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      KCI등재 SCOPUS SCIE

      Therapeutic Effect of Acer tegmentosum Maxim Twig Extract in Bile Duct Ligation-Induced Acute Cholestasis in Mice

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      https://www.riss.kr/link?id=A108472155

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      다국어 초록 (Multilingual Abstract)

      Cholestatic liver disease, or cholestasis, is a condition characterized by liver inflammation and fibrosis following a bile duct obstruction and an intrahepatic accumulation of bile acids. Inhibiting inflammation is a promising therapeutic strategy fo...

      Cholestatic liver disease, or cholestasis, is a condition characterized by liver inflammation and fibrosis following a bile duct obstruction and an intrahepatic accumulation of bile acids. Inhibiting inflammation is a promising therapeutic strategy for cholestatic liver diseases. Acer tegmentosum Maxim extract (ATE) is best known for its anti-inflammatory and antioxidative properties. In this study, we investigated the effects of ATE on liver injury and fibrosis in mice with bile duct ligation (BDL)-induced cholestasis through analysis of gene expression, cytokines, and histological examination. Oral administration of ATE (20 or 50 mg/kg) for 14 days significantly attenuated hepatocellular necrosis compared to vehicle-treated BDL mice, which was accompanied by the reduced level of serum bile acids and bilirubin. We determined that ATE treatment reduced liver inflammation, oxidative stress, and fibrosis. These beneficial effects of ATE were concurrent with the decreased expression of genes involved in the NF-κB pathway, suggesting that the anti-inflammatory effect of ATE could be a possible mechanism against cholestasis-associated liver injury. Our findings substantiate ATE's role as an alternative therapeutic agent for cholestasis-induced liver injury and fibrosis.

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      참고문헌 (Reference) 논문관계도

      1 Ha H, "Water extract of Acer tegmentosum reduces bone destruction by inhibiting osteoclast differentiation and function" 19 : 3940-3954, 2014

      2 Fu Y, "The novel Chinese medicine JY5formula alleviates hepatic fibrosis by inhibiting the Notch signaling pathway" 12 : 671152-, 2021

      3 Terziroli Beretta-Piccoli B, "The challenges of primary biliary cholangitis : What is new and what needs to be done" 105 : 102328-, 2019

      4 Tacke F, "Targeting hepatic macrophages to treat liver diseases" 66 : 1300-1312, 2017

      5 Ye Q, "Salidroside inhibits CCl4-induced liver fibrosis in mice by reducing activation and migration of HSC induced by liver sinusoidal endothelial cell-derived exosomal SphK1" 12 : 677810-, 2021

      6 Li H, "Salidroside improves high-fat diet-induced non-alcoholic steatohepatitis by regulating the gut microbiota-bile acid-farnesoid X receptor axis" 124 : 109915-, 2020

      7 Feng J, "Salidroside ameliorates autophagy and activation of hepatic stellate cells in mice via NF-jB and TGF-b1/Smad3 pathways" 12 : 1837-1853, 2018

      8 Yang ZR, "Salidroside alleviates oxidative stress in the liver with non-alcoholic steatohepatitis in rats" 17 : 16-, 2016

      9 Kim TW, "Protective effect of the aqueous extract from the root of Platycodon grandiflorum on cholestasis-induced hepatic injury in mice" 50 : 1473-1478, 2012

      10 Bai Y, "Production of salidroside in metabolically engineered Escherichia coli" 4 : 6640-, 2014

      1 Ha H, "Water extract of Acer tegmentosum reduces bone destruction by inhibiting osteoclast differentiation and function" 19 : 3940-3954, 2014

      2 Fu Y, "The novel Chinese medicine JY5formula alleviates hepatic fibrosis by inhibiting the Notch signaling pathway" 12 : 671152-, 2021

      3 Terziroli Beretta-Piccoli B, "The challenges of primary biliary cholangitis : What is new and what needs to be done" 105 : 102328-, 2019

      4 Tacke F, "Targeting hepatic macrophages to treat liver diseases" 66 : 1300-1312, 2017

      5 Ye Q, "Salidroside inhibits CCl4-induced liver fibrosis in mice by reducing activation and migration of HSC induced by liver sinusoidal endothelial cell-derived exosomal SphK1" 12 : 677810-, 2021

      6 Li H, "Salidroside improves high-fat diet-induced non-alcoholic steatohepatitis by regulating the gut microbiota-bile acid-farnesoid X receptor axis" 124 : 109915-, 2020

