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腺苷受体对大鼠回肠升、降神经反射反应的调节作用。

Modulatory effect of adenosine receptors on the ascending and descending neural reflex responses of rat ileum.

作者信息

Storr Martin, Thammer Jutta, Dunkel Ralf, Schusdziarra Volker, Allescher Hans-Dieter

机构信息

Department of Internal Medicine II, Technical University of Munich, Ismaningerstrasse 22, 81675 Munich, Germany.

出版信息

BMC Neurosci. 2002 Dec 20;3:21. doi: 10.1186/1471-2202-3-21.

Abstract

BACKGROUND

Adenosine is known to act as a neuromodulator by suppressing synaptic transmission in the central and peripheral nervous system. Both the release of adenosine within the small intestine and the presence of adenosine receptors on enteric neurons have been demonstrated. The aim of the present study was to characterize a possible involvement of adenosine receptors in the modulation of the myenteric reflex. The experiments were carried out on ileum segments 10 cm in length incubated in an single chambered organ bath, and the reflex response was initiated by electrical stimulation (ES).

RESULTS

ES caused an ascending contraction and a descending relaxation followed by a contraction. All motility responses to ES were completely blocked by tetrodotoxin, indicating that they are mediated by neural mechanisms. Atropine blocked the contractile effects, whereas the descending relaxation was significantly increased. The A1 receptor agonist N6-cyclopentyladenosine increased the ascending contraction, whereas the ascending contraction was reduced by the A1 receptor antagonist 8-cyclopentyl-1,3-dipropylxanthine. Activation of the A1 receptor further reduced the descending relaxation and the latency of the peristaltic reflex. The A2B receptor antagonist alloxazine increased ascending contraction, whereas descending relaxation remained unchanged. For A2A and A3 receptors, we found contradictory effects of the agonists and antagonists, thus there is no clear physiological role for these receptors at this time.

CONCLUSIONS

This study suggests that the myenteric ascending and descending reflex response of the rat small intestine is modulated by release of endogenous adenosine via A1 receptors.

摘要

背景

已知腺苷通过抑制中枢和外周神经系统的突触传递来发挥神经调质的作用。小肠内腺苷的释放以及肠神经元上腺苷受体的存在均已得到证实。本研究的目的是确定腺苷受体在肌间反射调节中可能的作用。实验在单腔器官浴槽中孵育的10厘米长的回肠段上进行,反射反应由电刺激(ES)引发。

结果

电刺激引起先升后降的收缩,随后是一次收缩。对电刺激的所有运动反应均被河豚毒素完全阻断,表明它们是由神经机制介导的。阿托品阻断了收缩效应,而降性松弛显著增强。A1受体激动剂N6-环戊基腺苷增加了升性收缩,而A1受体拮抗剂8-环戊基-1,3-二丙基黄嘌呤则降低了升性收缩。A1受体的激活进一步缩短了降性松弛和蠕动反射的潜伏期。A2B受体拮抗剂咯嗪增加了升性收缩,而降性松弛保持不变。对于A2A和A3受体,我们发现激动剂和拮抗剂的作用相互矛盾,因此目前这些受体尚无明确的生理作用。

结论

本研究表明,大鼠小肠的肌间升性和降性反射反应受内源性腺苷通过A1受体释放的调节。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f066/139982/2bc556aa9ece/1471-2202-3-21-1.jpg

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