Increased expression of kisspeptin and GnRH forms in the brain of scombroid fish during final ovarian maturation and ovulation
© Selvaraj et al.; licensee BioMed Central Ltd. 2012
Received: 31 May 2012
Accepted: 22 August 2012
Published: 27 August 2012
Kisspeptins (Kiss) are prime players in the control of reproductive function through their regulation of gonadotropin-releasing hormone (GnRH) expression in the brain. The experimental scombroid fish, chub mackerel (Scomber japonicus) expresses two kiss (kiss1 and kiss2) and three gnrh (gnrh1, gnrh2, and gnrh3) forms in the brain. In the present study, we analyzed expression changes of kiss and gnrh mRNAs in the brain and corresponding GnRH peptides in the brain and pituitary during final ovarian maturation (FOM) and ovulation.
Female fish possessing late vitellogenic oocytes were injected with GnRH analogue to induce FOM and ovulation. Fish were observed for daily spawning activities and sampled one week post-injection at germinal vesicle migration (GVM), oocyte hydration, ovulation, and post-ovulatory time periods. Changes in relative mRNA levels of kiss and gnrh forms in the brain were determined using quantitative real-time PCR. Changes in GnRH peptides in the brain and pituitary were analyzed using time-resolved fluoroimmunoassay.
Both kiss1 and kiss2 mRNA levels in the brain were low at late vitellogenic stage and increased significantly during the GVM period. However, kiss1 mRNA levels decreased during oocyte hydration before increasing again at ovulatory and post-ovulatory periods. In contrast, kiss2 mRNA levels decreased at ovulatory and post-ovulatory periods. Levels of gnrh1 mRNA in the brain increased only during post-ovulatory period. However, levels of gnrh2 and gnrh3 mRNAs were elevated during GVM and then, decreased during oocyte hydration before increasing again at ovulatory period. During post-ovulatory period, both gnrh2 and gnrh3 mRNA levels declined. Peptide levels of all three GnRH forms in the brain were elevated during GVM and oocyte hydration; their levels were significantly lower during late vitellogenic, ovulatory, and post-ovulatory periods. In contrast, pituitary GnRH peptide levels did not show any significant fluctuations, with the GnRH1 peptide levels being many-fold higher than the GnRH2 and GnRH3 forms.
The results indicate increased expression of multiple Kiss and GnRH forms in the brain and suggest their possible involvement in the regulation of FOM and ovulation in captive female chub mackerel.
KeywordsKisspeptins Kiss GnRH Mackerel Brain Pituitary Spawning cycle
In vertebrates, including teleosts, reproductive processes are regulated by the precise coordination of neuroendocrine hormones acting through the brain-pituitary-gonad (BPG) axis. A neurohormone, gonadotropin-releasing hormone (GnRH), plays a central role by stimulating the synthesis and release of the pituitary gonadotropins (GtHs). These pituitary GtHs, follicle-stimulating hormone (FSH) and luteinizing hormone (LH), act on the gonads to stimulate steroidogenesis, which is responsible for progression of ovarian growth and maturation [1, 2]. However, in recent years, kisspeptins, a member of the RF-amide family, have been shown to act as an upstream endogenous regulator of GnRH neurons in mammals [3, 4]. Recent studies indicate that their role in teleostean fish is also conserved [5, 6]. Kisspeptins primarily act at the level of GnRH neurons, which express kisspeptin receptor (GPR54 or Kiss1r) [7, 8].
Studies in teleosts have revealed the presence of multiple kisspeptin forms (Kiss1, Kiss2) in the brain . Moreover, teleosts brain expresses multiple GnRH forms (GnRH1, GnRH2, and GnRH3) with one or two forms regulating pituitary function [9, 10]. These multiplicities have complicated our understanding of their physiological roles in the gonadal growth and maturation in teleosts, especially in females as they exhibit different forms of reproductive dysfunctions when reared in captivity .
The experimental scombroid fish model, chub mackerel (Scomber japonicus), is a multiple batch-spawning pelagic fish. It is one of the most commercially important marine fish species in Japan. This species has been targeted for aquaculture in recent years owing to a sharp decline in the wild population, high consumer demand, use in the tuna fishing industry as bait, and high early growth potential . In southwestern Japan, wild-caught fish are being used for aquaculture production in sea pens . However, vitellogenic females fail to undergo final ovarian maturation (FOM) and ovulation in aquaculture conditions [13, 14]. Therefore, characterization and understanding of neuroendocrine pathways acting via BPG axis is critical to clarify the reproductive dysfunction in female chub mackerel . Our group already standardized a protocol based on sustained GnRH analogue delivery system to induce FOM and ovulation in outdoor tanks during natural spawning season (April-June) . This system allows us to sample fish at different stages of FOM and ovulation.
