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      An Ultrasonographic Study of Ovarian Antral Follicular Dynamics in Prepubertal Gilts During the Expected Activation of the Hypothalamo-pituitary-ovarian Axis

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          Abstract

          Daily transrectal ultrasonography was carried out in eight 4–5-month-old Polish Large White × Polish Landrace gilts for 42 days to monitor the growth of individual ovarian antral follicles ≥2 mm in diameter. In total, 52.4 ± 16.2 and 123.0 ± 6.7 follicles per gilt (mean ± SD) that grew to ≥4 mm were identified during the first and second 21-day study periods, respectively (P<0.01). Four follicular waves (defined as the synchronous growth of a group of follicles from 2–3 mm to ≥4 mm) emerged during the first period, and five waves emerged during the second period. The maximum diameters attained by the largest follicles of waves were 5.7 ± 0.6 and 7.0 ± 0.5 mm (first and second periods, respectively; P<0.01). The present results provide direct evidence for the rhythmic, wave-like pattern of antral follicle recruitment in prepubertal gilts. The number of follicles and maximum diameter they attain increase significantly during the expected activation of the hypothalamo-pituitary-ovarian axis in prepubescent gilts.

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          Most cited references23

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          Reproductive cycles in pigs.

          The oestrous cycle in pigs spans a period of 18-24 days. It consists of a follicular phase of 5-7 days and a luteal phase of 13-15 days. During the follicular phase, small antral follicles develop into large, pre-ovulatory follicles. Being a polytocous species, the pig may ovulate from 15 to 30 follicles, depending on age, nutritional status and other factors. During the luteal phase, follicle development is less pronounced, although there is probably a considerable turnover of primordial to early antral follicles that fail to further develop due to progesterone inhibition of gonadotrophic hormones. Nevertheless, formation of the early antral follicle pool during this stage probably has a major impact on follicle dynamics in the follicular phase in terms of number and quality of follicles. Generally, gilts are mated at their second or third estrous cycle after puberty. After farrowing, pigs experience a lactational anoestrus period, until they are weaned and the follicular phase is initiated, resulting in oestrus and ovulation 4-7 days after weaning. This paper describes the major endocrine processes during the follicular and luteal phases that precede and follow ovulation. The role of nutrition and metabolic status on these processes are briefly discussed.
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            Characteristics of ovarian follicle development in domestic animals.

            In most domestic animals the later stages of follicle development occurs in a wave-like pattern during oestrous cycles (cattle, sheep, goats, horses and buffalo) or periods of reproductive activity (llamas and camels). A follicle wave is the organized development of a cohort of gonadotrophin-dependent follicles all of which initially increase in size, but most of which subsequently regress and die by atresia (subordinate follicles). The number of remaining (dominant) follicles is specific to the species and is indicative of litter size. Follicle waves develop during both luteal and follicular phases and it is the dominant follicle(s) of the last follicular wave that ovulates. However, there are cases where dominant follicles from the last two follicle waves can ovulate (sheep and goats). There are exceptions to the organized wave-like pattern of follicle growth where follicle development is apparently continuous (pigs and chickens). In these animals many follicles develop to intermediate diameters and at specific times follicles that are destined to ovulate are selected from this pool and continue growing to ovulation. Understanding the pattern of follicle development in different species is increasingly important for designing improved methods to manipulate reproduction in domestic animals.
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              Follicular dynamics during the ovulatory season in goats.

              Growth and regression of ovarian follicles>or=3 mm were studied by transrectal ultrasonography for 4 interovulatory intervals in each of 5 Saanen goats. The observed number of growing identified 4-mm follicles per day differed (P or=6 mm followed a pattern of significant peaks on Days 0 (ovulation), 4,8 and 14. A follicular wave was defined by consecutive days of entry of follicles>or=6 mm into the wave, and the day of emergence was defined as the first day that the >or=6 mm follicles were 3 mm. In 15 of 20 (75%) interovulatory intervals, 1 wave emerged during each of Day -2 to Day 1 (Wave 1); Days 2 to 5 (Wave 2); Days 6 to 9 (Wave 3); and Days 10 to 15 (Wave 4). Ovulation occurred during Wave 4. The mean days of emergence of Waves 1 to 4 were Days -1, 4, 8 and 13, respectively. However, in 5 of these 15 interovulatory intervals, 50% of the apparent waves merged or were continuous so that a distinction could not be made between 2 waves. The largest follicle grew to a larger (P<0.05) maximum diameter for Waves 1 (8.7+/-0.3 mm) and 4 (9.7+/-0.3 mm) than for Waves 2 (7.2+/-0.2 mm) and 3 (7.3+/-0.2 mm). The following observations suggested that the phenomenon of follicular dominance was more common during Waves 1 and 4 than during Waves 2 and 3: 1) the interwave intervals (days) were longer (P<0.05) for Waves 1 (3.4+/-0.2) and 4 (4.3+/-0.6) than for Waves 2 and 3 (2.5+/-0.2 for each wave) and 2) the correlation between maximum diameter of largest follicle and the subsequent interwave interval was significant for Waves 1 and 4 but not for Waves 2 and 3. The 5 remaining interovulatory intervals were irregular and involved more than 4 waves, including 2 interovulatory intervals with prolonged follicular phases (14 and 21) and failures of ovulation. In conclusion, the predominant follicular-wave pattern was 4 waves with ovulation from Wave 4, and apparent follicular dominance was expressed during some follicular waves, especially during Waves 1 and 4.
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                Author and article information

                Journal
                J Reprod Dev
                J. Reprod. Dev
                JRD
                The Journal of Reproduction and Development
                The Society for Reproduction and Development
                0916-8818
                1348-4400
                26 May 2013
                August 2013
                : 59
                : 4
                : 409-414
                Affiliations
                [1) ]Department of Swine and Small Ruminant Breeding, University of Agriculture, 30-059 Cracow, Poland
                [2) ]Department of Biomedical Sciences, Ontario Veterinary College, University of Guelph, Ontario N1G 2W1, Canada
                Author notes
                Correspondence: T Schwarz (e-mail: rzschwar@ 123456cyf-kr.edu.pl )
                Article
                2012-181
                10.1262/jrd.2012-181
                3944353
                23708742
                058c1a3c-3e43-4d5e-ae12-63401849e141
                ©2013 Society for Reproduction and Development

                This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License.

                History
                : 05 December 2012
                : 22 March 2013
                Categories
                Technology Report

                antral follicle,follicular dynamics,gilt,pig,prepubertal,ultrasonography

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