Gastroprotective effects of montelukast andNigella sativaoil against corticosteroid-induced gastric damage: they are much more than antiasthmatic drugs

Author:

Rizk Fatma H.1,Ibrahim Marwa A.A.2,Abd-Elsalam Marwa M.3,Soliman Nema A.4,Abd-Elsalam Sherief M.5

Affiliation:

1. Department of Physiology, Faculty of Medicine, Tanta University, Egypt.

2. Department of Histology, Faculty of Medicine, Tanta University, Egypt.

3. Department of Histology, Faculty of Medicine, Kafr-Elsheikh University, Egypt.

4. Department of Biochemistry, Faculty of Medicine, Tanta University, Egypt.

5. Department of Tropical Medicine, Faculty of Medicine, Tanta University, Egypt.

Abstract

Corticosteroids are used to treat a variety of diseases like bronchial asthma. However, long-term corticosteroids have a gastric ulcerogenic potential. Montelukast (MTK) and Nigella sativa oil (NSO) are used in treatment of bronchial asthma. Previous studies showed that MTK and NSO had gastroprotective effects in other models of gastric ulcer. The present study assesses synergistic gastroprotective effects of both drugs in dexamethasone (DXM)-induced gastric damage. Fifty male rats were divided into 5 groups: normal control (I), DXM group (II), MTK + DXM group (III), NSO + DXM group (IV), MTK + NSO + DXM group (V). After 7 days, stomachs were removed for biochemical analysis and histological examinations. Significant increases in malondialdehyde (MDA) level, superoxide dismutase (SOD) activity, myeloperoxidase (MPO) activity, and proliferating cell nuclear antigen (PCNA) positive cells, with significant decreases in mucus secretion were detected in DXM-treated group compared with group I. Meanwhile, significant decreases of MDA level, MPO activity, and PCNA positive cells and significant increases in mucus secretion were detected in treated groups compared with group II. SOD activity significantly decreased in group V compared with group II. We could conclude that administration of either MTK or NSO or both with DXM counteracts DXM-induced gastric lesions.

Publisher

Canadian Science Publishing

Subject

Physiology (medical),Pharmacology,General Medicine,Physiology

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