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1.
J Comp Physiol B ; 190(1): 49-62, 2020 01.
Artigo em Inglês | MEDLINE | ID: mdl-31858229

RESUMO

Nonapeptides and their receptors regulate a diverse range of physiological processes. We assessed the contractile responsiveness of uteri from the squamate viviparous-oviparous species pair, Pseudemoia entrecasteauxii and Lampropholis guichenoti, as well as the bimodally reproductive species, Saiphos equalis, to arginine vasopressin (AVP). We assessed the resulting uterine contractility as a function of pregnancy status, species and parity mode. We also measured mRNA abundance for the nonapeptide receptor, oxytocin receptor (oxtr), in uteri from P. entrecasteauxii and L. guichenoti and compared expression across pregnancy status and parity mode. We found that pregnant uteri exhibited a significantly greater contractile response to AVP than non-pregnant uteri in all three lizard species studied. Cross-species comparisons revealed that uteri from viviparous P. entrecasteauxii were significantly more responsive to AVP than uteri from oviparous L. guichenoti during both pregnant and non-pregnant states. Conversely, for non-pregnant S. equalis, uteri from viviparous individuals were significantly less responsive to AVP than uteri from oviparous individuals, while during pregnancy, there was no difference in AVP contractile responsiveness. There was no difference in expression of oxtr between L. guichenoti and P. entrecasteauxii, or between pregnant and non-pregnant individuals within each species. We found no significant correlation between oxtr expression and AVP contractile responsiveness. These findings indicate that there are differences in nonapeptide signalling across parity mode and suggest that in these lizards, labour may be triggered either by an increase in plasma nonapeptide concentration, or by an increase in expression of a different nonapeptide receptor from the vasopressin-like receptor family.


Assuntos
Arginina Vasopressina/farmacologia , Lagartos/fisiologia , Oviparidade/fisiologia , Contração Uterina/efeitos dos fármacos , Viviparidade não Mamífera/fisiologia , Sequência de Aminoácidos , Animais , Feminino , Lagartos/embriologia , Lagartos/genética , Lagartos/metabolismo , Oviparidade/efeitos dos fármacos , Ocitocina/metabolismo , Gravidez , Receptores de Ocitocina/genética , Receptores de Ocitocina/metabolismo , Reprodução/efeitos dos fármacos , Homologia de Sequência , Viviparidade não Mamífera/efeitos dos fármacos
2.
Mar Environ Res ; 113: 80-7, 2016 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-26613261

RESUMO

Pregnant eelpout were exposed via the water to known endocrine disrupting compounds (EDCs) to clarify if EDCs could be causing the increased eelpout fry malformation frequencies observed in coastal areas receiving high anthropogenic input. The presence of a teratogenic window for estrogen-induced malformations was also investigated by starting the exposure at different times during eelpout pregnancy. Both 17α-ethinylestradiol (EE2) (17.8 ng/L) and pyrene (0.5 µg/L) significantly increased fry malformation frequency whereas 4-t-octylphenol (4-t-OP) up to 14.3 µg/L did not. Vitellogenin was significantly induced by EE2 (5.7 and 17.8 ng/L) but not by 4-t-OP and pyrene. A critical period for estrogen-induced fry malformations was identified and closed between 14 and 22 days post fertilization (dpf). Exposure to 17ß-estradiol (E2) between 0 and 14 dpf caused severe malformations and severity increased the closer exposure start was to fertilization, whereas malformations were absent by exposure starting later than 14 dpf. Data on ovarian fluid volume and larval length supported the suggested teratogenic window. Larval mortality also increased when exposure started right after fertilization.


Assuntos
Embrião não Mamífero/efeitos dos fármacos , Etinilestradiol/toxicidade , Perciformes/anormalidades , Perciformes/embriologia , Fenóis/toxicidade , Anormalidades Múltiplas/induzido quimicamente , Anormalidades Múltiplas/veterinária , Animais , Relação Dose-Resposta a Droga , Desenvolvimento Embrionário , Congêneres do Estradiol , Feminino , Doenças dos Peixes/induzido quimicamente , Larva/efeitos dos fármacos , Projetos Piloto , Viviparidade não Mamífera/efeitos dos fármacos , Poluentes Químicos da Água/toxicidade
3.
Environ Sci Technol ; 48(24): 14668-76, 2014 Dec 16.
Artigo em Inglês | MEDLINE | ID: mdl-25380199

