
Flores, C.M.6
-
91
-
-
0030440971
-
Characterization of two cloned human CB1 cannabinoid receptor isoforms
-
Rinaldi-Carmona M, Calandra B, Shire D, Bouaboula M, Oustric D, Barth F, Casellas P, Ferrara P, Le Fur G (1996a) Characterization of two cloned human CB1 cannabinoid receptor isoforms. J Pharmacol Exp Ther 278:871-878
-
(1996)
J Pharmacol Exp Ther
, vol.278
, pp. 871-878
-
-
Rinaldi-Carmona, M.1
Calandra, B.2
Shire, D.3
Bouaboula, M.4
Oustric, D.5
Barth, F.6
Casellas, P.7
Ferrara, P.8
Le Fur, G.9
-
92
-
-
0029912522
-
Characterization and distribution of binding sites for [3H]-SR141716A, a selective brain (CB1) cannabinoid receptor antagonist, in rodent brain
-
Rinaldi-Carmona M, Pialot F, Congy C, Redon E, Barth F, Bachy A, Brelière J-C, Soubrié P, Le Fur G (1996b) Characterization and distribution of binding sites for [3H]-SR141716A, a selective brain (CB1) cannabinoid receptor antagonist, in rodent brain. Life Sci 58:1239-1247
-
(1996)
Life Sci
, vol.58
, pp. 1239-1247
-
-
Rinaldi-Carmona, M.1
Pialot, F.2
Congy, C.3
Redon, E.4
Barth, F.5
Bachy, A.6
Brelière, J.-C.7
Soubrié, P.8
Le Fur, G.9
-
93
-
-
0036799373
-
Anandamide is a partial agonist at native vanilloid receptors in acutely isolated mouse trigeminal sensory neurons
-
Roberts LA, Christie MJ, Connor M (2002) Anandamide is a partial agonist at native vanilloid receptors in acutely isolated mouse trigeminal sensory neurons. Br J Pharmacol 137:421-428
-
(2002)
Br J Pharmacol
, vol.137
, pp. 421-428
-
-
Roberts, L.A.1
Christie, M.J.2
Connor, M.3
-
94
-
-
33745280979
-
Interleukin-2- suppression by 2-arachidonyl glycerol is mediated through peroxisome proliferator-activated receptor γ independently of cannabinoid receptors 1 and 2
-
Rockwell CE, Snider NT, Thompson JT, Heuvel JPV, Kaminski NE (2006) Interleukin-2- suppression by 2-arachidonyl glycerol is mediated through peroxisome proliferator-activated receptor γ independently of cannabinoid receptors 1 and 2. Mol Pharmacol 70:101-111
-
(2006)
Mol Pharmacol
, vol.70
, pp. 101-111
-
-
Rockwell, C.E.1
Snider, N.T.2
Thompson, J.T.3
Heuvel, J.4
Kaminski, N.E.5
-
95
-
-
0035116496
-
Structure-activity relationship for the endogenous cannabinoid, anandamide, and certain of its analogues at vanilloid receptors in transfected cells and vas deferens
-
Ross RA, Gibson TM, Brockie HC, Leslie M, Pashmi G, Craib SJ, Di Marzo V, Pertwee RG (2001) Structure-activity relationship for the endogenous cannabinoid, anandamide, and certain of its analogues at vanilloid receptors in transfected cells and vas deferens. Br J Pharmacol 132:631-640
-
(2001)
Br J Pharmacol
, vol.132
, pp. 631-640
-
-
Ross, R.A.1
Gibson, T.M.2
Brockie, H.C.3
Leslie, M.4
Pashmi, G.5
Craib, S.J.6
Di Marzo, V.7
Pertwee, R.G.8
-
96
-
-
66949171814
-
Inhibition of human recombinant T-type calcium channels by the endocannabinoid N-arachidonoyl dopamine
-
Ross HR, Gilmore AJ, Connor M (2009) Inhibition of human recombinant T-type calcium channels by the endocannabinoid N-arachidonoyl dopamine. Br J Pharmacol 156:740-750
-
(2009)
Br J Pharmacol
, vol.156
, pp. 740-750
-
-
Ross, H.R.1
Gilmore, A.J.2
Connor, M.3
-
97
-
-
35649015179
-
The orphan receptor GPR55 is a novel cannabinoid receptor
