• 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

Hyperlipemia: a role in regulating UCP3 gene expression in skeletal muscle during cancer cachexia?

作者信息

Busquets S, Carbó N, Almendro V, Figueras M, López-Soriano F J, Argilés J M

机构信息

Cancer Research Group, Departament de Bioquímica i Biologia Molecular, Facultat de Biologia, Universitat de Barcelona, Diagonal 645, 08071 Barcelona, Spain.

出版信息

FEBS Lett. 2001 Sep 14;505(2):255-8. doi: 10.1016/s0014-5793(01)02815-0.

DOI:10.1016/s0014-5793(01)02815-0
PMID:11566186
Abstract

Rats bearing the Yoshida AH-130 ascites hepatoma showed an increased expression of both uncoupling protein-2 (UCP2) (two-fold) and UCP3 (three- to four-fold) in skeletal muscle (both soleus and gastrocnemius). The increase in mRNA content was associated with increased circulating concentrations of fatty acids (two-fold), triglyceride (two-fold) and cholesterol (1.9-fold). Administration of nicotinic acid to tumor-bearing rats abolishes the hyperlipidemic increase associated with tumor burden. The vitamin treatment also resulted in a decreased UCP3 gene expression in soleus muscle but not in gastrocnemius. It is concluded that circulating fatty acids may be involved in the regulation of UCP3 gene expression in aerobic muscles during experimental cancer cachexia. Since the UCP3 protein could have a role in energy expenditure, it may be suggested that hypolipidemic agents may have a beneficial role in the treatment of the cachectic syndrome.

摘要

相似文献

1
Hyperlipemia: a role in regulating UCP3 gene expression in skeletal muscle during cancer cachexia?
FEBS Lett. 2001 Sep 14;505(2):255-8. doi: 10.1016/s0014-5793(01)02815-0.
2
Interorgan signaling between adipose tissue metabolism and skeletal muscle uncoupling protein homologs: is there a role for circulating free fatty acids?脂肪组织代谢与骨骼肌解偶联蛋白同系物之间的器官间信号传导:循环游离脂肪酸是否发挥作用?
Diabetes. 1998 Nov;47(11):1693-8. doi: 10.2337/diabetes.47.11.1693.
3
Skeletal muscle UCP2 and UCP3 gene expression in a rat cancer cachexia model.
FEBS Lett. 1998 Oct 9;436(3):415-8. doi: 10.1016/s0014-5793(98)01178-8.
4
Skeletal muscle UCP3 and UCP2 gene expression in response to inhibition of free fatty acid flux through mitochondrial beta-oxidation.骨骼肌中解偶联蛋白3(UCP3)和解偶联蛋白2(UCP2)基因表达对通过线粒体β-氧化的游离脂肪酸通量抑制的反应。
Pflugers Arch. 1999 Sep;438(4):452-7. doi: 10.1007/s004249900080.
5
Increased gene expression of brown fat uncoupling protein (UCP)1 and skeletal muscle UCP2 and UCP3 in MAC16-induced cancer cachexia.MAC16诱导的癌症恶病质中棕色脂肪解偶联蛋白(UCP)1以及骨骼肌UCP2和UCP3的基因表达增加。
Cancer Res. 2000 May 1;60(9):2405-10.
6
Increased adipose expression of the uncoupling protein-3 gene by thiazolidinediones in Wistar fatty rats and in cultured adipocytes.噻唑烷二酮类药物使Wistar肥胖大鼠及培养的脂肪细胞中解偶联蛋白-3基因的脂肪表达增加。
Diabetes. 1998 Nov;47(11):1809-14. doi: 10.2337/diabetes.47.11.1809.
7
Changes in FAT/CD36, UCP2, UCP3 and GLUT4 gene expression during lipid infusion in rat skeletal and heart muscle.大鼠骨骼肌和心肌脂质输注期间FAT/CD36、UCP2、UCP3和GLUT4基因表达的变化
Int J Obes Relat Metab Disord. 2002 Jun;26(6):838-47. doi: 10.1038/sj.ijo.0802005.
8
Altered gene expression of uncoupling protein-2 and -3 in stroke-prone spontaneously hypertensive rats.易卒中型自发性高血压大鼠中解偶联蛋白-2和-3的基因表达改变
J Hypertens. 2000 Sep;18(9):1233-8. doi: 10.1097/00004872-200018090-00009.
9
Skeletal muscle heterogeneity in fasting-induced upregulation of genes encoding UCP2, UCP3, PPARgamma and key enzymes of lipid oxidation.禁食诱导下骨骼肌中编码解偶联蛋白2(UCP2)、解偶联蛋白3(UCP3)、过氧化物酶体增殖物激活受体γ(PPARγ)及脂质氧化关键酶的基因上调的异质性
Pflugers Arch. 2002 Oct;445(1):80-6. doi: 10.1007/s00424-002-0879-9. Epub 2002 Jul 17.
10
Post-starvation gene expression of skeletal muscle uncoupling protein 2 and uncoupling protein 3 in response to dietary fat levels and fatty acid composition: a link with insulin resistance.饥饿后骨骼肌解偶联蛋白2和解偶联蛋白3的基因表达对膳食脂肪水平和脂肪酸组成的响应:与胰岛素抵抗的联系
Diabetes. 1999 Feb;48(2):436-41. doi: 10.2337/diabetes.48.2.436.

