Journal
NEUROSCIENCE LETTERS
Volume 503, Issue 2, Pages 93-99Publisher
ELSEVIER IRELAND LTD
DOI: 10.1016/j.neulet.2011.08.015
Keywords
Phosphodiesterase III inhibitor; Cerebral ischemia; Inflammation; Cytokines; apoptosis
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Funding
- IRCCS Centro Neurolesi Bonino-Pulejo, Messina, Italy
- Italian Ministry of Health
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Olprinone hydrochloride, a specific phosphodiesterase Ill inhibitor, has anti-inflammatory effects in addition to its inotropic and vasodilatory effects. The purpose of this study was to examine the beneficial effects of olprinone on cerebral ischemia reperfusion injury. In the present study, we examined the detailed mechanisms underlying the inhibitory effects of olprinone on inflammatory and apoptotic responses induced by middle cerebral artery occlusion (MCAo) in rats. Focal cerebral ischemia was induced by transient MCAo in the right hemisphere, via the external carotid artery into the internal carotid to block the origin of the median carotid artery. The rats were subjected to artery occlusion (2 h) followed by reperfusion (22 h). Olprinone was administered 5 min before reperfusion. MCAo-induced cerebral ischemia was associated with an increase in inducible nitric oxide synthase expression, nitrotyrosine formation, as well as IL-1 beta expression and ICAM-1 expression in ischemic regions. Olprinone treatment showed marked reduction in infarct size compared with control rats. These expressions were markedly inhibited by olprinone treatment. We also demonstrated that olprinone reduces levels of apoptosis (TUNEL, Bax and Bcl-2 expression) resulting in a reduction in the infarct volume in ischemia-reperfusion brain injury. Based on these findings we propose that olprinone would be useful in lowering the risk of damage or improving function in ischemia-reperfusion brain injury-related disorders. (C) 2011 Elsevier Ireland Ltd. All rights reserved.
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