Effect of Nano-eugenol and Aerobic Exercise Against the Streptozotocin Toxicity and Inflammatory Mediators P38-MAPK, NPY, and A-Rα2A in the Dorsal Root Ganglia of Diabetic Rats

Q4 Pharmacology, Toxicology and Pharmaceutics
Abbas Shareghi boroujeni, K. J. Dehkordi, G. Sharifi, F. Taghian, Z. Mazaheri
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引用次数: 3

Abstract

Background: The aim of this study was to investigate the effects of nano-eugenol combined with aerobic exercise against the streptozotocin toxicity and inflammatory mediators P38-MAPK, NPY and A-Rα2A in the dorsal root ganglia of diabetic rats. Methods: Twenty-five, 8-week-old Wistar male rats were divided into 5 groups: 1) normal control group (normal model); 2) diabetic control group (diabetic model); 3), diabetic + exercise group (diabetic+exercise model); 4) diabetic group + nano-eugenol (diabetic+nano model); and 5) diabetic + exercise + nano-eugenol (diabetic+exercise+nano model). Diabetes was induced in the experimental groups 2 through 5 by the intraperitoneal injection of streptozotocin at 4mg/100 grams of the rats’ body weight. The nano-eugenol supplement was also gavaged into the supplement groups 4 and 5 only. Groups 3 and 5 exercised progressively at a speed of 8 to 20 meter/min for 5 to 30 min, five days a week over the 8-week study duration. Results: The diabetic rats that exercised and were treated with the nano-eugenol, showed a significant decrease in P38-MAPK gene expression compared to the normal model group (P=0.001). The study of the therapeutic modalities also showed that only the diabetic + exercise + nano-eugenol group showed a significant increase in NPY and A-Rα2A genes compared to the normal model (P=0.001). Conclusion: Based on the results, the use of nano-eugenol supplementation combined with aerobic exercise is likely to be effective in controlling the neurological damages due to diabetes by negatively regulating the P38-MAPK gene while positively regulating the NPY and A-Rα2A genes in the DRG region.
纳米丁香酚和有氧运动对糖尿病大鼠背根神经节中链脲佐菌素毒性及炎症介质P38-MAPK、NPY和a - r - α 2a的影响
背景:本研究旨在探讨纳米丁香酚联合有氧运动对糖尿病大鼠背根神经节链脲佐菌素毒性和炎症介质P38-MAPK、NPY和A-Rα2A的影响。方法:25只8周龄Wistar雄性大鼠分为5组:1)正常对照组(正常模型);2) 糖尿病对照组(糖尿病模型);3) 糖尿病+运动组(糖尿病+运动模型);4) 糖尿病组+纳米丁香酚(糖尿病+纳米模型);5)糖尿病+运动+纳米丁香酚(糖尿病+运动+nano模型)。实验组2-5通过腹膜内注射4mg/100g大鼠体重的链脲佐菌素诱导糖尿病。纳米丁香酚补充剂也仅被灌胃到补充剂组4和5中。第3组和第5组在8周的研究期间每周5天,以8至20米/分钟的速度进行5至30分钟的渐进式运动。结果:运动和纳米丁香酚治疗的糖尿病大鼠,与正常模型组相比,P38-MAPK基因表达显著降低(P=0.001)。治疗模式的研究还表明,只有糖尿病+运动+纳米丁香酚组的NPY和a-Rα2A基因与正常模型相比显著增加(P=0.001,纳米丁香酚补充与有氧运动相结合的使用可能通过负调控P38-MAPK基因而正调控DRG区域的NPY和A-Rα。
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来源期刊
Iranian Journal of Toxicology
Iranian Journal of Toxicology Environmental Science-Health, Toxicology and Mutagenesis
CiteScore
1.60
自引率
0.00%
发文量
24
审稿时长
9 weeks
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