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首页> 外文期刊>American Journal of Physiology >Inhibitory effect of central dopamine on basal pancreatic secretion in conscious rats.
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Inhibitory effect of central dopamine on basal pancreatic secretion in conscious rats.

机译:中枢多巴胺对清醒大鼠基础胰腺分泌的抑制作用。

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We examined the role and the peripheral mechanism of action of central dopamine on basal pancreatic exocrine secretion in conscious rats. Rats were fitted with bile and pancreatic catheters to collect bile and pancreatic juice separately and also with a left lateral brain ventricle and external jugular vein catheters. After 90-min basal collection, the D1- and D2-receptor antagonists (Sch-23390 and eticlopride, respectively) and dopamine were administered into the lateral brain ventricle. Sch-23390 (30, 100, and 300 nmol/rat), but not eticlopride (300 nmol/rat), stimulated pancreatic fluid and protein secretion. Dopamine (30, 100, and 300 nmol/rat) inhibited pancreatic secretion lose dependently. Pretreatment with Sch-23390 prevented the inhibitory effect of dopamine. Intravenously injected Sch-23390 or dopamine had no effect on pancreatic secretion. The inhibitory effect of dopamine was blocked by bretylium, an inhibitor of norepinephrine release, and phentolamine, an alpha-blocker, but not by vagotomy. The beta-antagonist propranolol alone significantly inhibited basal pancreatic secretion, and dopamine did not modify the inhibitory effect of propranolol. The proton pump inhibitor omeprazole partially but not completely reduced the inhibition by dopamine. These results suggest that central dopamine inhibits pancreatic exocrine secretion via D1-like receptors and that the inhibitory effect is mediated via sympathetic nerves, especially alpha-adrenoceptors.
机译:我们研究了中枢多巴胺对清醒大鼠基础胰腺外分泌分泌的作用及其外围机制。大鼠装有胆汁和胰导管以分别收集胆汁和胰液,还装有左脑侧脑室和颈外静脉导管。基础收集90分钟后,将D1和D2受体拮抗剂(分别为Sch-23390和艾托必利)和多巴胺施用于脑外侧脑室。 Sch-23390(30、100和300 nmol /大鼠),而非依替普利(300 nmol /大鼠),可刺激胰液和蛋白质分泌。多巴胺(30、100和300 nmol /大鼠)抑制胰脏分泌失落。 Sch-23390的预处理可防止多巴胺的抑制作用。静脉注射Sch-23390或多巴胺对胰腺分泌没有影响。多巴胺的抑制作用被去甲肾上腺素释放抑制剂布雷替尼和α-阻滞剂酚妥拉明阻断,但迷走神经切断术并未阻断。单独使用β-拮抗剂普萘洛尔可显着抑制基础胰腺分泌,而多巴胺不会改变普萘洛尔的抑制作用。质子泵抑制剂奥美拉唑部分但不完全降低多巴胺的抑制作用。这些结果表明中枢多巴胺通过D1样受体抑制胰腺外分泌分泌,并且抑制作用是通过交感神经,尤其是α-肾上腺素能受体介导的。

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