The Endocannabinoid Peptide RVD-Hemopressin Is a TRPV1 Channel Blocker

Neurotransmission is critical for brain function, allowing neurons to communicate through neurotransmitters and neuropeptides. RVD-hemopressin (RVD-Hp), a novel peptide identified in noradrenergic neurons, modulates cannabinoid receptors CB1 and CB2. Unlike hemopressin (Hp), which induces anxiogenic behaviors via transient receptor potential vanilloid 1 (TRPV1) activation, RVD-Hp counteracts these effects, suggesting that it may block TRPV1. This study investigates RVD-Hp's role as a TRPV1 channel blocker using HEK293 cells expressing TRPV1-GFP. Calcium imaging and patch-clamp recordings demonstrated that RVD-Hp reduces TRPV1-mediated calcium influx and TRPV1 ion currents. Molecular docking and dynamics simulations indicated that RVD-Hp interacts with TRPV1's selectivity filter, forming stable hydrogen bonds and van der Waals contacts, thus preventing ion permeation. These findings highlight RVD-Hp's potential as a therapeutic agent for conditions involving TRPV1 activation, such as pain and anxiety.

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Publication Details

Journal
Biomolecules
Published
2024-09-08
DOI
https://doi.org/10.3390/biom14091134
Citations
1
Primary Topic
Biochemical effects in animals
Type
article
Field-Weighted Citation Impact
0.33

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article

The Endocannabinoid Peptide RVD-Hemopressin Is a TRPV1 Channel Blocker

Valeria Márquez‐Miranda, Fernando Hinostroza, Ingrid Carvacho, Ingrid Araya‐Durán et al.
1 citations
Biomolecules
Biochemical effects in animals
0.33
article

The Endocannabinoid Peptide RVD-Hemopressin Is a TRPV1 Channel Blocker

Valeria Márquez‐Miranda, Fernando Hinostroza, Ingrid Carvacho, Ingrid Araya‐Durán, Isabel Vidal-Beltrán, Constanza Suárez-Suárez, Sebastián González-Pérez, Sebastián Vergara
article en
1 citations

Abstract

Neurotransmission is critical for brain function, allowing neurons to communicate through neurotransmitters and neuropeptides. RVD-hemopressin (RVD-Hp), a novel peptide identified in noradrenergic neurons, modulates cannabinoid receptors CB1 and CB2. Unlike hemopressin (Hp), which induces anxiogenic behaviors via transient receptor potential vanilloid 1 (TRPV1) activation, RVD-Hp counteracts these effects, suggesting that it may block TRPV1. This study investigates RVD-Hp's role as a TRPV1 channel blocker using HEK293 cells expressing TRPV1-GFP. Calcium imaging and patch-clamp recordings demonstrated that RVD-Hp reduces TRPV1-mediated calcium influx and TRPV1 ion currents. Molecular docking and dynamics simulations indicated that RVD-Hp interacts with TRPV1's selectivity filter, forming stable hydrogen bonds and van der Waals contacts, thus preventing ion permeation. These findings highlight RVD-Hp's potential as a therapeutic agent for conditions involving TRPV1 activation, such as pain and anxiety.

BiomoleculesVol. 14(9)
Universidad Andrés Bello (CL), Catholic University of the Maule (CL), Millennium Institute for Integrative Biology (CL), University of Valparaíso (CL)
Agencia Nacional de Investigación y Desarrollo, Comisión Nacional de Investigación Científica y Tecnológica
Good health and well-being
Openalex Percentile: Top 38%
Biochemical effects in animals
0.33
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