Basic Research
Copyright ©The Author(s) 2004. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Jan 1, 2004; 10(1): 100-104
Published online Jan 1, 2004. doi: 10.3748/wjg.v10.i1.100
Effect of Qingyitang on activity of intracellular Ca2+ -Mg2+ -ATPase in rats with acute pancreatitis
Ying Qiu, Yong-Yu Li, Shu-Guang Li, Bo-Gen Song, Gui-Fen Zhao
Ying Qiu, Bo-Gen Song, Gui-Fen Zhao, Department of Pathology, Medical School of Tongji University, Shanghai 200331, China
Yong-Yu Li, Department of Pathophysiology, Medical School of Tongji University, Shanghai 200331, China
Shu-Guang Li, Department of Prevention Medicine, Medical School of Tongji University, Shanghai 200331, China
Author contributions: All authors contributed equally to the work.
Supported by National Natural Science Foundation of China, No. 30060031
Correspondence to: Yong-Yu Li, Department of Pathophysiology, Medical School of Tongji University, 500 Zhennan Road, Shanghai 200331, China. liyyu@163.net
Telephone: +86-21-68537254 Fax: + 86-21-62846993
Received: March 3, 2003
Revised: May 1, 2003
Accepted: May 21, 2003
Published online: January 1, 2004
Abstract

AIM: To study the change of intracellular calcium-magnesium ATPase (Ca2+ -Mg2+ -ATPase) activity in pancreas, liver and kidney tissues of rats with acute pancreatitis (AP), and to investigate the effects of Qingyitang (QYT) (Decoction for clearing the pancreas) and tetrandrine (Tet) and vitamin E (VitE) on the activity of Ca2+ -Mg2+ -ATPase.

METHODS: One hundred and five Sprague-Dawley rats were randomly divided into: normal control group, AP group, treatment group with QYT (1 mL/100 g) or Tet (0.4 mL/100 g) or VitE (100 mg/kg). AP model was prepared by a retrograde injection of sodium taurocholate into the pancreatic duct. Tissues of pancreas, liver and kidney of the animals were taken at 1 h, 5 h, 10 h respectively after AP induction, and the activity of Ca2+ -Mg2+ -ATPase was studied using enzyme-histochemistry staining. Meanwhile, the expression of Ca2+ -Mg2+ -ATPase of the tissues was studied by RT-PCR.

RESULTS: The results showed that the positive rate of Ca2+ -Mg2+ -ATPase in AP group (8.3%, 25%, 29.2%) was lower than that in normal control group (100%) in all tissues (P < 0.01), the positive rate of Ca2+ -Mg2+ -ATPase in treatment group with QYT (58.3%, 83.3%, 83.3%), Tet (50.0%, 70.8%, 75.0%) and VitE (54.2%, 75.0%, 79.2%) was higher than that in AP group (8.3%, 25.0%, 29.2%) in all tissues (P < 0.01). RT-PCR results demonstrated that in treatment groups Ca2+ -Mg2+ -ATPase gene expression in pancreas tissue was higher than that in AP group at the observing time points, and the expression at 5 h was higher than that at 1 h. The expression of Ca2+ -Mg2+ -ATPase in liver tissue was positive, but without significant difference between different groups.

CONCLUSION: The activity and expression of intracellular Ca2+ -Mg2+ -ATPase decreased in rats with AP, suggesting that Ca2+ -Mg2+ -ATPase may contribute to the occurrence and development of cellular calcium overload in AP. QYT, Tet and VitE can increase the activity and expression of Ca2+ -Mg2+ -ATPase and may relieve intracellular calcium overload to protect the tissue and cells from injuries.

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