scholarly journals The development and vascularisation of the corpus luteum in the mouse and rabbit

The development of the corpus luteum from the ruptured follicle has been the subject of a very large number of memoirs. Of these the most important have been summarised by Van der Stricht (1912) up to 1912 and more recently by Hill and Gatenby (1926) and Corner (1919), so that no useful purpose would be served by recapitulating in detail the controversial discussions contained in them. Many of the older papers are not based on a complete series of early stages of early stages of corpora lutea, since either the material was not available, or else the writers were unable to diagnose accurately the time of œstus. Sobotta (1890, 1897), Cohn (1903), Marshall (1904, 1925), and van der Stricht 91912), however, drew their conclusions from a series of accurately dated ovaries, as have more recent workers (Cornern 1919; Drips, 1919; Hill and Gatenby, 1926; Kurashige, 1927; Long and Evans, 1922; and Watrin, 1924). It is now generally agreed-and has been shown conclusively in the work of Hill and Gatenby (1926)-that the lutein cells are formed by the enlargement of the follicullar epithelium. The fate of the theca interna cells, which surround the mature follicle prior to ovulation, is still a matter of dispute, and the problem is complicated by histological species differences. There seems no reasonable doubt, however, that these elements take part in the formation of the corpus luteum, since, in numerous cases, the typical fat containing cells, closely associated with the vascular connective tissue, can be distiguished among the follicular lutein cells after ovulation. It remains to be decided whether or not they persist as functional elements, and retain their individuality.

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.


1968 ◽  
Vol 57 (3) ◽  
pp. 386-394 ◽  
Author(s):  
E. Østergaard ◽  
J. Starup

ABSTRACT 144 fertile women were treated cyclically with a daily dose of 5 mg of 6-methyl-6-dehydro-17α-acetoxyprogesterone (megestrol acetate) + 0.1 mg of 17α-ethynyl-oestradiol-3-methylether (mestranol) for a period of 1 to 24 months. The excretion of pregnanediol on days 21 to 23 never exceeded 0.9 mg/day, and there was no correlation between the excretion of pregnanediol and the length of the treatment period. In 62 fertile women it was shown by laparotomy, that inhibition of ovulation was extremely reliable when treatment with megestrol acetate + mestranol was initiated at the latest on day 7. If the treatment was started later than day 7 then the inhibition of ovulation was increasingly unreliable, and from day 10 there was no inhibition of ovulation. As could be expected the excretion of pregnanediol on day 23 was invariably low in all patients who did not show any sign of recent ovulation. More surprising was the finding of a low excretion of pregnanediol in 6 patients in whom fresh corpora lutea were found at laparotomy on day 24. This finding might be due either to an impaired function of the corpus luteum or to an influence of the steroids on the metabolism of progesterone or on the analysis used for the determination of pregnanediol. This problem has been the subject of more detailed studies. 16 fertile women underwent laparotomy on days 24 to 26, and in the cycle in which the laparotomy was performed, treatment was initiated on day 10 or later with megestrol acetate only, mestranol only, or the combination of both substances. All patients showed fresh corpora lutea. It was observed that not only megestrol acetate + mestranol, but also megestrol acetate only suppressed the excretion of pregnanediol in the late part of the cycle when treatment was initiated before ovulation, whereas mestranol only caused no decrease in the pregnanediol excretion. If treatment with megestrol acetate + mestranol was started after ovulation then the excretion of pregnanediol was not suppressed, but the luteal phase was shorter than usual. In addition, it was observed in 3 postmenopausal women, that megestrol acetate caused no significant changes in the excretion of pregnanediol following intramuscular administration of progesterone. It is therefore concluded that the low excretion of pregnanediol observed during treatment with megestrol acetate + mestranol in patients showing fresh corpora lutea, is due to an impaired function of the corpus luteum and not to a change in the metabolism of progesterone. Furthermore, it appears that megestrol acetate is responsible for this effect.


The parts played by the various reproductive organs in causing the growth of the mammary gland and the secretion of milk have been the subject of much recent investigation. Most of the work has been done with the rabbit, and the changes which occur in its mammary glands have been studied very minutely. The causes of the growth changes in the gland during the first part of pregnancy are now conclusively shown to be due to the influence of the corpus luteum. These changes in the rabbit culminate at about the 16th day after coitus; after this time in pseudo-pregnant rabbits ( i. e ., rabbits which have had coitus and developed corpora lutea, but have not become pregnant) the gland undergoes atrophy. If the growth changes of the mammary glands of a series of pregnant and pseudo-pregnant rabbits be compared, it will be seen that the changes are similar until about the 16th day, at which period in the pseudo-pregnant condition the gland begins to atrophy, while in the pregnant animal the gland becomes much thicker, increasing rapidly in weight from the 24th to the 30th day.


