Effect of antioxidant protection by p-coumaric acid on low-density lipoprotein cholesterol oxidation.
Zang-LY; Cosma-G; Gardner-H; Shi-XL; Castranova-V; Vallyathan-V
Am J Physiol, Cell Physiol 2000 Oct; 279(4):C954-C960
Mechanisms in which p-coumaric acid (CA) acts as an antioxidant are not well understood. This study investigated whether CA can act as a direct scavenger of reactive oxygen species (ROS) and whether it minimizes the oxidation of low-density lipoprotein (LDL). Rats were administered CA in drinking water at low or high doses for 10, 21, and 30 days (uptakes were 29 and 317 mg/day, respectively). Blood levels of 8-epiprostaglandin F-2 alpha were monitored as a marker of LDL oxidation. Oral administration of CA (317 mg/day) for 30 days significantly inhibited LDL oxidation. CA also reduced LDL cholesterol levels in serum but had no effect on levels of high-density lipoprotein cholesterol. In vitro studies that used electron spin resonance in combination with spin trapping techniques were used to determine the ability of CA to scavenge ROS and alter LDL oxidation. CA effectively scavenged . OH in a dose-dependent manner. IC50 and maximum velocity for CA scavenging of . OH were 4.72 mu M and 1.2 mu M/s, respectively, with a rate constant of 1.8 X 10(11) M-1.s(-1). Our studies suggest that the antioxidant properties of CA may involve the direct scavenging of ROS such as OH.
Mathematical-models; Statistical-analysis; Standards; Animal-studies; Oxidative-processes; Oxidation; Lipid-peroxidation; Lipids; Analytical-processes; Analytical-Method;
Author Keywords: hydroxyl radical; lipid peroxidation; reactive oxygen species
V Vallyathan, Pathology and Physiology Research Branch, Health Effects Laboratory Division, National Institute for Occupational Safety and Health, 1095 Willowdale Rd., Morgantown, WV 26505-2888
American Journal of Physiology: Cell Physiology