Interplay between endocannabinoid and endovanilloid mechanisms in fear conditioning
The transient receptor potential cation channel, subfamily V (vanilloid), member 1 (TRPV1) mediates pain perception to thermal and chemical stimuli in peripheral neurons. The cannabinoid receptor type 1 (CB ), on the other hand, promotes analgesia in both the periphery and the brain. TRPV1 and CB ha...
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Published in | Acta Neuropsychiatrica Vol. 36; no. 5; pp. 255 - 264 |
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Main Authors | , , , |
Format | Journal Article Book Review |
Language | English |
Published |
Cambridge, UK
Cambridge University Press
01.10.2024
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Subjects | |
Online Access | Get full text |
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Summary: | The transient receptor potential cation channel, subfamily V (vanilloid), member 1 (TRPV1) mediates pain perception to thermal and chemical stimuli in peripheral neurons. The cannabinoid receptor type 1 (CB
), on the other hand, promotes analgesia in both the periphery and the brain. TRPV1 and CB
have also been implicated in learned fear, which involves the association of a previously neutral stimulus with an aversive event. In this review, we elaborate on the interplay between CB
receptors and TRPV1 channels in learned fear processing.
We conducted a PubMed search for a narrative review on endocannabinoid and endovanilloid mechanisms on fear conditioning.
TRPV1 and CB
receptors are activated by a common endogenous agonist, arachidonoyl ethanolamide (anandamide), Moreover, they are expressed in common neuroanatomical structures and recruit converging cellular pathways, acting in concert to modulate fear learning. However, evidence suggests that TRPV1 exerts a facilitatory role, whereas CB
restrains fear responses.
TRPV1 and CB
seem to mediate protective and aversive roles of anandamide, respectively. However, more research is needed to achieve a better understanding of how these receptors interact to modulate fear learning. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 ObjectType-Review-3 content type line 23 |
ISSN: | 0924-2708 1601-5215 1601-5215 |
DOI: | 10.1017/neu.2023.54 |