      7 Feng J, "Salidroside ameliorates autophagy and activation of hepatic stellate cells in mice via NF-jB and TGF-b1/Smad3 pathways" 12 : 1837-1853, 2018

      8 Yang ZR, "Salidroside alleviates oxidative stress in the liver with non-alcoholic steatohepatitis in rats" 17 : 16-, 2016

      9 Kim TW, "Protective effect of the aqueous extract from the root of Platycodon grandiflorum on cholestasis-induced hepatic injury in mice" 50 : 1473-1478, 2012

      10 Bai Y, "Production of salidroside in metabolically engineered Escherichia coli" 4 : 6640-, 2014

      11 Li HY, "Plant-based foods and their bioactive compounds on fatty liver disease : Effects, mechanisms, and clinical application" 2021 : 6621644-, 2021

      12 Qiu LX, "Novel insights into the mechanisms whereby isoflavones protect against fatty liver disease" 21 : 1099-1107, 2015

      13 Trauner M, "New therapeutic concepts in bile acid transport and signaling for management of cholestasis" 65 : 1393-1404, 2017

      14 Beuers U, "New paradigms in the treatment of hepatic cholestasis : From UDCA to FXR, PXR and beyond" 62 : S25-S37, 2015

      15 He G, "NF-jB and STAT3—Key players in liver inflammation and cancer" 21 : 159-168, 2011

      16 Smolka V, "Long-term follow-up of children and adolescents with primary sclerosing cholangitis and autoimmune sclerosing cholangitis" 15 : 412-418, 2016

      17 Choi GE, "Inhibitory effect of Acer tegmentosum maxim extracts on P. gingivalis LPS-induced periodontitis" 109 : 104529-, 2020

      18 Woolbright BL, "Inflammation and cell death during cholestasis : The evolving role of bile acids" 19 : 215-228, 2019

      19 Woolbright BL, "Inflammation : Cause or consequence of chronic cholestatic liver injury" 137 : 111133-, 2020

      20 Lee CH, "Histone deacetylase 8 inhibition alleviates cholestatic liver injury and fibrosis" 183 : 114312-, 2021

      21 Park HS, "Hepatoprotective effects of an Acer tegmentosum Maxim extract through antioxidant activity and the regulation of autophagy" 239 : 111912-, 2019

      22 Fursule RA, "Hepatoprotective and antioxidant activity of Phaseolus trilobus, Ait on bile duct ligation induced liver fibrosis in rats" 129 : 416-419, 2010

      23 Barkin JA, "Endoscopic management of primary sclerosing cholangitis" 16 : 842-850, 2017

      24 Yang G, "Effect of Acer tegmentosum bark on atopic dermatitis-like skin lesions in NC/Nga mice" 177 : 53-60, 2016

      25 Hao L, "ERRc suppression by Sirt6alleviates cholestatic liver injury and fibrosis" 5 : e137566-, 2020

      26 Allen K, "Bile acids induce inflammatory genes in hepatocytes : A novel mechanism of inflammation during obstructive cholestasis" 178 : 175-186, 2011

      27 Engin A, "Bile acid toxicity and protein kinases" 1275 : 229-258, 2021

      28 Li T, "Bile acid signaling in liver metabolism and diseases" 2012 : 754067-, 2012

      29 박현정 ; 심현수 ; 박송이 ; 심인섭, "Antidepressant effect and neural mechanism of Acer tegmentosum in repeated stress–induced ovariectomized female rats" 한국통합생물학회 24 (24): 205-213, 2020

      30 김억천 ; 김소헌 ; Shan-Ji Piao ; 김택중 ; 배기호 ; 김한성 ; 홍순선 ; 이병익 ; 남문석, "Antiangiogenic Activity of Acer tegmentosum Maxim Water Extract in Vitro and in Vivo" 대한의학회 30 (30): 979-987, 2015

      31 배의진 ; 류재하 ; 박병현 ; 배은주, "Angelica keiskei Root Extract Attenuates Bile Duct Ligation-Induced Liver Injury in Mice" 한국식품영양과학회 25 (25): 435-442, 2022

      32 Cho HH, "Acer tegmentosum Maxim inhibits adipogenesis in 3T3-L1 adipocytes and attenuates lipid accumulation in obese rats fed a high-fat diet" 12 : 3753-, 2020

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