• 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

相似文献

1
Normal food intake and body weight in mice lacking the G protein-coupled receptor GPR39.缺乏G蛋白偶联受体GPR39的小鼠的正常食物摄入量和体重
Endocrinology. 2007 Feb;148(2):501-6. doi: 10.1210/en.2006-1275. Epub 2006 Nov 9.
2
GPR39 signaling is stimulated by zinc ions but not by obestatin.GPR39信号传导由锌离子刺激,而非由肥胖抑制素刺激。
Endocrinology. 2007 Jan;148(1):13-20. doi: 10.1210/en.2006-0933. Epub 2006 Sep 7.
3
Lack of obestatin effects on food intake: should obestatin be renamed ghrelin-associated peptide (GAP)?胃饥饿素抑制素对食物摄入无影响:胃饥饿素抑制素应更名为胃饥饿素相关肽(GAP)吗?
Regul Pept. 2007 Jun 7;141(1-3):1-7. doi: 10.1016/j.regpep.2006.12.023. Epub 2007 Jan 12.
4
Altered gastrointestinal and metabolic function in the GPR39-obestatin receptor-knockout mouse.GPR39-胃泌酸调节素受体基因敲除小鼠的胃肠和代谢功能改变
Gastroenterology. 2006 Oct;131(4):1131-41. doi: 10.1053/j.gastro.2006.07.009.
5
Obestatin, a peptide encoded by the ghrelin gene, opposes ghrelin's effects on food intake.肥胖抑制素是一种由胃饥饿素基因编码的肽,它能对抗胃饥饿素对食物摄入的影响。
Science. 2005 Nov 11;310(5750):996-9. doi: 10.1126/science.1117255.
6
GPR39, a receptor of the ghrelin receptor family, plays a role in the regulation of glucose homeostasis in a mouse model of early onset diet-induced obesity.GPR39,胃饥饿素受体家族的受体,在早期发病饮食诱导肥胖小鼠模型中,在调节葡萄糖稳态方面发挥作用。
J Neuroendocrinol. 2011 Jun;23(6):490-500. doi: 10.1111/j.1365-2826.2011.02132.x.
7
Comment on "Obestatin, a peptide encoded by the ghrelin gene, opposes ghrelin's effects on food intake".对“胃饥饿素基因编码的一种肽——肥胖抑制素,对抗胃饥饿素对食物摄入的影响”的评论
Science. 2007 Feb 9;315(5813):766; author reply 766. doi: 10.1126/science.1135047.
8
Obestatin does not activate orphan G protein-coupled receptor GPR39.胃饥饿素不激活孤儿G蛋白偶联受体GPR39。
Biochem Biophys Res Commun. 2006 Dec 8;351(1):21-5. doi: 10.1016/j.bbrc.2006.09.141. Epub 2006 Oct 19.
9
Changes in obestatin gene and GPR39 receptor expression in peripheral tissues of rat models of obesity, type 1 and type 2 diabetes.肥胖、1型和2型糖尿病大鼠模型外周组织中肥胖抑制素基因及GPR39受体表达的变化
J Diabetes. 2017 Apr;9(4):353-361. doi: 10.1111/1753-0407.12417. Epub 2016 Jul 28.
10
Effects of obestatin on energy balance and growth hormone secretion in rodents.肥胖抑制素对啮齿动物能量平衡及生长激素分泌的影响。
Endocrinology. 2007 Jan;148(1):21-6. doi: 10.1210/en.2006-0915. Epub 2006 Sep 28.