The chub mackerel brain expresses kiss1 and kiss2. During the seasonal ovarian cycle, kiss2 mRNA levels decrease during vitellogenic and ovarian regression stages . Also, the presence of three GnRH forms, namely GnRH1, GnRH2, and GnRH3 (previously seabream GnRH, chicken GnRH-II, and salmon GnRH forms, respectively ) in the brain were demonstrated previously [19, 20]. An increase in the pituitary peptide levels of GnRH1 was observed during ovarian growth and regression stages , in agreement with our immunocytochemical observation of dense GnRH1-immunoreactive (ir) fibers localized close to FSH- and LH-producing cells in the pituitary . In female gilthead seabream (Sparus aurata), which also express three GnRH forms as that of chub mackerel, an increase in the levels of all three forms of GnRH-encoding mRNAs in the brain was reported during FOM . In the present study, to clarify the possible involvement of kisspeptin and GnRH system in the regulation of FOM and ovulation, we analyzed the expression profiles of kiss and gnrh mRNAs in the brain as well as corresponding GnRH peptides in the pituitary of chub mackerel after initial administration of GnRH analogue.
Fish and tissue sampling
Adult chub mackerel (2-year-old) were caught from the wild using purse seine during autumn 2008 and reared for six months in sea pens at a fish farm in the Oita prefecture, Kyushu Island. During the following spawning season (April-June), fish were transferred to Fishery Research Laboratory of Kyushu University and moved into 3-ton outdoor concrete tanks circulated with running seawater. The fish were acclimated and reared under natural photoperiod and temperature. Our previous studies indicated that female chub mackerel fail to undergo FOM and ovulation spontaneously in this captive system [13, 14]. An induced spawning protocol based on sustained release GnRH delivery system was adopted from previous study .
After 3 days of acclimation, fish were anaesthetized with 2-phenoxyethanol (100 mg/l) and females with late vitellogenic oocytes (600–650 μm in diameter) were selected by ovarian biopsy using a plastic catheter tube (2 mm internal diameter), as described previously [13, 16]. Males oozing milt under gentle abdominal pressure were selected. After selection of required number of females and males, intramuscular injection with the GnRH agonist (D-Ala6, des-Gly10)-LHRH ethylamide (Sigma-Aldrich, St. Louis, USA) at 400 μg/kg body weight were performed on April 30th, May 13th, May 21st, and May 22nd, 2009 to obtain different ovarian stages, namely germinal vesicle migration (GVM), oocyte hydration (HY), ovulation (OV), and post-ovulation (POV), respectively. The sampling times were 13.00, 16.00, 20.00, and 6.00 h of the day, respectively. In all cases, injections were performed at 11.00 h. Sampling times were fixed based on our previous data on time course of FOM and ovulation in chub mackerel induced by GnRHa . Fish sampling for the analysis was performed on day 8, based on previous reports showing the decline in the plasma concentration of GnRH agonist on day 5 after intramuscular injection with the GnRH agonist suspended in coconut oil in Plaice, Pleuronectes platessa[22, 23]. The first spawning was observed 34–36 h post-injection, and subsequent daily spawning occurred between 22.00 and 24.00 h. In the following experimental system, daily spawning of chub mackerel is observed for 20–30 days during the spawning season, when the water temperature ranged between 18-23°C (Yoneda et al., unpublished observations). The late vitellogenic (LV) stage fish were sampled before the start of induced spawning experiment.
Fork length, body weight, and gonadosomatic index of female chub mackerel analyzed in the study period
Fork length (cm)
33.6 ± 0.4
Body weight (g)
7.3 ± 1.4
Fork length (cm)
33.5 ± 0.5
34.6 ± 0.8
34.9 ± 0.5
33.2 ± 0.4
35.3 ± 1.3
Body weight (g)
578.6 ± 30.0
659.9 ± 44.0
513.5 ± 19.3
694.7 ± 94.4
6.7 ± 0.8
4.5 ± 0.66
8.2 ± 1.8
6.9 ± 1.2
8.0 ± 2.7
After fixation, ovary samples from each fish were dehydrated in a series of ethanol solutions up to 100%, embedded in paraffin, and sectioned at 5–7 μm using a Leica RM 2155 rotary microtome (Leica, Germany). Sections were stained with hematoxylin and counterstained with eosin. The stained tissues were subsequently observed under a light microscope. Chub mackerel show asynchronous ovarian development, and ovarian stages were thus classified based on the developmental stages of first clutch oocytes as (1) LV, (2) GVM, (3) HY, (4) OV, and (5) POV.