1992 ◽  
Vol 135 (3) ◽  
pp. 589-NP ◽  
Author(s):  
T. Tamura ◽  
J. Kitawaki ◽  
T. Yamamoto ◽  
Y. Osawa ◽  
S. Kominami ◽  
...  

ABSTRACT Immunohistochemical localization of 17α-hydroxylase/C17–20 lyase (P-45017α,lyase) and aromatase cytochrome P-450 (P-450arom) in normal human ovaries during the menstrual cycle was studied using specific polyclonal antibodies which were raised against corresponding enzymes. In the follicular phase of matured follicles, P-45017α,lyase was localized in theca interna cells and P-450arom in granulosa cells. P-45017α,lyase was expressed in theca interna cells before P-450arom was expressed in granulosa cells. The corpus luteum showed immunoreactivity to both enzymes and, after menstruation, immunoreactivity decreased gradually until it could not be detected in the corpus albicans. In corpus luteum graviditatis the immunoreactivity continued to be expressed strongly. In some atretic follicles, P-45017α,lyase and/or P-450arom continued to be expressed. In the stromal layer, P-45017α,lyase was detected in secondary interstitial cells, which originated from the theca interna of atretic follicles, and P-450arom was detected in hilar cells. Immunoreactivity to both enzymes was also detected in oocytes of developing follicles. These results are consistent with the two cell theory in the human ovary. They also suggest that androgens and oestrogens are produced not only by follicles and corpora lutea but also by stroma and oocytes. Journal of Endocrinology (1992) 135, 589–595


1996 ◽  
Vol 148 (3) ◽  
pp. 435-446 ◽  
Author(s):  
G Meduri ◽  
M T Vu Hai ◽  
A Jolivet ◽  
S Takemori ◽  
S Kominami ◽  
...  

Abstract Previous studies have shown a heterogeneous expression of LH receptors in various structures of the porcine ovary. Specially striking was the existence in the preovulatory follicle of inner layers of theca interna cells devoid of LH receptor and the confinement in the corpus luteum of the LH receptor to the external cellular layers. In the present study, we have compared the steroidogenic capabilities of LH receptor-positive and -negative cells using immunocytochemistry for side-chain cleavage P450, 3β-hydroxysteroid-dehydrogenase, 17α-hydroxylase P450 and aromatase P450. We have also examined, using the same methods, the evolution of the various cell types after ovulation and during the development of the corpus luteum. In preovulatory follicles the inner layers of theca cells which were not labelled with anti-LH receptor antibodies appeared to express the steroidogenic enzymes in a way similar to that of the outer LH receptor-positive cell layers. Ovulation per se did not change the distribution of LH receptors (present in the outer luteal cells and in the granulosa) or of steroidogenic enzymes. However, 48 h after follicular rupture there was a marked decrease in overall labelling with anti-LH receptor antibody, and especially a disappearance of immunostaining in the luteal cells of granulosa origin. In the mid-luteal phase (6 days after ovulation), the receptor content seemed to increase in the peripheral luteal cells derived from the theca but the receptor did not reappear in the granulosa-derived luteal cells. Thus the down-regulation of LH receptor appeared to be reversible in the external thecal layers but irreversible in the granulosa cells. Furthermore, the distribution of the various steroidogenic enzymes in the corpora lutea delineated granulosa-derived from theca-derived cells and showed that only the external layers of the latter expressed the LH receptor. These results showed the existence in the preovulatory follicle of two theca interna regions expressing the same steroidogenic enzymes but possibly submitted to a different hormonal control. Furthermore, the cells derived from these two regions as well as the cells of granulosa origin showed a distinct pattern of variation of LH receptivity during the development of the corpus luteum. During these studies we also observed that, in the interstitial tissue, only a minority of cells which derived from remnants of atretic follicles expressed both the LH receptor and the steroidogenic enzymes. Journal of Endocrinology (1996) 148, 435–446


2005 ◽  
Vol 33 (06) ◽  
pp. 395-403 ◽  
Author(s):  
M. Thumes ◽  
M. Holsteg ◽  
K. Failing ◽  
H. Bostedt ◽  
R. Hospes

