Dominance status is associated with a variation in cannabinoid receptor 1 expression and amphetamine reward

The rewarding effects of psychostimulants appear to be distinct between dominant and subordinate individuals. In turn, the endocannabinoid system is an important modulator of drug reward in the nucleus accumbens and medial prefrontal cortex, however the connection with social dominance is yet to be...

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Published inPharmacology, biochemistry and behavior Vol. 221; p. 173483
Main Authors Migliaro, Martin, Sánchez-Zavaleta, Rodolfo, Soto-Tinoco, Eva, Ruiz-Contreras, Alejandra E., Méndez-Díaz, Mónica, Herrera-Solís, Andrea, Pérez de la Mora, Miguel, Prospéro-García, Oscar E.
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.11.2022
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Abstract The rewarding effects of psychostimulants appear to be distinct between dominant and subordinate individuals. In turn, the endocannabinoid system is an important modulator of drug reward in the nucleus accumbens and medial prefrontal cortex, however the connection with social dominance is yet to be established. Male rats were classified as dominant or subordinate on the basis of their spontaneous agonistic interactions and drug reward was assessed by means of conditioned place preference with amphetamine (AMPH). In addition, the expression of CB1R, CB2R, FAAH1, and DAGLa was quantified from accumbal and cortical tissue samples. Our findings demonstrate that dominant rats required a lesser dose of AMPH to acquire a preference for the drug-associated compartment, thereby suggesting a higher sensitivity to the rewarding effects of AMPH. Furthermore, dominants exhibited a lower expression of CB1R in the medial prefrontal cortex and nucleus accumbens. This study illustrates how CBR1 expression could differentiate the behavioral phenotypes associated to social dominance. •Dominant rats are more sensitive to the rewarding effects of d-amphetamine.•Higher sensitivity of dominants to the rewarding effects of d-amphetamine cannot be attributed to anxiety.•Dominant rats have a lower endogenous expression of CB1R in the mPFC and the NAc.
AbstractList The rewarding effects of psychostimulants appear to be distinct between dominant and subordinate individuals. In turn, the endocannabinoid system is an important modulator of drug reward in the nucleus accumbens and medial prefrontal cortex, however the connection with social dominance is yet to be established. Male rats were classified as dominant or subordinate on the basis of their spontaneous agonistic interactions and drug reward was assessed by means of conditioned place preference with amphetamine (AMPH). In addition, the expression of CB1R, CB2R, FAAH1, and DAGLa was quantified from accumbal and cortical tissue samples. Our findings demonstrate that dominant rats required a lesser dose of AMPH to acquire a preference for the drug-associated compartment, thereby suggesting a higher sensitivity to the rewarding effects of AMPH. Furthermore, dominants exhibited a lower expression of CB1R in the medial prefrontal cortex and nucleus accumbens. This study illustrates how CBR1 expression could differentiate the behavioral phenotypes associated to social dominance.
The rewarding effects of psychostimulants appear to be distinct between dominant and subordinate individuals. In turn, the endocannabinoid system is an important modulator of drug reward in the nucleus accumbens and medial prefrontal cortex, however the connection with social dominance is yet to be established. Male rats were classified as dominant or subordinate on the basis of their spontaneous agonistic interactions and drug reward was assessed by means of conditioned place preference with amphetamine (AMPH). In addition, the expression of CB1R, CB2R, FAAH1, and DAGLa was quantified from accumbal and cortical tissue samples. Our findings demonstrate that dominant rats required a lesser dose of AMPH to acquire a preference for the drug-associated compartment, thereby suggesting a higher sensitivity to the rewarding effects of AMPH. Furthermore, dominants exhibited a lower expression of CB1R in the medial prefrontal cortex and nucleus accumbens. This study illustrates how CBR1 expression could differentiate the behavioral phenotypes associated to social dominance. •Dominant rats are more sensitive to the rewarding effects of d-amphetamine.•Higher sensitivity of dominants to the rewarding effects of d-amphetamine cannot be attributed to anxiety.•Dominant rats have a lower endogenous expression of CB1R in the mPFC and the NAc.
ArticleNumber 173483
Author Herrera-Solís, Andrea
Ruiz-Contreras, Alejandra E.
Prospéro-García, Oscar E.
Migliaro, Martin
Pérez de la Mora, Miguel
Sánchez-Zavaleta, Rodolfo
Méndez-Díaz, Mónica
Soto-Tinoco, Eva
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  fullname: Herrera-Solís, Andrea
  organization: Laboratorio de Efectos Terapéuticos de los Cannabinoides, Subdirección de Investigación Biomédica, Hospital General Dr. Manuel Gea González, Ciudad de México, Mexico
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  givenname: Miguel
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  fullname: Pérez de la Mora, Miguel
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  organization: Laboratorio de Cannabinoides, Departamento de Fisiología, Facultad de Medicina, Universidad Nacional Autónoma de México, Ciudad de México, Mexico
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Keywords CB2R
Dominance status
Sub
eCBS
Social brain
PRE
Dom
DAGLa
EPM
Drug reward
AG
DP
NAc
mPFC
Endocannabinoid system
LIRL
TEST
FAAH1
HIWL
AMPH
Psychostimulant
MDS
A-CPP
CB1R
Language English
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PublicationTitle Pharmacology, biochemistry and behavior
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Snippet The rewarding effects of psychostimulants appear to be distinct between dominant and subordinate individuals. In turn, the endocannabinoid system is an...
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StartPage 173483
SubjectTerms Amphetamine - pharmacology
Animals
CB1R
Central Nervous System Stimulants - metabolism
Central Nervous System Stimulants - pharmacology
Dominance status
Drug reward
Endocannabinoid system
Male
Nucleus Accumbens - metabolism
Psychostimulant
Rats
Receptor, Cannabinoid, CB1 - genetics
Reward
Social brain
Title Dominance status is associated with a variation in cannabinoid receptor 1 expression and amphetamine reward
URI https://dx.doi.org/10.1016/j.pbb.2022.173483
https://www.ncbi.nlm.nih.gov/pubmed/36270348
Volume 221
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