Quantitative real-time PCR analysis of kiss and gnrh mRNAs in the brain
List of primers used for real-time PCR expression analysis of kiss and gnrh mRNAs
Nucleotide sequences (5′-3′)
Mac. Kiss1 RT Fw
Mac. Kiss1 RT Rv
Mac. Kiss2 RT Fw
Mac. Kiss2 RT Rv
Mac. RT sbGnRH Fw
Mac. RT sbGnRH Rv
Mac. RT cGnRH-II Fw
Mac. RT cGnRH-II Rv
Mac. RT sGnRH Fw
Mac. RT sGnRH Rv
Time-resolved fluoroimmunoassay analysis of GnRH peptides in the brain and pituitary
Brain and pituitary extracts were prepared following the protocol described earlier [26, 27]. Brain and pituitary GnRH peptide levels were measured using a previously developed time-resolved fluoroimmunoassay (TR-FIA) system to quantify levels of GnRH1 (sbGnRH form), GnRH2 (cGnRH-II form), and GnRH3 (sGnRH form) in tissue extracts [28, 29]. Parallelism between the typical standard curves of each GnRH peptide and the corresponding competition curves of sample extracts of chub mackerel was confirmed with serially two-fold-diluted standards and sample extracts in TR-FIA assay buffer . The detection range, minimum detectable limit, and cross reactivity data are presented in our recent publication . The intra- and interassay CV values of TR-FIA for GnRH1 were 9.0% and 19.6%, those for GnRH2 were 7.5% and 5.8%, and those for GnRH3 were 7.4% and 10.3%. GnRH peptide levels in the brain and pituitary samples are expressed as ng/mg tissue and ng/pituitary, respectively.
All data are represented as the mean ± standard error of the mean. Changes in the levels of kiss and gnrh mRNAs in the brain and GnRH peptides in the brain and pituitary during different ovarian stages were analyzed by one-way ANOVA, followed by Tukey’s multiple comparison test. p<0.05 was considered significant and different letters in figures represent significant differences between different ovarian stages. All analyses were conducted in GraphPad Prism4.
Changes in kiss1 and kiss2 mRNA levels in the brain
Changes in gnrh1, gnrh2, and gnrh3 mRNA levels in the brain
Changes in GnRH1, GnRH2, and GnRH3 peptide levels in the brain and pituitary
Pituitary peptide levels of all three GnRH forms did not show any significant differences among different ovarian stages (See Additional file 1: Figure S1).
The present study is part of a series of works targeted towards understanding the molecular basis of chub mackerel reproduction with the aim of correcting reproductive dysfunction in captivity [15, 17, 19, 20, 31]. In the present study, after GnRHa administration to fish, first spawning was observed 34–36 h post-injection and subsequent daily spawning occurred between 22.00 and 24.00 h till day 7 post-injection. Based on the previous reports demonstrating significant decline in the plasma concentration of GnRH agonist on day 5 after intramuscular injection with the GnRH agonist suspended in coconut oil in the Plaice [22, 23], results of the present study likely indicate an endogenous profile of female chub mackerel undergoing FOM and ovulation in captivity.
It was interesting to find that both kiss1 and kiss2 mRNA levels in the brain peaked during FOM stage. However, it has been previously demonstrated that kiss1 levels did not show any fluctuation and kiss2 levels remained low during late vitellogenic and post-spawning periods in female chub mackerel . These results suggest an ovarian stage dependent expression of kiss1 and kiss2 in the brain of chub mackerel. Similar observations on differential expression changes of kiss mRNAs in the brain at different reproductive stages of other teleosts were reported previously. Biran et al.  have found that in female zebrafish (Danio rerio), kiss1 mRNA levels in the brain gradually increased during the first 2–8 weeks of life to peak in fish with large mature vitellogenic follicles at 12 weeks. Subsequently, Kitahashi et al.  found both kiss1 and kiss2 mRNA levels in the brain peaked 30 days after fertilization and remained high during puberty and adulthood. In grass pufferfish (Takifugu niphobles), expressing only kiss2, mRNA levels peaked in the brain and pituitary of adult mature and spawning females . Similarly, in the brain of mature female striped bass (Morone saxatilis), both kiss1 and kiss2 mRNAs, including levels of their receptors gpr54-1 and gpr54-2, were found to be significantly increased in comparison to juvenile and prepubertal fish . In female Senegalese sole (Solea senegalensis), Mechaly et al.  found highest kiss2 mRNA expression in the forebrain and midbrain either before or during the spawning season. However, in Atlantic cod (Gadus morhua), kiss2 mRNA expression in the brain was elevated in the vitellogenic females . Based on these results, we hypothesize that increased kiss mRNA levels in the brain are likely involved in the regulation of FOM and ovulation in chub mackerel. Future studies on the investigation of kiss expression in the brain of naturally spawning female chub mackerel will help to clarify the proposed hypothesis.
