van Dam B, Demirci C, Reitsma H J, van Lambalgen A A, van den Bos G C, Tangelder G J, Stehouwer C D
Department of Internal Medicine, Institute for Cardiovascular Research, Vrije Universiteit, Amsterdam, The Netherlands.
Int J Exp Diabetes Res. 2000;1(3):221-32. doi: 10.1155/edr.2000.221.
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 age-matched controls (n = 8), basal inside diameters of A2-A4 arterioles and the reactivity to topically applied acetylcholine and nitroprusside, before and after N(G)-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.
一氧化氮(NO)活性的变化可能在微血管血流早期增加中起重要作用,而微血管血流增加与糖尿病微血管病变的发病机制有关。我们在6周链脲佐菌素诱导的糖尿病大鼠(n = 6)和年龄匹配的对照大鼠(n = 8)的原位斜方肌制备中,评估了N(G)-硝基-L-精氨酸处理前后A2 - A4小动脉的基础内径以及对局部应用乙酰胆碱和硝普钠的反应性。在糖尿病大鼠中,A2 - A4小动脉的胆碱能血管舒张功能完好。链脲佐菌素诱导的糖尿病大鼠A3和A4小动脉的基础直径显著更高。A3小动脉基础直径增加部分归因于NO对基础直径的贡献增加。链脲佐菌素诱导的糖尿病大鼠中,A2小动脉对硝普钠的反应受损,但A3和A4小动脉未受损。因此,本研究表明,链脲佐菌素诱导糖尿病6周后,NO活性和敏感性发生改变。这些链脲佐菌素诱导的变化具有解剖学特异性,对于小动脉而言,取决于它们在血管树中的位置。