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慢性吗啡治疗对蛋白激酶C活性的影响:与布托啡诺的比较及对阿片类耐受的意义

Influence of chronic morphine treatment on protein kinase C activity: comparison with butorphanol and implication for opioid tolerance.

作者信息

Narita M, Makimura M, Feng Y, Hoskins B, Ho I K

机构信息

Department of Pharmacology and Toxicology, University of Mississippi Medical Center, Jackson 39216-4505.

出版信息

Brain Res. 1994 Jul 4;650(1):175-9. doi: 10.1016/0006-8993(94)90224-0.

Abstract

The aim of this study was to determine whether chronic opioid treatment could influence the protein kinase C (PKC) activity in the rat brain. Chronic morphine (microns agonist) but not butorphanol (mu/delta/kappa mixed agonist) treatment enhanced cytosolic PKC activity in the pons/medulla, but not in the cytosolic fractions of cortex and midbrain regions. Concomitant administration of the opioid receptor antagonist, naloxone, blocked the PKC upregulation by chronic morphine. Chronic administration of morphine and butorphanol produced no change in the membrane PKC activity. Antinociceptive tolerance to morphine but not to butorphanol was developed under these conditions. These results suggest that chronic morphine administration leads to an upregulation of the cytosolic PKC activity in the pons/medulla through repeated activation of mu opioid receptors and that the PKC upregulation in this specific area may contribute to the morphine tolerance.

摘要

本研究的目的是确定慢性阿片类药物治疗是否会影响大鼠脑中蛋白激酶C(PKC)的活性。慢性吗啡(μ激动剂)治疗可增强脑桥/延髓中细胞溶质PKC的活性,但丁丙诺啡(μ/δ/κ混合激动剂)治疗则无此作用,且在皮质和中脑区域的细胞溶质部分也未增强。同时给予阿片受体拮抗剂纳洛酮可阻断慢性吗啡引起的PKC上调。慢性给予吗啡和丁丙诺啡对膜PKC活性无影响。在这些条件下,对吗啡产生了抗伤害感受耐受性,但对丁丙诺啡未产生耐受性。这些结果表明,慢性给予吗啡通过反复激活μ阿片受体导致脑桥/延髓中细胞溶质PKC活性上调,且该特定区域的PKC上调可能导致吗啡耐受性。

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