메뉴 건너뛰기




Volumn 123, Issue 3, 2013, Pages 256-266

K-685, a TRPV1 antagonist, blocks PKC-sensitized TRPV1 activation and improves the inflammatory pain in a rat complete Freund's adjuvant model

Author keywords

Complete Freund's adjuvant (CFA); Inflammation; Pain; Protein kinase C (PKC); TRPV1 antagonist

Indexed keywords

ANALGESIC AGENT; DICLOFENAC; FREUND ADJUVANT; K 685; MITOGEN ACTIVATED PROTEIN KINASE; N (3 HYDROXY 2 OXO 1,2,3,4 TETRAHYDRO 5 QUINOLYL) 5 (4 ISOPROPOXYPHENYL) 5 (4 TRIFLUOROMETHYLPHENYL) 2,4 PENTADIENAMIDE; PROTEIN KINASE C; UNCLASSIFIED DRUG; VANILLOID RECEPTOR 1;

EID: 84890508541     PISSN: 13478613     EISSN: 13478648     Source Type: Journal    
DOI: 10.1254/jphs.13088FP     Document Type: Article
Times cited : (10)

References (32)
  • 5
    • 0004906771 scopus 로고    scopus 로고
    • Direct activation of capsaicin receptors by products of lipoxygenases: Endogenous capsaicin-like substances
    • Hwang SW, Cho H, Kwak J, Lee SY, Kang CJ, Jung J, et al. Direct activation of capsaicin receptors by products of lipoxygenases: endogenous capsaicin-like substances. Proc Natl Acad Sci U S A 2000;97:6155-6160.
    • (2000) Proc Natl Acad Sci U S A , vol.97 , pp. 6155-6160
    • Hwang, S.W.1    Cho, H.2    Kwak, J.3    Lee, S.Y.4    Kang, C.J.5    Jung, J.6
  • 6
    • 0038190980 scopus 로고    scopus 로고
    • N-oleoyldopamine, a novel endogenous capsaicin-like lipid that produces hyperalgesia
    • Chu CJ, Huang SM, De Petrocellis L, Bisogno T, Ewing SA, Miller JD, et al. N-oleoyldopamine, a novel endogenous capsaicin-like lipid that produces hyperalgesia. J Biol Chem. 2003;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
  • 7
    • 0023898089 scopus 로고
    • Local effector functions of capsaicin-sensitive sensory nerve endings: Involvement of tachykinins, calcitonin gene-related peptide and other neuropeptides
    • Holzer P. Local effector functions of capsaicin-sensitive sensory nerve endings: involvement of tachykinins, calcitonin gene-related peptide and other neuropeptides. Neuroscience. 1988; 24:739-768.
    • (1988) Neuroscience , vol.24 , pp. 739-768
    • Holzer, P.1
  • 8
    • 33747235382 scopus 로고    scopus 로고
    • Inflammatory pain: The cellular basis of heat hyperalgesia
    • Huang J, Zhang X, McNaughton PA. Inflammatory pain: the cellular basis of heat hyperalgesia. Curr Neuropharmacol. 2006;4:197-206.
    • (2006) Curr Neuropharmacol , vol.4 , pp. 197-206
    • Huang, J.1    Zhang, X.2    McNaughton, P.A.3
  • 12
    • 33646769105 scopus 로고    scopus 로고
    • Sensitization of TRPV1 by EP1 and IP reveals peripheral nociceptive mechanism of prostaglandins
    • Moriyama T, Higashi T, Togashi K, Iida T, Segi E, Sugimoto Y, et al. Sensitization of TRPV1 by EP1 and IP reveals peripheral nociceptive mechanism of prostaglandins. Mol Pain. 2005;1:3.
    • (2005) Mol Pain , vol.1 , pp. 3
    • Moriyama, T.1    Higashi, T.2    Togashi, K.3    Iida, T.4    Segi, E.5    Sugimoto, Y.6
  • 13
    • 69449091027 scopus 로고    scopus 로고
    • Protein kinase D isoforms are expressed in rat and mouse primary sensory neurons and are activated by agonists of protease-activated receptor 2
    • Amadesi S, Grant AD, Cottrell GS, Vaksman N, Poole DP, Rozengurt E, et al. Protein kinase D isoforms are expressed in rat and mouse primary sensory neurons and are activated by agonists of protease-activated receptor 2. J Comp Neurol. 2009;516:141-156.
    • (2009) J Comp Neurol , vol.516 , pp. 141-156
