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美加明对体内颈动脉体化学感受器对生理和药理刺激反应的影响。

Effects of mecamylamine on responses of carotid body chemoreceptors in vivo to physiological and pharmacological stimuli.

作者信息

Sampson S R

出版信息

J Physiol. 1971 Feb;212(3):655-66. doi: 10.1113/jphysiol.1971.sp009348.

Abstract
  1. Effects of mecamylamine on the spontaneous discharge rate of afferent fibres of carotid body chemoreceptors in vivo and their responses to ACh, NaCN, HCl and hypoxia were studied in sixteen cats.2. Cats were anaesthetized with sodium pentobarbitone, paralysed with gallamine triethiodide and artificially ventilated. Chemoreceptor excitants were injected into the common carotid artery; mecamylamine was given intravenously.3. Mecamylamine, 230 mug/kg or greater, failed to diminish either the rate of spontaneous discharge of carotid body chemoreceptors at high arterial oxygen tensions (greater than 130 mm Hg), or the responses of these receptors to NaCN (0.5-25 mug), HCl or hypoxic blood.4. Responses of chemoreceptor afferent fibres to ACh (1.0-50 mug) in the same preparations were either completely abolished or considerably reduced by mecamylamine.5. These data do not support the hypothesis of a cholinergic mechanism for the initiation of chemosensory discharges in the carotid body, either at rest or in response to stimuli such as NaCN, acid or hypoxia.
摘要
  1. 在16只猫身上研究了美加明对体内颈动脉体化学感受器传入纤维自发放电率及其对乙酰胆碱、氰化钠、盐酸和低氧反应的影响。

  2. 猫用戊巴比妥钠麻醉,用三碘季铵酚使其麻痹,并进行人工通气。化学感受器兴奋药注入颈总动脉;美加明静脉给药。

  3. 230微克/千克或更高剂量的美加明,既不能降低高动脉氧分压(大于130毫米汞柱)时颈动脉体化学感受器的自发放电率,也不能降低这些感受器对氰化钠(0.5 - 25微克)、盐酸或低氧血的反应。

  4. 在相同的标本中,化学感受器传入纤维对乙酰胆碱(1.0 - 50微克)的反应被美加明完全消除或显著降低。

  5. 这些数据不支持在静息状态或对诸如氰化钠、酸或低氧等刺激作出反应时,颈动脉体化学感觉放电起始存在胆碱能机制的假说。

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Mecamylamine and its mode of action.美加明及其作用方式。
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