Solgi Torab, Amiri Iraj, Asl Sara Soleimani, Saidijam Massoud, Seresht Banafsheh Mirzaei, Artimani Tayebe
Department of Anatomy, School of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran.
Endometrium and Endometriosis Research Center, Hamadan University of Medical Sciences, Hamadan, Iran.
Int J Reprod Biomed. 2021 Aug 16;19(7):589-598. doi: 10.18502/ijrm.v19i7.9465. eCollection 2021 Jul.
Cerium dioxide nanoparticles (CNPs) due to the antidiabetic and antioxidant activities are proposed for the treatment of oxidative stress-associated diseases.
To examine the impact of CNPs on hyperglycemia-induced apoptosis and oxidative stress in the testis of diabetic rats.
Twenty-four male rats were divided into four groups (n = 6/each) as diabetic rats, CNPs group, diabetic + CNPs rats, and controls. The control group was fed only mouse food and water. Rats became diabetic through receiving streptozotocin (STZ) 60 mg/kg. CNPs were given to the rats at a dose of 30 mg/kg daily for 2 wk. Malondialdehyde and total thiol group (TTG) levels were measured using spectrofluorometer. Expression of b-cell lymphoma protein 2-associated X protein () and b-cell lymphoma protein 2 () were investigated using quantitative real-time polymerase chain reaction. Western blot analysis was used to examine caspase 3 protein levels.
The content of malondialdehyde significantly increased in the STZ-diabetic rats, while TTG levels demonstrated a remarkable decrease. Caspase-3, , and / mRNA ratio raised significantly in the STZ-diabetic rats. On the other hand, mRNA levels reduced in the testis of diabetic rats (p = 0.006). Intervention with CNPs caused a substantial increase in the TTG levels, while the malondialdehyde contents, caspase-3, levels, as well as mRNA ratio were considerably decreased following CNPs treatment. Administration of CNPs increased mRNA levels of (p 0.0001).
CNPs treatment attenuates testicular apoptosis and oxidative stress induced by diabetes. This nanoparticle might be suggested for the treatment of diabetes-associated reproductive disorders.
由于二氧化铈纳米颗粒(CNPs)具有抗糖尿病和抗氧化活性,因此被提议用于治疗与氧化应激相关的疾病。
研究CNPs对糖尿病大鼠睾丸中高血糖诱导的细胞凋亡和氧化应激的影响。
将24只雄性大鼠分为四组(每组n = 6),即糖尿病大鼠组、CNPs组、糖尿病 + CNPs大鼠组和对照组。对照组仅给予鼠粮和水。通过腹腔注射链脲佐菌素(STZ)60 mg/kg使大鼠患糖尿病。以30 mg/kg的剂量每日给大鼠灌胃CNPs,持续2周。使用荧光分光光度计测量丙二醛和总巯基(TTG)水平。采用定量实时聚合酶链反应研究b细胞淋巴瘤蛋白2相关X蛋白()和b细胞淋巴瘤蛋白2()的表达。使用蛋白质免疫印迹分析检测半胱天冬酶3蛋白水平。
STZ诱导的糖尿病大鼠丙二醛含量显著增加,而TTG水平显著降低。STZ诱导的糖尿病大鼠中半胱天冬酶-3、和/ mRNA比值显著升高。另一方面,糖尿病大鼠睾丸中的mRNA水平降低(p = 0.006)。CNPs干预导致TTG水平大幅增加,而CNPs处理后丙二醛含量、半胱天冬酶-3、水平以及mRNA比值均显著降低。给予CNPs可使的mRNA水平升高(p 0.0001)。
CNPs治疗可减轻糖尿病诱导的睾丸细胞凋亡和氧化应激。这种纳米颗粒可能对治疗糖尿病相关的生殖系统疾病有帮助。