Morin C, Rousseau E, Blier PU, Fortin S. Effect of docosahexaenoic acid monoacylglyceride on systemic hypertension and cardiovascular dysfunction. Am J Physiol Heart Circ Physiol 309: H93-H102, 2015. First published April 24, 2015 doi:10.1152/ajpheart.00823.2014 Fatty acid supplementation has been associated with lower blood pressure. Cardiovascular diseases are also known to be linked directly to an increase in -6 and a reduction in -3 fatty acid levels in blood circulation and tissues. To determine the effect of docosahexaenoic acid monoglycerides (MAG-DHA) on blood pressure, lipid profiles, and vascular remodeling in rats fed a high-fat/high-carbohydrate (HFHC) diet. Studies were performed in male rats subjected to 8 wk of HFHC diet supplemented or not with 3 g/day MAG-DHA. After 8 wk of daily MAG-DHA treatment, rats in the HFHC ϩ MAG-DHA group had lower arterial blood pressure and heart rate compared with the HFHC group. Moreover, MAG-DHA prevented the increase aortic wall thickness, whereas lipid analysis of aortic tissues revealed an increase in DHA/AA ratio correlated with the production of resolvin D2 and D3 metabolites. Histological analysis revealed that MAG-DHA prevented the development of LVH in the HFHC group. Serum lipid profile analysis further showed a decrease in total cholesterol (TC) and LDL, including very low-density lipoprotein (VLDL) and triglyceride (TG) levels, together with an increase in HDL levels after 8 wk of MAG-DHA treatment compared with the HFHC group. Furthermore, daily MAG-DHA treatment resulted in reduced proinflammatory marker levels such as CRP, IL-6, TNF␣, and IL-1. Altogether, these findings revealed that per os administration of MAG-DHA prevents HFHC-diet induced hypertension and LVH in rats. docosahexaenoic acid; hypertension; cardiac hypertrophy; inflammation DESPITE AGGRESSIVE TREATMENT with current therapies, hypertension and heart failure remain major public health problems due to poor quality of life, frequent hospitalizations, and death (5). New therapeutic approaches are needed to prevent the development of heart failure and reverse the progression of established dysfunction. Current evidence from experimental animal studies, epidemiological studies, and clinical trials suggests that -3 polyunsaturated fatty acids (n-3 PUFA) of marine origin may be protective against cardiovascular disease (5, 26). For example, McLennan et al. (27) reported that docosahexaenoic acid (DHA) was more effective than eicosapentaenoic acid (EPA) in delaying the development of hypertension in spontaneously hypertensive rats (SHR). Moreover, DHA inhibited ischemia-induced cardiac arrhythmias at low dietary intakes in Hooded Wistar rats (27), whereas in the stroke-prone SHR model, dietary DHA intake was found to prevent the development of hypertension (20). Other studies also found that treatment with a mixture of DHA and EPA in animal models of chronic left ventricular (LV) dysfunction resulted in beneficial effects on pressure overload-induced cardiac disease (7,11,12,27,41).Epidemio...