TY - JOUR
T1 - Functional analysis of kisspeptin peptides in adult immature chub mackerel (Scomber japonicus) using an intracerebroventricular administration method
AU - Ohga, Hirofumi
AU - Selvaraj, Sethu
AU - Adachi, Hayato
AU - Imanaga, Yui
AU - Nyuji, Mitsuo
AU - Yamaguchi, Akihiko
AU - Matsuyama, Michiya
N1 - Funding Information:
We are also grateful to Sanny David Lumayno, Naoki Sugihara, Shugo Igarashi, Ryoko Kodama, and Kayo Yashiki for their assistance during fish sampling. This work was supported by a grant for scientific research ( 23658163 ) from the Ministry of Education, Culture, Sports, Science, and Technology (MEXT) , and through 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.
PY - 2014/2/21
Y1 - 2014/2/21
N2 - In vertebrates (including teleosts), the pivotal hierarchical factor in the control of gonadotropin secretion is the hypothalamic gonadotropin-releasing hormone (GnRH) decapeptide, which regulates the release of pituitary follicle-stimulating hormone (FSH) and luteinizing hormone (LH). Recently, kisspeptins encoded by the Kiss1 gene have been shown to act as upstream endogenous regulators of GnRH neurons in mammals. The chub mackerel (Scomber japonicus) brain expresses two kiss genes (kiss1 and kiss2) that show sexually dimorphic expression profiles during the seasonal gonadal cycle. In the present study, we evaluated the biological potency of kisspeptin peptides to induce transcriptional changes in gnrh1 (hypophysiotropic GnRH form in this species), fshβ and lhβ during the immature stage of adult chub mackerel (2+ years old). Synthetic Kiss1 pentadecapeptide (Kiss1-15) or Kiss2 dodecapeptide (Kiss2-12) at a dose of 100. ng were administered into the intracerebroventricular (ICV) region, and brains were sampled at 6 and 12. h post-injection. In female fish, gnrh1 levels decreased in the presence of both kisspeptin peptides at 12. h post-injection. No significant variation was observed in male fish. In contrast, ICV administration of Kiss2-12 (but not Kiss1-15) significantly increased fshβ and lhβ mRNAs at 12. h post-injection compared to a saline injected control in both sexes. These results suggested that synthetic Kiss2-12 could induce transcriptional changes in gnrh1 and gths.
AB - In vertebrates (including teleosts), the pivotal hierarchical factor in the control of gonadotropin secretion is the hypothalamic gonadotropin-releasing hormone (GnRH) decapeptide, which regulates the release of pituitary follicle-stimulating hormone (FSH) and luteinizing hormone (LH). Recently, kisspeptins encoded by the Kiss1 gene have been shown to act as upstream endogenous regulators of GnRH neurons in mammals. The chub mackerel (Scomber japonicus) brain expresses two kiss genes (kiss1 and kiss2) that show sexually dimorphic expression profiles during the seasonal gonadal cycle. In the present study, we evaluated the biological potency of kisspeptin peptides to induce transcriptional changes in gnrh1 (hypophysiotropic GnRH form in this species), fshβ and lhβ during the immature stage of adult chub mackerel (2+ years old). Synthetic Kiss1 pentadecapeptide (Kiss1-15) or Kiss2 dodecapeptide (Kiss2-12) at a dose of 100. ng were administered into the intracerebroventricular (ICV) region, and brains were sampled at 6 and 12. h post-injection. In female fish, gnrh1 levels decreased in the presence of both kisspeptin peptides at 12. h post-injection. No significant variation was observed in male fish. In contrast, ICV administration of Kiss2-12 (but not Kiss1-15) significantly increased fshβ and lhβ mRNAs at 12. h post-injection compared to a saline injected control in both sexes. These results suggested that synthetic Kiss2-12 could induce transcriptional changes in gnrh1 and gths.
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U2 - 10.1016/j.neulet.2013.12.072
DO - 10.1016/j.neulet.2013.12.072
M3 - Article
C2 - 24412259
AN - SCOPUS:84892841967
SN - 0304-3940
VL - 561
SP - 203
EP - 207
JO - Neuroscience Letters
JF - Neuroscience Letters
ER -