HISTOCHEMICAL DEMONSTRATION OF OXIDATIVE ENZYMES IN THE ADENOHYPOPHYSIS OF THE PIG, WITH PARTICULAR REFERENCE TO THE PARS INTERMEDIA

1967 ◽  
Vol 39 (3) ◽  
pp. 351-359 ◽  
Author(s):  
A. HOWE ◽  
A. J. THODY

SUMMARY The adenohypophysis of the pig was examined histochemically for the presence of 11 oxidative enzymes, namely: 1.1.1.27 l-lactate: NAD oxidoreductase, 1.1.1.30 d-3-hydroxybutyrate: NAD oxidoreductase, 1.1.1.37 l-malate: NAD oxidoreductase, 1.1.1.41 threo-ds-isocitrate: NAD oxidoreductase (decarboxylating), 1.1.1.42 threo-ds-isocitrate: NADP oxidoreductase (decarboxylating), 1.1.1.49 d-glucose-6-phosphate: NADP oxidoreductase, 1.1.99.5 l-glycerol-3-phosphate: (acceptor) oxidoreductase, 1.3.99.1 succinate: (acceptor) oxidoreductase, 1.4.1.2 l-glutamate: NAD oxidoreductase (deaminating), 1.6.99.1 reduced-NADP: (acceptor) oxidoreductase, 1.6.99.3 reduced-NAD: (acceptor) oxidoreductase. With the exception of 1.1.1.30 d-3-hydroxybutyrate: NAD oxidoreductase, activity was found throughout the adenohypophysis for all these enzymes. A comparison was made with the activity for these enzymes in liver. In the adenohypophysis, the pars tuberalis exhibited the highest activity for all enzymes, generally equal to or greater than that shown by the liver. The pars intermedia and the pars anterior showed similar activity for these enzymes, in general of a lower order than that given by the liver. The pattern of enzyme distribution in the pars intermedia is described; high activity for 1.1.1.37 l-malate: NAD oxidoreductase, 1.1.1.27 l-lactate: NAD oxidoreductase, 1.6.99.3 reduced-NAD: (acceptor) oxidoreductase, 1.6.99.1 reduced-NADP: (acceptor) oxidoreductase was shown by cells lining cysts and the pituitary cleft. The findings are discussed in relation to the possible association of these enzymes with secretory function.

Author(s):  
Eva Horvath ◽  
Kalman Kovacs

The human pituitary gland consists of two major components: the adenohypophysis comprising the hormone producing cells of the pars anterior, pars intermedia, and pars tuberalis, and the neurohypophysis, also called pars nervosa or posterior lobe (1). In contrast to most mammalian species, the human gland has no anatomically distinct pars intermedia (2). The exclusively proopiomelanocortin (POMC)-producing cells of the pars intermedia are sandwiched between the anterior and posterior lobes in the majority of mammals, whereas in the human they are incorporated within the pars anterior, thereby constituting the pars distalis (3). The pars tuberalis is a minor upward extension of the adenohypophysis attached to the exterior of the lower pituitary stalk. In this chapter we deal only with adenohypophyseal tumours. Histologically, the adenohypophysis consists of a central median (or mucoid) wedge flanked by the two lateral wings. The hormone-producing cell types are distributed in an uneven, but characteristic manner. The cells are arranged within evenly sized acini surrounded by a delicate but well-defined reticulin fibre network giving the pituitary its distinct architecture (4). In the center of the acini is the long-neglected pituitary follicle composed of the agranular nonendocrine folliculo-stellate cells (5).


1936 ◽  
Vol s2-78 (312) ◽  
pp. 637-651
Author(s):  
N. H. HOWES

1. The structure of the pituitary of the adult skate is described. 2. This gland shows two distinct regions of growth which can be correlated with increase of size of the animal. 3. The pars anterior can be subdivided into three regions differing by the staining reactions of their constituent cells: (a) an anterior region where deep-purple chromaphil cells are found; (b) a middle, where they are faintly basiphil; and (c) a posterior, where they are mainly acidophil. 4. It is suggested that these regions are homologous with the pars tuberalis, basiphil, and oxyphil areas respectively of the pars anterior of the mammalian pituitary. 5. The oxyphil cells show an iodine-leucobase reaction similar to that given by the oxyphil cells of the ox pituitary. 6. The ventral lobe is a completely separate structure from the pars intermedia, although it may run along the ventral surface of the latter for some distance. 7. The histology of the neuro-intermediate lobe is described.