Recent studies suggest that the expression of kisspeptin receptor appears to have a more critical role in regulating the reproductive processes than its ligand . In sheep, administration of kisspeptin decapeptides (Kiss1-10) was shown to regulate expression of kisspeptin receptors in the brain . Similarly, in a prepubertal yellowtail kingfish (Seriola lalandi), administration of Kiss2-10 showed a significant dose-dependent response in the relative mRNA expression of kisspeptin receptor (Kiss2r) . Interestingly, in zebrafish, habenula kiss1 neurons were shown to coexpress kisspeptin receptor (kissr1) [33, 40]. Further, administration of Kiss1-10 was shown to decrease habenula kiss1 mRNA expression, suggesting autocrine regulation of the kiss1 gene in the zebrafish . In light of the above, we have recently isolated two isoforms of kisspeptin receptors from the brain of chub mackerel (Ohga et al., unpublished observations). Future analyses on the expression changes of kisspeptin receptors at different reproductive stages and ligand-receptor binding affinity will help to further clarify the role of kisspeptin system in the control of reproductive processes in chub mackerel. Recently, for the first time in fish, Beck et al.  revealed that exogenous administration of kisspeptin peptides has potential to accelerate gonadal development in the basses of the family Moronidae, and their hybrid. In line with the above report, functional studies of the effects of kisspeptin peptides on inducing gonadal growth and maturation in chub mackerel merits investigation.
Chub mackerel show asynchronous type of ovarian development, containing two or three clutches of vitellogenic oocytes of different diameters . During spawning season, only a small percentage of first clutch late vitellogenic oocytes undergo FOM, hydration, ovulation, and spawning with successive progression of mid and early vitellogenic oocytes [16, 43]. Interestingly, kiss1 but not kiss2 expression in the brain was found to increase during ovulatory and post-ovulatory periods, when the second clutch of vitellogenic oocytes is likely to undergo FOM on the following day (See Additional file 2: Figure S2). Our previous study  showed that during late vitellogenic and post-spawning periods, kiss2 but not kiss1 expression in the brain decreased. The post-spawning period analyzed in our previous study  corresponds to termination of spawning season (August) and ovaries contain mainly atretic oocytes with degenerated late-vitellogenetic oocytes. In contrast, the post-ovulatory period analyzed in the present study corresponds to spawning season (April-June) and ovaries contain post-ovulatory follicles with two or three clutches of vitellogenic oocytes. Moreover, it is likely that these fish undergo repetitive spawning activity before termination of spawning season. These results suggest differential expression changes of kiss1 and kiss2 in the brain in response to unknown factors. The gonadal sex steroids have been demonstrated to act in the regulation of kisspeptin expression in the brain of mammals and teleosts [44, 45]. For instance, among teleost fishes expressing two kiss forms (kiss1 and kiss2), ovarian estrogen has been shown to regulate region specific kiss expression in the brain. In the brain of medaka (Oryzias latipes), only kiss1 neurons in the nucleus ventral tuberis (NVT) have shown to be up-regulated by ovarian estrogen [46, 47]. However, in the brain of goldfish (Carassius auratus), only kiss2 neurons in the preoptic area were shown to be up-regulated by ovarian estrogen . Interestingly, in the prepubertal zebrafish, estradiol treatment was shown to enhance expression of both kiss1 and kiss2. Future studies on the localization of kiss expression in the brain and role of sex steroids on the regulation of kiss expression will help to further define the significance of differential expression changes of kiss1 and kiss2 in the brain of chub mackerel.
Presently, for chub mackerel there is no anatomical evidence to show that kisspeptin system is directly or indirectly involved in the regulation of GnRH neurons. For the first time, Parhar et al.  demonstrated coexpression of kisspeptin receptor in GnRH1, GnRH2, and GnRH3 neurons in Nile tilapia (Oreochromis niloticus). Subsequently, Nocillado et al.  found a positive correlation in the brain expression pattern of kisspeptin receptor and GnRH in female grey mullet (Mugil cephalus). In zebrafish, kisspeptin immunoreactive axonal fibers were shown to interact with hypophysiotropic GnRH3 neuronal systems . Also, in the brain of female red seabream, expression changes of kiss2 mRNA were shown to correlate with number of GnRH1-immunoreactive neurons . Recently, in striped bass, kisspeptin receptor was colocalized in GnRH1 neurons, indicating direct influence of kisspeptin on regulation of GnRH1 neuronal system . In the present study, we found that an increase in kiss1 and kiss2 mRNA levels coincided with an increase in gnrh2 and gnrh3 levels in the brain, including the peptide levels of all three GnRH forms during FOM. These findings, including the data of other studies, suggest that the role of kisspeptins in the regulation of GnRH neuronal system is likely conserved in the chub mackerel and merits future investigation on the colocalization of kisspeptin and GnRH system.