-
Ryberg E, Larsson N, Sjogren S, Hjorth S, Hermansson N-O, Leonova J, Elebring T, Nilsson K, Drmota T, Greasley PJ (2007) The orphan receptor GPR55 is a novel cannabinoid receptor. Br J Pharmacol 152:1092-1101
-
(2007)
Br J Pharmacol
, vol.152
, pp. 1092-1101
-
-
Ryberg, E.1
Larsson, N.2
Sjogren, S.3
Hjorth, S.4
Hermansson, N.-O.5
Leonova, J.6
Elebring, T.7
Nilsson, K.8
Drmota, T.9
Greasley, P.J.10
-
98
-
-
33644820331
-
Activation of large-conductance, Ca2þ- activated Kþ channels by cannabinoids
-
Sade H, Muraki K, Ohya S, Hatano N, Imaizumi Y (2006) Activation of large-conductance, Ca2þ- activated Kþ channels by cannabinoids. Am J Physiol Cell Physiol 290:C77-C86
-
(2006)
Am J Physiol Cell Physiol
, vol.290
, pp. C77-C86
-
-
Sade, H.1
Muraki, K.2
Ohya, S.3
Hatano, N.4
Imaizumi, Y.5
-
99
-
-
0034740567
-
Despite substantial degradation, 2-arachidonoylglycerol is a potent full efficacy agonist mediating CB1 receptor-dependent G-protein activation in rat cerebellar membranes
-
Savinainen JR, Järvinen T, Laine K, Laitinen JT (2001) Despite substantial degradation, 2-arachidonoylglycerol is a potent full efficacy agonist mediating CB1 receptor-dependent G-protein activation in rat cerebellar membranes. Br J Pharmacol 134:664-672
-
(2001)
Br J Pharmacol
, vol.134
, pp. 664-672
-
-
Savinainen, J.R.1
Järvinen, T.2
Laine, K.3
Laitinen, J.T.4
-
101
-
-
0030593443
-
Cannabinoid receptor stimulation of guanosine- 50-O-(3-[35S]thio)triphosphate binding in rat brain membranes
-
Selley DE, Stark S, Sim LJ, Childers SR (1996) Cannabinoid receptor stimulation of guanosine- 50-O-(3-[35S]thio)triphosphate binding in rat brain membranes. Life Sci 59:659-668
-
(1996)
Life Sci
, vol.59
, pp. 659-668
-
-
Selley, D.E.1
Stark, S.2
Sim, L.J.3
Childers, S.R.4
-
102
-
-
0031051583
-
Structural requirements for binding of anandamide-type compounds to the brain cannabinoid receptor
-
Sheskin T, Hanuš L, Slager J, Vogel Z, Mechoulam R (1997) Structural requirements for binding of anandamide-type compounds to the brain cannabinoid receptor. J Med Chem 40:659-667
-
(1997)
J Med Chem
, vol.40
, pp. 659-667
-
-
Sheskin, T.1
Hanuš, L.2
Slager, J.3
Vogel, Z.4
Mechoulam, R.5
-
103
-
-
0030425575
-
Evaluation of binding in a transfected cell line expressing a peripheral cannabinoid receptor (CB2): Identification of cannabinoid receptor subtype selective ligands
-
2): identification of cannabinoid receptor subtype selective ligands. J Pharmacol Exp Ther 278:989-999
-
(1996)
J Pharmacol Exp Ther
, vol.278
, pp. 989-999
-
-
Showalter, V.M.1
Compton, D.R.2
Martin, B.R.3
Abood, M.E.4
-
104
-
-
81055130228
-
The major central endocannabinoid directly acts at GABAA receptors
-
Sigel E, Baur R, Rácz I, Marazzi J, Smart TG, Zimmer A, Gertsch J (2011) The major central endocannabinoid directly acts at GABAA receptors. Proc Natl Acad Sci U S A 108:18150-18155
-
(2011)
Proc Natl Acad Sci U S A
, vol.108
, pp. 18150-18155
-
-
Sigel, E.1
Baur, R.2
Rácz, I.3
Marazzi, J.4
Smart, T.G.5
Zimmer, A.6
Gertsch, J.7
-
105
-
-
0029120593
-
In vitro autoradiography of receptor-activated G proteins in rat brain by agonist-stimulated guanylyl 50-[γ-[35S]thio]triphosphate binding
