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[Abstract Title]. - Society for Neuroscience

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Topic: B.11.b. Cell biology and signalling<br />

Support: CIHR<br />

OMHF<br />

<strong>Title</strong>: Citalopram mediated neural progenitor cell proliferation and survival<br />

Authors: *A. S. PETTIT, S. A. L. BENNETT;<br />

Dept Biochem, Micro, Immuno, Univ. of Ottawa, Ottawa, ON, Canada<br />

<strong>Abstract</strong>: Depression is associated with a decreased hippocampal volume that correlates with<br />

the length of the depressive episode. Converging evidence suggests that this pathology results<br />

from both progressive loss of neurons and glia and impaired regeneration. Successful<br />

amelioration of the depressive phenotype by chronic antidepressant treatment correlates with an<br />

increase in neural progenitor cell (NPC) proliferation and maturation in experimental models of<br />

disease matching the kinetics of clinical antidepressant efficacy. These correlations have led<br />

researchers to hypothesize that neurogenesis is required <strong>for</strong> antidepressant drug action.<br />

Citalopram, a selective serotonin reuptake inhibitor, is one of the most widely prescribed<br />

antidepressants on the market to date. Few studies have examined the impact of citalopram on<br />

cell proliferation and maturation in the subgranular zone (SGZ) of the dentate gyrus of the<br />

hippocampus, one of the primary sites of neurogenesis in the adult mammalian brain. Using<br />

halogenated thymidine analogue labeling, we have studied the effect of subchronic (7 or 14 day)<br />

and chronic (28 day) citalopram treatment on NPC proliferation and survival in the SGZ of<br />

wildtype mice identifying the progenitor subtypes responsive to antidepressant treatment.<br />

Disclosures: A.S. Pettit , None; S.A.L. Bennett, None.<br />

Poster<br />

241. Glial Neuronal Interactions<br />

Time: Sunday, November 16, 2008, 1:00 pm - 5:00 pm<br />

Program#/Poster#: 241.11/G5<br />

Topic: B.11.b. Cell biology and signalling<br />

Support: NINDS, NIH Intramural Funds<br />

<strong>Title</strong>: Site specific phosphorylation of human septin 5 (sept5) at serine 327 by cyclin dependent<br />

kinase 5 regulates secretion

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