Immunolocalization of the Anti-Müllerian Hormone (AMH) in Caprine Follicles and the Effects of AMH onIn VitroCulture of Caprine Pre-antral Follicles Enclosed in Ovarian Tissue

2016 ◽  
Vol 51 (2) ◽  
pp. 212-219 ◽  
Author(s):  
RMP Rocha ◽  
LF Lima ◽  
AA Carvalho ◽  
RN Chaves ◽  
MP Bernuci ◽  
...  
Keyword(s):  
Ovarian Tissue ◽  
Antral Follicles

Vitrification of bovine ovarian tissue: effect of perforated antral follicles on the structural preservation of follicles

2017 ◽  
Vol 26 (5) ◽  
pp. 1183-1188
Author(s):  
A. Mogheiseh ◽  
F. Namazi ◽  
M. Kafi ◽  
S. Safarinejad ◽  
M. Azari ◽  
...  
Keyword(s):  
Ovarian Tissue ◽  
Antral Follicles ◽  
Structural Preservation ◽  
Tissue Effect

PLASMA LEVELS OF OESTROGEN AND PROGESTERONE IN PREGNANT AND LACTATING HAMSTERS

1974 ◽  
Vol 63 (1) ◽  
pp. 125-135 ◽  
Author(s):  
RICHARD BARANCZUK ◽  
G. S. GREENWALD
Keyword(s):  
Plasma Levels ◽  
Post Partum ◽  
Ovarian Tissue ◽  
Foetal Death ◽  
Antral Follicles ◽  
Peripheral Plasma ◽  
Progesterone Secretion ◽  
Baseline Levels ◽  
The One ◽  
Normal Gestation

SUMMARY Oestrone (OE1), oestradiol (OE2) and progesterone were measured by radioimmunoassay in the same samples of peripheral plasma from pregnant and lactating hamsters. The levels of progesterone during most of pregnancy did not exceed the values found during the first 2 days of the oestrous cycle. However, on day 14 of pregnancy (2 days before parturition) the level of progesterone abruptly increased to 29 ng/ml and fell rapidly thereafter. Hysterectomy on day 12 of pregnancy resulted in baseline levels of progesterone ( < 2 ng/ml) on day 13 and no peak in progesterone comparable to the one observed on day 14 of normal gestation. Injecting progesterone on day 14 or later prolonged gestation and caused maternal and foetal death. Oestradiol concentration showed peaks on days 7 (67·3 pg/ml), 11 (117·6 pg/ml) and 14 (81·8 pg/ml) of pregnancy and dropped precipitously between days 14 and 16 of pregnancy. The highest values obtained on day 11 correlated with the maximal proliferation of antral follicles. The abrupt decline of oestrogen concentration at parturition is different from the pattern found in the mouse and rat but is consistent with the lack of post-partum ovulation in the hamster. Injecting 50–150 μg oestradiol cyclopentylpropionate between days 12 and 16 did not interfere with parturition by the morning of day 16. Oestrone was detectable throughout pregnancy; the levels were lower than for OE2. In general, the oestrogen patterns were parallel. During lactation, progesterone secretion remained relatively constant at about 10–11 ng/ml, presumably synthesized by the hypertrophied interstitium which is the dominant ovarian tissue. In most instances OE1 and OE2 were not detectable during lactation, consistent with the absence of antral follicles.

scholarly journals Function of Cryopreserved Cat Ovarian Tissue after Autotransplantation

Animals ◽  
2019 ◽  
Vol 9 (12) ◽  
pp. 1065 ◽  
Author(s):  
Janice M. V. Vilela ◽  
Ellen C. R. Leonel ◽  
Liudimila P. Gonçalves ◽  
Raísa E. G. Paiva ◽  
Rodrigo S. Amaral ◽  
...  
Keyword(s):  
Subcutaneous Tissue ◽  
Ovarian Tissue ◽  
Fibrous Tissue ◽  
Ovarian Tissue Cryopreservation ◽  
Post Transplantation ◽  
Fresh Tissue ◽  
Tissue Samples ◽  
Antral Follicles ◽  
Ovarian Cortex ◽  
Tissue Cryopreservation

The aim of this study was to assess a slow-freezing protocol of cat ovarian tissue cryopreservation using autotransplantation. Four adult queens were ovariohysterectomized and the ovaries were fragmented and cryopreserved. After one week, the grafts were thawed and autografted to the subcutaneous tissue of the dorsal neck of each queen, then randomly removed after 7, 14, 28, 49, and 63 days after transplantation. Percentages of morphologically normal primordial and growing follicles (MNFs) were 88% and 97%, respectively, in fresh tissue samples (fresh controls), and 74% and 100%, respectively, immediately after thawing (cryo D0). No MNFs were found after 49 days of transplantation. In both fresh control and cryo D0 fragments, granulosa cells were frequently in proliferation. Two morphologically normal antral follicles were detected in one queen on Day 28 post-transplantation. Connective tissue fibers increased, suggesting replacement of active ovarian cortex by fibrous tissue. Tissue vascularization was observed at 7 days after grafting, and wide blood vessels were clearly visible on Days 49 and 63. In conclusion, although follicular survival was low after cryopreservation and grafting of cat ovarian tissue, follicles were able to develop up to the antral stage, which is an encouraging outcome.

