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Therapeutic potential of digitoflavone on diabetic nephropathy: nuclear factor erythroid 2-related factor 2-dependent
Yang Yang1, Gang Chen1, Xiaolan Cheng1
1Laboratory of Cellular and Molecular Biology, Jiangsu Province Academy of Traditional Chinese Medicine, Nanjing 210028, Jiangsu, China.
Abstract:
Nuclear factor erythroid 2-related factor 2 (Nrf2) has emerged as a therapeutic target in many diseases, because it can induce antioxidant enzymes and other cytoprotective enzymes. Moreover, some Nrf2 activators have strong anti-inflammatory activities. Oxidative stress and inflammation are major components involved in the pathology of diabetic nephropathy. In the present study, we evaluated the Nrf2-dependent anti-oxidative and anti-inflammatory effects of digitoflavone in streptozotocin-induced diabetic nephropathy. The molecular mechanisms of digitoflavone were investigated in vitro using SV40-transformed mouse mesangial cells (SV40-Mes13). For the in vivo experiment, diabetes was induced in Nrf2+/+ and Nrf2-/- mice by STZ injection, and digitoflavone was administered 2 weeks after the STZ injection. Digitoflavone induced Nrf2 activation and decreased oxidative damage, inflammation, TGF-β1 expression, extracellular matrix protein expression, and mesangial cell hyperplasia in SV40-Mes13 cells. Digitoflavone-treated Nrf2+/+ mice, but not Nrf2-/- mice, showed attenuated common metabolic disorder symptoms, improved renal performance, minimized pathological alterations, and decreased oxidative damage, inflammatory gene expression, inflammatory cell infiltration, TGF-β1 expression, and extracellular matrix protein expression. Our results show that the anti-oxidative and anti-inflammatory effects of digitoflavone are mediated by Nrf2 activation and that digitoflavone can be used therapeutically to improve metabolic disorders and relieve renal damage induced by diabetes.
Insights
Digitoflavone activates Nuclear factor erythroid 2-related factor 2 (Nrf2), reducing oxidative stress and inflammation in diabetic nephropathy. This therapeutic effect is Nrf2-dependent, offering potential for treating diabetic kidney damage.
Area of Science:
- Nephrology
- Pharmacology
- Molecular Biology
Background:
- Diabetic nephropathy involves oxidative stress and inflammation.
- Nuclear factor erythroid 2-related factor 2 (Nrf2) regulates antioxidant and cytoprotective enzymes.
- Nrf2 activators show anti-inflammatory potential.
Purpose of the Study:
- To evaluate the Nrf2-dependent anti-oxidative and anti-inflammatory effects of digitoflavone in diabetic nephropathy.
- To investigate the therapeutic potential of digitoflavone in a mouse model of diabetic kidney disease.
Main Methods:
- In vitro studies using mouse mesangial cells (SV40-Mes13).
- In vivo studies using streptozotocin (STZ)-induced diabetic Nrf2+/+ and Nrf2-/- mice.
- Administration of digitoflavone and assessment of various biomarkers and pathological changes.
Main Results:
- Digitoflavone activated Nrf2, reducing oxidative damage, inflammation, TGF-β1, extracellular matrix deposition, and mesangial cell hyperplasia in vitro.
- In vivo, digitoflavone attenuated metabolic disorders, improved renal function, and reduced kidney damage in Nrf2+/+ mice, but not in Nrf2-/- mice.
- Key findings demonstrate Nrf2-mediated protective effects against diabetic nephropathy.
Conclusions:
- The anti-oxidative and anti-inflammatory effects of digitoflavone are mediated through Nrf2 activation.
- Digitoflavone shows therapeutic promise for improving metabolic disorders and alleviating diabetic nephropathy.
- Nrf2 activation is crucial for digitoflavone's renoprotective effects in diabetes.
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