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肾上腺素能受体激动剂和阻滞剂对颈动脉体化学感受性抑制的作用。

Effects of adrenoceptor stimulating and blocking agents on carotid body chemosensory inhibition.

作者信息

Llados F, Zapata P

出版信息

J Physiol. 1978 Jan;274:501-9. doi: 10.1113/jphysiol.1978.sp012163.

Abstract
  1. The effects of alpha- and beta-adrenoceptor agonists and antagonists on chemosensory discharges originating from carotid bodies in situ were studied in anaesthetized cats.2. Noradrenaline (NA) injections commonly resulted in increased frequency of carotid nerve chemosensory discharge, an effect ascribed to reduced blood flow through the glomus, and reduced or eliminated by alpha-adrenergic block.3. NA injections occasionally produced an initial reduction of chemosensory discharge frequency, which was however less intense and of shorter duration than that caused by dopamine. This effect of NA is not mediated by alpha-adrenoceptors, since it is not blocked by dibenamine, but probably by low affinity for dopamine receptors.4. Dopamine and apomorphine-elicited chemosensory inhibition were not affected by low doses of phenoxybenzamine, which blocked NA-evoked hypertensive reactions.5. Higher doses of phenoxybenzamine and dibenamine produced a displacement to the right of dose-response curves for dopamine- and apormorphine-elicited chemosensory inhibition. However, this interference by alpha-adrenergic blockers was attributed to the resultant hypotension, since it was reversed upon restoration of blood pressure.6. Isoprenaline, a beta-adrenergic agonist, did not induce chemosensory inhibition, whilst beta-adrenergic blockers (propranolol and dichloroisoproterenol) did not modify dopamine- and apomorphine-elicited chemosensory inhibition.7. These results provide further support for the hypothesis that chemosensory inhibition could be mediated by specific dopamine receptors, distinct from alpha- and beta-adrenoceptors.
摘要
  1. 在麻醉猫身上研究了α和β肾上腺素能激动剂及拮抗剂对源自原位颈动脉体的化学感受性放电的影响。

  2. 注射去甲肾上腺素(NA)通常会导致颈动脉神经化学感受性放电频率增加,这种效应归因于通过球状体的血流减少,并且可被α肾上腺素能阻滞所减弱或消除。

  3. 注射NA偶尔会使化学感受性放电频率最初降低,然而这种降低的强度比多巴胺引起的要小且持续时间更短。NA的这种效应不是由α肾上腺素能受体介导的,因为它不会被双苄胺阻断,但可能是由于对多巴胺受体的低亲和力。

  4. 低剂量的苯氧苄胺可阻断NA诱发的高血压反应,但不影响多巴胺和阿扑吗啡引起的化学感受性抑制。

  5. 较高剂量的苯氧苄胺和双苄胺使多巴胺和阿扑吗啡引起的化学感受性抑制的剂量反应曲线向右移位。然而,α肾上腺素能阻滞剂的这种干扰归因于由此导致的低血压,因为在血压恢复后这种干扰就会逆转。

  6. β肾上腺素能激动剂异丙肾上腺素不会诱导化学感受性抑制,而β肾上腺素能阻滞剂(普萘洛尔和二氯异丙肾上腺素)不会改变多巴胺和阿扑吗啡引起的化学感受性抑制。

  7. 这些结果为化学感受性抑制可能由不同于α和β肾上腺素能受体的特定多巴胺受体介导这一假说提供了进一步的支持。

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J Histochem Cytochem. 1971 Oct;19(10):621-6. doi: 10.1177/19.10.621.
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