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      KCI등재 SCOPUS SCIE

      A Comparison of Short- and Long-Term Soy Protein Isolate Intake and Its Ability to Reduce Liver Steatosis in Obese Zucker Rats Through Modifications of Genes Involved in Inflammation and Lipid Transport

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      https://www.riss.kr/link?id=A107982750

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      다국어 초록 (Multilingual Abstract)

      Obesity can lead to several health disorders including nonalcoholic fatty liver disease (NAFLD), the aggregation of lipids within hepatocytes, and consequent inflammation of the liver tissue. Previously, we reported that feeding obese Zucker rats with...

      Obesity can lead to several health disorders including nonalcoholic fatty liver disease (NAFLD), the aggregation of lipids within hepatocytes, and consequent inflammation of the liver tissue. Previously, we reported that feeding obese Zucker rats with soy protein isolate (SPI) can reduce liver steatosis. To understand how SPI reduced liver steatosis, we conducted global gene expression analysis on liver samples obtained from these rats after short- (8 weeks) and long-term SPI feeding (16 weeks). We compared and contrasted these data using Ingenuity Pathway Analysis (IPA) software. This study focused mainly on target molecules that could be participating in inflammation processes and lipid metabolism that are well-known components of NAFLD. Inflammatory response was predicted to be inhibited in animals fed the SPI diet at both 8 and 16 weeks of experiment. This general prediction was based on negative activation z scores obtained through IPA (z score < −2.0, P < .00001) for eight aspects of immune function/inflammatory response. Lipid metabolism was predicted to be strongly enhanced in rats fed the SPI diet for 16 weeks than for 8 weeks. This prediction was based on positive activation z scores (z scores >2.0, P < .00001) of eight functions involved in lipid transport and metabolism. We observed that the longer the rats were fed the SPI diet, the more beneficial it resulted against NAFLD. Based on our findings, the predicted reductions in inflammatory mechanisms while enhancing lipid transport out of the liver could be the reasons behind the reduction of liver steatosis.

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      참고문헌 (Reference)

      1 Woodcock JM, "Three residues in the common beta chain of the human GM-CSF, IL-3 and IL-5receptors are essential for GM-CSF and IL-5 but not IL-3 high affinity binding and interact with Glu21 of GM-CSF" 13 : 5176-5185, 1994

      2 Uchimura K, "The serine protease prostasin regulates hepatic insulin sensitivity by modulating TLR4 signalling" 5 : 3428-3440, 2014

      3 Buzzetti E, "The multiple-hit pathogenesis of non-alcoholic fatty liver disease(NAFLD)" 65 : 1038-1048, 2016

      4 Meighan-Mantha RL, "The mitogeninducible Fn14 gene encodes a type I transmembrane protein that modulates fibroblast adhesion and migration" 274 : 33166-33176, 1999

      5 Garlanda C, "The interleukin-1family : Back to the future" 39 : 1003-1018, 2013

      6 Feng SL, "The Fn14 immediate-early response gene is induced during liver regeneration and highly expressed in both human and murine hepatocellular carcinomas" 156 : 1253-1261, 2000

      7 Jiang S, "TRIM24 suppresses development of spontaneous hepatic lipid accumulation and hepatocellular carcinoma in mice" 62 : 371-379, 2015

      8 Reza Hakkak, "Short- and Long-Term Soy Diet Versus Casein Protects Liver Steatosis Independent of the Arginine Content" 한국식품영양과학회 18 (18): 1274-1280, 2015

      9 Chen S, "Resveratrol improves insulin resistance, glucose and lipid metabolism in patients with nonalcoholic fatty liver disease : A randomized controlled trial" 47 : 226-232, 2015

      10 Park JK, "Quantitative analysis of NPTX2hypermethylation is a promising molecular diagnostic marker for pancreatic cancer" 35 : e9-e15, 2007

      1 Woodcock JM, "Three residues in the common beta chain of the human GM-CSF, IL-3 and IL-5receptors are essential for GM-CSF and IL-5 but not IL-3 high affinity binding and interact with Glu21 of GM-CSF" 13 : 5176-5185, 1994

      2 Uchimura K, "The serine protease prostasin regulates hepatic insulin sensitivity by modulating TLR4 signalling" 5 : 3428-3440, 2014

      3 Buzzetti E, "The multiple-hit pathogenesis of non-alcoholic fatty liver disease(NAFLD)" 65 : 1038-1048, 2016

      4 Meighan-Mantha RL, "The mitogeninducible Fn14 gene encodes a type I transmembrane protein that modulates fibroblast adhesion and migration" 274 : 33166-33176, 1999

      5 Garlanda C, "The interleukin-1family : Back to the future" 39 : 1003-1018, 2013

      6 Feng SL, "The Fn14 immediate-early response gene is induced during liver regeneration and highly expressed in both human and murine hepatocellular carcinomas" 156 : 1253-1261, 2000

      7 Jiang S, "TRIM24 suppresses development of spontaneous hepatic lipid accumulation and hepatocellular carcinoma in mice" 62 : 371-379, 2015

      8 Reza Hakkak, "Short- and Long-Term Soy Diet Versus Casein Protects Liver Steatosis Independent of the Arginine Content" 한국식품영양과학회 18 (18): 1274-1280, 2015

      9 Chen S, "Resveratrol improves insulin resistance, glucose and lipid metabolism in patients with nonalcoholic fatty liver disease : A randomized controlled trial" 47 : 226-232, 2015

