• Title/Summary/Keyword: Reproductive Cycle

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Sexual Maturation and Reproduction Cycle of the Bat Star, Asterina pectinifera (Echinodermata: Asteroidae) (별불가사리, Asterina pectinifera의 성 성숙과 생식주기)

  • Cho, In-Young;Lee, Jung-Sik;Yoo, Myoung-Suk
    • Korean Journal of Fisheries and Aquatic Sciences
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    • v.39 no.1
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    • pp.27-34
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    • 2006
  • Sexual maturation and reproductive cycle of the bat star Asterina pectinifera were investigated by histological method. Specimens were collected monthly in Donghwari, Gosunggun, Korea from January 2004 to February 2005. The bat star was dioecious. The gonads are composed of a number of gametogenic follicles. The gonadosomatic index (GSI) of female and male were reached the maximum in July (5.72, 4.54) and the minimum in December (0.89) and January, February (0.51), and the gonad index (GI) of female and male were reached the maximum in July (3.53, 3.91) and the minimum in August (0.95) and October to December (1.0), respectively. The main spawning was from August to September. The reproductive cycle of the bat star could be divided into five stages: in the female, inactive (November-February), early active (January February), late active (March-June), ripe (July), spent and degenerative (August-November) and in the male, inactive (November-February), early active (January-March), late active (April-June), ripe (July), spent and degenerative (August-October), respectively.

The Chronic and Unpredictable Stress Suppressed Kisspeptin Expression during Ovarian Cycle in Mice

  • Kim, Seung-Joon
    • Journal of Animal Reproduction and Biotechnology
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    • v.34 no.1
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    • pp.40-49
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    • 2019
  • Chronic and unpredictable stress can disrupt the female reproductive system by suppression for secretion of gonadotrophin-releasing hormone (GnRH) and gonadotrophin, resulted in ovarian malfunction and infertility. In the recent days, kisspeptin has been highly highlighted as a hypothalamic peptide which directly stimulates synthesis and release for GnRH. However, in spite of the key role of kisspeptin in the female reproductive system, little information is still available on the changes of its expression during ovarian cycle under stressed condition. Therefore, we induced chronic and unpredictable stress series to the female mice to analyze kisspeptin expression in the brain and ovary. Stressed mice exhibited changes of behavior and body weight gain during the stress assessment, which suggested that the present stress model in mice was successfully established. In the brain level, kisspeptin expression was attenuated than control. In the ovary level, the stressed mice displayed irregularly shrunk oocytes with broken zona pellucida throughout the follicle stages, pyknotic granulosa cells, decreased number of developing follicles and increased number of atretic follicles than the control. In case of kisspeptin expression in the whole ovary tissue, the expression level was decreased in the stressed mice. In detail, the less intensity of kisspeptin expression in the antral follicles phase was observed in the stressed mice than control mice, indicating that local function of kisspeptin during ovary cycle is highly associated with development of ovarian follicles. We expect that the present study has important implications for the fields of reproductive biology.

Reproductive Cycle of the Venus Fish, Aphycypris chinensis (왜몰개, Aphyocypris chinensis의 생식주기)

  • Lee, Sung-Kyu;Choi, Shin-Sok;Yeom, Dong-Hyuk
    • Korean Journal of Ecology and Environment
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    • v.33 no.4 s.92
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    • pp.395-404
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    • 2000
  • The gonadosomatic index (GSI), hepatosomatic Index (HSI), egg size distribution, gonad development and reproductive characteristics of venus fish, Aphyocypris chinensis, were examined during March 1997- March 1998 in agricultural waterways of the Sedo-myun, Puyo county, Chungnam Province, Korea. Annual reproductive cycle was classified into the following five successive phases by monthly changes in GSI and the characteristics of ovary: quiescent phase (January- February), secondary growing and mature phase (March-May), ripe and spawning phase (June-July), degenerating and resting phase (August-September) and primary growing phase (October-December). The hepatosomatic index (HSI) showed clear seasonal pattern with two separate peaks. However, it exhibited a negative correlation to changes of GSI values. The regression analysis suggested that fecundity showed a strong positive linear relationship ($r^2\;=\;0.91$, n = 34) with body weight. The sex ratio of female to male was 1.4 : 1 in the natural population during the study. The minimum reproductive size of female and male venus fish was 38 mm and 33 mm in fork length, respectively.

