Iskender Hatice, Dokumacioglu Eda, Terim Kapakin Kubra Asena, Bolat Ismail, Mokhtare Behzat, Hayirli Armagan, Yenice Guler
Faculty of Healthy Sciences, Department of Nutrition and Dietetics, Artvin Coruh University, 08000 Artvin, Turkey.
Department of Pathology, Faculty of Veterinary Medicine, Ataturk University, Erzurum, Turkey.
J Diabetes Metab Disord. 2023 Jan 28;22(1):581-590. doi: 10.1007/s40200-022-01178-x. eCollection 2023 Jun.
Diabetes mellitus (DM) is an important public health problem all over the world, considering its complications and increasing prevalence. Oleanolic acid (OA) has anti-diabetic property via modulating glucose metabolism and acting as 5'-adenosine monophosphate (AMP)-activated protein kinase (AMPK) / Sirtuin-1 (SIRT-1) activator and Interleukin 6 (IL-6) / Nuclear factor kappa B (NF-κB) inhibitor. This research questioned if the OA treatment amliorates the hepatic inflammatory profile in the diabetic rats.
Twenty-eight male Sprague Dawley rats were first subjected to either no diabetes induction (healthy) or diabetes induction by i.p. injection of 50 mg/kg streptozotocin. Then rats in both groups were treated with either tap water or OA (5 mg/kg) within 1 ml tap water by oral gavage for 21 days.
The diabetic rats had higher hepatic MDA (2.88x) and serum AST (2.01x), ALP (2.22x), and ALT (4.27x) levels and 50% lower hepatic SOD level than the healthy rats. The OA treatment significantly reversed these antioxidant parameters in the diabetic rats. The diabetic rats had lower AMPK (85%) and hepatic SIRT-1 (47%) levels and higher hepatic NF-κB (53%) and IL-6 (34%) levels than the healthy rats. Comparing with the health rats, the OA treatment increased hepatic SIRT-1 level, but tended to increase hepatic AMPK level and decrease hepatic NF-κB and IL-6 levels in the diabetic rats. It was also partially effective to ameliorate degenerative changes and necrosis in the diabetic rats.
The OA treatment can be considered to alleviate oxidative stress and reduce severity of inflammation in hepatocytes in the diabetic subjects.
考虑到糖尿病(DM)的并发症及其患病率不断上升,它是一个全球性的重要公共卫生问题。齐墩果酸(OA)具有抗糖尿病特性,可通过调节葡萄糖代谢以及作为5'-单磷酸腺苷(AMP)激活的蛋白激酶(AMPK)/沉默调节蛋白1(SIRT-1)激活剂和白细胞介素6(IL-6)/核因子κB(NF-κB)抑制剂发挥作用。本研究探讨了OA治疗是否能改善糖尿病大鼠的肝脏炎症特征。
28只雄性Sprague Dawley大鼠首先分为未诱导糖尿病组(健康组)或腹腔注射50mg/kg链脲佐菌素诱导糖尿病组。然后,两组大鼠分别通过口服灌胃给予1ml自来水中的自来水或OA(5mg/kg),持续21天。
与健康大鼠相比,糖尿病大鼠的肝脏丙二醛(MDA)水平更高(2.88倍),血清天冬氨酸氨基转移酶(AST)、碱性磷酸酶(ALP)和丙氨酸氨基转移酶(ALT)水平更高(分别为2.01倍、2.22倍和4.27倍),肝脏超氧化物歧化酶(SOD)水平低50%。OA治疗显著逆转了糖尿病大鼠的这些抗氧化参数。与健康大鼠相比,糖尿病大鼠的AMPK水平较低(85%),肝脏SIRT-1水平较低(47%),肝脏NF-κB水平较高(53%),IL-6水平较高(34%)。与健康大鼠相比,OA治疗可提高糖尿病大鼠肝脏SIRT-1水平,但倾向于提高肝脏AMPK水平,并降低肝脏NF-κB和IL-6水平。它对改善糖尿病大鼠的退行性变化和坏死也有部分效果。
OA治疗可被认为能减轻糖尿病患者肝细胞的氧化应激并降低炎症严重程度。