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血清素诱导兔股动脉血管收缩:由5-HT2血清素能受体和α1-肾上腺素能受体共同介导。

Serotonin-induced vasoconstriction in rabbit femoral artery: mediation by both 5-HT2 serotonergic and alpha 1-adrenoceptors.

作者信息

Grandaw P P, Purdy R E

机构信息

Department of Pharmacology, College of Medicine, University of California, Irvine 92717, USA.

出版信息

J Cardiovasc Pharmacol. 1996 Jun;27(6):854-60. doi: 10.1097/00005344-199606000-00013.

Abstract

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.

摘要

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。

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