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一氧化氮(NO)在控制灌注离体犬回肠环形肌运动中的作用位点。

Sites of nitric oxide (NO) actions in control of circular muscle motility of the perfused isolated canine ileum.

作者信息

Fox-Threlkeld J E, Woskowska Z, Daniel E E

机构信息

School of Nursing, Faculty of Health Sciences, McMaster University, Hamilton, ON Canada.

出版信息

Can J Physiol Pharmacol. 1997 Dec;75(12):1340-9.

PMID:9534944
Abstract

In the isolated intra-arterially perfused canine ileum, N omega -nitro-L-arginine (L-NNA, 3 x 10(-4) M) increased tonic and phasic motor activity of the circular muscle. As has previously been shown, L-NNA enhanced contractions to electrical field stimulation at sites proximal to the serosal electrodes and converted initial relaxation when present at distal sites to contraction. L-NNA shifted the acetylcholine dose-response curve to the left and amplified the response to low-dose acetylcholine. Following L-NNA, addition of 10(-5) M sodium nitroprusside (NO donor) returned the tonic and phasic activity, the electrical field stimulation responses, and the acetylcholine dose-response curve to control values. Tetrodotoxin (TTX, 10(-6) M) increased tone (less than L-NNA) and abolished responses to both electrical field stimulation and motor activity induced by prior L-NNA. Subsequent L-NNA did not alter TTX-induced tonic motor responses. TTX also shifted the acetylcholine dose-response curve leftward and increased the responses to low-dose acetylcholine. After TTX, sodium nitroprusside returned the low-dose acetylcholine responses to control values and, after L-NNA, failed to restore them to control values. After L-NNA and TTX, sodium nitroprusside restored responses to low-dose acetylcholine to control values, Thus, removal of inhibition of the release of excitatory neurotransmitters, not removal of actions of NO on the muscle, accounted for the increases in tonic and phasic activity from L-NNA. Uninhibited release of excitatory transmitters augmented circular muscle responses to low-dose acetylcholine. TTX eliminated effects of excitatory transmitters, allowing exogenous NO to reduce low-dose acetylcholine contractions. No treatment affected the maximum responses to acetylcholine, produced by a contractile mechanism independent of muscle excitability and unaffected by exogenous NO or release of neurotransmitters.

摘要

在离体动脉内灌注的犬回肠中,Nω-硝基-L-精氨酸(L-NNA,3×10⁻⁴ M)增加了环行肌的紧张性和相性运动活性。如先前所示,L-NNA增强了浆膜电极近端部位对电场刺激的收缩,并将远端部位原本的舒张转变为收缩。L-NNA使乙酰胆碱剂量-反应曲线向左移动,并放大了对低剂量乙酰胆碱的反应。给予L-NNA后,添加10⁻⁵ M硝普钠(NO供体)可使紧张性和相性活性、电场刺激反应以及乙酰胆碱剂量-反应曲线恢复至对照值。河豚毒素(TTX,10⁻⁶ M)增加了张力(小于L-NNA),并消除了对电场刺激以及先前L-NNA诱导的运动活性的反应。随后给予的L-NNA并未改变TTX诱导的紧张性运动反应。TTX也使乙酰胆碱剂量-反应曲线向左移动,并增加了对低剂量乙酰胆碱的反应。给予TTX后,硝普钠使低剂量乙酰胆碱反应恢复至对照值,而给予L-NNA后,未能将其恢复至对照值。在给予L-NNA和TTX后,硝普钠将低剂量乙酰胆碱反应恢复至对照值。因此,L-NNA导致紧张性和相性活性增加的原因是去除了对兴奋性神经递质释放的抑制,而非去除了NO对肌肉的作用。兴奋性神经递质的无抑制释放增强了环行肌对低剂量乙酰胆碱的反应。TTX消除了兴奋性神经递质的作用,使外源性NO能够减少低剂量乙酰胆碱引起的收缩。没有任何处理影响乙酰胆碱的最大反应,该最大反应由独立于肌肉兴奋性且不受外源性NO或神经递质释放影响的收缩机制产生。

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