Abstract | OBJECTIVE: STUDY DESIGN: Experimental study. PLACE AND DURATION OF STUDY: Department of Biochemistry, University of Karachi from December 2007 to February 2008. METHODOLOGY: The study was conducted on thirty six locally bred male Albino Wistar rats. Freshly prepared amino acids (Val and Trp) were added in the drinking water of rats on alternate days and haloperidol at doses of 5.0 mg/kg or saline were injected twice daily for three weeks following one week of withdrawal. Locomotor/ exploratory activities were scored in activity boxes and open field apparatuses. Catalepsy was monitored on an inclined surface. The animals tested for locomotor activity and catalepsy for two weeks follow-up post- injections plus one week of drug withdrawal were decapitated to collect mPFC regions of rat brain for neurochemical analysis by high performance liquid chromatography with electrochemical detection (HPLC-EC). RESULTS: There was significant increase (p<0.01) in locomotor activity in rats orally supplemented with Val and Trp following one week of drug withdrawal from repeated administration. Marked reduction in cataleptogenic effects of the drug was also observed. Significant (p<0.01) increases in the brain Trp and mPFC 5-HT metabolism in Val and Trp supplemented animals were also noticed. CONCLUSION: These findings help to demonstrate the effect of dietary amino acids, in particular, Trp to potentiate mPFC serotonergic modulation of neuroleptic activity.
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Authors | Farhat Batool, Shoaib Ahmed, Darakhshan Jabeen Haleem |
Journal | Journal of the College of Physicians and Surgeons--Pakistan : JCPSP
(J Coll Physicians Surg Pak)
Vol. 19
Issue 3
Pg. 139-45
(Mar 2009)
ISSN: 1022-386X [Print] Pakistan |
PMID | 19268010
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Serotonin
- Tryptophan
- Valine
- Haloperidol
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Topics |
- Animals
- Catalepsy
(chemically induced)
- Dietary Supplements
- Frontal Lobe
(metabolism)
- Haloperidol
(pharmacology)
- Male
- Rats
- Rats, Wistar
- Serotonin
(metabolism)
- Substance Withdrawal Syndrome
(physiopathology)
- Tryptophan
(pharmacology)
- Valine
(pharmacology)
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