-
Sim LJ, Selley DE, Childers SR (1995) In vitro autoradiography of receptor-activated G proteins in rat brain by agonist-stimulated guanylyl 50-[γ-[35S]thio]triphosphate binding. Proc Natl Acad Sci U S A 92:7242-7246
-
(1995)
Proc Natl Acad Sci U S A
, vol.92
, pp. 7242-7246
-
-
Sim, L.J.1
Selley, D.E.2
Childers, S.R.3
-
106
-
-
0033984992
-
The endogenous lipid anandamide is a full agonist at the human vanilloid receptor (HVR1)
-
Smart D, Gunthorpe MJ, Jerman JC, Nasir S, Gray J, Muir AI, Chambers JK, Randall AD, Davis JB (2000) The endogenous lipid anandamide is a full agonist at the human vanilloid receptor (hVR1). Br J Pharmacol 129:227-230
-
(2000)
Br J Pharmacol
, vol.129
, pp. 227-230
-
-
Smart, D.1
Gunthorpe, M.J.2
Jerman, J.C.3
Nasir, S.4
Gray, J.5
Muir, A.I.6
Chambers, J.K.7
Randall, A.D.8
Davis, J.B.9
-
107
-
-
0028291118
-
The pharma- cological activity of anandamide, a putative endogenous cannabinoid, in mice
-
Smith PB, Compton DR, Welch SP, Razdan RK, Mechoulam R, Martin BR (1994) The pharma- cological activity of anandamide, a putative endogenous cannabinoid, in mice. J Pharmacol Exp Ther 270:219-227
-
(1994)
J Pharmacol Exp Ther
, vol.270
, pp. 219-227
-
-
Smith, P.B.1
Compton, D.R.2
Welch, S.P.3
Razdan, R.K.4
Mechoulam, R.5
Martin, B.R.6
-
108
-
-
0029866824
-
A lysine residue of the cannabinoid receptor is critical for receptor recognition by several agonists but not WIN55212-2
-
Song Z-H, Bonner TI (1996) A lysine residue of the cannabinoid receptor is critical for receptor recognition by several agonists but not WIN55212-2. Mol Pharmacol 49:891-896
-
(1996)
Mol Pharmacol
, vol.49
, pp. 891-896
-
-
Song, Z.-H.1
Bonner, T.I.2
-
109
-
-
34748905313
-
The endocannabinoid anandamide inhibits the function of α4β2 nicotinic acetylcholine receptors
-
Spivak CE, Lupica CR, Oz M (2007) The endocannabinoid anandamide inhibits the function of α4β2 nicotinic acetylcholine receptors. Mol Pharmacol 72:1024-1032
-
(2007)
Mol Pharmacol
, vol.72
, pp. 1024-1032
-
-
Spivak, C.E.1
Lupica, C.R.2
Oz, M.3
-
110
-
-
84862697350
-
Blockade ofβ-cell KATP channels by the endocannabinoid, 2-arachidonoylglycerol
-
Spivak CE, Kim W, Liu Q-R, Lupica CR, Doyle ME (2012) Blockade of β-cell KATP channels by the endocannabinoid, 2-arachidonoylglycerol. Biochem Biophys Res Commun 423:13-18
-
(2012)
Biochem Biophys Res Commun
, vol.423
, pp. 13-18
-
-
Spivak, C.E.1
Kim, W.2
Liu, Q.-R.3
Lupica, C.R.4
Doyle, M.E.5
-
111
-
-
33947697100
-
Biochemistry and pharmacology of endovanilloids
-
Starowicz K, Nigam S, Di Marzo V (2007) Biochemistry and pharmacology of endovanilloids. Pharmacol Ther 114:13-33
-
(2007)
Pharmacol Ther
, vol.114
, pp. 13-33
-
-
Starowicz, K.1
Nigam, S.2
Di Marzo, V.3
-
112
-
-
9944235039
-
Binding affinity and agonist activity of putative endogenous cannabinoids at the human neocortical CB1 receptor
-
Steffens M, Zentner J, Honegger J, Feuerstein TJ (2005) Binding affinity and agonist activity of putative endogenous cannabinoids at the human neocortical CB1 receptor. Biochem Pharmacol 69:169-178
-
(2005)
Biochem Pharmacol
, vol.69
, pp. 169-178
-
-
Steffens, M.1
Zentner, J.2
Honegger, J.3
Feuerstein, T.J.4
-
113
-
-
0030870722
