Antiapoptotic and antioxidative effects of cerium oxide nanoparticles on the testicular tissues of streptozotocin-induced diabetic rats: An experimental study

Publish Year: 1400
نوع سند: مقاله ژورنالی
زبان: English
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JR_IJRM-19-7_001

تاریخ نمایه سازی: 2 شهریور 1400

Abstract:

Background: Cerium dioxide nanoparticles (CNPs) due to the antidiabetic and antioxidant activities are proposed for the treatment of oxidative stress-associated diseases. Objective: To examine the impact of CNPs on hyperglycemia-induced apoptosis and oxidative stress in the testis of diabetic rats. Materials and Methods: Twenty-four male rats were divided into four groups (n = ۶/each) as diabetic rats, CNPs group, diabetic + CNPs rats, and controls. The control group was fed only with mouse food and water. Rats became diabetic through receiving streptozotocin (STZ) ۶۰ mg/kg. CNPs were given to the rats at a dose of ۳۰ mg/kg daily for two weeks. Malondialdehyde and total thiol group (TTG) levels were measured using spectrofluorometer. Expression of b-cell lymphoma protein ۲-associated X protein (BAX) and b-cell lymphoma protein ۲ (Bcl-۲) were investigated using quantitative real-time polymerase chain reaction. Western blot analysis was used to examine caspase ۳ protein levels. Results: The content of malondialdehyde significantly increased in the STZ-diabetic rats, while TTG levels demonstrated a remarkable decrease. Caspase-۳, BAX, and BAX/Bcl-۲ mRNA ratio raised significantly in the STZ-diabetic rats. On the other hand, Bcl-۲ mRNA levels reduced in the testis of diabetic rats (p = ۰.۰۰۶). Intervention with CNPs caused a substantial increase in the TTG levels, while the malondialdehyde contents, caspase-۳, BAX levels, as well as BAX/Bcl-۲ mRNA ratio were considerably decreased following CNPs treatment. Administration of CNPs increased mRNA levels of Bcl-۲ (p < ۰.۰۰۰۱). Conclusion: CNPs treatment attenuates testicular apoptosis and oxidative stress induced by diabetes. This nanoparticle might be suggested for the treatment of diabetes-associated reproductive disorders.

Authors

Torab solgi

Department of Anatomy, School of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran.

Iraj Amiri

Endometrium and Endometriosis Research Center, Hamadan University of Medical Sciences, Hamadan, Iran.

Sara Soleimani Asl

Endometrium and Endometriosis Research Center, Hamadan University of Medical Sciences, Hamadan, Iran.

Massoud Saidijam

Research Center for Molecular Medicine, Hamadan University of Medical Sciences, Hamadan, Iran.

Banafsheh Mirzaei seresht

Endometrium and Endometriosis Research Center, Hamadan University of Medical Sciences, Hamadan, Iran.

Tayebe Artimani

Endometrium and Endometriosis Research Center, Hamadan University of Medical Sciences, Hamadan, Iran.

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