4.7 Article

Gastroprotective effect of andrographolide sodium bisulfite against indomethacin-induced gastric ulceration in rats

Journal

INTERNATIONAL IMMUNOPHARMACOLOGY
Volume 26, Issue 2, Pages 384-391

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.intimp.2015.04.025

Keywords

Andrographolide sodium bisulfite; Indomethacin; Gastric ulcer; Antioxidant; Apoptosis; Rats

Funding

  1. National Natural Science Foundation of China [81173534]
  2. Science and Technology Planning Project of Guangdong Province [2012A080202002, 2013A022100001]
  3. Guangdong International Cooperation Project [2012B050300002]
  4. Science and Technological Program for Dongguan's Higher Education, Science and Research
  5. Health Care Institutions [2012105102009]
  6. Ph.D. Programs Foundation of Ministry of Education of China [20134425110009]
  7. Science and Technology Innovation Project of Guangdong Provincial Department of Education [2013KJCX0045]
  8. Central Finance of China in Support of the Development of Local Colleges and University [276(2014)]
  9. Science and technology cooperation projects among Hong Kong, Macao [2014DFH30010]
  10. Science and technology cooperation projects among Hong Kong, Taiwan [2014DFH30010]

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Andrographolide sodium bisulfite (ASB), a water-soluble sulfonate of andrographolide has been shown to possess anti-inflammatory, antipyretic and analgesic activities. However, there is no report on the gastroprotective effect of ASB against indomethacin-induced gastric-ulcer. Here we investigated the possible anti-ulcerogenic potential of ASB and the underlying mechanism against indomethacin-induced gastric ulcer in rats. The ulcer area, histopathological assessment, contents of gastric mucosal glutathione (GSH), catalase (CAT), superoxide dismutase (SOD), malonaldehyde (MDA) and prostaglandin E-2 (PGE(2)) were examined. In addition, cyclooxygenase-1 (COX-1), cyclooxygenase-2 (COX-2) mRNA expression and immunohistochemical evaluation of HSP70, Bcl-2 and Bax proteins were also investigated. Results indicated that ASB pre-treatment significantly reduced the ulcer areas induced by indomethacin compared with the vehicle group. The gastric levels of GSH, CAT and SOD were markedly increased by ASB while the level of MDA was decreased. In addition, ASB pretreatment significantly promoted the gastric PGE2 levels and up-regulated the COX-1 and COX-2 mRNA expression in comparison with the vehicle group. Immunohistochemistry analysis showed obvious up-regulation of HSP70 and Bcl-2 protein expression while suppression of Bax protein in the gastric tissue of ASB-pretreated group. Taken together, these-findings indicated that the gastroprotective effect of ASB might be associated with the improvement of antioxidative status, activation of COX-mediated PGE2 synthesis, down-regulation of Bax proteins and upregulation of Bcl-2 and HSP70 proteins. ASB might have the potential for further development as a promising alternative for antiulcer treatment. (C) 2015 Elsevier B.V. All rights reserved.

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