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己氟铵与大鼠膈肌胆碱能受体的脱敏相互作用。

The desensitizing interaction of hexafluorenium with the cholinergic receptor in the diaphragm of the rat.

作者信息

Scaf A H, Langendijk J W

出版信息

Arch Int Pharmacodyn Ther. 1977 Feb;225(2):196-207.

PMID:849069
Abstract
  1. The interaction of hexafluorenium with acetylcholine, carbachol and suxamethonium with regard to the depolarization of the end-plate of rat diaphragm was studied. The depolarization was measured with the moving meniscus technique of Fatt. The competitive antagonist d-tubocurarine was included in the studies. 2. Hexafluorenium inhibited acetylcholinesterase in the end-plate. 3. The receptors in the end-plate were desensitized by carbachol and suxamethonium. Hexafluorenium enhanced the desensitization by suxamethonium. d-Tubocurarine had no direct influence on desensitization 4. The desensitization of the receptors in rat diaphragm is compatible with a cyclic model of desensitization. 5. The desensitizing interaction of hexafluorenium with the receptors may explain the non-competitive antagonism with depolarizing drugs with regard to the depolarization of the end-plate and the synergism with these drugs with regard to the paralysis of the indirectly stimulated muscle reported earlier. 6. The affinities of carbachol, suxamethonium and d-tubocurarine to the sensitive receptors are 4.9, 5.2 and 6.8, respectively.
摘要
  1. 研究了六氟铵与乙酰胆碱、卡巴胆碱和琥珀酰胆碱在大鼠膈神经终板去极化方面的相互作用。采用法特的移动弯月面技术测量去极化。研究中包括竞争性拮抗剂d -筒箭毒碱。2. 六氟铵抑制终板中的乙酰胆碱酯酶。3. 卡巴胆碱和琥珀酰胆碱使终板中的受体脱敏。六氟铵增强了琥珀酰胆碱引起的脱敏作用。d -筒箭毒碱对脱敏没有直接影响。4. 大鼠膈神经终板中受体的脱敏与脱敏的循环模型相符。5. 六氟铵与受体的脱敏相互作用可能解释了先前报道的在终板去极化方面与去极化药物的非竞争性拮抗作用以及在间接刺激肌肉麻痹方面与这些药物的协同作用。6. 卡巴胆碱、琥珀酰胆碱和d -筒箭毒碱对敏感受体的亲和力分别为4.9、5.2和6.8。

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