TY - JOUR
T1 - Huangqi decoction inhibits hyperglycemia-induced podocyte apoptosis by down-regulated nox4/p53/bax signaling in vitro and in vivo
AU - Li, Zezheng
AU - Deng, Wenjuan
AU - Cao, Aili
AU - Zang, Yingjun
AU - Wang, Yunman
AU - Wang, Hao
AU - Wang, Li
AU - Peng, Wen
N1 - Publisher Copyright:
© 2019, E-Century Publishing Corporation. All rights reserved.
PY - 2019
Y1 - 2019
N2 - Background: Podocyte dysfunction is associated with the progression of diabetic nephropathy (DN). Huangqi decoction (HQD), a traditional Chinese medical formula, has been used to improve diabetes-related syndrome in China. The present study was to investigate the protective effect of HQD on podocyte apoptosis and the underlying molecular mechanism. Methods: Podocyte was used to measure the efficacy of HQD on cell apoptosis, activities of NADPH oxidases, ROS generation and mitochondrial membrane potential (MMP), and the activation of Nox4/p53/Bax signaling pathway with HQD treatment were also investigated in vitro. Renal pathological morphology, renal function, podocyte apoptosis and Nox4/p53/Bax signaling pathway were investigated with STZ-induced diabetic mice in vivo. Results: HQD increased the cell proliferation and MMP level, while the ROS production and activities of NADPH oxidases were decreased. Meanwhile, Nox4/p53/Bax signaling was down-regulated. Contrarily, overexpression of Nox4 or p53 significantly abolished those efficacies of HQD. Accordingly, in vivo study showed that the progressive albuminuria, glomerulosclerosis and loss of podocytes were significantly alleviated with HQD treatment in diabetic mice, which paralleled by the marked inhibition of Nox4/p53/Bax signaling. Conclusion: Collectively, we provide further evidence that HQD had a renoprotective effect in preventing podocyte apoptosis, which was mediated at least in part by down-regulation of Nox4/p53/Bax signaling.
AB - Background: Podocyte dysfunction is associated with the progression of diabetic nephropathy (DN). Huangqi decoction (HQD), a traditional Chinese medical formula, has been used to improve diabetes-related syndrome in China. The present study was to investigate the protective effect of HQD on podocyte apoptosis and the underlying molecular mechanism. Methods: Podocyte was used to measure the efficacy of HQD on cell apoptosis, activities of NADPH oxidases, ROS generation and mitochondrial membrane potential (MMP), and the activation of Nox4/p53/Bax signaling pathway with HQD treatment were also investigated in vitro. Renal pathological morphology, renal function, podocyte apoptosis and Nox4/p53/Bax signaling pathway were investigated with STZ-induced diabetic mice in vivo. Results: HQD increased the cell proliferation and MMP level, while the ROS production and activities of NADPH oxidases were decreased. Meanwhile, Nox4/p53/Bax signaling was down-regulated. Contrarily, overexpression of Nox4 or p53 significantly abolished those efficacies of HQD. Accordingly, in vivo study showed that the progressive albuminuria, glomerulosclerosis and loss of podocytes were significantly alleviated with HQD treatment in diabetic mice, which paralleled by the marked inhibition of Nox4/p53/Bax signaling. Conclusion: Collectively, we provide further evidence that HQD had a renoprotective effect in preventing podocyte apoptosis, which was mediated at least in part by down-regulation of Nox4/p53/Bax signaling.
KW - Diabetic nephropathy
KW - Huangqi decoction
KW - Mitochondrial dysfunction
KW - Nox4/p53/Bax signaling
KW - Oxidative stress
KW - Podocytes apoptosis
UR - http://www.scopus.com/inward/record.url?scp=85067430773&partnerID=8YFLogxK
M3 - Article
AN - SCOPUS:85067430773
SN - 1943-8141
VL - 11
SP - 3195
EP - 3212
JO - American Journal of Translational Research
JF - American Journal of Translational Research
IS - 5
M1 - AJTR0085336
ER -