Document Detail


Chronic lamotrigine does not alter the turnover of arachidonic acid within brain phospholipids of the unanesthetized rat: implications for the treatment of bipolar disorder.
MedLine Citation:
PMID:  17487474     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
RATIONALE: Drugs that are effective in treating the manic phase of bipolar disorder (lithium, carbamazepine, and valproate) upon chronic administration to rats decrease the turnover of arachidonic acid in their brain phospholipids. Lamotrigine may not be effective in the manic phase, but is effective in delaying the depressive phase and for treating rapid cycling bipolar disorder. Thus, lamotrigine provides a pharmacological tool to differentiate if downregulation of arachidonic acid turnover is specific to drugs effective in the manic phase of bipolar disorder.
MATERIALS AND METHODS: To test this hypothesis, rats were administered lamotrigine (10 mg kg(-1) day(-1)) or vehicle intragastrically once daily for 42 days. In the unanesthetized rat, [1-(14)C]arachidonic acid was infused intravenously and arterial blood plasma was sampled until the animal was killed at 5 min, and its microwaved brain was subjected to chemical and radiotracer analysis.
RESULTS: Using equations from our fatty acid model, we found that chronic lamotrigine compared with vehicle did not alter the net incorporation rate of plasma arachidonic acid into brain phospholipids, nor did it alter the turnover of arachidonic acid within brain phospholipids.
CONCLUSION: Chronic lamotrigine, which is effective in the depressive phase or rapid cycling bipolar disorder does not alter brain arachidonic acid turnover in the unanesthetized rat. These results are consistent with the hypothesis that drugs effective in treating the manic phase of bipolar disorder decrease brain arachidonic acid turnover.
Authors:
Ho-Joo Lee; Jagadeesh S Rao; Lisa Chang; Stanley I Rapoport; Richard P Bazinet
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Publication Detail:
Type:  Journal Article; Research Support, N.I.H., Intramural     Date:  2007-05-09
Journal Detail:
Title:  Psychopharmacology     Volume:  193     ISSN:  0033-3158     ISO Abbreviation:  Psychopharmacology (Berl.)     Publication Date:  2007 Sep 
Date Detail:
Created Date:  2007-07-30     Completed Date:  2007-10-23     Revised Date:  2013-08-21    
Medline Journal Info:
Nlm Unique ID:  7608025     Medline TA:  Psychopharmacology (Berl)     Country:  Germany    
Other Details:
Languages:  eng     Pagination:  467-74     Citation Subset:  IM    
Affiliation:
Brain Physiology and Metabolism Section, National Institute on Aging, National Institutes of Health, Bethesda, MD 20892, USA. hojoolee@mail.nih.gov
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MeSH Terms
Descriptor/Qualifier:
Acyl Coenzyme A / metabolism
Animals
Antimanic Agents / pharmacology*
Arachidonic Acid / metabolism*
Bipolar Disorder / drug therapy*
Brain / drug effects,  metabolism*
Disease Models, Animal
Down-Regulation
Male
Phospholipids / metabolism
Random Allocation
Rats
Rats, Inbred F344
Triazines / pharmacology*
gamma-Aminobutyric Acid / drug effects,  metabolism
Chemical
Reg. No./Substance:
0/Acyl Coenzyme A; 0/Antimanic Agents; 0/Phospholipids; 0/Triazines; 506-32-1/Arachidonic Acid; 56-12-2/gamma-Aminobutyric Acid; U3H27498KS/lamotrigine

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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