In several teleosts, either mRNA or peptide levels of the hypophysiotropic GnRH form, i.e., GnRH1 in teleosts expressing three GnRH forms, and mainly GnRH3 in the case of those expressing two forms, have been shown to fluctuate significantly during ovarian maturation or spawning season [10, 53]. However, in the brain of gilthead seabream expressing three GnRH forms and showing asynchronous type of ovarian development as that of chub mackerel, elevation in the levels of all three GnRH mRNAs and plasma LH were found 8h before spawning, when the germinal vesicle was located next to the micropyle of the oocyte . This is in agreement with the findings of present study showing elevations in the levels of gnrh2 and gnrh3 mRNAs, including the peptide levels of GnRH1, GnRH2, GnRH3 forms in the brain during FOM stage, germinal vesicle migration (7-10h before spawning). In the chub mackerel, we did not find any significant rise in gnrh1 mRNA levels except during post-ovulatory period. However, it is interesting to note that this increase also coincided with an increase in the mRNA levels of pituitary gonadotropin subunits (gpα fshβ lhβ) analyzed in the same fish samples . These results suggest that the stimulatory signal of gnrh1 contributing to increased pituitary lhβ levels resulting in FOM, would have initiated 14-17h before spawning in the chub mackerel. Since GnRH1 peptide levels were many-fold higher in the brain and pituitary of female chub mackerel during the FOM and ovulation stages, we propose GnRH1 form as the predominant regulator of maturation and spawning in chub mackerel. This is further supported by our previous data showing a dominant role of GnRH1 form in the regulation of vitellogenesis in chub mackerel .
The present study revealed significant fluctuations in the levels of two kiss mRNAs in the brain during the FOM and ovulatory periods. Further, levels of all three gnrh mRNAs and their peptides in the brain were found to fluctuate during FOM and ovulatory periods. These results indicate increased expression of multiple Kiss and GnRH forms in the brain and suggest their possible involvement in the regulation of FOM and ovulation in captive female chub mackerel. Future studies on the expression of kiss and gnrh mRNAs and changes in their peptide levels in the brain of naturally spawning female chub mackerel will be important to understanding their role in the reproductive dysfunction of captive fish.
We thank Mr. Akira Tabuchi of the School of Marine Biosciences, Kitasato University, for his kind help with the GnRH peptides measurement. This research was funded by a subproject on studies on the prediction and application of fish species alternation (SUPRFISH) financed by the Agriculture, Forestry and Fisheries Research Council (AFFRC) of Japan, as part of the Population Outbreak of Marine Life (POMAL) Project and a grant for scientific research (23658163) from the Ministry of Education, Culture, Sports, Science and Technology (MEXT) to MM. The first author SS is supported by the Japan Society for the Promotion of Science (JSPS) postdoctoral fellowship (P11406) for foreign researchers.
- Nagahama Y, Yamashita M: Regulation of oocyte maturation in fish. Dev Growth Differ. 2008, S1: S195-S219.View ArticleGoogle Scholar
- Yaron Z, Gur G, Melamed P, Rosenfeld H, Elizur A, Levavi-Sivan B: Regulation of fish gonadotropins. Int Rev Cytol. 2003, 225: 131-185.View ArticlePubMedGoogle Scholar
- Colledge WH: Kisspeptins and GnRH neuronal signalling. Trends Endocrinol Metab. 2009, 20: 115-121. 10.1016/j.tem.2008.10.005.View ArticlePubMedGoogle Scholar
- Hameed S, Jayasena CN, Dhillo WS: Kisspeptin and fertility. J Endocrinol. 2011, 208: 97-105. 10.1677/JOE-10-0265.View ArticlePubMedGoogle Scholar
- Elizur A: The Kiss1/GPR54 system in fish. Peptides. 2009, 30: 164-170. 10.1016/j.peptides.2008.08.018.View ArticlePubMedGoogle Scholar
- Tena-Sempere M, Felip A, Gómez A, Zanuy S, Carillo M: Comparative insights of the kisspeptin/kisspeptin receptor system: lessons from non-mammalian vertebrates. Gen Comp Endocrinol. 2012, 175: 234-243. 10.1016/j.ygcen.2011.11.015.View ArticlePubMedGoogle Scholar
