메뉴 건너뛰기




Volumn 171, Issue 1, 2014, Pages 253-264

G protein-gated inwardly rectifying potassium (KIR3) channels play a primary role in the antinociceptive effect of oxycodone, but not morphine, at supraspinal sites

Author keywords

opioid receptor; antinociception; G protein gated inwardly rectifying potassium channel; morphine; oxycodone

Indexed keywords

FENTANYL CITRATE; G PROTEIN COUPLED INWARDLY RECTIFYING POTASSIUM CHANNEL; MORPHINE; OPIATE; OXYCODONE; POTASSIUM CHANNEL BLOCKING AGENT; SMALL INTERFERING RNA; TERTIAPIN Q; UNCLASSIFIED DRUG;

EID: 84890283022     PISSN: 00071188     EISSN: 14765381     Source Type: Journal    
DOI: 10.1111/bph.12441     Document Type: Article
Times cited : (20)

References (37)
  • 1
    • 84890299573 scopus 로고    scopus 로고
    • The Concise Guide to PHARMACOLOGY 2013/14: Overview
    • Alexander SPH, et al. (2013). The Concise Guide to PHARMACOLOGY 2013/14: Overview. Br J Pharmacol 170: 1449-1867.
    • (2013) Br J Pharmacol , vol.170 , pp. 1449-1867
    • Alexander, S.P.H.1
  • 3
    • 33747816123 scopus 로고    scopus 로고
    • In vivo blood-brain barrier transport of oxycodone in the rat: Indications for active influx and implications for pharmacokinetics/ pharmacodynamics
    • Bostrom E, Simonsson US, Hammarlund-Udenase M, (2006). In vivo blood-brain barrier transport of oxycodone in the rat: indications for active influx and implications for pharmacokinetics/pharmacodynamics. Drug Metab Dispos 34: 1624-1631.
    • (2006) Drug Metab Dispos , vol.34 , pp. 1624-1631
    • Bostrom, E.1    Simonsson, U.S.2    Hammarlund-Udenase, M.3
  • 4
    • 39749132196 scopus 로고    scopus 로고
    • Blood-brain barrier transport helps to explain discrepancies in in vivo potency between oxycodone and morphine
    • Bostrom E, Hammarlund-Udenase M, Simonsson US, (2008). Blood-brain barrier transport helps to explain discrepancies in in vivo potency between oxycodone and morphine. Anesthesiology 108: 495-505.
    • (2008) Anesthesiology , vol.108 , pp. 495-505
    • Bostrom, E.1    Hammarlund-Udenase, M.2    Simonsson, U.S.3
  • 5
    • 0025808619 scopus 로고
    • Dissociation of opioid receptor upregulation and functional supersensitivity
    • Chang SC, Lutfy K, Sierra V, Yoburn BC, (1991). Dissociation of opioid receptor upregulation and functional supersensitivity. Pharmacol Biochem Behav 38: 853-859.
    • (1991) Pharmacol Biochem Behav , vol.38 , pp. 853-859
    • Chang, S.C.1    Lutfy, K.2    Sierra, V.3    Yoburn, B.C.4
  • 7
    • 0030819187 scopus 로고    scopus 로고
    • Controlled-release oxycodone and morphine in cancer related pain
    • Heiskanen T, Kalso E, (1997). Controlled-release oxycodone and morphine in cancer related pain. Pain 73: 37-45.
    • (1997) Pain , vol.73 , pp. 37-45
    • Heiskanen, T.1    Kalso, E.2
  • 8
    • 0023874505 scopus 로고
    • Pertussis toxin inhibits antinociception produced by intrathecal injection of morphine, noradrenaline and baclofen
    • Hoehn K, Reid A, Sawynok J, (1988). Pertussis toxin inhibits antinociception produced by intrathecal injection of morphine, noradrenaline and baclofen. Eur J Pharmacol 27: 65-72.
    • (1988) Eur J Pharmacol , vol.27 , pp. 65-72
    • Hoehn, K.1    Reid, A.2    Sawynok, J.3
  • 9
    • 0034105966 scopus 로고    scopus 로고
    • Osteroprotegerin blocks bone cancer-induced skeletal destruction, skeletal pain and pain-induced neurochemical reorganization of the spinal cord
    • Honore P, Lugar NM, Sabino MAC, Schwei MJ, Rogers SD, Mash DB, et al. (2000). Osteroprotegerin blocks bone cancer-induced skeletal destruction, skeletal pain and pain-induced neurochemical reorganization of the spinal cord. Nat Med 6: 521-528.
