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乙酰胆碱和多巴胺对家兔颈动脉化学感受性活动的影响。

The effects of acetylcholine and dopamine on carotid chemosensory activity in the rabbit.

作者信息

Docherty R J, McQueen D S

出版信息

J Physiol. 1979 Mar;288:411-23.

Abstract
  1. Intracarotid (I.C.) injection of either acetylcholine (ACh) or dopamine inhibited spontaneous chemosensory activity recorded from the peripheral cut end of the sinus nerve in the anaesthetized rabbit. 2. High doses of ACh (greater than or equal to 50 micrograms I.C.) evoked a slight increase in discharge which preceded the inhibition. This excitation was attributable to a nicotinic action of the drug since it was abolished by mecamylamine. 3. The muscarinic agonist bethanechol inhibited chemoreceptor activity, an effect which was blocked by high doses of atropine, as was the inhibition caused by ACh. Dopamine-induced inhibition was unaffected by atropine. 4. Atropine, in doses sufficient to abolish the vasodepressor effect of ACh, only slightly reduced the inhibitory action of ACh on the chemoreceptors. Also, the vasodilators sodium nitrite and sodium nitroprusside did not appreciably alter chemosensory discharge. It seems unlikely, therefore, that the inhibitory response to ACh is secondary to vascular changes. 5. The inhibitory response to dopamine, but not that to ACh, was blocked by the dopamine antagonist alpha-flupenthixol. This implies that inhibition of chemosensory activity evoked by exogenous ACh was not secondary to dopamine release. 6. The implications of the results are discussed, particularly with regard to the possible physiological role of ACh as a modulator of carotid chemosensory activity.
摘要
  1. 向麻醉兔的颈内动脉注射乙酰胆碱(ACh)或多巴胺,均可抑制从窦神经外周切断端记录到的自发化学感受活动。2. 高剂量的ACh(颈内注射大于或等于50微克)在抑制作用之前会引起放电轻微增加。这种兴奋归因于药物的烟碱样作用,因为它可被美加明消除。3. 毒蕈碱激动剂氨甲酰甲胆碱抑制化学感受器活动,高剂量阿托品可阻断此效应,ACh引起的抑制作用也可被其阻断。多巴胺诱导的抑制作用不受阿托品影响。4. 阿托品剂量足以消除ACh的血管减压作用时,仅轻微降低ACh对化学感受器的抑制作用。此外,血管扩张剂亚硝酸钠和硝普钠并未明显改变化学感受放电。因此,对ACh的抑制反应似乎不太可能继发于血管变化。5. 多巴胺拮抗剂α-氟奋乃静可阻断对多巴胺的抑制反应,但不能阻断对ACh的抑制反应。这意味着外源性ACh引起的化学感受活动抑制并非继发于多巴胺释放。6. 讨论了这些结果的意义,特别是关于ACh作为颈动脉化学感受活动调节剂的可能生理作用。
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ef5/1281435/ade6a3d21b64/jphysiol00752-0425-a.jpg

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