引用本文的文献

1
The Mystery Actor in the Neuroendocrine Theater: Who Really Knows Obestatin? Central Focus on Hypothalamic-Pituitary Axes.神经内分泌舞台上的神秘角色:究竟谁了解肥胖抑制素?聚焦下丘脑 - 垂体轴
Int J Mol Sci. 2025 Jul 31;26(15):7395. doi: 10.3390/ijms26157395.
2
The zinc receptor, ZnR/GPR39, modulates taste sensitivity by regulating ion secretion in mouse salivary gland.锌离子受体ZnR/GPR39通过调节小鼠唾液腺中的离子分泌来调节味觉敏感性。
iScience. 2025 Jan 28;28(2):111912. doi: 10.1016/j.isci.2025.111912. eCollection 2025 Feb 21.
3
Systematical identification of regulatory GPCRs by single-cell trajectory inference reveals the role of ADGRD1 and GPR39 in adipogenesis.
通过单细胞轨迹推断对调节性G蛋白偶联受体进行系统鉴定揭示了ADGRD1和GPR39在脂肪生成中的作用。
Sci China Life Sci. 2025 Apr;68(4):1057-1072. doi: 10.1007/s11427-024-2732-8. Epub 2025 Jan 14.
4
Signaling pathway mechanisms of neurological diseases induced by G protein-coupled receptor 39.G 蛋白偶联受体 39 诱导的神经疾病的信号通路机制。
CNS Neurosci Ther. 2023 Jun;29(6):1470-1483. doi: 10.1111/cns.14174. Epub 2023 Mar 21.
5
Inhibition of GPR39 restores defects in endothelial cell-mediated neovascularization under the duress of chronic hyperglycemia: Evidence for regulatory roles of the sonic hedgehog signaling axis.在慢性高血糖的压力下,抑制 GPR39 可恢复内皮细胞介导的血管新生缺陷: sonic hedgehog 信号轴的调节作用证据。
Proc Natl Acad Sci U S A. 2023 Jan 3;120(1):e2208541120. doi: 10.1073/pnas.2208541120. Epub 2022 Dec 27.
6
GPR39 Deficiency Impairs Memory and Alters Oxylipins and Inflammatory Cytokines Without Affecting Cerebral Blood Flow in a High-Fat Diet Mouse Model of Cognitive Impairment.在高脂饮食诱导的认知障碍小鼠模型中,GPR39基因缺失损害记忆,改变氧化脂质和炎性细胞因子水平,但不影响脑血流量。
Front Cell Neurosci. 2022 Jul 6;16:893030. doi: 10.3389/fncel.2022.893030. eCollection 2022.
7
Alterations of Serum Magnesium Concentration in Animal Models of Seizures and Epilepsy-The Effects of Treatment with a GPR39 Agonist and Knockout of the Gene.癫痫发作和癫痫动物模型中血清镁浓度的变化——GPR39 激动剂治疗和基因敲除的影响。
Cells. 2022 Jun 21;11(13):1987. doi: 10.3390/cells11131987.
8
Control of coronary vascular resistance by eicosanoids via a novel GPCR.通过新型 G 蛋白偶联受体对冠状动脉阻力的控制。
Am J Physiol Cell Physiol. 2022 May 1;322(5):C1011-C1021. doi: 10.1152/ajpcell.00454.2021. Epub 2022 Apr 6.
9
Role of GPR39 in Neurovascular Homeostasis and Disease.GPR39 在神经血管稳态和疾病中的作用。
Int J Mol Sci. 2021 Jul 30;22(15):8200. doi: 10.3390/ijms22158200.
10
The Zinc-Sensing Receptor GPR39 in Physiology and as a Pharmacological Target.锌感应受体GPR39的生理学功能及其作为药理学靶点的研究
Int J Mol Sci. 2021 Apr 8;22(8):3872. doi: 10.3390/ijms22083872.

缺乏G蛋白偶联受体GPR39的小鼠的正常食物摄入量和体重

Normal food intake and body weight in mice lacking the G protein-coupled receptor GPR39.

作者信息

Tremblay Frédéric, Perreault Mylène, Klaman Lori D, Tobin James F, Smith Erica, Gimeno Ruth E

机构信息

Cardiovascular and Metabolic Diseases, Wyeth Research, 200 Cambridge Park Drive (T4007E), Cambridge, Massachusetts 02140, USA.

出版信息

Endocrinology. 2007 Feb;148(2):501-6. doi: 10.1210/en.2006-1275. Epub 2006 Nov 9.

DOI:10.1210/en.2006-1275
PMID:17095592
Abstract

It has been recently proposed that obestatin, a peptide encoded by the ghrelin gene, reduces food intake by activating the orphan G protein-coupled receptor GPR39. To gain further insights into the role of GPR39 in body weight homeostasis, we characterized the phenotype of mice with targeted disruption of the GPR39 gene. Body weight, adiposity, and food intake were found to be similar between GPR39(+/+) and GPR39(-/-) mice. Furthermore, fasting glucose and insulin levels were similar between both genotypes. Injection of obestatin peptide (1 micromol/kg, ip) obtained from multiple sources did not consistently inhibit food intake in wild-type mice after an overnight fast, and no difference in food intake was observed between wild-type and GPR39 knockout mice after injection of the peptide. Finally, ectopic expression of GPR39 in HEK293T cells revealed a constitutive activation of the receptor that was unaffected by stimulation with obestatin. Our phenotypic characterization suggests that GPR39 is not a major modulator of food intake in mice, although a more subtle role cannot be excluded. The role of GPR39 in normal physiology requires further study and should be conducted independently of the function of obestatin.

摘要

最近有人提出,胃饥饿素基因编码的一种肽——肥胖抑制素,通过激活孤儿G蛋白偶联受体GPR39来减少食物摄入量。为了进一步深入了解GPR39在体重稳态中的作用,我们对GPR39基因靶向破坏的小鼠的表型进行了特征分析。发现GPR39(+/+)和GPR39(-/-)小鼠之间的体重、肥胖程度和食物摄入量相似。此外,两种基因型之间的空腹血糖和胰岛素水平也相似。从多个来源获得的肥胖抑制素肽(1微摩尔/千克,腹腔注射)在过夜禁食后并不能持续抑制野生型小鼠的食物摄入量,注射该肽后野生型小鼠和GPR39基因敲除小鼠之间的食物摄入量没有差异。最后,GPR39在HEK293T细胞中的异位表达显示该受体存在组成性激活,且不受肥胖抑制素刺激的影响。我们的表型特征分析表明,GPR39不是小鼠食物摄入量的主要调节因子,尽管不能排除其有更微妙的作用。GPR39在正常生理学中的作用需要进一步研究,且应独立于肥胖抑制素的功能进行研究。