    • (2000) Nat Med , vol.6 , pp. 521-528
    • Honore, P.1    Lugar, N.M.2    Sabino, M.A.C.3    Schwei, M.J.4    Rogers, S.D.5    Mash, D.B.6
  • 10
    • 0034282114 scopus 로고    scopus 로고
    • Involvement of G-protein-activated rectifying K (GIRK) channels in opioid-induced analgesia
    • Ikeda K, Kobayashi T, Kumanishi T, Niki H, Yano R, (2000). Involvement of G-protein-activated rectifying K (GIRK) channels in opioid-induced analgesia. Neurosci Res 38: 113-116.
    • (2000) Neurosci Res , vol.38 , pp. 113-116
    • Ikeda, K.1    Kobayashi, T.2    Kumanishi, T.3    Niki, H.4    Yano, R.5
  • 11
    • 0032558390 scopus 로고    scopus 로고
    • A novel high-affinity inhibitor for inward-rectifier K+ channels
    • Jin W, Lu Z, (1998). A novel high-affinity inhibitor for inward-rectifier K+ channels. Biochemistry 37: 13291-13299.
    • (1998) Biochemistry , vol.37 , pp. 13291-13299
    • Jin, W.1    Lu, Z.2
  • 13
    • 84876361883 scopus 로고    scopus 로고
    • Contribution of oxycodone and its metabolites to the overall analgesic effect after oxycodone administration
    • Klimas R, Witticke D, El Fallsh S, Mikus G, (2013). Contribution of oxycodone and its metabolites to the overall analgesic effect after oxycodone administration. Expert Opin Drug Metab Toxicol 9: 517-528.
    • (2013) Expert Opin Drug Metab Toxicol , vol.9 , pp. 517-528
    • Klimas, R.1    Witticke, D.2    El Fallsh, S.3    Mikus, G.4
  • 14
    • 0033010778 scopus 로고    scopus 로고
    • Bone tumors in the pelvis presenting growth during pregnancy
    • Komiya S, Zenmyo M, Inoue A, (1999). Bone tumors in the pelvis presenting growth during pregnancy. Arch Orthop Trauma Surg 119: 22-29.
    • (1999) Arch Orthop Trauma Surg , vol.119 , pp. 22-29
    • Komiya, S.1    Zenmyo, M.2    Inoue, A.3
  • 16
    • 33749175958 scopus 로고    scopus 로고
    • Antinociception by spinal and systemic oxycodone: Why does the route make a difference? in vitro and in vivo studies in rats
    • Lemberg KK, Kontinen VK, Siiskonen AO, Viljakka KM, Yli-Kauhaluoma JT, Korpi ER, et al. (2006). Antinociception by spinal and systemic oxycodone: why does the route make a difference? In vitro and in vivo studies in rats. Anesthesiology 105: 801-812.
    • (2006) Anesthesiology , vol.105 , pp. 801-812
    • Lemberg, K.K.1    Kontinen, V.K.2    Siiskonen, A.O.3    Viljakka, K.M.4    Yli-Kauhaluoma, J.T.5    Korpi, E.R.6
  • 17
    • 77954331629 scopus 로고    scopus 로고
    • Guidelines for reporting experiments involving animals: The ARRIVE guidelines
    • McGrath J, Drummond G, McLachlan E, Kilkenny C, Wainwright C, (2010). Guidelines for reporting experiments involving animals: the ARRIVE guidelines. Br J Pharmacol 160: 1573-1576.
    • (2010) Br J Pharmacol , vol.160 , pp. 1573-1576
    • McGrath, J.1    Drummond, G.2    McLachlan, E.3    Kilkenny, C.4    Wainwright, C.5
  • 18
    • 0031775956 scopus 로고    scopus 로고
    • Partial sciatic nerve injury in the mouse as a model of neuropathic pain: Behavioral and neuroanatomical correlates
    • Malmberg AB, Basbaum AI, (1998). Partial sciatic nerve injury in the mouse as a model of neuropathic pain: behavioral and neuroanatomical correlates. Pain 76: 215-222.
    • (1998) Pain , vol.76 , pp. 215-222
    • Malmberg, A.B.1    Basbaum, A.I.2
  • 19
    • 0037147624 scopus 로고    scopus 로고
    • Hyperalgesia and blunted morphine analgesia in G protein-gated potassium channel subunit knockout mice
    • Marker CL, Cintora SC, Roman MI, Stoffel M, Wickman K, (2002). Hyperalgesia and blunted morphine analgesia in G protein-gated potassium channel subunit knockout mice. Neuroreport 20: 2509-2513.