Zusammenfassung Ziel der Untersuchung: Überprüfung der Wirksamkeit von DL-Cloprostenol vs. D-Cloprostenol in der Östrusinduktion bei Milchrindern. Probanden und Methoden: Das Probandenkollektiv umfasste 134 Rinder im Durchschnittsalter von 4,0 ± 0,5 Jahren (99 in Laktation, 35 Färsen). Vor alternierender Injektion zweier Cloprostenolpräparate (Gruppe A: DL-Cloprostenol, 500 μg, n = 70; Gruppe B: D-Cloprostenol, 150 μg, n = 64) wurde die Progesteronkonzentration im Serum bestimmt. Gynäkologische Kontrollen erfolgten 0–3 d post injectionem (p. inj.), wobei die als inseminationsfähig beurteilten Probanden (n = 123) am dritten Tag besamt wurden. Ergebnisse: In beiden Gruppen kam es bis zum dritten Tag p. inj. zu einer deutlichen Konsistenzänderung oder Regression der Corpora lutea (p ≤ 0,001). Die Lysis eines C. l. periodicum verlief bei Kühen markanter als bei Färsen (p ≤ 0,017). Insgesamt war D-Cloprostenol dem DL-Cloprostenol hier leicht überlegen. Am dritten Tag p. inj. wiesen 67,1% (A) bzw. 71,9% (B) der Probanden gut ausgeprägte Östrusanzeichen auf. Als inseminationsfähig wurden 94,3% (A) und 89,1% (B) der Tiere eingestuft. Ein geringer Präparateunterschied bestand hinsichtlich des Graviditätsresultates. Bei einem C. l. persistens verlief die Regression weniger progressiv als bei einem C. l. periodicum (p ≤ 0,024). Signifikante Wechselwirkungen zwischen den Einflussfaktoren Präparat und Indikation einerseits sowie für die übrigen gynäkologischen Kriterien andererseits ergaben sich nicht. Bei den Probanden mit prostaglandininduziertem Zyklus nach einem C. l. persistens lag die Graviditätsrate nach der 1. KB deutlich niedriger (31,9%) als bei Tieren nach Lysis eines C. l. periodicum (52,4%, p = 0,08). Schlussfolgerungen und klinische Relevanz: Der Einsatz von D-Cloprostenol erbringt im Wesentlichen die Resultate wie der von DL-Cloprostenol. Eine Überlegenheit konnte jedoch für die Progressivität der lytischen Wirkung des D-Cloprostenols festgestellt werden. Kühe mit C. l. persistens reagierten präparateunabhängig weniger intensiv als solche mit C. l. periodicum.


1968 ◽  
Vol 59 (2_Suppl) ◽  
pp. S35-S51 ◽  
Author(s):  
B. L. Lobel ◽  
E. Levy

ABSTRACT Activities of various hydrolases and dehydrogenases were studied during the formation, development and involution of cyclic corpora lutea and in the corpora lutea of early pregnancy. At 24 hours postovulation the luteal cells, whether of granulosal or thecal origin, contained demonstrable levels of Δ5-3β-hydroxysteroid dehydrogenase and the NADP and NADPH2 diaphorases. During the period of proliferation and cellular growth, enzymic activities in the luteal cells were moderate at first, and then increased. In the mature corpus luteum, activities of the dehydrogenases occurred in all luteal cells but were most intense in the large polymorphic luteal cells. Activities of hydrolytic enzymes, low in the immediate postovulatory period, increased with the development of the vascular system. Enzymic characteristics of corpora lutea of gestation were similar to those of cyclic corpora, except for phosphorylase activity which was observed in luteal cells in gestational corpora, but confined to the vascular walls in cyclic corpora. No increase in activities of 17β- and 20β-hydroxysteroid dehydrogenases (above those seen in pre-ovulatory follicles) were observed after incubation of sections of either mature cyclic or gestational corpora. Involution of cyclic corpora lutea began with degenerative changes in the blood vessels: pyknosis of the endothelial cell nuclei and a sudden decline in activities of hydrolytic enzymes in the vascular walls. Subsequently, the luteal cells showed a sharp decrease in activities of the dehydrogenases as well as other signs of regressive change. The cytochemical findings are discussed in relation to biochemical observations on steroid synthesis by the bovine corpus luteum.


