## Abstract Epidemiological studies indicate that nonsteroidal anti‐inflammatory drugs (NSAIDs) are neuroprotective, although the mechanisms underlying their beneficial effect remain largely unknown. Given their well‐known adverse effects, which of the NSAIDs is the best for neurodegenerative disea
Downregulation of in vitro neurotoxicity of brain macrophages by prostaglandin E2 and a β-adrenergic agonist
✍ Scribed by Clotilde Théry; Alexandre Dobbertin; Dr. Michel Mallat
- Publisher
- John Wiley and Sons
- Year
- 1994
- Tongue
- English
- Weight
- 412 KB
- Volume
- 11
- Category
- Article
- ISSN
- 0894-1491
No coin nor oath required. For personal study only.
✦ Synopsis
Brain macrophages (BM), a subpopulation of microglia, have the ability to kill neurons by producing reactive oxygen intermediates. Cocultures of neurons and macrophages derived from the cerebral cortex of rat embryos were used to look for regulation of BM neurotoxicity. Isoproterenol (lop7 M), a p-adrenergic agonist, induced a significant inhibition of BM neurotoxicity and this effect was abolished in the presence of propranolol, a P-adrenergic antagonist. BM neurotoxicity was also reduced in the presence of prostaglandin E, (lo-', lop6 M), a metabolite derived from arachidonic acid. These results suggest endogenous mechanisms of neuroprotection operating either during development or following lesions. Q 1994 Wiley-Liss, Inc.
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