Summary. Electron microscopic examination of the intrinsic autonomic ganglia of the rat pancreas revealed the presence of small cells, when compared to the principal ganglionic neurons, within a particular type of ganglia. The small cells were often located in clusters around fenestrated capillaries, but their most striking characteristic was the presence of catecholamine-like granules distributed throughout the cytoplasm. The possible implication of this new source of catecholamines, acting either as interneurons or as neuroendocrine cells, is discussed in the light of a local regulatory mechanism for islet secretion.Key words: Autonomic nervous system, intrinsic ganglia, small granulated cells, catecholamines, islets of Langerhans, electron microscopy.Certain of the physiologic responses of the endocrine pancreas are mediated by sympathetic discharge via direct stimulation from the central nervous system [1,2]. However, we have recently observed that the glucagon response to glucopenia in the isolated perfused rat pancreas can be largely blocked by phentolamine [3]. Although we concluded that this alpha-adrenergically mediated response to glucopenia must reflect norepinephfine release from severed perinsular sympathetic nerve endings independent of the central nervous system, and since there is no other known source of catecholamines in the pancreas, we undertook a search for an alternative source of catecholamines. In this report we present ultrastructural evidence for a second source of catecholamines based on the demonstration of small cells containing catecholamine-like granules within the intrinsic autonomic ganglia of the rat pancreas.
Materials and methodsThree normal albino rats (SiVZ strain, body weight 110 160 g) were used in this study. Under ether anaesthesia the animals were perfused through the left ventricle with 1% glutaraldehyde and 1% paraformaldehyde in 0.1 tool/1 phosphate buffer (pH 7.4) after rinsing of the circulation with 0.9% NaC1 solution. After fixation, small samples of both ventral and dorsal parts of the pancreas were dissected out, postfixed in 2% buffered OsO4, dehydrated and embedded in Epon. Pancreatic ganglia were identified on 1 ~tm thick toluidine blue stained sections. After staining with uranyl acetate and lead citrate, ultrathin sections were viewed in a Philips EM 301 electron microscope. For the quantitative analysis, the volume density of the different components of 8 ganglia (principal neurons, small granulated cells, satellite cells and blood capillaries) was determined on semithin sections using the point-counting method [4]. Data for each component were expressed as % of the total volume density occupied by the 8 ganglia. In the small granulated cells, the size (nm) and density (number/p~m 2) of the vesicles was quantified on electron micrographs at 55 000 magnification, calibrated with a Fullham reference grid, 2160lines/ram (Schenectady, NY, USA).
ResultsIn both duodenal and splenic parts of the pancreas (Fig. 1), two types of autonomic ganglia were observed. On...