The effect of maternal caffeine ingestion on pancreatic function in the neonatal rat

Abstract

Summary. Pancreatic function was investigated in neonatal suckling offspring of caffeine-ingesting dams, with or without maternal sucrose supplementation, throughout pregnancy and lactation. In offspring of rats ingesting caffeine without sucrose supplementation, there was initial hyperinsulinaemia, followed by a progressive fall of plasma insulin to subnormal levels. This fall in plasma insulin coincided with depletion of pancreatic insulin stores. Both the fall in plasma insulin and depletion of pancreatic insulin stores were prevented by sucrose supplementation of caffeine-ingesting dams. Offspring of dams fed sucrose alone and control offspring also maintained pancreatic insulin stores and circulating insulin levels over the first 14 days of postnatal life. Pancreases from offspring of caffeine-exposed animals tested in vitro showed enhanced sensitivity of the insulin release process to glucose. This was reflected in the glucose concentration required to elicit half-maximal insulin release (2.4 ___ 0.2 mmol/1 for caffeine offspring, 2.3 + 0.2 mmol/1 for caffeine with sucrose, 3.8 _+ 0.3 mmol/1 for sucrose and 4.1 + 0.3 mmol/1 for control offspring, mean +_ SEM). In contrast, offspring of sucrose-supplemented (with or without caffeine) dams showed increased sensitivity of the proinsulin biosynthetic process to glucose, whereas offspring of dams ingesting caffeine alone showed no significant enhancement of the biosynthetic process compared with control offspring. Thus enhanced sensitivity of the insulin secretory process to glucose without a change in the sensitivity of the biosynthetic process in the offspring of the caffeine ingesting (nonsucrose supplemented) dams could explain the progressive depletion of pancreatic insulin stores and eventual hypoinsulinaemia seen in this group.

Effect of islet activating protein on glucose tolerance, insulin secretion and insulin responsiveness in the NZO mouse

“…Islets were isolated from non-fasted NZO mice as described above, homogenized at 4 ~ with the addition of sucrose containing medium (final sucrose concentration 150 retool/l), as described previously [27]. The homogenates were diluted 1 : 1000 and assayed for insulin as described previously [26].…”