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健康豚鼠与经电离辐射的豚鼠结肠对某些致痉剂及其拮抗剂反应性的比较研究。

Comparative studies of colon reactivity of healthy and ionization-radiated guinea-pigs to some spasmogens and their antagonists.

作者信息

Petkov V, Todorov S, Donev N, Belokonski I

出版信息

Acta Physiol Pharmacol Bulg. 1978;4(1):26-37.

PMID:726912
Abstract

Comparative studies were carried out of the contractile effects of acetylcholine (1 X 10(-6) M), histamine (1 X 10(-6) M), serotonin (1 X 10(-5) M), nicotine (1 X 10(-5) M), BaCl2 (1 X 10(-3) M) and of the influence on the induced contractions caused by the antagonists of these spasmogens, namely: atropin (1 X 10(-6) M), dipenhydramine (1 X 10(-6) M), benzyloxygramine (1 X 10(-5) M), hexamethonium (1 X 10(-5) M) and papaverine (1 x 10(-5) M) on isolated segment of guinea-pig colon. Experimental acute radiation sickness is found to induce considerable changes in the reactivity of the intestinal smooth-muscle preparation used to the spasmogens applied and to their antagonists. Depending on the nature of the pharmacological agents, the degree of development of the experimental acute radiation sickness, and on other factors, the changes in the reactivity to the drugs tested revealed very great qualitative and quantitative differences. The following more definite changes could be pointed out. The spastic effects of serotonin and BaCl2 were potentiated, while the spastic effects of histamine and nicotine showed a tendency toward decrease. Under conditions of acute radiation sickness tha antagonistic effect of atropine to acetylcholine was intensified, while the antagonistic effects of benzyloxygramine to serotonin, of hexamethonium to nicotine and of papaverine to BaCl2, grew weaker. Diphenhydramine showed potentiated antagonistic effect to histamine on the 72nd h after radiation. Certain possibilities are discussed concerning the mechanisms underlying the changes in the reactivity of the intestinal smooth muscle to pharmacological agents, induced by acute radiation sickness.

摘要

对乙酰胆碱(1×10⁻⁶M)、组胺(1×10⁻⁶M)、5-羟色胺(1×10⁻⁵M)、尼古丁(1×10⁻⁵M)、氯化钡(1×10⁻³M)的收缩作用以及这些致痉剂拮抗剂,即阿托品(1×10⁻⁶M)、苯海拉明(1×10⁻⁶M)、苄氧胺(1×10⁻⁵M)、六甲铵(1×10⁻⁵M)和罂粟碱(1×10⁻⁵M)对豚鼠结肠离体段诱发收缩的影响进行了比较研究。发现实验性急性放射病会使所用肠平滑肌制剂对所施加的致痉剂及其拮抗剂的反应性发生相当大的变化。根据药理剂的性质、实验性急性放射病的发展程度以及其他因素,对所测试药物反应性的变化显示出非常大的质和量的差异。可以指出以下更明确的变化。5-羟色胺和氯化钡的痉挛作用增强,而组胺和尼古丁的痉挛作用呈下降趋势。在急性放射病条件下,阿托品对乙酰胆碱的拮抗作用增强,而苄氧胺对5-羟色胺、六甲铵对尼古丁、罂粟碱对氯化钡的拮抗作用减弱。苯海拉明在放射后第72小时对组胺显示出增强的拮抗作用。讨论了急性放射病引起肠平滑肌对药理剂反应性变化的潜在机制的某些可能性。

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Acta Physiol Pharmacol Bulg. 1978;4(1):26-37.
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