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Am J Physiol Heart Circ Physiol 293: H3602-H3607, 2007. First published September 21, 2007; doi:10.1152/ajpheart.00098.2007
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Cannabidiol, a nonpsychoactive Cannabis constituent, protects against myocardial ischemic reperfusion injury

Ronen Durst,1 Haim Danenberg,1 Ruth Gallily,2 Raphael Mechoulam,3 Keren Meir,4 Etty Grad,1 Ronen Beeri,1 Thea Pugatsch,1 Elizabet Tarsish,1 and Chaim Lotan1

1Cardiology Department and 4Pathology Department, Hadassah Hebrew University Medical Center, 2Lautenberg Center for General and Tumor Immunology, and 3Department of Medicinal Chemistry and Natural Products, Pharmacy School, Hebrew University Medical School, Jerusalem, Israel

Submitted 24 January 2007 ; accepted in final form 19 September 2007

Cannabidiol (CBD) is a major, nonpsychoactive Cannabis constituent with anti-inflammatory activity mediated by enhancing adenosine signaling. Inasmuch as adenosine receptors are promising pharmaceutical targets for ischemic heart diseases, we tested the effect of CBD on ischemic rat hearts. For the in vivo studies, the left anterior descending coronary artery was transiently ligated for 30 min, and the rats were treated for 7 days with CBD (5 mg/kg ip) or vehicle. Cardiac function was studied by echocardiography. Infarcts were examined morphometrically and histologically. For ex vivo evaluation, CBD was administered 24 and 1 h before the animals were killed, and hearts were harvested for physiological measurements. In vivo studies showed preservation of shortening fraction in CBD-treated animals: from 48 ± 8 to 39 ± 8% and from 44 ± 5 to 32 ± 9% in CBD-treated and control rats, respectively (n = 14, P < 0.05). Infarct size was reduced by 66% in CBD-treated animals, despite nearly identical areas at risk (9.6 ± 3.9 and 28.2 ± 7.0% in CBD and controls, respectively, P < 0.001) and granulation tissue proportion as assessed qualitatively. Infarcts in CBD-treated animals were associated with reduced myocardial inflammation and reduced IL-6 levels (254 ± 22 and 2,812 ± 500 pg/ml in CBD and control rats, respectively, P < 0.01). In isolated hearts, no significant difference in infarct size, left ventricular developed pressures during ischemia and reperfusion, or coronary flow could be detected between CBD-treated and control hearts. Our study shows that CBD induces a substantial in vivo cardioprotective effect from ischemia that is not observed ex vivo. Inasmuch as CBD has previously been administered to humans without causing side effects, it may represent a promising novel treatment for myocardial ischemia.

ischemia-reperfusion; myocardial infarction; cannabinoids; pharmacotherapy



Address for reprint requests and other correspondence: R. Durst, Cardiac Echo Lab, Massachusetts General Hospital, Blake 2, Rm. 255, 55 Fruit St., Boston, MA 02114 (e-mail: rdurst{at}partners.org)




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