scholarly journals Ovarian characteristics in sheep with multiple fecundity genes

Reproduction ◽  
2017 ◽  
Vol 153 (2) ◽  
pp. 233-240 ◽  
Author(s):  
Kenneth P McNatty ◽  
Derek A Heath ◽  
Zaramasina Clark ◽  
Karen Reader ◽  
Jennifer L Juengel ◽  
...  

Ewes heterozygous for combinations of the Inverdale (FecXI; I+), Booroola (FecB; B+) and Woodlands (FecX2W; W+) mutations have ovulation rates higher than each mutation separately. The aims of the experiments described herein were to examine the ovarian phenotypes in I+B+ and I+B+W+ ewes and to compare these with the appropriate ++ (controls), I+ and BB animals available for this study. The mean ± s.e.m. ovulation rates in the ++ (n = 23), I+ (10), I+B+ (7), I+B+W+ (10) and BB (3) animals were 1.8 ± 0.1, 2.5 ± 0.2, 6.6 ± 1.0, 9.6 ± 0.9 and 9.7 ± 0.9 respectively. The maximum number of granulosa cells per follicle in the ++ and I+ genotypes was accumulated after exceeding 5 mm diameter, whereas in I+B+, I+B+W+ and BB animals, this was achieved when follicles reached >2–3 mm. The number of putative preovulatory follicles, as assessed from those with LH-responsive granulosa cells, 24 h after the induction of luteolysis, was higher (P < 0.01) in the I+B+ and I+B+W+ compared to the ++ and I+ genotypes. The median follicular diameters of these follicles in the ++, I+, I+B+, I+B+W+ and BB genotypes were 6, 5, 3, 3 and 3 mm respectively. The total number of granulosa cells in the putative preovulatory follicles when added together, and total mass of luteal tissue, did not differ between the genotypes. Thus, despite large ovulation rate differences between animals with one or more fecundity genes, the total cell compositions over all preovulatory follicles and corpora lutea, when added together, are similar to that from the one or two such follicles in the wild types.

1974 ◽  
Vol 54 (1) ◽  
pp. 29-33 ◽  
Author(s):  
J. J. DUFOUR ◽  
M. H. FAHMY

Follicular and luteal changes during the first half of pregnancy were studied using 47 Yorkshire (Y), 52 Landrace (Ld) and 44 Lacombe (Lc) sows examined at 23, 42 and 63 days of pregnancy. Follicular fluid weight was greater in Lc than in Y (20%) and Ld (8%) sows. The mean follicular weight for all breeds increased by 22.6% (P < 0.05) from day 23 to day 42 of pregnancy. Yorkshire sows had significantly more small (1–2 mm) follicles than Lc and Ld sows. The average number of small follicles for all breeds was 117 at day 23 and remained unchanged at day 42, but was 20.5% higher (P < 0.01) at day 63. The number of medium (3–5 mm) follicles was similar in the three breeds, whereas that of large follicles (6–10 mm) was greater in Lc than in Y and Ld sows. The number of medium and large follicles increased with the advance in pregnancy. The ovulation rate as measured by the number of corpora lutea was 15.1 in Ld and 14.1 in Y and Lc. Luteal tissue weight was less in Y than in Ld and Lc sows. The weight of luteal tissue increased with advancing pregnancy.


1993 ◽  
Vol 138 (2) ◽  
pp. 315-325 ◽  
Author(s):  
K. P. McNatty ◽  
N. L. Hudson ◽  
D. A. Heath ◽  
L. Shaw ◽  
L. Blay ◽  
...  

