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Montelukast attenuates lipopolysaccharide-induced cardiac injury in rats
- Source :
- Human & Experimental Toxicology. 35:388-397
- Publication Year :
- 2015
- Publisher :
- SAGE Publications, 2015.
-
Abstract
- This study investigates the possible protective effects of montelukast (MNT) against lipopolysaccharide (LPS)-induced cardiac injury, in comparison to dexamethasone (DEX), a standard anti-inflammatory. Male Sprague Dawley rats (160–180 g) were assigned to five groups ( n = 8/group): (1) control; (2) LPS (10 mg/kg, intraperitoneal (i.p.)); (3) LPS + MNT (10 mg/kg, per os (p.o.)); (4) LPS + MNT (20 mg/kg, p.o.); and (5) LPS + DEX (1 mg/kg, i.p.). Twenty-four hours after LPS injection, heart/body weight (BW) ratio and percent survival of rats were determined. Serum total protein, creatine kinase muscle/brain (CK-MB), alkaline phosphatase (ALP), and lactate dehydrogenase (LDH) activities were measured. Heart samples were taken for histological assessment and for determination of malondialdehyde (MDA) and glutathione (GSH) contents. Cardiac tumor necrosis factor α (TNF-α) expression was evaluated immunohistochemically. LPS significantly increased heart/BW ratio, serum CK-MB, ALP, and LDH activities and decreased percent survival and serum total protein levels. MDA content increased in heart tissues with a concomitant reduction in GSH content. Immunohistochemical staining of heart specimens from LPS-treated rats revealed high expression of TNF-α. MNT significantly reduced percent mortality and suppressed the release of inflammatory and oxidative stress markers when compared with LPS group. Additionally, MNT effectively preserved tissue morphology as evidenced by histological evaluation. MNT (20 mg/kg) was more effective in alleviating LPS-induced heart injury when compared with both MNT (10 mg/kg) and DEX (1 mg/kg), as evidenced by decrease in positive staining by TNF-α immunohistochemically, decrease MDA, and increase GSH content in heart tissue. This study demonstrates that MNT might have cardioprotective effects against the inflammatory process during endotoxemia. This effect can be attributed to its antioxidant and/or anti-inflammatory properties.
- Subjects :
- Cyclopropanes
Lipopolysaccharides
Male
0301 basic medicine
Heart Diseases
Lipopolysaccharide
Health, Toxicology and Mutagenesis
Inflammation
Acetates
Sulfides
Pharmacology
Toxicology
medicine.disease_cause
Dexamethasone
Rats, Sprague-Dawley
03 medical and health sciences
chemistry.chemical_compound
Malondialdehyde
medicine
Animals
Creatine Kinase, MB Form
Montelukast
L-Lactate Dehydrogenase
Tumor Necrosis Factor-alpha
business.industry
Body Weight
Heart
Blood Proteins
Organ Size
General Medicine
Alkaline Phosphatase
Glutathione
Rats
030104 developmental biology
chemistry
Immunology
Quinolines
medicine.symptom
business
Oxidative stress
medicine.drug
Subjects
Details
- ISSN :
- 14770903 and 09603271
- Volume :
- 35
- Database :
- OpenAIRE
- Journal :
- Human & Experimental Toxicology
- Accession number :
- edsair.doi.dedup.....ceb02a6e055d0bb3e0863d269a1d37bd