RESUMO

Elevated frequencies of malformations among the offspring of Baltic eelpout (Zoarces viviparus) have been observed in aquatic environments receiving high anthropogenic input suggesting that manmade chemicals could be the causative agent. However, causal links between exposure to chemicals and abnormal development have never been confirmed in laboratory experiments. The purpose of this study was to investigate if exposure to 17ß-estradiol (E2) causes abnormal development in larvae of the viviparous eelpout. Wild female eelpout were collected immediately after fertilization and exposed to E2 concentrations ranging from 5.7 to 133 ng L(-1) for 6 weeks in a flow through test system. The experiment shows that E2 concentrations of 53.6 and 133 ng L(-1) cause severe abnormal development among eelpout embryos. Reduced amount of ovarian fluid and increased weight of the ovarian sac indicate disturbance of ovarian function. Female plasma concentrations of E2 and vitellogenin increase in a monotonic concentration-response relationship with significant induction in the low concentration range. Our findings support the plausibility that the abnormal development among eelpout embryos encountered in monitoring programs may actually be caused by exposure to chemicals in the environment.


Assuntos
Embrião não Mamífero/efeitos dos fármacos , Estradiol/toxicidade , Perciformes/embriologia , Poluentes Químicos da Água/toxicidade , Anormalidades Múltiplas/induzido quimicamente , Anormalidades Múltiplas/veterinária , Animais , Relação Dose-Resposta a Droga , Estradiol/análise , Estradiol/sangue , Feminino , Doenças dos Peixes/induzido quimicamente , Larva/efeitos dos fármacos , Mortalidade , Vitelogeninas/sangue , Viviparidade não Mamífera/efeitos dos fármacos , Poluentes Químicos da Água/análise , Poluentes Químicos da Água/sangue
4.
J Exp Zool B Mol Dev Evol ; 318(2): 148-58, 2012 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-22532476

RESUMO

Structural and functional changes to the uterus associated with maintenance of pregnancy are controlled primarily by steroid hormones such as progesterone. We tested the hypothesis that progesterone regulates uterine structural changes during pregnancy in the viviparous skink, Pseudemoia entrecasteauxii, by treating pregnant females with the progesterone receptor antagonist mifepristone at different stages of pregnancy. Expression and distribution of progesterone receptor was determined using Western blot and immunohistochemistry. During early pregnancy, mifepristone treatment resulted in altered uterine epithelial cell surface morphology and high embryo mortality, but did not affect females at mid and late stages of pregnancy. Females treated with mifepristone in early pregnancy exhibited abnormal uterine epithelial cell morphology such as lateral blebbing and presence of wide gaps between cells indicating loss of intercellular attachment. Chorioallantoic membranes of the embryo were not affected by mifepristone treatment. Two isoforms (55 kDa and 100 kDa) of progesterone receptor were identified using immunoblots and both isoforms were localized to the nucleus of uterine epithelial cells. The 55 kDa isoform was expressed throughout pregnancy, whereas the 100 kDa isoform was expressed during mid and especially late pregnancy. In P. entrecasteauxii, mifepristone may prevent successful embryo attachment in early pregnancy through its effects on uterine epithelial cells but may have little effect on pregnancy once the maternal-embryo structural relationship is established.


Assuntos
Embrião não Mamífero/efeitos dos fármacos , Antagonistas de Hormônios/farmacologia , Lagartos , Mifepristona/farmacologia , Receptores de Progesterona/metabolismo , Útero/efeitos dos fármacos , Viviparidade não Mamífera , Animais , Western Blotting , Eletroforese em Gel de Poliacrilamida , Embrião não Mamífero/anatomia & histologia , Embrião não Mamífero/metabolismo , Feminino , Imuno-Histoquímica , Lagartos/anatomia & histologia , Lagartos/fisiologia , Microscopia Eletrônica de Varredura , Útero/anatomia & histologia , Útero/metabolismo , Viviparidade não Mamífera/efeitos dos fármacos , Viviparidade não Mamífera/fisiologia
5.
Ecology ; 91(5): 1494-505, 2010 May.
Artigo em Inglês | MEDLINE | ID: mdl-20503881

RESUMO

Life-history traits are very sensitive to extreme environmental conditions, because resources that need to be invested in somatic maintenance cannot be invested in reproduction. Here we examined female life-history traits in the Mexican livebearing fish Poecilia mexicana from a variety of benign surface habitats, a creek with naturally occurring toxic hydrogen sulfide (H2S), a sulfidic cave, and a non-sulfidic cave. Previous studies revealed pronounced genetic and morphological divergence over very small geographic scales in this system despite the absence of physical barriers, suggesting that local adaptation to different combinations of two selection factors, toxicity (H2S) and darkness, is accompanied by very low rates of gene flow. Hence, we investigated life-history divergence between these populations in response to the selective pressures of darkness and/or toxicity. Our main results show that toxicity and darkness both select for (or impose constraints on) the same female trait dynamics: reduced fecundity and increased offspring size. Since reduced fecundity in the sulfur cave population was previously shown to be heritable, we discuss how divergent life-history evolution may promote further ecological divergence: for example, reduced fecundity and increased offspring autonomy are clearly beneficial in extreme environments, but fish with these traits are outcompeted in benign habitats.


