Effects of Pithecellobium Jiringa Ethanol Extract against Ethanol-Induced Gastric Mucosal Injuries in Sprague-Dawley Rats.docVIP
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Effects of Pithecellobium Jiringa Ethanol Extract against Ethanol-Induced Gastric Mucosal Injuries in Sprague-Dawley Rats
Molecules 2012, 17, 2796-2811; doi:10.3390/moleculeOPEN ACCESS
molecules
ISSN 1420-3049
/journal/molecules
Article
Effects of Pithecellobium Jiringa Ethanol Extract
against Ethanol-Induced Gastric Mucosal Injuries
in Sprague-Dawley Rats
Ibrahim Abdel Aziz Ibrahim 1,*, Suhailah Wasmn Qader 2, Mahmood Ameen Abdulla 3,
Amal R. Nimir 4, Siddig Ibrahim Abdelwahab 5 and Fouad Hussain AL-Bayaty 6
1
Department of Pharmacology, Faculty of Medicine, Universiti Teknology MARA,
Shah Alam 40450, Malaysia
2
Department of Biological Science, Faculty of Biosciences and Bioengineering,
University of Technology Malaysia, UTM Skudai 81310, Johor, Malaysia;
E-Mail: suhaylaqadir@
3
Department of Molecular Medicine, Faculty of Medicine, University of Malaya,
Kuala Lumpur 50603, Malaysia; E-Mail: mahmood955@
4
Division of Basic Medical Sciences, Faculty of Medicine, Cyberjaya University College of Medical
Sciences (CUCMS), Cyberjaya 63000, Selangor, Malaysia; E-Mail: aralmadi@
5
Department of Pharmacy, Faculty of Medicine, University of Malaya, Kuala Lumpur 50603,
Malaysia; E-Mail: siddigroa@
6
Department of Restorative Dentistry, Faculty of Dentistry, Universiti Technology MARA,
Shah Alam 40450, Malaysia; E-Mail: dribm74@
* Author to whom correspondence should be addressed; E-Mail: jjurishi@;
ibrahimabdel@.my; Tel.: +6-03-55-442-973; Fax: +6-03-55-442-831.
Received: 31 December 2011; in revised form: 23 February 2012 / Accepted: 23 February 2012 /
Published: 6 March 2012
Abstract: Current anti-gastric ulcer agents have side effects, despite the progression and
expansion of advances in treatment. This study aimed to investigate the gastroprotective
mechanisms of Pithecellobium jiringa ethanol extract against ethanol-induced gastric
mucosal ulcers in rats. For this purpose, Sprague Dawley rats were randomly divided into
five groups: Group 1 (normal control) rats were orally administered with vehicle
(carboxymethyl cellulose),
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