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大鼠脊髓中的血管紧张素II及其交感兴奋作用。

Angiotensin II in the spinal cord of the rat and its sympatho-excitatory effects.

作者信息

Lewis D I, Coote J H

机构信息

Department of Physiology, Medical School, University of Birmingham, UK.

出版信息

Brain Res. 1993 Jun 18;614(1-2):1-9. doi: 10.1016/0006-8993(93)91010-p.

Abstract

Immunohistochemical studies have shown there is a dense angiotensin-like immunoreactivity of terminals in the sympathetic region of the thoracic and lumbar spinal cord. In the present study measurements were made of the concentration of angiotensin in the spinal cord of rats using radioimmunoassay following two different extraction procedures. These gave concentrations of angiotensin as mean of 108 and 161 pg.g-1 tissue wet weight. Angiotensin II given intrathecally or microinjected into the spinal cord caused an increase in postganglionic sympathetic nerve activity which was blocked by prior application of saralasin. Angiotensin III was without effect. Intracellular recordings from sympathetic preganglionic neurones in-vitro in slices of neonate rat spinal cord showed that angiotensin II produced an increase of excitability of the neurones by a slow depolarisation without the generation of action potentials. This effect still occurred in the presence of TTX. Angiotensin II also could increase synaptic activity, both EPSPs and IPSPs as well as a synaptically induced slow depolarisation being observed suggesting that presympathetic interneurones are also sensitive to the peptide. The evidence indicates that if angiotensin is released from nerve terminals surrounding sympathetic neurones it will enhance the gain of the neurone so that it could more easily be discharged by other excitatory inputs.

摘要

免疫组织化学研究表明,在胸段和腰段脊髓的交感神经区域,终末存在密集的血管紧张素样免疫反应性。在本研究中,采用两种不同的提取方法后,通过放射免疫分析法对大鼠脊髓中血管紧张素的浓度进行了测量。这些方法测得的血管紧张素浓度分别为每克组织湿重108皮克和161皮克的平均值。鞘内注射或微量注射到脊髓中的血管紧张素II会导致节后交感神经活动增加,而预先应用沙拉新可阻断这种增加。血管紧张素III则无此作用。在新生大鼠脊髓切片中对交感神经节前神经元进行体外细胞内记录显示,血管紧张素II通过缓慢去极化使神经元兴奋性增加,而不产生动作电位。在存在河豚毒素的情况下,这种效应仍然会出现。血管紧张素II还可增加突触活动,观察到兴奋性突触后电位(EPSP)和抑制性突触后电位(IPSP)以及突触诱导的缓慢去极化,这表明交感神经节前中间神经元对该肽也敏感。证据表明,如果血管紧张素从交感神经元周围的神经终末释放,它将增强神经元的增益,使其更容易被其他兴奋性输入所激发。

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