Kim Sung Jin, Kang Seong-Il, Lee Nari, Oh Jung Min, Kim Hiyoung, Lee Mi-Gi, Song Ji Hoon, Shin Myoung-Sook
College of Korean Medicine, Gachon University, Seongnam 13120, Republic of Korea.
Jeju Institute of Korean Medicine, Jeju-si 63309, Republic of Korea.
Pharmaceuticals (Basel). 2025 Jul 28;18(8):1129. doi: 10.3390/ph18081129.
This study evaluated the immunoenhancing effects of extract in a cyclophosphamide-induced immunosuppressed mouse model. Jeju was processed via hot water extraction and 20% ethanol extraction. For immunosuppression induction, 7-week-old male BALB/c mice received intraperitoneal CPA injections (150 mg/kg, day -3; 110 mg/kg, day -1), followed by oral administration of hot water extract (ARE-W) and ethanol extract (ARE-E) at 100 and 300 mg/kg for 14 days. Oral administration of ARE-W and ARE-E was started on day 0, immediately following the final CPA injection on day -1. Immune function was assessed through body weight changes, spleen weight, NK cell activity, IFN-γ production, and splenic lymphocyte proliferation. Results demonstrated that CPA treatment induced comprehensive immune dysfunction, while extracts significantly ameliorated these immunosuppressive conditions. Notably, ARE-W (300 mg/kg) significantly enhanced NK cell cytotoxicity against tumor cells and IFN-γ production compared to the CPA group, and effectively restored spleen weight and lymphocyte proliferation. ARE-E also exhibited dose-dependent immune function recovery; however, ARE-W showed superior efficacy across most immune parameters. These findings suggest that extract, particularly ARE-W, effectively restores immune function in immunosuppressed conditions, indicating potential application as a natural functional material for ameliorating immunosuppression caused by cancer treatment or immune diseases.
本研究在环磷酰胺诱导的免疫抑制小鼠模型中评估了提取物的免疫增强作用。济州提取物通过热水提取和20%乙醇提取制备。为诱导免疫抑制,7周龄雄性BALB/c小鼠腹腔注射环磷酰胺(第-3天150 mg/kg;第-1天110 mg/kg),随后以100和300 mg/kg的剂量口服热水提取物(ARE-W)和乙醇提取物(ARE-E),持续14天。ARE-W和ARE-E的口服给药于第0天开始,即在第-1天最后一次注射环磷酰胺后立即进行。通过体重变化、脾脏重量、自然杀伤细胞活性、γ干扰素产生和脾淋巴细胞增殖来评估免疫功能。结果表明,环磷酰胺治疗导致全面的免疫功能障碍,而提取物显著改善了这些免疫抑制状况。值得注意的是,与环磷酰胺组相比,ARE-W(300 mg/kg)显著增强了自然杀伤细胞对肿瘤细胞的细胞毒性和γ干扰素的产生,并有效恢复了脾脏重量和淋巴细胞增殖。ARE-E也表现出剂量依赖性的免疫功能恢复;然而,在大多数免疫参数方面,ARE-W显示出更好的疗效。这些发现表明,提取物,特别是ARE-W,能在免疫抑制条件下有效恢复免疫功能,表明其作为一种天然功能材料在改善癌症治疗或免疫疾病引起的免疫抑制方面具有潜在应用价值。