scholarly journals HISTOCHEMICAL STUDIES ON GLYCOSIDASES OF THE RAT OVARY AND PLACENTA

1965 ◽  
Vol 13 (5) ◽  
pp. 396-403 ◽  
Author(s):  
D. BULMER

In the rat ovary and placenta the distribution of β-glucuronidase and β-galactosidase activities shown by the 6-bromo-2-naphthol post-coupling methods differs markedly from the distribution of β-glucuronidase activity which is indicated by the Fishman-Baker ferric hydroxyquinoline technique. In the ovary the intense reactions in interstitial cells and luteal cells with the post-coupling methods may be partly due to diffusion of intermediate reaction product. In the placenta a distribution is indicated for both glycosidases which is similar to the distribution pattern of acid phosphatase and organophosphate-resistant esterase. It is unlikely that the granular reactions obtained in some situations with the post-coupling methods can be regarded as an exact cytological localization of enzyme activity. The simultaneous coupling method for acetylglucosaminidase shows strong reactions in ovarian macrophages and atretic follicles, with weaker activity in corpora lutea, interstitial cells, and theca interna. In the placenta the visceral endoderm and decidua are strongly reactive, with weaker activity in the metrial gland and trophoblast. In some situations the reaction product is deposited in granular from, probably on the surface of lysosomal particles.

1916 ◽  
Vol s2-61 (244) ◽  
pp. 433-473
Author(s):  
CHAS. H. O'DONOGHUE

The Corpus Luteum (a) Follicular Wall--The membrana granulosa in the three species, P. cinereus, T. vulpecula, and D. aurita, is composed of typical polygonal cells arranged three or four cells deep around the ripe follicle. The theca folliculi also calls for no special comment in any case. It is composed of internal and external layers, does not contain any included interstitial cells, and its cells are always readily distinguishable from membrana granulosa cells. (b) The Formation of the Corpus Luteum--The corpus luteum in P. cinereus is formed by the irruption of both layers of the theca folliculi, which burst through the membrana granulosa and form a lining on its inner side. This method of formation is similar to that in P. obesula, P. nasuta, and M. ruficollis. The ripe follicle in T. vulpecula collapses when the ovum is extruded, and the central cavity is at once obliterated. The theca folliculi is drawn in with the membrana granulosa, which it penetrates, and the connective tissue becomes irregularly distributed through the body. It is unlike the process in any other marsupial so far examined, but to a certain extent resembles that in the mouse. In D. aurita the thecal irruptions do not at once go through the membrana granulosa, but push it before them until the central cavity is practically filled in, and then they break through and form the central plug of connective tissue. In one example, a very early stage, mitoses were found in the cells of the membrana granulosa, as was also the case in P. obesula and P. nasuta. (c) The fully formed Corpus Luteum.--The corpus luteum in P. cinereus remains hollow even when fully grown, and the central cavity does not get filled in until some time after the birth of the young, apparently not until the gland has started to decline. This condition is apparently unique. In T. vulpecula the corpus luteum is fairly typical when full grown, save that its connective tissue is much more irregularly arranged than in other marsupials. The condition of the corpus in D. aurita is very similar to that in D. viverrinus In no case is the membrana granulosa shed, nor does the theca interna contribute to the lutein cells of the corpus luteum. The Interstitial Tissue. There is present in the ovary of certain species of marsupials a tissue which corresponds histologically to the interstitial tissue in the ovary of the higher mammals. The cells are always distinguishable from ordinary stroma cells, cells of the theca interna, old lutein cells, or the cells of an atresic follicle, and there is no evidence that any of the last three are at any time transformed into interstitial cells. Such cells are present in the pouch young of T. vulpecula before they could have been derived from any of the sources suggested above. Interstitial tissue is to be regarded as a tissue suigeneris, although it is possible that it may originate from modified stroma cells at a very early stage. The tissue is irregularly distributed in the various species of marsupials, and it is worthy of note that it is present in all the Diprotodontia and absent in the Polyprotodontia so far examined. It may be present only as a few small groups of cells or in such quantity as to form by far the largest part of the bulk of the ovary, excluding corpora lutea, as, for example, in P. penicillata. The tissue has a typical glandular appearance, but no satisfactory account of its function has yet been put forward, and in view of this and its irregularity it is preferable not to call it a gland, but retain the term interstitial tissue or cells.


