Nephroprotective Effects of Curcumin in Murine Models of Focal and Segmental Glomerulosclerosis.

IF 2.9 4区 医学 Q2 PHARMACOLOGY & PHARMACY Pharmacology Pub Date : 2025-01-08 DOI:10.1159/000543293
Sufia Husain, Nervana Mustafa Kamal Bayoumy, Fatima Noor, Hanan Hagar
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Abstract

Introduction: This study aims to explore the reno-protective effect of Curcumin in focal and segmental glomerulosclerosis (FSGS) in Murine models, a common chronic glomerulopathy that leads to end stage renal disease.

Methods: Adult Wistar rats were used in this experiment. One group was treated with intravenous Adriamycin (ADR) injection to induce FSGS similar to that seen in humans and a second group was co-administered ADR and Curcumin (ADR-CUR). Saline treated rats served as controls. Renal injury was assessed by measuring the levels of serum creatinine, blood urea nitrogen (BUN), triglyceride and urinary protein. The homogenates of renal cortex were used to estimate the renal content of the inflammatory marker, tumor necrosis factor-a (TNF-a); oxidative stress marker, Malonaldehyde (MDA); and two anti-oxidants superoxide dismutase (SOD) and reduced glutathione (GSH). In addition, the rat kidneys were harvested by ends of week-8 and week-12 and examined for histological abnormalities.

Results: The ADR-treated rats showed biochemical and histological evidence of FSGS, in the form of proteinuria, elevated serum creatinine, BUN and triglycerides, elevated renal TNF-a and MDA, and segmental glomerulosclerosis. The ADR-CUR treated rats showed significant correction of all these variables. Co-administration with Curcumin resulted in improvement of the proteinuria, serum creatinine, BUN and triglyceride. The renal tissue levels of anti-oxidants SOD and GSH increased and that of TNF-a and MDA decreased and the histology revealed reduction in the extent of segmental glomerulosclerosis. The FSGS associated renal damage was notably antagonized by curcumin treatment.

Conclusion: Our findings confirm the reno-protective effects of Curcumin as a potential therapeutic agent in protection against the progression of FSGS and indicate that it is mitigated by inhibition of oxidant injury and inflammation and also by promotion of antioxidants. Curcumin ameliorated the ADR-induced FSGS in murine models. It may be a promising compound in the treatment of FSGS in human subjects. More human studies are needed to further elucidate its effects in FSGS.

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姜黄素在局灶性和节段性肾小球硬化小鼠模型中的肾保护作用。
本研究旨在探讨姜黄素在小鼠局灶性和节段性肾小球硬化(FSGS)模型中的肾保护作用,FSGS是一种常见的慢性肾小球病变,可导致终末期肾脏疾病。方法:采用成年Wistar大鼠进行实验。一组采用静脉注射阿霉素(ADR)诱导与人类相似的FSGS,另一组采用ADR和姜黄素(ADR- cur)联合用药。生理盐水处理的大鼠作为对照。通过测定血清肌酐、血尿素氮(BUN)、甘油三酯和尿蛋白水平来评估肾损伤。用肾皮质匀浆测定肾脏炎症标志物肿瘤坏死因子-a (TNF-a)的含量;氧化应激标志物丙二醛(MDA);两种抗氧化剂超氧化物歧化酶(SOD)和还原性谷胱甘肽(GSH)。此外,在第8周和第12周结束时摘取大鼠肾脏并检查组织学异常。结果:adr处理大鼠出现FSGS的生化和组织学证据,表现为蛋白尿、血清肌酐、BUN和甘油三酯升高、肾TNF-a和MDA升高、节段性肾小球硬化。ADR-CUR治疗的大鼠在所有这些变量上都有显著的校正。与姜黄素联合用药可改善蛋白尿、血清肌酐、尿素氮和甘油三酯。肾组织抗氧化剂SOD、GSH水平升高,TNF-a、MDA水平降低,组织学显示节段性肾小球硬化程度减轻。姜黄素可显著拮抗FSGS相关肾损害。结论:我们的研究结果证实了姜黄素作为一种潜在的治疗药物对FSGS进展的保护作用,并表明它可以通过抑制氧化损伤和炎症以及促进抗氧化剂来减轻。姜黄素可改善adr诱导的小鼠FSGS模型。它可能是一种有前途的化合物,用于治疗人类受试者的FSGS。需要更多的人体研究来进一步阐明其在FSGS中的作用。
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来源期刊
Pharmacology
Pharmacology 医学-药学
CiteScore
5.60
自引率
0.00%
发文量
52
审稿时长
6-12 weeks
期刊介绍: ''Pharmacology'' is an international forum to present and discuss current perspectives in drug research. The journal communicates research in basic and clinical pharmacology and related fields. It covers biochemical pharmacology, molecular pharmacology, immunopharmacology, drug metabolism, pharmacogenetics, analytical toxicology, neuropsychopharmacology, pharmacokinetics and clinical pharmacology. In addition to original papers and short communications of investigative findings and pharmacological profiles the journal contains reviews, comments and perspective notes; research communications of novel therapeutic agents are encouraged.
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