• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

链脲佐菌素诱导的糖尿病对大鼠7α-羟基-4-胆甾烯-3-酮特异性12α-羟化酶活性的影响。

Effect of streptozotocin-induced diabetes on the activity of 7 alpha-hydroxy-4-cholesten-3-one-specific 12 alpha-hydroxylase in rats.

作者信息

Kimura K, Ogura M

机构信息

Department of Biochemistry, Tottori University School of Medicine.

出版信息

Biol Chem Hoppe Seyler. 1988 Oct;369(10):1117-20. doi: 10.1515/bchm3.1988.369.2.1117.

DOI:10.1515/bchm3.1988.369.2.1117
PMID:3149485
Abstract

The activity of 12 alpha-hydroxylase in hepatic microsomes from normal, streptozotocin-induced diabetic, and insulin-treated diabetic rats was studied with 7 alpha-hydroxy-4-cholesten-3-one as a substrate. In the diabetic rats, the 12 alpha-hydroxylase activity was about 50% lower than in the normal rats. Treatment of the diabetics with insulin cancelled the reduction of the activity. These results show that an insulin-deficient state causes a paradoxical decrease in the activity of the key enzyme for cholic acid formation.

摘要

以7α-羟基-4-胆甾烯-3-酮为底物,研究了正常大鼠、链脲佐菌素诱导的糖尿病大鼠以及胰岛素治疗的糖尿病大鼠肝微粒体中12α-羟化酶的活性。糖尿病大鼠的12α-羟化酶活性比正常大鼠低约50%。用胰岛素治疗糖尿病大鼠可消除酶活性的降低。这些结果表明,胰岛素缺乏状态会导致胆酸形成关键酶的活性出现反常降低。

相似文献

1
Effect of streptozotocin-induced diabetes on the activity of 7 alpha-hydroxy-4-cholesten-3-one-specific 12 alpha-hydroxylase in rats.链脲佐菌素诱导的糖尿病对大鼠7α-羟基-4-胆甾烯-3-酮特异性12α-羟化酶活性的影响。
Biol Chem Hoppe Seyler. 1988 Oct;369(10):1117-20. doi: 10.1515/bchm3.1988.369.2.1117.
2
Decrease in the levels of a constitutive cytochrome P-450 (RLM5) in hepatic microsomes of diabetic rats.糖尿病大鼠肝微粒体中组成型细胞色素P-450(RLM5)水平降低。
Biochem Biophys Res Commun. 1987 Feb 13;142(3):623-30. doi: 10.1016/0006-291x(87)91460-4.
3
Increased activity of testosterone hydroxylases in liver microsomes of diabetic rats treated with insulin.胰岛素治疗的糖尿病大鼠肝脏微粒体中睾酮羟化酶活性增加。
Comp Biochem Physiol B. 1985;81(3):691-4. doi: 10.1016/0305-0491(85)90388-8.
4
Sex-dependent effect of streptozotocin-induced diabetes mellitus on hepatic steroid metabolism in the rat.链脲佐菌素诱导的糖尿病对大鼠肝脏类固醇代谢的性别依赖性影响。
Acta Endocrinol (Copenh). 1986 Feb;111(2):217-21. doi: 10.1530/acta.0.1110217.
5
Bile acids. LXXIII. Synthesis of analogs of 7 alpha-hydroxy-4-cholesten-3-one as substrates for hepatic steroid 12 alpha-hydroxylase.胆汁酸。第七十三篇。7α-羟基-4-胆甾烯-3-酮类似物作为肝脏类固醇12α-羟化酶底物的合成。
Steroids. 1984 Jul;44(1):95-101. doi: 10.1016/s0039-128x(84)80020-3.
6
Evidence for the presence of non-lipoprotein factors in diabetic serum capable of stimulating rat hepatic cholesterol-7 alpha-hydroxylase in vitro.有证据表明糖尿病血清中存在非脂蛋白因子,这些因子在体外能够刺激大鼠肝脏胆固醇7α-羟化酶。
Biochem Biophys Res Commun. 1984 Jun 29;121(3):743-8. doi: 10.1016/0006-291x(84)90741-1.
7
Insulin is a dominant suppressor of sterol 12 alpha-hydroxylase P450 (CYP8B) expression in rat liver: possible role of insulin in circadian rhythm of CYP8B.胰岛素是大鼠肝脏中固醇12α-羟化酶P450(CYP8B)表达的主要抑制因子:胰岛素在CYP8B昼夜节律中的可能作用。
J Biochem. 2000 Jan;127(1):57-64. doi: 10.1093/oxfordjournals.jbchem.a022584.
8
Cholesterol 7 alpha-hydroxylase of rat liver: an insulin sensitive enzyme.大鼠肝脏胆固醇7α-羟化酶:一种胰岛素敏感酶。
Biochem Biophys Res Commun. 1984 Nov 14;124(3):896-902. doi: 10.1016/0006-291x(84)91042-8.
9
Assays for cholesterol 7 alpha-hydroxylase and 12 alpha-hydroxylase using high performance liquid chromatography.
Steroids. 1985 Jun;45(6):539-50. doi: 10.1016/0039-128x(85)90018-2.
10
Complexation of cytochrome P-450 isozymes in hepatic microsomes from SKF 525-A-induced rats.来自SKF 525 - A诱导大鼠肝脏微粒体中细胞色素P - 450同工酶的络合作用。
Arch Biochem Biophys. 1988 May 1;262(2):381-8. doi: 10.1016/0003-9861(88)90202-0.

引用本文的文献

1
Bile acids in glucose metabolism and insulin signalling - mechanisms and research needs.胆汁酸在糖代谢和胰岛素信号转导中的作用——机制和研究需求。
Nat Rev Endocrinol. 2019 Dec;15(12):701-712. doi: 10.1038/s41574-019-0266-7. Epub 2019 Oct 15.