1986 ◽  
Vol 113 (4) ◽  
pp. 570-575 ◽  
Author(s):  
Firyal S. Khan-Dawood

Abstract. Immunoreactive oxytocin is detectable in the corpora lutea of women and cynomolgus monkeys by radioimmunoassay. To localize the presence of oxytocin and neurophysin I in ovarian tissues of subhuman primates, three corpora lutea and ovarian stromal tissues and two Fallopian tubes obtained during the menstrual cycle of the baboon and decidua from two pregnant baboons were examined using highly specific antisera against either oxytocin or neurophysin I and preoxidase-antiperoxidase light microscopy immunohistochemistry. Oxytocin-like as well as neurophysin I-like immunoreactivities were found in some cells of all the corpora lutea only, but could not be demonstrated in ovarian stromal tissues, Fallopian tubes and decidua. Specificity of the immunocytochemical reaction was further confirmed by immunoabsorption of the antiserum with excess oxytocin or neurophysin, after which the immunoreactivities for both oxytocin and neurophysin in the luteal tissue were negative. Similar controls using normal rabbit serum gave no positive staining for either oxytocin or neurophysin. Counterstaining of the positive immunoreactivities for oxytocin and neurophysin I with Mayer's haematoxylin and eosin demonstrated clearly that the oxytocin and neurophysin I appeared as granular material mainly within the cytoplasm of the luteal cells. The localization of immunoreactive oxytocin and neurophysin I in the corpus luteum of the baboon demonstrates directly the presence of these two neurohypophysial peptides within primate luteal cells and suggests their local production.


1991 ◽  
Vol 19 (01) ◽  
pp. 61-64 ◽  
Author(s):  
Satoshi Usuki

The effect of herbal components of Tokishakuyakusan on somatomedin C/insulin-like growth factor I (IGF-1) level in medium from rat corpora lutea incubated in vitro was examined. Hoelen + peony root + Japanese angelica root, hoelen + peony root, hoelen + Japanese angelica root or peony root + Japanese angelica root decreased the IGF-1 level. The data suggest that constituent herbal components of Tokishakuyakusan regulate the IGF-1 level by rat corpora lutea.


1987 ◽  
Vol 112 (2) ◽  
pp. 317-322 ◽  
Author(s):  
J. E. Sánchez-Criado ◽  
K. Ochiai ◽  
I. Rothchild

ABSTRACT Adult female rats were hypophysectomized and their pituitary glands autotransplanted beneath the left kidney capsule on day 2 (day 1 was the day of ovulation). In such rats the pituitary secretes prolactin fairly constantly and the corpora lutea secrete progesterone for several months. To induce the luteolytic effect of prolactin the rats were first injected s.c. with 2-bromo-α-ergocryptine (CB-154) on cycle days 12, 13 and 14 (i.e. 10, 11 and 12 days after operation) to depress prolactin secretion, and then with CB-154 vehicle (70% ethanol) daily until cycle day 21, to allow prolactin secretion to resume. One ovary was removed from each rat on day 15 and the remaining one on day 22. The mean (± s.e.m.) weight of the corpora lutea on day 15 was 1·46±0·06 mg and 0·98±0·07 mg on day 22 (n = 17). In contrast, rats in which the CB-154 treatment was maintained to day 21 had corpora lutea which weighed 1·31 ±0·09 on day 15 and 1·47 ±0·08 mg on day 22 (n = 15). To investigate whether indomethacin, a prostaglandin synthesis inhibitor, affected the luteolytic action of prolactin, the experiment was repeated, but on day 15 (after the removal of one ovary) the groups in which CB-154 treatment was stopped, as well as the group in which CB-154 treatment was maintained, were each divided into two groups. In one, indomethacin-containing silicone elastomer wafers and, in the other, blank silicone elastomer wafers, were placed within the bursa of the remaining ovary. There were no differences in corpus luteum weight on day 15 among any of these groups and the two groups of the first experiment. There was no significant difference in corpus luteum weight between day 15 and day 22 in any of the six groups except for the two groups treated with the CB-154 vehicle and not with indomethacin. Thus, treatment with indomethacin prevented the fall in corpus luteum weight associated with the discontinuation of CB-154 treatment. Serum prolactin levels fell until day 15 in all rats and remained low in those in which the CB-154 treatment was maintained to day 21, but returned to control values in those treated with vehicle after day 14. Serum progesterone levels fell and remained low in all groups. Indomethacin treatment had no effect on the levels of either serum prolactin or progesterone. We conclude that some of the pharmacological effects of indomethacin are to prevent prolactin-induced luteolysis, and we suggest that prolactin induces rapid regression of the corpus luteum by stimulating intraluteal prostaglandin production or by being necessary for the effect of luteolytic prostaglandins. J. Endocr. (1987) 112, 317–322


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