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논문 기본 정보

자료유형
학술저널
저자정보
Cheol Park (Dong-eui University) Hee-Jae Cha (Kosin University College of Medicine) Su-Hyun Hong (Dong-eui University College of Korean Medicine) Suhkmann Kim (Pusan National University) Heui-Soo Kim (Pusan National University) Yung Hyun Choi (Dong-eui University College of Korean Medicine)
저널정보
한국해양바이오학회 한국해양바이오학회지 한국해양바이오학회지 제12권 제1호
발행연도
2020.6
수록면
29 - 39 (11page)

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In this study, we investigated the inhibitory potential of an ethanol extract of Carpomitra costata (EECC) (Stackhouse) Batters, a brown alga, against neuroinflammatory responses in lipopolysaccharide (LPS)-stimulated BV2 microglia. Our results showed that EECC significantly suppressed the LPS-induced secretion of pro-inflammatory mediators, including nitric oxide (NO) and prostaglandin E2, with no significant cytotoxic effects. EECC also inhibited the LPS-induced expression of their regulatory enzymes, such as inducible NO synthase and cyclooxygenase-2. In addition, EECC downregulated the LPS-induced expression and production of the proinflammatory cytokines, tumor necrosis factor-α and interleukin-1β. In the mechanistic assessment of the antineuroinflammatory effects, EECC was found to inhibit the nuclear translocation and DNA binding of nuclear factor-kappa B (NF-κB) by disrupting the degradation of the κB-α inhibitor in the cytoplasm. Moreover, EECC effectively suppressed the enhanced expression of Toll-like receptor 4 (TLR4) and myeloid differentiation factor 88, as well as the binding of LPS to TLR4 in LPS-treated BV2 cells. Furthermore, EECC markedly reduced the LPS-induced generation of reactive oxygen species (ROS), demonstrating a strong antioxidative effect. Collectively, these results suggest that EECC repressed LPS-mediated inflammatory action in the BV2 microglia through the inactivation of NF-κB signaling by antagonizing TLR4 and/or preventing ROS accumulation. While further studies are needed to fully understand the anti-inflammatory effects associated with the antioxidant activity of EECC, the current findings suggest that EECC has a potential advantage in inhibiting the onset and treatment of neuroinflammatory diseases.

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Abstract
Introduction
Materials and Methods
Results
Discussion
Conclusion
References

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UCI(KEPA) : I410-ECN-0101-2020-472-000688317