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1.
Biomed Res Int ; 2015: 153573, 2015.
Artículo en Inglés | MEDLINE | ID: mdl-26581756

RESUMEN

The present study investigated the impact of zinc oxide nanoparticles (ZnONPs) on the oxidative status and sperm characteristics in diabetic rat testicular tissue. Forty male albino rats were used in this study; 10 of them served as a control and 30 rats were injected with a single dose (100 mg/kg) of streptozotocin intraperitoneally. They were subdivided into diabetic, diabetic + ZnONPs (10 mg/kg B.W.), and diabetic and cotreated with ZnONPs + insulin groups. The sperm count and motility were assessed. The activity and mRNA expression of superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPx), glutathione reductase (GRD), and Glutathion-S-Transferase (GST) were determined in the testicular tissue. Malondialdehyde (MDA) and reduced glutathione (GSH) levels were estimated in the testicular tissue. Sperm count and motility increased in ZnONPs treated diabetic rats. A significant increase in the activity and mRNA expression of SOD, CAT, GPx, GRD, and GST was shown in ZnONPs treated diabetic rats. MDA significantly decreased, while GSH increased in testicular tissue of ZnONPs treated diabetic rats. It was concluded that ZnONPs either alone or in combination with insulin have the ability to increase the sperm count and motility and protect the testicular tissue against the oxidative stress induced by diabetes in rats.


Asunto(s)
Antioxidantes/metabolismo , Diabetes Mellitus Experimental/metabolismo , Espermatozoides/metabolismo , Testículo/metabolismo , Animales , Catalasa/metabolismo , Diabetes Mellitus Experimental/enzimología , Diabetes Mellitus Experimental/patología , Glutatión Peroxidasa/metabolismo , Glutatión Reductasa/metabolismo , Glutatión Transferasa/metabolismo , Humanos , Peroxidación de Lípido/efectos de los fármacos , Hígado/efectos de los fármacos , Hígado/enzimología , Masculino , Nanopartículas/administración & dosificación , Nanopartículas/química , Estrés Oxidativo/efectos de los fármacos , Ratas , Espermatozoides/efectos de los fármacos , Espermatozoides/patología , Superóxido Dismutasa/metabolismo , Testículo/efectos de los fármacos , Testículo/patología , Óxido de Zinc/administración & dosificación , Óxido de Zinc/química
2.
Asian Pac J Cancer Prev ; 16(1): 103-8, 2015.
Artículo en Inglés | MEDLINE | ID: mdl-25640336

RESUMEN

Curcumin is widely used as a traditional medicine. This work was aimed to investigate its possible protective effect against chemically induced hepatocellular carcinoma (HCC) in rats. Fifty male albino rats were divided into five groups (n=10, each). The control group received a single dose of normal saline, the diethylnitrosamine (DENA) group received a single intra-peritoneal dose at 200mg/kg body weight, and the 3rd, 4th and 5th groups were given DENA and daily administrated curcunine (CUR) via intra-gastric intubation in doses of 300,200 and 100 mg/kg b.wt. respectively for 20 weeks. Serum, and liver samples were used for determination of alpha feto-protein (AFP), interleukin-2 (IL-2), interleukine-6 (IL-6), serum liver enzymes (AST, ALT, ALP and GGT) levels as well the activities and gene expression of glutathione peroxidise (GPx), glutathione reductase (GR), catalase (CAT) and super oxide dismutase (SOD). Curcumin significantly lowered the serum levels of AFP, IL-2 and IL-6, ALT, ALT, and malondialdehyde (MDA) as well gene expression of IL-2 and IL-6. In contrast it increased the gene expression and activities of Gpx, GRD, CAT and SOD. The protective effect of CUR against DEN-induced hepatocarcinogenesis in albino rats was proven.


Asunto(s)
Antioxidantes/uso terapéutico , Carcinoma Hepatocelular/prevención & control , Enfermedad Hepática Inducida por Sustancias y Drogas/tratamiento farmacológico , Curcumina/uso terapéutico , Neoplasias Hepáticas/prevención & control , Animales , Carcinoma Hepatocelular/inducido químicamente , Carcinoma Hepatocelular/tratamiento farmacológico , Catalasa/biosíntesis , Enfermedad Hepática Inducida por Sustancias y Drogas/prevención & control , Dietilnitrosamina/toxicidad , Glutatión Peroxidasa/biosíntesis , Glutatión Reductasa/biosíntesis , Interleucina-2/sangre , Interleucina-6/sangre , Hígado/efectos de los fármacos , Hígado/enzimología , Neoplasias Hepáticas/inducido químicamente , Neoplasias Hepáticas/tratamiento farmacológico , Masculino , Malondialdehído/sangre , Ratas , Superóxido Dismutasa/biosíntesis , alfa-Fetoproteínas/metabolismo
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