Korean Red Ginseng Water Extract Restores Impaired Endothelial Function by Inhibiting Arginase Activity in Aged Mice.
10.4196/kjpp.2014.18.2.95
- Author:
Kwanhoon CHOI
1
;
Jeongyeon YOON
;
Hyun Kyo LIM
;
Sungwoo RYOO
Author Information
1. Department of Biology, Kangwon National University, Chuncheon 200-701, Korea. ryoosw08@kangwon.ac.kr
- Publication Type:Original Article
- Keywords:
Aging;
Endothelial nitric oxide synthase;
Korean red ginseng extract;
Vasorelaxation
- MeSH:
Aging;
Animals;
Aorta;
Arginase*;
Cardiovascular Diseases;
Humans;
Lipid Peroxidation;
Male;
Mice*;
Mortality;
Nitric Oxide;
Nitric Oxide Synthase Type III;
Panax*;
Peroxynitrous Acid;
Plasma;
Reactive Oxygen Species;
Up-Regulation;
Vascular Diseases;
Vasoconstriction;
Vasodilation;
Water*
- From:The Korean Journal of Physiology and Pharmacology
2014;18(2):95-101
- CountryRepublic of Korea
- Language:English
-
Abstract:
Cardiovascular disease is the prime cause of morbidity and mortality and the population ages that may contribute to increase in the occurrence of cardiovascular disease. Arginase upregulation is associated with impaired endothelial function in aged vascular system and thus may contribute to cardiovascular disease. According to recent research, Korean Red Ginseng water extract (KRGE) may reduce cardiovascular disease risk by improving vascular system health. The purpose of this study was to examine mechanisms contributing to age-related vascular endothelial dysfunction and to determine whether KRGE improves these functions in aged mice. Young (10+/-3 weeks) and aged (55+/-5 weeks) male mice (C57BL/6J) were orally administered 0, 10, or 20 mg/mouse/day of KRGE for 4 weeks. Animals were sacrificed and the aortas were removed. Endothelial arginase activity, nitric oxide (NO) generation and reactive oxygen species (ROS) production, endothelial nitric oxide synthase (eNOS) coupling, vascular tension, and plasma peroxynitrite production were measured. KRGE attenuated arginase activity, restored nitric oxide (NO) generation, reduced ROS production, and enhanced eNOS coupling in aged mice. KRGE also improved vascular tension in aged vessels, as indicated by increased acetylcholine-induced vasorelaxation and improved phenylephrine-stimulated vasoconstriction. Furthermore, KRGE prevented plasma peroxynitrite formation in aged mice, indicating reduced lipid peroxidation. These results suggest KRGE exerts vasoprotective effects by inhibiting arginase activity and augmenting NO signaling and may be a useful treatment for age-dependent vascular diseases.
