beta-cell mass dynamics in Zucker diabetic fatty rats - Rosiglitazone prevents the rise in net cell death

The evolution of diabetes in the male leptin receptor-deficient (fa/fa) Zuc ker diabetic fatty (ZDF) rat is associated with disruption of normal islet architecture, beta -cell degranulation, and increased beta -cell death. It is unknown whether these changes precede or develop as a result of the incr easing plasma glucose, or whether the increased beta -cell death can be pre vented. Early intervention with thiazolidinediones prevents disruption of t he islet architecture. To determine the specific effects of rosiglitazone ( RSG) on beta -cell mass dynamics, male fa/fa (obese) and +/fa or +/+ (lean) rats age 6 weeks were fed either chow (control group [CN]) or chow mixed w ith rosiglitazone (RSG group) at a dosage of 10 mu mol kg(-1) body wt day(- 1). Rats were killed after 0, 2, 4, 6, or 10 weeks of treatment (at age 6, 8, 10, 12, or 16 weeks). Plasma glucose increased from 8.9 +/- 0.4 mmol/l a t 0 weeks to 34.2 +/- 1.8 mmol/l (P = 0.0001) at 6 weeks of treatment in ob ese CN rats and fell from 8.0 +/- 0.3 to 6.3 +/- 0.4 mmol/l in obese RSG ra ts (P = 0.02). beta -cell mass fell by 51% from 2 to 6 weeks of treatment ( ages 8-12 weeks) in obese CN rats (6.9 +/- 0.9 to 3.4 +/- 0.5 mg; P < 0.05) , whereas beta -cell mass was unchanged in obese RSG rats. At 10 weeks of t reatment (age 16 weeks), beta -cell mass in obese CN rats was only 56% of t hat of obese RSG rats (4.4 +/- 0.4 vs. 7.8 +/- 0.3 mg, respectively; P = 0. 0001). The beta -cell replication rate fell from a baseline value of 0.95 /- 0.12% in lean rats and 0.94 a 0.07% in obese rats (at 0 weeks) to simila r to0.3-0.5% in all groups by 6 weeks of treatment (age 12 weeks). After 10 weeks of treatment, beta -cell replication was higher in obese RSG rats th an in CN rats (0.59 +/- 0.14 vs. 0.28 +/- 0.05%, respectively; P < 0.02). A pplication of our mass balance model of beta -cell turnover indicated that net beta -cell death was fivefold higher in obese CN rats as compared with RSG rats after 6 weeks of treatment (age 12 weeks). The increase in beta -c ell death in obese CN rats during the 8-week observation period was well co rrelated with the increase in plasma glucose (r(2) = 0.90, P < 0.0001). The se results suggest that the development of hyperglycemia in ZDF rats is con comitant with increasing net alpha -cell death. beta -cell proliferation co mpensates for the increased beta -cell loss at a time when plasma glucose i s moderately elevated, but compensation ultimately fails and the plasma glu cose levels increase beyond similar to 20 mmol/l. Treatment with rosiglitaz one, previously shown to reduce insulin resistance, prevents the loss of be ta -cell mass in obese ZDF rats by maintaining beta -cell proliferation and preventing increased net beta -cell death.