    • (2002) Neuroreport , vol.20 , pp. 2509-2513
    • Marker, C.L.1    Cintora, S.C.2    Roman, M.I.3    Stoffel, M.4    Wickman, K.5
  • 20
    • 1642290744 scopus 로고    scopus 로고
    • Spinal G-protein-gated K+ channels formed by GIRK1 and GIRK2 subunits modulate thermal nociception and contribute to morphine analgesia
    • Marker CL, Stoffel M, Wickman K, (2004). Spinal G-protein-gated K+ channels formed by GIRK1 and GIRK2 subunits modulate thermal nociception and contribute to morphine analgesia. J Neurosci 17: 2806-2812.
    • (2004) J Neurosci , vol.17 , pp. 2806-2812
    • Marker, C.L.1    Stoffel, M.2    Wickman, K.3
  • 21
    • 0032454825 scopus 로고    scopus 로고
    • Breakthrough pain in cancer patients: Pathophysiology and treatment
    • Mercadante S, Arcuri E, (1998). Breakthrough pain in cancer patients: pathophysiology and treatment. Cancer Treat Rev 24: 425-432.
    • (1998) Cancer Treat Rev , vol.24 , pp. 425-432
    • Mercadante, S.1    Arcuri, E.2
  • 22
    • 70349506371 scopus 로고    scopus 로고
    • Morphine, oxycodone, and fentanyl exhibit different analgesic profiles in mouse pain models
    • Minami K, Hasegawa M, Ito H, Nakamura A, Tomii T, Matsumoto M, et al. (2009). Morphine, oxycodone, and fentanyl exhibit different analgesic profiles in mouse pain models. J Pharmacol Sci 111: 60-72.
    • (2009) J Pharmacol Sci , vol.111 , pp. 60-72
    • Minami, K.1    Hasegawa, M.2    Ito, H.3    Nakamura, A.4    Tomii, T.5    Matsumoto, M.6
  • 23
    • 0037422558 scopus 로고    scopus 로고
    • Contribution of GIRK2-mediated postsynaptic signaling to opiate and alpha2-adrenergic analgesia and analgesic sex differences
    • Mitrovic I, Margeta-Mitrovic M, Bader S, Stoffel M, Jan LY, Basbaum AI, (2003). Contribution of GIRK2-mediated postsynaptic signaling to opiate and alpha2-adrenergic analgesia and analgesic sex differences. Proc Nalt Acad Sci USA 100: 271-276.
    • (2003) Proc Nalt Acad Sci USA , vol.100 , pp. 271-276
    • Mitrovic, I.1    Margeta-Mitrovic, M.2    Bader, S.3    Stoffel, M.4    Jan, L.Y.5    Basbaum, A.I.6
  • 25
    • 84871576242 scopus 로고    scopus 로고
    • Differential activation of the μ-opioid receptor by oxycodone and morphine in pain-related brain regions in a bone cancer pain model
    • Nakamura A, Hasegawa M, Minami K, Kanbara T, Tomii T, Nishiyori A, et al. (2013). Differential activation of the μ-opioid receptor by oxycodone and morphine in pain-related brain regions in a bone cancer pain model. Br J Pharmacol 168: 375-388.
    • (2013) Br J Pharmacol , vol.168 , pp. 375-388
    • Nakamura, A.1    Hasegawa, M.2    Minami, K.3    Kanbara, T.4    Tomii, T.5    Nishiyori, A.6
  • 26
    • 40549115667 scopus 로고    scopus 로고
    • Comparative pharmacological profiles of morphine and oxycodone under a neuropathic pain-like state in mice: Evidence for less sensitivity to morphine
    • Narita M, Nakamura A, Ozaki M, Imai S, Miyoshi K, Suzuki M, et al. (2008). Comparative pharmacological profiles of morphine and oxycodone under a neuropathic pain-like state in mice: evidence for less sensitivity to morphine. Neuropsychopharmacology 33: 1097-1112.
    • (2008) Neuropsychopharmacology , vol.33 , pp. 1097-1112
    • Narita, M.1    Nakamura, A.2    Ozaki, M.3    Imai, S.4    Miyoshi, K.5    Suzuki, M.6
  • 27
    • 4544377830 scopus 로고    scopus 로고
    • Radiopharmaceutical therapy for palliation of bone pain from osseous metastases
    • Pandit-Taskar N, Batraki M, Divgi CR, (2004). Radiopharmaceutical therapy for palliation of bone pain from osseous metastases. J Nucl Med 45: 1358-1365.
    • (2004) J Nucl Med , vol.45 , pp. 1358-1365
