Pilc A, Enna S J
Life Sci. 1985 Sep 30;37(13):1183-94. doi: 10.1016/0024-3205(85)90129-8.
Experiments were undertaken to examine the characteristics of the adrenergic receptor-coupled cAMP system in rat brain slices. It was found that the potentiation of isoproterenol-stimulated cAMP accumulation by 6-fluoronorepinephrine, an alpha-adrenergic agonist, is largely dependent upon the degree of beta-receptor occupancy, with prazosin-sensitive alpha-adrenergic receptors contributing less to this interaction. Chronic administration of a variety of antidepressants decreased the potentiating interaction between 6-fluoronorepinephrine and isoproterenol even under conditions where there were no obvious effects on the alpha- or beta- adrenergic components themselves. Chronic administration of imipramine had no effect on the interaction between 6-fluoronorepinephrine and adenosine, suggesting that the drug selectively modifies the coupling between the alpha- and beta-adrenergic systems. The results suggest that antidepressants influence the coupling between 6-fluoronorepinephrine and isoproterenol receptors independent of any effect on the individual recognition sites.
开展实验以研究大鼠脑片肾上腺素能受体偶联环磷酸腺苷(cAMP)系统的特性。结果发现,α-肾上腺素能激动剂6-氟去甲肾上腺素对异丙肾上腺素刺激的cAMP积累的增强作用在很大程度上取决于β受体的占据程度,对哌唑嗪敏感的α-肾上腺素能受体对这种相互作用的贡献较小。长期给予多种抗抑郁药会降低6-氟去甲肾上腺素与异丙肾上腺素之间的增强相互作用,即使在对α-或β-肾上腺素能成分本身没有明显影响的情况下也是如此。长期给予丙咪嗪对6-氟去甲肾上腺素与腺苷之间的相互作用没有影响,这表明该药物选择性地改变了α-和β-肾上腺素能系统之间的偶联。结果表明,抗抑郁药影响6-氟去甲肾上腺素与异丙肾上腺素受体之间的偶联,而与对单个识别位点的任何影响无关。