Cardiovascular Research Advance Access originally published online on October 9, 2009
Cardiovascular Research 2009 84(3):341-342; doi:10.1093/cvr/cvp339
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Published on behalf of the European Society of Cardiology. All rights reserved. © The Author 2009. For permissions please email: journals.permissions@oxfordjournals.org.
Endocannabinoid signalling as an anti-inflammatory therapeutic target in atherosclerosis: does it work?
Institute for Transfusion Medicine, Hanover Medical School, Carl-Neuberg-Str. 1, 30625 Hanover, Germany
* Corresponding author. Tel: +49 511 532 6704/9714; fax: +49 511 532 2079. E-mail address: immenschuh.stephan@mh-hannover.de
This editorial refers to CB1 and CB2 cannabinoid receptors differentially regulate the production of reactive oxygen species by macrophages by K.H. Han et al., pp. 378–386, this issue.
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The endocannabinoid system is a physiological signalling network that has attracted major attention in recent years because of its therapeutic potential for the treatment of various pathological conditions, including cardiovascular disease. More specifically, targeted modulation of the major receptors of this system, the G-protein-coupled cannabinoid 1 (CB1) and cannabinoid 2 (CB2) receptors, has been implicated in the protection against atherosclerosis. Accumulating evidence suggests that specific blockage of these receptors may have beneficial effects on classical cardiovascular risk factors such as hypercholesterolaemia, obesity, and impaired glucose tolerance.1 In a pioneering report, it was demonstrated that low levels of the cannabinoid derivative delta-9-tetrahydrocannabinoid reduced the progression of
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Cardiovasc Res 2009 84: 378-386.[Abstract] [Full Text] [PDF]