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1.
Laboratory Animal Research ; : 48-48, 2018.
Article Dans Anglais | WPRIM | ID: wpr-713479

Résumé

In this article, So-Young Park is inadvertently omitted from the listed author names. In the Acknowledgement section, funding source is incorrectly cited and has been changed upon request of authors.

2.
Laboratory Animal Research ; : 105-113, 2017.
Article Dans Anglais | WPRIM | ID: wpr-204555

Résumé

Ginsenosides from Panax ginseng are well known for their diverse pharmacological effects including antithrombotic activity. Since adventitious roots of mountain ginseng (ARMG) also contain various ginsenosides, blood flow-improving effects of the dried powder and extract of ARMG were investigated. Rats were orally administered with dried powder (PARMG) or ethanol extract (EARMG) of ARMG (125, 250 or 500 mg/kg) or aspirin (30 mg/kg, a reference control) for 3 weeks. Forty min after the final administration, carotid arterial thrombosis was induced by applying a 70% FeCl₃-soaked filter paper outside the arterial wall for 5 min, and the blood flow was monitored with a laser Doppler probe. Both PARMG and EARMG delayed the FeCl₃-induced arterial occlusion in a dose-dependent manner, doubling the occlusion time at high doses. In mechanism studies, a high concentration of EARMG inhibited platelet aggregation induced by collagen in vitro. In addition, EARMG improved the blood lipid profiles, decreasing triglyceride and cholesterol levels. Although additional action mechanisms remain to be clarified, it is suggested that ARMG containing high amount of ginsenosides such as Rg₃ improves blood flow not only by inhibiting oxidative thrombosis, but also by modifying blood lipid profiles.


Sujets)
Animaux , Rats , Acide acétylsalicylique , Cholestérol , Collagène , Éthanol , Ginsénosides , Techniques in vitro , Panax , Agrégation plaquettaire , Thrombose , Triglycéride
3.
Laboratory Animal Research ; : 171-179, 2016.
Article Dans Anglais | WPRIM | ID: wpr-94495

Résumé

Anti-atherosclerosis effects of perilla oil were investigated, in comparison with lovastatin, in rabbits fed a high-cholesterol diet (HCD). Hypercholesterolemia was induced in rabbits by feeding the HCD containing 0.5% cholesterol and 1% corn oil, and perilla oil (0.1 or 0.3%) was added to the diet containing 0.5% cholesterol for 10 weeks. HCD greatly increased blood total cholesterol and low-density lipoproteins, and caused thick atheromatous plaques, covering 74% of the aortic wall. Hyper-cholesterolemia also induced lipid accumulation in the liver and kidneys, leading to lipid peroxidation. Perilla oil not only attenuated hypercholesterolemia and atheroma formation, but also reduced fat accumulation and lipid peroxidation in hepatic and renal tissues. The results indicate that perilla oil prevents atherosclerosis and fatty liver by controlling lipid metabolism, and that it could be the first choice oil to improve diet-induced metabolic syndrome.


Sujets)
Lapins , Athérosclérose , Cholestérol , Huile de maïs , Régime alimentaire , Stéatose hépatique , Hypercholestérolémie , Rein , Métabolisme lipidique , Peroxydation lipidique , Lipoprotéines LDL , Foie , Lovastatine , Perilla , Plaque d'athérosclérose
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