The protective effects of Δ9-tetrahydrocannabinol against inflammation and oxidative stress in rat liver with fructose-induced hyperinsulinemia
被引:9
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作者:
Beydogan, Alisa Bahar
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机构:
Istanbul Univ, Fac Cerrahpasa Med, Dept Med Biol, TR-34098 Istanbul, TurkeyIstanbul Univ, Fac Cerrahpasa Med, Dept Med Biol, TR-34098 Istanbul, Turkey
Beydogan, Alisa Bahar
[1
]
Coskun, Zeynep Mine
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机构:
Istanbul Bilim Univ, Fac Arts & Sci, Dept Mol Biol & Genet, Istanbul, TurkeyIstanbul Univ, Fac Cerrahpasa Med, Dept Med Biol, TR-34098 Istanbul, Turkey
Coskun, Zeynep Mine
[2
]
Bolkent, Sema
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Istanbul Univ, Fac Cerrahpasa Med, Dept Med Biol, TR-34098 Istanbul, TurkeyIstanbul Univ, Fac Cerrahpasa Med, Dept Med Biol, TR-34098 Istanbul, Turkey
Bolkent, Sema
[1
]
机构:
[1] Istanbul Univ, Fac Cerrahpasa Med, Dept Med Biol, TR-34098 Istanbul, Turkey
[2] Istanbul Bilim Univ, Fac Arts & Sci, Dept Mol Biol & Genet, Istanbul, Turkey
Objectives A large amount of fructose is metabolized in the liver and causes hepatic functional damage. Delta(9)-tetrahydrocannabinol (THC) is known as a therapeutic agent for clinical and experimental applications. The study aims to investigate the effects of THC treatment on inflammation, lipid profiles and oxidative stress in rat liver with hyperinsulinemia. Methods Sprague-Dawley rats were divided into groups: control, fructose (10% fructose in drinking water for 12 weeks), THC (1.5 mg/kg/day for the last 4 weeks, intraperitoneally) and fructose+THC groups. Biochemical parameters were measured spectrophotometrically. ELISA method was used for insulin measurement. Apoptosis and inflammation markers were detected by the streptavidin-biotin peroxidase method. Key findings The consumptions of food and fluid are inversely proportional to fructose and non-fructose groups. Insulin levels were the highest in fructose group. The reduced glutathione-S-transferase level significantly increased in fructose + THC group compared with fructose group. Total cholesterol level in the fructose + THC group was higher than the fructose group. Caspase-3 and NF-kappa beta immunopositive cell numbers increased in fructose + THC rats compared with fructose group. The number of IL-6 immunopositive cell decreased in fructose + THC group compared with fructose group. Conclusions According to the result, long-term and low-dose THC administration may reduce hyperinsulinemia and inflammation in rats to some extent.
机构:
Bellinson Hosp, Dept Med D, Rabin Med Ctr, Petah Tiqwa, Israel
Bellinson Hosp, Rabin Med Ctr, Liver Inst, Petah Tiqwa, Israel
Rabin Med Ctr, Dept Gastroenterol, Petah Tiqwa, IsraelBellinson Hosp, Dept Med D, Rabin Med Ctr, Petah Tiqwa, Israel
Schmilovitz-Weiss, H.
Hoclihauser, E.
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Felsenstein Med Res Ctr, Cardiac Res Lab, Dept Cardiothorac Surg, Petah Tiqwa, IsraelBellinson Hosp, Dept Med D, Rabin Med Ctr, Petah Tiqwa, Israel
Hoclihauser, E.
Pappo, O.
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Beilinson Med Ctr, Rabin Med Ctr, Dept Histopathol, Petah Tiqwa, IsraelBellinson Hosp, Dept Med D, Rabin Med Ctr, Petah Tiqwa, Israel
Pappo, O.
Yitzhaki, S.
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机构:Bellinson Hosp, Dept Med D, Rabin Med Ctr, Petah Tiqwa, Israel
Yitzhaki, S.
Ackerman, Z.
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机构:
Hadassah Univ Hosp, Dept Med, IL-91240 Jerusalem, IsraelBellinson Hosp, Dept Med D, Rabin Med Ctr, Petah Tiqwa, Israel
Ackerman, Z.
Cheporko, Y.
