Cannabidiol binding and negative allosteric modulation at the cannabinoid type 1 receptor in the presence of delta-9-tetrahydrocannabinol: An In Silico study

被引:46
作者
Chung, Hery [1 ]
Fierro, Angelica [2 ]
Pessoa-Mahana, C. David [1 ]
机构
[1] Pontificia Univ Catolica Chile, Fac Chem, Pharm Dept, Santiago, Chile
[2] Pontificia Univ Catolica Chile, Fac Chem, Organ Chem Dept, Santiago, Chile
来源
PLOS ONE | 2019年 / 14卷 / 07期
关键词
CRYSTAL-STRUCTURE; CB1; RECEPTORS; WEB SERVER; HELIX; 8; TETRAHYDROCANNABINOL; ENDOCANNABINOIDS; PHARMACOLOGY; ACTIVATION; RESIDUES; DYNAMICS;
D O I
10.1371/journal.pone.0220025
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Recent evidence has raised in discussion the possibility that cannabidiol can act as a negative allosteric modulator of the cannabinoid type 1 receptor. Here we have used computational methods to study the modulation exerted by cannabidiol on the effects of delta-9-tetrahydrocannabinol in the cannabinoid receptor type 1 and the possibility of direct receptor blockade. We propose a putative allosteric binding site that is located in the N-terminal region of receptor, partially overlapping the orthosteric binding site. Molecular dynamics simulations reveled a coordinated movement involving the outward rotation of helixes 1 and 2 and subsequent expansion of the orthosteric binding site upon cannabidiol binding. Finally, changes in the cytoplasmic region and high helix 8 mobility were related to impaired receptor internalization. Together, these results offer a possible explanation to how cannabidiol can directly modulate effects of delta-9-tetrahydrocannabinol on the cannabinoid receptor type 1.
引用
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页数:18
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