Heat shock proteins 27 and 70 contribute to the protection of Schisandrin B against d-galactosamine-induced liver injury in mice

Author:

Gao Zhiying1,Zhang Jishun2,Li Libo3,Shen Longqing4,Li Qingyi3,Zou Yu3,Du Xiaohui3,Zhao Zhibo4

Affiliation:

1. Polygenic Disease Institute, Qiqihar Medical University, 333 Bukui Street, Jianhua District, Qiqihar 161006, P. R. China.

2. Department of Gastroenterology and Hepatology, Beijing Chaoyang Hospital, Capital Medical University, 5 Jingyuan Road, Shijingshan District, Beijing 100043, P. R. China.

3. Department of Pharmacology, Qiqihar Medical University, 333 Bukui Street, Jianhua District, Qiqihar 161006, P. R. China.

4. School of Basic Medicine, Qiqihar Medical University, 333 Bukui Street, Jianhua District, Qiqihar 161006, P. R. China.

Abstract

Schisandrin B is a hepatoprotective component isolated from a traditional Chinese herb, Schisandra chinensis (Turcz.) Baill. This study determined the effect of Schisandrin B on d-galactosamine -induced liver injury and the role of heat shock proteins 27 and 70 against liver injury in mice. Acute liver injury was induced by intraperitoneal injection of d-galactosamine to mice, and Schisandrin B was given orally. The protein and gene expression of heat shock proteins 27 and 70 were detected by western blot and real-time quantitative polymerase chain reaction, respectively. Liver tissues were subjected to histological evaluation, and the activities of alanine aminotransferase and aspartate aminotransferase in the serum were measured. Pretreatment of Schisandrin B significantly attenuated d-galactosamine-induced liver injury in mice. This result was evidenced by improved alteration of histopathological hepatic necrosis and reduced alanine aminotransferase and aspartate aminotransferase activities in the serum. The hepatoprotective effect was accompanied with overexpression of heat shock proteins 27 and 70 both at the protein and mRNA levels. However, the aforementioned actions of Schisandrin B were all markedly suppressed by the heat shock protein inhibitor quercetin. Heat shock proteins 27 and 70 were involved in the protective effect of Schisandrin B against d-galactosamine-induced liver injury in mice.

Publisher

Canadian Science Publishing

Subject

Physiology (medical),Pharmacology,General Medicine,Physiology

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