Reproduction ◽  
2000 ◽  
pp. 375-385 ◽  
Author(s):  
K Sundfeldt ◽  
Y Piontkewitz ◽  
H Billig ◽  
L Hedin

The cadherins and their cytoplasmic counterparts, the catenins, form the adherens junctions, which are of importance for tissue integrity and barrier functions. The development and maturation of the ovarian follicle is characterized by structural changes, which require altered expression or function of the components involved in cell-cell contacts. The present study examined the cell-specific localization and temporal expression of epithelial cadherin (E-cadherin) and alpha- and beta-catenin during follicular development, ovulation and corpus luteum formation in the immature gonadotrophin- and oestrogen-stimulated rat ovary. Immunohistochemistry and immunoblotting demonstrated the expression of E-cadherin in theca and interstitial cells of immature ovaries before and after injection of equine chorionic gonadotrophin (eCG). E-cadherin was not detected in granulosa cells, except in the preantral follicles located to the inner region of the ovary. The content of E-cadherin in theca and interstitial cells decreased after an ovulatory dose of hCG. Granulosa cells of apoptotic follicles did not express E-cadherin. Oestrogen treatment (diethylstilboestrol) of immature rats for up to 3 days did not result in a measurable expression of E-cadherin in granulosa cells. alpha- and beta-catenin were expressed in all ovarian compartments. The concentration of beta-catenin was constant during the follicular phase, whereas the content of alpha-catenin decreased in granulosa cells after treatment with diethylstilboestrol or hCG. The expression of alpha-catenin was also reduced in theca and interstitial cells after hCG. alpha- and beta-catenin were present in most ovarian cells at all stages of folliculogenesis. Therefore, the catenins have the potential to associate with different members of the cadherin family and to participate in the regulation of cytoskeletal structures and intracellular signalling. The restricted expression of E-cadherin in granulosa cells of preantral follicles indicates a role in the recruitment of these follicles to subsequent cycles. The specific decrease of alpha-catenin in granulosa cells and the reduction of both alpha-catenin and E-cadherin in theca cells of ovulatory follicles might reflect some of the molecular changes in cell-cell adhesion associated with ovulation and luteinization.


2019 ◽  
Vol 242 (2) ◽  
pp. 115-124 ◽  
Author(s):  
Raul Riquelme ◽  
Freddy Ruz ◽  
Artur Mayerhofer ◽  
Hernán E Lara

An increase in the sympathetic tone in the rat ovary induces a polycystic ovary (PCOS-like) phenotype. No information exists about its impact on fertility. In contrast, increased follicular development and improved fertility in rats were found after pharmacological inhibition of acetylcholinesterase, which increased intraovarian acetylcholine (ACh). Now, we studied the impact of sympathetic stress, followed by a recovery period without stress, on the cholinergic and noradrenergic systems of the rat ovary and on fertility. To activate ovarian sympathetic nerves, female Sprague–Dawley rats were exposed to cold stress (4°C/3 h day for 28 days; first period), followed by a 28-day period without cold stress (second period). No changes in estrous cyclicity during the first period was found. At the end of this period, ovarian levels of NA and ACh were increased. Morphometric analysis showed lower numbers of secondary and antral follicles, enhanced follicular atresia and fewer corpora lutea. Plasma progesterone was lower and testosterone was higher than that in controls. At end of the second period, ovarian ACh levels had returned to control levels, but NA levels remained elevated. The second period was also characterized by the presence of cystic follicles in the ovary, by elevated plasma testosterone and estradiol levels, while progesterone levels were decreased. Estrous cyclicity and ovulation during that period were irregular and fertility decreased. Thus, cold stress initially activated both ovarian noradrenergic and cholinergic system. After stress, the ovary did not fully recover and activation of the noradrenergic system persisted and correlated with cystic ovarian morphology and decreased fertility.


