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The Journal of Clinical Investigation logoLink to The Journal of Clinical Investigation
. 1998 Feb 15;101(4):899–904. doi: 10.1172/JCI368

Impaired pancreatic beta cell function in the fetal GK rat. Impact of diabetic inheritance.

P Serradas 1, M N Gangnerau 1, M H Giroix 1, C Saulnier 1, B Portha 1
PMCID: PMC508638  PMID: 9466985

Abstract

The Goto-Kakisaki (GK) rat is a genetic model of non-insulin-dependent diabetes. At 21.5 d of age we found that GK fetuses had an increased plasma glucose concentration, a decreased plasma insulin level, and a reduced pancreatic beta cell mass. To investigate the beta cell function during fetal life we used a hyperglycemic clamp protocol applied to the mothers, which allowed us to obtain a steady-state hyperglycemia in the corresponding fetuses. At variance, with Wistar (W) fetuses, plasma insulin concentration in GK fetuses did not rise in response to hyperglycemia. In contrast, GK fetal pancreas released insulin in response to glucose in vitro to the same extent as W fetal pancreas. Such a discrepancy between the in vivo and in vitro results suggests that the lack of pancreatic reactivity to glucose as seen in vivo is extrinsic to the fetal GK beta cell. Finally, the importance of gestational hyperglycemia was investigated by performing crosses between GK and W rats. Fetuses issued from crosses between W mother and GK father or GK mother and W father had a beta cell mass close to normal values and were still able to increase their plasma insulin levels in response to hyperglycemia in vivo. Our data suggest that hyperglycemia in utero does not influence the severity of the decrease of the beta cell mass or the lack of the insulin secretory response to glucose in the fetal GK rat. Moreover they indicate that conjunction of GK genes originating from both parents is necessary in order for these defects to be fully expressed.

