| Literature DB >> 23219792 |
Satoshi Okuyama1, Sona Minami, Naoko Shimada, Nahomi Makihata, Mitsunari Nakajima, Yoshiko Furukawa.
Abstract
Cerebral ischemia causes delayed neuronal cell death in the hippocampus resulting in sequential cognitive impairments. Hyper-activated inflammation following ischemia is one of the etiologies for delayed neuronal cell death. In the present study, using a transient global ischemia mouse model, we showed that auraptene (AUR), a citrus coumarin, effectively inhibited microglia activation, cyclooxygenase-2 expression by astrocytes, and neuronal cell death in the hippocampus following ischemic insults. These results suggest that AUR acts as a neuroprotective agent in the ischemic brain, which may be mediated by suppression of the inflammatory response.Entities:
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Year: 2012 PMID: 23219792 DOI: 10.1016/j.ejphar.2012.11.043
Source DB: PubMed Journal: Eur J Pharmacol ISSN: 0014-2999 Impact factor: 4.432