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CGS 9896对大鼠应激性胃溃疡的影响。

Effect of CGS 9896 on stress-induced gastric ulcer in rat.

作者信息

Najim R A, Karim K H

机构信息

Department of Pharmacology, College of Medicine, University of Baghdad, Iraq.

出版信息

Clin Exp Pharmacol Physiol. 1990 Feb;17(2):157-161. doi: 10.1111/j.1440-1681.1990.tb01298.x.

DOI:10.1111/j.1440-1681.1990.tb01298.x
PMID:2109664
Abstract
  1. The effects of CGS 9896, a partial benzodiazepine agonist, and chlordiazepoxide, a full benzodiazepine agonist, on stress-induced gastric ulcers as well as blood glucose were compared. 2. Ulceration in the glandular stomach was induced by 2 h restraint at 4 degrees C. 3. CGS 9896 reduced significantly the ulcer parameters but did not affect blood glucose. The effect of CGS 9896 was dose-dependently blocked by the benzodiazepine antagonist flumazepil. 4. Chlordiazepoxide reduced the ulcer parameters but increased blood glucose. 5. Since CGS 9896 lacks sedative effects but reduced ulcer parameters, the anti-ulcer and sedative effects of drugs acting at benzodiazepine receptors are disassociated. 6. Benzodiazepine-induced hyperglycaemia does not play a major role in the anti-ulcer effects.
摘要
  1. 比较了部分苯二氮䓬激动剂CGS 9896和完全苯二氮䓬激动剂氯氮䓬对应激诱导的胃溃疡以及血糖的影响。2. 通过在4℃下约束2小时诱导腺胃溃疡。3. CGS 9896显著降低溃疡参数,但不影响血糖。苯二氮䓬拮抗剂氟马西尼剂量依赖性地阻断了CGS 9896的作用。4. 氯氮䓬降低溃疡参数,但升高血糖。5. 由于CGS 9896缺乏镇静作用但降低了溃疡参数,作用于苯二氮䓬受体的药物的抗溃疡和镇静作用是分离的。6. 苯二氮䓬诱导的高血糖在抗溃疡作用中不起主要作用。

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Effect of CGS 9896 on stress-induced gastric ulcer in rat.CGS 9896对大鼠应激性胃溃疡的影响。
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A benzodiazepine receptor inverse agonist inhibits stress-induced ulcer formation.一种苯二氮䓬受体反向激动剂可抑制应激诱导的溃疡形成。
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Benzodiazepines reduce gastric ulcers induced in rats by stress.苯二氮䓬类药物可减轻应激诱导的大鼠胃溃疡。
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Investigation of the actions of the benzodiazepine antagonists Ro 15-1788 and CGS 8216 using the schedule-controlled behavior of rats.利用大鼠的程序控制行为研究苯二氮䓬拮抗剂Ro 15 - 1788和CGS 8216的作用。
Pharmacol Biochem Behav. 1986 Sep;25(3):537-41. doi: 10.1016/0091-3057(86)90137-1.

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