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Molecular Mechanisms and Treatment Strategies in Diabetic Nephropathy: New Avenues for Calcium Dobesilate—Free Radical Scavenger and Growth Factor Inhibition

机译:糖尿病肾病的分子机制和治疗策略:苯磺酸硅钙的新途径-自由基清除剂和生长因子抑制

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摘要

Diabetic nephropathy is one of the most important microvascular complications of diabetes mellitus and is responsible for 40–50% of all cases of end stage renal disease. The therapeutic strategies in diabetic nephropathy need to be targeted towards the pathophysiology of the disease. The earlier these therapeutic strategies can bring about positive effects on vascular changes and prevent the vasculature in patients with diabetes from deteriorating, the better the renal function can be preserved. Studies evaluating anti-inflammatory and antioxidative strategies in diabetic nephropathy demonstrate the need and value of these novel treatment avenues. CaD is an established vasoactive and angioprotective drug that has shown a unique, multitarget mode of action in several experimental studies and in different animal models of diabetic microvascular complications. On the molecular level, CaD reduces oxidative stress and inhibits growth factors such as fibroblast growth factor and vascular endothelial growth factors. Recent findings have demonstrated a strong rationale for its use in reducing urine albumin excretion rate and markers of inflammation as well as improving endothelial function. Its beneficial effects make it an attractive therapeutic compound especially in the early stages of the disease. These findings, although promising, need further confirmation in prospective clinical trials with CaD.
机译:糖尿病肾病是糖尿病最重要的微血管并发症之一,占所有终末期肾脏疾病病例的40–50%。糖尿病肾病的治疗策略需要针对该疾病的病理生理学。这些治疗策略越早对血管变化产生积极影响并防止糖尿病患者的脉管系统恶化,就可以更好地保留肾脏功能。评估糖尿病性肾病中抗炎和抗氧化策略的研究证明了这些新颖治疗途径的必要性和价值。 CaD是一种成熟的血管活性和血管保护药物,在多项实验研究和糖尿病微血管并发症的不同动物模型中均显示出独特的多靶点作用模式。在分子水平上,CaD减少氧化应激并抑制生长因子,例如成纤维细胞生长因子和血管内皮生长因子。最近的发现证明了其在降低尿白蛋白排泄率和炎症标志物以及改善内皮功能方面的强大理由。它的有益作用使其成为有吸引力的治疗化合物,尤其是在疾病的早期阶段。这些发现尽管很有希望,但在前瞻性CaD临床试验中需要进一步证实。

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