Seong Hye Rim, Wang Cuicui, Irfan Muhammad, Kim Young Eun, Jung Gooyoung, Park Sung Kyeong, Kim Tae Myoung, Choi Ehn-Kyoung, Rhee Man Hee, Kim Yun-Bae
College of Veterinary Medicine, Chungbuk National University, Cheongju, Republic of Korea.
College of Veterinary Medicine, Kyungpook National University, Daegu, Republic of Korea.
J Ginseng Res. 2022 Sep;46(5):683-689. doi: 10.1016/j.jgr.2022.01.001. Epub 2022 Jan 12.
Since ginsenosides exert an anti-thrombotic activity, blood flow-improving effects of DK-MGAR101, an extract of mountain ginseng adventitious roots (MGAR) containing various ginsenosides, were investigated in comparison with an extract of Korean Red Ginseng (ERG).
In Sprague-Dawley rats orally administered with DK-MGAR101 or ERG, oxidative carotid arterial thrombosis was induced with FeCl (35%), and their blood flow and occlusion time were measured. To elucidate underlying mechanisms, the cytoprotective activities on rat aortic endothelial cells (RAOECs) exposed to hydrogen peroxide (HO) were confirmed. In addition, the inhibitory activities of DK-MGAR101 and ERG on agonist-induced platelet aggregation, thromboxane B production, and ATP granule release from stimulated platelets as well as blood coagulation were analyzed.
DK-MGAR101 containing high concentrations of Rb1, Rg1, Rg3, Rg5, and Rk1 ginsenosides (55.07 mg/g) was more effective than ERG (ginsenosides 8.45 mg/g) in protecting RAOECs against HO cytotoxicity. DK-MGAR101 was superior to ERG not only in suppressing platelet aggregation, thromboxane B production, and granule release, but also in delaying blood coagulation, FeCl-induced arterial occlusion, and thrombus formation.
The results indicate that DK-MGAR101 prevents blood vessel occlusion by suppressing platelet aggregation, thrombosis, and blood coagulation, in addition to endothelial cell injury.
由于人参皂苷具有抗血栓形成活性,因此对含多种人参皂苷的山参不定根提取物(MGAR)DK-MGAR101与高丽红参提取物(ERG)的血流改善作用进行了比较研究。
给Sprague-Dawley大鼠口服DK-MGAR101或ERG,用35%的FeCl3诱导氧化型颈动脉血栓形成,并测量其血流和闭塞时间。为阐明潜在机制,确认了对暴露于过氧化氢(H2O2)的大鼠主动脉内皮细胞(RAOECs)的细胞保护活性。此外,分析了DK-MGAR101和ERG对激动剂诱导的血小板聚集、血栓素B生成、刺激血小板的ATP颗粒释放以及血液凝固的抑制活性。
含有高浓度Rb1、Rg1、Rg3、Rg5和Rk1人参皂苷(55.07mg/g)的DK-MGAR101在保护RAOECs免受H2O2细胞毒性方面比ERG(人参皂苷8.45mg/g)更有效。DK-MGAR101不仅在抑制血小板聚集、血栓素B生成和颗粒释放方面优于ERG,而且在延迟血液凝固、FeCl3诱导的动脉闭塞和血栓形成方面也更优。
结果表明,DK-MGAR101除了可防止内皮细胞损伤外,还可通过抑制血小板聚集、血栓形成和血液凝固来预防血管闭塞。