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Acute Cocaine Differentially Induces PKA Phosphorylation Substrates in Male and Female Rats | OMICS International | Abstract
ISSN: 2155-6105

Journal of Addiction Research & Therapy
Open Access

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Research Article

Acute Cocaine Differentially Induces PKA Phosphorylation Substrates in Male and Female Rats

Wei-Lun Sun1, Luyi Zhou2, Arbi Nazarian1, Vanya Quinones- Jenab1,3 and Shirzad Jenab1,3*

1Department of Psychology and Biopsychology and Behavioral Neuroscience, City University of New York, New York 10065, USA

2Biological Sciences and Biology, PhD Programs, City University of New York, New York, USA

3Biopsychology and Behavioral Neuroscience and Biology PhD Programs, City University of New York, New York, USA

Corresponding Author:
Dr. Shirzad Jenab
Department of Psychology
Hunter College of the City University
of New York, New York 10065, USA
Tel: +1-212-772-5732
Fax: +1-212-772-4619
E-mail: [email protected]

Received date: June 15, 2015 Accepted date: July 30, 2015 Published date: August 06, 2015

Citation: Sun WL, Nazarian A, Jenab S, Zhou L, Jenaba VQ (2015) Acute Cocaine Differentially Induces PKA Phosphorylation Substrates in Male and Female Rats. J Addict Res Ther 6:236. doi:10.4172/2155-6105.1000236

Copyright: © 2015 Sun WL, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Abstract

Background: Sex differences in intracellular dopamine pathways may contribute to the known sex differences in psychomotor responses to cocaine and differential development of dependence. This study aimed to determine whether there are sex differences in the activation of the extracellular signal-regulated kinases (ERK1/2, or p44/p42 MAPK) and PKA phosphorylation-dependent substrates in the nucleus accumbens (NAcc) of male and female rats at baseline or after acute cocaine administration.

Methods: 60-day-old male and female Fischer rats were injected with saline or cocaine (30 mg/kg) and sacrificed 5, 15, 30, 45 or 90 minutes later. Total locomotor activity, Stereotypic, rearing, and ambulatory behaviors was measured for 90 minutes using a two-frame automated Photobeam Activity

Results: Similar to our previous findings, total locomotor activities were higher in female rats after this single cocaine administration. Females had higher levels of phosphorylated PKA substrates after cocaine administration, and this change lasted longer and had a greater magnitude than in cocaine treated male rats. Furthermore, although cocaine administration increased the phosphorylation of ERK proteins, there were no sex differences in p-ERK protein levels either at baseline or after acute cocaine administration.

Conclusion: Taken together, these findings suggest that sex differences in basal and cocaine-induced alterations in PKA signaling activity in the NAcc may contribute to sex differences in psychomotor responses to cocaine. However, not all the components of the DA-intracellular signaling pathway maybe heightened in female rats as ERK phosphorylation patterns did not differ between the sexes.

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