Establishment of a rat model of uric acid nephropathy
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  • YAN Meixia

    YAN Meixia

    1. State Key Laboratory of Dampness Syndrome of Chinese Medicine, the Second Affiliated Hospital of Guangzhou University of Chinese Medicine, (the Second Clinical Medical College of Guangzhou University of Chinese Medicine), Guangzhou 510006, China. 2. Department of Nephrology, Henan Provincial People’s Hospital, Department of Nephrology of Central China Fuwai Hospital, Zhengzhou 450003. 3. Department of Nephrology, Guangdong Provincial Hospital of Chinese Medicine, Guangzhou 510006.
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  • HUO Shuai

    HUO Shuai

    1. State Key Laboratory of Dampness Syndrome of Chinese Medicine, the Second Affiliated Hospital of Guangzhou University of Chinese Medicine, (the Second Clinical Medical College of Guangzhou University of Chinese Medicine), Guangzhou 510006, China. 2. Department of Nephrology, Henan Provincial People’s Hospital, Department of Nephrology of Central China Fuwai Hospital, Zhengzhou 450003.4. Department of Nephrology, Henan Provincial People’s Hospital, Department of Nephrology of Central Fuwai Hospital, Zhengzhou 450003.
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  • TIAN Ruimin

    TIAN Ruimin

    1. State Key Laboratory of Dampness Syndrome of Chinese Medicine, the Second Affiliated Hospital of Guangzhou University of Chinese Medicine, (the Second Clinical Medical College of Guangzhou University of Chinese Medicine), Guangzhou 510006, China. 2. Department of Nephrology, Henan Provincial People’s Hospital, Department of Nephrology of Central China Fuwai Hospital, Zhengzhou 450003. 3. Department of Nephrology, Guangdong Provincial Hospital of Chinese Medicine, Guangzhou 510006.5. Guangdong Provincial Key Laboratory of Chinese Medicine for Prevention and Treatment of Refractory Chronic Diseases, Guangzhou 51006.
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  • XU Peng

    XU Peng

    1. State Key Laboratory of Dampness Syndrome of Chinese Medicine, the Second Affiliated Hospital of Guangzhou University of Chinese Medicine, (the Second Clinical Medical College of Guangzhou University of Chinese Medicine), Guangzhou 510006, China. 2. Department of Nephrology, Henan Provincial People’s Hospital, Department of Nephrology of Central China Fuwai Hospital, Zhengzhou 450003. 3. Department of Nephrology, Guangdong Provincial Hospital of Chinese Medicine, Guangzhou 510006.5. Guangdong Provincial Key Laboratory of Chinese Medicine for Prevention and Treatment of Refractory Chronic Diseases, Guangzhou 51006.
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  • LI Chuang

    LI Chuang

    1. State Key Laboratory of Dampness Syndrome of Chinese Medicine, the Second Affiliated Hospital of Guangzhou University of Chinese Medicine, (the Second Clinical Medical College of Guangzhou University of Chinese Medicine), Guangzhou 510006, China. 2. Department of Nephrology, Henan Provincial People’s Hospital, Department of Nephrology of Central China Fuwai Hospital, Zhengzhou 450003. 3. Department of Nephrology, Guangdong Provincial Hospital of Chinese Medicine, Guangzhou 510006.5. Guangdong Provincial Key Laboratory of Chinese Medicine for Prevention and Treatment of Refractory Chronic Diseases, Guangzhou 51006.
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  • HU Tianxiang

    HU Tianxiang

    2.Department of Nephrology, Henan Provincial People’s Hospital, Department of Nephrology of Central China Fuwai Hospital, Zhengzhou 450003. 3. Department of Nephrology, Guangdong Provincial Hospital of Chinese Medicine, Guangzhou 510006.
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  • CHEN Dahao

    CHEN Dahao

    1. State Key Laboratory of Dampness Syndrome of Chinese Medicine, the Second Affiliated Hospital of Guangzhou University of Chinese Medicine, (the Second Clinical Medical College of Guangzhou University of Chinese Medicine), Guangzhou 510006, China. 2. Department of Nephrology, Henan Provincial People’s Hospital, Department of Nephrology of Central China Fuwai Hospital, Zhengzhou 450003. 3. Department of Nephrology, Guangdong Provincial Hospital of Chinese Medicine, Guangzhou 510006.
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  • CHEN Xiaoling

