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According to the earlier concept, the paraganglia of man are believed to degenerate during the first postnatal years after their dominance during the fetal period. Clinical case reports on persisting paraganglia led us to extensive exploration of surgical material obtained from urological and gynecological surgery. The formaldehyde induced fluorescence (FIF) was used for tracing the catecholamine containing tissues. The fluorescence intensities were recorded with a Leitz MPV 2 microspectrophotometer. Solitary, small paraganglia were found in all patients studied. They were especially frequent in the walls of the urinary bladder and in the connective tissue surrounding the urogenital organs. The intensity of the fluorescence was comparable to pharmacological standard of 10(-2) M noradrenaline and at the same level as the FIF of human fetal paraganglia. All cells of the paraganglionic clusters exhibited FIF and no signs of degeneration could be observed. It is suggested that the paraganglia of man do not degenerate postnatally but persist as a remarcable catecholamine reservoir, which might be of physiological importance.

Synaptosomes from one day old and adult rat brain were studied. Specific cytochemical methods for demonstrating monoaminergic (MA) nerve endings were used. Permanganate fixation after preincubation with 5-OHDA or alpha-methyl-NA demonstrated MA synaptosomes. Their number was small in the adult (less than 1 %) and still smaller in the one day old rat brain. The MA synaptosomes from developing rats were different from the adult ones. The large amount of endoplasmic reticulum in developing synaptosomes suggests that granular vesicles are formed from endoplasmic reticulum in nerve endings.

Potassium permanganate fixative is usually employed at pH 7.0. At this pH the amines in the granules of the adrenal medullary cells do not react with permanganate. When the pH was adjusted to 5.0, electron dense precipitates were seen in the amine granules of part of the medullary cells, probably noradrenalin containing cells.

A new combination of freeze-drying, formaldehyde induced fluorescence method for catecholamines and autoradiography of water soluble substances was developed and tested with different tissues containing biogenic amines. The freeze-dried tissue pieces were fixed with vaporours paraformaldehyde and OsO4 before embedding procedure. The effect of OsO4-vapour on the formaldehyde induced fluorescence was tested. The method produces semi-thin sections in which the fluorescence is well preserved and the tissue lightly stained with OsO4 which also fixes the steroid hormones used for radioautography.

Three types of monoamine-storing cells were fixed with permanganates and analyzed ultrastructurally. The SIF cells contained the typical granulated vesicles characteristic of monoamines. On the other hand, both the catecholamine-storing cells in the adrenal medulla and the mast cells were devoid of a dense core in their monoamine vesicles. This is surprising, since permanganate is considered a reliable means of demonstrating monoamines at the fine structural level. The significance of this finding is discussed against the close relationship between SIF cells and cells of the adrenal medulla. Because permanganate as a fixative is widely used in monoamine fine structural cytochemistry, the present findings undoubtedly need further clarification.