Cannabinoid type-1 receptor signaling in central serotonergic neurons regulates anxiety-like behavior and sociability

The endocannabinoid system possesses neuromodulatory functions by influencing the release of various neurotransmitters, including γ-aminobutyric acid (GABA) and glutamate. A functional interaction between endocannabinoids and the serotonergic system has already been suggested. Previously, we showed...

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Main Authors: Beat eLutz, Martin eHäring, Vanessa eEnk, Alejandro eAparisi Rey, Sebastian eLoch, Inigo eRuiz De Azua, Krisztina eMonory, Tillmann eWeber, Dusan eBartsch
Format: Article
Language:English
Published: Frontiers Media S.A. 2015-09-01
Series:Frontiers in Behavioral Neuroscience
Subjects:
Online Access:http://journal.frontiersin.org/Journal/10.3389/fnbeh.2015.00235/full
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author Beat eLutz
Martin eHäring
Vanessa eEnk
Alejandro eAparisi Rey
Sebastian eLoch
Inigo eRuiz De Azua
Krisztina eMonory
Tillmann eWeber
Dusan eBartsch
author_facet Beat eLutz
Martin eHäring
Vanessa eEnk
Alejandro eAparisi Rey
Sebastian eLoch
Inigo eRuiz De Azua
Krisztina eMonory
Tillmann eWeber
Dusan eBartsch
author_sort Beat eLutz
collection DOAJ
description The endocannabinoid system possesses neuromodulatory functions by influencing the release of various neurotransmitters, including γ-aminobutyric acid (GABA) and glutamate. A functional interaction between endocannabinoids and the serotonergic system has already been suggested. Previously, we showed that cannabinoid type 1 (CB1) receptor mRNA and protein are localized in serotonergic neurons of the raphe nuclei, implying that the endocannabinoid system can modulate serotonergic functions. In order to substantiate the physiological role of the CB1 receptor in serotonergic neurons of the raphe nuclei, we generated serotonergic (5-HT) neuron-specific CB1 receptor-deficient mice, using the Cre/loxP system with a tamoxifen-inducible Cre recombinase under the control of the regulatory sequences of the tryptophan hydroxylase 2 gene (TPH2-CreERT2), thus, restricting the recombination to 5-HT neurons of the central nervous system. Applying several different behavioral paradigms, we revealed that mice lacking the CB1 receptor in serotonergic neurons are more anxious and less sociable than control littermates. Thus, we were able to show that functional CB1 receptor signaling in central serotonergic neurons modulates distinct behaviors in mice.
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spelling doaj.art-c48efe2446d64f95aaf35891c4e1d35c2022-12-21T17:57:59ZengFrontiers Media S.A.Frontiers in Behavioral Neuroscience1662-51532015-09-01910.3389/fnbeh.2015.00235155948Cannabinoid type-1 receptor signaling in central serotonergic neurons regulates anxiety-like behavior and sociabilityBeat eLutz0Martin eHäring1Vanessa eEnk2Alejandro eAparisi Rey3Sebastian eLoch4Inigo eRuiz De Azua5Krisztina eMonory6Tillmann eWeber7Dusan eBartsch8University Medical Center of the Johannes Gutenberg University MainzUniversity Medical Center of the Johannes Gutenberg University MainzUniversity Medical Center of the Johannes Gutenberg University MainzUniversity Medical Center of the Johannes Gutenberg University MainzUniversity Medical Center of the Johannes Gutenberg University MainzUniversity Medical Center of the Johannes Gutenberg University MainzUniversity Medical Center of the Johannes Gutenberg University MainzCentral Institute of Mental HealthCentral Institute of Mental HealthThe endocannabinoid system possesses neuromodulatory functions by influencing the release of various neurotransmitters, including γ-aminobutyric acid (GABA) and glutamate. A functional interaction between endocannabinoids and the serotonergic system has already been suggested. Previously, we showed that cannabinoid type 1 (CB1) receptor mRNA and protein are localized in serotonergic neurons of the raphe nuclei, implying that the endocannabinoid system can modulate serotonergic functions. In order to substantiate the physiological role of the CB1 receptor in serotonergic neurons of the raphe nuclei, we generated serotonergic (5-HT) neuron-specific CB1 receptor-deficient mice, using the Cre/loxP system with a tamoxifen-inducible Cre recombinase under the control of the regulatory sequences of the tryptophan hydroxylase 2 gene (TPH2-CreERT2), thus, restricting the recombination to 5-HT neurons of the central nervous system. Applying several different behavioral paradigms, we revealed that mice lacking the CB1 receptor in serotonergic neurons are more anxious and less sociable than control littermates. Thus, we were able to show that functional CB1 receptor signaling in central serotonergic neurons modulates distinct behaviors in mice.http://journal.frontiersin.org/Journal/10.3389/fnbeh.2015.00235/fullAnxietyRaphe NucleiSerotoninsociabilityCB1 receptor
spellingShingle Beat eLutz
Martin eHäring
Vanessa eEnk
Alejandro eAparisi Rey
Sebastian eLoch
Inigo eRuiz De Azua
Krisztina eMonory
Tillmann eWeber
Dusan eBartsch
Cannabinoid type-1 receptor signaling in central serotonergic neurons regulates anxiety-like behavior and sociability
Frontiers in Behavioral Neuroscience
Anxiety
Raphe Nuclei
Serotonin
sociability
CB1 receptor
title Cannabinoid type-1 receptor signaling in central serotonergic neurons regulates anxiety-like behavior and sociability
title_full Cannabinoid type-1 receptor signaling in central serotonergic neurons regulates anxiety-like behavior and sociability
title_fullStr Cannabinoid type-1 receptor signaling in central serotonergic neurons regulates anxiety-like behavior and sociability
title_full_unstemmed Cannabinoid type-1 receptor signaling in central serotonergic neurons regulates anxiety-like behavior and sociability
title_short Cannabinoid type-1 receptor signaling in central serotonergic neurons regulates anxiety-like behavior and sociability
title_sort cannabinoid type 1 receptor signaling in central serotonergic neurons regulates anxiety like behavior and sociability
topic Anxiety
Raphe Nuclei
Serotonin
sociability
CB1 receptor
url http://journal.frontiersin.org/Journal/10.3389/fnbeh.2015.00235/full
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