1972 ◽  
Vol 69 (1) ◽  
pp. 141-152 ◽  
Author(s):  
A. Zmigrod ◽  
H. R. Lindner ◽  
S. A. Lamprecht

ABSTRACT Progesterone underwent extensive reductive metabolism when incubated with a microsomal preparation from rat ovaries in the presence of NADPH. The major products formed were 3β-hydroxy-5α-pregnan-20-one, 5α-pregnane-3,20-dione and 5α-pregnane-3β,20α-diol. Newly formed corpora lutea of pregnancy were almost devoid of any microsomal A-ring reducing activity (5α-reductase and a 3β-hydroxysteroid dehydrogenase) and of soluble 20α-hydroxysteroid dehydrogenase. The behaviour of the A-ring reducing enzymes paralleled that of 20α-ol dehydrogenase in that their activity (i) was high during the oestrous cycle; (ii) declined between the third and seventh day of pregnancy; and (iii) increased sharply in corpora lutea of pregnancy when ergocornine – a drug blocking pituitary prolactin secretion – was given to the rats, yet remained low when prolactin and ergocornine were administered concurrently. However, the A-ring reducing activity did not show the sharp pre-partum rise exhibited by 20α-ol dehydrogenase, thus deviating from a pattern compatible with a co-ordinate control of the three enzymes involved in the metabolic inactivation of progesterone. Contrary to a report in the literature, 5α-pregnane-3,20-dione (20 mg/rat/day) was found to be ineffective when tested for pregnancy or deciduoma supporting activity in ovariectomized rats. The microsomal reductases, if indeed operative in vivo, may restrict the availability of progesterone as an oestrogen precursor.


1994 ◽  
Vol 31 (1) ◽  
pp. 82-92 ◽  
Author(s):  
B. Biolatti ◽  
M. Castagnaro ◽  
E. Bollo ◽  
S. Appino ◽  
G. Re

Pathologic findings, lectin histochemistry, and nuclear estrogen receptors were studied in the reproductive organs of gilts treated with clenbuterol. A ration containing 1 ppm of clenbuterol was fed for 40 days to four Landrace x Large white, 9-month-old gilts, weighing 134 to 172 kg at slaughter (gilt Nos. 5–8). Four gilts (Nos. 1–4) served as controls. Treated animals had macroscopic lesions characterized by microcystic ovaries and uterine atrophy. Histopathologic lesions included atretic degeneration of many ovarian follicles, complete absence of functional corpora lutea, a reduction in the number of endometrial glands, and a decrease in cytoplasmic volume of endometrial and glandular epithelial cells. In ovaries, uterus, and vagina lectin histochemistry, performed with thirteen different biotinylated lectins, revealed a different staining distribution between control and treated gilts. The binding pattern of Ricinus communis agglutinin-1 (RCA-I) and -II (RCA-II) in the ovaries of control gilts, displayed labeling of cytoplasm in theca interna cells of Graafian follicles. There was no labeling of the same cells in treated gilts. Labeling patterns with Griffonia simplicifolia agglutinin-I (GS-I), Phaseolus vulgaris agglutinin (PHA), RCA-I and RCA-II documented a difference in the vascularis of the theca interna between Graafian follicles of control and treated gilts. The GS-1 and Ulex europaeus agglutinin-I (UEA-I) binding patterns in uterus and vagina of treated gilts when compared to control gilts suggested that there was a block of the cycling activity in the proliferative stage. Immunohistochemical staining for estrogen receptors in the endometrium was positive in all but one treated gilts, and negative to weakly positive in control gilts. Serum progesterone concentrations were decreased in treated animals when compared to control: estradiol concentrations were similar in both group of gilts. Cystic ovaries, uterine atrophy, and reduction in progesterone concentrations suggested that clenbuterol changed ovarian hormonal activity in treated animals.


1979 ◽  
Vol 07 (04) ◽  
pp. 333-344 ◽  
Author(s):  
Moo Rim Byung

An investigation was conducted to delineate the fine structure of steroid-producing ovarian theca interna cells following administration of Korean Panax ginseng to rats for 60 days. The cytoplasmic changes were observed in the ginseng-treated theca interna cells, increased number, size and density of the mitochondria, and increased size of the smooth surfaced endoplasmic reticulum, the rough surfaced endoplasmic reticulum and the Golgi apparatus. The nucleus and nucleolus were slightly enlarged and increased numbers of dense bodies were seen whereas lipid droplets were decreased in number. The changes may result from hyperfunction of the steroid-producing cells. Morphologic changes seen may represent stimulating effects on the steroid-producing cells of the theca interna in ginseng-treated animals.


