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Design and optimization strategies for the development of new drugs that treat chronic kidney disease

机译:治疗慢性肾病的新药开发的设计与优化策略

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Introduction: Chronic kidney disease (CKD) is characterized by increased risks of progression to end-stage kidney disease requiring dialysis and cardiovascular mortality, predicted to be among the five top causes of death by 2040. Only the design and optimization of novel strategies to develop new drugs to treat CKD will contain this trend. Current therapy for CKD includes nonspecific therapy targeting proteinuria and/or hypertension and cause-specific therapies for diabetic kidney disease, autosomal dominant polycystic kidney disease, glomerulonephritides, Fabry nephropathy, hemolytic uremic syndrome and others.Areas covered: Herein, the authors review the literature on new drugs under development for CKD as well as novel design and development strategies.Expert opinion: New therapies for CKD have become a healthcare priority. Emerging therapies undergoing clinical trials are testing expanded renin-angiotensin system blockade with double angiotensin receptor/endothelin receptor blockers, SGLT2 inhibition, and targeting inflammation, the immune response, fibrosis and the Nrf2 transcription factor. Emerging therapeutic targets include cell senescence, complement activation, Klotho expression preservation and microbiota. Novel approaches include novel model systems that can be personalized (e.g. organoids), unbiased systems biology-based identification of new therapeutic targets, drug databases that speed up drug identification and repurposing, nanomedicines that improve drug delivery and RNA targeting to expand the number of targetable proteins.
机译:介绍:慢性肾病(CKD)的特点是提高需要透析和心血管死亡率的进展的风险,预计将成为2040年的五个最高原因之一。只有设计和优化发展的新战略治疗CKD的新药将包含这一趋势。 CKD的目前疗法包括靶向蛋白尿和/或高血压的非特异性疗法和糖尿病肾病的原因特异性疗法,常染色体占优势性多囊肾疾病,肾盂酮,法布里肾病,溶血性尿毒症综合征和其他溶血性尿毒症综合征。覆盖:本文,作者审查了文献关于CKD开发的新药物以及新颖的设计与发展策略.Pert意见:CKD的新疗法已成为医疗保健优先权。正在进行临床试验的新兴疗法正在使用双血管紧张素受体/内皮素受体阻断剂,SGLT2抑制和靶向炎症,免疫应答,纤维化和NRF2转录因子进行渗透性疗法。新兴治疗靶标包括细胞衰老,补体激活,Klotho表达保存和微生物酵母。新方法包括可以是个性化的新型模型系统(例如有机体),基于无偏的系统生物学的新治疗目标鉴定,药物数据库加速药物鉴定和重新扫描,纳米胺的纳米核苷酸,可改善药物递送和靶向靶向的RNA靶向扩大靶向的靶向蛋白质。

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