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Drug Chem Toxicol ; 39(4): 432-8, 2016 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-26864947

RESUMEN

Methamphetamine (METH) is known to damage neurons and induce psychosis. It can also induce apoptosis in seminiferous tubules and affect sperm quality. The present study was carried out to investigate the effect of a rat model of METH addiction on sperm quality and expression of progesterone receptors (PR) and estrogen receptors (ER) in the testis. Sperm quality parameters including sperm motility, sperm morphology and sperm concentration were examined. Protein and gene expressions PR, ERα and ERß were studied using immunohistochemistry and reverse transcriptase-polymerase chain reaction, respectively. The percentages of normal sperm motility and normal sperm morphology were significantly decreased in animals receiving METH, especially in escalating dose (ED METH) and escalating dose-binge (ED-binge METH) groups when compared with control. In addition, sperm concentrations in ED METH and ED-binge METH groups were numerically decreased. PR, ERα and ERß immunoreactive cells were significantly decreased in spermatogonia, spermatogenic cells and especially in Sertoli cells in all METH-treated groups. Furthermore, messenger RNA expression of PR, ERα and ERß were also significantly decreased in all METH-treated animals. These results indicate that METH can induce abnormal sperm quality. These changes of sperm quality may relate to the reduction of PR, ERα and ERß expressions in male germ cells and Sertoli cells which are essential for spermatogenesis and development of sperm.


Asunto(s)
Receptor alfa de Estrógeno/metabolismo , Metanfetamina/toxicidad , Receptores de Progesterona/metabolismo , Espermatozoides/efectos de los fármacos , Testículo/efectos de los fármacos , Trastornos Relacionados con Anfetaminas/metabolismo , Animales , Relación Dosis-Respuesta a Droga , Receptor alfa de Estrógeno/genética , Receptor beta de Estrógeno/genética , Receptor beta de Estrógeno/metabolismo , Expresión Génica/efectos de los fármacos , Inmunohistoquímica , Masculino , Ratas Sprague-Dawley , Receptores de Progesterona/genética , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa , Motilidad Espermática/efectos de los fármacos , Espermatozoides/patología , Testículo/patología
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