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Effect of electromagnetic field exposure on the reproductive system

  • Gye, Myung-Chan;Park, Chan-Jin
    • Clinical and Experimental Reproductive Medicine
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    • v.39 no.1
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    • pp.1-9
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    • 2012
  • The safety of human exposure to an ever-increasing number and diversity of electromagnetic field (EMF) sources both at work and at home has become a public health issue. To date, many in vivo and in vitro studies have revealed that EMF exposure can alter cellular homeostasis, endocrine function, reproductive function, and fetal development in animal systems. Reproductive parameters reported to be altered by EMF exposure include male germ cell death, the estrous cycle, reproductive endocrine hormones, reproductive organ weights, sperm motility, early embryonic development, and pregnancy success. At the cellular level, an increase in free radicals and $[Ca^{2+}]i$ may mediate the effect of EMFs and lead to cell growth inhibition, protein misfolding, and DNA breaks. The effect of EMF exposure on reproductive function differs according to frequency and wave, strength (energy), and duration of exposure. In the present review, the effects of EMFs on reproductive function are summarized according to the types of EMF, wave type, strength, and duration of exposure at cellular and organism levels.

Gonadal Development and Reproductive Cycle of the Ark shell Scapharca subcrenata (Bivalvia: Arcidae) from Yeoja Bay (여자만 새꼬막 Scapharca subcrenata의 생식소 발달과 생식주기)

  • Kim, Sung-Yeon;Shin, Yun-Kyung;Lim, Han-Kue;Lee, Won-Chan
    • Journal of Aquaculture
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    • v.21 no.4
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    • pp.252-258
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    • 2008
  • Gonadal development and reproductive cycle of the ark shell Scarpharca subcrenata were investigated by histological observations. Samples were collected monthly from March 2007 to February 2008 in the Yeoja Bay, Yeosu, Jeollanam-do, Korea. S. subcrenata was dioecious. The gonads consist of a number of oogenic follicle and acinus. Monthly changes in the gonad index reached a maximum in June and a minimum in September. Monthly changes in the condition index reached a maximum in April and a minimum in September. The reproductive cycle of this species can be divided into five successive stages: early active stage (January to April), late active stage (March to June), ripe stage (May to August), spent stage (July to September) and recovery and resting stage (September to March). The main spawning of S. subcrenata occurred in July and August in Yeoja Bay. The sex ratio of female to male was not significantly different from 1:1.

Gametogenesis and Reproductive Cycle of the Murex Shell Ceratostoma rorifluum(Neogastropoda: Muricidae) (패류 맵사리(Ceratostoma rorifluum)의 생식세포형성과 생식주기)

  • Lee, Ju-Ha
    • Korean Journal of Fisheries and Aquatic Sciences
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    • v.41 no.4
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    • pp.253-260
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    • 2008
  • Gonadal development, gametogenesis, reproductive cycle, spawning, relative weight of flesh, and onset of sexual maturity of the murex shell, Ceratostoma rorifluum, collected from the rocky intertidal zone of Daehang-ri, Buan-gun, Jeollabuk-do, Korea were investigated monthly from January to December 2005 both cytologically and histologically. The gonads were widely placed on the digestive gland located in the posterior spiral fleshy part in the shell. C. rorifluum had separate sexes, and was an internal fertilizer. The sex ratio of females to males was approximately 1:1. The ovary and testis contained a great number of oogenic follicles and spermatogenic tubules, respectively. The oogonia and fully ripe oocytes were $15-19{\mu}m$ and $150-160{\mu}m$ in diameter, respectively, and the cytoplasm of the ripe oocytes contained a number of yolk granules. The relative weight of flesh reached a maximum in August($39.35{\pm}0.40%$), and then decreased rapidly in November($32.75{\pm}1.20%$). The percentages of female and male snails at first sexual maturity with shell heights ranging from 12.1-14.0 mm were 60.0% and 52.9%, respectively, while 100% of the snails of both sexes with shell heights over 18.1 mm were reproductively active. Based on the gonadal development and histological observations, the reproductive cycle of the snail could be categorized into five successive stages: early active(December to May), late active(March to July), ripe(June to September), spawning(July to October), and recovery(October to March). C. rorifluum spawned once a year between July and October, and the majority of spawning occurred in September when the seawater temperature exceeded $23.5^{\circ}C$.

Reproductive Cycle of the Melanin Snail, Semisulcospira libertina libertina (다슬기(Semisulcospira libertina libertina)의 번식주기)

  • 장영진;장해진;민병화;방인철
    • Development and Reproduction
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    • v.4 no.2
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    • pp.175-180
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    • 2000
  • The reproductive cycle of ovoviviparous melania snail, Semisulcospira libeytina libertina was studied in the valley near Naewon Temple in Yangsan, Korea. Water temperature (WT) of the habitat ranged from 1.3$^{\circ}C$ to 22.5$^{\circ}C$ The meat weight rate (MWR) reached the maximum with the beginning of WT increase in March and the minimum in August. Monthly changes in average oocyte diameter showed the maximum (249.6$\pm$2.6 ${\mu}{\textrm}{m}$) in July and the minimum (134.3$\pm$2.8 ${\mu}{\textrm}{m}$) in December S. libertina libertina seemed to be a year-round breeder except for mid-summer and mid-winter. Two main reproductive cycle of the species could be divided into five successive stages: multiplicative (March, October), growing (April and May, November), mature (June and July, December), ovulation (August, January), parturition (September and October, March to May) and resting (September, February) stages in female and multiplicative (March, October), growing (April, November), mature (March to June, December), copulatory (July and August, January), resting (September, February) stages in male.

