首页> 美国卫生研究院文献>British Journal of Pharmacology and Chemotherapy >Effect of M40403 treatment of diabetic rats on endoneurial blood flow motor nerve conduction velocity and vascular function of epineurial arterioles of the sciatic nerve
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Effect of M40403 treatment of diabetic rats on endoneurial blood flow motor nerve conduction velocity and vascular function of epineurial arterioles of the sciatic nerve

机译:M40403对糖尿病大鼠的治疗对坐骨神经神经内膜血流量运动神经传导速度和血管神经功能的影响

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摘要

class="enumerated" style="list-style-type:decimal">To further explore the effect of antioxidants in preventing diabetes-induced vascular and neural dysfunction we treated streptozotocin-induced diabetic rats daily with subcutaneous injections of 10 mg kg−1 of M40403 (n=11) and compared the results obtained from 17 control rats and 14 untreated diabetic rats. M40403 is a manganese(II) complex with a bis(cyclo-hexylpyridine)-substituted macrocyclic ligand that was designed to be a selective functional mimetic of superoxide dismutase. Thus, M40403 provides a useful tool to evaluate the roles of superoxide in disease states.Treatment with M40403 significantly improved diabetes-induced decrease in endoneurial blood flow, acetylcholine-mediated vascular relaxation in arterioles that provide circulation to the region of the sciatic nerve, and motor nerve conduction velocity (P<0.05). M40403 treatment also reduced the appearance of superoxide in the aorta and epineurial vessels and peroxynitrite in epineurial vessels. Treating diabetic rats with M40403 reduced the diabetes-induced increase in thiobarbituric acid reactive substances in serum but did not prevent the decrease in lens glutathione level. Treating diabetic rats with M40403 did not improve sciatic nerve Na+/K+ ATPase activity or the sorbitol, fructose or myo-inositol content of the sciatic nerve.These studies provide additional evidence that diabetes-induced oxidative stress and the generation of superoxide and perhaps peroxynitrite may be partially responsible for the development of diabetic vascular and neural complications.
机译:class =“ enumerated” style =“ list-style-type:decimal”> <!-list-behavior =枚举前缀-word = mark-type = decimal max-label-size = 0-> 为了进一步探讨抗氧化剂在预防糖尿病引起的血管和神经功能障碍中的作用,我们每天皮下注射10μmgkg −1 M40403(n = 11)来治疗链脲佐菌素诱导的糖尿病大鼠,并比较从17只对照大鼠和14只未治疗的糖尿病大鼠获得的结果。 M40403是具有双(环己基吡啶)取代的大环配体的锰(II)配合物,被设计为超氧化物歧化酶的选择性功能模拟物。因此,M40403为评估超氧化物在疾病状态中的作用提供了有用的工具。 用M40403治疗可显着改善糖尿病引起的神经内膜血流量减少,乙酰胆碱介导的小动脉血管舒张,从而为血液循环提供动力。坐骨神经区域和运动神经传导速度(P <0.05)。 M40403处理还减少了主动脉和肾小管血管中超氧化物的出现以及肾小管血管中过氧亚硝酸盐的出现。用M40403治疗糖尿病大鼠可减少糖尿病引起的血清硫代巴比妥酸反应性物质的增加,但不能阻止晶状体谷胱甘肽水平的降低。用M40403治疗糖尿病大鼠并不能改善坐骨神经Na + / K + ATPase的活性或坐骨神经的山梨糖醇,果糖或肌醇含量。 这些研究提供了额外的证据,表明糖尿病引起的氧化应激以及超氧化物和过氧亚硝酸盐的产生可能是糖尿病血管和神经并发症发展的部分原因。

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