Laboratory of Efficacy Research, Korea Ginseng Corporation, 30 Gajeong-ro, Shinseong- dong, Yuseong-gu, 34128, Daejeon, Republic of Korea.
Infectious Disease Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), 125 Gwahak-ro, Yuseong- gu, 34141, Daejeon, Republic of Korea.
BMC Complement Med Ther. 2022 Nov 4;22(1):284. doi: 10.1186/s12906-022-03736-5.
Although Korean Red Ginseng (KRG) is safe, this finding was only evaluated in 3-mo-long studies. Its safety was verified through a 6-mo KRG administration clinical study, but long-term studies beyond 6 mo are insufficient. This study investigated the safety and efficacy of 12-mo KRG administration.
In this study, 300 mg/kg of KRG was administered to male and female Sprague Dawley rats for 4, 8, and 12 mo to evaluate its efficacy and safety. Clinical signs, including pathological examination and haematological analyses, were observed. Flow cytometric analyses were utilised to analyse spleen and thymus immune cell counts after 12 mo. Proteomic analysis of the sera was performed using a nanospray-interfaced mass spectrometer with an 11-plex Tandem Mass Tag (TMT) labelling system. Bioinformatic analysis was then performed using Ingenuity Pathway Analysis and PANTHER. Data are available via ProteomeXchange with identifier PXD032036.
No significant body and organ weight changes were observed, and haematological and serum biochemical analyses did not show clinical significance. The effectiveness of long-term KRG administration was confirmed through increased immune cell distribution and activity. Changes in proteins correlated with viral infection reduction were confirmed through proteomic analysis.
The results suggested that 12-mo KRG intake is safe, improves immune system activity, and reduces viral infections with no significant changes in toxicological aspects.
虽然红参(KRG)是安全的,但这一发现仅在为期 3 个月的研究中得到评估。通过为期 6 个月的 KRG 给药临床研究验证了其安全性,但超过 6 个月的长期研究还不够。本研究调查了 KRG 给药 12 个月的安全性和疗效。
在这项研究中,雄性和雌性 Sprague Dawley 大鼠给予 300mg/kg 的 KRG,进行 4、8 和 12 个月的治疗,以评估其疗效和安全性。观察临床症状,包括病理检查和血液学分析。流式细胞术分析用于分析 12 个月后脾和胸腺免疫细胞计数。使用纳喷雾接口质谱仪和 11 重串联质量标签(TMT)标记系统对血清进行蛋白质组分析。使用 IPA 和 PANTHER 进行生物信息学分析。数据可通过 ProteomeXchange 以标识符 PXD032036 获得。
未观察到体重和器官重量的显著变化,血液学和血清生化分析也未显示出临床意义。通过增加免疫细胞分布和活性证实了长期 KRG 给药的有效性。通过蛋白质组分析证实了与病毒感染减少相关的蛋白质变化。
这些结果表明,12 个月的 KRG 摄入是安全的,可提高免疫系统的活性,并减少病毒感染,而毒理学方面没有明显变化。