Department of Integrative Biotechnology, Sungkyunkwan University, 2066 Seobu-ro, Suwon 16419, Republic of Korea.
Laboratory of Natural Products Efficacy Research, Korea Ginseng Corporation, 30 Gajeong-ro, Shinseong-dong, Yuseong-gu, Daejeon 34128, Republic of Korea.
Am J Chin Med. 2023;51(6):1361-1384. doi: 10.1142/S0192415X23500623. Epub 2023 Jul 25.
Few studies have reported the therapeutic effects of Korean red ginseng (KRG) against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). However, the positive effects of KRG on other viruses have been reported and the effects of KRG on pulmonary inflammatory diseases have also been studied. Therefore, this study investigated the therapeutic effects of KRG-water extract (KRG-WE) in a pseudo-type SARS-CoV-2 (PSV)-induced lung injury model. Constructing the pseudovirus, human angiotensin-converting enzyme 2 (hACE2) transgenic mice were infected via intranasal injection that had been orally administered with KRG-WE for six weeks. After 7-days post infection (dpi), the antiviral effects of KRG-WE were confirmed, followed by real-time polymerase chain reaction (PCR), western blot analysis, flow cytometric analysis, and an enzyme-linked immunoassay (ELISA). KRG-WE significantly inhibited an increase in immunoglobulin caused by PSV. Furthermore, KRG-WE effectively suppressed alveolar macrophages (AMs) inside the lungs and helped normalize the population of other immune cells. In addition, virus-induced gene expression and inflammatory signals such as nuclear factor-kappa B and other upstream molecules were downregulated. Moreover, KRG-WE also normalized gene expression and protein activity in the spleen. In conclusion, KRG-WE reduced AMs, normalized the immune response, and decreased the expression of inflammatory genes and activation of signaling pathway phosphorylation, thereby exhibiting anti-inflammatory effects and attenuating lung damage.
鲜有研究报道红参(KRG)对严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)的治疗作用。然而,已有研究报道了 KRG 对其他病毒的积极作用,以及 KRG 对肺部炎症性疾病的影响。因此,本研究探讨了 KRG 水提取物(KRG-WE)在假型 SARS-CoV-2(PSV)诱导的肺损伤模型中的治疗作用。构建假病毒后,通过鼻腔内注射感染 hACE2 转基因小鼠,同时用 KRG-WE 灌胃六周。感染后 7 天(dpi),确认 KRG-WE 的抗病毒作用,然后进行实时聚合酶链反应(PCR)、western blot 分析、流式细胞术分析和酶联免疫吸附试验(ELISA)。KRG-WE 显著抑制 PSV 引起的免疫球蛋白增加。此外,KRG-WE 有效抑制肺内肺泡巨噬细胞(AMs),有助于恢复其他免疫细胞的群体。此外,病毒诱导的基因表达和核因子-κB 等上游分子的炎症信号被下调。此外,KRG-WE 还使脾脏中的基因表达和蛋白活性正常化。总之,KRG-WE 减少了 AMs,使免疫反应正常化,降低了炎症基因的表达和信号通路磷酸化的激活,从而表现出抗炎作用并减轻肺损伤。