B. vanDam, C. Demirci, H. Reitsma, A. V. van Lambalgen, G. C. van den Bos, G. Tangelder, C. Stehouwer
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引用次数: 8
摘要
一氧化氮活性的变化可能在微血管流动的早期增加中起重要作用,微血管流动与糖尿病微血管病变的发病机制有关。我们在6周的链脲唑霉素糖尿病大鼠(n = 6)和对照组(n = 8)的斜方肌原位制备中,评估了ng -硝基- l -精氨酸前后,A2-A4小动脉的基本内径和对乙酰胆碱和硝普苷外用的反应性。糖尿病大鼠A2-A4小动脉胆碱能血管舒张功能完好。链脲佐菌素糖尿病大鼠A3和A4小动脉基底直径明显增大。A3小动脉基底直径增加的部分原因是一氧化氮对基底直径的贡献增加。链脲佐菌素糖尿病大鼠对硝普塞的反应在A2小动脉中受损,但在A3和A4小动脉中没有受损。因此,本研究表明,在链脲佐菌素诱导的糖尿病6周后,NO活性和敏感性发生了改变。这些链脲佐菌素引起的变化在解剖学上是特异性的,对于小动脉来说,这取决于它们在血管树中的位置。
Alterations in Nitric Oxide Activity and Sensitivity in Early Streptozotocin-Induced Diabetes Depend on Arteriolar Size
Changes in NO activity may play an important role in the early increase in microvascular flow that has been implicated in the pathogenesis of diabetic microangiopathy. We assessed, in the in situ spinotrapezius muscle preparation of 6 weeks' streptozotocin-diabetic rats (n = 6) and of agematched controls (n = 8), basal inside diameters of A2–A4 arterioles and the reactivity to topically applied acetylcholine and nitroprusside, before and after NG-nitro-L-arginine. In diabetic rats, cholinergic vasodilatation in A2–A4 arterioles was intact. Basal diameter in A3 and A4 arterioles was significantly higher in streptozotocin-diabetic rats. The increased basal diameter in A3 arterioles was partially due to an increased contribution of NO to basal diameter. The response to nitroprusside was impaired in streptozotocin-diabetic rats in A2, but not in A3 and A4 arterioles. Thus, this study shows that NO activity and sensitivity are altered after 6 weeks of streptozotocin-induced diabetes. These streptozotocin-induced changes are anatomically specific and, for arterioles, depend on their position within the vascular tree.