Creatine supplementation increases soleus muscle creatine content and lowers the insulinogenic index in an animal model of inherited type 2 diabetes
Open accessAbstract
Creatine supplementation may exert beneficial effects on muscle performance and facilitate peripheral glucose disposal in both rats and human subjects. The present study was undertaken to explore the effects of creatine supplementation on the ATP, creatine, phosphocreatine and glycogen content of white and red gastrocnemius and soleus muscles and on blood D-glucose and plasma insulin concentrations before and during an intravenous glucose tolerance test in Goto-Kakizaki rats, a current animal model of inherited type 2 diabetes mellitus. Creatine supplementation increased muscle creatine content, especially in the soleus muscle of young rats (+35.5-/+15.8%; d.f.=10; p<0.05), and lowered the insulinogenic index, i.e. the paired ratio between plasma insulin and blood D-glucose concentrations. The latter change was mainly attributable to a lowering of plasma insulin concentration. It is proposed, therefore, that creatine supplementation may improve the sensitivity to insulin in extrapancreatic sites in the present animal model of type 2 diabetes.
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Creatine supplementation has been reported to enhance glycemic control.
“enhance glycemic control [132, 203–205];”
From International Society of Sports Nutrition position stand: safety and efficacy of creatine supplementation in exercise, sport, and medicine (2017) · cites this paper as [204]
The Introduction says creatine intake may improve whole-body glucose homeostasis, and the Discussion suggests that a lower insulinogenic index in creatine-supplemented diabetic rats may reflect improved insulin sensitivity. However, the Blood D-glucose and plasma insulin concentrations section reports no significant difference in blood glucose between supplemented and control rats during the glucose tolerance test. The paper therefore supports a possible metabolic benefit, but not demonstrated improvement in glycemic control in its own experiment. (LLM, conf=0.86)
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- Authors
- Op't Eijnde, B., Jijakli, H., Hespel, P., & Malaisse, W.
- Affiliations
- Université Libre de Bruxelles (BE)
- KU Leuven (BE)
- Corresponding author
- Malaisse, Willy
- Venue
- International Journal of Molecular Medicine
- Publisher
- Spandidos Publications
- Published
- 2006-06-01
- Volume
- 17
- Issue
- 6
- Pages
- 1077-84
- ISSN
- 1107-3756 (ISSN-L)
- 1791-244X
- OpenAlex
- W2064355103
- Cited by
- 29
- References
- 8
- Citations by year
- 2026: 1 · 2025: 1 · 2023: 1 · 2021: 4 · 2020: 1 · 2019: 1 · 2018: 1 · 2017: 1 · 2016: 1 · 2012: 1
- FWCI
- 1.03
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- International Journal of Molecular Medicine (publishedVersion)
- PubMed (publishedVersion)
- Dépôt institutionnel de l'Université libre de Bruxelles (Université Libre de Bruxelles) (submittedVersion)
- Acta Physiologica
- Funders
- Fonds Wetenschappelijk Onderzoek
- Vlaamse regering
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Muscle metabolism and nutrition
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Metabolism, Diabetes, and Cancer
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Natural Antidiabetic Agents Studies
- Keywords
- creatine supplementation, type 2 diabetes, insulin resistance, insulinogenic index, soleus muscle, gastrocnemius, phosphocreatine, muscle glycogen, ATP levels, Goto-Kakizaki rats, glucose tolerance, plasma insulin
- MeSH terms
- Adenosine Triphosphate, Animals, Blood Glucose, Body Weight, Creatine, Diabetes Mellitus, Type 2, Disease Models, Animal, Eating, Glucose Tolerance Test, Glycogen, Insulin, Male, Rats, Inbred Strains, Muscle, Skeletal, Rats
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