-
A second endogenous cannabinoid that modulates long- term potentiation
-
Stella N, Schweitzer P, Piomelli D (1997) A second endogenous cannabinoid that modulates long- term potentiation. Nature 388:773-778
-
(1997)
Nature
, vol.388
, pp. 773-778
-
-
Stella, N.1
Schweitzer, P.2
Piomelli, D.3
-
114
-
-
0029860393
-
Enzymatic synthesis of oleamide (Cis-9,10-octadenoamide), an endogenous sleep-inducing lipid, by rat brain microsomes
-
Sugiura T, Kondo S, Kodaka T, Tonegawa T, Nakane S, Yamashita A, Ishima Y, Waku K (1996) Enzymatic synthesis of oleamide (cis-9,10-octadenoamide), an endogenous sleep-inducing lipid, by rat brain microsomes. Biochem Mol Biol Int 40:931-938
-
(1996)
Biochem Mol Biol Int
, vol.40
, pp. 931-938
-
-
Sugiura, T.1
Kondo, S.2
Kodaka, T.3
Tonegawa, T.4
Nakane, S.5
Yamashita, A.6
Ishima, Y.7
Waku, K.8
-
115
-
-
35648985645
-
Cannabinoid activation of PPARα; a novel neuroprotective mechanism
-
Sun Y, Alexander SPH, Garle MJ, Gibson CL, Hewitt K, Murphy SP, Kendall DA, Bennett AJ (2007) Cannabinoid activation of PPARα; a novel neuroprotective mechanism. Br J Pharmacol 152:734-743
-
(2007)
Br J Pharmacol
, vol.152
, pp. 734-743
-
-
Sun, Y.1
Alexander, S.2
Garle, M.J.3
Gibson, C.L.4
Hewitt, K.5
Murphy, S.P.6
Kendall, D.A.7
Bennett, A.J.8
-
116
-
-
0031808129
-
Mutation of a highly conserved aspartate residue in the second transmembrane domain of the cannabinoid receptors, CB1 and CB2, disrupts G-protein coupling
-
2, disrupts G-protein coupling. J Pharmacol Exp Ther 285:651-658
-
(1998)
J Pharmacol Exp Ther
, vol.285
, pp. 651-658
-
-
Tao, Q.1
Abood, M.E.2
-
117
-
-
79954952532
-
Endocannabinoids modulate human epidermal keratinocyte proliferation and survival via the sequential engagement of cannabinoid receptor-1 and transient receptor potential vanilloid-1
-
Toth BI, Dobrosi N, Dajnoki A, Czifra G, Oláh A, Szollosi AG, Juhász I, Sugawara K, Paus R, Bíro T (2011) Endocannabinoids modulate human epidermal keratinocyte proliferation and survival via the sequential engagement of cannabinoid receptor-1 and transient receptor potential vanilloid-1. J Invest Dermatol 131:1095-1104
-
(2011)
J Invest Dermatol
, vol.131
, pp. 1095-1104
-
-
Toth, B.I.1
Dobrosi, N.2
Dajnoki, A.3
Czifra, G.4
Oláh, A.5
Szollosi, A.G.6
Juhász, I.7
Sugawara, K.8
Paus, R.9
Bíro, T.10
-
118
-
-
84892749496
-
Pregnenolone can protect the brain from cannabis intoxication
-
Vallée M, Vitiello S, Bellocchio L, Hébert-Chatelain E, Monlezun S, Martin-Garcia E, Kasanetz F, Baillie GL, Panin F, Cathala A, Roullot-Lacarrière V, Fabre S, Hurst DP, Lynch DL, Shore DM, Deroche-Gamonet V, Spampinato U, Revest JM, Maldonado R, Reggio PH, Ross RA, Marsicano G, Piazza PV (2014) Pregnenolone can protect the brain from cannabis intoxication. Science 343:94-98
-
(2014)
Science
, vol.343
, pp. 94-98
-
-
Vallée, M.1
Vitiello, S.2
Bellocchio, L.3
Hébert-Chatelain, E.4
Monlezun, S.5
Martin-Garcia, E.6
Kasanetz, F.7
Baillie, G.L.8
Panin, F.9
Cathala, A.10
Roullot-Lacarrière, V.11
Fabre, S.12
Hurst, D.P.13
Lynch, D.L.14
Shore, D.M.15
Deroche-Gamonet, V.16
Spampinato, U.17
Revest, J.M.18
Maldonado, R.19
Reggio, P.H.20
Ross, R.A.21
Marsicano, G.22
Piazza, P.V.23
more..