- Parhar IS, Ogawa S, Sakuma Y: Laser-captured single digoxigenin-labeled neurons of gonadotropin releasing hormone types reveal a novel G protein-coupled receptor (Gpr54) during maturation in cichlid fish. Endocrinology. 2003, 145: 3613-3618.View ArticleGoogle Scholar
- Parhar I, Ogawa S, Kitahashi T: RFamide peptides as mediators in environmental control of GnRH neurons. Prog Neurobiol. 2012, 98: 176-196. 10.1016/j.pneurobio.2012.05.011.View ArticlePubMedGoogle Scholar
- Kah O, Lethimonier C, Somoza G, Guilgur LG, Vaillant C, Lareyre JJ: GnRH and GnRH receptors in metazoan: a historical, comparative, and evolutive perspective. Gen Comp Endocrinol. 2007, 153: 346-364. 10.1016/j.ygcen.2007.01.030.View ArticlePubMedGoogle Scholar
- Okubo K, Nagahama Y: Structural and functional evolution of gonadotropin-releasing hormone in vertebrates. Acta Physiol. 2008, 193: 3-15. 10.1111/j.1748-1716.2008.01832.x.View ArticleGoogle Scholar
- Zohar Y, Muñoz-Cueto JA, Elizur A, Kah O: Neuroendocrinology of reproduction in teleost fish. Gen Comp Endocrinol. 2010, 165: 438-455. 10.1016/j.ygcen.2009.04.017.View ArticlePubMedGoogle Scholar
- Mendiola D, Yamashita Y, Matsuyama M, Alvarez P, Tanaka M: Scomber japonicus, H. is a better candidate species for juvenile production activities than Scomber scombrus. L. Aqua Res. 2008, 39: 1122-1127. 10.1111/j.1365-2109.2008.01959.x.View ArticleGoogle Scholar
- Shiraishi T, Ohta K, Yamaguchi A, Yoda M, Chuda H, Matsuyama M: Reproductive parameters of the chub mackerel Scomber japonicus estimated from human chorionic gonadotropin induced final oocyte maturation and ovulation in captivity. Fish Sci. 2005, 71: 531-542.View ArticleGoogle Scholar
- Matsuyama M, Shiraishi T, Sundaray JK, Rahman MA, Ohta K, Yamaguchi A: Steroidogenesis in ovarian follicles of chub mackerel, Scomber japonicus. Zool Sci. 2005, 22: 101-110. 10.2108/zsj.22.101.View ArticlePubMedGoogle Scholar
- Nyuji M, Selvaraj S, Kitano H, Ohga H, Yoneda M, Shimizu A, Kaneko K, Yamaguchi A, Matsuyama M: Changes in the expression of pituitary gonadotropin subunits during reproductive cycle of multiple spawning female chub mackerel Scomber japonicus. Fish Physiol Biochem. 2012, 38: 883-897. 10.1007/s10695-011-9576-y.View ArticlePubMedGoogle Scholar
- Shiraishi T, Ketkar SD, Kitano H, Nyuji M, Yamaguchi A, Matsuyama M: Time course of final oocyte maturation and ovulation in chub mackerel Scomber japonicus induced by hCG and GnRHa. Fish Sci. 2008, 74: 764-769. 10.1111/j.1444-2906.2008.01587.x.View ArticleGoogle Scholar
- Selvaraj S, Kitano H, Fujinaga Y, Ohga H, Yoneda M, Yamaguchi A, Shimizu A, Matsuyama M: Molecular characterization, tissue distribution, and mRNA expression profiles of two Kiss genes in the adult male and female chub mackerel (Scomber japonicus) during different gonadal stages. Gen Comp Endocrinol. 2010, 169: 28-38. 10.1016/j.ygcen.2010.07.011.View ArticlePubMedGoogle Scholar
- Fernald RD, White RB: Gonadotropin-releasing hormone genes: phylogeny, structure, and functions. Front Neuroendocrinol. 1999, 20: 224-240. 10.1006/frne.1999.0181.View ArticlePubMedGoogle Scholar
- Selvaraj S, Kitano H, Fujinaga Y, Amano M, Takahashi A, Shimizu A, Yoneda M, Yamaguchi A, Matsuyama M: Immunological characterization and distribution of three GnRH forms in the brain and pituitary gland of chub mackerel (Scomber japonicus). Zool Sci. 2009, 26: 828-839. 10.2108/zsj.26.828.View ArticlePubMedGoogle Scholar
- Selvaraj S, Kitano H, Amano M, Nyuji M, Kaneko K, Yamaguchi A, Matsuyama M: Molecular characterization and expression profiles of three GnRH forms in the brain and pituitary of adult chub mackerel (Scomber japonicus) maintained in captivity. Aquaculture. 2012, 356/35: 200-210.View ArticleGoogle Scholar
- Gothilf Y, Meiri I, Elizur A, Zohar Y: Preovulatory changes in the levels of three gonadotropin-releasing hormone-encoding messenger ribonucleic acids (mRNAs), gonadotropin beta-subunit mRNAs, plasma gonadotropin, and steroids in the female gilthead seabream, Sparus aurata. Biol Reprod. 1997, 57: 1145-1154. 10.1095/biolreprod57.5.1145.View ArticlePubMedGoogle Scholar
- Vermeirssen ELM, Scott AP, Mylonas CC, Zohar Y: Gonadotrophin-releasing hormone agonist stimulates milt fluidity and plasma concentrations of 17,20β-dihydroxylated and 5β-reduced, 3α-hydroxylated C21 steroids in male plaice (Pleuronectes platessa). Gen Comp Endocrinol. 1998, 112: 163-177. 10.1006/gcen.1998.7132.View ArticlePubMedGoogle Scholar
