Cellular and Molecular Physiology Laboratory (CMPL), Division of Obstetrics and Gynaecology, School of Medicine, Faculty of Medicine, Pontificia Universidad Católica de Chile, Santiago 8330024, Chile.
School of Medical Technology, Health Sciences Faculty, Universidad San Sebastian, Lientur 1457, Concepción 4080871, Chile.
Mol Aspects Med. 2017 Jun;55:26-44. doi: 10.1016/j.mam.2017.01.007. Epub 2017 Jan 31.
Adenosine as well as agonists and antagonists for the four adenosine receptor subtypes (A1R, A2AR, A2BR and A3R) play a role in several key physiological and pathophysiological processes, including the regulation of vascular tone, thrombosis, immune response, inflammation, and angiogenesis. This review focuses on the adenosine-mediated regulation of lipid availability in the cell and in the systemic circulation as well in humans and animal models. Therefore, adenosine, mainly by acting on A1R, inhibits lipolysis activity, leading to reduction of the circulating fatty acid levels. This nucleoside can also participate in the early development of atherosclerosis by inhibiting the formation of foam cells via stimulation of cholesterol efflux through A2AR expressed on macrophages and reduction of the inflammatory process by activating A2AR and A2BR. Adenosine also appears to modulate intracellular cholesterol availability in Niemann-Pick type C1 disease and Alzheimer disease via A2AR and A3, respectively. Remarkably, the role of adenosine receptors in the regulation of plasma total cholesterol and triglyceride levels has been studied in animal models. Thus, an anti-atherogenic role for A2BR as well as a pro-atherogenic role of A2AR and A1 have been proposed; A3R has not been shown to participate in the control of lipid levels or the development of atherosclerosis. Surprisingly, and despite the role of A2A in the inhibition of foam cell formation among isolated cells, this receptor appears to be pro-atherogenic in mice. Remarkably, the role of adenosine receptors in human dyslipidaemia and atherosclerosis must to be elucidated. Additionally, it has been reported that increased lipid levels impair the effects of adenosine/adenosine receptors in controlling vascular tone, and we speculate on the possibility that this impairment could be due to alterations in the composition of the membrane microdomains where the adenosine receptors are located. Finally, a possible role for adenosine/adenosine receptors in the phenomena of dyslipidaemia in pregnancy has been proposed.
腺苷以及四种腺苷受体亚型(A1R、A2AR、A2BR 和 A3R)的激动剂和拮抗剂在几种关键的生理和病理生理过程中发挥作用,包括血管张力调节、血栓形成、免疫反应、炎症和血管生成。这篇综述重点介绍了腺苷在细胞和全身循环中调节脂质可用性的作用,以及在人类和动物模型中的作用。因此,腺苷主要通过作用于 A1R 抑制脂肪分解活性,导致循环脂肪酸水平降低。这种核苷还可以通过刺激巨噬细胞上表达的 A2AR 促进胆固醇流出,以及通过激活 A2AR 和 A2BR 减少炎症过程,参与动脉粥样硬化的早期发展。腺苷还通过 A2AR 和 A3 分别在尼曼-匹克 C1 病和阿尔茨海默病中调节细胞内胆固醇的可用性。值得注意的是,在动物模型中已经研究了腺苷受体在调节血浆总胆固醇和甘油三酯水平中的作用。因此,提出了 A2BR 的抗动脉粥样硬化作用以及 A2AR 和 A1 的促动脉粥样硬化作用;A3R 尚未被证明参与脂质水平的控制或动脉粥样硬化的发展。令人惊讶的是,尽管 A2A 在分离细胞中抑制泡沫细胞形成方面发挥作用,但该受体在小鼠中似乎具有促动脉粥样硬化作用。值得注意的是,腺苷受体在人类血脂异常和动脉粥样硬化中的作用必须阐明。此外,据报道,脂质水平升高会损害腺苷/腺苷受体在控制血管张力方面的作用,我们推测这种损害可能是由于位于腺苷受体的膜微区的组成发生变化所致。最后,有人提出腺苷/腺苷受体可能在妊娠期间血脂异常现象中发挥作用。