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影响环核苷酸代谢的药物对缓激肽和去-Arg9-缓激肽诱导的离体大鼠十二指肠舒张和收缩的作用。

Effects of the agents affecting cyclic nucleotide metabolism on the bradykinin- and des-Arg9-bradykinin-induced relaxations and contractions in isolated rat duodenum.

作者信息

Oztürk Y

机构信息

Department of Pharmacology, Faculty of Pharmacy, Anadolu University, Eskişehir, Turkey.

出版信息

Gen Pharmacol. 1994 Nov;25(7):1389-95. doi: 10.1016/0306-3623(94)90163-5.

Abstract
  1. Bradykinin and related kinins possess two different types of action (consisting of relaxation and contraction) in the isolated rat duodenum via their specific receptors. However, the mechanisms of these actions have not been fully elucidated. The present study was undertaken to investigate the effects of the agents affecting cyclic nucleotide metabolism on bradykinin-induced relaxations and on bradykinin- and des-Arg9-bradykinin-induced contractions. 2. Des-Arg9-bradykinin, B1 receptor agonist, and high concentrations of bradykinin elicited dose-dependent contractile responses in the rat duodenum, while low concentrations of bradykinin caused a dose-dependent relaxation in this tissue. 3. Nicotinic acid, an inhibitor of adenylate cyclase, inhibited the relaxation of rat duodenum induced by bradykinin at low concentrations in a non-competitive manner. However, the inhibitory efficacy of nicotinic acid against bradykinin was limited by 39.9% and this inhibition was not further increased by higher concentrations of nicotinic acid up to 10(-3) M. 4. Imidazole, an activator of cyclic nucleotide phosphodiesterase, caused a slight inhibition of the relaxant responses to low concentrations of bradykinin and of the contractile responses to des-Arg9-bradykinin and high concentrations of bradykinin in isolated rat duodenum. These inhibitions were also limited in efficacies and not increased by higher concentrations of imidazole. 5. Methylene blue, an agent that inhibits soluble guanylate cyclase, suppressed the contractions of rat duodenum induced by des-Arg9-bradykinin and high concentrations of bradykinin in a non-competitive manner. Again, these inhibitions were limited and further increase in the inhibitory efficacy was not observed in spite of increasing the methylene blue concentrations.(ABSTRACT TRUNCATED AT 250 WORDS)
摘要
  1. 缓激肽及相关激肽通过其特异性受体在离体大鼠十二指肠中具有两种不同类型的作用(包括舒张和收缩)。然而,这些作用的机制尚未完全阐明。本研究旨在探讨影响环核苷酸代谢的药物对缓激肽诱导的舒张以及缓激肽和去-Arg9-缓激肽诱导的收缩的影响。2. 去-Arg9-缓激肽、B1受体激动剂以及高浓度的缓激肽在大鼠十二指肠中引发剂量依赖性的收缩反应,而低浓度的缓激肽则导致该组织出现剂量依赖性的舒张。3. 烟酸,一种腺苷酸环化酶抑制剂,以非竞争性方式抑制低浓度缓激肽诱导的大鼠十二指肠舒张。然而,烟酸对缓激肽的抑制效力受限,为39.9%,且高达10(-3)M的更高浓度烟酸并未进一步增强这种抑制作用。4. 咪唑,一种环核苷酸磷酸二酯酶激活剂,对离体大鼠十二指肠中低浓度缓激肽诱导的舒张反应以及去-Arg9-缓激肽和高浓度缓激肽诱导的收缩反应产生轻微抑制。这些抑制作用在效力上也有限,且更高浓度的咪唑并未增强抑制效果。5. 亚甲蓝,一种抑制可溶性鸟苷酸环化酶的药物,以非竞争性方式抑制去-Arg9-缓激肽和高浓度缓激肽诱导的大鼠十二指肠收缩。同样,这些抑制作用有限,尽管增加亚甲蓝浓度,也未观察到抑制效力进一步增强。(摘要截断于250字)

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