- Scott AP, Witthames PR, Vermeirssen ELM, Carolsfeld J: Prolonged-release gonadotropin-releasing hormone analogue implants enhance oocyte final maturation and ovulation, and increase plasma concentrations of sulphated C21 steroids in North Sea plaice. J Fish Biol. 1999, 55: 316-328.Google Scholar
- Larionov A, Krause A, Miller W: A standard curve based method for relative real time PCR data processing. BMC Bioinformatics. 2005, 62: 1-16.Google Scholar
- Bustin S, Benes V, Garson J, Hellemans J, Huggett J, Kubista M, Mueller R, Nolan T, Pfaffl M, Shipley G, Vandesompele J, Wittwer C: The MIQE guidelines: minimal information for publication of quantitative real-time PCR experiments. Clin Chem. 2009, 55: 611-622. 10.1373/clinchem.2008.112797.View ArticlePubMedGoogle Scholar
- Okuzawa K, Amano M, Kobayashi M, Aida K, Hanyu I, Hasegawa Y, Miyamoto K: Differences in salmon GnRH and chicken GnRH-II contents in discrete brain areas of male and female rainbow trout according to age and stage of maturity. Gen Comp Endocrinol. 1990, 80: 116-126. 10.1016/0016-6480(90)90155-F.View ArticlePubMedGoogle Scholar
- Pham KX, Amano M, Amiya N, Kurita Y, Yamamori K: Distribution of three GnRHs in the brain and pituitary of the wild Japanese flounder Paralichthys olivaceus. Fish Sci. 2006, 72: 89-94. 10.1111/j.1444-2906.2006.01121.x.View ArticleGoogle Scholar
- Yamada H, Amano M, Okuzawa K, Chiba H, Iwata M: Maturational changes in brain contents of salmon GnRH in rainbow trout as measured by a newly developed time-resolved fluoroimmunoassay. Gen Comp Endocrinol. 2002, 126: 136-143. 10.1006/gcen.2002.7791.View ArticlePubMedGoogle Scholar
- Amano M, Yamanome T, Yamada H, Okuzawa K, Yamamori K: Effects of photoperiod on gonadotropin-releasing hormone levels in the brain and pituitary of underyearling male barfin flounder. Fish Sci. 2004, 70: 812-818. 10.1111/j.1444-2906.2004.00874.x.View ArticleGoogle Scholar
- Shiraishi T, Ketkar SD, Katoh Y, Nyuji M, Yamaguchi A, Matsuyama M: Spawning frequency of the Tsushima current subpopulation of chub mackerel Scomber japonicus off Kyushu, Japan. Fish Sci. 2009, 75: 649-655. 10.1007/s12562-009-0094-0.View ArticleGoogle Scholar
- Nyuji M, Shiraishi T, Selvaraj S, In VV, Kitano H, Yamaguchi A, Okamoto K, Onoue S, Shimizu A, Matsuyama M: Immunoreactive changes in pituitary FSH and LH cells during seasonal reproductive and spawning cycles of female chub mackerel Scomber japonicus. Fish Sci. 2011, 77: 731-739. 10.1007/s12562-011-0380-5.View ArticleGoogle Scholar
- Biran J, Ben-Dor S, Levavi-Sivan B: Molecular identification and functional characterization of the kisspeptin/kisspeptin receptor system in lower vertebrates. Biol Reprod. 2008, 79: 776-786. 10.1095/biolreprod.107.066266.View ArticlePubMedGoogle Scholar
- Kitahashi T, Ogawa S, Parhar IS: Cloning and expression of kiss2 in the zebrafish and medaka. Endocrinology. 2009, 150: 821-831.View ArticlePubMedGoogle Scholar
- Md S, Motohashi E, Doi H, Ando H: Elevation of Kiss2 and its receptor gene expression in the brain and pituitary of grass puffer during the spawning season. Gen Comp Endocrinol. 2010, 169: 48-57. 10.1016/j.ygcen.2010.07.008.View ArticleGoogle Scholar
- Zmora N, Stubblefield J, Zulperi Z, Biran J, Levavi-Sivan B, Muñoz-Cueto JA, Zohar Y: Differential and Gonad Stage-Dependent Roles of Kisspeptin1 and Kisspeptin2 in Reproduction in the Modern Teleosts. Morone Species. Biol Reprod. 2012, 86: 177-View ArticlePubMedGoogle Scholar
- Mechaly AS, Viñas J, Piferrer F: Sex-specific changes in the expression of kisspeptin, kisspeptin receptor, gonadotropins and gonadotropin receptors in the Senegalese sole (Solea senegalensis) during a full reproductive cycle. Comp Biochem Physiol Part A. 2012, 162: 364-371. 10.1016/j.cbpa.2012.04.003.View ArticleGoogle Scholar
- Cowan M, Davie A, Migaud H: Photoperiod effects on the expression of kisspeptin and gonadotropin genes in Atlantic cod, Gadus morhua, during first maturation. Comp Biochem Physiol Part A. 2012, 163: 82-94. 10.1016/j.cbpa.2012.05.191.View ArticleGoogle Scholar
