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Decreased ß-cell volume and insulin secretion but preserved glucose tolerance in a growth hormone insensitive pig model.
Laane, Laeticia; Renner, Simone; Kemter, Elisabeth; Stirm, Michael; Rathkolb, Birgit; Blutke, Andreas; Bidlingmaier, Martin; de Angelis, Martin Hrabe; Wolf, Eckhard; Hinrichs, Arne.
Afiliación
  • Laane L; Chair for Molecular Animal Breeding and Biotechnology, Gene Center and Department of Veterinary Sciences, LMU Munich, Munich, Germany.
  • Renner S; Center for Innovative Medical Models (CiMM), LMU Munich, Oberschleißheim, Germany.
  • Kemter E; Chair for Molecular Animal Breeding and Biotechnology, Gene Center and Department of Veterinary Sciences, LMU Munich, Munich, Germany.
  • Stirm M; Center for Innovative Medical Models (CiMM), LMU Munich, Oberschleißheim, Germany.
  • Rathkolb B; German Center for Diabetes Research (DZD), Neuherberg, Germany.
  • Blutke A; Chair for Molecular Animal Breeding and Biotechnology, Gene Center and Department of Veterinary Sciences, LMU Munich, Munich, Germany.
  • Bidlingmaier M; Center for Innovative Medical Models (CiMM), LMU Munich, Oberschleißheim, Germany.
  • de Angelis MH; German Center for Diabetes Research (DZD), Neuherberg, Germany.
  • Wolf E; Chair for Molecular Animal Breeding and Biotechnology, Gene Center and Department of Veterinary Sciences, LMU Munich, Munich, Germany.
  • Hinrichs A; Center for Innovative Medical Models (CiMM), LMU Munich, Oberschleißheim, Germany.
Pituitary ; 2024 Jul 03.
Article en En | MEDLINE | ID: mdl-38960990
ABSTRACT

PURPOSE:

Growth hormone (GH) is a central regulator of ß-cell proliferation, insulin secretion and sensitivity. Aim of this study was to investigate the effect of GH insensitivity on pancreatic ß-cell histomorphology and consequences for metabolism in vivo.

METHODS:

Pancreata from pigs with growth hormone receptor deficiency (GHR-KO, n = 12) were analyzed by unbiased quantitative stereology in comparison to wild-type controls (WT, n = 12) at 3 and 7-8.5 months of age. In vivo secretion capacity for insulin and glucose tolerance were assessed by intravenous glucose tolerance tests (ivGTTs) in GHR-KO (n = 3) and WT (n = 3) pigs of the respective age groups.

RESULTS:

Unbiased quantitative stereological analyses revealed a significant reduction in total ß-cell volume (83% and 73% reduction in young and adult GHR-KO vs. age-matched WT pigs; p < 0.0001) and volume density of ß-cells in the pancreas of GHR-KO pigs (42% and 39% reduction in young and adult GHR-KO pigs; p = 0.0018). GHR-KO pigs displayed a significant, age-dependent increase in the proportion of isolated ß-cells in the pancreas (28% in young and 97% in adult GHR-KO vs. age-matched WT pigs; p = 0.0009). Despite reduced insulin secretion in ivGTTs, GHR-KO pigs maintained normal glucose tolerance.

CONCLUSION:

GH insensitivity in GHR-KO pigs leads to decreased ß-cell volume and volume proportion of ß-cells in the pancreas, causing a reduced insulin secretion capacity. The increased proportion of isolated ß-cells in the pancreas of GHR-KO pigs highlights the dependency on GH stimulation for proper ß-cell maturation. Preserved glucose tolerance accomplished with decreased insulin secretion indicates enhanced sensitivity for insulin in GH insensitivity.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Pituitary Asunto de la revista: ENDOCRINOLOGIA Año: 2024 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Pituitary Asunto de la revista: ENDOCRINOLOGIA Año: 2024 Tipo del documento: Article País de afiliación: Alemania
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