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Gonadal Development and Reproductive Cycle of the North Pacific Seastar, Asterias amurensis(Echinodermata: Asteroidea) (아무르불가사리, Asterias amurensis의 생식소 발달과 생식주기)

  • Kim, Hyun-Ju;Yoo, Myoung-Suk;Bae, Hea-Ja
    • Development and Reproduction
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    • v.10 no.1
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    • pp.33-39
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    • 2006
  • Gonadal development and reproductive cycle of the North Pacific seastar, Asterias amurensis captured from the Gosung, Gyeongsangnamdo, between November 2003 and February 2005, was investigated monthly changes of gonadosomatic index(GSI), gonadal development and oocyte size-frequency distribution. Monthly changes of GSI values showed similar trends in female and male. GSI values were reached the maximum in March($3.88{\pm}3.04$ in female, $0.87{\pm}0.57$ in male), and then gradually decreased. Based on the monthly changes of GSI, histological observation of gonadal development, reproductive cycle was divided into following successive stage: growing stage(October to January), mature stage(February to March), spent stage(March to April), degeneration and resorption stage(April to May), recovery stage(July to September). based on these result, this species seemed to have a synchronous oocyte development and one spawning season a year.

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Changes in Plasma Sex Steroid and Cortisol Levels during Annual Reproductive Cycle of Ribbed Gunnel, Dictyosoma burgeri

  • Hwang, In Joon;Kim, Sung Yeon;Kim, Hyung Bae;Baek, Hea Ja
    • Development and Reproduction
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    • v.16 no.4
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    • pp.279-287
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    • 2012
  • We investigated the changes in plasma sex steroid hormones, testosterone (T), estradiol-$17{\beta}$ ($E_2$), 17,$20{\beta}$-dihydroxy-4-pregnen-3-one ($17{\alpha}20{\beta}P$), 11-ketotestosterone (11KT) and cortisol levels from ribbed gunnel, Dictyosoma burgeri in associated with annual reproductive cycle. The gonadosomatic index (GSI) of females increased from November, peaked in February and decreased rapidly from March. The GSI of males also increased from November, peaked in January and then decreased gradually. In females, $E_2$ levels increased and remained high from December to February. The levels of T showed a similar tendency and correlated ($r_s$=0.898, p<0.01) with $E_2$ levels. The levels of $17{\alpha}20{\beta}P$ increased rapidly in February ($4.78{\pm}1.01ng/ml$) and peaked in July ($5.08{\pm}0.65ng/ml$). Cortisol level was peaked in March and correlated with $17{\alpha}20{\beta}P$ levels ($r_s$=0.696, p<0.01). In males, the levels of T was peaked in January and then decreased rapidly. The levels of 11KT were remained high from October to January. On the other hand, the levels of $17{\alpha}20{\beta}P$ fluctuated during reproductive cycle. These results suggest that plasma sex steroids in ribbed gunnels have annual periodicity, and that cortisol may involve in maturation of females.

Gonadal Development and Reproductive Cycle of the Rabbitfish (Siganus canaliculatus) (흰점독가시치 (Siganus canaliculatus)의 생식소 발달 및 생식주기)

  • HWANG Hyung Kyu;PARK Chang Beom;KANG Yong Jin;LEE Jong Ha;RHO Sum;LEE Yong Don
    • Korean Journal of Fisheries and Aquatic Sciences
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    • v.37 no.5
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    • pp.393-399
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    • 2004
  • Annual reproductive cycle of Siganus canaliculatus was studied based on monthly variation of gonadosomatic index (GSI) and histological changes of gonads. Samples were monthly collected by a set net along the southern coast of Jeju Island, Korea from January to December, 1996. Variation of the monthly mean GSI values showed similar trends in female and male. The GSI values increased from June and reached a peak in the spawning season in July $(9.65{\pm}1.96\;in\;females,\;10.00{\pm}4.27\;in\;males)$, and decreased rapidly thereafter. Female hepatosomatic index (HSI) values ranged from $1.26{\pm}0.22\;(in\;April)\;to\;2.34{\pm}0.39$ (in July), and male HSI values ranged from $1.27{\pm}0.21\;(in\;April)\;to\;1.87{\pm}0.30$ (in October). Annual reproductive cycle was classified into the following successive stages: in female, growing stage (from February to June), mature stage (from June to July), ripe and spawning stage (from July to August), recovery stage (from August to March); and in male, growing stage (from January to June), mature stage (from June to July), ripe and spent stage (from July to August), and recovery stage (from August to April). Based on these data, this species has a group-synchronous oocyte development and one spawning season a year.