Effect of Agmatine on Non-Alcoholic Fatty Liver Disease Induced by Type 2 Diabetes in Rats

Samar F Miski, M. Ahmad, A. Esmat
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引用次数: 1

Abstract

Aim: To determine the potential hepatoprotective effect of Agmatine (AGM) on NAFLD-induced by Type 2 diabetes mellitus (T2DM) in rats. Study design: Forty male Wistar rats weighing from (200 -250 g) were distributed at random into five groups (8 rats per group): group 1 as control; group 2 as untreated-T2DM; groups 3 & 4 as T2DM cotreated with AGM (40 & 80 mg/kg/d), while group 5 T2DM cotreated with Silymarin (100 mg/kg/d). Place and duration of study: Department of Pharmacology, Faculty of Medicine, king Abdul-Aziz University; between October 2020 and January 2021. Methodology: A rat model of T2DM with NAFLD complication was established by feeding rats with 10% fructose in drinking water and intraperitoneally injecting them with a single low dose of streptozotocin (STZ) (45mg/kg). The fasting blood glucose was detected, serum levels of hepatic biomarkers were all assessed. Moreover, histopathological examination was performed by hematoxylin and eosin (H&E) staining. Original Research Article Miski et al.; JPRI, 33(31A): 127-134, 2021; Article no.JPRI.68688 128 Results: STZ induced T2DM in rats causes a significant (p<0.05, n=8) rise in serum levels of FBG, ALT, AST, TB, TC, TG, and LDL in comparison with the corresponding control group. Co-treatment with AGM (40 & 80 mg/kg) and silymarin significantly alleviated hyperglycemia and amended hepatic biomarkers that was reflected on improved histopathological changes. Conclusion: The current data suggest that oral AGM co-treatment could have a hepatoprotective effect against T2DM associated with NAFLD in rats. Further investigations are recommended to elucidate molecular mechanisms accountable for the useful effects of AGM on hepatocytes.
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胍丁氨酸对2型糖尿病大鼠非酒精性脂肪肝的影响
目的:探讨Agmatine (AGM)对2型糖尿病(T2DM)大鼠nafld的潜在保护作用。研究设计:体重(200 ~ 250 g)的雄性Wistar大鼠40只,随机分为5组(每组8只):第一组为对照组;2组为未经治疗的t2dm;3、4组为T2DM, AGM共处理组(40、80 mg/kg/d),水飞蓟素共处理组(100 mg/kg/d)。学习地点和时间:阿卜杜勒-阿齐兹国王大学医学院药学系;2020年10月至2021年1月。方法:以10%果糖灌胃大鼠,腹腔注射低剂量链脲佐菌素(STZ) (45mg/kg),建立T2DM合并NAFLD大鼠模型。检测空腹血糖,评估血清肝脏生物标志物水平。采用苏木精和伊红(H&E)染色进行组织病理学检查。Miski et al.;地球物理学报,33(31):127-134,2021;文章no.JPRI。68688 128结果:STZ诱导T2DM大鼠血清FBG、ALT、AST、TB、TC、TG、LDL水平较对照组显著升高(p<0.05, n=8)。AGM(40和80 mg/kg)和水飞蓟素共同治疗可显著缓解高血糖和改善肝脏生物标志物,这反映在改善的组织病理学变化上。结论:目前的数据表明,口服AGM联合治疗对大鼠T2DM合并NAFLD具有肝保护作用。建议进一步研究以阐明AGM对肝细胞有益作用的分子机制。
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