Effects of red ginseng on the regulation of cyclooxygenase-2 of spleen cells in whole-body gamma irradiated mice.

Hyun Jung Koo, Seon-A Jang, Kwang-Hee Yang, Se Chan Kang, Seung Namkoong, Tae-Hyung Kim, Do Thi Thu Hang, Eun-Hwa Sohn
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引用次数: 17

Abstract

Exposure to gamma radiation causes a wide range of biological damage and alterations, including oxidative stress, inflammation and cancer. This study aimed to identify the radioprotective effect of Korean red ginseng extract (RG) against whole-body gamma-irradiation (γIR) in mice and the regulatory mechanisms of the radiosensitive gene in spleen, cyclooxygenase-2 (COX-2). RG was administered intraperitoneally (i.p.) or orally (p.o.) to C57BL/6 mice for five days, which were then exposed to 6.5 Gy of (137)Cs-γIR. Thymus and spleen were harvested after three days, and organ size and COX-2 expression of the spleen using Western blotting, were examined. γIR shrank both organs and RG recovered the size of thymus but not spleen. RG also significantly inhibited the increased expression of COX-2 induced by γIR. These results were similar following both routes of RG administration, however i.p. RG administration was more effective, thus it was used in progressive studies. In terms of COX-2 expression related intracellular factors, we found here that γIR activated the p38 MAPK, PI3K/Akt and HO-1 but not NF-κB or Nrf2. Activated p38 MAPK, PI3K/Akt and HO-1 were down-regulated by RG while the RG-induced COX-2 expression was only related to HO-1 activation. These results suggest that RG supplementation provides protective effects against radiation-induced inflammation and cancer, and its potential to be utilized in clinical trials and functional foods.

红参对γ辐照小鼠脾脏细胞环氧化酶-2的调节作用。
暴露于伽马辐射会引起广泛的生物损伤和改变,包括氧化应激、炎症和癌症。本研究旨在探讨红参提取物(RG)对小鼠全身γ辐照(γIR)的辐射防护作用及脾脏放射敏感基因环氧合酶-2 (COX-2)的调控机制。RG经腹腔(i.p.)或口服(p.o.)给C57BL/6小鼠5天,然后暴露于6.5 Gy的(137)Cs-γIR中。3天后取胸腺和脾脏,用Western blotting检测脏器大小和脾脏COX-2表达。γ - ir使两脏器均缩小,RG使胸腺大小恢复,脾脏未恢复。RG还能显著抑制γ - ir诱导的COX-2表达升高。两种RG给药方式的结果相似,但口服RG更有效,因此用于进行性研究。在COX-2表达相关的细胞内因子方面,我们发现γIR可激活p38 MAPK、PI3K/Akt和HO-1,但不能激活NF-κB或Nrf2。激活的p38 MAPK、PI3K/Akt和HO-1被RG下调,而RG诱导的COX-2表达仅与HO-1激活有关。这些结果表明,补充RG对辐射引起的炎症和癌症具有保护作用,并有可能用于临床试验和功能食品。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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