-
119
-
-
0033816899
-
Influence of cannabinoids on the delayed rectifier in freshly dissociated smooth muscle cells of the rat aorta
-
Van den Bossche I, Vanheel B (2000) Influence of cannabinoids on the delayed rectifier in freshly dissociated smooth muscle cells of the rat aorta. Br J Pharmacol 131:85-93
-
(2000)
Br J Pharmacol
, vol.131
, pp. 85-93
-
-
Van Den Bossche, I.1
Vanheel, B.2
-
120
-
-
66249127223
-
The endocannabinoid anandamide inhibits potassium conductance in rat cortical astrocytes
-
Vignali M, Benfenati V, Caprini M, Anderova M, Nobile M, Ferroni S (2009) The endocannabinoid anandamide inhibits potassium conductance in rat cortical astrocytes. Glia 57:791-806
-
(2009)
Glia
, vol.57
, pp. 791-806
-
-
Vignali, M.1
Benfenati, V.2
Caprini, M.3
Erova, M.4
Nobile, M.5
Ferroni, S.6
-
121
-
-
0027315816
-
Anandamide, a brain endogenous compound, interacts specifically with cannabinoid receptors and inhibits adenylate cyclase
-
Vogel Z, Barg J, Levy R, Saya D, Heldman E, Mechoulam R (1993) Anandamide, a brain endogenous compound, interacts specifically with cannabinoid receptors and inhibits adenylate cyclase. J Neurochem 61:352-355
-
(1993)
J Neurochem
, vol.61
, pp. 352-355
-
-
Vogel, Z.1
Barg, J.2
Levy, R.3
Saya, D.4
Heldman, E.5
Mechoulam, R.6
-
122
-
-
46249108439
-
Integrin clustering enables anandamide-induced Ca2þ signaling in endothelial cells via GPR55 by protection against CB1-receptor-triggered repression
-
Waldeck-Weiermair M, Zoratti C, Osibow K, Balenga N, Goessnitzer E, Waldhoer M, Malli R, Graier WF (2008) Integrin clustering enables anandamide-induced Ca2þ signaling in endothelial cells via GPR55 by protection against CB1-receptor-triggered repression. J Cell Sci 121:1704-1717
-
(2008)
J Cell Sci
, vol.121
, pp. 1704-1717
-
-
Waldeck-Weiermair, M.1
Zoratti, C.2
Osibow, K.3
Balenga, N.4
Goessnitzer, E.5
Waldhoer, M.6
Malli, R.7
Graier, W.F.8
-
123
-
-
79952437809
-
Enhancement of apamin-sensitive medium afterhyperpolarization current by anandamide and its role in excitability control in cultured hippocampal neurons
-
Wang W, Zhang K, Yan S, Li A, Hu X, Zhang L, Liu C (2011) Enhancement of apamin-sensitive medium afterhyperpolarization current by anandamide and its role in excitability control in cultured hippocampal neurons. Neuropharmacology 60:901-909
-
(2011)
Neuropharmacology
, vol.60
, pp. 901-909
-
-
Wang, W.1
Zhang, K.2
Yan, S.3
Li, A.4
Hu, X.5
Zhang, L.6
Liu, C.7
-
124
-
-
38549146611
-
Anandamide inhibition of 5-HT3A receptors varies with receptor density and desensitization
-
Xiong W, Hosoi M, Koo B-N, Zhang L (2008) Anandamide inhibition of 5-HT3A receptors varies with receptor density and desensitization. Mol Pharmacol 73:314-322
-
(2008)
Mol Pharmacol
, vol.73
, pp. 314-322
-
-
Xiong, W.1
Hosoi, M.2
Koo, B.-N.3
Zhang, L.4
-
125
-
-
84859556161
-
A common molecular basis for exogenous and endogenous cannabinoid potentiation of glycine receptors
-
Xiong W, Wu X, Li F, Cheng K, Rice KC, Lovinger DM, Zhang L (2012) A common molecular basis for exogenous and endogenous cannabinoid potentiation of glycine receptors. J Neurosci 32:5200-5208
