Leptin—Much More Than a Satiety Signal
Abstract
Much attention has focused on the effects of leptin as a central satiety agent. There is now a significant amount of evidence that leptin is active in the periphery. This review focuses on the ability of leptin to modify insulin sensitivity, tissue metabolism, stress responses, and reproductive function. Leptin's effect on several of these systems is mediated via the hypothalamic-pituitary axis. Therefore, although in vitro studies provide evidence for direct effects on specific tissues and metabolic pathways, it is essential to consider the interactions between leptin and other regulatory factors in vivo. Little is known about the regulation of peripheral receptor expression or the production of binding proteins. Both of these factors determine the bioactivity of circulating leptin and have the potential to induce a peripheral resistance to leptin, similar to the central “leptin resistance” observed in obese subjects. Future research will clarify which of the endocrine and metabolic actions of peripheral leptin are of physiological relevance and which should be considered a pharmacological manipulation.
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To date there is limited evidence that leptin mediates thermogenesis via the SNS in humans.
“In addition, leptin, released by white adipocytes, regulates energy balance by effects on the hypothalamus that lead to inhibition of food intake and increased thermogenesis via activation of the SNS, though to date there is limited evidence that leptin mediates thermogenesis via the SNS in humans 66–70.”
From Cellular bioenergetics as a target for obesity therapy (2010) · cites this paper as [69]
Leptin, released by white adipocytes, regulates energy balance by effects on the hypothalamus that lead to inhibition of food intake and increased thermogenesis via activation of the SNS.
“In addition, leptin, released by white adipocytes, regulates energy balance by effects on the hypothalamus that lead to inhibition of food intake and increased thermogenesis via activation of the SNS, though to date there is limited evidence that leptin mediates thermogenesis via the SNS in humans 66–70.”
From Cellular bioenergetics as a target for obesity therapy (2010) · cites this paper as [69]
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References 274 · Cited by 222
- Authors
- Harris, R. B. S.
- Affiliations
- Pennington Biomedical Research Center (US)
- Corresponding author
- Harris, Ruth B. S.
- ORCID
- Harris, Ruth B. S.
- Venue
- Annual Review of Nutrition
- Publisher
- Annual Reviews
- Published
- 2000-07
- Volume
- 20
- Issue
- 1
- Pages
- 45-75
- ISSN
- 0199-9885 (ISSN-L)
- 1545-4312
- OpenAlex
- W2164384489
- Semantic Scholar
- 86536c8884f75bcb8ad5f457c52caa9855f1ab68
- Cited by
- 222
- References
- 274
- Citations by year
- 2025: 1 · 2024: 5 · 2023: 2 · 2022: 3 · 2021: 4 · 2020: 4 · 2019: 8 · 2018: 4 · 2017: 2 · 2016: 9 · 2015: 10 · 2014: 4 · 2013: 11 · 2012: 6
- FWCI
- 2.13
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Annual Review of Nutrition (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institute of Diabetes and Digestive and Kidney Diseases (R01DK053903)
- 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 › Reproductive Medicine › Hypothalamic control of reproductive hormones
- Keywords
- leptin, insulin sensitivity, tissue metabolism, stress response, reproductive function, hypothalamic-pituitary axis, leptin resistance, obesity, satiety
- MeSH terms
- Insulin Secretion, Adipose Tissue, Animals, Growth Substances, Humans, Insulin, Nutritional Status, Obesity, Reproduction, Satiation, Stress, Physiological, Leptin
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