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花生四烯酸乙醇胺及相关脂质的有组织贩运。

Organized trafficking of anandamide and related lipids.

作者信息

Yates Marla L, Barker Eric L

机构信息

The Department of Medicinal Chemistry and Molecular Pharmacology, Purdue University School of pharmacy and Phramceutical Sciences, West Lafayette, Indiana, USA.

出版信息

Vitam Horm. 2009;81:25-53. doi: 10.1016/S0083-6729(09)81002-9.

Abstract

N-arachidonylethanolamide (anandamide or AEA) is an endogenous long-chain fatty acid ethanolamide with activity at both the cannabinoid 1 (CB(1)) and cannabinoid 2 (CB(2)) receptors, as well as the transient receptor potential vanilloid 1 (TRPV1) receptor. Whereas the mechanisms for both AEA biosynthesis and metabolism are fairly well established, the manner by which AEA is accumulated into cells remains controversial. The overwhelming majority of scientific reports indicate that this lipid neuromodulator is taken into cells via a facilitated process. Some reports have suggested that AEA uptake occurs by facilitated diffusion. Recent evidence indicates that AEA uptake may occur via endocytosis, contesting the premise that passive diffusion is the mechanism by which AEA transverses the plasma membrane. This chapter serves as an introduction to the endocannabinoid field with an emphasis on the various proposed mechanisms for the cellular uptake of endocannabinoids and other related hydrophobic molecules.

摘要

N-花生四烯酰乙醇胺(花生四烯酸乙醇胺或AEA)是一种内源性长链脂肪酸乙醇胺,对大麻素1(CB(1))和大麻素2(CB(2))受体以及瞬时受体电位香草酸亚型1(TRPV1)受体均具有活性。虽然AEA生物合成和代谢的机制已相当明确,但AEA在细胞内积累的方式仍存在争议。绝大多数科学报告表明,这种脂质神经调节剂是通过易化过程进入细胞的。一些报告提出,AEA的摄取是通过易化扩散发生的。最近的证据表明,AEA的摄取可能通过内吞作用发生,这对被动扩散是AEA穿过质膜的机制这一前提提出了质疑。本章作为内源性大麻素领域的介绍,重点阐述了内源性大麻素和其他相关疏水分子细胞摄取的各种提出的机制。

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