Protetive effects of anemoside B4 on kidney tissue of rats with chronic renal failure and its mechanism
10.13481/j.1671-587x.20200116
- Author:
Xianghui GUO
1
Author Information
1. Department of Emergency Medicine, Affiliated Tangshan Workers' Hospital, Hebei Medical University
- Publication Type:Journal Article
- Keywords:
Anemoside B4;
Apoptosis;
Chronic renal failure;
Inflammatory cytokine;
Oxidative stress enzyme;
Serum urine cratinine
- From:
Journal of Jilin University(Medicine Edition)
2020;46(1):90-95
- CountryChina
- Language:Chinese
-
Abstract:
Objective: To investigate the effects of anemoside B4 on the blood oxygen stress, inflanmation state and the expressions of apoptosis-related proteins in kidney tissue of the rats with chronic renal failure (CRF), and to illuminate the mechanism of anemoside B4 in protecting the kidney tissue of the CRF rats. Methods: A total of 75 SD male rats were divided into control group, model group, positive control group, low dose of anemoside B4 group and high dose of anemoside B4 group. The CRF rat models were established by continuous administration of adenine for 21 d. After successful modeling, the rats in low and high doses of anemoside B4 groups were given 1 and 2 mg · kg-1 anemoside B4 by gavage and the rats in positive control group were given 0.5 mg · kg-1 dexamethasone, lasted for 28 d; the rats in control group and model group were given the same amount of normal saline. Biochemical analyzer was used to detect serum urine creatinine (Scr) and urea nitrogen (BUN) levels. The kit method was used to detect the activity of superoxide dismutase (SOD) and the levels of malondialdehyde (MDA) in kidney tissue of the rats. ELISA was used to detect the levels of interleukin-1β (IL-1β), interleukin-6 (IL-6) and tumor necrosis factro-α (TNF-α) in kidney tissue of the rats. Western blotting method was used to detect the activation of PI3K/Akt pathway and the expression levels of apopotosis-related proteins Bcl-2, Bax and Caspase-3 in kindey tissue. Results: Compared with control group, the serum Scr and BUN levels of the rats in model group were increased (P<0.01), the number of normal glomerulus and renal corpuscles were decreased, the activity of SOD in kidney tissue was decreased (P<0.01), the levels of MDA, IL-1β, IL-6 and TNF-α were increased (P< 0.01), the expression levels of Bax and Caspase-3 proteins were increased (P<0.01), and the expression levels of p-Akt and Bcl-2 proteins were decreased (P<0.01). Compared with model group, the serum Scr and BUN levels of the rats in positive control group, low and high doses of anemoside B4 groups were significantly decreased (P< 0.01), the number of normal glomerulus and renal corpuscles were increased significantly, the activities of SOD in kidney tissue were increased significantly (P<0.01), the levels of MDA, IL-lβ, IL-6, and TNF-α were significantly decreased (P<0.01), the protein expression levels of Bax and Caspase-3 were decreased significantly (P<0.01), and the expression levels of p-Akt and Bcl-2 proteins were increased significantly (P<0.01). Conclusion: Anemoside B4 can protect the renal tissue injury by reducing the levels of Scr and BUN in serum, reducing oxidative stress response, reducing the release of inflammatory factors, and activating the PI3K/Akt pathway of renal tissue.
