Key result
Magnolol exhibits cell-type specific and dose-related cardiovascular protective effects, including protection against ischemic/reperfusion injury, reduction of atherosclerosis, and inhibition of platelet aggregation.
Magnolol exhibits pleiotropic, dose-dependent cardiovascular protective effects in preclinical models, highlighting its potential as a preventive agent.
Hypothesis-generating for magnolol in cardioprotection; leaves open clinical translation pending human trials.
Magnolia officinalis has been widely used in traditional Chinese medicine. Magnolol, an active component isolated from Magnolia officinalis, is known to be a cardiovascular protector since 1994. The multiplex mechanisms of magnolol on cardiovascular protection depends on cell types and dosages, and will be reviewed and discussed in this article. Magnolol under low and moderate dosage possesses the ability to protect heart from ischemic/reperfusion injury, reduces atherosclerotic change, protects endothelial cell against apoptosis and inhibits neutrophil-endothelial adhesion. The moderate to high concentration of magnolol mainly acts on smooth muscle cells and platelets. Magnolol induces apoptosis in vascular smooth muscle cells at moderate concentration and inhibits proliferation at moderate and high concentration. High concentration of magnolol also abrogates platelet activation, aggregation and thrombus formation. Magnolol also serves as an smooth muscle relaxant only upon the high concentration. Oral intake of magnolol to reach the therapeutic level for cardiovascular protection is applicable, thus makes magnolol an agent of great potential for preventing cardiovascular diseases in high-risk patients.
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Ho et al. (2012) conducted a review in Cardiovascular diseases. Magnolol was evaluated. Magnolol exhibits cell-type specific and dose-related cardiovascular protective effects, including protection against ischemic/reperfusion injury, reduction of atherosclerosis, and inhibition of platelet aggregation.
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