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1.
Reprod Domest Anim ; 58(9): 1214-1224, 2023 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-37386932

RESUMEN

The incidence of male fertility disorders has increased greatly due to various genetic and lifestyle factors. Recently, it has been hypothesized that vitamin D may be involved with idiopathic infertility. The goal of the study was to determine the effect and relationship between blood vitamin D metabolites, intracellular sperm vitamin D levels, and gene expression of 1-α-hydroxylase and VDR, with regard to semen quality. Seventy volunteers aged 25-45 were involved in the study. According to spermogram analysis, participants were stratified into normozoospermic control group, non-normozoospermic target group, and oligoasthenoteratozoospermic group. Vitamin D metabolites (total 25-hydroxycholecalciferol, 1,25-dihydroxycholecalciferol) in blood and spermatozoa were determined by ELISA. Free and bioavailable 25-hydroxycholecalciferol were calculated using the Vermeulen equation. mRNA expression of VDR and 1-α hydroxylase was evaluated by qPCR. Free and bioavailable 25-hydroxycholecalciferol were significantly higher in the control group compared to the target group and compared to the oligoasthenoteratozoospermic group . Intracellular sperm 1,25-dihydroxycholecalciferol was higher in the control group compared to the target group. The mRNA levels of 1- α-hydroxylase were significantly higher in the control samples, while VDR expression was significantly higher in the target group. Significant positive correlations were established between free and bioavailable 25-hydroxycholecalciferol with sperm motility and morphology. Vitamin D metabolites in blood and intracellular sperm 1,25-dihydroxycholecalciferol seem to exert beneficial effects on sperm motility and morphology. Regarding sperm quality, these effects are more pronounced in the free and bioavailable 25OHD compared to the total 25OHD in blood. Higher expression of 1-α-hydroxylase likely leads to higher intracellular levels of 1,25-dihydroxycholecalciferol, which could contribute to sperm motility and morphology. Higher VDR expression may be a compensatory mechanism related to lower intracellular sperm 1,25-dihydroxycholecalciferol.


Asunto(s)
Calcitriol , Receptores de Calcitriol , Masculino , Animales , Receptores de Calcitriol/genética , Receptores de Calcitriol/metabolismo , Calcitriol/metabolismo , Calcifediol/metabolismo , Análisis de Semen/veterinaria , Motilidad Espermática , Semen/metabolismo , Vitamina D/metabolismo , Espermatozoides , ARN Mensajero/metabolismo , Expresión Génica , Oxigenasas de Función Mixta/genética , Oxigenasas de Función Mixta/metabolismo
2.
Arch Physiol Biochem ; 127(4): 327-336, 2021 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-31291758

RESUMEN

CONTEXT: Sulphurous mineral waters (SMW) have a wide range of applications. Sulphur content of mineral waters is considered as possible determinant for their anti-inflammatory or pro-inflammatory effects. OBJECTIVE: To explore the healing properties of Varna basin mineral water by analysing possible antioxidative and anti-inflammatory effects. MATERIALS AND METHODS: An intervention with Varna SMW intake was performed with healthy volunteers. Total thiols, total glutathione and its fractions, reactive oxygen metabolites, malondialdehyde, intracellular adhesion molecule (ICAM-1) and vascular cell adhesion molecule (VCAM-1) were measured. Expression of γ-gluthamyl-cysteinyl ligase (GCL) and sICAM-1 genes was also analysed. RESULTS: A significantly increased total glutathione and total thiols were observed at the end of the intervention. GCL and sICAM-1 gene expressions were increased after the intervention. CONCLUSION: SMW consumption improved redox status of the body. We suggested that these beneficial effects may be attributed to the established high levels of sulphur-containing compounds in Varna mineral water.


Asunto(s)
Biomarcadores/análisis , Regulación de la Expresión Génica/efectos de los fármacos , Inflamación/prevención & control , Aguas Minerales/administración & dosificación , Estrés Oxidativo/efectos de los fármacos , Azufre/farmacología , Adulto , Anciano , Antiinflamatorios/farmacología , Antioxidantes/farmacología , Femenino , Voluntarios Sanos , Humanos , Inflamación/patología , Molécula 1 de Adhesión Intercelular/genética , Molécula 1 de Adhesión Intercelular/metabolismo , Masculino , Persona de Mediana Edad , Encuestas y Cuestionarios , Factores de Transcripción/genética , Factores de Transcripción/metabolismo , Molécula 1 de Adhesión Celular Vascular/genética , Molécula 1 de Adhesión Celular Vascular/metabolismo
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