Effects of the histone deacetylase inhibitor sodium butyrate in models of depression and anxiety

Gundersen, BB; Blendy, JA

HERO ID

1455815

Reference Type

Journal Article

Year

2009

Language

English

PMID

19393671

HERO ID 1455815
In Press No
Year 2009
Title Effects of the histone deacetylase inhibitor sodium butyrate in models of depression and anxiety
Authors Gundersen, BB; Blendy, JA
Journal Neuropharmacology
Volume 57
Issue 1
Page Numbers 67-74
Abstract Histone modification, which affects the rate of transcription without altering DNA sequence, occurs in response to various psychiatric drugs and in several models of psychiatric disease. As increases in histone acetylation have been seen after treatment with antidepressants, we investigated whether directly increasing histone acetylation using a histone deacetylase inhibitor would have antidepressant effects. We administered sodium butyrate (NaB, 100 mg/kg, i.p.) to mice acutely (3 injections over 24 h) or chronically (twice daily for 21 days) and subjected them to a number of behavioral tests of antidepressant response. This dose of NaB had no effect on overall locomotor activity after either acute or chronic treatment. Acutely treated mice showed an increase in immobility in the forced-swim test (FST) and an increase in latency to consume in the novel environment of the novelty-induced hypophagia (NIH) paradigm, an anxiogenic effect. The effect of NaB on anxiety did not generalize to another test, the elevated zero maze, where it had no effect. Chronic treatment with NaB had no effect on latency to consume in the NIH or immobility in the FST. However, this dose did alter histone acetylation in the hippocampus. While H4 acetylation increased in the hippocampus 30 min following acute NaB, chronic treatment caused a decrease in AcH4. There were no changes in AcH3 following either treatment. While changes in chromatin structure may be involved in the mechanism of action of antidepressant drugs, these data suggest that increasing histone acetylation pharmacologically is not sufficient to produce antidepressant effects.
Doi 10.1016/j.neuropharm.2009.04.008
Pmid 19393671
Wosid WOS:000267711400009
Is Certified Translation No
Dupe Override No
Comments Source: Web of Science WOS:000267711400009
Is Public Yes
Language Text English
Keyword Depression; Sodium butyrate; Histone acetylation; Anxiety; Novelty-induced hypophagia; Mouse