Chen Yijun, Weng Wenci, Zhang Haiyang, Rong Guangli, Yu Xuewen, Wei Qing, Shao Mumin, Cai Yuchun, Han Pengxun, Sun Huili
Department of Nephrology, Shenzhen Traditional Chinese Medicine Hospital, The Fourth Clinical Medical College of Guangzhou University of Chinese Medicine Shenzhen 518033, Guangdong, China.
Department of Nephrology, Shenzhen Traditional Chinese Medicine Hospital Affiliated with Nanjing University of Chinese Medicine Shenzhen 518000, Guangdong, China.
Am J Transl Res. 2022 Jan 15;14(1):211-222. eCollection 2022.
Previous studies have demonstrated that both artemether and enalapril are effective in treating diabetic nephropathy (DN). However, the effects and underlying mechanisms of their combination in treating DN remain unknown. The experimental DN model was induced by injecting streptozotocin (STZ) into male C57BL/6J mice. Mice were randomly allocated to the Type 1 diabetes control (T1D-ctrl), STZ, STZ + artemether (STZ + Art), STZ + enalapril (STZ + ACEi), or STZ + artemether + enalapril (STZ + Art + ACEi) group. The interventions lasted for 8 weeks. At the end of the experiment, related urine and serum biochemical values, such as urinary albumin excretion (UAE) and fasting blood glucose (FBG), were measured. In addition, blood pressure (BP) and kidney morphologic changes were also evaluated. The expression of oxidative stress related molecules, such as catalase, acetylated SOD2 (k68) and acetylated SOD2 (k122) in the kidney were measured. Results: combination therapy showed more pronounced effects in reducing UAE, FBG, and BP than any single drug. Typical diabetic kidney injuries, such as heavier kidney weight, and glomerular and tubular hypertrophy, were also further alleviated by combination therapy. Combination therapy also up-regulated the expression of catalase and down-regulated the expression of acetylated SOD2 (k68) and acetylated SOD2 (k122). Combination therapy with artemether and enalapril exhibited renoprotective effects in STZ-induced T1D mice superior to a single drug. The mechanism might be associated with their synergistic effects in enhancing antioxidant defense.
先前的研究表明,蒿甲醚和依那普利在治疗糖尿病肾病(DN)方面均有效。然而,它们联合治疗DN的效果及潜在机制仍不清楚。通过向雄性C57BL/6J小鼠注射链脲佐菌素(STZ)诱导建立实验性DN模型。将小鼠随机分为1型糖尿病对照组(T1D-ctrl)、STZ组、STZ+蒿甲醚(STZ+Art)组、STZ+依那普利(STZ+ACEi)组或STZ+蒿甲醚+依那普利(STZ+Art+ACEi)组。干预持续8周。实验结束时,测量相关的尿液和血清生化值,如尿白蛋白排泄量(UAE)和空腹血糖(FBG)。此外,还评估了血压(BP)和肾脏形态学变化。检测肾脏中过氧化氢酶、乙酰化超氧化物歧化酶2(k68)和乙酰化超氧化物歧化酶2(k122)等氧化应激相关分子的表达。结果:联合治疗在降低UAE、FBG和BP方面比任何单一药物都有更显著的效果。联合治疗还进一步减轻了典型的糖尿病肾脏损伤,如肾脏重量增加、肾小球和肾小管肥大。联合治疗还上调了过氧化氢酶的表达,下调了乙酰化超氧化物歧化酶2(k68)和乙酰化超氧化物歧化酶2(k122)的表达。蒿甲醚和依那普利联合治疗对STZ诱导的1型糖尿病小鼠具有优于单一药物的肾脏保护作用。其机制可能与其在增强抗氧化防御方面的协同作用有关。