Cited by 150Adipokines, Inflammation, and Metabolic DiseasesRegulation of Appetite and ObesityAdipose Tissue and Metabolism

Brain Adipocytokine Action and Metabolic Regulation

Ahima, Rexford S., Qi, Yong, Singhal, Neel S., Jackson, Malaka B., Scherer, Philipp E.·2006·Diabetes

Abstract

Adipose tissue secretes factors that control various physiological systems. The fall in leptin during fasting mediates hyperphagia and suppresses thermogenesis, thyroid and reproductive hormones, and immune system. On the other hand, rising leptin levels in the fed state stimulate fatty acid oxidation, decrease appetite, and limit weight gain. These divergent effects of leptin occur through neuronal circuits in the hypothalamus and other brain areas. Leptin also regulates the activities of enzymes involved in lipid metabolism, e.g., AMP-activated protein kinase and stearoyl-CoA desaturase-1, and also interacts with insulin signaling in the brain. Adiponectin enhances fatty acid oxidation and insulin sensitivity, in part by stimulating AMP-activated protein kinase phosphorylation and activity in liver and muscle. Moreover, adiponectin decreases body fat by increasing energy expenditure and lipid catabolism. These effects involve peripheral and possibly central mechanisms. Adipose tissue mediates interconversion of steroid hormones and secretes proinflammatory cytokines, vasoactive peptides, and coagulation and complement proteins. Understanding the actions of these “adipocytokines” will provide insight into the pathogenesis and treatment of obesity and related diseases.

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Crossref · 10.2337/db06-s018

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  • Obesity is associated with dysregulated signaling systems, such as leptin and insulin resistance, as well as increased signaling through proinflammatory cytokines and pathways activated by oxidative and endoplasmatic reticulum stress.

    “Obesity is associated with dysregulated signaling systems, such as leptin and insulin resistance, as well as increased signaling through proinflammatory cytokines and pathways activated by oxidative and endoplasmatic reticulum stress ([3](#B3)).”

    From Food reward, hyperphagia, and obesity (2011) · cites this paper as [3]

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References 103 · Cited by 150

Authors
Ahima, R. S., Qi, Y., Singhal, N. S., Jackson, M. B., & Scherer, P. E.
Affiliations
  • University of Pennsylvania (US)
  • Children's Hospital of Philadelphia (US)
  • Albert Einstein College of Medicine (US)
Venue
Diabetes
Published
2006-12-01
Volume
55
Issue
Supplement_2
Pages
S145-S154
ISSN
  • 0012-1797 (ISSN-L)
  • 1939-327X
OpenAlex
W2136861985
Cited by
150
References
103
Citations by year
2026: 2 · 2025: 1 · 2024: 8 · 2023: 4 · 2022: 7 · 2021: 3 · 2020: 4 · 2019: 5 · 2018: 10 · 2017: 4 · 2016: 7 · 2015: 2 · 2014: 7 · 2013: 9 · 2012: 12
FWCI
1.32
Type
journal article
Language
en
Open access
closed
Locations
  • Diabetes (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • National Institutes of Health (1r03ey014935-01)
  • National Eye Institute (R03-EY014935)
  • National Institute of Diabetes and Digestive and Kidney Diseases (R01 DK 55758, P01-DK49210, R01-DK62348, R01DK055758, P01DK049210, R01DK062348, P30 DK 19525, R24DK071030, P30DK019525)
Topics
  • Health Sciences › Medicine › Epidemiology › Adipokines, Inflammation, and Metabolic Diseases
  • Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Regulation of Appetite and Obesity
  • Health Sciences › Medicine › Physiology › Adipose Tissue and Metabolism
Keywords
adipokines, leptin, adiponectin, hypothalamus, AMPK, stearoyl-CoA desaturase 1, insulin signaling, fatty acid oxidation, energy expenditure, lipid metabolism, obesity, hyperphagia, thermogenesis, inflammatory cytokines, adipose tissue hormones
MeSH terms
Adipose Tissue, Animals, Blood Glucose, Brain, Fasting, Glucose, Humans, Neuropeptides, Obesity, Leptin, Mice, Adiponectin

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