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分离的胃平滑肌细胞上的胃动素受体。

Motilin receptors on isolated gastric smooth muscle cells.

作者信息

Louie D S, Owyang C

机构信息

Department of Internal Medicine, University of Michigan Medical Center, Ann Arbor 48109.

出版信息

Am J Physiol. 1988 Feb;254(2 Pt 1):G210-6. doi: 10.1152/ajpgi.1988.254.2.G210.

Abstract

Motilin has a stimulating effect on gastrointestinal motility. The mechanism of its action is not known. Direct and neuronal effects have been postulated. To determine if receptors are present on smooth muscle cells we investigated the effect of synthetic porcine motilin and its interaction with acetylcholine on isolated guinea pig gastric smooth muscle cells. Motilin elicited a dose-dependent contraction of gastric smooth muscle cells. Minimal (8.3 +/- 1.3%) and maximal (33.9 +/- 2.4%) responses were observed at 10(-12) and 10(-6) M, respectively. The ED50 of motilin was 10(-9) M. Acetylcholine also elicited a dose-response muscle contraction with a maximal response observed at 10(-7) M. Atropine (10(-7) M) completely inhibited the maximal response to acetylcholine but did not have any effect on the contractile response to motilin. In addition, dibutyryl guanosine 3',5'-cyclic monophosphate (10(-3) M) and substance P antagonist, spantide (10(-4) M), also did not inhibit the action of motilin. Acetylcholine (10(-11) M) shifted the dose-response curve of motilin to the left by 1.5 log units. The maximal response to the combination of motilin (10(-6) M) and acetylcholine (10(-11) M) was 32 +/- 3.2%, which was similar to the maximal response to motilin alone. It is concluded that distinct motilin and muscarinic receptors are present on guinea pig gastric smooth muscle cells. The interaction between motilin and acetylcholine is additive and not potentiative.

摘要

胃动素对胃肠蠕动有刺激作用。其作用机制尚不清楚。有人提出了直接作用和神经作用的假设。为了确定平滑肌细胞上是否存在受体,我们研究了合成猪胃动素的作用及其与乙酰胆碱对分离的豚鼠胃平滑肌细胞的相互作用。胃动素引起胃平滑肌细胞剂量依赖性收缩。分别在10^(-12)和10^(-6)M时观察到最小(8.3±1.3%)和最大(33.9±2.4%)反应。胃动素的半数有效剂量为10^(-9)M。乙酰胆碱也引起剂量反应性肌肉收缩,在10^(-7)M时观察到最大反应。阿托品(10^(-7)M)完全抑制了对乙酰胆碱的最大反应,但对胃动素的收缩反应没有任何影响。此外,二丁酰鸟苷3',5'-环一磷酸(10^(-3)M)和P物质拮抗剂,spantide(10^(-4)M),也不抑制胃动素的作用。乙酰胆碱(10^(-11)M)使胃动素的剂量反应曲线向左移动1.5个对数单位。胃动素(10^(-6)M)和乙酰胆碱(10^(-11)M)组合的最大反应为32±3.2%,与单独使用胃动素的最大反应相似。结论是豚鼠胃平滑肌细胞上存在不同的胃动素和毒蕈碱受体。胃动素和乙酰胆碱之间的相互作用是相加的,而不是增强的。

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