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本文引用的文献

1
CREB mediates brain serotonin regulation of bone mass through its expression in ventromedial hypothalamic neurons.CREB 通过其在腹内侧下丘脑神经元中的表达介导大脑血清素对骨量的调节。
Genes Dev. 2010 Oct 15;24(20):2330-42. doi: 10.1101/gad.1977210.
2
Insulin signaling in osteoblasts integrates bone remodeling and energy metabolism.成骨细胞中的胰岛素信号转导整合了骨重塑和能量代谢。
Cell. 2010 Jul 23;142(2):296-308. doi: 10.1016/j.cell.2010.06.003.
3
Hematopoietic origin of pathological grooming in Hoxb8 mutant mice.Hoxb8 突变小鼠病理性梳理行为的造血起源。
Cell. 2010 May 28;141(5):775-85. doi: 10.1016/j.cell.2010.03.055.
4
Pharmacological inhibition of gut-derived serotonin synthesis is a potential bone anabolic treatment for osteoporosis.抑制肠道来源的血清素合成是骨质疏松症潜在的骨合成代谢治疗方法。
Nat Med. 2010 Mar;16(3):308-12. doi: 10.1038/nm.2098. Epub 2010 Feb 7.
5
Serotonin release and uptake in the gastrointestinal tract.胃肠道中的血清素释放和摄取。
Auton Neurosci. 2010 Feb 16;153(1-2):47-57. doi: 10.1016/j.autneu.2009.08.002. Epub 2009 Sep 2.
6
The transcription factor ATF4 regulates glucose metabolism in mice through its expression in osteoblasts.转录因子ATF4通过其在成骨细胞中的表达来调节小鼠的葡萄糖代谢。
J Clin Invest. 2009 Sep;119(9):2807-17. doi: 10.1172/JCI39366. Epub 2009 Aug 10.
7
Impaired gastric acidification negatively affects calcium homeostasis and bone mass.胃酸分泌受损会对钙稳态和骨量产生负面影响。
Nat Med. 2009 Jun;15(6):674-81. doi: 10.1038/nm.1963.
8
Lrp5 controls bone formation by inhibiting serotonin synthesis in the duodenum.Lrp5通过抑制十二指肠中血清素的合成来控制骨形成。
Cell. 2008 Nov 28;135(5):825-37. doi: 10.1016/j.cell.2008.09.059.
9
Luminal regulation of normal and neoplastic human EC cell serotonin release is mediated by bile salts, amines, tastants, and olfactants.正常和肿瘤性人类肠嗜铬细胞5-羟色胺释放的管腔调节由胆汁盐、胺类、味觉剂和嗅觉剂介导。
Am J Physiol Gastrointest Liver Physiol. 2008 Aug;295(2):G260-72. doi: 10.1152/ajpgi.00056.2008. Epub 2008 Jun 12.
10
Pulmonary hypertension: therapeutic targets within the serotonin system.肺动脉高压:5-羟色胺系统内的治疗靶点
Br J Pharmacol. 2008 Oct;155(4):455-62. doi: 10.1038/bjp.2008.241. Epub 2008 Jun 9.

胃肠道在控制骨量积累中的重要性。

The importance of the gastrointestinal tract in the control of bone mass accrual.

机构信息

Department of Genetics and Development, Columbia University, New York, New York, USA.

出版信息

Gastroenterology. 2011 Aug;141(2):439-42. doi: 10.1053/j.gastro.2011.06.011. Epub 2011 Jun 17.

DOI:10.1053/j.gastro.2011.06.011
PMID:21699800
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4902797/
Abstract

One of the least anticipated and less heralded outcomes of mouse genetics has been to rediscover whole organism physiology. Among the many unexpected findings that it has brought to our attention has been the realization that gut-derived serotonin is a hormone-inhibiting bone formation. The importance of this discovery presented in this review is 2-fold. First, it provides a molecular explanation for 2 human genetic diseases-osteoporosis, pseudoglioma, and high bone mass syndrome; second, it suggests a novel and anabolic way to treat osteoporosis. These findings illustrate the importance of the gastrointestinal tract in the regulation of organ physiology at yet another extraluminal site.

摘要

老鼠遗传学最出人意料和鲜为人知的结果之一是重新发现了整个生物体生理学。它引起了我们的注意,其中许多意想不到的发现之一是,肠道衍生的血清素是一种抑制骨形成的激素。本文综述的重要性有两个方面。首先,它为两种人类遗传疾病——骨质疏松症、假神经胶质瘤和高骨量综合征提供了分子解释;其次,它提示了一种治疗骨质疏松症的新的合成代谢方法。这些发现说明了胃肠道在调节另一个腔外器官生理学中的重要性。