School of Laboratory Medicine and Medical Sciences, College of Health Sciences, University of KwaZulu-Natal, Durban, South Africa.
School of Chemistry and Physics, College of Engineering and Sciences, University of KwaZulu-Natal, Pietermaritzburg, South Africa.
Biomed Pharmacother. 2020 Sep;129:110483. doi: 10.1016/j.biopha.2020.110483. Epub 2020 Jul 10.
Diabetic renal injury advances through different stages of structural and functional changes in the glomerulus, therefore treatment during the pre-diabetic state could be used as therapeutic target in the management and prevention of diabetic nephropathy (DN). Once diagnosed, dietary interventions and pharmacological therapy have been recommended to manage DN and pre-diabetic related complications. However, poor patient compliance still results, therefore newer alternative drugs are required. High fat high carbohydrates (HFHC) diet was used to induce pre-diabetes for 20 weeks. After the induction, pre-diabetic rats were randomly allocated to respective treatment groups. Subcutaneous ruthenium(II) Schiff base complex injection (15 mg/kg) was administered to pre-diabetic rats in both the presence and absence of dietary intervention once a day every third day for 12 weeks. The administration of ruthenium(II) complex resulted in reduced blood glucose, aldosterone, fluid intake and urinary output which correlated with a restoration in plasma and urinary electrolytes along with plasma antioxidants concentration. Furthermore, there was a decrease in kidney injury molecule-1 (KIM-1) concentration, albumin excretion rate (AER) albumin creatinine ratio (ACR) and mRNA expression of podocin in urine in ruthenium-treated pre-diabetic rats. Ruthenium(II) Schiff base complex ameliorated renal function while preventing the progression of DN in prediabetic-treated rats.
糖尿病肾病(DN)的发生和发展是一个连续的过程,在肾小球的结构和功能发生改变之前,会经历不同的阶段。因此,在糖尿病前期进行治疗,可能成为管理和预防 DN 的靶点。一旦被诊断为糖尿病,就会建议采用饮食干预和药物治疗来管理 DN 和相关的糖尿病前期并发症。然而,由于患者的依从性较差,仍需要新的替代药物。本研究采用高脂肪高碳水化合物(HFHC)饮食诱导 20 周的糖尿病前期。诱导成功后,将糖尿病前期大鼠随机分配到各自的治疗组。在存在和不存在饮食干预的情况下,每天给糖尿病前期大鼠皮下注射钌(II)席夫碱络合物(15mg/kg),每三天一次,共 12 周。钌(II)络合物的给药导致血糖、醛固酮、液体摄入和尿液输出减少,这与血浆和尿液电解质以及血浆抗氧化剂浓度的恢复相关。此外,在钌处理的糖尿病前期大鼠中,尿液中的肾损伤分子-1(KIM-1)浓度、白蛋白排泄率(AER)、白蛋白肌酐比(ACR)和 podocin 的 mRNA 表达降低。钌(II)席夫碱络合物改善了肾功能,同时阻止了糖尿病前期大鼠 DN 的进展。