      10 Park JK, "Quantitative analysis of NPTX2hypermethylation is a promising molecular diagnostic marker for pancreatic cancer" 35 : e9-e15, 2007

      11 Hales CM, "Prevalence of obesity and severe obesity among adults : United States, 2017–2018" 360 : 1-8, 2020

      12 Kakino S, "Pivotal role of TNF-a in the development and progression of nonalcoholic fatty liver disease in a murine model" 50 : 80-87, 2018

      13 Fang YL, "Pathogenesis of nonalcoholic fatty liver disease in children and adolescence: From ‘‘two hit theory’’ to ‘‘multiple hit model.’’" 24 : 2974-2983, 2018

      14 Gu J, "Nonalcoholic lipid accumulation and hepatocyte malignant transformation" 4 : 123-130, 2016

      15 Moschen AR, "Non-alcoholic steatohepatitis : A microbiota-driven disease" 24 : 537-545, 2013

      16 Castan˜o-Rodrı´guez N, "NAFLD, Helicobacter species and the intestinal microbiome" 31 : 657-668, 2017

      17 Kincaid HJ, "Microbiome-immune-metabolic axis in the epidemic of childhood obesity : Evidence and opportunities" 21 : 1-13, 2020

      18 Kawano Y, "Mechanisms of hepatic triglyceride accumulation in non-alcoholic fatty liver disease" 48 : 434-441, 2013

      19 Mortazavi A, "Mapping and quantifying mammalian transcriptomes by RNASeq" 5 : 621-628, 2008

      20 Kozaczek M, "Liver transcriptomic analysis after short- and longterm feeding of soy protein isolate and its ability to reduce liver steatosis in obese zucker rats" University of Arkansas 2020

      21 Auguet T, "Liver lipocalin 2 expression in severely obese women with non alcoholic fatty liver disease" 121 : 119-124, 2013

      22 Tilg H, "Interleukin-1 and inflammasomes in alcoholic liver disease/acute alcoholic hepatitis and nonalcoholic fatty liver disease/nonalcoholic steatohepatitis" 64 : 955-965, 2016

      23 Hotamisligil GS, "Inflammation, metaflammation and immunometabolic disorders" 542 : 177-185, 2017

      24 Sun Z, "IL-33-ST2 axis in liver disease : Progression and challenge" 2017 : 5314213-, 2017

      25 Zaiss MM, "IL-1b suppresses innate IL-25 and IL-33 production and maintains helminth chronicity" 9 : e1003531-, 2013

      26 Mirea AM, "IL-1 family cytokine pathways underlying NAFLD : Towards new treatment strategies" 24 : 458-471, 2018

      27 Freese K, "Histone deacetylase expressions in hepatocellular carcinoma and functional effects of histone deacetylase inhibitors on liver cancer cells in vitro" 11 : 1587-, 2019

      28 Charrez B, "Hepatocellular carcinoma and non-alcoholic steatohepatitis : The state of play" 22 : 2494-2502, 2016

      29 Francisco-Cruz A, "Granulocyte-macrophage colony-stimulating factor : Not just another haematopoietic growth factor" 31 : 774-, 2014

      30 Pejnovic N, "Galectin-3 and IL-33/ST2 axis roles and interplay in dietinduced steatohepatitis" 22 : 9706-9717, 2016

      31 Alwahsh SM, "Diet high in fructose leads to an overexpression of lipocalin-2 in rat fatty liver" 20 : 1807-1821, 2014

      32 Niederreiter L, "Cytokines and fatty liver diseases" 2 : 14-20, 2018

      33 Kozaczek M, "Comparison of liver gene expression by RNAseq and PCR analysis after 8 weeks of feeding soy protein isolate-or casein-based diets in an obese liver steatosis rat model" 10 : 8218-8229, 2019

      34 Kern PA, "Adiponectin expression from human adipose tissue : Relation to obesity, insulin resistance, and tumor necrosis factor-a expression" 52 : 1779-1785, 2003

      35 Tilg H, "A role for IL-1 inhibitors in the treatment of non-alcoholic fatty liver disease (NAFLD)?" 29 : 103-106, 2020

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2023 평가예정 해외DB학술지평가 신청대상 (해외등재 학술지 평가)
      2020-01-01 평가 등재학술지 유지 (해외등재 학술지 평가) KCI등재
      2014-06-24 학회명변경 한글명 : 한국식품영양과학회지 -> 한국식품영양과학회
      영문명 : Journal of the Korean Society of Food Science and Nutrition -> The Korean Society of Food Science and Nutrition
      KCI등재
      2014-04-02 학회명변경 한글명 : 한국식품영양과학회 -> 한국식품영양과학회지
      영문명 : 미등록 -> Journal of the Korean Society of Food Science and Nutrition
      KCI등재
      2013-10-01 평가 SCOPUS 등재 (등재유지) KCI등재
      2010-01-01 평가 SCI 등재 (등재유지) KCI등재
      2007-01-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      2006-01-01 평가 등재후보 1차 PASS (등재후보1차) KCI등재후보
      2005-01-20 학술지등록 한글명 : Journal of Medicinal Food
      외국어명 : Journal of Medicinal Food
      KCI등재후보
      2005-01-20 학술지등록 한글명 : Journal of Medicinal Food
      외국어명 : Journal of Medicinal Food
      KCI등재후보
      2004-01-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      학술지 인용정보

      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 1.88 0.33 1.35
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      1.09 0.84 0.536 0.08
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