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中枢给予心房利钠因子可减少大鼠胆汁分泌。

Centrally applied atrial natriuretic factor diminishes bile secretion in the rat.

作者信息

Bianciotti L G, Vatta M S, Vescina C, Trippodi V, Sabbatini M E, Fernandez B E

机构信息

Cátedra de Fisiopatología, Facultad de Farmacia y Bioquímica, Universidad de Buenos Aires, Junín 956, 5 Piso, 1113, Buenos Aires, Argentina.

出版信息

Regul Pept. 2001 Dec 15;102(2-3):127-33. doi: 10.1016/s0167-0115(01)00310-x.

Abstract

Little is known about the role of centrally applied peptides in the regulation of bile secretion. We previously reported that the intravenous injection of atrial natriuretic factor (ANF) reduces bile acid dependent flow without affecting portal venous pressure in the rat. In the present work, we studied the effects of centrally applied ANF on bile secretion and the possible pathways involved. Rats were cannulated in the brain lateral ventricle for the administration of 1, 10 and 100 ng/microl ANF. After 1 week, the common bile duct was cannulated and bile samples were collected every 15 min for 60 min after the administration of ANF. The excretion rate of various biliary components was assessed. Bile secretion experiments were also performed after bilateral truncal vagotomy or atropine administration to evaluate the participation of a vagal pathway. In addition, the role of the sympathetic system was addressed by combined administration of propranolol and phentolamine. Centrally applied ANF did not modify blood pressure but diminished bile flow and bile acid output. It also reduced sodium and potassium secretion but did not modify protein or phospholipid excretion. Neither bilateral truncal vagotomy nor atropine administration abolished ANF response. Furthermore, combined administration of adrenergic antagonists did not alter ANF inhibitory effect on bile flow. In conclusion, centrally applied ANF reduced bile acid dependent flow not through a vagal or adrenergic pathway in the rat, suggesting the involvement of a peptidergic pathway.

摘要

关于中枢应用肽类在胆汁分泌调节中的作用,人们所知甚少。我们先前报道,静脉注射心房利钠因子(ANF)可降低大鼠胆汁酸依赖性胆汁流量,而不影响门静脉压力。在本研究中,我们研究了中枢应用ANF对胆汁分泌的影响以及可能涉及的途径。将大鼠的脑侧脑室插管,以给予1、10和100 ng/微升的ANF。1周后,将胆总管插管,在给予ANF后每15分钟收集一次胆汁样本,共收集60分钟。评估各种胆汁成分的排泄率。在双侧迷走神经干切断术或给予阿托品后也进行胆汁分泌实验,以评估迷走神经途径的参与情况。此外,通过联合给予普萘洛尔和酚妥拉明来探讨交感神经系统的作用。中枢应用ANF不会改变血压,但会减少胆汁流量和胆汁酸输出。它还会减少钠和钾的分泌,但不会改变蛋白质或磷脂的排泄。双侧迷走神经干切断术或给予阿托品均未消除ANF的反应。此外,联合给予肾上腺素能拮抗剂不会改变ANF对胆汁流量的抑制作用。总之,中枢应用ANF在大鼠中不是通过迷走神经或肾上腺素能途径来减少胆汁酸依赖性胆汁流量的,这表明存在一条肽能途径。

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