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1.
J Exp Zool A Ecol Integr Physiol ; 333(9): 619-628, 2020 11.
Article in English | MEDLINE | ID: mdl-32851786

ABSTRACT

This study evaluated the effects of food availability on the transcript levels of genes related to reproduction and growth in the sapphire devil (Chrysiptera cyanea), a tropical damselfish. Nonbreeding fish were reared at high-food (HF) and low-food (LF) levels for 4 weeks under long-days. Vitellogenic oocytes could be observed in the ovaries of the HF group. The quantitative polymerase chain reaction analysis revealed that lhß and cyp19b in the brains, vtg and igf1 in the livers and cyp19a in the ovaries of HF fish were significantly higher than that of LF fish, suggesting that estradiol-17ß (E2) synthesis in the ovary and brain is activated when suitable permissive factors are available to fish. Food limitation lowered hepatic igf1 and dio2, suggesting that the TH-IGF1 signaling system functions in the liver, and that food availability altered hepatic deiodination activities related to intercellular levels of thyroid hormones. Hepatic dio2 significantly decreased when fish were immersed for 3 days in E2-containing seawater; this suggests that E2 impedes the conversion of T4 to T3 in the liver. Our study shows that igf1 was upregulated in accordance with HF-induced vitellogenesis but downregulated by E2 treatment, suggesting that igf1 is bidirectional and altered by maturational status. Once vitellogenesis begins under a suitable range of proximal factors, fish need to maintain their nutritional status because food availability is a permissive factor for their reproduction.


Subject(s)
Food , Perciformes/physiology , Vitellogenesis/physiology , Animal Nutritional Physiological Phenomena , Animals , Brain/metabolism , Estradiol/metabolism , Estradiol/pharmacology , Female , Insulin-Like Growth Factor I/metabolism , Liver/drug effects , Liver/metabolism , Ovary/metabolism , Perciformes/genetics , Perciformes/metabolism , Thyroid Hormones/genetics , Thyroid Hormones/metabolism , Transcriptome , Vitellogenesis/radiation effects
2.
J Photochem Photobiol B ; 183: 57-63, 2018 Jun.
Article in English | MEDLINE | ID: mdl-29684721

ABSTRACT

The negative effects of ambient ultraviolet (UVA) on the water environment have been recently highlighted; UVA can create deleterious effects by stimulating stress on pelagic organisms. Little is known about UVA effects on oocyte characteristics of female fish. In the present study we explored the effects of exposure to ecologically relevant levels of simulated UVA radiation on ovaries of two major strains WT (HdrR) and P53 (-/-) of medaka (Oryzias latipes) mature female. Fish were assigned to control and three UVA-exposed groups as (15 min, 30 min, and 60 min/day) for three days and sample selection was 24 h and 14 days after exposure. Histological alterations and oocyte atresia percentage were analyzed in the UVA-exposed fish compared to control. Alteration comprised hyperthrophied follicular cells with increased thickness, breakdown of egg chorion (zona radiata), damage of cortical alveoli, and distorted nucleus and cytoplasm. The atresia percentages significantly increased with higher UVA exposure dose and time for both the wild type and the p53 deficient fish. The wild type displayed significantly higher oocyte atresia percentage than the p53 mutant. These results suggested that UVA exposure provoked histological alterations in both p53 and WT medaka oocytes leading to follicular atresia, which reduce female reproductive ability and larval production. UVA oocyte response showed p53 dependent and independent histological alteration, however, the p53 mutant was less sensitive to UVA than the wild type in medaka fish.


Subject(s)
Ultraviolet Rays , Vitellogenesis/radiation effects , Animals , Female , Fish Proteins/deficiency , Fish Proteins/genetics , Oocytes/metabolism , Oocytes/radiation effects , Oryzias/genetics , Oryzias/growth & development , Ovary/pathology , Tumor Suppressor Protein p53/deficiency , Tumor Suppressor Protein p53/genetics
3.
Gen Comp Endocrinol ; 221: 86-93, 2015 Sep 15.
Article in English | MEDLINE | ID: mdl-25712829

ABSTRACT

The gonadotropic system and ovarian growth and development were studied during vitellogenesis in female Atlantic salmon subjected to either simulated natural photoperiod and ambient water temperature (NL-amb), or an accelerating photoperiod (short day of LD8:16 from May 10) combined with either warmed (ca 2°C above ambient; 8L-warm) or cooled water (ca 2°C below ambient; 8L-cold) from May to September. Monthly samples were collected from 10 females/group for determination of transcript levels of pituitary gonadotropin subunits (fshb and lhb) and ovarian gonadotropin receptors (fshr and lhr), plasma sex steroids (testosterone: T and estradiol-17ß: E2), gonadosomatic index (GSI) and oocyte size. Short day in combination with either warmed or cooled water induced an earlier increase in pituitary fshb and lhb levels compared with NL-amb controls, and advanced ovarian growth and the seasonal profiles of T, E2. By contrast only minor effects were seen of the photothermal treatments on ovarian fshr and lhr. The 8L-cold had earlier increase in fshb, lhb and E2, but similar oocyte and gonadal growth as 8L-warm, suggesting that the 8L-cold group tried to compensate for the lower water temperature during the period of rapid gonadal growth by increasing fshb and E2 production. Both the 8L-warm and 8L-cold groups showed incomplete ovulation in a proportion of the females, possibly due to the photoperiod advancement resulting in earlier readiness of spawning occurring at a higher ambient temperature, or due to some reproductive dysfunction caused by photothermal interference with normal neuroendocrine regulation of oocyte development and maturation.


Subject(s)
Gonadal Steroid Hormones/blood , Gonadotropins, Pituitary/metabolism , Light , Oocytes/cytology , Ovary/metabolism , Receptors, Gonadotropin/metabolism , Salmo salar/metabolism , Temperature , Vitellogenesis , Animals , Estradiol/blood , Female , Follicle Stimulating Hormone/genetics , Follicle Stimulating Hormone/metabolism , Oocytes/metabolism , Ovary/radiation effects , Ovulation/radiation effects , Pituitary Gland/metabolism , RNA, Messenger/genetics , RNA, Messenger/metabolism , Salmo salar/blood , Salmo salar/genetics , Steroids/blood , Steroids/metabolism , Testosterone/blood , Vitellogenesis/drug effects , Vitellogenesis/radiation effects
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