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The Antioxidant and Anti-inflammatory Effects of Abalone Intestine Digest, Haliotis discus hannai in RAW 264.7 Macrophages
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  • The Antioxidant and Anti-inflammatory Effects of Abalone Intestine Digest, Haliotis discus hannai in RAW 264.7 Macrophages
  • The Antioxidant and Anti-inflammatory Effects of Abalone Intestine Digest, Haliotis discus hannai in RAW 264.7 Macrophages
저자명
Qian. Zhong-Ji,Kim. Sun-Ae,Lee. Jun-Sik,Kim. Hak-Ju,Choi. Il-Whan,Jung. Won-Kyo
간행물명
Biotechnology and bioprocess engineering
권/호정보
2012년|17권 3호|pp.475-484 (10 pages)
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한국생물공학회
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정기간행물|ENG|
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이 논문은 한국과학기술정보연구원과 논문 연계를 통해 무료로 제공되는 원문입니다.
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기타언어초록

Abalone is a marine gastropod and an important fishery and food industrial resource that is massively maricultured in Asia, Africa, Australia, and America. However, the health beneficial effects of abalone have rarely been reported. In the present study, we examine the antioxidant and anti-inflammatory effects of abalone Haliotis discus hannai in macrophage cells. The results showed that abalone intestine digest (AID) has antioxidant activities against lipid peroxidation, ROS stress and DNA damage in $H_2O_2$-treated RAW264.7 macrophages. In the lipopolysaccharide (LPS)-induced macrophages, AID suppresses LPS-induced production of nitric oxide (NO) via inducible nitric oxide synthase (iNOS) expression in a dose-dependent manner. It also significantly reduced the generation of proinflammatory cytokines, such as interleukin (IL-$1{eta}$), tumor necrosis factor (TNF)-${alpha}$, and IL-6. Furthermore, AID significantly suppresses the phosphorylation of mitogen-activated protein kinases (MAPKs) such as ERK, JNK, and p38. These results indicated that AID inhibits oxidative damage by ROS and LPS-induced inflammatory response via blocking the MAPK signaling pathway in murine macrophages. The potent antioxidant and anti-inflammatory effects of abalone intestine as byproducts from fishery manufacturing may suggest the possibility of high valuable utilization and application as a nutraceutical and therapeutic substance.