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Tripterygium glycosides improve abnormal lipid deposition in nephrotic syndrome rat models
Bidan Zheng1, Dongfang Lu1, Xiuping Chen1
1Guangdong Provincial Key Laboratory of Clinical Research on Traditional Chinese Medicine Syndrome, The Second Clinical Medical College, Guangzhou University of Chinese Medicine, Guangzhou, China.
Objective:
The purpose of this study was to determine the effect of tripterygium glycosides (TGs) on regulating abnormal lipid deposition in nephrotic syndrome (NS) rats.
Methods:
Sprague-Dawley (SD) rats were injected with 6 mg/kg doxorubicin to construct nephrotic syndrome models (n = 6 per group), and then administered with TGs (10 mg/kg·d-1), prednisone (6.3 mg/kg·d-1), or pure water for 5 weeks. Biomedical indexes, such as urine protein/creatinine ratio (PCR), blood urea nitrogen (BUN), serum creatinine (Scr), serum albumin (SA), triglycerides (TG), total cholesterol (TC)were investigated to evaluate the renal injury of rats. H&E staining experiment was used to assess the pathological alterations. Oil Red O staining was used to assess the level of renal lipid deposition. Malondialdehyde (MDA) and glutathione (GSH) were measured to assess the extent of oxidative damage to the kidney. TUNEL staining was used to assess the status of apoptosis in the kidney. Western blot analysis was performed to examine the levels of relevant intracellular signaling molecules.
Results:
After treatment with TGs, those tested biomedical indexes were significantly improved, and the extent of kidney tissue pathological changes and lipid deposition in the kidney was diminished. Treatment with TGs decreased renal oxidative damage and apoptosis. Regarding the molecular mechanism, TGs significantly increased the protein expression levels of Bcl-2 but decreased the levels of CD36, ADFP, Bax, and Cleaved caspase-3.
Conclusion:
TGs alleviates renal injury and lipid deposition induced by doxorubicin, suggesting that it may be a new strategy for reducing renal lipotoxicity in NS.
Insights
Tripterygium glycosides (TGs) reduce kidney damage and abnormal lipid deposition in nephrotic syndrome (NS) rats. This study suggests TGs may offer a new therapeutic strategy for reducing renal lipotoxicity in NS patients.
Area of Science:
- Nephrology
- Pharmacology
- Biochemistry
Background:
- Nephrotic syndrome (NS) is characterized by abnormal lipid deposition and renal injury.
- Doxorubicin-induced nephropathy is a common model for studying NS.
- Understanding the mechanisms of renal lipotoxicity is crucial for developing effective treatments.
Purpose of the Study:
- To investigate the therapeutic effect of tripterygium glycosides (TGs) on regulating abnormal lipid deposition in nephrotic syndrome (NS) rats.
- To evaluate the impact of TGs on renal injury, oxidative stress, and apoptosis in a doxorubicin-induced NS rat model.
- To explore the molecular mechanisms underlying the protective effects of TGs.
Main Methods:
- Nephrotic syndrome was induced in Sprague-Dawley rats using doxorubicin.
- Rats were treated with TGs, prednisone, or water for 5 weeks.
- Biomedical indexes, renal pathology, lipid deposition, oxidative damage, apoptosis, and protein expression were assessed.
Main Results:
- TGs significantly improved biomedical indexes and reduced pathological changes and lipid deposition in the kidneys.
- TGs treatment decreased renal oxidative damage and apoptosis.
- TGs modulated the expression of key proteins involved in apoptosis and lipid metabolism, including Bcl-2, CD36, ADFP, Bax, and Cleaved caspase-3.
Conclusions:
- Tripterygium glycosides (TGs) effectively alleviate renal injury and lipid deposition induced by doxorubicin in NS rats.
- TGs demonstrate potential as a novel therapeutic strategy for mitigating renal lipotoxicity in NS.
- The findings highlight the therapeutic promise of TGs in managing nephrotic syndrome.
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