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The COX‐2 inhibitors, meloxicam and nimesulide, suppress neurogenesis in the adult mouse brain
Author(s) -
Goncalves Maria Beatriz,
Williams EmmaJane,
Yip Ping,
YáñezMuñoz Rafael J,
Williams Gareth,
Doherty Patrick
Publication year - 2010
Publication title -
british journal of pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.432
H-Index - 211
eISSN - 1476-5381
pISSN - 0007-1188
DOI - 10.1111/j.1476-5381.2009.00618.x
Subject(s) - neurogenesis , subventricular zone , progenitor cell , neural stem cell , hippocampus , biology , neuroscience , microglia , olfactory bulb , stem cell , microbiology and biotechnology , immunology , central nervous system , inflammation
Background and purpose:  In adults, neurogenesis persists in the hippocampus and the subventricular zone (SVZ), and this is important for learning and memory. Inhibitors of COX‐2 suppress ischaemia‐induced neurogenesis in the hippocampus. Here, we have determined the effects of COX‐2 inhibitors on neurogenesis throughout the normal adult mouse brain. Experimental approach:  Young adult mice were treated with COX‐2 inhibitors, and the proliferation of neural progenitor cells was measured in the SVZ and hippocampus. In addition, the local uptake of lentiviral vectors in the rostral migratory stream enabled the formation of new neurons in the olfactory bulb (OB) to be assessed. Key results:  The COX‐2 inhibitor meloxicam suppressed progenitor cell proliferation in the SVZ and hippocampus. A significant decrease in the appearance of new neurons in the OB was also observed. Similar effects on progenitor proliferation in the SVZ were seen with nimesulide. The absence of COX‐2 expression in the proliferating progenitors in vivo , and the lack of effect of the COX‐2 inhibitors on the growth rate of a cultured progenitor cell line, suggest that the effect is indirect. The specific expression of COX‐2 in resting microglia that closely associate with the proliferating progenitor cells provides for a possible site of action. Conclusions and implications:  Treatment with a COX‐2 inhibitor results in a substantial inhibition of adult neurogenesis. Studies on human tissues are warranted in order to determine if this effect extends to humans, and whether inhibition of neurogenesis should be considered as an adverse effect of these drugs.

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