    • Amadesi, S.1    Grant, A.D.2    Cottrell, G.S.3    Vaksman, N.4    Poole, D.P.5    Rozengurt, E.6
  • 14
    • 0035810934 scopus 로고    scopus 로고
    • Potentiation of capsaicin receptor activity by metabotropic ATP receptors as a possible mechanism for ATP-evoked pain and hyperalgesia
    • Tominaga M, Wada M, Masu M. Potentiation of capsaicin receptor activity by metabotropic ATP receptors as a possible mechanism for ATP-evoked pain and hyperalgesia. Proc Natl Acad Sci U S A. 2001;98:6951-6956.
    • (2001) Proc Natl Acad Sci U S A , vol.98 , pp. 6951-6956
    • Tominaga, M.1    Wada, M.2    Masu, M.3
  • 15
    • 0036291431 scopus 로고    scopus 로고
    • Activation of protein kinase C sensitizes human VR1 to capsaicin and to moderate decreases in pH at physiological temperatures in Xenopus oocytes
    • Crandall M, Kwash J, Yu W, White G. Activation of protein kinase C sensitizes human VR1 to capsaicin and to moderate decreases in pH at physiological temperatures in Xenopus oocytes. Pain. 2002;98:109-117.
    • (2002) Pain , vol.98 , pp. 109-117
    • Crandall, M.1    Kwash, J.2    Yu, W.3    White, G.4
  • 16
    • 0034700494 scopus 로고    scopus 로고
    • Induction of vanilloid receptor channel activity by protein kinase C
    • Premkumar LS, Ahern GP. Induction of vanilloid receptor channel activity by protein kinase C. Nature. 2000;408:985-990.
    • (2000) Nature , vol.408 , pp. 985-990
    • Premkumar, L.S.1    Ahern, G.P.2
  • 17
    • 0035425705 scopus 로고    scopus 로고
    • Protein kinase C activation potentiates gating of the vanilloid receptor VR1 by capsaicin, protons, heat and anandamide
    • Vellani V, Mapplebeck S, Moriondo A, Davis JB, McNaughton PA. Protein kinase C activation potentiates gating of the vanilloid receptor VR1 by capsaicin, protons, heat and anandamide. J Physiol. 2001;534:813-825.
    • (2001) J Physiol , vol.534 , pp. 813-825
    • Vellani, V.1    Mapplebeck, S.2    Moriondo, A.3    Davis, J.B.4    McNaughton, P.A.5
  • 18
    • 0037134417 scopus 로고    scopus 로고
    • Direct phosphorylation of capsaicin receptor VR1 by protein kinase Cepsilon and identification of two target serine residues
    • Numazaki M, Tominaga T, Toyooka H, Tominaga M. Direct phosphorylation of capsaicin receptor VR1 by protein kinase Cepsilon and identification of two target serine residues. J Biol Chem. 2002;277:13375-13378.
    • (2002) J Biol Chem , vol.277 , pp. 13375-13378
    • Numazaki, M.1    Tominaga, T.2    Toyooka, H.3    Tominaga, M.4
  • 19
    • 0000396616 scopus 로고    scopus 로고
    • A novel nociceptor signaling pathway revealed in protein kinase C epsilon mutant mice
    • Khasar SG, Lin YH, Martin A, Dadgar J, McMahon T, Wang D, et al. A novel nociceptor signaling pathway revealed in protein kinase C epsilon mutant mice. Neuron. 1999;24:253-260.
    • (1999) Neuron , vol.24 , pp. 253-260
    • Khasar, S.G.1    Lin, Y.H.2    Martin, A.3    Dadgar, J.4    McMahon, T.5    Wang, D.6
  • 20
    • 53149147776 scopus 로고    scopus 로고
    • Protein kinase C epsilon contributes to basal and sensitizing responses of TRPV1 to capsaicin in rat dorsal root ganglion neurons
    • Srinivasan R, Wolfe D, Goss J, Watkins S, de Groat WC, Sculptoreanu A, et al. Protein kinase C epsilon contributes to basal and sensitizing responses of TRPV1 to capsaicin in rat dorsal root ganglion neurons. Eur J Neurosci. 2008;28:1241-1254.
    • (2008) Eur J Neurosci , vol.28 , pp. 1241-1254
    • Srinivasan, R.1    Wolfe, D.2    Goss, J.3    Watkins, S.4    De Groat, W.C.5    Sculptoreanu, A.6
  • 21
