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Article

The Gastroprotective Role of Acanthus ilicifolius – A Study to Unravel the Underlying Mechanism of Anti-Ulcer Activity

by
K. T. Mani SENTHIL KUMAR
1,
Zothan PUIA
1,
Samir K. SAMANTA
1,
Rajiv BARIK
1,
Arnab DUTTA
1,
Bapi GORAIN
1,
Dilip K. ROY
1,
Dipan ADHIKARI
1,
Sanmoy KARMAKAR
1 and
Tuhinadri SEN
1,2,*
1
Department of Pharmaceutical Technology, Jadavpur University, Kolkata 700032, India
2
School of Natural Product Studies, Jadavpur University, Kolkata 700032, India
*
Author to whom correspondence should be addressed.
Sci. Pharm. 2012, 80(3), 701-718; https://doi.org/10.3797/scipharm.1108-11
Submission received: 13 August 2011 / Accepted: 18 June 2012 / Published: 18 June 2012

Abstract

Acanthus ilicifolius (Acanthaceae), a mangrove medicinal plant, is widely used by the local inhabitants of the Sundarbans (India) to treat a variety of diseases. As a part of our continued search for novel bioactive products from mangrove medicinal plants, we were able to document the anti-inflammatory effects of this plant. In the present study, we have performed a detailed evaluation of the gastroprotective activity of the methanolic extract of Acanthus ilicifolius using different models of gastric ulceration. Unlike the conventional non-steroidal anti-inflammatory drugs, a methanolic extract of Acanthus ilicifolius leaves (MEAL) possessing significant anti-inflammatory properties, as revealed from our previous studies displayed in rats in dosages of 200 mg and 400 mg / kg BW after intraperitoneal administration, showed significant protective activity (anti-ulcer activity) against the gastric lesions induced by aspirin, indomethacin, stress, ethanol, and pylorus ligation. In pylorus-ligated rats, administration of Methanolic extract of Acanthus ilicifolius leaves (MEAL) significantly decreased gastric volume, acidity, and peptic activity. Moreover, pre-treatment with MEAL significantly restored the levels of reduced glutathione (GSH) and the antioxidant enzyme superoxide dismutase (SOD), catalase (CAT), and glutathione peroxidase (GPX), along with significant inhibition of both lipid peroxidation and myeloperoxidase (MPO) activity in pylorus-ligated animals. Ulceration induced with ethanol was significantly inhibited with MEAL, and the extract also resulted in the reduction of both lipid peroxidation and myelo-peroxidase activity. Furthermore, in this experimental model, administration of MEAL improved the activities of SOD, CAT, GSH, and GPX. A similar pattern of action was also noticed in cold-restraint stress-induced (CRS) ulceration, where MEAL pre-treatment inhibited CRS-induced ulceration, improved the status of antioxidant enzymes, and also reduced the level of lipid peroxides. These results suggest that extracts of the leaves of Acanthus ilicifolius may exhibit anti-ulcer activities additional to the anti-inflammatory properties.
Keywords: Acanthus ilicifolius; Sundarban mangroves; Ulcer protection; Dual inhibitor Acanthus ilicifolius; Sundarban mangroves; Ulcer protection; Dual inhibitor

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MDPI and ACS Style

SENTHIL KUMAR, K.T.M.; PUIA, Z.; SAMANTA, S.K.; BARIK, R.; DUTTA, A.; GORAIN, B.; ROY, D.K.; ADHIKARI, D.; KARMAKAR, S.; SEN, T. The Gastroprotective Role of Acanthus ilicifolius – A Study to Unravel the Underlying Mechanism of Anti-Ulcer Activity. Sci. Pharm. 2012, 80, 701-718. https://doi.org/10.3797/scipharm.1108-11

AMA Style

SENTHIL KUMAR KTM, PUIA Z, SAMANTA SK, BARIK R, DUTTA A, GORAIN B, ROY DK, ADHIKARI D, KARMAKAR S, SEN T. The Gastroprotective Role of Acanthus ilicifolius – A Study to Unravel the Underlying Mechanism of Anti-Ulcer Activity. Scientia Pharmaceutica. 2012; 80(3):701-718. https://doi.org/10.3797/scipharm.1108-11

Chicago/Turabian Style

SENTHIL KUMAR, K. T. Mani, Zothan PUIA, Samir K. SAMANTA, Rajiv BARIK, Arnab DUTTA, Bapi GORAIN, Dilip K. ROY, Dipan ADHIKARI, Sanmoy KARMAKAR, and Tuhinadri SEN. 2012. "The Gastroprotective Role of Acanthus ilicifolius – A Study to Unravel the Underlying Mechanism of Anti-Ulcer Activity" Scientia Pharmaceutica 80, no. 3: 701-718. https://doi.org/10.3797/scipharm.1108-11

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