Fiorillo C D, Williams J T
Vollum Institute, Oregon Health Sciences University, Portland 97201, USA.
J Neurosci. 1996 Feb 15;16(4):1479-85. doi: 10.1523/JNEUROSCI.16-04-01479.1996.
In rat locus coeruleus (LC) neurons, alpha 2 adrenoceptors, mu-opioid and somatostatin receptors all activate the same potassium conductance. Chronic treatment with morphine causes a loss of sensitivity that is specific to the mu-opioid response, with no change in the alpha 2 adrenoceptor-mediated response. Acute desensitization induced by opioid, somatostatin, and alpha 2-adrenoceptor agonists was studied in brain slices of rat LC using intracellular recording. A supramaximal concentration of the opioid agonist Met5-enkephalin induced a profound homologous desensitization but little heterologous desensitization to an alpha 2-adrenoceptor agonist (UK 14304) or somatostatin. All desensitized currents showed partial recovery. A supramaximal concentration of UK14304 caused a relatively small amount of desensitization. Although little interaction was observed among inhibitory G-protein-coupled receptors, activation of an excitatory receptor had marked effects on inhibitory responses. Muscarinic agonists, which produce an inward current in LC neurons, reduced the magnitude of agonist-induced outward currents and increased both the rate and amount of opioid desensitization. Muscarinic activation did not alter desensitization of alpha 2-adrenoceptor responses. Acute desensitization shares several characteristics with the tolerance induced by chronic morphine treatment of animals.
在大鼠蓝斑(LC)神经元中,α2肾上腺素能受体、μ阿片受体和生长抑素受体均激活相同的钾离子电导。吗啡长期治疗会导致对μ阿片反应特有的敏感性丧失,而α2肾上腺素能受体介导的反应无变化。使用细胞内记录法,在大鼠LC脑片中研究了阿片类药物、生长抑素和α2肾上腺素能受体激动剂诱导的急性脱敏作用。阿片类激动剂Met5-脑啡肽的超最大浓度诱导了深度同源脱敏,但对α2肾上腺素能受体激动剂(UK 14304)或生长抑素的异源脱敏作用很小。所有脱敏电流均显示出部分恢复。UK14304的超最大浓度引起相对少量的脱敏。尽管在抑制性G蛋白偶联受体之间未观察到明显相互作用,但兴奋性受体的激活对抑制性反应有显著影响。毒蕈碱激动剂在LC神经元中产生内向电流,降低了激动剂诱导的外向电流幅度,并增加了阿片类药物脱敏的速率和程度。毒蕈碱激活并未改变α2肾上腺素能受体反应的脱敏作用。急性脱敏与慢性吗啡处理动物诱导的耐受性具有若干共同特征。