메뉴 건너뛰기




Volumn 65, Issue 4, 2014, Pages 525-530

Effects of synthetic analogues of human opiorphin on rat brain opioid receptors

Author keywords

Met enkephalin Arg Phe; Opioid receptors; Peptidase inhibition; Radioligand binding; Rat brain membranes

Indexed keywords

ENKEPHALIN-MET, ARG(6)-PHE(7)-; GLUTAMINYL-ARGINYL-PHENYLALANYL-SERYL-ARGININE; METENKEPHALIN; OLIGOPEPTIDE; OPIATE RECEPTOR; SALIVA PROTEIN;

EID: 84906859516     PISSN: 08675910     EISSN: 18991505     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (11)

References (14)
  • 1
    • 33845200443 scopus 로고    scopus 로고
    • Human opiorphin, a natural antinociceptive modulator of opioid-dependent pathways
    • Wisner A, Dufour E, Messaoudi M, et al. Human opiorphin, a natural antinociceptive modulator of opioid-dependent pathways. Proc Natl Acad Sci USA 2006; 103: 17979-17984.
    • (2006) Proc Natl Acad Sci USA , vol.103 , pp. 17979-17984
    • Wisner, A.1    Dufour, E.2    Messaoudi, M.3
  • 2
    • 84865373183 scopus 로고    scopus 로고
    • Opiorphin highly improves the specific binding and affinity of MERF and MEGY to rat brain opioid receptors
    • Toth F, Toth G, Benyhe S, Rougeot C, Wollemann M. Opiorphin highly improves the specific binding and affinity of MERF and MEGY to rat brain opioid receptors. Regul Pept 2012; 178: 71-75.
    • (2012) Regul Pept , vol.178 , pp. 71-75
    • Toth, F.1    Toth, G.2    Benyhe, S.3    Rougeot, C.4    Wollemann, M.5
  • 3
    • 0030611354 scopus 로고    scopus 로고
    • Met5- enkephalin-Arg6-Phe7, an endo-genous neuropeptide, binds to multiple opioid and nonopioid sites in rat brain
    • Benyhe S, Farkas J, Toth G, Wollemann M. Met5- enkephalin-Arg6-Phe7, an endo-genous neuropeptide, binds to multiple opioid and nonopioid sites in rat brain. J Neurosci Res 1997; 48: 249-258.
    • (1997) J Neurosci Res , vol.48 , pp. 249-258
    • Benyhe, S.1    Farkas, J.2    Toth, G.3    Wollemann, M.4
  • 5
    • 0031940531 scopus 로고    scopus 로고
    • Effects of three peptidase inhibitors, amastatin, captopril and phosphoramidon, on the hydrolysis of [Met5]-enkephalin- Arg6-Phe7 and other opioid peptides
    • Hiranuma T, Kitamura K, Taniguchi T, et al. Effects of three peptidase inhibitors, amastatin, captopril and phosphoramidon, on the hydrolysis of [Met5]-enkephalin- Arg6-Phe7 and other opioid peptides. Naunyn Schmiedebergs Arch Pharmacol 1998; 357: 276-282.
    • (1998) Naunyn Schmiedebergs Arch Pharmacol , vol.357 , pp. 276-282
    • Hiranuma, T.1    Kitamura, K.2    Taniguchi, T.3
  • 6
    • 0032437267 scopus 로고    scopus 로고
    • Protection against dynorphin-(1-8) hydrolysis in membrane preparations by the combination of amastatin, captopril and phosphoramidon
    • Hiranuma T, Kitamura K, Taniguchi T, et al. Protection against dynorphin-(1-8) hydrolysis in membrane preparations by the combination of amastatin, captopril and phosphoramidon. J Pharmacol Exp Ther 1998; 286: 863-869.
    • (1998) J Pharmacol Exp Ther , vol.286 , pp. 863-869
    • Hiranuma, T.1    Kitamura, K.2    Taniguchi, T.3
  • 7
    • 0037336859 scopus 로고    scopus 로고
    • Peptidases prevent mu-opioid receptor internalization in dorsal horn neurons by endogenously released opioids
    • Song B, Marvizon JCG. Peptidases prevent mu-opioid receptor internalization in dorsal horn neurons by endogenously released opioids. J Neurosci 2003; 23: 1847-1858.
    • (2003) J Neurosci , vol.23 , pp. 1847-1858
    • Song, B.1    Marvizon, J.C.G.2
  • 8
    • 84906871228 scopus 로고    scopus 로고