引用本文的文献

1
Cancer-Mediated Muscle Cachexia: Etiology and Clinical Management.癌症介导的肌肉恶病质:病因学与临床管理
Trends Endocrinol Metab. 2021 Jun;32(6):382-402. doi: 10.1016/j.tem.2021.03.007. Epub 2021 Apr 19.
2
An automatic diagnostic system based on deep learning, to diagnose hyperlipidemia.一种基于深度学习的自动诊断系统,用于诊断高脂血症。
Diabetes Metab Syndr Obes. 2019 May 3;12:637-645. doi: 10.2147/DMSO.S198547. eCollection 2019.
3
The emerging role of skeletal muscle oxidative metabolism as a biological target and cellular regulator of cancer-induced muscle wasting.
骨骼肌氧化代谢作为癌症诱导的肌肉萎缩的生物学靶点和细胞调节因子的新作用。
Semin Cell Dev Biol. 2016 Jun;54:53-67. doi: 10.1016/j.semcdb.2015.11.005. Epub 2015 Dec 1.
4
Cachexia: a problem of energetic inefficiency.恶病质:能量利用效率低下的问题。
J Cachexia Sarcopenia Muscle. 2014 Dec;5(4):279-86. doi: 10.1007/s13539-014-0154-x. Epub 2014 Aug 15.
5
Cancer cachexia is associated with a decrease in skeletal muscle mitochondrial oxidative capacities without alteration of ATP production efficiency.癌症恶病质与骨骼肌线粒体氧化能力下降有关,而不影响 ATP 生成效率。
J Cachexia Sarcopenia Muscle. 2012 Dec;3(4):265-75. doi: 10.1007/s13539-012-0071-9. Epub 2012 May 31.
6
Cancer cachexia.癌症恶病质
J Oral Maxillofac Pathol. 2011 Sep;15(3):257-60. doi: 10.4103/0973-029X.86670.
7
Energy homeostasis and cachexia in chronic kidney disease.慢性肾脏病中的能量稳态与恶病质
Pediatr Nephrol. 2006 Dec;21(12):1807-14. doi: 10.1007/s00467-006-0194-3. Epub 2006 Aug 1.
8
Long-term dietary high protein intake up-regulates tissue specific gene expression of uncoupling proteins 1 and 2 in rats.长期高蛋白质饮食可上调大鼠解偶联蛋白1和2的组织特异性基因表达。
Eur J Nutr. 2005 Oct;44(7):414-21. doi: 10.1007/s00394-004-0545-4. Epub 2004 Dec 28.