ABSTRACT This study in ewes examined the effects on ovarian function of a pulsatile regimen of ovine FSH (NIADDK-oFSH-17) administered over a 24- to 28-day period beginning on day 1 of the oestrous cycle (day 0 = oestrus). The FSH (1·66 μg or 5·00 μg) was administered i.v. over a 1-min interval once every hour throughout the treatment period. In other ewes ovine LH (NIDDK-oLH-23) was administered (10 μg once every 2 h) for 24–28 days together with oFSH (1·66 μg/h). Compared with untreated controls (n = 19 ewes), FSH alone at both doses (n = 19 ewes/dose) as well as the FSH +LH treatment (n=10) led to significant increases in the plasma concentrations of FSH (P <0·01), ovarian weight (P <0·05) and ovulation rate (P <0·01) but there was no change in the mean weight of individual corpora lutea (CL). Exogenous FSH at the high but not the low dose alone or with LH stimulated a significant overall increase in plasma inhibin concentrations (P <0·05). The geometric mean (and 95% confidence limits) ovulation rates in the high FSH (i.e. 5·00 μg/h), low FSH (i.e. 1·66 μg/h), low FSH+LH, and control treatment groups were 15·3 (9·3, 24·8), 3·7 (2·1, 6·0), 3·7 (2·5, 5·8) and 1·4 (1·2, 1·7) respectively. The FSH or FSH+LH treatments did not alter the total numbers of antral follicles (≥1 mm diameter). However, the high but not the low FSH or low FSH + LH treatment led to significant increases in the mean numbers of large follicles (i.e. >4·5 mm diameter; P<0·01) and a higher proportion of non-atretic antral follicles. Highly significant linear relationships were found between the mean plasma concentrations of FSH or inhibin and the ovulation rate (FSH: r=0·74, P<0·0001; inhibin: r=0·93, P<0·0001). Highly significant linear relationships were also found between the plasma concentrations of FSH or inhibin and the number of large follicles (i.e. >4·5 mm diameter; FSH, r=0·78, P<0·0001; inhibin, r=0·80, P<0·0001) and between the plasma concentrations of inhibin and the number of granulosa cells in large follicles (r=0·78, P<0·0001). After the high FSH but not the low FSH treatment there were significant increases in both FSH- and LH-induced responsiveness in granulosa cells with respect to cyclic AMP synthesis in vitro. In the high FSH treatment group, granulosa cells from 1–2·5 mm diameter follicles were responsive to LH whereas, in the low FSH or FSH + LH treatment groups and the controls, granulosa cells were not responsive to LH until the follicles were >4·5 mm in diameter. FSH or FSH+ LH treatment did not lead to increases in aromatase activity in granulosa cells (i.e. when expressed on a per cell basis) or to increases in oestradiol in follicular fluid. Collectively these results show that chronic increases in plasma FSH concentrations influence, in a dose–responsive manner, the size distribution of antral follicles, the proportion of non-atretic follicles, the number of follicles with peak aromatase activity and the ovulation rate, without altering the total number of antral follicles, the granulosa cell composition of individual follicles or the sizes of individual CL. Exogenous FSH treatment at high but not low doses enhanced the sensitivities of granulosa cells to both FSH and LH in vitro. Increases in plasma FSH also led to higher concentrations of plasma inhibin as a consequence of an increase in the number of large follicles and thus the number of granulosa cells. Journal of Endocrinology (1993) 138, 315–325


2010 ◽  
Vol 22 (1) ◽  
pp. 360
Author(s):  
M. I. Cueto ◽  
F. Pereyra-Bonnet ◽  
P. Silvestre ◽  
A. E. Gibbons

The aim of the study was to assess possible variations in superovulatory yields due to different FSH treatments at 2 times of the year. Superovulation and embryo recovery were performed during the breeding (n = 63) andnonbreeding (n = 46) seasons in Merino ewes located at 41°S latitude. Animals were kept under the same conditions, housed outdoors in a sheltered and covered pen, and were fed a liveweight maintenance ration. All animals received 60-mg medroxyprogesterone acetate intravaginal sponges (Progespon®, Syntex, Buenos Aires, Argentina) for 14 days. Ewes were then randomly assigned to 2 different superovulatory treatments: classic (n = 74) and one shot (n = 35) in both seasons. Classic superovulatory treatment consisted of 7 decreasing doses (2 × 48 mg, 2 × 24 mg, 2 × 20 mg, and1 × 16 mg NIH-FSH-P1)ofFSH (Folltropin®-V, Bioniche, Belleville, Ontario, Canada), administered twice daily from 48 h before to 24 h after pessary removal. A dose of eCG (300 IU; Novormon®, Syntex) was administered at progestagen removal. One shot superovulatory treatment consisted of a single dose of FSH (70 mg NIH-FSH-P1) plus 300 UI of eCG injected at pessary withdrawal. Embryo donors were inseminated by laparoscopy with frozen-thawed semen (100 × 106 spz) 12 h after the onset of estrus. Surgical embryo recovery was done on Day 7 after sponge withdrawal and embryos were graded for quality according to morphology (Grade 1 = excellent or good; Grade 2 = fair; Grade 3 = poor; and Grade 4 = dead or degenerated; IETS 1998). A 2 × 2 factorial ANOVA was used to test the main effects (season and superovulatory treatment) and interactions. There were no significant differences in the proportion of responding ewes (>3 corpora lutea), ovulation rate, and recovered Grades 1 to 2 embryos between the breeding and nonbreeding season (Table 1; P > 0.05). However, number of recovered ova/embryos and ova/embryo recovery rate were higher during the breeding season compared with the nonbreeding season, whereas the percentage of nonfertilized ova was lower in the breeding season than in the nonbreeding season (P < 0.05). Analysis of data comparing superovulatory treatments showed that the proportion of responding ewes, ovulation rate, recovered embryos, and recovered Grades 1 to 2 embryos were lower for the one shot treatment than for the classic treatment (P < 0.05). Embryo recovery rate and nonfertilization rate did not differ between treatments (P > 0.05). It was concluded that there was an increase in the number of total recovered ova/embryos during the breeding season compared with the nonbreeding season, although the number of recovered good-quality embryos was not affected. The use of multiple FSH injections produced a higher number of total recovered and viable embryos in Merino sheep than the one shot superovulatory treatment. Table 1.Embryo yields in ewes submitted to superovulation


