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脂联素受体1可抵抗去卵巢小鼠血清骨钙素和GPRC6A表达的下降。

Adiponectin receptor 1 resists the decline of serum osteocalcin and GPRC6A expression in ovariectomized mice.

作者信息

Lin Yuan-Yu, Chen Ching-Yi, Ding Shih-Torng

机构信息

Department of Animal Science and Biotechnology, Tunghai University, Taichung, Taiwan.

Department of Animal Science and Technology, National Taiwan University, Taipei, Taiwan.

出版信息

PLoS One. 2017 Dec 1;12(12):e0189063. doi: 10.1371/journal.pone.0189063. eCollection 2017.

DOI:10.1371/journal.pone.0189063
PMID:29194451
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5711023/
Abstract

Hormonal changes that cause metabolic complications are a common problem in postmenopausal women. Adiponectin and osteocalcin are cytokines associated with glucose regulatory and insulin sensitized function in postmenopausal stages. The current study investigated the role of adiponectin signaling and osteocalcin mediated function in glucose metabolism in ovariectomized mice. In a mouse menopausal-related metabolic disorder model, overexpression of adiponectin receptor 1 improved glucose tolerance and caused resistance to body weight increase and decline of serum osteocalcin. Furthermore, adiponectin receptor 1 transgenic ovariectomized mice had higher GPRC6A (the putative osteocalcin receptor) expression in muscle tissue. Immunofluorescence indicated that GPRC6A and adiponectin receptor 1 were co-localized in mouse muscle tissues. The present finding suggested adiponectin receptor 1 can mediate the improvement of glucose metabolism by osteocalcin in ovariectomized mice. Our findings imply the possibility to ameliorate menopause-induced metabolic disorder by GPRC6A and adiponectin signaling.

摘要

导致代谢并发症的激素变化是绝经后女性的常见问题。脂联素和骨钙素是与绝经后阶段葡萄糖调节和胰岛素敏感性功能相关的细胞因子。当前研究调查了脂联素信号传导和骨钙素介导的功能在去卵巢小鼠葡萄糖代谢中的作用。在小鼠绝经相关代谢紊乱模型中,脂联素受体1的过表达改善了葡萄糖耐量,并导致对体重增加和血清骨钙素下降的抵抗。此外,脂联素受体1转基因去卵巢小鼠在肌肉组织中具有更高的GPRC6A(假定的骨钙素受体)表达。免疫荧光表明GPRC6A和脂联素受体1在小鼠肌肉组织中共定位。目前的发现表明脂联素受体1可以介导骨钙素对去卵巢小鼠葡萄糖代谢的改善作用。我们的研究结果意味着通过GPRC6A和脂联素信号传导改善绝经诱导的代谢紊乱的可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e929/5711023/1eb4c741ce76/pone.0189063.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e929/5711023/de86d5e3a505/pone.0189063.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e929/5711023/f06a87522226/pone.0189063.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e929/5711023/9ad006675b46/pone.0189063.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e929/5711023/1eb4c741ce76/pone.0189063.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e929/5711023/de86d5e3a505/pone.0189063.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e929/5711023/f06a87522226/pone.0189063.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e929/5711023/9ad006675b46/pone.0189063.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e929/5711023/1eb4c741ce76/pone.0189063.g004.jpg

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本文引用的文献

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Cell Signal. 2015 Mar;27(3):532-44. doi: 10.1016/j.cellsig.2014.12.018. Epub 2015 Jan 3.
2
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Maturitas. 2014 Sep;79(1):86-90. doi: 10.1016/j.maturitas.2014.06.008. Epub 2014 Jun 18.
3
Adiponectin receptor 1 regulates bone formation and osteoblast differentiation by GSK-3β/β-catenin signaling in mice.
脂联素受体1通过GSK-3β/β-连环蛋白信号通路调节小鼠的骨形成和成骨细胞分化。
Bone. 2014 Jul;64:147-54. doi: 10.1016/j.bone.2014.03.051. Epub 2014 Apr 5.
4
Bone-specific insulin resistance disrupts whole-body glucose homeostasis via decreased osteocalcin activation.骨特异性胰岛素抵抗通过减少骨钙素的激活作用破坏全身葡萄糖稳态。
J Clin Invest. 2014 Apr;124(4):1-13. doi: 10.1172/JCI72323. Epub 2014 Mar 18.
5
Regulation of adiponectin multimerization, signaling and function.脂联素多聚化、信号传导及功能的调控
Best Pract Res Clin Endocrinol Metab. 2014 Jan;28(1):25-31. doi: 10.1016/j.beem.2013.06.003. Epub 2013 Jul 5.
6
Role of adiponectin in mediating the association of osteocalcin with insulin resistance and type 2 diabetes: a cross sectional study in pre- and post-menopausal women.脂联素在介导骨钙素与胰岛素抵抗及2型糖尿病关联中的作用:一项针对绝经前和绝经后女性的横断面研究
Arch Physiol Biochem. 2014 May;120(2):73-9. doi: 10.3109/13813455.2013.877488. Epub 2014 Jan 9.
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