    • Pandit-Taskar, N.1    Batraki, M.2    Divgi, C.R.3
  • 28
    • 33644756719 scopus 로고    scopus 로고
    • Comparison of the antinociceptive response to morphine and morphine-like compounds in male and female Sprague-Dawley rats
    • Peckham EM, Traynor JR, (2006). Comparison of the antinociceptive response to morphine and morphine-like compounds in male and female Sprague-Dawley rats. J Pharmacol Exp Ther 316: 1195-1201.
    • (2006) J Pharmacol Exp Ther , vol.316 , pp. 1195-1201
    • Peckham, E.M.1    Traynor, J.R.2
  • 29
    • 0032899247 scopus 로고    scopus 로고
    • Breakthrough pain: Characteristics and impact in patients with cancer pain
    • Portenoy RK, Payne D, Jacobsen P, (1999). Breakthrough pain: characteristics and impact in patients with cancer pain. Pain 81: 129-134.
    • (1999) Pain , vol.81 , pp. 129-134
    • Portenoy, R.K.1    Payne, D.2    Jacobsen, P.3
  • 30
    • 0025167399 scopus 로고
    • A novel behavioral model of neuropathic pain disorders produced in rats by partial sciatic nerve injury
    • Seltzer D, Dubner R, Shir Y, (1990). A novel behavioral model of neuropathic pain disorders produced in rats by partial sciatic nerve injury. Pain 43: 205-218.
    • (1990) Pain , vol.43 , pp. 205-218
    • Seltzer, D.1    Dubner, R.2    Shir, Y.3
  • 32
    • 44949131642 scopus 로고    scopus 로고
    • Oxycodone controlled-release as first-choice therapy for moderate-to-severe cancer pain in Italian patients: Results of an open-label, multicentre, observational study
    • Silvestri B, Bandieri E, Del Prete S, Ianniello GP, Micheletto G, Dambrosio M, et al. (2008). Oxycodone controlled-release as first-choice therapy for moderate-to-severe cancer pain in Italian patients: results of an open-label, multicentre, observational study. Clin Drug Investig 28: 399-407.
    • (2008) Clin Drug Investig , vol.28 , pp. 399-407
    • Silvestri, B.1    Bandieri, E.2    Del Prete, S.3    Ianniello, G.P.4    Micheletto, G.5    Dambrosio, M.6
  • 33
    • 0037392850 scopus 로고    scopus 로고
    • Morphine blood-brain barrier transport is influenced by probenecid co-administration
    • Tunblad K, Jonsson EN, Hammarlund-Udenaes M, (2003). Morphine blood-brain barrier transport is influenced by probenecid co-administration. Pharm Res 20: 618-623.
    • (2003) Pharm Res , vol.20 , pp. 618-623
    • Tunblad, K.1    Jonsson, E.N.2    Hammarlund-Udenaes, M.3
  • 35
    • 0031780851 scopus 로고    scopus 로고
    • Efficacy of oxycodone in neuropathic pain: A randomized trial in postherpetic neuralgia
    • Watson CP, Babul N, (1998). Efficacy of oxycodone in neuropathic pain: a randomized trial in postherpetic neuralgia. Neurology 50: 1837-1841.
    • (1998) Neurology , vol.50 , pp. 1837-1841
    • Watson, C.P.1    Babul, N.2
  • 36
    • 0020599793 scopus 로고
    • Substantia gelatinosa neurons hyperpolarized in vitro by encephalin
    • Yoshimura M, North RA, (1983). Substantia gelatinosa neurons hyperpolarized in vitro by encephalin. Nature 305: 529-530.
    • (1983) Nature , vol.305 , pp. 529-530
    • Yoshimura, M.1    North, R.A.2
  • 37
    • 79958796157 scopus 로고    scopus 로고
    • Naringin directly activates inwardly rectifying potassium channels at an overlapping binding site to tertiapin-Q
    • Yow TT, Pera E, Absalom N, Heblinski M, Johnston GA, Hanrahan JR, et al. (2011). Naringin directly activates inwardly rectifying potassium channels at an overlapping binding site to tertiapin-Q. Br J Pharmacol 163: 1017-1033.
    • (2011) Br J Pharmacol , vol.163 , pp. 1017-1033
    • Yow, T.T.1    Pera, E.2    Absalom, N.3    Heblinski, M.4    Johnston, G.A.5    Hanrahan, J.R.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.