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Maternal Western-style diet affects offspring islet composition and function in a non-human primate model of maternal over-nutrition.
Elsakr, Joseph M; Dunn, Jennifer C; Tennant, Katherine; Zhao, Sifang Kathy; Kroeten, Karly; Pasek, Raymond C; Takahashi, Diana L; Dean, Tyler A; Velez Edwards, Digna R; McCurdy, Carrie E; Aagaard, Kjersti M; Powers, Alvin C; Friedman, Jacob E; Kievit, Paul; Gannon, Maureen.
Afiliação
  • Elsakr JM; Department of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, TN, USA.
  • Dunn JC; Department of Veterans Affairs Tennessee Valley, Nashville, TN, USA; Department of Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.
  • Tennant K; Division of Cardiometabolic Health, Oregon National Primate Research Center, Beaverton, OR, USA.
  • Zhao SK; Vanderbilt Epidemiology Center, Vanderbilt University Medical Center, Nashville, TN, USA.
  • Kroeten K; Vanderbilt Summer Diabetes Research Program, Vanderbilt University, Nashville, TN, USA.
  • Pasek RC; Department of Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.
  • Takahashi DL; Division of Cardiometabolic Health, Oregon National Primate Research Center, Beaverton, OR, USA.
  • Dean TA; Division of Cardiometabolic Health, Oregon National Primate Research Center, Beaverton, OR, USA.
  • Velez Edwards DR; Vanderbilt Epidemiology Center, Vanderbilt University Medical Center, Nashville, TN, USA; Department of Biomedical Informatics, Department of Obstetrics and Gynecology, Vanderbilt University Medical Center, Nashville, TN, USA.
  • McCurdy CE; Department of Human Physiology, University of Oregon, Eugene, OR, 97403, USA.
  • Aagaard KM; Department of Obstetrics and Gynecology, Division of Maternal-Fetal Medicine, Baylor College of Medicine, Houston, TX, 77030, USA.
  • Powers AC; Department of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, TN, USA; Department of Veterans Affairs Tennessee Valley, Nashville, TN, USA; Department of Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.
  • Friedman JE; Department of Pediatrics, Department of Biochemistry and Molecular Genetics, University of Colorado School of Medicine, Aurora, CO, USA.
  • Kievit P; Division of Cardiometabolic Health, Oregon National Primate Research Center, Beaverton, OR, USA.
  • Gannon M; Department of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, TN, USA; Department of Veterans Affairs Tennessee Valley, Nashville, TN, USA; Department of Medicine, Vanderbilt University Medical Center, Nashville, TN, USA; Department of Cell and Developmental Biology, Vanderbil
Mol Metab ; 25: 73-82, 2019 07.
Article em En | MEDLINE | ID: mdl-31036449
ABSTRACT

OBJECTIVE:

In humans, offspring of women who are overweight or obese are more likely to develop metabolic disease later in life. Studies in lower animal species reveal that a calorically-dense maternal diet is associated with alterations in islet cell mass and function. The long-term effects of maternal diet on the structure and function of offspring islets with characteristics similar to humans are unknown. We used a well-established non-human primate (NHP) model to determine the consequences of exposure to Western-Style Diet (WSD) in utero and during lactation on islet cell mass and function in the offspring.

METHODS:

Female Japanese Macaques (Macaca fuscata) were fed either control (CTR) or WSD before and throughout pregnancy and lactation. Offspring were weaned onto CTR or WSD to generate four different groups based on maternal/offspring diets CTR/CTR, WSD/CTR, CTR/WSD, and WSD/WSD. Offspring were analyzed at three years of age. Pancreatic tissue sections were immunolabelled to measure α- and ß-cell mass and proliferation as well as islet vascularization. Live islets were also isolated to test the effects of WSD-exposure on islet function ex vivo. Offspring glucose tolerance was correlated with various maternal characteristics.

RESULTS:

α-cell mass was reduced as a result of maternal WSD exposure. α-cell proliferation was reduced in response to offspring WSD. Islet vasculature did not differ among the diet groups. Islets from WSD/CTR offspring secreted a greater amount of insulin in response to glucose ex vivo. We also found that maternal glucose tolerance and parity correlated with offspring glucose tolerance.

CONCLUSIONS:

Maternal WSD exposure results in persistently decreased α-cell mass in the three-year old offspring. WSD/CTR islets secreted greater amounts of insulin ex vivo, suggesting that these islets are primed to hyper-secrete insulin under certain metabolic stressors. Although WSD did not induce overt impaired glucose tolerance in dams or offspring, offspring born to mothers with higher glucose excursions during a glucose tolerance test were more likely to also show higher glucose excursions.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Efeitos Tardios da Exposição Pré-Natal / Ilhotas Pancreáticas / Fenômenos Fisiológicos da Nutrição Materna / Dieta Ocidental Tipo de estudo: Prognostic_studies Limite: Animals / Female / Humans / Male / Pregnancy Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Efeitos Tardios da Exposição Pré-Natal / Ilhotas Pancreáticas / Fenômenos Fisiológicos da Nutrição Materna / Dieta Ocidental Tipo de estudo: Prognostic_studies Limite: Animals / Female / Humans / Male / Pregnancy Idioma: En Ano de publicação: 2019 Tipo de documento: Article