Beta-cell mass and proliferation following late fetal and early postnatal malnutrition in the rat
- PMID: 9754832
- DOI: 10.1007/s001250051038
Beta-cell mass and proliferation following late fetal and early postnatal malnutrition in the rat
Abstract
We have recently shown that maternal food restriction during late pregnancy in rats decreased beta-cell mass in the offspring at birth, without altering beta-cell proliferation. The aim of the present work was to determine: 1) whether sustained maternal undernutrition until weaning (R group) more dramatically alters beta-cell mass in the offspring and if normal food supply from weaning until adulthood could reverse the deleterious effects and; 2) if altered beta-cell proliferation was responsible for the decreased beta-cell mass. Beta-cell fraction and proliferative capacity were determined during the suckling period and at adult age after ad libitum feeding from weaning in the R animals and in age-matched controls (C group). At day 21, the offspring born and nursed by food-restricted mothers (R animals) showed a 66% reduction in beta-cell mass and number, which did not increase from birth to weaning, although beta-cell proliferation remained normal. At 3 months of age, R animals had 35% decreased beta-cell fraction, with a 50% decrease in the head of the pancreas. In that area, beta-cell proliferation was similar to that of the controls. In the tail of the pancreas, beta-cell fraction was only slightly impaired but beta-cell proliferation was increased by 37%, as compared with the controls. This increase was associated with a shift in islet size distribution towards medium and large islets compared with the head of pancreas from these R animals. No regional variations of beta-cell fraction, proliferation or islet size distribution were observed in adult control animals. In conclusion, prolonged malnutrition until weaning impairs beta-cell development but not beta-cell proliferation. Subsequent re-nutrition is followed by increased beta-cell proliferation but this is insufficient to fully restore beta-cell mass.
Similar articles
-
The impact of IUGR on pancreatic islet development and β-cell function.J Endocrinol. 2017 Nov;235(2):R63-R76. doi: 10.1530/JOE-17-0076. Epub 2017 Aug 14. J Endocrinol. 2017. PMID: 28808079 Free PMC article. Review.
-
In utero undernutrition impairs rat beta-cell development.Diabetologia. 1997 Oct;40(10):1231-4. doi: 10.1007/s001250050812. Diabetologia. 1997. PMID: 9349607
-
Impaired beta-cell regeneration in perinatally malnourished rats: a study with STZ.FASEB J. 2000 Dec;14(15):2611-7. doi: 10.1096/fj.00-0015com. FASEB J. 2000. PMID: 11099480
-
Impaired development of pancreatic beta-cell mass is a primary event during the progression to diabetes in the GK rat.Diabetologia. 1997 Aug;40(8):916-25. doi: 10.1007/s001250050768. Diabetologia. 1997. PMID: 9267986
-
Endocrine pancreas development is altered in foetuses from rats previously showing intra-uterine growth retardation in response to malnutrition.Diabetologia. 2002 Mar;45(3):394-401. doi: 10.1007/s00125-001-0767-4. Diabetologia. 2002. PMID: 11914745
Cited by
-
The intrauterine metabolic environment modulates the gene expression pattern in fetal rat islets: prevention by maternal taurine supplementation.Diabetologia. 2008 May;51(5):836-45. doi: 10.1007/s00125-008-0956-5. Epub 2008 Mar 3. Diabetologia. 2008. PMID: 18311556
-
The impact of IUGR on pancreatic islet development and β-cell function.J Endocrinol. 2017 Nov;235(2):R63-R76. doi: 10.1530/JOE-17-0076. Epub 2017 Aug 14. J Endocrinol. 2017. PMID: 28808079 Free PMC article. Review.
-
Effect of Postnatal Nutritional Environment Due to Maternal Diabetes on Beta Cell Mass Programming and Glucose Intolerance Risk in Male and Female Offspring.Biomolecules. 2021 Jan 28;11(2):179. doi: 10.3390/biom11020179. Biomolecules. 2021. PMID: 33525575 Free PMC article.
-
Genetic evidence of the programming of beta cell mass and function by glucocorticoids in mice.Diabetologia. 2011 Feb;54(2):350-9. doi: 10.1007/s00125-010-1898-2. Epub 2010 Sep 21. Diabetologia. 2011. PMID: 20857084
-
Higher glycolytic capacities in muscle of carnivorous rainbow trout juveniles after high dietary carbohydrate stimulus at first feeding.Nutr Metab (Lond). 2019 Nov 9;16:77. doi: 10.1186/s12986-019-0408-x. eCollection 2019. Nutr Metab (Lond). 2019. PMID: 31728152 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
