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New Advances in Adaptive Thermogenesis: UCP1 and Beyond.适应性生热的新进展:解耦蛋白 1 及其他。
Cell Metab. 2019 Jan 8;29(1):27-37. doi: 10.1016/j.cmet.2018.11.002. Epub 2018 Nov 29.
2
Mechanisms underlying UCP1 dependent and independent adipocyte thermogenesis.UCP1 依赖性和非依赖性脂肪细胞产热的机制。
Obes Rev. 2019 Feb;20(2):241-251. doi: 10.1111/obr.12796. Epub 2018 Nov 18.
3
Serotonin signals through a gut-liver axis to regulate hepatic steatosis.血清素通过肠-肝轴传递信号以调节肝脂肪变性。
Nat Commun. 2018 Nov 16;9(1):4824. doi: 10.1038/s41467-018-07287-7.
4
De novo NAD synthesis enhances mitochondrial function and improves health.从头合成 NAD 可增强线粒体功能并改善健康。
Nature. 2018 Nov;563(7731):354-359. doi: 10.1038/s41586-018-0645-6. Epub 2018 Oct 24.
5
Nucleus of the Solitary Tract Serotonin 5-HT Receptors Modulate Food Intake.孤束核 5-羟色胺能受体调节摄食。
Cell Metab. 2018 Oct 2;28(4):619-630.e5. doi: 10.1016/j.cmet.2018.07.017. Epub 2018 Aug 23.
6
Cardiovascular Safety of Lorcaserin in Overweight or Obese Patients.盐酸氯卡色林在超重或肥胖患者中的心血管安全性。
N Engl J Med. 2018 Sep 20;379(12):1107-1117. doi: 10.1056/NEJMoa1808721. Epub 2018 Aug 26.
7
Abnormal absorptive colonic motor activity in germ-free mice is rectified by butyrate, an effect possibly mediated by mucosal serotonin.无菌小鼠结肠吸收运动异常可被丁酸盐纠正,这种作用可能是通过黏膜内 5-羟色胺介导的。
Am J Physiol Gastrointest Liver Physiol. 2018 Nov 1;315(5):G896-G907. doi: 10.1152/ajpgi.00237.2017. Epub 2018 Aug 10.
8
A population of gut epithelial enterochromaffin cells is mechanosensitive and requires Piezo2 to convert force into serotonin release.肠上皮嗜铬细胞群体具有机械敏感性,需要 Piezo2 将力转化为 5-羟色胺释放。
Proc Natl Acad Sci U S A. 2018 Aug 7;115(32):E7632-E7641. doi: 10.1073/pnas.1804938115. Epub 2018 Jul 23.
9
Inhibition of Serotonin Synthesis Induces Negative Hepatic Lipid Balance.血清素合成的抑制会导致肝脏脂质平衡呈负向变化。
Diabetes Metab J. 2018 Jun;42(3):233-243. doi: 10.4093/dmj.2017.0084. Epub 2018 Apr 25.
10
Multifaceted Roles of Beige Fat in Energy Homeostasis Beyond UCP1.米色脂肪在解偶联蛋白 1 之外的能量平衡中的多方面作用。
Endocrinology. 2018 Jul 1;159(7):2545-2553. doi: 10.1210/en.2018-00371.

血清素在调节代谢中的新作用:古老分子的新意义。

Emerging Roles for Serotonin in Regulating Metabolism: New Implications for an Ancient Molecule.

机构信息

Division of Endocrinology and Metabolism, Department of Medicine, McMaster University, Hamilton, Ontario, Canada.

Centre for Metabolism, Obesity and Diabetes Research, McMaster University, Hamilton, Ontario, Canada.

出版信息

Endocr Rev. 2019 Aug 1;40(4):1092-1107. doi: 10.1210/er.2018-00283.

DOI:10.1210/er.2018-00283
PMID:30901029
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6624793/
Abstract

Serotonin is a phylogenetically ancient biogenic amine that has played an integral role in maintaining energy homeostasis for billions of years. In mammals, serotonin produced within the central nervous system regulates behavior, suppresses appetite, and promotes energy expenditure by increasing sympathetic drive to brown adipose tissue. In addition to these central circuits, emerging evidence also suggests an important role for peripheral serotonin as a factor that enhances nutrient absorption and storage. Specifically, glucose and fatty acids stimulate the release of serotonin from the duodenum, promoting gut peristalsis and nutrient absorption. Serotonin also enters the bloodstream and interacts with multiple organs, priming the body for energy storage by promoting insulin secretion and de novo lipogenesis in the liver and white adipose tissue, while reducing lipolysis and the metabolic activity of brown and beige adipose tissue. Collectively, peripheral serotonin acts as an endocrine factor to promote the efficient storage of energy by upregulating lipid anabolism. Pharmacological inhibition of serotonin synthesis or signaling in key metabolic tissues are potential drug targets for obesity, type 2 diabetes, and nonalcoholic fatty liver disease (NAFLD).

摘要

血清素是一种演化上古老的生物胺,在数亿年的时间里对维持能量平衡起着至关重要的作用。在哺乳动物中,中枢神经系统产生的血清素通过增加对棕色脂肪组织的交感神经驱动来调节行为、抑制食欲和促进能量消耗。除了这些中枢回路外,新出现的证据还表明,外周血清素作为一种增强营养吸收和储存的因素具有重要作用。具体来说,葡萄糖和脂肪酸刺激十二指肠释放血清素,促进肠道蠕动和营养吸收。血清素也进入血液并与多个器官相互作用,通过促进肝脏和白色脂肪组织中的胰岛素分泌和从头脂肪生成,为能量储存做好准备,同时减少脂肪分解和棕色和米色脂肪组织的代谢活性。总的来说,外周血清素作为一种内分泌因子,通过上调脂质合成代谢来促进能量的有效储存。在关键代谢组织中抑制血清素合成或信号传递可能是肥胖、2 型糖尿病和非酒精性脂肪性肝病 (NAFLD) 的潜在药物靶点。