Ceballos-Gutiérrez Adriana, Rodríguez-Hernández Alejandrina, Álvarez-Valadez María Del Rosario, Limón-Miranda Saraí, Andrade Felipa, Figueroa-Gutiérrez Alejandro, Díaz-Reval Irene, Apolinar-Iribe Alejandro, Castro-Sánchez Luis, Alamilla Javier, Sánchez-Pastor Enrique, Virgen-Ortiz Adolfo
Facultad de Medicina, Universidad de Colima, Colima 28040, Mexico.
Centro Universitario de Investigaciones Biomédicas, Universidad de Colima, Colima 28045, Mexico.
Nanomaterials (Basel). 2021 Sep 7;11(9):2319. doi: 10.3390/nano11092319.
ZnO nanoparticles (ZnONPs) have been shown to have therapeutic potential in some diseases such as diabetes and cancer. However, concentration-dependent adverse effects have also been reported. Studies which evaluate the effects of ZnONPs on the cardiovascular system are scarce. This study aimed to evaluate the cardiovascular effects of a low dose of ZnONPs administered chronically in healthy rats. Changes in dyslipidemia biomarkers, blood pressure, aortic wall structure, vascular contractility, and expression of cannabinoid receptors in the aorta wall were evaluated. Healthy rats were divided into two groups: control or treated (one, two, and three months). The treated rats received an oral dose of 10 mg/kg/day. The results showed that treatment with ZnONPs induced dyslipidemia from the first month, increasing atherosclerosis risk, which was confirmed by presence of atherosclerotic alterations revealed by aorta histological analysis. In in vitro assays, ZnONPs modified the aorta contractile activity in response to the activation of cannabinoid receptors (CB and CB). The expression of CB and CB was modified as well. Moreover, ZnONPs elicited an increase in blood pressure. In conclusion, long-time oral administration of ZnONPs induce dyslipidemia and atherosclerosis eliciting alterations in aorta contractility, CB and CB receptors expression, and an increase in blood pressure in healthy rats.
氧化锌纳米颗粒(ZnONPs)已被证明在某些疾病如糖尿病和癌症中具有治疗潜力。然而,浓度依赖性的不良反应也有报道。评估ZnONPs对心血管系统影响的研究很少。本研究旨在评估长期给予低剂量ZnONPs对健康大鼠心血管系统的影响。评估了血脂异常生物标志物、血压、主动脉壁结构、血管收缩性以及主动脉壁中大麻素受体表达的变化。健康大鼠分为两组:对照组或治疗组(1个月、2个月和3个月)。治疗组大鼠口服剂量为10mg/kg/天。结果表明,从第一个月起,ZnONPs治疗就诱导了血脂异常,增加了动脉粥样硬化风险,主动脉组织学分析显示的动脉粥样硬化改变证实了这一点。在体外试验中,ZnONPs改变了主动脉对大麻素受体(CB1和CB2)激活的收缩活性。CB1和CB2的表达也发生了改变。此外,ZnONPs导致血压升高。总之,长期口服ZnONPs会诱导血脂异常和动脉粥样硬化,引起主动脉收缩性、CB1和CB2受体表达的改变,并导致健康大鼠血压升高。