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某些拟胆碱药物对豚鼠盲肠离体绦虫的作用。

The actions of some cholinomimetic drugs on the isolated taenia of the guinea-pig caecum.

作者信息

Hobbiger F, Mitchelson F, Rand M J

出版信息

Br J Pharmacol. 1969 May;36(1):53-69. doi: 10.1111/j.1476-5381.1969.tb08303.x.

Abstract
  1. The actions on the taenia of 4-(m-chlorophenylcarbamoyloxy)-2-butynyl-trimethylammonium chloride (McN-A-343), N-benzyl-3-pyrrolidyl acetate methobromide (AHR-602), tetramethylammonium (TMA) and choline phenyl ether have been examined and compared with the actions of acetylcholine, nicotine and 1,1-dimethyl-4-phenylpiperazinium (DMPP).2. Responses of the taenia to these agonists are quantitatively and often qualitatively dependent on the tone of the preparation. A method is described which makes allowance for the effect of tone on heights of contractions.3. Acetylcholine, McN-A-343 and AHR-602 produced only contractions; TMA produced contractions or biphasic responses; and choline phenyl ether, nicotine and DMPP produced contractions, relaxations or biphasic responses.4. The mode of action of these compounds has been analysed by means of hyoscine, ganglion-blocking drugs, tetrodotoxin and local anaesthetics.5. It is concluded that acetylcholine, McN-A-343, AHR-602, TMA and choline phenyl ether act on muscarinic receptors in the smooth muscle. Choline phenyl ether has an additional action on nicotinic receptors of cholinergic neurones. Nicotine and DMPP act on nicotinic receptors of cholinergic neurones and of inhibitory neurones. An action on the latter is sometimes also seen with TMA and choline phenyl ether.6. With nicotine or DMPP, and TMA or choline phenyl ether in the presence of hyoscine, part of the contraction phase of biphasic responses (in which a contraction follows relaxation) is best explained as being triggered by the initial relaxation-that is, as a "rebound contraction".7. None of the compounds tested appeared to exert an atropine-sensitive action on neurones.8. In the presence of hyoscine high concentrations of agonists can act on sites not involved with lower concentrations.
摘要
  1. 已对4-(间氯苯基氨甲酰氧基)-2-丁炔基-三甲基氯化铵(McN-A-343)、N-苄基-3-吡咯烷基乙酸甲酯溴化物(AHR-602)、四甲铵(TMA)和胆碱苯醚对绦虫的作用进行了研究,并与乙酰胆碱、尼古丁和1,1-二甲基-4-苯基哌嗪鎓(DMPP)的作用进行了比较。

  2. 绦虫对这些激动剂的反应在数量上,且常常在质量上取决于标本的张力。本文描述了一种方法,该方法考虑到了张力对收缩高度的影响。

  3. 乙酰胆碱、McN-A-343和AHR-602仅产生收缩;TMA产生收缩或双相反应;胆碱苯醚、尼古丁和DMPP产生收缩、舒张或双相反应。

  4. 已通过东莨菪碱、神经节阻断药物、河豚毒素和局部麻醉药对这些化合物的作用方式进行了分析。

  5. 得出的结论是,乙酰胆碱、McN-A-343、AHR-602、TMA和胆碱苯醚作用于平滑肌中的毒蕈碱受体。胆碱苯醚对胆碱能神经元的烟碱受体有额外作用。尼古丁和DMPP作用于胆碱能神经元和抑制性神经元的烟碱受体。TMA和胆碱苯醚有时对后者也有作用。

  6. 使用尼古丁或DMPP,以及在东莨菪碱存在下的TMA或胆碱苯醚时,双相反应(其中收缩继以舒张)的部分收缩期最好解释为由初始舒张触发,即作为“反跳性收缩”。

  7. 所测试的化合物似乎均未对神经元发挥阿托品敏感作用。

  8. 在东莨菪碱存在的情况下,高浓度的激动剂可作用于与低浓度时所涉及部位不同的位点。

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Secondary excitation of intestinal smooth muscle.肠道平滑肌的继发性兴奋
Br J Pharmacol. 1971 Feb;41(2):213-26. doi: 10.1111/j.1476-5381.1971.tb08023.x.

本文引用的文献

2
Reversal of nicotine action on the intestine by atropine.阿托品对尼古丁肠道作用的逆转。
Br J Pharmacol Chemother. 1951 Jun;6(2):311-7. doi: 10.1111/j.1476-5381.1951.tb00644.x.
6
INHIBITION OF INTESTINAL SMOOTH MUSCLE.肠平滑肌的抑制
Aust J Exp Biol Med Sci. 1965 Jun;43:277-90. doi: 10.1038/icb.1965.27.

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