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胰岛素对正常、糖尿病及治疗后糖尿病大鼠肝脏和培养的大鼠肝细胞载脂蛋白B生成的影响。

Insulin effects on apolipoprotein B production by normal, diabetic and treated-diabetic rat liver and cultured rat hepatocytes.

作者信息

Sparks J D, Sparks C E, Miller L L

机构信息

Department of Pathology, University of Rochester School of Medicine and Dentistry, NY 14642.

出版信息

Biochem J. 1989 Jul 1;261(1):83-8. doi: 10.1042/bj2610083.

DOI:10.1042/bj2610083
PMID:2673217
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1138784/
Abstract
  1. The effect of insulin on apolipoprotein (apo B) secretion was studied in 24 h recirculating liver perfusions of isolated normal, diabetic and insulin-treated diabetic rats. In single perfusions from each group apo B accumulated in the media in a linear fashion. 2 In perfusions of normal rat livers, when the medium contained insulin plus cortisol, apo B production was significantly inhibited (by 35.8%), demonstrating a hormone effect on apo B secretion. 3. In perfusions of diabetic-rat livers, apo B production was decreased to 11.8% of normal when the medium contained no hormones, and was not significantly changed by the addition of insulin plus cortisol to the medium, suggesting that the hormone effect on apo B secretion is missing in long-term hypoinsulinaemic states. 4. Treatment of diabetic rats with daily insulin injection restored apo B production and restored the effect of insulin plus cortisol in the medium to inhibit apo B secretion during perfusion. 5. Parallel studies of apo B secretion with insulin alone, cortisol alone and insulin plus cortisol in the medium were performed in primary cultures of hepatocytes to compare results from liver perfusions. 6. Apo B secretion by hepatocytes from normal, diabetic and treated-diabetic rats was inhibited (by 36.8%, 57.1% and 57.9% respectively) when insulin alone was added to the medium. 7. Insulin plus cortisol inhibited apo B secretion by hepatocytes from normal and treated diabetic rats (by 30.2% and 47.2% respectively), but failed to inhibit apo B secretion by hepatocytes from diabetic rats.
摘要
  1. 在对正常、糖尿病及胰岛素治疗的糖尿病大鼠进行24小时离体肝脏再循环灌注实验中,研究了胰岛素对载脂蛋白(apo B)分泌的影响。在每组的单次灌注中,apo B以线性方式在培养基中蓄积。2. 在正常大鼠肝脏灌注实验中,当培养基中含有胰岛素加皮质醇时,apo B的产生受到显著抑制(抑制35.8%),表明激素对apo B分泌有影响。3. 在糖尿病大鼠肝脏灌注实验中,当培养基中不含激素时,apo B的产生降至正常水平的11.8%,向培养基中添加胰岛素加皮质醇后,其产生无显著变化,这表明在长期低胰岛素血症状态下,激素对apo B分泌的影响缺失。4. 每天给糖尿病大鼠注射胰岛素进行治疗,可恢复apo B的产生,并恢复培养基中胰岛素加皮质醇在灌注期间抑制apo B分泌的作用。5. 在肝细胞原代培养中,对培养基中单独使用胰岛素、单独使用皮质醇以及胰岛素加皮质醇时的apo B分泌进行了平行研究,以比较肝脏灌注实验的结果。6. 当培养基中单独添加胰岛素时,正常、糖尿病及胰岛素治疗的糖尿病大鼠肝细胞的apo B分泌均受到抑制(分别抑制36.8%、57.1%和57.9%)。7. 胰岛素加皮质醇抑制正常及胰岛素治疗的糖尿病大鼠肝细胞的apo B分泌(分别抑制30.2%和47.2%),但未能抑制糖尿病大鼠肝细胞的apo B分泌。

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Insulin effects on apolipoprotein B production by normal, diabetic and treated-diabetic rat liver and cultured rat hepatocytes.胰岛素对正常、糖尿病及治疗后糖尿病大鼠肝脏和培养的大鼠肝细胞载脂蛋白B生成的影响。
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本文引用的文献

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Protein measurement with the Folin phenol reagent.使用福林酚试剂进行蛋白质测定。
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Transitory increase in fat content and size of liver induced by insulin in alloxandiabetic rats.胰岛素诱导的四氧嘧啶糖尿病大鼠肝脏脂肪含量和大小的短暂增加。
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Lipoprotein secretion by isolated perfused livers from streptozotocin-diabetic rats.链脲佐菌素诱导的糖尿病大鼠离体灌注肝脏的脂蛋白分泌
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The effect of fasting on the secretion of lipoproteins and two forms of apo B by perfused rat liver.
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Effects of insulin and glucose on very low density lipoprotein triglyceride secretion by cultured rat hepatocytes.胰岛素和葡萄糖对培养的大鼠肝细胞极低密度脂蛋白甘油三酯分泌的影响。
J Clin Invest. 1982 Jul;70(1):63-73. doi: 10.1172/jci110604.
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Hypolipidemia.血脂过低
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Diabetes and atherosclerosis: an overview.糖尿病与动脉粥样硬化:概述
Diabetes. 1981;30(Suppl 2):1-7. doi: 10.2337/diab.30.2.s1.
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Hepatic production of VLDL-triglycerides. Dependence of portal substrate and insulin concentration.肝脏极低密度脂蛋白甘油三酯的生成。门静脉底物及胰岛素浓度的依赖性。
Horm Metab Res. 1980 Dec;12(12):688-94. doi: 10.1055/s-2007-999233.