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Changes in the size and number of secretion granules in the rat exocrine pancreas induced by feeding or stimulation in vitro

A morphometric study

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Summary

The size, number and volume per cell of secretion granules in rat exocrine pancreas have been measured using stereological techniques. The changes which occur as a result of feeding starved animals (90 min) or stimulating lobular fragments in vitro with carbachol are documented. In fasted animals mean acinar cell volume was estimated as 1670 μm3 and the cells contained an average of around 450 secretion granules with a corrected mean diameter of 0.70 μm. They occupied around 7% of cell volume. After feeding mean cell volume was about 1300 μm3 and the cells contained an average of about 190 granules per cell with a mean diameter of 0.58 μm. They occupied 3% of cell volume. A shift in the size frequency distribution of granule diameters occurred as a result of feeding. In vitro experiments in which lobules were induced to secrete with carbachol (10μM, 3 h, 37° C) had a similar effect. Mean cell volume was reduced from around 1760 μm3 to 1360 μm3, mean granule number from around 420 per cell to 180 per cell and the volume density of granules was reduced from about 8% to 3% of cell volume. There was no significant change in mean granule diameter or shift in the size-frequency distribution of granule diameters. Incubation of tissues with cycloheximide (1 mM, 3 h, 37° C) did not prevent secretion by carbachol but it prevented replacement of granules. As a consequence, depletion by carbachol was greater in the presence of cycloheximide, the granules being reduced to around 110 per cell and to only 2.5% of cell volume. We conclude that feeding causes a preferential loss of larger granules and that during secretion replacement of granules occurs. Some of these granules are smaller than those evident in the glands of starved animals.

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Aughsteen, A.A., Cope, G.H. Changes in the size and number of secretion granules in the rat exocrine pancreas induced by feeding or stimulation in vitro. Cell Tissue Res. 249, 427–436 (1987). https://doi.org/10.1007/BF00215527

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