α-硫辛酸对1型糖尿病大鼠脑组织MDA含量及组织学的影响

Rania Arif Mahfud, D. Lyrawati, Imam Sarwono
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引用次数: 2

摘要

背景。糖尿病性神经病是一种可以影响锥体细胞和海马神经元细胞的疾病。硫辛酸在涉及活性氧(ROS)的病理条件下有效,包括在大脑中。目标。探讨ALA对糖尿病雄性Wistar大鼠脑氧化应激的影响。方法。本研究采用真实实验设计和纯后测对照组。将30只雄性大鼠随机分为5组:不含ALA的正常大鼠(NTA)、不含ALA的糖尿病大鼠(DTA)、ALA给药80 mg、ALA给药200 mg、ALA给药500 mg/kg/d。ALA治疗小鼠,每天口服一次。以60 mg/kg体重单次腹腔注射链脲佐菌素(STZ)诱导大鼠糖尿病。用分光光度法测定脑内丙二醛(MDA)含量。用苏木精和伊红染色评价脑结构(海马锥体细胞)。结果。DTA组、DA80组、DA200组MDA水平高于NTA组,但MDA值差异无统计学意义(p = 0.260)。NTA组、DA80组和DA200组与MDA呈弱正相关(r = 0.327)。NTA与DTA在锥体细胞结构上无差异。结论。ALA治疗4周后,糖尿病脑内氧化应激无明显降低。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
EFFECT OF ALPHA LIPOIC ACID ON MDA LEVELS AND HISTOLOGY OF BRAIN IN TYPE 1 DM
Background. Diabetic neuropaty is a condition that can affect pyramidal cells and neuronal cells in the  hippocampus. Alpha lipoic acid is effective in pathological conditions where ROS (Reactive Oxygen Species)  have been implicated, include in brain. Objective. To investigate effects of ALA on oxidative stress in diabetic brain of male Wistar rats. Methods. True experimental design and Posttest Only Control Group are used in this study. Thirty male rats were randomly divided into 5 groups: normal rats without ALA (NTA), diabetic rats without ALA (DTA), diabetic rats with ALA 80 mg, ALA dose 200 mg, and ALA dose 500 mg/kg/day. ALA therapy in mice conducted orally once a day. Diabetes was induced in rats by single intraperitonial injection of streptozotocin (STZ) at 60 mg/kg body weight. The content of malondialdehyde (MDA) in the brain was measured by spectrophotometeric assays. Brain structure (pyramidal cell in hippocampus) was assessed by staining with hematoxylin and eosin. Results. MDA levels in the DTA, DA80 and DA200 is greater than the levels of MDA in the NTA group, but not statistically significant at the MDA values (p = 0,260). Test-Product Moment Pearson correlation showed a weak positive relationship and not significant (r = 0,327) between the groups of NTA, DA80 and DA200 with MDA. No differences pyramidal cell structure between NTA and DTA. Conclusion. The treatment for 4 weeks with ALA had not reduced oxidative stress in diabetic brain.
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