    • Structure-activity relationship study and function-based peptidomimetic design of human opiorphin with improved bioavailability property and unaltered analgesic activity
    • doi.org/10.4172/2167- 0501.1000122
    • Bogeas A, Dufour E, Bisson J-F, Messaoudi M, Rougeot C. Structure-activity relationship study and function-based peptidomimetic design of human opiorphin with improved bioavailability property and unaltered analgesic activity. Biochem Pharmacol 2013; 2: 3. doi.org/10.4172/2167- 0501.1000122.
    • (2013) Biochem Pharmacol , vol.2 , Issue.3
    • Bogeas, A.1    Dufour, E.2    Bisson, J.-F.3    Messaoudi, M.4    Rougeot, C.5
  • 9
    • 77957069134 scopus 로고    scopus 로고
    • Human opiorphin is a naturally occurring antidepressant acting selectively on enkephalin dependent delta-opioid pathways
    • Javelot H, Messaoudi M, Garnier S, Rougeot C. Human opiorphin is a naturally occurring antidepressant acting selectively on enkephalin dependent delta-opioid pathways. J Physiol Pharmacol 2010; 61: 355-362.
    • (2010) J Physiol Pharmacol , vol.61 , pp. 355-362
    • Javelot, H.1    Messaoudi, M.2    Garnier, S.3    Rougeot, C.4
  • 10
    • 0028170058 scopus 로고
    • Characterization of [3H]Met-enkephalin-Arg6-Phe7-binding to opioid receptors in frog brain membrane preparations
    • Wollemann M, Farkas J, Toth G, Benyhe S. Characterization of [3H]Met-enkephalin-Arg6-Phe7-binding to opioid receptors in frog brain membrane preparations. J Neurochem 1994; 63: 1460-1465.
    • (1994) J Neurochem , vol.63 , pp. 1460-1465
    • Wollemann, M.1    Farkas, J.2    Toth, G.3    Benyhe, S.4
  • 11
    • 0016822591 scopus 로고
    • Different effects of protein modifying reagents on receptor binding of opiate agonists and antagonists
    • Pasternak GW, Wilson HA, Snyder SH. Different effects of protein modifying reagents on receptor binding of opiate agonists and antagonists. Mol Pharmacol 1975; 11: 340-351.
    • (1975) Mol Pharmacol , vol.11 , pp. 340-351
    • Pasternak, G.W.1    Wilson, H.A.2    Snyder, S.H.3
  • 12
    • 77957034700 scopus 로고    scopus 로고
    • Systemically active opiorphin is a potent yet non-addictive analgesic without drug tolerance effects
    • Rougeot C, Robert F, Menz L, Bisson JF, Messaoudi M. Systemically active opiorphin is a potent yet non-addictive analgesic without drug tolerance effects. J Physiol Pharmacol 2010; 61: 483-490.
    • (2010) J Physiol Pharmacol , vol.61 , pp. 483-490
    • Rougeot, C.1    Robert, F.2    Menz, L.3    Bisson, J.F.4    Messaoudi, M.5
  • 13
    • 84873433898 scopus 로고    scopus 로고
    • Exogenous melatonin abolishes thermal hyperalgesia in neuropathic pain. The role of the opioid system and benzodiazepine-GABAergic mechanism
    • Zurowski D, Nowak L, Machowska A, Wordliczek J, Thor PJ. Exogenous melatonin abolishes thermal hyperalgesia in neuropathic pain. The role of the opioid system and benzodiazepine-GABAergic mechanism. J Physiol Pharmacol 2012; 63: 641-647.
    • (2012) J Physiol Pharmacol , vol.63 , pp. 641-647
    • Zurowski, D.1    Nowak, L.2    Machowska, A.3    Wordliczek, J.4    Thor, P.J.5
  • 14
    • 84855743814 scopus 로고    scopus 로고
    • Central corticotrophin-realising factor (CRF) may attenuate somatic pain sensitivity through involvement of glucocorticoids
    • Yarushkina NI, Bagaeva TR, Filaretova LP. Central corticotrophin-realising factor (CRF) may attenuate somatic pain sensitivity through involvement of glucocorticoids. J Physiol Pharmacol 2011; 62: 541-548.
    • (2011) J Physiol Pharmacol , vol.62 , pp. 541-548
    • Yarushkina, N.I.1    Bagaeva, T.R.2    Filaretova, L.P.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.