Cited by 352Regulation of Appetite and ObesityDiabetes Treatment and ManagementNeuropeptides and Animal Physiology

Effects of GLP-1 on appetite and weight

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Shah, Meera, Vella, Adrian·2014·Reviews in Endocrine and Metabolic Disorders

Abstract

Glucagon-like peptide 1 (GLP-1) is a cleavage product of the pre-proglucagon gene which is expressed in the α-cells of the pancreas, the L-cells of the intestine, and neurons located in the caudal brainstem and hypothalamus. GLP-1 is of relevance to appetite and weight maintenance because it has actions on the gastrointestinal tract as well as the direct regulation of appetite. It delays gastric emptying and gut motility in humans. In addition, interventricular injections of GLP-1 inhibit food intake, independent of the presence of food in the stomach or gastric emptying. Peripherally administered GLP-1 also affects the central regulation of feeding. It is therefore the synergistic actions of GLP-1 in the gut and brain, acting on both central and peripheral receptors that seem responsible for the effects of the hormone on satiety.

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  • GLP-1RAs were originally approved for diabetes treatment with the notable side effect of pronounced weight loss.

    “Glucagon like peptide-1 receptor agonists (GLP-1RA) are a class of medications that were originally approved for diabetes treatment with the notable side effect of pronounced weight loss.23–25”

    From The Effect of Semaglutide and GLP-1 RAs on Risk of Nonarteritic Anterior Ischemic Optic Neuropathy (2025) · cites this paper as [23]

    Section 5 says GLP-1 receptor agonists were FDA-approved for type 2 diabetes and consistently produced weight loss compared with controls. But Section 7 describes their effect on weight as “relatively small but significant,” so “pronounced weight loss” overstates the source. (LLM, conf=0.90)

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Research works printed but not linked: 61

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Cited by

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Authors
Shah, M., & Vella, A.
Affiliations
Mayo Clinic (US)
Corresponding author
Vella, Adrian
Venue
Reviews in Endocrine and Metabolic Disorders
Published
2014-05-09
Volume
15
Issue
3
Pages
181-187
ISSN
  • 1389-9155 (ISSN-L)
  • 1573-2606
OpenAlex
W2073295531
Cited by
352
References
13
Citations by year
2026: 40 · 2025: 68 · 2024: 41 · 2023: 50 · 2022: 34 · 2021: 43 · 2020: 21 · 2019: 23 · 2018: 14 · 2017: 6 · 2016: 2 · 2015: 7 · 2014: 2 · 2013: 1
FWCI
0.64
Type
journal article
Language
en
Open access
Locations
  • Reviews in Endocrine and Metabolic Disorders (publishedVersion)
  • PubMed (publishedVersion)
  • Europe PMC (PubMed Central) (acceptedVersion)
  • PubMed Central (acceptedVersion)
Funders
  • Bristol-Myers Squibb
  • Sanofi
  • Daiichi-Sankyo
  • National Institutes of Health (UL1TR000135)
  • National Institute of Diabetes and Digestive and Kidney Diseases (DK82396, P30DK050456, DK TR000135, R01DK082396, DK-78646, R01DK078646)
  • National Center for Advancing Translational Sciences
  • Daiichi Sankyo Europe
Topics
  • Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Regulation of Appetite and Obesity
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes Treatment and Management
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuropeptides and Animal Physiology
Keywords
glucagon-like peptide-1, appetite regulation, weight maintenance, satiety, gastric emptying, intestinal motility, dietary intake, central regulation of feeding, preproglucagon, alpha cells, intestinal L cells, hypothalamus, brainstem neurons
MeSH terms
Appetite, Body Weight, Eating, Gastric Emptying, Humans, Glucagon-Like Peptide 1

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