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1.
Gen Comp Endocrinol ; 239: 71-79, 2016 12 01.
Artigo em Inglês | MEDLINE | ID: mdl-26519761

RESUMO

Testicular receptor 2 (TR2; also known as Nr2c1) is one of the first orphan nuclear receptors identified and known to regulate various physiological process with or without any ligand. In this study, we report the cloning of full length nr2c1 and its expression analysis during gonadal development, seasonal testicular cycle and after human chorionic gonadotropin (hCG) induction. In addition, in situ hybridization (ISH) was performed to localize nr2c1 transcripts in adult testis and whole catfish (1day post hatch). Tissue distribution and gonadal ontogeny studies revealed high expression of nr2c1 in developing and adult testis. Early embryonic stage-wise expression of nr2c1 seems to emphasize its importance in cellular differentiation and development. Substantial expression of nr2c1 during pre-spawning phase and localization of nr2c1 transcripts in sperm/spermatids were observed. Significant upregulation after hCG induction indicate that nr2c1 is under the regulation of gonadotropins. Whole mount ISH analysis displayed nr2c1 expression in notochord indicating its role in normal vertebrate development. Taken together, our findings suggest that nr2c1 may have a plausible role in the testicular and embryonic development of catfish.


Assuntos
Peixes-Gato/genética , Peixes-Gato/metabolismo , Desenvolvimento Embrionário , Membro 1 do Grupo C da Subfamília 2 de Receptores Nucleares/genética , Membro 1 do Grupo C da Subfamília 2 de Receptores Nucleares/metabolismo , Testículo/metabolismo , Animais , Peixes-Gato/embriologia , Gonadotropina Coriônica/farmacologia , Clonagem Molecular , Embrião não Mamífero , Perfilação da Expressão Gênica , Regulação da Expressão Gênica no Desenvolvimento , Humanos , Masculino , Estações do Ano , Distribuição Tecidual
2.
Environ Toxicol Pharmacol ; 37(3): 1006-14, 2014 May.
Artigo em Inglês | MEDLINE | ID: mdl-24742880

RESUMO

Endocrine disrupting chemicals have raised public concern, since their effects have been found to interfere with the physiological systems of various organisms, especially during critical stage of development and reproduction. Endosulfan and malathion, pesticides widely used for agricultural purposes, have been known to disrupt physiological functions in aquatic organisms. The current work analyzes the effects of endosulfan (2.5 parts per billion [ppb]) and malathion (10 ppb) on the reproductive physiology of catfish (Clarias batrachus) by evaluating protein expression profiles after 21 days of exposure. The proteomic profile of testis and ovary after exposure to endosulfan showed downregulation of proteins such as ubiquitin and Esco2, and upregulation in melanocortin-receptor-2 respectively. Malathion exposed ovary showed upregulated prolactin levels. Identification of proteins differentially expressed in gonads due to the exposure to these pesticides may serve as crucial indications to denote their disruptive effects at the level of proteins.


Assuntos
Endossulfano/toxicidade , Proteínas de Peixes/metabolismo , Inseticidas/toxicidade , Malation/toxicidade , Ovário/efeitos dos fármacos , Testículo/efeitos dos fármacos , Animais , Peixes-Gato/metabolismo , Feminino , Masculino , Ovário/metabolismo , Proteômica , Testículo/metabolismo
3.
Ecotoxicol Environ Saf ; 102: 210-9, 2014 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-24468447

RESUMO

Pesticides like malathion have the potential to disrupt development and reproduction of aquatic organisms including fishes. To investigate the likely consequences of malathion exposure at low doses in juvenile catfish, Clarias batrachus, we studied the expression pattern of genes encoding certain transcription factors, activin A, sex steroid or orphan nuclear receptors and steroidogenic enzymes which are known to be involved in gonadal development along with histological changes. To compare further, we also analyzed certain brain specific genes related to gonadal axis. Fifty days post hatch catfish fingerlings were exposed continuously to 1 and 10 µg/L of malathion for 21 days. Results from these experiments indicated that transcript levels of various genes were altered by the treatments, which may further affect the gonadal development either directly or indirectly through brain. Histological analysis revealed slow progression of spermatogenesis in testis, while in ovary, the oil droplet oocytes were found to be higher after treatment (10 µg/L). Our findings revealed that the exposure of malathion, even at low doses, hinder or modulate early gonadal development differentially by targeting gene expression pattern of transcription factors, activin A, sex steroid or orphan nuclear receptors and steroidogenic enzymes with an evidence on histological changes. Further, some of the genes showed differential expression at the level of brain in male and female sex after the exposure of malathion.


Assuntos
Encéfalo/efeitos dos fármacos , Peixes-Gato/fisiologia , Regulação da Expressão Gênica/efeitos dos fármacos , Malation/toxicidade , Ovário/efeitos dos fármacos , Testículo/efeitos dos fármacos , Poluentes Químicos da Água/toxicidade , Animais , Peixes-Gato/genética , Peixes-Gato/metabolismo , Feminino , Masculino , Ovário/crescimento & desenvolvimento , Ovário/metabolismo , Reprodução/efeitos dos fármacos , Testículo/crescimento & desenvolvimento , Testículo/metabolismo , Fatores de Transcrição/genética
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