1972 ◽  
Vol 23 (5) ◽  
pp. 851 ◽  
Author(s):  
AO Trounson ◽  
NW Moore

Peppin Merino ewes selected for (T group) and against (0 group) multiple births over a number of generations were used in an experiment designed to study the effect of selection on ovulation rate, response to exogenous gonadotrophin (1300 i.u. pregnant mare serum gonadotrophin—PMSG), and their ability to support one or more embryos of their own or the other group. Fertilized eggs, collected following treatment of donors with PMSG, were transferred within and between groups at a rate of one and three per recipient. Recipients were not treated with PMSG. The mean ovulation rates of T and 0 recipients were 2.03 and 1.13, and the mean ovulatory response to PMSG of T ewes was almost 50 % greater than that of O ewes (4.76 v. 3.29 corpora lutea). The survival to birth of transferred eggs was affected by both the selection group of the egg and the selection group of the recipient, and by the number of eggs transferred. More O than T recipients lambed (77 % v. 45 %); and within O recipients, intergroup transfers were more successful than intragroup transfers (94 % v. 54% ewes lambed). A similar but not significant difference was observed in T group recipients (54% v. 38% lambed). Where three eggs were transferred, neither the selection group of the recipient nor that of the egg had any effect upon the incidence of multiple births. It is concluded that selection has operated primarily on ovulation rate, and there was some evidence of heterosis in intergroup transfers.


1975 ◽  
Vol 84 (1) ◽  
pp. 113-117 ◽  
Author(s):  
A. J. Mackenzie ◽  
T. N. Edey

SUMMARYPrenatal mortality was examined in 74 primiparous Merino ewes which, after hand mating to fertile rams on the second oestrus following synchronization, were allocated to two groups. One group of 38 ewes was confined to yards and restricted to approximately 30% of their maintenance requirement for 14 days while the other group of 36 remained at pasture. The degree and timing of prenatal loss was assessed by corpora lutea counts, pregnancy diagnosis about day 40, returns to service and lambing records.The mean ovulation rate was 1·06 and the 19-day non-return rate was 87·8%. Pregnancy failed in a higher proportion of the underfed ewes (45·0%) than in the control ewes (30·8%) but this difference did not reach significance. Of the ewes returning to service, significantly more did so with cycles longer than 19 days in the underfed group (9/12) than in the control group (2/8), indicating that in the latter stages, the treatment may have been detrimental to embryo survival.In a second experiment, ovulation rate and prenatal mortality, assessed as in the first experiment, were studied in 85 mature Merino ewes subjected to the following nutritional treatments: HH, control; HL, 30% submaintenance feeding for 14 days following mating; LH, 15% submaintenance feeding for 7 days prior to mating; LL, both submaintenance treatments.Acute undernutrition prior to mating (LH) had no effect on ovulation rate or prenatal mortality. Ovulation rates were low over all groups (mean 1·09) and thus precluded any valid examination of ovulation rate and body weight relationships. The right ovary was significantly more active in producing ova than the left in all groups (P < 0·05). Although ova wastage was apparently higher in. the post-mating undernutrition groups (HL, 44%; LL, 48%; LH, 50%) than in the control group (HH, 35%), the differences were not significant. An increased incidence of extended (> 19 days) first-return cycle lengths in group LL provided some evidence of induced prenatal mortality.In so far as the experiments can be considered together, they indicate that if body weights are comparable, primiparous 1½-year-old ewes are not necessarily more susceptible than mature ewes to prenatal mortality induced by severe short-term undernutrition.