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机构:
Felsenstein Med Res Ctr, Cardiac Res Lab, Dept Cardiothorac Surg, Petah Tiqwa, IsraelBellinson Hosp, Dept Med D, Rabin Med Ctr, Petah Tiqwa, Israel
Cheporko, Y.
Shainberg, A.
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机构:
Bar Ilan Univ, Fac Life Sci, Ramat Gan, IsraelBellinson Hosp, Dept Med D, Rabin Med Ctr, Petah Tiqwa, Israel
Shainberg, A.
Grossman, E.
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机构:
Chaim Sheba Med Ctr, Internal Med D & Hypertens Unit, IL-52621 Tel Hashomer, IsraelBellinson Hosp, Dept Med D, Rabin Med Ctr, Petah Tiqwa, Israel
Grossman, E.
Leibovitz, A.
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机构:Bellinson Hosp, Dept Med D, Rabin Med Ctr, Petah Tiqwa, Israel
Leibovitz, A.
Ben-Ari, Z.
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机构:
Bellinson Hosp, Rabin Med Ctr, Liver Inst, Petah Tiqwa, IsraelBellinson Hosp, Dept Med D, Rabin Med Ctr, Petah Tiqwa, Israel
机构:
Nanjing Univ, Sch Life Sci, State Key Lab Pharmaceut Biotechnol, Nanjing 210023, Peoples R ChinaNanjing Univ, Sch Life Sci, State Key Lab Pharmaceut Biotechnol, Nanjing 210023, Peoples R China
Yang, Yan-Zi
Liu, Zhi-Hong
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机构:
Nanjing Univ, Sch Life Sci, State Key Lab Pharmaceut Biotechnol, Nanjing 210023, Peoples R ChinaNanjing Univ, Sch Life Sci, State Key Lab Pharmaceut Biotechnol, Nanjing 210023, Peoples R China
Liu, Zhi-Hong
Wang, Shan-Chun
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机构:
Chia Tai Tianqing Pharmaceut Grp Co LTD, Jiangsu Key Lab Targeted Antiviral Res, Nanjing 210023, Peoples R ChinaNanjing Univ, Sch Life Sci, State Key Lab Pharmaceut Biotechnol, Nanjing 210023, Peoples R China
Wang, Shan-Chun
Zhang, Xi-Quan
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机构:
Chia Tai Tianqing Pharmaceut Grp Co LTD, Jiangsu Key Lab Targeted Antiviral Res, Nanjing 210023, Peoples R ChinaNanjing Univ, Sch Life Sci, State Key Lab Pharmaceut Biotechnol, Nanjing 210023, Peoples R China
Zhang, Xi-Quan
Xu, Hong-Jiang
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机构:
Chia Tai Tianqing Pharmaceut Grp Co LTD, Jiangsu Key Lab Targeted Antiviral Res, Nanjing 210023, Peoples R ChinaNanjing Univ, Sch Life Sci, State Key Lab Pharmaceut Biotechnol, Nanjing 210023, Peoples R China
Xu, Hong-Jiang
Yang, Ling
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机构:
Chia Tai Tianqing Pharmaceut Grp Co LTD, Jiangsu Key Lab Targeted Antiviral Res, Nanjing 210023, Peoples R ChinaNanjing Univ, Sch Life Sci, State Key Lab Pharmaceut Biotechnol, Nanjing 210023, Peoples R China
Yang, Ling
Kong, Ling-Dong
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机构:
Nanjing Univ, Sch Life Sci, State Key Lab Pharmaceut Biotechnol, Nanjing 210023, Peoples R ChinaNanjing Univ, Sch Life Sci, State Key Lab Pharmaceut Biotechnol, Nanjing 210023, Peoples R China
机构:
Ankang City Ctr Hosp, Dept Hemodialysis, Ankang 725000, Peoples R ChinaAnkang City Ctr Hosp, Dept Hemodialysis, Ankang 725000, Peoples R China
Cheng Xiaoli
Qiu Linwei
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机构:
Shandong Univ, Shandong Prov ENT Hosp, Dept Endocrinol, Jinan 250022, Peoples R ChinaAnkang City Ctr Hosp, Dept Hemodialysis, Ankang 725000, Peoples R China
Qiu Linwei
Wang Fen
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机构:
Beijing Univ Chinese Med, Affiliated Hosp 3, Dept Endocrinol, Beijing 100029, Peoples R ChinaAnkang City Ctr Hosp, Dept Hemodialysis, Ankang 725000, Peoples R China