2021
DOI: 10.1021/acs.jcim.1c00893
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TRPV1 Activation by Anandamide via a Unique Lipid Pathway

Abstract: The capsaicin receptor, transient receptor potential vanilloid type 1 (TRPV1), is a polymodal channel that has been implicated in the perception of pain and can be modulated by a variety of cannabinoid ligands. Here we report TRPV1 channel activation by the endocannabinoid, anandamide (AEA), in a unique, peripheral binding site via extended MD simulations. These results aim to expand the understanding of TRPV1 and assist in the development of new TRPV1 modulators.

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Cited by 9 publications
(3 citation statements)
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“…In addition to acting on CB1 and CB2, AEA activates the ionotropic TRPV1 channel, resulting in the opening of the ion channel and Ca 2+ influx [312,[326][327][328][329][330][331], the Gprotein-coupled receptor GPR55 [332,333], and the cation channel TRPA1 [334], while it inhibits the TRPM8 channel [334]. In addition, AEA activates PPARγ, and 2-AG activates PPARα [335].…”
Section: Endogenous Receptors For Aea and 2-agmentioning
confidence: 99%
“…In addition to acting on CB1 and CB2, AEA activates the ionotropic TRPV1 channel, resulting in the opening of the ion channel and Ca 2+ influx [312,[326][327][328][329][330][331], the Gprotein-coupled receptor GPR55 [332,333], and the cation channel TRPA1 [334], while it inhibits the TRPM8 channel [334]. In addition, AEA activates PPARγ, and 2-AG activates PPARα [335].…”
Section: Endogenous Receptors For Aea and 2-agmentioning
confidence: 99%
“…The naphthyl moiety at the end of the tail displays pi-pi interactions with both Y487 and Y445 (Figure 2B). The additional interactions of 1288208 could aid in the stability of the ligand in the tunnel from an external standpoint, allowing the headgroup more time in the tunnel, potentially triggering channel activation as previously hypothesized from MD simulations (Muller et al, 2020(Muller et al, , 2021.…”
Section: Cross-agonist Virtual Screeningmentioning
confidence: 81%
“…In this regard, the recent finding that CBD has a profile consistent with a negative modulation of CB1R signaling both at a cellular and nuclear level ( Laprairie et al, 2015 ) offers a significant and welcome insight. Interestingly both AEA and CBD act as direct agonists of TRPV1 (and TRPV2) channels ( Bisogno et al, 2001 ; Muller et al, 2021 ); TRPV1, in particular, is ideally located in the hippocampal CA1 region to modulate excitatory glutamate signaling. Intriguingly upon the following exposure, CBD rapidly desensitizes the TRPV1 channel ( Anderson et al, 2022 ) and, thus, may reduce neuronal hyperexcitation ( Chávez et al, 2010 ; Etemad et al, 2022 ).…”
Section: Discussionmentioning
confidence: 99%