Roles of the interorgan neuronal network in the development of metabolic syndrome

Kenji Uno

Research output: Contribution to journalArticle

1 Citation (Scopus)

Abstract

Metabolic processes in different tissues and remote organs are under coordinated systemic regulation, allowing adaptation to a variety of external circumstances. Neuronal signals as well as humoral factors, such as nutrients, growth factors, and hormones, have attracted increasing attention for their roles in this interorgan metabolic network, responsible for the maintenance of metabolic homeostasis at the whole-body level. These interorgan communications within an organism are considered to be diverse and, in fact, we identified previously unknown neuronal relay systems originating in the liver which modulate energy, glucose, and lipid metabolism. Furthermore, when nutrient overload is prolonged, these neuronal mechanisms, which function as an endogenous defense system against obesity development, contribute to the pathophysiological states of metabolic syndrome characterized by obesity-associated features. Therefore, these interorgan neuronal systems are considered to be possible molecular targets for treating metabolic syndrome. We herein review the precise mechanisms underlying the functions of the mammalian interorgan neuronal network, especially the pathways from the liver to several other organs, focusing on their significance and roles in the development of metabolic syndrome.

Original languageEnglish
Pages (from-to)205-211
Number of pages7
JournalDiabetology International
Volume7
Issue number3
DOIs
Publication statusPublished - 2016 Sep 1

Keywords

  • Amino acids
  • Hypertension
  • Hypertriglyceridemia
  • Interorgan neuronal network
  • Metabolic syndrome
  • PPARγ
  • mTOR

ASJC Scopus subject areas

  • Internal Medicine
  • Endocrinology, Diabetes and Metabolism

Fingerprint Dive into the research topics of 'Roles of the interorgan neuronal network in the development of metabolic syndrome'. Together they form a unique fingerprint.

  • Cite this