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Montelukast, a Cysteinyl Leukotriene Receptor-1 Antagonist, Dose- and Time-Dependently Protects against Focal Cerebral Ischemia in Mice.
- Source :
- Pharmacology; 2005, Vol. 73 Issue 1, p31-40, 10p
- Publication Year :
- 2005
-
Abstract
- Our previous studies showed that cysteinyl leukotriene receptor-1 (CysLT<subscript>1</subscript>) antagonist pranlukast has a neuroprotective effect on cerebral ischemia in rats and mice. However, whether the neuroprotective effect of pranlukast is its special action or a common action of CysLT<subscript>1</subscript> receptor antagonists remains to be clarified. This study was performed to determine whether montelukast, another CysLT<subscript>1</subscript> receptor antagonist, has the neuroprotective effect on focal cerebral ischemia in mice, and to observe its dose- and time-dependent properties. Permanent focal cerebral ischemia was induced by middle cerebral artery occlusion (MCAO). Montelukast was injected intraperitoneally either as multiple doses (once a day for 3 days and 30 min before MCAO) or as a single dose (at 30 min before, 30 min after, or 1 h after MCAO), respectively, and pranlukast and edaravone were used as controls. The neurological deficits, infarct volumes, brain edema, neuron density, and Evans blue extravasation in the brain were determined 24 h after MCAO. Pretreatments with multiple doses or a single dose of montelukast (0.1 and 1.0 mg/kg) before MCAO significantly attenuated all the ischemic insults. Post-treatment with a single dose of montelukast (0.1 and 1.0 mg/kg) at 30 min after MCAO also significantly decreased brain edema and infarct volume, but not neurological deficits. However, post-treatment with a single dose of montelukast at 1 h after MCAO had no significant effect. Pranlukast showed the same effects as montelukast, but edaravone attenuated the ischemic insults only with multiple doses before MCAO. Thus, montelukast has a dose- and time-dependent neuroprotective effect on permanent focal cerebral ischemia in mice, with an effective dose range of 0.1–1.0 mg/kg and a therapeutic window of 30 min. These findings further support the therapeutic potential of CysLT<subscript>1</subscript> receptor antagonists in the treatment of cerebral ischemia at earlier phases. Copyright © 2005 S. Karger AG, Basel [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 00317012
- Volume :
- 73
- Issue :
- 1
- Database :
- Complementary Index
- Journal :
- Pharmacology
- Publication Type :
- Academic Journal
- Accession number :
- 15327961
- Full Text :
- https://doi.org/10.1159/000081072