Protective Effects of Total Flavonoids from Lysimachia christinae on Calcium Oxalate-Induced Oxidative Stress in a Renal Cell Line and Renal Tissue

Author:

Wang Jian1ORCID,Chen Jia-Jian1,Huang Jia-Hao1,Lv Bo-Dong234,Huang Xiao-Jun23,Hu Qing23,Fu Jun23,Huang Wen-Jie23,Tao Ting-Ting235ORCID

Affiliation:

1. The Second Clinical Medical College, Zhejiang Chinese Medical University, 310053 Hangzhou, China

2. Department of Urology, The Second Affiliated Hospital of Zhejiang Chinese Medical University, 310005 Hangzhou, China

3. Zhejiang Provincial Key Laboratory of Traditional Chinese Medicine, 310053 Hangzhou, China

4. Andrology Laboratory on Integration of Chinese and Western Medicine, Zhejiang Provincial Key Laboratory of Traditional Chinese Medicine, 310053 Hangzhou, China

5. Zhejiang Provincial Key Laboratory of Sexual function of Integrated Traditional Chinese and Western Medicine, 310053 Hangzhou, China

Abstract

Oxidative stress (OS) in renal tubular epithelial cells (RTECs) is induced by calcium oxalate (CaOx) stones and plays an important role in the pathology of CaOx nephrolithiasis. The nuclear factor-E2-related factor 2 (Nrf2)/antioxidant response element (ARE) pathway is an important endogenous antioxidant pathway. Flavonoids are compounds with 2-phenylchromone as the basic mother nucleus and are natural antioxidant components of Lysimachia christinae. Our previous studies demonstrated that the total flavonoids from L. christinae (TFL) reduced calcium and oxalic acid concentrations in urine, thus inhibiting CaOx stone formation. We also showed that TFL can reduce OS in renal tissue. However, whether TFL inhibit the formation of CaOx stones through the Nrf2/ARE pathway requires further investigation. Here, we found that TFL protected against injury to a renal cell line and renal tissue, reduced CaOx-induced OS in renal tissue, and reduced CaOx crystal formation. In addition, TFL significantly increased nuclear Nrf2 and the expression of the downstream antioxidant genes heme oxygenase 1 (HO-1) and NAD(P)H quinone oxidoreductase 1 (NQO-1). Furthermore, TFL increased superoxide dismutase (SOD) activity and decreased the malondialdehyde (MDA) content, thereby alleviating OS in RTECs. Silencing Nrf2 expression blocked the protective effect of TFL on CaOx-induced OS. Taken together, our findings indicate that TFL reduce CaOx-induced OS in renal tissue by activating the Nrf2/ARE pathway.

Funder

National Natural Science Foundation of China

Publisher

Hindawi Limited

Subject

Complementary and alternative medicine

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