Nakajima T, Naitoh F, Kuruma I
Eur J Pharmacol. 1977 Jan 21;41(2):163-9. doi: 10.1016/0014-2999(77)90205-9.
Dopamine, apomorphine, isoproterenol and norepinephrine all increased the concentration of adenosine 3',5'-monophosphate in the rat kidney particulate preparation, which was composed of tubules, glomeruli and blood vessels. The concentrations of dopamine, apomorphine, isoproterenol and norepinephrine causing a half-maximal increase were 50, 83, 0.1 and 10 muM, respectively. The alpha-blocker, phentolamine, at a concentration as high as 1 mM, did not significantly reduce the effect of these drugs on the adenosine 3',5'-monophosphate concentration. The beta-blocker, propranolol (50 muM), blocked the effect of isoproterenol and norepinephrine, but not that of dopamine. The effect of dopamine was selectively blocked by spiroperidol (50 muM), a dopamine receptor antagonist, whereas the effects of isoproterenol and norepinephrine was not blocked by spiroperidol. These results suggest that in the rat kidney particulate preparation there is a specific dopamine receptor which can lead to the increase in the concentration of adenosine 3',5'-monophosphate.
多巴胺、阿扑吗啡、异丙肾上腺素和去甲肾上腺素均能增加大鼠肾脏微粒体制剂中3',5'-环磷酸腺苷的浓度,该制剂由肾小管、肾小球和血管组成。引起最大效应一半时的多巴胺、阿扑吗啡、异丙肾上腺素和去甲肾上腺素的浓度分别为50、83、0.1和10 μM。α受体阻滞剂酚妥拉明在高达1 mM的浓度下,并未显著降低这些药物对3',5'-环磷酸腺苷浓度的影响。β受体阻滞剂普萘洛尔(50 μM)可阻断异丙肾上腺素和去甲肾上腺素的作用,但不阻断多巴胺的作用。多巴胺的作用可被多巴胺受体拮抗剂螺哌啶醇(50 μM)选择性阻断,而异丙肾上腺素和去甲肾上腺素的作用则不被螺哌啶醇阻断。这些结果表明,在大鼠肾脏微粒体制剂中存在一种特异性多巴胺受体,它可导致3',5'-环磷酸腺苷浓度升高。