1923 ◽  
Vol s2-67 (266) ◽  
pp. 257-292
Author(s):  
G. R. DE BEER

1. The hypophysis of Petromyzon arises as a solid ingrowth. 2. The depression in which the hypophysis and olfactory organs come to lie is formed by the great expansion of the upper lip in conjunction with the sides of the anterior surface of the head. 3. The beginning of the histological differentiation of the glandular elements takes place from a solid strand before the appearance of any cavity. 4. The hypophysial cavity arises late as a split in the thickness of the hypophysis, and afterwards extends in both directions communicating forwards with the external depression. 5. The homologue of the pars tuberalis is probably to be found in the ‘Uebergangsteil’ of Stendell, a chromophobe portion situated between the pars anterior and pars intermedia. 6. The hypophysis of Amia is derived from the ectoderm, thus agreeing with all other known forms. 7. It arises outside the stomodaeum on the anterior surface of the head. 8. It is a solid ingrowth which loses all connexion with its point of origin, and within which the hypophysial cavity makes its appearance at a later stage. 9. Outside and in front of the stomodaeum is probably the primitive position of origin of the hypophysis, without connexion with either mouth or nose. 10. In Selachians and Amniotes where the fore-brain is early very large and the cranial flexure pronounced, the hypophysis arises further posteriorly and so is included in the hollow of the stomodaeum. 11. Although probably primitively hollow, the rudiment of the hypophysis is often solid. Such diversity is brought about by embryonic developmental conditions, perhaps the distance separating the rudiment from the infundibulum.


In a previous contribution (Hogben and Slome, 1931) evidence was brought forward to show that the white background response does not depend on the same mechanism of coordination as the black background response, which is produced by reflex liberation of a hormone (“B” substance) of the pars intermedia in the pituitary gland; and experiments pointing to the existence of another internal secretion (“W” substance), connected directly or indirectly with the activity of the pars tuberalis, were described. The existence of separate receptor components of the retina controlling the two systems was left for subsequent enquiry. Of two possible hypotheses concerning the nature of the receptive mechanism, the most likely one is illustrated diagrammatically in fig. 1. In normal situations, when an animal is illuminated on a black background, light can only fall on the floor of the retina. If it is aquatic, the maximum divergence of any two rays which strike the eye is twice the critical angle for air and water, so that in the absence of reflexion of rays from sur­rounding objects below the surface of separation all rays will presumably be brought to a sharp focus in shallow water. There are thus three distinct possibilities which arise from the way in which the animal is illuminated if, as in Xenopus , the eyes are situated on the top of the head: ( a ) in darkness no part of the retina is stimulated, the same being true of the eyeless animal; ( b ) when the animal is exposed to a black background only a sharply localized region of the retina is stimulated; ( c ) when the animal is exposed to a white background the whole of the retina is illuminated owing to the scattering of rays in all directions from the surroundings. For convenience of description the usual black back­ground situation will be described hereafter as one in which only the “floor” of the retina is stimulated, and the white background situation as one in which the floor and the “ periphery ” of the retina are both stimulated together. If then, the receptor elements of the floor and periphery initiate different systems of reflex arcs the phenomena of the background response in Amphibia and Reptiles may be interpreted as follows. In Reptiles we may suppose that stimulation of floor reflexly excites the melanophores to expand, while stimulation of peripheral photoreceptors excites them to contract, being presumably prepotent in the final common path. In Amphibia two alternatives may be con­sidered: ( a ) that floor elements reflexly excite liberation of “B” and that peripheral photoreceptors, being prepotent, reflexly inhibit libera­tion of “B"; ( b ) that floor elements reflexly excite liberation of “B”, and peripheral photoreceptors reflexly excite production of the antago­nistic substance “W” in quantity sufficient to over-ride the effect of “B”. The crucial test of the truth of the general hypothesis that the floor and peripheral elements of the retina initiate different processes of coordina­tion was suggested by Keeble and Gamble (1904-6) in their experiments on Crustacea. If it is true, a normal animal illuminated from below in a black tank with a white top should react in exactly the same way as a normal animal when illuminated in a black tank from above. On the other hand, a normal animal illuminated from below in a black tank with a black top should react like an eyeless animal in the same situation, because the floor elements would not be subject to stimulation. The experiment may be varied as indicated below. In order to obtain signi­ficant results two classes of precautions must be carefully observed. One is that the physical dimensions of the tank must not exceed certain limits, since the maximal divergence of two rays is rigidly fixed when an animal is illuminated from above. The other is that there must be no air-water interface to permit reflexion of the incident rays downwards. Aside from the fact that no bubbles must be allowed to collect, this condition presents a practical difficulty if the animal has to come to the surface to breathe.


