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肾上腺素能受体激动剂和拮抗剂对五肽胃泌素诱导的胃液分泌的作用是否归因于它们对组胺形成的影响?

Can the actions of adrenoceptor agonists and antagonists on pentagastrin-induced gastric secretion be due to their effects of histamine formation?

作者信息

Curwain B P, Holton P, McIsaac R L, Spencer J

出版信息

Br J Pharmacol. 1974 Jun;51(2):217-23. doi: 10.1111/j.1476-5381.1974.tb09650.x.

Abstract

1 The effects of some adrenoceptor agonists and antagonists which have been reported to affect histamine formation in leucocytes (Assem & Feigenbaum, 1972) have been investigated on gastric secretion in conscious dogs with Heidenhain pouches.2 Submaximal secretion in response to pentagastrin was enhanced by propranolol (0.1-1.0 mg/kg i.v.) and phenylephrine (1.0 mug kg(-1) min(-1) i.v. for 20 min), which increase histamine formation, and was decreased by phentolamine (2 mg/kg i.v.) and isoprenaline (0.05-0.2 mug kg(-1) min(-1) i.v. for 30 min), which decrease histamine formation. Practolol (2 mg/kg i.v.), which has no effect on histamine formation, had no effect on secretion.3 Acid secretion in response to histamine was either unaffected or affected in the opposite direction by these drugs.4 The effects of the drugs on pentagastrin-induced secretion were not secondary to changes in mucosal blood flow (radioactive aniline clearance).5 The results are consistent with the hypothesis that acid secretion in response to pentagastrin involves the formation of endogenous histamine.

摘要
  1. 一些据报道可影响白细胞中组胺生成的肾上腺素能受体激动剂和拮抗剂(Assem和Feigenbaum,1972年)对具有海登海因小胃的清醒犬胃分泌的影响已被研究。

  2. 普萘洛尔(静脉注射0.1 - 1.0毫克/千克)和去氧肾上腺素(静脉注射1.0微克/千克·分钟,持续20分钟)可增强对五肽胃泌素的次最大分泌,这两种药物会增加组胺生成;而酚妥拉明(静脉注射2毫克/千克)和异丙肾上腺素(静脉注射0.05 - 0.2微克/千克·分钟,持续30分钟)可降低对五肽胃泌素的次最大分泌,这两种药物会减少组胺生成。对组胺生成无影响的心得宁(静脉注射2毫克/千克)对分泌也无影响。

  3. 这些药物对组胺诱导的胃酸分泌要么无影响,要么产生相反的影响。

  4. 这些药物对五肽胃泌素诱导分泌的影响并非继发于黏膜血流的变化(放射性苯胺清除率)。

  5. 结果与以下假设一致,即对五肽胃泌素的胃酸分泌涉及内源性组胺的生成。

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5
Effect of propranolol on gastric acid secretion in rats.普萘洛尔对大鼠胃酸分泌的影响。
Br J Pharmacol. 1972 Sep;46(1):170-1. doi: 10.1111/j.1476-5381.1972.tb06860.x.

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