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右芬氟拉明导致大鼠回肠中血清素释放增加。

Increased release of serotonin from rat ileum due to dexfenfluramine.

作者信息

Rezaie-Majd Shahrzad, Murar Jozef, Nelson Daniel P, Kelly Rosemary F, Hong Zhigang, Lang Irene M, Varghese Anthony, Weir E Kenneth

机构信息

Department of Medicine, Veterans Administration Medical Center, University of Minnesota, Minneapolis 55417, USA.

出版信息

Am J Physiol Regul Integr Comp Physiol. 2004 Nov;287(5):R1209-13. doi: 10.1152/ajpregu.00191.2004. Epub 2004 Jul 8.

Abstract

Plasma levels of serotonin are elevated in primary pulmonary hypertension even after bilateral lung transplantation, suggesting a possible etiologic role. Serotonin is released primarily from the small intestine. Anorectic agents, such as dexfenfluramine, which can cause pulmonary hypertension, are known to inhibit potassium channels in vascular smooth muscle cells. We examined the hypothesis that dexfenfluramine may stimulate release of serotonin from the ileum by inhibition of K+ channels. In an isolated loop of rat ileum perfused with a physiological salt solution, the administration of dexfenfluramine, its major metabolite D-norfenfluramine, the potassium channel blocker 4-aminopyridine (5 mM), and caffeine (30 mM) increased serotonin levels in the venous effluent. Potassium chloride (60 mM) tended to increase serotonin levels. In genetically susceptible individuals, dexfenfluramine may induce pulmonary hypertension by increasing cytosolic calcium in enterochromaffin cells of the small intestine, thus releasing serotonin and causing vasoconstriction. This work indicates that dexfenfluramine and its major metabolite d-norfenfluramine can increase serotonin release from the small intestine.

摘要

即使在双侧肺移植后,原发性肺动脉高压患者的血浆血清素水平仍会升高,这表明其可能具有病因学作用。血清素主要从小肠释放。已知能导致肺动脉高压的食欲抑制剂,如右芬氟拉明,可抑制血管平滑肌细胞中的钾通道。我们检验了右芬氟拉明可能通过抑制钾通道刺激回肠释放血清素的假说。在用生理盐溶液灌注的大鼠离体回肠袢中,给予右芬氟拉明、其主要代谢产物D -去甲芬氟拉明、钾通道阻滞剂4 -氨基吡啶(5 mM)和咖啡因(30 mM)可使静脉流出液中的血清素水平升高。氯化钾(60 mM)倾向于增加血清素水平。在基因易感性个体中,右芬氟拉明可能通过增加小肠肠嗜铬细胞中的胞质钙来诱导肺动脉高压,从而释放血清素并引起血管收缩。这项研究表明,右芬氟拉明及其主要代谢产物D -去甲芬氟拉明可增加小肠血清素的释放。

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