271. Effect of season on sow ovarian morphology

2008 ◽  
Vol 20 (9) ◽  
pp. 71
Author(s):  
M. Bertoldo ◽  
P. K. Holyoake ◽  
G. Evans ◽  
C. G. Grupen
Keyword(s):  
Ovarian Tissue ◽  
Developmental Competence ◽  
Corpora Lutea ◽  
Ovarian Weight ◽  
Antral Follicles ◽  
Oocyte Developmental Competence ◽  
Ovarian Morphology ◽  
The Difference ◽  
Seasonal Infertility ◽  
Farrowing Rate

Reduced farrowing rate caused by embryonic mortality is a manifestation of seasonal infertility in pigs. The ability of the oocyte to mature, be fertilised and sustain embryonic development is acquired gradually by the oocyte throughout folliculogenesis. This study was undertaken to determine if seasonal differences in ovarian morphology are associated with reduced reproductive performance displayed during seasonal infertility. Sows culled after weaning were sourced from two genetically distinct herds (Farms A and B). Pairs of ovaries were collected from sows 4 days post-weaning during winter (n = 131) and summer (n = 275). Ovarian weight (Farm A only) and the numbers of small (3–4 mm) and large (5–8 mm) follicles were assessed (Farms A and B). Data did not follow normality and was analysed using the Mann–Whitney test. Mean ovarian weight per sow during winter (20.0 ± 1.3 g) was significantly heavier than that during summer (15.3 ± 0.8 g; P < 0.05). Farm A ovaries had a greater total number of antral follicles in winter compared with summer, and a greater number of antral follicles in winter compared with Farm B ovaries (P < 0.05). In Farm A ovaries, the proportion of follicles that were large was greater in summer compared with winter (78% v. 66%; P < 0.05), but the follicular distribution did not change with season in Farm B ovaries. While the findings demonstrate that ovarian weight was greater in winter compared with summer, they suggest that this difference was not the result of changes in the number or distribution of surface antral follicles. The difference in ovarian weight is possibly due to differences in ovarian tissue resulting from regressed corpora lutea. Further studies are being undertaken to assess the effect of season on oocyte developmental competence and the steroid content of follicular fluid isolated from small and large follicles.

scholarly journals Gene Expression in Granulosa Cells From Small Antral Follicles From Women With or Without Polycystic Ovaries

2019 ◽  
Vol 104 (12) ◽  
pp. 6182-6192 ◽  
Author(s):  
Lisa Ann Owens ◽  
Stine Gry Kristensen ◽  
Avi Lerner ◽  
Georgios Christopoulos ◽  
Stuart Lavery ◽  
...  
Keyword(s):  
Gene Expression ◽  
Granulosa Cells ◽  
Polycystic Ovary ◽  
Ovarian Tissue ◽  
Polycystic Ovaries ◽  
Vitro Fertilization ◽  
Antral Follicles ◽  
Oocyte Aspiration ◽  
And Function

Abstract Context Polycystic ovary syndrome (PCOS) is the most common cause of anovulation. A key feature of PCOS is arrest of follicles at the small- to medium-sized antral stage. Objective and Design To provide further insight into the mechanism of follicle arrest in PCOS, we profiled (i) gonadotropin receptors; (ii) characteristics of aberrant steroidogenesis; and (iii) expression of anti-Müllerian hormone (AMH) and its receptor in granulosa cells (GCs) from unstimulated, human small antral follicles (hSAFs) and from granulosa lutein cells (GLCs). Setting GCs from hSAFs were collected at the time of cryopreservation of ovarian tissue for fertility preservation and GLCs collected during oocyte aspiration before in vitro fertilization/intracytoplasmic sperm injection. Participants We collected hSAF GCs from 31 women (98 follicles): 10 with polycystic ovaries (PCO) and 21 without. GLCs were collected from 6 women with PCOS and 6 controls undergoing IVF. Main Outcome Measures Expression of the following genes: LHCGR, FSHR, AR, INSR, HSD3B2, CYP11A1, CYP19, STAR, AMH, AMHR2, FST, INHBA, INHBB in GCs and GLCs were compared between women with PCO and controls. Results GCs in hSAFs from women with PCO showed higher expression of LHCGR in a subset (20%) of follicles. Expression of FSHR (P < 0.05), AR (P < 0.05), and CYP11A1 (P < 0.05) was lower, and expression of CYP19A1 (P < 0.05), STAR (P < 0.05), HSD3B2 (P = NS), and INHBA (P < 0.05) was higher in PCO GCs. Gene expression in GL cells differed between women with and without PCOS but also differed from that in GCs. Conclusions Follicle arrest in PCO is characterized in GCs by differential regulation of key genes involved in follicle growth and function.

