Adiponectin acts in the brain to decrease body weight
Abstract
Adiponectin (ADP) is an adipocyte hormone involved in glucose and lipid metabolism. We detected a rise in ADP in cerebrospinal fluid after intravenous (i.v.) injection, consistent with brain transport. In contrast to leptin, intracerebroventricular (i.c.v.) administration of ADP decreased body weight mainly by stimulating energy expenditure. Full-length ADP, mutant ADP with Cys39 replaced with serine, and globular ADP were effective, whereas the collagenous tail fragment was not. Lep(ob/ob) mice were especially sensitive to i.c.v. and systemic ADP, which resulted in increased thermogenesis, weight loss and reduction in serum glucose and lipid levels. ADP also potentiated the effect of leptin on thermogenesis and lipid levels. While both hormones increased expression of hypothalamic corticotropin-releasing hormone (CRH), ADP had no substantial effect on other neuropeptide targets of leptin. In addition, ADP induced distinct Fos immunoreactivity. Agouti (A(y)/a) mice did not respond to ADP or leptin, indicating the melanocortin pathway may be a common target. These results show that ADP has unique central effects on energy homeostasis.
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Adiponectin improves the metabolic profile in leptin deficient ob/ob mice by overall increasing energy expenditure, despite not triggering a reduction in food intake.
“Importantly, adiponectin has been shown to improve the metabolic profile in leptin deficient ob/ob mice by overall increasing energy expenditure, despite not triggering a reduction in food intake 131.”
From Inter‐organ communication: a gatekeeper for metabolic health (2019) · cites this paper as [131]
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References 27 · Cited by 809
- Authors
- Qi, Y., Takahashi, N., Hileman, S. M., Patel, H. R., Berg, A. H., Pajvani, U. B., Scherer, P. E., & Ahima, R. S.
- Affiliations
- University of Pennsylvania (US)
- West Virginia University (US)
- Albert Einstein College of Medicine (US)
- Corresponding author
- Ahima, Rexford S
- ORCID
- Venue
- Nature Medicine
- Published
- 2004-04-11
- Volume
- 10
- Issue
- 5
- Pages
- 524-529
- ISSN
- 1078-8956 (ISSN-L)
- 1546-170X
- OpenAlex
- W2081393100
- Cited by
- 809
- References
- 27
- Citations by year
- 2026: 11 · 2025: 9 · 2024: 15 · 2023: 27 · 2022: 18 · 2021: 43 · 2020: 28 · 2019: 35 · 2018: 30 · 2017: 38 · 2016: 40 · 2015: 37 · 2014: 35 · 2013: 46 · 2012: 54
- FWCI
- 18.01
- Type
- journal article
- Language
- en
- Update notices
- erratum (2004-06-01)
- Open access
- closed
- Locations
- Nature Medicine (publishedVersion)
- PubMed (publishedVersion)
- Funders
- University of Pennsylvania
- National Institutes of Health
- National Institute of General Medical Sciences (T32GM07288, T32GM007288)
- National Institute of Diabetes and Digestive and Kidney Diseases (R01 DK 55758, R01-DK62348, R01DK055758, R01DK062348, P30 DK 19525, P30DK019525)
- Topics
- Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Regulation of Appetite and Obesity
- Health Sciences › Medicine › Epidemiology › Adipokines, Inflammation, and Metabolic Diseases
- Health Sciences › Medicine › Physiology › Adipose Tissue and Metabolism
- Keywords
- adiponectin, brain, body weight regulation, energy expenditure, thermogenesis, leptin, leptin resistance, Fos expression, melanocortin pathway, cerebrospinal fluid, energy homeostasis, glycolipid metabolism, agouti mice
- MeSH terms
- Animals, Body Weight, Brain, Drug Synergism, Energy Metabolism, Injections, Intraventricular, Mice, Inbred C57BL, Mice, Mutant Strains, Mice, Obese, Proteins, Recombinant Proteins, Leptin, Intercellular Signaling Peptides and Proteins, Mice, Adiponectin, Agouti Signaling Protein
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