1965 ◽  
Vol 31 (3) ◽  
pp. 279-287 ◽  
Author(s):  
B. A. YOUNG ◽  
C. L. FOSTER ◽  
E. CAMERON

SUMMARY The ultrastructure of the adenohypophysis of the rabbit is described preliminary to reporting changes after experimental procedures. Fixation by perfusing with gluteraldehyde enabled selected regions of the gland to be removed with accuracy. Separate descriptions of the pars distalis proper, zona tuberalis, pars tuberalis and pars intermedia are therefore included. In the pars distalis proper four types of granular cell were recognized although their function cannot be accurately determined. For convenience, therefore, they have been designated 1, 2, 3 and 4. In addition a fifth type of cell (type 5) is described which is also present in the other areas. This cell, as well as having possible phagocytic functions, appears to be concerned in the formation of a perivascular channel. Two types of cell are recognized in the zona tuberalis, which are similar in appearance to the 3 and 4 cells of the pars distalis, although not necessarily identical in function. The characteristic cells of the pars tuberalis are rich in cytoplasmic RNA and contain large numbers of intracellular fibrils. It is suggested that the ribosomes are concerned in the synthesis of a sedentary protein which may take the form of the microfibrils. The pars intermedia contains a predominant cell type with large granules of varying density. The relationship of these granules to the specific hormone is discussed.


1964 ◽  
Vol 24 (3) ◽  
pp. 247-256 ◽  
Author(s):  
Kensaku KAWAKATSU ◽  
Masahiko MORI ◽  
Tsuneo MIZUSHIMA ◽  
Hisaaki MAKINO

1966 ◽  
Vol 14 (1) ◽  
pp. 84-93 ◽  
Author(s):  
TAKENORI HASHIMOTO ◽  
M. S. BURSTONE

Enzyme histochemical studies of normal and burned mouse skin as well as those treated with methylcholanthrene or 2,4-dinitro-1-chlorobenzene revealed that the irritant (or stimulus) carcinogenic or noncarcinogenic, initially results in a more distinct polarization2 of the localization of oxidative enzymes including glucose 6-phosphate dehydrogenase (predominant in the upper layers of the hypertrophic epidermis) and DPN-dependent dehydrogenases, succinic dehydrogenase and cytochrome oxidase in the lower layers. Subsequently, only the carcinogen disrupted the polarization pattern. Methylcholanthrene-induced squamous cell carcinomas were classified from a histochemical standpoint according to the following three types: (1) those well differentiated and having a distinctly polarized pattern of oxidative enzymes; (2) those showing disruption of the polarization pattern and marked activity of oxidative enzymes; and (3) those that were undifferentiated and characterized by absence of a polarized pattern and weak activity of oxidative enzymes. Type 1 showed an enzyme distribution pattern resembling that of the inflammatory hypertrophic epidermis; type 2 was similar in enzymatic pattern to the advancing proximal portion of the regenerating epidermis; and type 3 was similar enzyme-histochemically to the undifferentiated epithelium of the early embryo skin. Thus, a great variation in the distribution pattern of enzyme activities appears during the carcinogenesis process.


1973 ◽  
Vol 136 (3) ◽  
pp. 649-658 ◽  
Author(s):  
Alan V. Emes ◽  
Harold Hassall

1. Soluble and mitochondrial forms of histidine–pyruvate aminotransferase were separated from rat liver preparations by chromatography on DEAE-cellulose. 2. These enzymes were characterized with respect to substrate specificity, substrate affinity, pH optimum, stability and molecular weight by chromatography on Sephadex G-200. 3. Each enzyme has a relatively broad specificity showing significant activity towards l-phenylalanine and l-tyrosine and catalysing transamination with a number of monocarboxylic 2-oxo acids. 2-Oxoglutarate is not a substrate for either enzyme. 4. The molecular weights of the two enzymes, by chromatography on Sephadex G-200, are in the range 130000–150000. 5. The formation in vitro of imidazolyl-lactate from imidazolylpyruvate and NADH was demonstrated by using liver preparations. 6. From a study of imidazolyl-lactate–NAD+oxidoreductase activity after electrophoresis of liver preparations on polyacrylamide gel, and from an examination of the activity of l-lactate–NAD+oxidoreductase (EC 1.1.1.27) towards imidazolylpyruvate, it is concluded that this latter enzyme is responsible for the formation of imidazolyl-lactate in the liver. 7. Preparations of bacteria obtained from rat faeces form imidazolylpropionate from l-histidine and urocanate without further subculture. The amount of imidazolylpropionate formed is increased under anaerobic conditions and more so in an atmosphere of H2. It is suggested that the gut flora of the rat contribute largely, if not exclusively, to the formation of imidazolylpropionate normally found in the urine.


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