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Reveals that apolipoprotein A-I fractions mediate high-density lipoprotein protection against atherosclerosis via reverse cholesterol transport, suggesting new targets for cardiovascular disease.
HDL metabolism and its relationship to atherosclerosis is a complex topic, though notable advances have been made. First, HDL clearly has an anti-atherogenic action. Second, this action is due to some fraction/s containing apoA-I but not apoA-II. Third, some of the molecular mechanisms involved in two key anti-atherogenic functions of HDL have been defined: reverse cholesterol transport and prevention of LDL oxidative modification. These advances may permit the development of effective strategies, complementing those already available, for treating and preventing atherothrombotic cardiovascular diseases.
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Ribas et al. (2002) studied this question.
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