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Activation of CGRP neurons in the parabrachial nucleus suppresses addictive behavior.
- Source :
-
Proceedings of the National Academy of Sciences of the United States of America [Proc Natl Acad Sci U S A] 2024 Jun 11; Vol. 121 (24), pp. e2401929121. Date of Electronic Publication: 2024 Jun 06. - Publication Year :
- 2024
-
Abstract
- Punishment such as electric shock or physical discipline employs a mixture of physical pain and emotional distress to induce behavior modification. However, a neural circuit that produces behavior modification by selectively focusing the emotional component, while bypassing the pain typically induced by peripheral nociceptor activation, is not well studied. Here, we show that genetically silencing the activity of neurons expressing calcitonin gene-related peptide (CGRP) in the parabrachial nucleus blocks the suppression of addictive-like behavior induced by footshock. Furthermore, activating CGRP neurons suppresses not only addictive behavior induced by self-stimulating dopamine neurons but also behavior resulting from self-administering cocaine, without eliciting nocifensive reactions. Moreover, among multiple downstream targets of CGRP neurons, terminal activation of CGRP in the central amygdala is effective, mimicking the results of cell body stimulation. Our results indicate that unlike conventional electric footshock, stimulation of CGRP neurons does not activate peripheral nociceptors but effectively curb addictive behavior.<br />Competing Interests: Competing interests statement:The authors declare no competing interest.
- Subjects :
- Animals
Mice
Male
Dopaminergic Neurons metabolism
Dopaminergic Neurons physiology
Cocaine pharmacology
Behavior, Animal physiology
Parabrachial Nucleus metabolism
Parabrachial Nucleus physiology
Calcitonin Gene-Related Peptide metabolism
Neurons metabolism
Neurons physiology
Behavior, Addictive metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1091-6490
- Volume :
- 121
- Issue :
- 24
- Database :
- MEDLINE
- Journal :
- Proceedings of the National Academy of Sciences of the United States of America
- Publication Type :
- Academic Journal
- Accession number :
- 38843183
- Full Text :
- https://doi.org/10.1073/pnas.2401929121