We have previously shown that nicotinamide protects against energy depletion and decreases infarction in a rat model of cerebral ischemia [1, 2]. It is known that postischemic cell-mediated neuroinflammation exaggerates the initial brain insult caused by ischemia. Herein, we explored whether nicotinamide mitigates the cellular inflammatory response after transient focal cerebral ischemia for 90 min in rats. Nicotinamide (NICO, 500 mg/kg) or vehicle was given intravenously at reperfusion onset. Immunohistochemistry and flow cytometric analysis were used to evaluate the cellular inflammatory response at 48 hr after reperfusion. Relative to controls, NICO-treated animals resulted in significantly decreased macrophages (4.57(x105)±3.00 vs. 2.83(x105)±1.42) and T lymphocytes (0.74(x105)±0.57 vs. 0.28(x105)±1.42) in the bloodstream (P>0.05). Treatment with NICO also significantly decreased the cellular inflammatory response in the ischemic hemisphere. Specifically, melatonin effectively decreased the extent of neutrophil emigration (Ly6G-positive/CD45-positive) and macrophage/activated microglial infiltration (CD11b-positive/CD45-positive) by 55% (P<0.01) and 66% (P<0.01), respectively. In addition, NICO significantly decreased the population composition of T lymphocyte (CD3-positive/CD45-positive; P<0.001) by 39%. This NICO-mediated decrease in the cellular inflammatory response was accompanied by both reduced brain infarction by 34% (P<0.05) and improved surviving neurons in penumbral cortex and caudoputamen by 112% (P<0.005) and 250% (P<0.001), respectively. Thus, intravenous administration of NICO upon reperfusion effectively decreased the emigration of circulatory neutrophils, T-lymphocytes and macrophages/monocytes into the injured brain and inhibited focal microglial activation following cerebral ischemia-reperfusion. The finding demonstrates nicotinamide's inhibitory ability against the cellular inflammatory response after cerebral ischemia-reperfusion, and further supports its pleuripotent neuroprotective actions suited as a therapy of candidate for further clinical trials in the context of ischemic stroke.
|頁（從 - 到）||BP07-06M|
|期刊||Journal of Cerebral Blood Flow and Metabolism|
|出版狀態||Published - 2007 十一月 13|
All Science Journal Classification (ASJC) codes
- Clinical Neurology
- Cardiology and Cardiovascular Medicine