Grandaw P P, Purdy R E
Department of Pharmacology, College of Medicine, University of California, Irvine 92717, USA.
J Cardiovasc Pharmacol. 1996 Jun;27(6):854-60. doi: 10.1097/00005344-199606000-00013.
We determined the receptors mediating the contractile response of the rabbit femoral artery to serotonin in isolated vascular rings mounted in tissue baths for the measurement of isometric contraction. Serotonin elicited a biphasic concentration-response curve (CRC). The threshold and maximal concentrations of the first phase were 0.03 and 3 microM, respectively. The respective values for the second phase were 10 and 1,000 microM. Benextramine, a selective, irreversible alpha-adrenoceptor antagonist, eliminated the second phase. Similar results were obtained with benextramine in femoral arteries acutely denervated with 6-hydroxydopamine (6-OHDA). In contrast, the reversible, competitive 5-HT2 antagonist ketanserin shifted the first phase of the serotonin CRC to the right ina concentration-dependent manner but had little or no effect on the second phase. No evidence for functional alpha 2-adrenoceptors was found. We conclude that the first phase of the serotonin CRC in rabbit femoral artery was mediated predominantly by 5-HT2 receptors and that the second phase was mediated by alpha 1-adrenoceptors.
我们测定了介导兔股动脉对5-羟色胺收缩反应的受体,实验采用安装在组织浴中的离体血管环,以测量等长收缩。5-羟色胺引发了双相浓度-反应曲线(CRC)。第一相的阈值浓度和最大浓度分别为0.03 μM和3 μM。第二相的相应值分别为10 μM和1000 μM。选择性、不可逆的α-肾上腺素能受体拮抗剂苄非他明消除了第二相。在用6-羟基多巴胺(6-OHDA)急性去神经的股动脉中,苄非他明也得到了类似结果。相比之下,可逆性、竞争性5-HT2拮抗剂酮色林以浓度依赖性方式使5-羟色胺CRC的第一相右移,但对第二相几乎没有影响。未发现功能性α2-肾上腺素能受体的证据。我们得出结论,兔股动脉中5-羟色胺CRC的第一相主要由5-HT2受体介导,第二相由α1-肾上腺素能受体介导。