Reproduction ◽  
2002 ◽  
pp. 527-533 ◽  
Author(s):  
H Cardenas ◽  
WF Pope ◽  

Treatment with testosterone increases ovulation rate in pigs. The present study was conducted to examine the effects of 5alpha-dihydrotestosterone (DHT), a non-aromatizable androgen receptor ligand, on ovulation rate and amounts of androgen receptor and FSH receptor mRNAs in postpubertal gilts. In Expt 1, ovulation rate in response to daily i.m. injections of 0, 6, 60 or 600 microg DHT kg(-1) body weight from day 13 of the oestrous cycle (day 0 = day 1 of oestrus) to the following oestrus increased with each dose of DHT (P < 0.05). The mean increase in number of corpora lutea ranged from approximately three to 17 over the three dosages of DHT. In Expt 2, gilts treated daily with 60 microg DHT kg(-1) body weight during the early follicular phase (from day 13 to day 16), coincident with follicular recruitment, or the late follicular phase (day 17 to oestrus), had higher (P < 0.05) rates of ovulation compared with gilts that received vehicle, and were not different from gilts treated with DHT from day 13 to oestrus. Percentage recovery of day 3 embryos was not altered when gilts were treated from day 13 to day 16 or from day 17 to oestrus; however, treatment of gilts with DHT from day 13 to oestrus decreased recovery of day 3 (Expt 1) or day 11 (Expt 2) conceptuses. Daily administration of 6 microg DHT kg(-1) body weight to gilts from day 13 of the oestrous cycle to the following oestrus (Expt 3) did not affect the relative amounts of androgen receptor mRNA, but increased (P < 0.05) the amounts of FSH receptor mRNA in preovulatory follicles as determined by RT-PCR. The results of these experiments indicate that androgens may regulate ovulation rate in gilts. One of the roles of androgens might be regulation of the amounts of FSH receptor mRNA in ovarian follicles.


1971 ◽  
Vol 68 (1_Suppl) ◽  
pp. S295-S317 ◽  
Author(s):  
William Hansel

ABSTRACT Simplified methods for incubating luteal tissues have been developed. Progesterone biosynthesis in washed, minced bovine luteal tissue is stimulated by added bovine LH. The response is linear in the range 2–200 ng added LH per ml of medium. The use of covariance analysis to correct for differences in time elapsing between mincing the tissue and the beginning of incubation reduces the standard error of the mean and results in marked improvement in the indices of precision. Progesterone biosynthesis in washed, minced bovine luteal tissues appears specific for LH; no other pituitary hormones give a response, and the response is completely negated by adding anti-bovine LH serum to the incubation medium. Prior treatment of cattle from which the incubated corpora lutea are obtained with various levels of human chorionic gonadotrophin, results in greatly increased luteal tissue weights. However, this tissue has a markedly reduced sensitivity to LH added in vitro. No conclusive evidence was found for a feedback inhibition of progesterone on its own synthesis in this system. The incubation system developed is sensitive enough to serve as a bioassay for LH in biological tissues and fluids. Preliminary data suggest that a simplified protein binding assay can be successfully used to measure the progestins synthesized by minced, washed bovine luteal tissue in response to added bovine LH.


1978 ◽  
Vol 26 (2) ◽  
pp. 177-184 ◽  
Author(s):  
N. Sefidbakht ◽  
M. S. Mostafavi ◽  
A. Farid

ABSTRACTKarakul, Mehraban, Naeini and Bakhtiari sheep were checked twice a day for oestrus using aproned rams and were laparotomized within 5 to 16 h of the end of every second oestrous period. Oestrus was observed for 12 monthly periods commencing on 21 April.The Mehraban breed with 1 -6 oestrous periods per month was less seasonal in its breeding activity (P<0·01) than the other breeds. Four-year-old ewes were more sexually active (P<0·01) than 3-year-old ewes (1·48 v. 1·28 oestrous periods per month). Seasonal variation in the sexual activity of the ewes was observed (P<001); the peak of activity in July to January was followed by a steady decline in February and March to a low in April and May, and then a steep recovery phase in June. There was only limited sexual activity for at least 4 months (March to June).The overall mean cycle length was 17·8 days (14 to 23 days), and the means for the four breeds were 17·6, 17·8, 17·8 and 17·9. The oestrous cycle was longer (P<0·05) during the period from December t o February than during that from June to August.The overall mean duration of the oestrous period was 36·9 h and the means for the four breeds were 35·2, 38·0, 37·4 and 37·1 h, respectively (P<0·05). The duration showed some monthly variation (P<0·01) but did not follow a special seasonal pattern. The ovulation rates for the four breeds were 1·07, 1·13,0·94 and 0·95 respectively, (P<0·01). There was a non-significant decline in the mean ovulation rate from March to June. Right ovaries were more active than left ovaries as judged by the observation of a higher average number of corpora lutea per ewe per laparotomy (0·58 v. 0·43, P<001).