    CHEN Xiaoling

    1. State Key Laboratory of Dampness Syndrome of Chinese Medicine, the Second Affiliated Hospital of Guangzhou University of Chinese Medicine, (the Second Clinical Medical College of Guangzhou University of Chinese Medicine), Guangzhou 510006, China. 2. Department of Nephrology, Henan Provincial People’s Hospital, Department of Nephrology of Central China Fuwai Hospital, Zhengzhou 450003. 3. Department of Nephrology, Guangdong Provincial Hospital of Chinese Medicine, Guangzhou 510006.
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  • MAO Wei

    MAO Wei

    1. State Key Laboratory of Dampness Syndrome of Chinese Medicine, the Second Affiliated Hospital of Guangzhou University of Chinese Medicine, (the Second Clinical Medical College of Guangzhou University of Chinese Medicine), Guangzhou 510006, China. 2. Department of Nephrology, Henan Provincial People’s Hospital, Department of Nephrology of Central China Fuwai Hospital, Zhengzhou 450003. 3. Department of Nephrology, Guangdong Provincial Hospital of Chinese Medicine, Guangzhou 510006.6. Guangdong Provincial Key Laboratory of Clinical Research on Traditional Chinese Medicine Syndrome, Guangzhou 51006
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Affiliation:

1. State Key Laboratory of Dampness Syndrome of Chinese Medicine, the Second Affiliated Hospital of Guangzhou University of Chinese Medicine, (the Second Clinical Medical College of Guangzhou University of Chinese Medicine), Guangzhou 510006, China. 2. Department of Nephrology, Henan Provincial People’s Hospital, Department of Nephrology of Central China Fuwai Hospital, Zhengzhou 450003. 3. Department of Nephrology, Guangdong Provincial Hospital of Chinese Medicine, Guangzhou 510006. 4. Department of Nephrology, Henan Provincial People’s Hospital, Department of Nephrology of Central Fuwai Hospital, Zhengzhou 450003. 5. Guangdong Provincial Key Laboratory of Chinese Medicine for Prevention and Treatment of Refractory Chronic Diseases, Guangzhou 51006. 6. Guangdong Provincial Key Laboratory of Clinical Research on Traditional Chinese Medicine Syndrome, Guangzhou 51006

Clc Number:

R-33

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    Abstract:

    Objective Establish a reasonable and stable rat model of uric acid nephropathy to provide a pathological model for screening, research, and treatment of uric acid nephropathy. Methods Experimental rats were randomly divided into three model groups and a control group. Model mice were administrated orally with 750 mg / kg oteracil potassium combined with 150 mg / kg low dose uric acid (M-A), 750 mg / kg oteracil potassium combined with 300 mg / kg medium dose uric acid (M-B), or 750 mg / kg oteracil potassium combined with 600 mg / kg high dose uric acid (M- B). After continuous intragastric administration for 4 weeks, changes in blood uric acid, blood creatinine, urea nitrogen, triglycerides, cholesterol and other indicators as well as pathological changes of the kidneys were observed for 4 weeks. Results Compared with the control group, the serum uric acid of the three model groups was significantly higher (P< 0.01, P<0.05, P<0.05), serum creatinine of the M-B and M-C groups was increased significantly (P<0.05, P<0. 01), triglycerides of the M-B group were significantly lower (P<0.05). Renal pathology scores of M-B and M-C groups were significantly higher those of the control group (P<0.01). Masson staining of morphology showed that, in comparison with the control group, kidney damage was more obvious in the three model groups ( P< 0.05, P< 0.01, P< 0.01 ). Immunohistochemical staining of inflammation marker CD68 showed that, compared with the control group, its expression was increased of in three model groups (P<0. 05, P<0. 01, P<0. 01). Expression of epithelial cell marker E-Cadherin was significantly reduced in M-B and M-C groups in comparison with to the control group ( P< 0.01 ). Expression of myofibroblast marker protein α-SMA was increased the three model groups compared with the control group (P<0.05, P< 0.01, P<0.01). Conclusions Oteracil potassium (750 mg / kg) combined with the middle dose of uric acid (300 mg / kg) is ideal to establish a rat model of uric acid nephropathy.

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History
  • Received:January 28,2021
  • Online: April 12,2022
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