Cited by 26Pharmacology and Obesity TreatmentRegulation of Appetite and ObesityDiabetes Treatment and Management

Potential use of exenatide for the treatment of obesity

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Folli, Franco, Guardado Mendoza, Rodolfo·2011·Expert Opinion on Investigational Drugs

Abstract

INTRODUCTION: Obesity is a major health threat in the Western world because of its high incidence and prevalence, and its association with metabolic and cardiovascular disease as well as cancer. The reduction of food intake in obese patients can be achieved only transiently (generally for no longer than 6 months), in the absence of concomitant pharmacological therapy. Only bariatric surgery provides a means to increase satiety and/or decrease nutrient absorption in obese patients, in the long term. AREAS COVERED: This article reviews the available pharmacological treatments for obesity as well as the pharmacology and mechanism of action of exenatide in obese type 2 diabetic patients. EXPERT OPINION: Exenatide is a potential new candidate treatment for obesity, possibly in combination with other hormones that increase satiety (leptin) and slow gastric emptying (amylin).

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Crossref · 10.1517/13543784.2011.630660

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  • Many currently used anti-obesity drugs have limited clinical use because of safety or effectiveness concerns.

    “However, given the safety or effectiveness concerns of anti-obesity drugs, many of the currently used drugs have limited clinical use.”
  • EX has a relatively short half-life of 2.4 hours, detectable in plasma within 15 minutes after administration and still detectable 15 hours after a single subcutaneous injection >0.2 μg/kg.

    “EX has a relatively short half-life of 2.4 hours, which can be detected in plasma within 15 minutes after administration, and can still be detected 15 hours after a single subcutaneous injection > 0.2 µg/kg (12).”
  • EX is a synthetic product of exendin-4 with multiple hypoglycemic mechanisms: inhibiting glucagon release from α cells, slowing gastric emptying, decreasing appetite, and increasing glucose-dependent insulin secretion.

    “As the first GLP-1R agonist approved for T2DM, EX is a new class of compound and a synthetic product of exendin-4, which is a compound naturally derived from the Gila monster and has multiple hypoglycemic mechanisms: inhibiting of glucagon release from α cells, slowing of gastric emptying, decreasing appetite and increasing glucose-dependent insulin secretion (12, 46, 47).”

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Authors
Folli, F., & Guardado Mendoza, R.
Affiliations
  • The University of Texas at San Antonio Health Science Center (US)
  • University of Guanajuato, Division of Health Sciences, Department of Medicine and Nutrition, León, Gto, México
Venue
Expert Opinion on Investigational Drugs
Published
2011-10-24
Volume
20
Issue
12
Pages
1717-1722
ISSN
  • 1354-3784 (ISSN-L)
  • 1744-7658
OpenAlex
W1968389922
Cited by
26
References
52
Citations by year
2026: 1 · 2025: 5 · 2024: 2 · 2023: 5 · 2022: 1 · 2020: 2 · 2018: 1 · 2015: 1 · 2014: 2 · 2013: 4 · 2012: 2
FWCI
1.84
Type
journal article
Language
en
Open access
Locations
  • Expert Opinion on Investigational Drugs (publishedVersion)
  • PubMed (publishedVersion)
  • PubMed Central (acceptedVersion)
Funders
National Institute of Diabetes and Digestive and Kidney Diseases (R01DK080148)
Topics
  • Health Sciences › Medicine › Pharmacology › Pharmacology and Obesity Treatment
  • Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Regulation of Appetite and Obesity
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes Treatment and Management
Keywords
exenatide, obesity treatment, GLP-1 receptor agonists, satiety hormones, leptin, amylin, gastric emptying, type 2 diabetes, bariatric surgery
MeSH terms
Exenatide, Diabetes Mellitus, Type 2, Eating, Humans, Hypoglycemic Agents, Obesity, Peptides, Venoms, Bariatric Surgery

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