2003 ◽  
Vol 179 (2) ◽  
pp. 195-203 ◽  
Author(s):  
F Shi ◽  
PS LaPolt

FoxO1 is a transcription factor implicated in a growing number of physiological processes, including apoptosis, cell cycle progression, and insulin signaling. Recent findings indicate that FSH and growth factors influence ovarian functions in part through regulation of FoxO1. The present study utilized immunohistochemical analysis to determine the ovarian localization and regulation of FoxO1 protein levels in neonatal rats, immature rats during gonadotropin-induced follicular development, ovulation, and luteinization, and in spontaneously developing ovarian cysts of aging rats. In postnatal rats, FoxO1 immunoreactivity was very faint in ovaries of 5- and 10-day-old females. In contrast, strong immunoreactivity was observed in granulosa cells of larger developing follicles at 25 days of age. To stimulate follicle development, immature female rats received equine chorionic gonadotropin (eCG) followed 52 h later by an ovulatory dose of human chorionic gonadotropin (hCG). Prior to gonadotropin treatment, moderate FoxO1 immunoreactivity was observed in granulosa cells of small follicles. Subsequently, treatment with eCG markedly decreased FoxO1 protein levels in granulosa cells of healthy antral and preovulatory follicles. Interestingly, FoxO1 staining was observed in cumulus and antral, but not mural granulosa cells of preovulatory follicles. Induction of ovulation and luteinization with hCG further decreased ovarian FoxO1 levels, with no staining evident in corpora lutea. At all time points, the most intensive FoxO1 staining was observed in granulosa cells of atretic follicles, with predominantly nuclear localization. Similarly, while FoxO1 levels were low in granulosa cells of preovulatory follicles in proestrous rats, FoxO1 staining was intense in granulosa cells of spontaneously developing cystic follicles in aged, acyclic females. Together, these findings indicate that FoxO1 is expressed in a regulated, cell-specific manner during ovarian follicular development, atresia and luteinization, suggesting roles in these physiological processes.


Reproduction ◽  
2018 ◽  
Vol 156 (3) ◽  
pp. R57-R67 ◽  
Author(s):  
Adam J Ziecik ◽  
Emilia Przygrodzka ◽  
Beenu M Jalali ◽  
Monika M Kaczmarek

The new corpora lutea (CLs) in pigs are formed from the preovulatory follicles after the luteinizing hormone (LH) surge. However, total autonomy and independence of CLs from LH up to Day 12 of cycle has recently been questioned. Transformation of estrous cycle CL to CL of pregnancy initiated by embryonic signals requires not only the cessation of prostaglandin F2 (PGF2α) supply to the luteal tissue but also needs the CL to overcome luteolytic acquisition and/or changing its sensitivity to PGF2αduring Days 12–14 of pregnancy. The luteolytic cascade is prevented by inhibition of lymphocyte infiltration and leucocyte recruitment, limitation of cell apoptosis, upregulation of pregnancy-associated genes and an enhanced antiluteolytic role of PGE2. Our ‘two-signal switch hypothesis’ highlights the importance ofpostPGF2αand PGE2receptor signaling pathways activation in CLs during luteolysis and rescue. The ‘luteolytic switch’ involves increased expression of many regression mediators and activation of thepostPTGFR signaling pathway. The ‘rescue switch’ initiated by embryonic signals – estradiol 17β and PGE2– inducespostPTGER2/4 pathway, turning the ‘luteolytic switch’ off and triggering activity of genes responsible for CL maintenance. In mid and late pregnancy, CLs are maintained by LH and the synergistic action of metabolic hormones. This paper provides an outline of recent views on CL regression, rescue and maintenance during pregnancy in pigs that conflict with previous paradigms and highlights new findings regarding the actions of prostaglandins, role of microRNAs (miRNA) and immune system and signaling pathways governing the life cycle of porcine CL.


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