DC Field | Value | Language |
---|---|---|
dc.contributor.author | Yo Sep Hwang | - |
dc.contributor.author | Jeewon Lim | - |
dc.contributor.author | Hyang Ran Yoon | - |
dc.contributor.author | S H Park | - |
dc.contributor.author | A Kim | - |
dc.contributor.author | Jun-Pil Jang | - |
dc.contributor.author | Hee Jun Cho | - |
dc.contributor.author | Hee Gu Lee | - |
dc.date.accessioned | 2024-01-12T16:32:50Z | - |
dc.date.available | 2024-01-12T16:32:50Z | - |
dc.date.issued | 2024 | - |
dc.identifier.issn | 1661-6596 | - |
dc.identifier.uri | https://oak.kribb.re.kr/handle/201005/33311 | - |
dc.description.abstract | Sepsis is a systemic inflammatory syndrome that results in multiple-organ failure caused by a dysregulated host immune response to microbial infection. Astragali complanati semen extract (ACSE) exhibits pharmacological activities, including antioxidant, anticancer, antiaging, and anti-diabetes effects. It is widely used in traditional medicine to treat liver and kidney diseases; however, the protective effect of ACSE on sepsis and its mechanisms are unknown. In the present study, we investigated the anti-inflammatory effects and potential mechanisms of the action of ACSE on sepsis. We show that ACSE improved survival rates in mouse models of acute sepsis induced by CLP (cecal ligation and puncture) and LPS stimulation. ACSE administration decreased aspartate aminotransferase (AST) and alanine aminotransferase (ALT) in sepsis-induced mice. Furthermore, ACSE reduced the levels of nitric oxide (NO), tumor necrosis factor-α (TNF-α), interleukin-1β (IL-1β), and interleukin-6 (IL-6) in the serum of septic mice. ACSE treatment inhibited the expression of these proinflammatory genes in LPS-stimulated J774 macrophages. Moreover, ACSE inhibited the phosphorylation of the IκB kinase (IKK) and the nuclear translocation of p65 NF-κB by LPS stimulation in macrophages. These results reveal the mechanism underlying the protective effect of ACSE against sepsis by inhibiting NF-κB activation and suggest that ACSE could be a potential therapeutic candidate to treat acute inflammatory diseases. | - |
dc.publisher | MDPI | - |
dc.title | Astragalus complanatus ethanol attenuates septic shock by exerting anti-inflammatory effects on macrophages | - |
dc.title.alternative | Astragalus complanatus ethanol attenuates septic shock by exerting anti-inflammatory effects on macrophages | - |
dc.type | Article | - |
dc.citation.title | International Journal of Molecular Sciences | - |
dc.citation.number | 1 | - |
dc.citation.endPage | 384 | - |
dc.citation.startPage | 384 | - |
dc.citation.volume | 25 | - |
dc.contributor.affiliatedAuthor | Yo Sep Hwang | - |
dc.contributor.affiliatedAuthor | Jeewon Lim | - |
dc.contributor.affiliatedAuthor | Hyang Ran Yoon | - |
dc.contributor.affiliatedAuthor | Jun-Pil Jang | - |
dc.contributor.affiliatedAuthor | Hee Jun Cho | - |
dc.contributor.affiliatedAuthor | Hee Gu Lee | - |
dc.contributor.alternativeName | 황요셉 | - |
dc.contributor.alternativeName | 임지원 | - |
dc.contributor.alternativeName | 윤향란 | - |
dc.contributor.alternativeName | 박성훈 | - |
dc.contributor.alternativeName | 김애영 | - |
dc.contributor.alternativeName | 장준필 | - |
dc.contributor.alternativeName | 조희준 | - |
dc.contributor.alternativeName | 이희구 | - |
dc.identifier.bibliographicCitation | International Journal of Molecular Sciences, vol. 25, no. 1, pp. 384-384 | - |
dc.identifier.doi | 10.3390/ijms25010384 | - |
dc.subject.keyword | Astragalus complanatus | - |
dc.subject.keyword | Sepsis | - |
dc.subject.keyword | Inflammation | - |
dc.subject.keyword | Macrophages | - |
dc.subject.keyword | NF-κB | - |
dc.subject.local | Astragalus complanatus | - |
dc.subject.local | sepsis | - |
dc.subject.local | Sepsis | - |
dc.subject.local | Inflammation | - |
dc.subject.local | inflammation | - |
dc.subject.local | nflammation | - |
dc.subject.local | macrophage | - |
dc.subject.local | macrophages | - |
dc.subject.local | Macrophage | - |
dc.subject.local | Macrophages | - |
dc.subject.local | NFkappaB | - |
dc.subject.local | NFκB | - |
dc.subject.local | Nf-κB | - |
dc.subject.local | Nf-κb | - |
dc.subject.local | Nuclear factor (NF)-κB | - |
dc.subject.local | Nuclear factor kappa B | - |
dc.subject.local | Nuclear factor kappaB | - |
dc.subject.local | Nuclear factor κB | - |
dc.subject.local | Nuclear factor κB (NF-κB) | - |
dc.subject.local | Nuclear factor-kappa B | - |
dc.subject.local | Nuclear factor-kappa B (NF-κB) | - |
dc.subject.local | Nuclear factor-kappaB | - |
dc.subject.local | Nuclear factor-κB | - |
dc.subject.local | Nuclear factor-κb | - |
dc.subject.local | NF-kB | - |
dc.subject.local | NF-kappa B | - |
dc.subject.local | NF-kappaB | - |
dc.subject.local | NF-ΚB | - |
dc.subject.local | NF-κ B | - |
dc.subject.local | NF-κB | - |
dc.subject.local | NF-κB (nuclear factor kappa-B) | - |
dc.subject.local | nuclear factor kappa B | - |
dc.subject.local | nuclear factor κB | - |
dc.subject.local | nuclear factor-kappaB | - |
dc.subject.local | nuclear factor-kappaB (NF-κB) | - |
dc.subject.local | nuclear factor-κB | - |
dc.subject.local | nuclear factorκB | - |
dc.description.journalClass | Y | - |
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