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Author Notes:

Michael A. Nader, Ph.D., Department of Physiology and Pharmacology, Wake Forest University School of Medicine, 546 NRC, Medical Center Boulevard, Winston-Salem, NC 27157-1083, Email: mnader@wakehealth.edu.

M.A.N., S.H.N., P.W.C. and N.V.R. designed the experiments.

N.V.R., R.W.G and B.L.B. performed the behavioral studies, including intravenous catheterization.

H.D.G. analyzed the PET data, J.R.K. assisted with the social housing manipulations, P.K.G., H.M.L.D., D.M. and S.G. were involved in the synthesis of both radiotracers and B.A.R. was responsible for the statistical analyses.

The manuscript was written by M.A.N. with assistance from S.H.N., P.W.C., R.W.G, B.L.B. and J.R.K.

We would like to thank Cora Lee Wetherington for comments on an earlier version of this manuscript and Jennifer Sandridge, Michelle Icenhower, Susan Martelle, Whitney Wilson, Tonya Calhoun, Dewayne Cairnes, Kim Black, Holly Smith and Li Wu for excellent technical assistance.

The CSF samples were analyzed by Dr. John Mann at the New York State Psychiatric Institute.

Financial Disclosures: There are no financial disclosures or conflicts of interest to report for any author.

Subject:

Research Funding:

This research was supported by the National Institute on Drug Abuse Grant DA 017763.

Keywords:

  • Science & Technology
  • Life Sciences & Biomedicine
  • Neurosciences
  • Psychiatry
  • Neurosciences & Neurology
  • Dopamine
  • females
  • PET imaging
  • gender differences
  • social rank
  • vulnerability
  • POSITRON-EMISSION-TOMOGRAPHY
  • CYNOMOLGUS MONKEYS
  • RHESUS-MONKEYS
  • NUCLEUS-ACCUMBENS
  • SEX-DIFFERENCES
  • HOUSED MONKEYS
  • ABUSE
  • RATS
  • TRANSPORTER
  • AGGRESSION

SOCIAL DOMINANCE IN FEMALE MONKEYS: DOPAMINE RECEPTOR FUNCTION AND COCAINE REINFORCEMENT

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Journal Title:

Biological Psychiatry

Volume:

Volume 72, Number 5

Publisher:

, Pages 414-421

Type of Work:

Article | Post-print: After Peer Review

Abstract:

Background: Brain imaging and behavioral studies suggest an inverse relationship between dopamine (DA) D2/D3 receptors and vulnerability to cocaine abuse, although most research has used males. For example, male monkeys that become dominant in a social group have significant elevations in D2/D3 receptor availability and are less vulnerable to cocaine reinforcement. Methods: DA D2/D3 receptor availability was assessed in female cynomolgus monkeys (n = 16) with positron emission tomography (PET) while they were individually housed, 3 months after stable social hierarchies had formed, and again when individually housed. In addition, PET was used to examine changes in dopamine transporter (DAT) availability after social hierarchy formation. After imaging studies were complete, monkeys received implantation with indwelling intravenous catheters and self-administered cocaine (.001-.1 mg/kg/injection) under a fixed-ratio 30 schedule of reinforcement. Acquisition of cocaine reinforcement occurred when response rates were significantly higher than when saline was self-administered. Results: Neither DAT nor D2/D3 receptor availability in the caudate nucleus and putamen was predictive of social rank, but both significantly changed after formation of social hierarchies. DA D2/D3 receptor availability significantly increased in females that became dominant, whereas DAT availability decreased in subordinate females. Dominant female monkeys acquired cocaine reinforcement at significantly lower doses than subordinate monkeys. Conclusions: The relationship between D2/D3 receptor availability and vulnerability to cocaine reinforcement seems, on the basis of these findings, opposite in females and males. These data indicate that the social environment profoundly affects the DA system but does so in ways that have different functional consequences for females than for males.

Copyright information:

© 2012 Society of Biological Psychiatry.

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