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Modulation by peripheral opioids of basal and distension-stimulated gastric acid secretion in the rat.

机译:外周阿片对大鼠基础和扩张刺激胃酸分泌的调节。

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摘要

1. The influence of opioids in modulating gastric acid secretory responses has been investigated in the continuously perfused stomach of the anaesthetized rat. 2. Intravenous administration of morphine (0.75-3 mg kg-1) or the peripherally acting enkephalin analogue, BW443C (0.75-3 mg kg-1), substantially augmented acid secretion in basal conditions. These effects were significantly inhibited by the opioid antagonists naloxone (1 mg kg-1) and the peripherally acting N-methylnalorphine (2 mg kg-1). When administered alone, neither opioid antagonist influenced basal acid output. 3. Acid secretory responses to different levels of gastric distension (5-20 cmH2O) were significantly and dose-dependently reduced in rats pretreated with morphine (3 mg kg-1) or BW443C (1.5 mg kg-1). Previous administration of either naloxone or N-methyl nalorphine reversed the inhibitory effects of opioids on gastric acid secretion stimulated by distension. Likewise, blockade of opioid receptors with naloxone or N-methylnalorphine significantly increased acid output induced by distension. 4. Levels of serum gastrin in control animals were not increased after intragastric distension (20 cmH2O). Pretreatment with BW443C (1.5 mg kg-1) did not modify the levels of gastrin present during basal or distension stimulated conditions. 5. Pretreatment with morphine or BW443C did not influence the acid responses to i.v. injection of pentagastrin (100 micrograms kg-1), histamine (5 mg kg-1) or carbachol (4 micrograms kg-1). Acid secretion induced by i.v. administration of 2-deoxy-D-glucose (150 mg kg-1) was reduced in rats pretreated with morphine but not with BW443C. Gastric secretory responses to insulin (0.3 i.u. kg-1) were not modified by i.v. morphine.(ABSTRACT TRUNCATED AT 250 WORDS)
机译:1.在麻醉大鼠的连续灌胃中,研究了阿片类药物在调节胃酸分泌反应中的作用。 2.静脉内注射吗啡(0.75-3 mg kg-1)或外周作用脑啡肽类似物BW443C(0.75-3 mg kg-1),在基础条件下可大大增加酸的分泌。阿片拮抗剂纳洛酮(1 mg kg-1)和外围作用的N-甲基纳洛啡(2 mg kg-1)显着抑制了这些作用。当单独给药时,两种阿片拮抗剂均不会影响基础酸的输出。 3.在吗啡(3 mg kg-1)或BW443C(1.5 mg kg-1)预处理的大鼠中,对不同水平的胃胀(5-20​​ cmH2O)的酸分泌反应显着且剂量依赖性降低。先前施用纳洛酮或N-甲基纳洛啡可逆转阿片类药物对扩张刺激的胃酸分泌的抑制作用。同样,用纳洛酮或N-甲基纳洛啡阻断阿片受体可显着增加由扩张引起的酸输出。 4.胃内扩张(20 cmH2O)后,对照组动物的血清胃泌素水平没有增加。用BW443C(1.5 mg kg-1)预处理不会改变基础或扩张刺激条件下胃泌素的水平。 5.用吗啡或BW443C预处理不影响酸对静脉注射的反应。注射五肽胃泌素(100微克kg-1),组胺(5毫克kg-1)或卡巴胆碱(4微克kg-1)。 i.v.诱导的酸分泌使用吗啡但未使用BW443C预处理的大鼠减少了2-脱氧-D-葡萄糖(150 mg kg-1)的给药。静脉注射未改变对胰岛素的胃分泌反应(0.3 i.u. kg-1)。吗啡(摘要截断为250个字)

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