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Selected References

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  1. Abdel-Halim S. M., Guenifi A., Luthman H., Grill V., Efendic S., Ostenson C. G. Impact of diabetic inheritance on glucose tolerance and insulin secretion in spontaneously diabetic GK-Wistar rats. Diabetes. 1994 Feb;43(2):281–288. doi: 10.2337/diab.43.2.281. [DOI] [PubMed] [Google Scholar]
  2. Aerts L., Van Assche F. A. Is gestational diabetes an acquired condition? J Dev Physiol. 1979 Jun;1(3):219–225. [PubMed] [Google Scholar]
  3. Bihoreau M. T., Ktorza A., Kinebanyan M. F., Picon L. Impaired glucose homeostasis in adult rats from hyperglycemic mothers. Diabetes. 1986 Sep;35(9):979–984. doi: 10.2337/diab.35.9.979. [DOI] [PubMed] [Google Scholar]
  4. Bisbis S., Bailbe D., Tormo M. A., Picarel-Blanchot F., Derouet M., Simon J., Portha B. Insulin resistance in the GK rat: decreased receptor number but normal kinase activity in liver. Am J Physiol. 1993 Nov;265(5 Pt 1):E807–E813. doi: 10.1152/ajpendo.1993.265.5.E807. [DOI] [PubMed] [Google Scholar]
  5. Bliss C. R., Sharp G. W. A critical period in the development of the insulin secretory response to glucose in fetal rat pancreas. Life Sci. 1994;55(6):423–427. doi: 10.1016/0024-3205(94)90053-1. [DOI] [PubMed] [Google Scholar]
  6. Eriksson U., Andersson A., Efendić S., Elde R., Hellerström C. Diabetes in pregnancy: effects on the foetal and newborn rat with particular regard to body weight, serum insulin concentration and pancreatic contents of insulin, glucagon and somatostatin. Acta Endocrinol (Copenh) 1980 Jul;94(3):354–364. doi: 10.1530/acta.0.0940354. [DOI] [PubMed] [Google Scholar]
  7. Freychet P., Roth J., Neville D. M., Jr Monoiodoinsulin: demonstration of its biological activity and binding to fat cells and liver membranes. Biochem Biophys Res Commun. 1971 Apr 16;43(2):400–408. doi: 10.1016/0006-291x(71)90767-4. [DOI] [PubMed] [Google Scholar]
  8. GOODNER C. J., FREINKEL N. Carbohydrate metabolism in pregnancy. IV. Studies on the permeability of the rat placenta to I-131 insulin. Diabetes. 1961 Sep-Oct;10:383–392. doi: 10.2337/diab.10.5.383. [DOI] [PubMed] [Google Scholar]
  9. Gauguier D., Bihoreau M. T., Picon L., Ktorza A. Insulin secretion in adult rats after intrauterine exposure to mild hyperglycemia during late gestation. Diabetes. 1991 Dec;40 (Suppl 2):109–114. doi: 10.2337/diab.40.2.s109. [DOI] [PubMed] [Google Scholar]
  10. Gauguier D., Nelson I., Bernard C., Parent V., Marsac C., Cohen D., Froguel P. Higher maternal than paternal inheritance of diabetes in GK rats. Diabetes. 1994 Feb;43(2):220–224. doi: 10.2337/diab.43.2.220. [DOI] [PubMed] [Google Scholar]
  11. Girard J. R., Kervran A., Soufflet E., Assan R. Factors affecting the secretion of insulin and glucagon by the rat fetus. Diabetes. 1974 Apr;23(4):310–317. doi: 10.2337/diab.23.4.310. [DOI] [PubMed] [Google Scholar]
  12. Giroix M. H., Vesco L., Portha B. Functional and metabolic perturbations in isolated pancreatic islets from the GK rat, a genetic model of noninsulin-dependent diabetes. Endocrinology. 1993 Feb;132(2):815–822. doi: 10.1210/endo.132.2.8425496. [DOI] [PubMed] [Google Scholar]
  13. Kervran A., Randon J., Girard J. R. Dynamics of glucose-induced plasma insulin increase in the rat fetus at different stages of gestation. Effects of maternal hypothermia and fetal decapitation. Biol Neonate. 1979;35(5-6):242–248. doi: 10.1159/000241180. [DOI] [PubMed] [Google Scholar]
  14. Kikuchi M., Rabinovitch A., Blackard W. G., Renold A. E. Perifusion of pancreas fragments. A system for the study of dynamic aspects of insulin secretion. Diabetes. 1974 Jun;23(6):550–559. doi: 10.2337/diab.23.6.550. [DOI] [PubMed] [Google Scholar]
  15. Movassat J., Saulnier C., Portha B. Beta-cell mass depletion precedes the onset of hyperglycaemia in the GK rat, a genetic model of non-insulin-dependent diabetes mellitus. Diabete Metab. 1995 Dec;21(5):365–370. [PubMed] [Google Scholar]
  16. Nolan C. J., Proietto J. The set point for maternal glucose homeostasis is lowered during late pregnancy in the rat: the role of the islet beta-cell and liver. Diabetologia. 1996 Jul;39(7):785–792. doi: 10.1007/s001250050511. [DOI] [PubMed] [Google Scholar]
  17. Picarel-Blanchot F., Berthelier C., Bailbé D., Portha B. Impaired insulin secretion and excessive hepatic glucose production are both early events in the diabetic GK rat. Am J Physiol. 1996 Oct;271(4 Pt 1):E755–E762. doi: 10.1152/ajpendo.1996.271.4.E755. [DOI] [PubMed] [Google Scholar]
  18. Picon L., Montané M. Glycémies foetale et maternelle chez la ratte à divers stades de la gestation. Action de l'insuline injectée au foetus sur sa glycémie. C R Acad Sci Hebd Seances Acad Sci D. 1968 Aug 19;267(8):860–863. [PubMed] [Google Scholar]
  19. Portha B., Serradas P., Bailbé D., Suzuki K., Goto Y., Giroix M. H. Beta-cell insensitivity to glucose in the GK rat, a spontaneous nonobese model for type II diabetes. Diabetes. 1991 Apr;40(4):486–491. doi: 10.2337/diab.40.4.486. [DOI] [PubMed] [Google Scholar]
  20. Rhoten W. B. Insulin secretory dynamics during development of rat pancreas. Am J Physiol. 1980 Jul;239(1):E57–E63. doi: 10.1152/ajpendo.1980.239.1.E57. [DOI] [PubMed] [Google Scholar]
  21. Serradas P., Giroix M. H., Saulnier C., Gangnerau M. N., Borg L. A., Welsh M., Portha B., Welsh N. Mitochondrial deoxyribonucleic acid content is specifically decreased in adult, but not fetal, pancreatic islets of the Goto-Kakizaki rat, a genetic model of noninsulin-dependent diabetes. Endocrinology. 1995 Dec;136(12):5623–5631. doi: 10.1210/endo.136.12.7588317. [DOI] [PubMed] [Google Scholar]
  22. Triadou N., Portha B., Picon L., Rosselin G. Experimental chemical diabetes and pregnancy in the rat. Evolution of glucose tolerance and insulin response. Diabetes. 1982 Jan;31(1):75–79. doi: 10.2337/diab.31.1.75. [DOI] [PubMed] [Google Scholar]

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