- Nocillado JN, Biran J, Lee YY, Levavi-Sivan B, Mechaly AS, Zohar Y, Elizur A: The Kiss2 receptor (Kiss2r) gene in southern bluefin tuna, Thunnus maccoyii and in yellowtail kingfish, Seriola lalandi – functional analysis and isolation of transcript variants. Mol Cell Endocrinol. 362: 211-220.Google Scholar
- Li Q, Roa A, Clarke IJ, Smith JT: Seasonal variation in the gonadotropin-releasing hormone response to kisspeptin in sheep: possible kisspeptin regulation of the kisspeptin receptor. Neuroendocrinology. in pressGoogle Scholar
- Ogawa S, Ng KW, Ramadasan PN, Nathan FM, Parhar IS: Habenular Kiss1 neurons modulate the serotonergic system in the brain of zebrafish. Endocrinology. 2012, 153: 2398-2407. 10.1210/en.2012-1062.View ArticlePubMedGoogle Scholar
- Beck BH, Fuller SA, Peatman E, McEntire ME, Darwish A, Freeman DW: Chronic exogenous kisspeptin administration accelerates gonadal development in basses of the genus Morone. Comp Biochem Physiol Part A. 2012, 162: 265-273. 10.1016/j.cbpa.2012.03.019.View ArticleGoogle Scholar
- Murua H, Saborido-Rey F: Female reproductive strategies of marine fish species of the North Atlantic. J NW Atl Fish Sci. 2003, 33: 23-31.View ArticleGoogle Scholar
- Yamada T, Aoki I, Mitani I: Spawning time, spawning frequency and fecundity of Japanese chub mackerel, Scomber japonicus in the waters around the Izu islands, Japan. Fish Res. 1998, 38: 83-89. 10.1016/S0165-7836(98)00113-1.View ArticleGoogle Scholar
- Garcia-Galiano D, Pinilla L, Tena-Sempere M: Sex steroids and the control of the kiss1 system: developmental roles and major regulatory actions. J Neuroendocrinol. 2012, 24: 22-34. 10.1111/j.1365-2826.2011.02230.x.View ArticlePubMedGoogle Scholar
- Kanda S, Oka Y: Evolutionary insights into the steroid sensitive kiss1 and kiss2 neurons in the vertebrate brain. Front Endocrin. 2012, 3: 28-View ArticleGoogle Scholar
- Kanda S, Akazome Y, Matsunaga T, Yamamoto N, Yamada S, Tsukamura H, Maeda K, Oka Y: Identification of KiSS-1 product kisspeptin and steroid-sensitive sexually dimorphic kisspeptin neurons in medaka (Oryzias latipes). Endocrinology. 2008, 149: 2467-2476. 10.1210/en.2007-1503.View ArticlePubMedGoogle Scholar
- Mitani Y, Kanda S, Akazome Y, Zempo B, Oka Y: Hypothalamic Kiss1 but not Kiss2 neurons are involved in estrogen feedback in medaka (Oryzias latipes). Endocrinology. 2010, 151: 1751-1759. 10.1210/en.2009-1174.View ArticlePubMedGoogle Scholar
- Kanda S, Karigo T, Oka Y: Steroid sensitive kiss2 neurones in the goldfish: evolutionary insights into the duplicate kisspeptin gene-expressing neurones. J Neuroendocrinol. 2012, 24: 897-906. 10.1111/j.1365-2826.2012.02296.x.View ArticlePubMedGoogle Scholar
- Biran J, Palevitch O, Ben-Dor S, Levavi-Sivan B: Neurokinin Bs and neurokinin B receptors in zebrafish-potential role in controlling fish reproduction. PNAS. 2012, 109: 10269-10274. 10.1073/pnas.1119165109.PubMed CentralView ArticlePubMedGoogle Scholar
- Nocillado JN, Levavi-Sivan B, Carrick F, Elizur A: Temporal expression of G-protein-coupled receptor 54 (GPR54), gonadotropin-releasing hormones (GnRH), and dopamine receptor D2 (drd2) in pubertal female grey mullet, Mugil cephalus. Gen Comp Endocrinol. 2007, 150: 278-287. 10.1016/j.ygcen.2006.09.008.View ArticlePubMedGoogle Scholar
- Servili A, Page YL, Leprince J, Caraty A, Escobar S, Parhar IS, Seong JY, Vaudry H, Kah O: Organization of two independent kisspeptin systems derived from evolutionary-ancient kiss genes in the brain of zebrafish. Endocrinology. 2011, 152: 1527-1540. 10.1210/en.2010-0948.View ArticlePubMedGoogle Scholar
- Shimizu Y, Tomikawa J, Hirano K, Nanikawa Y, Akazome Y, Kanda S, Kazeto Y, Okuzawa K, Uenoyama Y, Ohkura S, Tsukamura H, Maeda KI, Gen K, Oka Y, Yamamoto N: Central distribution of kiss2 neurons and peri-pubertal changes in their expression in the brain of male and female red seabream Pagrus major. Gen Comp Endocrinol. 2012, 175: 432-442. 10.1016/j.ygcen.2011.11.038.View ArticlePubMedGoogle Scholar
- Amano M: Reproductive biology of salmoniform and pleuronectiform fishes with special reference to gonadotropin-releasing hormone (GnRH). Aqua-Biosci Monogr. 2010, 3: 39-72. 10.5047/absm.2010.00302.0039.View ArticleGoogle Scholar
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