• 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

糖尿病大鼠心脏中泛酸的代谢

Metabolism of pantothenic acid in hearts of diabetic rats.

作者信息

Beinlich C J, Robishaw J D, Neely J R

机构信息

Geisinger Clinic, Weis Center for Research, Danville, PA 17822.

出版信息

J Mol Cell Cardiol. 1989 Jul;21(7):641-9. doi: 10.1016/0022-2828(89)90605-6.

DOI:10.1016/0022-2828(89)90605-6
PMID:2795660
Abstract

The metabolism of pantothenic acid (Pa) by cardiac muscle was studied in normal and diabetic rats. Tissue levels of Coenzyme A (CoA) are elevated in the heart during early (6 to 12 h) diabetes, remains at a high level for several days, and then returns to normal or below normal levels. The increase in total tissue CoA mainly occurs in myocytes as indicated by isolation of cardiac myocytes from control and diabetic animals and measuring their content of CoA. The CoA concentration increased from 37 to 93 microM in the cytosolic compartment and from 2.0 to 2.6 mM in the mitochondrial matrix. These effects of diabetes were reversed by insulin treatment. CoA synthesis in hearts removed from control rats and perfused in vitro was stimulated by including in the perfusate Pa, cysteine and dithiothreitol, but no exogenous energy substrate. This stimulated in vitro rate of CoA synthesis was reduced in hearts removed from diabetic animals, and the reduction increased with duration of diabetes. The reduced rate in diabetic hearts resulted from both a decreased rate of Pa phosphorylation and decreased Pa transport. Transport of Pa into myocytes was decreased by as much as 80% in hearts from diabetic animals. The low transport rate was due to a decrease in Vmax with no apparent change in Km. Treatment of the isolated heart with insulin did not correct the diabetic-induced reduction in Pa transport. The transport rate in normal and diabetic hearts was not influenced by the type of energy substrate provided to the heart.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

研究了正常大鼠和糖尿病大鼠心肌中泛酸(Pa)的代谢情况。在糖尿病早期(6至12小时),心脏中辅酶A(CoA)的组织水平升高,持续数天保持在高水平,然后恢复到正常或低于正常水平。通过从对照动物和糖尿病动物中分离心肌细胞并测量其CoA含量表明,总组织CoA的增加主要发生在心肌细胞中。胞质区室中的CoA浓度从37微摩尔/升增加到93微摩尔/升,线粒体基质中的CoA浓度从2.0毫摩尔/升增加到2.6毫摩尔/升。胰岛素治疗可逆转糖尿病的这些影响。在体外灌注时,向灌注液中加入Pa、半胱氨酸和二硫苏糖醇,但不添加外源能量底物,可刺激从对照大鼠心脏中取出的心脏中CoA的合成。从糖尿病动物心脏中取出的心脏,这种体外刺激的CoA合成速率降低,且随着糖尿病持续时间的延长而增加。糖尿病心脏中合成速率降低是由于Pa磷酸化速率降低和Pa转运减少所致。糖尿病动物心脏中Pa向心肌细胞的转运减少了多达80%。转运速率低是由于Vmax降低,而Km无明显变化。用胰岛素处理离体心脏并不能纠正糖尿病引起的Pa转运减少。正常和糖尿病心脏的转运速率不受提供给心脏的能量底物类型的影响。(摘要截短于250字)

相似文献

1
Metabolism of pantothenic acid in hearts of diabetic rats.糖尿病大鼠心脏中泛酸的代谢
J Mol Cell Cardiol. 1989 Jul;21(7):641-9. doi: 10.1016/0022-2828(89)90605-6.
2
Myocardial metabolism of pantothenic acid in chronically diabetic rats.慢性糖尿病大鼠中泛酸的心肌代谢
J Mol Cell Cardiol. 1990 Mar;22(3):323-32. doi: 10.1016/0022-2828(90)91465-j.
3
Regulation of coenzyme A synthesis in heart muscle: effects of diabetes and fasting.
Am J Physiol. 1981 Apr;240(4):H606-11. doi: 10.1152/ajpheart.1981.240.4.H606.
4
Coenzyme A degradation in the heart: effects of diabetes and insulin.心脏中辅酶A的降解:糖尿病和胰岛素的影响。
J Mol Cell Cardiol. 1987 Mar;19(3):281-8. doi: 10.1016/s0022-2828(87)80595-3.
5
Effects of diabetes and fasting on pantothenic acid metabolism in rats.
Am J Physiol. 1981 Jun;240(6):E597-601. doi: 10.1152/ajpendo.1981.240.6.E597.
6
Coenzyme A metabolism in pantothenic acid-deficient rats.泛酸缺乏大鼠体内的辅酶A代谢
J Nutr. 1982 Jun;112(6):1144-50. doi: 10.1093/jn/112.6.1144.
7
Insulin effects on pantothenic acid uptake in isolated perfused working hearts from diabetic rats.胰岛素对糖尿病大鼠离体灌注工作心脏中泛酸摄取的影响。
Diabetes. 1988 Oct;37(10):1335-9. doi: 10.2337/diab.37.10.1335.
8
Fatty acid metabolism in hearts containing elevated levels of CoA.在辅酶A水平升高的心脏中的脂肪酸代谢。
Am J Physiol. 1986 Mar;250(3 Pt 2):H351-9. doi: 10.1152/ajpheart.1986.250.3.H351.
9
Rate-limiting step and control of coenzyme A synthesis in cardiac muscle.心肌中辅酶A合成的限速步骤及调控
J Biol Chem. 1982 Sep 25;257(18):10967-72.
10
Pantothenate kinase and control of CoA synthesis in heart.泛酸激酶与心脏中辅酶A合成的调控
Am J Physiol. 1984 Apr;246(4 Pt 2):H532-41. doi: 10.1152/ajpheart.1984.246.4.H532.

引用本文的文献

1
Coenzyme A biosynthesis: mechanisms of regulation, function and disease.辅酶 A 生物合成:调控机制、功能与疾病。
Nat Metab. 2024 Jun;6(6):1008-1023. doi: 10.1038/s42255-024-01059-y. Epub 2024 Jun 13.
2
Regulation of coenzyme A levels by degradation: the 'Ins and Outs'.辅酶 A 水平的降解调控:“内与外”。
Prog Lipid Res. 2020 Apr;78:101028. doi: 10.1016/j.plipres.2020.101028. Epub 2020 Mar 29.
3
Stable isotope labeling by essential nutrients in cell culture for preparation of labeled coenzyme A and its thioesters.
细胞培养中必需营养物的稳定同位素标记用于标记辅酶 A 及其硫酯的制备。
Anal Chem. 2011 Feb 15;83(4):1363-9. doi: 10.1021/ac1027353. Epub 2011 Jan 26.
4
Coenzyme A sequestration in rat hearts oxidizing ketone bodies.大鼠心脏中辅酶A隔离与酮体氧化
J Clin Invest. 1992 Mar;89(3):968-73. doi: 10.1172/JCI115679.