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大鼠离体胃片:一种用于研究胃酸分泌生理和药理学的体外模型。

The rat isolated stomach sheet; an in vitro model for the study of the physiology and pharmacology of gastric acid secretion.

作者信息

Spencer J

出版信息

J Pharmacol Methods. 1982 Nov;8(3):197-212. doi: 10.1016/0160-5402(82)90074-2.

Abstract

The development of an isolated stomach preparation from immature rats is described. Acid secretion was measured by titration of mucosal samples taken at 15 min intervals. Nonstimulated acid secretion was generally in the range 60-180 mumol H+g-1 wet weight of mucosa hr-1 and was maintained for up to 5.5 hr. A small proportion of stomachs (20%) had a higher level of spontaneous secretion which fell to the more usual low level within 1.5 hr. Pentagastrin (1.3 X 10(-8) M-1.3 X 10(-7) M), bethanechol (2 X 10(-6) M-3 X 10(-5) M), histamine (5 X 10(-6) M-5 X 10(-4) M) and theophylline (2 X 10(-4) M-1 X 10(-3) M) induced concentration-dependent stimulation of acid secretion. Linear log-dose response relationships were obtained for each of the four stimulants. The regression coefficients from each drug study, calculated over a similar increase in concentration, were not significantly different from one another. The maximal secretory rates recorded with the four secretagogues were comparable, range 152.5-226.0 mumol H+g-1hr-1. The methodology and results are compared with other mammalian in vitro stomach preparations currently used to study the physiology and pharmacology of gastric acid secretion.

摘要

本文描述了从未成熟大鼠制备离体胃标本的方法。通过每隔15分钟采集黏膜样本进行滴定来测量胃酸分泌。未刺激状态下的胃酸分泌一般在60 - 180 μmol H⁺·g⁻¹黏膜湿重·小时⁻¹范围内,并可持续长达5.5小时。一小部分胃(20%)有较高水平的自发分泌,在1.5小时内降至更常见的低水平。五肽胃泌素(1.3×10⁻⁸ M - 1.3×10⁻⁷ M)、氨甲酰甲胆碱(2×10⁻⁶ M - 3×10⁻⁵ M)、组胺(5×10⁻⁶ M - 5×10⁻⁴ M)和茶碱(2×10⁻⁴ M - 1×10⁻³ M)可诱导胃酸分泌的浓度依赖性刺激。四种刺激物均呈现线性对数剂量反应关系。在浓度类似增加范围内计算的每种药物研究的回归系数彼此之间无显著差异。四种促分泌剂记录的最大分泌率相当,范围为152.5 - 226.0 μmol H⁺·g⁻¹·小时⁻¹。将该方法和结果与目前用于研究胃酸分泌生理和药理的其他哺乳动物体外胃标本进行了比较。

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