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P物质对猫颈动脉化学感受器活动的影响。

Effects of substance P on carotid chemoreceptor activity in the cat.

作者信息

McQueen D S

出版信息

J Physiol. 1980 May;302:31-47. doi: 10.1113/jphysiol.1980.sp013228.

DOI:10.1113/jphysiol.1980.sp013228
PMID:6157809
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1282833/
Abstract
  1. The influence of substance P (SP) on spontaneous chemosensory discharge and on responses of the carotid chemoreceptors to various drugs has been investigated in pentobarbitone anaesthetized casts in which chemoreceptor activity was recorded from the peripheral end of a sectioned sinus nerve. 2. After an initial slight inhibition during the first 5--15 sec following the injection, SP (0.1--100 microgram I.A.) caused a dose-related increase in discharge which lasted for 45--300 sec in artificially ventilated cats, discharge being increased by about 50% on average. The increase was of shorter duration when the animals were allowed to breathe spontaneously. 3. The delayed increase in discharge was not secondary to the hypotension caused by SP, nor was it entirely due to changes in bronchomotor tone resulting from direct or indirect actions of SP, although such changes contributed to the response. It was not possible to determine whether the excitation was due to a direct effect of SP on the chemoreceptors. 4. Chemosensory excitation evoked by NaCN (5 microgram I.A.) was potentiated during I.A. infusions of SP and also 10--20 min after SP (10 microgram I.A.) had been injected. In contrast, responses to ACh (50 microgram I.A.) were inhibited. These effects may be due to a nicotinic-blocking action of SP on the carotid chemoreceptors. It was also found that the inhibitory action of dopamine (5 microgram I.A.) was reduced during SP infusion whereas that of 5-HT (10 microgram I.A.) was potentiated. 5. A sample of crude SP had effects on spontaneous chemoreceptor discharge and responses to NaCN and ACh which were qualitatively similar to those obtained using synthetic SP. 6. The physiological significance of the results is discussed and it is concluded that the interpretation depends upon whether or not SP is present in the cat's carotid body.
摘要
  1. 研究了P物质(SP)对自发化学感受性放电以及颈动脉化学感受器对各种药物反应的影响。实验采用戊巴比妥麻醉的猫,在切断的窦神经外周端记录化学感受器活动。2. 在注射后最初的5 - 15秒有轻微抑制,之后,腹腔注射0.1 - 100微克的SP可使放电呈剂量依赖性增加,在人工通气的猫中持续45 - 300秒,平均放电增加约50%。当动物自主呼吸时,增加的持续时间较短。3. 放电的延迟增加并非继发于SP引起的低血压,也不完全归因于SP直接或间接作用导致的支气管运动张力变化,尽管这些变化对反应有一定作用。无法确定兴奋是否是由于SP对化学感受器的直接作用。4. 腹腔注射5微克NaCN诱发的化学感受性兴奋在腹腔注射SP期间以及注射10 - 20分钟后增强。相反,对50微克ACh的反应受到抑制。这些作用可能是由于SP对颈动脉化学感受器的烟碱阻断作用。还发现,在输注SP期间,多巴胺(5微克腹腔注射)的抑制作用减弱,而5 - HT(10微克腹腔注射)的作用增强。5. 粗制SP样本对自发化学感受器放电以及对NaCN和ACh的反应,在性质上与合成SP相似。6. 讨论了结果的生理意义,并得出结论,其解释取决于猫的颈动脉体中是否存在SP。

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