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Effects of Korean Black Raspberry Wines on Hepatic Cholesterol Metabolism and Retinal Vascular Formation In Vitro
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  • Effects of Korean Black Raspberry Wines on Hepatic Cholesterol Metabolism and Retinal Vascular Formation In Vitro
  • Effects of Korean Black Raspberry Wines on Hepatic Cholesterol Metabolism and Retinal Vascular Formation In Vitro
저자명
Jun. Hee-Jin,Wen. Qingcheng,Lee. Ji-Hae,Jeun. Jung-Ae,Lee. Hwa-Jung,Lee. Kwang-Geun,Oh. Sea-Kwan,Lee. Sung-Joon
간행물명
Journal of the Korean Society for Applied Biological Chemistry
권/호정보
2012년|55권 2호|pp.249-257 (9 pages)
발행정보
한국응용생명화학회
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정기간행물|ENG|
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이 논문은 한국과학기술정보연구원과 논문 연계를 통해 무료로 제공되는 원문입니다.
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기타언어초록

Toxicity, antioxidant activity, and biological functionality of Korean black raspberry wine (KBRW) extracts on human ARPE-19 and HepG2 cells were determined using MTT and lipid/malonaldehyde (MA) assays and reverse transcription polymerase chain reaction (RT-PCR) as well as anti-obesity effect of KBRW extracts on various cancer cells. All samples inhibited MA formation by 38.0-88.0%. Bokbunja and Sanmaesu exerted greater inhibitory effect than other wines. Both cell lines were each treated with KBRW for 24 h, and viability was measured by MTT assay. No toxicity was found, even at 500 ${mu}g/mL$. Changes in gene expression for CYP7A1, low-density-lipoprotein (LDL) receptor, 3-hydrozy-3-methylglutaryl-CoA (HMG-CoA) reductase, and vescular endothelial growth factor (VEGF) were assessed by semi-quantitative RT-PCR. CYP7A1 and LDL receptor expressions in ARPE-19 cells were elevated, whereas HMG CoA reductase expression was decreased by Bokbunja and Sanmaesu. Expression of VEGF was decreased by Bokbunja but elevated by Sanmaesu. In HepG2 cells, gene expression was similar after Bokbunja and Sanmaesu treatments. CYP7A1 and HMG CoA expressions were elevated. LDL receptor expression was increased by Bokbunja but decreased by Sanmaesu. Bokbunja and Sanmaesu inhibited VEGF expression but elevated those of CYP7A1 and HMG CoA reductase. Bokbunja and Sanmaesu displayed anti-cholesterol effects that could be attributed to increased gene expression in CYP7A1 and HMG CoA reductase.