Zong Yuan, Zhou Xujiao, Cheng Jingyi, Yu Jian, Wu Jihong, Jiang Chunhui
Department of Ophthalmology and Vision Science, Eye and ENT Hospital, Fudan University, Shanghai, China.
Key Laboratory of Myopia of State Health Ministry, and Key Laboratory of Visual Impairment and Restoration of Shanghai, Shanghai, China.
Cell Physiol Biochem. 2017;43(5):2088-2101. doi: 10.1159/000484193. Epub 2017 Oct 23.
BACKGROUND/AIMS: Cannabinoids are vasoactive substances that act as key regulators of arterial tone in the blood vessels supplying peripheral tissues and the central nervous system. We therefore investigated the effect of cannabinoids on retinal capillaries and pericytes.
The effects of cannabinoids on capillary diameters were determined using an ex vivo whole-mount rat retinal model. Western blotting, quantitative PCR, and immunohistochemistry were performed to explore the underlying mechanism.
Endogenous cannabinoid 2-arachidonoylglycerol and anandamide and exogenous cannabinoid (R-(+)-WIN55212-2) dilated the noradrenaline-precontracted capillaries in a concentration-dependent manner (1 µM to 0.1 mM). The extent of vasorelaxation was positively correlated with changes in pericyte width. The effects of R-(+)-WIN55212-2 on vasorelaxation and pericyte width were inhibited by a cannabinoid receptor type-1 (CB1) antagonist, AM251 or rimonabant (SR141716A), the nitric oxide synthase inhibitor l-NAME, and the guanylate cyclase inhibitor ODQ. They were also abolished by the removal of the endothelium, but not by the cannabinoid receptor-2 antagonist SR144528, the endothelial cannabinoid receptor antagonist O-1918, or the cyclooxygenase inhibitor indomethacin.
The exogenous cannabinoid R-(+)-WIN55212-2 promotes the vasorelaxation of pericyte-containing rat retinal capillaries. This effect of R-(+)-WIN55212-2 is dependent on CB1 and the nitric oxide-cyclic guanosine monophosphate pathway, and requires an intact endothelium.
背景/目的:大麻素是血管活性物质,在外周组织和中枢神经系统供血血管中作为动脉张力的关键调节因子。因此,我们研究了大麻素对视网膜毛细血管和周细胞的作用。
使用离体大鼠视网膜全层模型测定大麻素对毛细血管直径的影响。进行蛋白质免疫印迹、定量聚合酶链反应和免疫组织化学以探究潜在机制。
内源性大麻素2-花生四烯酸甘油酯和花生四烯酸乙醇胺以及外源性大麻素(R-(+)-WIN55212-2)以浓度依赖性方式(1 μM至0.1 mM)使去甲肾上腺素预收缩的毛细血管扩张。血管舒张程度与周细胞宽度变化呈正相关。R-(+)-WIN55212-2对血管舒张和周细胞宽度的作用被大麻素1型受体(CB1)拮抗剂AM251或利莫那班(SR141716A)、一氧化氮合酶抑制剂L-NAME和鸟苷酸环化酶抑制剂ODQ抑制。去除内皮细胞也可消除这些作用,但大麻素2型受体拮抗剂SR144528、内皮大麻素受体拮抗剂O-1918或环氧化酶抑制剂吲哚美辛则无此作用。
外源性大麻素R-(+)-WIN55212-2促进含周细胞的大鼠视网膜毛细血管的血管舒张。R-(+)-WIN55212-2的这种作用依赖于CB1和一氧化氮-环磷酸鸟苷途径,且需要完整的内皮细胞。