Selley D E, Nestler E J, Breivogel C S, Childers S R
Department of Physiology and Pharmacology, Bowman Gray School of Medicine, Wake Forest University, Winston-Salem, NC 21757, USA.
Brain Res. 1997 Jan 23;746(1-2):10-8. doi: 10.1016/s0006-8993(96)01125-0.
The nucleus locus coeruleus is involved in the expression of opiate physical dependence and withdrawal, and has been characterized extensively with regard to chronic morphine-induced alterations in biochemical and electrophysiological responses. In the present study the effects of chronic morphine treatment on opioid receptor-coupled G-protein activity was investigated in membranes from rat locus coeruleus. Opioid agonists stimulated low Km GTPase activity with pharmacology consistent with mu receptors. Chronic morphine treatment resulted in decreases in both basal and opioid-stimulated low Km GTPase activity, with no change in the percent stimulation by agonist. The decrease in low Km GTPase activity appeared to be due to a decrease in the Vmax of the enzyme, with no change in the Km for GTP hydrolysis. These results were confirmed by assays of basal and opioid receptor-stimulated [35S]GTP gamma S binding in the presence of excess GDP. Thus, chronic morphine treatment apparently decreased inhibitory G-protein activity in the locus coeruleus without producing any detectable desensitization. These results suggest a potential adaptation at the receptor/transducer level which may contribute to other biochemical changes produced in the locus coeruleus by chronic morphine treatment.
蓝斑核参与阿片类物质身体依赖性和戒断反应的表达,并且在慢性吗啡诱导的生化和电生理反应改变方面已被广泛研究。在本研究中,研究了慢性吗啡处理对大鼠蓝斑核膜中阿片受体偶联G蛋白活性的影响。阿片类激动剂刺激低Km GTP酶活性,其药理学特性与μ受体一致。慢性吗啡处理导致基础和阿片类刺激的低Km GTP酶活性均降低,激动剂刺激百分比无变化。低Km GTP酶活性的降低似乎是由于该酶的Vmax降低,而GTP水解的Km没有变化。在过量GDP存在下,通过基础和阿片受体刺激的[35S]GTPγS结合测定证实了这些结果。因此,慢性吗啡处理明显降低了蓝斑核中的抑制性G蛋白活性,而没有产生任何可检测到的脱敏作用。这些结果表明在受体/转导水平上存在潜在的适应性变化,这可能导致慢性吗啡处理在蓝斑核中产生的其他生化变化。