Maxfield E K, Love A, Cotter M A, Cameron N E
Department of Biomedical Sciences, University of Aberdeen, Scotland, United Kingdom.
Am J Physiol. 1995 Sep;269(3 Pt 1):E530-7. doi: 10.1152/ajpendo.1995.269.3.E530.
Effects of the angiotensin II AT1 receptor antagonist ZD-7155 on nerve function, blood flow, capillarization, oxygenation, and regenerative capacity after injury were studied in streptozocin-diabetic rats. Deficits in saphenous sensory and sciatic motor conduction velocity measured after 1 or 2 mo of diabetes in anesthetized rats were prevented and corrected by ZD-7155. Sciatic resistance to hypoxic conduction failure, which was increased by 71% by 2 mo of diabetes, was attenuated by 39% with ZD-7155. Endoneurial capillary density, which was unaffected by diabetes, was increased by 34% with 2 mo of ZD-7155 treatment. Sciatic nutritive endoneurial blood flow, which was reduced by 45% by 2 mo of diabetes, remained in the nondiabetic range with ZD-7155. Mean endoneurial O2 tension was reduced 38% by diabetes, which was attenuated by ZD-7155. Punctate freeze damage of sciatic nerve caused complete fiber degeneration. Fourteen days postlesion, there was a 26% deficit in myelinated fiber regeneration distance after 2 mo of diabetes, which was prevented by ZD-7155 treatment from diabetes induction. Thus alterations in the renin-angiotensin system contribute to the neurovascular etiology of nerve dysfunction in experimental diabetes.
在链脲佐菌素诱导的糖尿病大鼠中,研究了血管紧张素II AT1受体拮抗剂ZD - 7155对损伤后神经功能、血流、毛细血管形成、氧合及再生能力的影响。ZD - 7155可预防并纠正麻醉大鼠糖尿病1或2个月后所测的隐神经感觉和坐骨神经运动传导速度的缺陷。糖尿病2个月使坐骨神经对缺氧传导衰竭的耐受性增加了71%,而ZD - 7155可使其降低39%。糖尿病对神经内膜毛细血管密度无影响,但ZD - 7155治疗2个月可使其增加34%。糖尿病2个月使坐骨神经的营养性神经内膜血流减少45%,而ZD - 7155可使其维持在非糖尿病范围内。糖尿病使神经内膜平均氧张力降低38%,ZD - 7155可使其减轻。坐骨神经点状冷冻损伤导致完全性纤维变性。损伤后14天,糖尿病2个月后有髓纤维再生距离有26%的缺陷,ZD - 7155治疗从糖尿病诱导开始即可预防此缺陷。因此,肾素 - 血管紧张素系统的改变促成了实验性糖尿病中神经功能障碍的神经血管病因。