    • 23044473189 scopus 로고    scopus 로고
    • A-425619 [1-Isoquinolin-5-yl-3-(4-trifluoromethyl-benzyl)-urea], a novel and selective transient receptor potential type V1 receptor antagonist, blocks channel activation by vanilloids, heat, and acid
    • El Kouhen R, Surowy CS, Bianchi BR, Neelands TR, McDonald HA, Niforatos W, et al. A-425619 [1-Isoquinolin-5-yl-3-(4-trifluoromethyl-benzyl)-urea], a novel and selective transient receptor potential type V1 receptor antagonist, blocks channel activation by vanilloids, heat, and acid. J Pharmacol Exp Ther. 2005;314:400-409.
    • (2005) J Pharmacol Exp Ther , vol.314 , pp. 400-409
    • El Kouhen, R.1    Surowy, C.S.2    Bianchi, B.R.3    Neelands, T.R.4    McDonald, H.A.5    Niforatos, W.6
  • 22
    • 23044496253 scopus 로고    scopus 로고
    • A-425619 [1-isoquinolin-5-yl-3-(4-trifluoromethyl-benzyl)-urea], a novel transient receptor potential type V1 receptor antagonist, relieves pathophysiological pain associated with inflammation and tissue injury in rats
    • Honore P, Wismer CT, Mikusa J, Zhu CZ, Zhong C, Gauvin DM, et al. A-425619 [1-isoquinolin-5-yl-3-(4-trifluoromethyl-benzyl)-urea], a novel transient receptor potential type V1 receptor antagonist, relieves pathophysiological pain associated with inflammation and tissue injury in rats. J Pharmacol Exp Ther. 2005;314:410-421.
    • (2005) J Pharmacol Exp Ther , vol.314 , pp. 410-421
    • Honore, P.1    Wismer, C.T.2    Mikusa, J.3    Zhu, C.Z.4    Zhong, C.5    Gauvin, D.M.6
  • 23
    • 0038128285 scopus 로고    scopus 로고
    • N-(4-Tertiarybutylphenyl)-4-(3-cholorphyridin-2-yl) tetrahydropyrazine- 1(2H)-carbox-amide (BCTC), a novel, orally effective vanilloid receptor 1 antagonist with analgesic properties: II. In vivo characterization in rat models of inflammatory and neuropathic pain
    • Pomonis JD, Harrison JE, Mark L, Bristol DR, Valenzano KJ, Walker K. N-(4-Tertiarybutylphenyl)-4-(3-cholorphyridin-2-yl) tetrahydropyrazine-1(2H)- carbox-amide (BCTC), a novel, orally effective vanilloid receptor 1 antagonist with analgesic properties: II. in vivo characterization in rat models of inflammatory and neuropathic pain. J Pharmacol Exp Ther. 2003;306:387-393.
    • (2003) J Pharmacol Exp Ther , vol.306 , pp. 387-393
    • Pomonis, J.D.1    Harrison, J.E.2    Mark, L.3    Bristol, D.R.4    Valenzano, K.J.5    Walker, K.6
  • 24
    • 79951977972 scopus 로고    scopus 로고
    • Amelioration of neuropathic pain by novel transient receptor potential vanilloid 1 antagonist AS1928370 in rats without hyperthermic effect
    • Watabiki T, Kiso T, Kuramochi T, Yonezawa K, Tsuji N, Kohara A, et al. Amelioration of neuropathic pain by novel transient receptor potential vanilloid 1 antagonist AS1928370 in rats without hyperthermic effect. J Pharmacol Exp Ther. 2011;336:743-750.
    • (2011) J Pharmacol Exp Ther , vol.336 , pp. 743-750
    • Watabiki, T.1    Kiso, T.2    Kuramochi, T.3    Yonezawa, K.4    Tsuji, N.5    Kohara, A.6
  • 25
    • 84880797755 scopus 로고    scopus 로고
    • The orally administered selective TRPV1 antagonist, JTS-653, attenuates chronic pain refractory to non-steroidal anti-inflammatory drugs in rats and mice including post-herpetic pain
    • Kitagawa Y, Tamai I, Hamada Y, Usui K, Wada M, Sakata M, et al. The orally administered selective TRPV1 antagonist, JTS-653, attenuates chronic pain refractory to non-steroidal anti-inflammatory drugs in rats and mice including post-herpetic pain. J Pharmacol Sci. 2013;122:128-137.
    • (2013) J Pharmacol Sci , vol.122 , pp. 128-137