2005 ◽  
Vol 185 (3) ◽  
pp. 561-575 ◽  
Author(s):  
Koji Y Arai ◽  
Hisashi Kishi ◽  
Satoshi Onodera ◽  
Wanzhu Jin ◽  
Gen Watanabe ◽  
...  

To elucidate changing patterns of inhibin/activin subunit mRNAs in the ovary of the golden hamster (Mesocricetus auratus) during the oestrous cycle, inhibin/activin subunit cDNAs of this species were cloned and ribonuclease protection assay and in situ hybridization were carried out. Inhibin α-subunit mRNA was localized in granulosa cells of primary, secondary, tertiary and atretic follicles throughout the 4-day oestrous cycle. It was also expressed in luteal cells on days 1 (oestrus), 2 (metoestrus) and 3 (dioestrus). βA-subunit mRNA was localized in granulosa cells of large secondary (>200 μm) and tertiary follicles throughout the oestrous cycle. βB-subunit mRNA was confined to granulosa cells of large secondary and tertiary follicles. Both α- and βA-subunit mRNAs were also found in ovarian interstitial cells and theca interna cells of tertiary and atretic follicles in the evening of day 4 (pro-oestrus). A striking increase in βA-subunit mRNA levels was also observed during the preovulatory period. The expression pattern of βA-subunit mRNA during the preovulatory period is unique and not found in other species. An i.v. injection of anti-luteinizing hormone-releasing hormone (LHRH) serum before the LH surge abolished the expression of α- and βA-subunit mRNAs in ovarian interstitial cells and theca interna cells. The treatment also abolished the preovulatory increase in βA-subunit mRNA. Furthermore, administration of human chorionic gonadotrophin (hCG), which followed the injection of anti-LHRH serum, restored the expression patterns of α- and βA-subunit mRNAs. The present study revealed that the golden hamster showed a unique expression pattern of βA-subunit mRNA in response to the LH surge.


Reproduction ◽  
2015 ◽  
Vol 150 (1) ◽  
pp. 11-20 ◽  
Author(s):  
Tonny Studsgaard Petersen ◽  
Martin Stahlhut ◽  
Claus Yding Andersen

Phosphodiesterases (PDEs) are important regulators of the intracellular cAMP concentration, which is a central second messenger that affects a multitude of intracellular functions. In the ovaries, cAMP exerts diverse functions, including regulation of ovulation and it has been suggested that augmented cAMP levels stimulate primordial follicle growth. The present study examined the gene expression, enzyme activity and immunolocalization of the different cAMP hydrolysing PDEs families in the rat ovary. Further, the effect of PDE4 inhibition on primordial follicle activation in cultured neonatal rat ovaries was also evaluated. We found varied expression of all eight families in the ovary with Pde7b and Pde8a having the highest expression each accounting for more than 20% of the total PDE mRNA. PDE4 accounted for 15–26% of the total PDE activity. Immunoreactive PDE11A was found in the oocytes and PDE2A in the corpora lutea. Incubating neonatal rat ovaries with PDE4 inhibitors did not increase primordial follicle activation or change the expression of the developing follicle markers Gdf9, Amh, Inha, the proliferation marker Mki67 or the primordial follicle marker Tmeff2. In addition, the cAMP analogue 8-bromo-cAMP did not increase AKT1 or FOXO3A phosphorylation associated with follicle activation or increase the expression of Kitlg known to be associated with follicle differentiation but did increase the Tmeff2, Mki67 and Inha expression in a dose-dependent manner. In conclusion, this study shows that both Pde7b and Pde8a are highly expressed in the rodent ovary and that PDE4 inhibition does not cause an increase in primordial follicle activation.


1964 ◽  
Vol 12 (9) ◽  
pp. 670-673 ◽  
Author(s):  
KÁROLY BALOGH

20α-Hydroxysteroid dehydrogenase activity was localized histochemically in the corpus luteum of the rat by using Nitro-BT as an indicator. Intensive enzyme activity was obseryed in the corpus luteum cells, especially during involution. The placenta and corpora lutea of pregnancy failed to reveal enzyme activity during the last week of gravidity. Other tissues, including endocrine glands, liver and kidneys were also negative. The Present method offers a possibility to identify the sites of progesterone metabolism in the rat ovary at the microscopic level.


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