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氨基胍治疗对糖尿病诱导的大鼠回肠肌间神经丛变化的影响。

Effect of aminoguanidine treatment on diabetes-induced changes in the myenteric plexus of rat ileum.

作者信息

Shotton Hannah R, Adams Ashok, Lincoln Jill

机构信息

Department of Anatomy and Developmental Biology, University College London, Gower Street, London WC1E 6BT, UK.

出版信息

Auton Neurosci. 2007 Mar 30;132(1-2):16-26. doi: 10.1016/j.autneu.2006.08.007. Epub 2006 Sep 20.

Abstract

The aim of this study was to investigate the ability of aminoguanidine (AG) to prevent diabetes-induced changes in nitric oxide synthase- (nNOS), vasoactive intestinal polypeptide- (VIP) and noradrenaline- (NA) containing nerves of the rat ileum using immunohistochemical and biochemical techniques. Diabetes was induced in adult male Wistar rats by a single intraperitoneal injection of streptozotocin (65 mg/kg). AG was administered in the drinking water to control (1.8 g/l) and diabetic (0.9 g/l) rats over a period of 8 weeks. Diabetes caused a significant increase in the thickness of nNOS-containing nerve fibres (p<0.001) in the circular muscle, in nNOS activity (p<0.05) and in the size distribution of nNOS-containing myenteric neurons (p<0.001). The thickness of VIP-containing nerve fibres was significantly greater (p<0.01) and there was a significant increase in varicosity size (p<0.01) and proportion of VIP-positive myenteric neurons (p<0.01) in diabetes. NA levels were significantly reduced (p<0.01) and the size of varicosities containing tyrosine hydroxylase (TH) was significantly increased (p<0.001) in diabetes. AG treatment completely or partially prevented the diabetes-induced increase in nNOS activity, in VIP-containing varicosity size, and in fibre width of both VIP- and nNOS-containing fibres in the circular muscle but had no effect on the diabetes-induced increase in nNOS-containing neuronal size or proportion of VIP-containing myenteric neurons. In contrast to VIP, AG treatment had no effect on the increase in TH-containing varicosity size in diabetes and also failed to prevent the decrease in NA levels induced by diabetes. These results indicate that AG treatment for neuropathy is not equally effective for all autonomic nerves supplying the ileum and that diabetes-induced changes in NA-containing nerves are particularly difficult to treat.

摘要

本研究旨在利用免疫组织化学和生化技术,研究氨基胍(AG)预防糖尿病引起的大鼠回肠中一氧化氮合酶(nNOS)、血管活性肠肽(VIP)和去甲肾上腺素(NA)能神经变化的能力。通过单次腹腔注射链脲佐菌素(65 mg/kg)诱导成年雄性Wistar大鼠患糖尿病。在8周的时间里,给对照大鼠(1.8 g/l)和糖尿病大鼠(0.9 g/l)饮用含AG的水。糖尿病导致环行肌中含nNOS神经纤维的厚度显著增加(p<0.001)、nNOS活性显著增加(p<0.05)以及含nNOS的肌间神经元大小分布显著增加(p<0.001)。糖尿病时,含VIP神经纤维的厚度显著增加(p<0.01),静脉曲张大小显著增加(p<0.01),VIP阳性肌间神经元比例显著增加(p<0.01)。糖尿病时,NA水平显著降低(p<0.01),含酪氨酸羟化酶(TH)的静脉曲张大小显著增加(p<0.001)。AG治疗完全或部分预防了糖尿病引起的nNOS活性增加、含VIP静脉曲张大小增加以及环行肌中含VIP和nNOS纤维的纤维宽度增加,但对糖尿病引起的含nNOS神经元大小增加或含VIP肌间神经元比例增加没有影响。与VIP不同,AG治疗对糖尿病时含TH静脉曲张大小的增加没有影响,也未能预防糖尿病引起的NA水平降低。这些结果表明,AG治疗神经病变对供应回肠的所有自主神经并非同样有效,且糖尿病引起的含NA神经变化尤其难以治疗。

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