    • Kitagawa, Y.1    Tamai, I.2    Hamada, Y.3    Usui, K.4    Wada, M.5    Sakata, M.6
  • 26
    • 84859805419 scopus 로고    scopus 로고
    • Discovery of novel 5,5-diarylpentadienamides as orally available transient receptor potential vanilloid 1 (TRPV1) antagonists
    • Saku O, Ishida H, Atsumi E, Sugimoto Y, Kodaira H, Kato Y, et al. Discovery of novel 5,5-diarylpentadienamides as orally available transient receptor potential vanilloid 1 (TRPV1) antagonists. J Med Chem. 2012;55:3436-3451.
    • (2012) J Med Chem , vol.55 , pp. 3436-3451
    • Saku, O.1    Ishida, H.2    Atsumi, E.3    Sugimoto, Y.4    Kodaira, H.5    Kato, Y.6
  • 27
    • 0038467306 scopus 로고    scopus 로고
    • N-(4-tertiarybutylphenyl)-4-(3-chloropyridin-2-yl)tetra-hydropyrazine- 1(2H)-carbox-amide (BCTC), a novel, orally effective vanilloid receptor 1 antagonist with analgesic properties: I. In vitro characterization and pharmacokinetic properties
    • Valenzano KJ, Grant ER, Wu G, Hachicha M, Schmid L, Tafesse L, et al. N-(4-tertiarybutylphenyl)-4-(3-chloropyridin-2-yl)tetra-hydropyrazine-1(2H) -carbox-amide (BCTC), a novel, orally effective vanilloid receptor 1 antagonist with analgesic properties: I. in vitro characterization and pharmacokinetic properties. J Pharmacol Exp Ther. 2003;306:377-386.
    • (2003) J Pharmacol Exp Ther , vol.306 , pp. 377-386
    • Valenzano, K.J.1    Grant, E.R.2    Wu, G.3    Hachicha, M.4    Schmid, L.5    Tafesse, L.6
  • 29
    • 77950861534 scopus 로고    scopus 로고
    • The role of ERK-1/2 in the N/OFQ-induced inhibition of delayed rectifier potassium currents
    • Wang W, Cui Q, Li Y, Li B, Yang X, Cui L, et al. The role of ERK-1/2 in the N/OFQ-induced inhibition of delayed rectifier potassium currents. Biochem Biophys Res Commun. 2010;394:1058-1062.
    • (2010) Biochem Biophys Res Commun , vol.394 , pp. 1058-1062
    • Wang, W.1    Cui, Q.2    Li, Y.3    Li, B.4    Yang, X.5    Cui, L.6
  • 30
    • 33748680717 scopus 로고    scopus 로고
    • TRPV1 receptors in the CNS play a key role in broad-spectrum analgesia of TRPV1 antagonists
    • Cui M, Honore P, Zhong C, Gauvin D, Mikusa J, Hernandez G, et al. TRPV1 receptors in the CNS play a key role in broad-spectrum analgesia of TRPV1 antagonists. J Neurosci. 2006; 26:9385-9393.
    • (2006) J Neurosci , vol.26 , pp. 9385-9393
    • Cui, M.1    Honore, P.2    Zhong, C.3    Gauvin, D.4    Mikusa, J.5    Hernandez, G.6
  • 31
    • 41749117999 scopus 로고    scopus 로고
    • Pharmacological blockade of the vanilloid receptor TRPV1 elicits marked hyperthermia in humans
    • Gavva NR, Treanor JJ, Garami A, Fang L, Surapaneni S, Akrami A, et al. Pharmacological blockade of the vanilloid receptor TRPV1 elicits marked hyperthermia in humans. Pain. 2008;136:202-210.
    • (2008) Pain , vol.136 , pp. 202-210
    • Gavva, N.R.1    Treanor, J.J.2    Garami, A.3    Fang, L.4    Surapaneni, S.5    Akrami, A.6
  • 32
    • 79954584227 scopus 로고    scopus 로고
    • Oral and cutaneous thermosensory profile of selective TRPV1 inhibition by ABT-102 in a randomized healthy volunteer trial
    • Rowbotham MC, Nothaft W, Duan WR, Wang Y, Faltynek C, McGaraughty S, et al. Oral and cutaneous thermosensory profile of selective TRPV1 inhibition by ABT-102 in a randomized healthy volunteer trial. Pain. 2011;152:1192-1200.
    • (2011) Pain , vol.152 , pp. 1192-1200
    • Rowbotham, M.C.1    Nothaft, W.2    Duan, W.R.3    Wang, Y.4    Faltynek, C.5    McGaraughty, S.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.