1. Isoliquiritigenin attenuates acute renal injury through suppressing oxidative stress, fibrosis and JAK2/STAT3 pathway in streptozotocin-induced diabetic rats
- Author
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Zheng Yang, Jie Wang, Leiming Sun, and Jiaying Zhang
- Subjects
STAT3 Transcription Factor ,GPX1 ,Cell Survival ,SOD2 ,Apoptosis ,Bioengineering ,oxidative damage ,Pharmacology ,Kidney ,medicine.disease_cause ,Applied Microbiology and Biotechnology ,Antioxidants ,Streptozocin ,Cell Line ,Diabetes Mellitus, Experimental ,Rats, Sprague-Dawley ,tgf-β/smad signaling pathway ,Diabetic nephropathy ,chemistry.chemical_compound ,Chalcones ,Fibrosis ,medicine ,Renal fibrosis ,Animals ,Inflammation ,business.industry ,diabetic nephropathy ,fibrosis ,General Medicine ,Acute Kidney Injury ,Janus Kinase 2 ,medicine.disease ,Streptozotocin ,isoliquiritigenin ,Disease Models, Animal ,Oxidative Stress ,Glucose ,chemistry ,Female ,Reactive Oxygen Species ,business ,Oxidation-Reduction ,TP248.13-248.65 ,Isoliquiritigenin ,Oxidative stress ,Research Article ,Research Paper ,Biotechnology ,medicine.drug - Abstract
The aim of the current study was to evaluate the protective effects and mechanisms of isoliquiritigenin (ISO) on acute renal injury. CCK-8 assays were applied to assess the effects of ISO at different doses (20, 40, and 80 μg/mL) on oxidative damage in human renal HK-2 cells incubated with high glucose. After the diabetic nephropathy (DN) rat model was established, the model animals were randomly assigned to saline-treated control, three model groups received the 10, 20 and 40 mg/kg ISO, respectively, using the healthy Sprague-Dawley (SD) rats as normal control. The blood biochemical indexes, renal functions, oxidative stress, morphological changes, fibrosis- and JAK2/STAT3-related factors in DN model rats were all assessed. The cellular viability of the renal HK-2 cells with oxidative damages were all markedly ameliorated via the incubation of ISO between 10 and 80 μg/mL compared with negative control. In addition, the significantly down-regulated ROS content and up-regulated expression levels of GSH, SOD2, and GPX1 were all observed in ISO-treated groups. Long-term administration of ISO at different doses in DN rats effectively improved general diabetic characteristics and renal morphology. Furthermore, long-term administration of ISO could ameliorate excessive oxidation stress, down-regulate the expression levels of renal fibrosis- and inflammation-related factors, as well as inhibit the JAK2/STAT3 signaling pathway. In conclusion, ISO at all three dosages could efficiently improve the renal injury induced by STZ via ameliorating renal fibrosis, oxidative stress, and inhibiting JAK2/STAT3 signaling pathways in the DN rats.
- Published
- 2021
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