Assuntos
Adaptação Fisiológica , Escuridão , Fenômenos Geológicos , Sulfeto de Hidrogênio/toxicidade , Poecilia/fisiologia , Viviparidade não Mamífera/fisiologia , Tecido Adiposo , Animais , Ecossistema , Feminino , Masculino , Reprodução/efeitos dos fármacos , Reprodução/fisiologia , Viviparidade não Mamífera/efeitos dos fármacos
6.
Horm Behav ; 51(3): 379-86, 2007 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-17274995

RESUMO

Although multiple condition dependence in dispersal is common, the proximate mechanisms that integrate information from multiple sources remain largely unknown. In the common lizard (Lacerta vivipara), earlier studies have shown that maternal plasma corticosterone level interacts with maternal phenotype to affect offspring phenotype and dispersal strategy, and may reflect the mother's external and/or internal environment. However, the mechanism by which these two types of environmental information are integrated has not been identified. We explored the possibility that the timing and duration of the corticosterone signal are the key factors by which the message is modulated. We found that the timing of corticosterone exposure affects the juvenile phenotype: an exposure to corticosterone early in development has negative effects on juvenile size, weight, and body condition, that can nevertheless be restored in the case of a prolonged exposure. The duration of corticosterone exposure affects the dispersal strategy, although the precise effect depends on the sex ratio of the clutch. That is, in female-biased clutches, a prolonged exposure during gestation promotes philopatry of juveniles, while a short exposure enhances their dispersal, a result that is consistent with kin competition theory. Therefore, our results demonstrate that while corticosterone titer may signal a mother's external and/or internal environment to her developing young, differences in the timing and duration of this endocrine signal produce offspring with specialized phenotypes that exhibit different dispersal strategies.


Assuntos
Migração Animal/efeitos dos fármacos , Corticosterona/farmacologia , Tamanho da Ninhada de Vivíparos/efeitos dos fármacos , Lagartos , Viviparidade não Mamífera/efeitos dos fármacos , Animais , Animais Recém-Nascidos , Peso Corporal/efeitos dos fármacos , Ecossistema , Feminino , Masculino , Mães , Análise de Sobrevida , Fatores de Tempo
7.
J Comp Physiol B ; 176(8): 783-92, 2006 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-16832686

RESUMO

The southern snow skink Niveoscincus microlepidotus is a viviparous alpine lizard with biennial reproduction, in which embryos are fully developed before winter but parturition is delayed until spring. We aimed to determine whether, in this species, in vitro uterine preparations are responsive to arginine vasotocin (AVT) and prostaglandin (PGF(2alpha)) in autumn and spring, and whether pre-treatment with the beta-adrenergic agonist isoproterenol decreases the effectiveness of AVT in stimulating uterine contractions. Using the spotted snow skink (Niveoscincus ocellatus), an annually breeding species, we aimed to determine influences of temperature and the beta-adrenergic system upon the response to AVT in vivo. In both N. microlepidotus and N. ocellatus females are more responsive to AVT than to PGF(2alpha), and that the response to AVT is decreased, but not prevented, by beta-adrenergic stimulation. In N. microlepidotus, uteri are equally responsive in both seasons to the hormones administered. In N. ocellatus environmental conditions, specifically, temperature, modulate the response to AVT in vivo with the time to parturition increasing as temperature decreases. We conclude that in these viviparous squamates the endocrine cascade leading to parturition is modulated by the beta-adrenergic system, and that this may reflect the mechanism by which the timing of parturition is tied to suitable environmental conditions.


Assuntos
Agonistas Adrenérgicos beta/farmacologia , Isoproterenol/farmacologia , Lagartos/fisiologia , Ocitócicos/farmacologia , Vasotocina/farmacologia , Viviparidade não Mamífera/efeitos dos fármacos , Animais , Dinoprosta/farmacologia , Feminino , Técnicas In Vitro , Temperatura , Contração Uterina/efeitos dos fármacos , Útero/efeitos dos fármacos , Útero/fisiologia
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