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苄胺及其代谢产物对大鼠离体灌注肠系膜动脉床反应的影响。

Effect of benzylamine and its metabolites on the responses of the isolated perfused mesenteric arterial bed of the rat.

作者信息

Elliott J, Callingham B A

机构信息

Department of Pharmacology, University of Cambridge, UK.

出版信息

J Auton Pharmacol. 1991 Oct;11(5):323-35. doi: 10.1111/j.1474-8673.1991.tb00256.x.

Abstract
  1. Semicarbazide-sensitive amine oxidase (SSAO) is an enzyme activity which can be found in the plasma membrane of rat vascular smooth muscle cells. We have investigated the possibility that the products of deamination by this enzyme, namely ammonia, hydrogen peroxide and the aldehyde, may be important in the modulation of the responses of vascular smooth muscle to extracellular stimuli. 2. The isolated perfused mesenteric arterial bed of the rat was used and dose-pressure response curves (DRC) to bolus injections of adrenaline (Ad) or ATP were plotted by non-linear curve fitting. The relaxant effects of carbachol (CCh), which releases endothelium dependent relaxing factor (ERDF), were studied by co-administering CCh with Ad. The effects of including the preferred SSAO substrate, benzylamine (BZ; 25 microM), in the perfusion fluid throughout the experiment and of inhibition of SSAO by treatment of rats with (E)-2-(3',4'-dimethoxyphenyl)-3-fluoroallylamine (MDL 72145; 1 mg kg-1) 1 h before dissection, have been studied. 3. Neither BZ nor SSAO inhibition affected the DRC to ATP. BZ shifted Ad responses to the left, inhibition of SSAO increased this shift indicating that the amine, but not its metabolites, were responsible for the potentiation of the responses to Ad. DRC to CCh showed a shift to the left and a significant decrease in the Hill slope with BZ, indicative of a potentiation of low doses of CCh more than high doses. Inhibition of SSAO prevented this change and so the metabolites of BZ deamination appeared to be involved in the potentiation. 4. Ammonia generated by SSAO may contribute to the production of EDRF or hydrogen peroxide may sensitize guanylate cyclase to stimulation by EDRF and so explain these findings.
摘要
  1. 氨基脲敏感胺氧化酶(SSAO)是一种可在大鼠血管平滑肌细胞质膜中发现的酶活性。我们研究了该酶脱氨基产物,即氨、过氧化氢和醛,在调节血管平滑肌对细胞外刺激反应中可能起重要作用的可能性。2. 使用大鼠离体灌注肠系膜动脉床,通过非线性曲线拟合绘制肾上腺素(Ad)或ATP推注的剂量-压力反应曲线(DRC)。通过将卡巴胆碱(CCh)与Ad共同给药,研究了释放内皮依赖性舒张因子(ERDF)的CCh的舒张作用。研究了在整个实验过程中在灌注液中加入首选的SSAO底物苄胺(BZ;25μM)以及在解剖前1小时用(E)-2-(3',4'-二甲氧基苯基)-3-氟烯丙胺(MDL 72145;1mg/kg)处理大鼠抑制SSAO的效果。3. BZ和SSAO抑制均未影响对ATP的DRC。BZ使Ad反应向左移动,SSAO抑制增强了这种移动,表明胺而非其代谢产物是Ad反应增强的原因。对CCh的DRC显示,BZ使其向左移动且Hill斜率显著降低,表明低剂量CCh比高剂量CCh增强作用更明显。抑制SSAO可防止这种变化,因此BZ脱氨基的代谢产物似乎参与了增强作用。4. SSAO产生的氨可能有助于EDRF的产生,或者过氧化氢可能使鸟苷酸环化酶对EDRF的刺激敏感,从而解释这些发现。

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