Qiu Y, Li YY, Li SG, Song BG, Zhao GF. Effect of Qingyitang on activity of intracellular Ca
2+ -Mg
2+ -ATPase in rats with acute pancreatitis.
World J Gastroenterol 2004;
10:100-4. [PMID:
14695778 PMCID:
PMC4717058 DOI:
10.3748/wjg.v10.i1.100]
[Citation(s) in RCA: 20] [Impact Index Per Article: 1.0] [Reference Citation Analysis] [Abstract] [MESH Headings] [Track Full Text] [Download PDF] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Indexed: 12/15/2022] Open
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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