Duchesnea indica Extract Ameliorates LPS-Induced Septic Shock in Mice

被引:3
|
作者
Lee, Yuan Yee [1 ]
Yuk, Heung Joo [2 ]
Saba, Evelyn [3 ]
Kim, Sung Dae [1 ]
Kim, Dong-Seon [2 ]
Kopalli, Spandana Rajendra [4 ]
Oh, Jae-Wook [5 ]
Rhee, Man Hee [1 ]
机构
[1] Kyungpook Natl Univ, Coll Vet Med, Daegu 41566, South Korea
[2] Korea Inst Oriental Med, Herbal Med Res Div, Daejeon 34054, South Korea
[3] Pir Mehr Ali Shah Arid Agr Univ, Fac Vet & Anim Sci, Dept Vet Biomed Sci, Rawalpindi 46000, Pakistan
[4] Sejong Univ, Dept Integrat Biosci & Biotechnol, Seoul 05006, South Korea
[5] Konkuk Univ, Dept Stem Cell & Regenerat Biotechnol, KIT, Seoul 05029, South Korea
基金
新加坡国家研究基金会;
关键词
NF-KAPPA-B; KOREAN RED GINSENG; ELLAGIC ACID; ANTIOXIDANT ACTIVITY; P38; MAPK; SEPSIS; CELLS; KB; INFLAMMATION; INHIBITION;
D O I
10.1155/2022/5783867
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
Objective. Duchesnea indica has been reported for its anti-inflammatory properties. However, its efficacy in sepsis has yet to be reported. In this study, we studied the ability of Duchesnea indica extract (DIE) to rescue mice from septic shock and sepsis. Methods. In vitro studies included the measurement of secreted nitric oxide, cell viability, gene and protein expression via real-time polymerase chain reaction and western blot, and confocal microscopy in RAW 264.7 cells. In vivo studies include a model of septic shock and sepsis in BALB/c mice induced by a lethal and sub-lethal dose of lipopolysaccharide (LPS). Results. DIE suppressed the expression of proinflammatory cytokines induced by LPS and prevented the translocation of NF kappa B into the nucleus of RAW 264.7 cells. It also prevented reactive oxygen species damage induced by LPS in murine bone marrow-derived macrophages. Models of sepsis and septic shock were established in BALB/c mice and DIE-rescued mice from septic shock. DIE also reversed the increase in tumor necrosis factor-alpha and nitrite levels in the serum of mice induced with sepsis. DIE also prevented the translocation of NF kappa B from the cytosol into the nucleus in murine lungs. Histopathological damage induced by sepsis was reversed in the testis, liver, and lungs of mice. Conclusion. In conclusion, DIE is a suitable candidate for development as a therapeutic agent for sepsis.
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页数:12
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