Aims/
hypothesis. In the Goto-Kakisaki rat, a genetic model of non-insulin dependent diabetes, we have recently reported that as early as
fetal age, there is a restriction of the beta-cell mass which is maintained in the adult animal and is detectable before the
onset of hyperglycaemia. It is therefore important to investigate the beta-cell growth potential in young Goto-Kakisaki rats.
Methods. We have studied in 4 and 7-day-old Goto-Kakisaki neonates: 1. the in vivo replication rate of the beta cell; 2. the occurrence
of beta-cell apoptosis; 3. the effectiveness of beta-cell regeneration after damage caused by neonatal treatment with streptozotocin.
Results. The replication rate in vivo of beta cells and the beta-cell apoptosis were similar in untreated Wistar and Goto-Kakisaki
neonates on days 4 and 7 whereas the total beta-cell masses were reduced to 50 % in the Goto-Kakisaki groups. Treatment with
streptozotocin reduced the total beta-cell mass to the same extent in both Wistar and Goto-Kakisaki rats on day 4 compared
with the corresponding normal values in Wistar and Goto-Kakisaki neonates. From day 4 to day 7, spontaneous beta-cell regeneration
was manifest in both groups. Compared with the Wistar streptozotocin group, the net value of the beta-cell mass added during
this period was more limited in the Goto-Kakisaki streptozotocin group, despite the replication activity of the residual beta
cells being increased in this group to the same extent as in the Wistar streptozotocin group.
Conclusion/
interpretation. We therefore suggest: 1. that the reduced beta-cell mass in the untreated neonatal Goto-Kakisaki rat does not appear to
reflect a reduction in the rate of beta-cell replication or an increased beta-cell death by apoptosis but is potentially due
to an impaired rate of beta-cell neogenesis, and 2. that beta-cell regeneration can be reactivated after streptozotocin insult
in the neonatal Goto-Kakisaki rat, although to a lesser extent compared with that in streptozotocin-treated Wistar neonates.
[Diabetologia (1999) 42: 1098–1106]
Keywords Regeneration - neogenesis - beta-cell proliferation - beta-cell apoptosis - GK rat - Type II diabetes.
Received: 8 January 1999 and in revised form: 26 February 1999