Plasma Cocaine Metabolite and Liver CYP450 3A4 Isoenzyme Levels as Indicators of Cocaine Dependence in Rats Treated with Nutritional Supplements

Author:

Gardner Natwaine Sherune1,Luke Kedon JS2,Wheatley Andrew O.2,De La Haye Winston G.2,Bahado-Singh Perceval2,Dilworth Lowell3,McGrowder Donovan A.4,Barton Everard2,Young Lauriann Elizabeth5,Salako-Akande Ajibike6,Morrison Errol7,Eldemire-Shearer Denise8,Lowe Henry9,Asemota Helen N.10

Affiliation:

1. Biotechnology Centre, UWI Mona, Kingston, Jamaica

2. UWI Mona, Kingston, Jamaica

3. Department of Pathology, UWI Mona, Kingston, Jamaica

4. Department of Pathology, Faculty of Medical Sciences, UWI Mona, Kingston, Jamaica

5. Department of Basic Medical Sciences, Faculty of Medical Sciences, UWI Mona, Kingston, Jamaica

6. Getwele Natureceuticals, Halethorpe, MD, USA

7. NCST, Kingston, Jamaica

8. Department of Community health, UWI Mona, Kingston, Jamaica

9. Bio-Tech R&D Institute, Kingston, Jamaica

10. Biotechnology Centre, UWI Mona, Kingston, Jamaica and UWI BMS - Biochemistry Section, Mona, Jamaica

Abstract

The effects that chronic cocaine administration (CCA) have on craving, cocaine metabolite concentrations and cytochrome P450 3A4 isoenzyme (CYP450 3A4) activities in Sprague-Dawley rats following the administration of Salako Nutritional Supplements (SNS) were examined. Five groups of fifty rats were used to assess the effect of the SNS following CCA. Craving was analyzed for each rat using a Conditioned Place Preference protocol. Blood samples were obtained at regular intervals and used to measure cocaine plasma metabolite levels. CYP450 3A4 activity was determined in the liver. Administration of the SNS reduced craving of cocaine significantly, upon discontinuing cocaine in the rats. Blood plasma analysis showing higher benzoylecgonine equilibrium and the CYP450 3A4 levels demonstrated that the SNS possibly aided in the removal of the stored metabolites indicative of increased metabolism of cocaine, enhanced by the Supplements. Results indicate that the SNS formulation reduces craving caused by CCA by increasing the liver CYP450 3A4 activity, resulting in better plasma clearance.

Publisher

IGI Global

Subject

General Engineering

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