FEBS Letters | |
Anandamide activates human platelets through a pathway independent of the arachidonate cascade | |
Menichelli, Adriana2  Maccarrone, Mauro1  Del Principe, Domenico2  Finazzi Agrò, Alessandro1  Bari, Monica1  | |
[1] Department of Experimental Medicine and Biochemical Sciences, University of Rome Tor Vergata, Via di Tor Vergata 135, I-00133 Rome, Italy;Department of Public Health and Cell Biology, University of Rome Tor Vergata, Via di Tor Vergata 135, I-00133 Rome, Italy | |
关键词: Anandamide; Arachidonate; Endocannabinoid; Lipoxygenase; Platelet; AnNH; anandamide (arachidonoylethanolamide); CB1/2; cannabinoid receptor 1/2; PaNH; palmitoylethanolamide; FAAH; fatty acid amide hydrolase; PMSF; phenylmethylsulfonyl fluoride; ASA; acetylsalicylic acid; NO; nitric oxide; SNP; sodium nitroprusside; SNAP; S-nitroso-N-acetylpenicillamine; SPER/NO; spermine NONOate; (13-H)ODNHEtOH; (13-hydroxy) linoleoylethanolamide; 15-/11-H(P)AnNH; 15-/11-hydro(pero)xy anandamide; PBS; phosphate-buffered saline; RP-HPLC; reversed phase high performance liquid chromatography; GAR-AP; goat anti-rabbit alkaline phosphatase conjugate; | |
DOI : 10.1016/S0014-5793(99)00308-7 | |
学科分类:生物化学/生物物理 | |
来源: John Wiley & Sons Ltd. | |
【 摘 要 】
Anandamide (arachidonoylethanolamide, AnNH) is shown to activate human platelets, a process which was not inhibited by acetylsalicylic acid (aspirin). Unlike AnNH, hydroperoxides generated thereof by lipoxygenase activity, and the congener (13-hydroxy)linoleoylethanolamide, were unable to activate platelets, though they counteracted AnNH-mediated stimulation. On the other hand, palmitoylethanolamide neither activated human platelets nor blocked the AnNH effects. AnNH inactivation by human platelets was afforded by a high-affinity transporter, which was activated by nitric oxide-donors up to 225% of the control. The internalized AnNH could thus be hydrolyzed by a fatty acid amide hydrolase (FAAH), characterized here for the first time.
【 授权许可】
Unknown
【 预 览 】
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