Development of antral follicles in human cryopreserved ovarian tissue following xenografting

2001 ◽  
Vol 16 (3) ◽  
pp. 417-422 ◽  
Author(s):  
D. A. Gook ◽  
B.A. McCully ◽  
D.H. Edgar ◽  
J.C. McBain
Keyword(s):  
Ovarian Tissue ◽  
Antral Follicles ◽  
Cryopreserved Ovarian Tissue

scholarly journals Successful in vitro culture of pre-antral follicles derived from vitrified murine ovarian tissue: oocyte maturation, fertilization, and live births

Reproduction ◽  
2011 ◽  
Vol 141 (2) ◽  
pp. 183-191 ◽  
Author(s):  
Xiaoqian Wang ◽  
Sally Catt ◽  
Mulyoto Pangestu ◽  
Peter Temple-Smith
Keyword(s):  
Cancer Patients ◽  
Oocyte Maturation ◽  
Ovarian Tissue ◽  
Blastocyst Stage ◽  
Ovarian Tissue Cryopreservation ◽  
Antral Follicles ◽  
Live Births ◽  
And Function ◽  
Tissue Cryopreservation

Cryopreservation of ovarian tissue is an important option for preserving the fertility of cancer patients undergoing chemotherapy and radiotherapy. In this study, we examined the viability and function of oocytes derivedin vitrofrom pre-antral follicles as an alternative method for restoring fertility. Pre-antral follicles (specified as secondary follicle with a diameter around 100–130 μm) were mechanically isolated from vitrified-warmed and fresh adult mouse ovarian tissues and cultured for 12 days followed by an ovulation induction protocol at the end of this period to initiate oocyte maturation. Oocytes were then released from these follicles, fertilizedin vitro, and cultured to the blastocyst stage and vitrified. After storage in liquid nitrogen for 2 weeks, groups of vitrified blastocysts were warmed and transferred into pseudo-pregnant recipient females. Although most of the isolated mouse pre-antral follicles from fresh (79.4%) and vitrified (75.0%) ovarian tissues survived the 12-dayin vitroculture period, significantly fewer mature oocytes developed from vitrified-warmed pre-antral follicles than from the fresh controls (62.2 vs 86.4%,P<0.05). No difference was observed in embryo cleavage rates between these two groups, but the proportion of embryos that developed into blastocysts in the vitrification group was only half that of the controls (24.2 vs 47.2%,P<0.05). Nevertheless, live births of healthy normal pups were achieved after transfer of vitrified blastocysts derived from both experimental groups. This study shows that successful production of healthy offspring using anin vitrofollicle culture system is feasible, and suggests that this procedure could be used in cancer patients who wish to preserve their fertility using ovarian tissue cryopreservation.

scholarly journals Influence Of Different Methods Of Operative Treatment On Ovarian Reserve.

2012 ◽  
Vol 3 ◽  
Author(s):  
V Simrok ◽  
Simrok Starcheva
Keyword(s):  
Blood Flow ◽  
Surgical Treatment ◽  
Polycystic Ovary Syndrome ◽  
Operative Treatment ◽  
Ovarian Reserve ◽  
Polycystic Ovary ◽  
Ovarian Tissue ◽  
Reserve Estimation ◽  
Ovary Syndrome ◽  
Antral Follicles

This research paper presents the results of ovarian reserve estimation for 125 women with the Polycystic Ovary Syndrome (PCOS) who have undergone various methods of surgical treatment - resection of the ovaries, thermokauterisation and drilling by laser (Ho-Yag). Ovarian reserve was estimated according to the amount of antral follicles, level of follitropin and Müllerian inhibiting substance (MIS), also named anti-Müllerian hormone (AMH). Blood flow in ovarian tissue was also examined after various methods of surgical treatment. The study has shown that the gentlest method of surgical treatment is drilling by Ho-Yag laser, which is least likely to injure the tissue of ovaries, and also this method is most effective in enhancing and preserving ovarian reserve.

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