Increased tryptophan hydroxylase immunoreactivity in the dorsal raphe nucleus of alcohol-dependent, depressed suicide subjects is restricted to the dorsal subnucleus
Considerable evidence suggests that alcoholics with co‐occurring depressive disorder are at greater risk for developing psychosocial problems particularly suicidal behavior. Moreover, dysfunction in serotonin (5‐HT) neurotransmission has been implicated in depression, suicide and alcoholism. In the...
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Published in | Synapse (New York, N.Y.) Vol. 60; no. 1; pp. 81 - 85 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Hoboken
Wiley Subscription Services, Inc., A Wiley Company
01.07.2006
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Subjects | |
Online Access | Get full text |
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Summary: | Considerable evidence suggests that alcoholics with co‐occurring depressive disorder are at greater risk for developing psychosocial problems particularly suicidal behavior. Moreover, dysfunction in serotonin (5‐HT) neurotransmission has been implicated in depression, suicide and alcoholism. In the present study, we measured the levels of tryptophan hydroxylase (TPH), the main synthetic enzyme of 5‐HT synthesis, in specific nuclei of the dorsal raphe (DR) in depressed suicide victims with alcohol dependence and matched psychiatrically normal controls. TPH immunoreactivity (IR) was quantified in frozen tissue sections containing the DR from 8 suicide victims with a diagnosis of major depression and alcohol dependence, and 8 psychiatrically normal control subjects by using immunoautoradiographic methods. We found that the levels of TPH‐IR were significantly increased by 46% in the dorsal subnucleus of the DR in depressed suicide victims with alcohol dependence when compared with controls. In contrast, TPH‐IR levels did not significantly differ in the other DR subnuclei between depressed, alcoholic suicide subjects, and controls. Our results indicate that abnormalities in 5‐HT biosynthesis in the brain of depressed alcoholic suicide subjects are restricted within distinct regions of the DR. Synapse 60:81–85, 2006. © 2006 Wiley‐Liss, Inc. |
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Bibliography: | ark:/67375/WNG-Q0J7R46B-Z ArticleID:SYN20278 NIH - No. P20RR17701 USPHS - No. MH57011 istex:FB3D03AC0123B379CBE566E651C4180B4EFCC831 Fonds de la recherche en santé du Québec (FRSQ) ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0887-4476 1098-2396 |
DOI: | 10.1002/syn.20278 |