-
(2012)
J Neurosci
, vol.32
, pp. 5200-5208
-
-
Xiong, W.1
Wu, X.2
Li, F.3
Cheng, K.4
Rice, K.C.5
Lovinger, D.M.6
Zhang, L.7
-
126
-
-
53149140992
-
Subunit-specific modulation of glycine receptors by cannabinoids and N-arachidonyl-glycine
-
Yang Z, Aubrey KR, Alroy I, Harvey RJ, Vandenberg RJ, Lynch JW (2008) Subunit-specific modulation of glycine receptors by cannabinoids and N-arachidonyl-glycine. Biochem Pharmacol 76:1014-1023
-
(2008)
Biochem Pharmacol
, vol.76
, pp. 1014-1023
-
-
Yang, Z.1
Aubrey, K.R.2
Alroy, I.3
Harvey, R.J.4
Vandenberg, R.J.5
Lynch, J.W.6
-
127
-
-
67649438808
-
International union of basic and clinical pharmacology. LXXIII. Nomenclature for the formyl peptide receptor (FPR) family
-
Ye RD, Boulay F, Wang JM, Dahlgren C, Gerard C, Parmentier M, Serhan CN, Murphy PM (2009) International union of basic and clinical pharmacology. LXXIII. Nomenclature for the formyl peptide receptor (FPR) family. Pharmacol Rev 61:119-161
-
(2009)
Pharmacol Rev
, vol.61
, pp. 119-161
-
-
Ye, R.D.1
Boulay, F.2
Wang, J.M.3
Dahlgren, C.4
Gerard, C.5
Parmentier, M.6
Serhan, C.N.7
Murphy, P.M.8
-
128
-
-
80052056760
-
Molecular sites for the positive allosteric modulation of glycine receptors by endocannabinoids
-
Yévenes GE, Zeilhofer HU (2011) Molecular sites for the positive allosteric modulation of glycine receptors by endocannabinoids. PLoS One 6:e23886
-
(2011)
Plos One
, vol.6
-
-
Yévenes, G.E.1
Zeilhofer, H.U.2
-
129
-
-
66449121455
-
Lipid G protein-coupled receptor ligand identification using β-arrestin PathHunterTM assay
-
Yin H, Chu A, Li W, Wang B, Shelton F, Otero F, Nguyen DG, Caldwell JS, Chen YA (2009) Lipid G protein-coupled receptor ligand identification using β-arrestin PathHunterTM assay. J Biol Chem 284:12328-12338
-
(2009)
J Biol Chem
, vol.284
, pp. 12328-12338
-
-
Yin, H.1
Chu, A.2
Li, W.3
Wang, B.4
Shelton, F.5
Otero, F.6
Nguyen, D.G.7
Caldwell, J.S.8
Chen, Y.A.9
-
130
-
-
0033614984
-
Vanilloid receptors on sensory nerves mediate the vasodilator action of anandamide
-
Zygmunt PM, Petersson J, Andersson DA, Chuang H, Sørgård M, Di Marzo V, Julius D, Hogestätt ED (1999) Vanilloid receptors on sensory nerves mediate the vasodilator action of anandamide. Nature 400:452-457
-
(1999)
Nature
, vol.400
, pp. 452-457
-
-
Zygmunt, P.M.1
Petersson, J.2
Ersson, D.A.3
Chuang, H.4
Sørgård, M.5
Di Marzo, V.6
Julius, D.7
Hogestätt, E.D.8
-
131
-
-
84891599659
-
Monoacylglycerols activate TRPV1—a link between phospholipase C and TRPV1
-
Zygmunt PM, Ermund A, Movahed P, Andersson DA, Simonsen C, Jonsson BAG, Blomgren A, Birnir B, Bevan S, Eschalier A, Mallet C, Gomis A, Hogestätt ED (2013) Monoacylglycerols activate TRPV1—a link between phospholipase C and TRPV1. PLoS One 8:e81618
-
(2013)
Plos One
, vol.8
-
-
Zygmunt, P.M.1
Ermund, A.2
Movahed, P.3
Ersson, D.A.4
Simonsen, C.5
Jonsson, B.6
Blomgren, A.7
Birnir, B.8
Bevan, S.9
Eschalier, A.10
Mallet, C.11
Gomis, A.12
Hogestätt, E.D.13
|