Zinc Oxide Nanoparticles Induce an Adverse Effect on Blood Glucose Levels Depending On the Dose and Route of Administration in Healthy and Diabetic Rats
Adolfo Virgen-Ortiz,
Alejandro Apolinar-Iribe,
Irene Díaz-Reval,
Hortensia Parra-Delgado,
Saraí Limón-Miranda,
Enrique Alejandro Sánchez-Pastor,
Luis Castro-Sánchez,
Santos Jesús Castillo,
Adan Dagnino-Acosta,
Edgar Bonales-Alatorre,
Alejandrina Rodríguez-Hernández
Affiliations
Adolfo Virgen-Ortiz
Centro Universitario de Investigaciones Biomédicas, Universidad de Colima, Colima C.P. 28045, Mexico
Alejandro Apolinar-Iribe
Departamento de Física, Universidad de Sonora, A.P. 1626, Hermosillo, Sonora C.P. 83000, Mexico
Irene Díaz-Reval
Centro Universitario de Investigaciones Biomédicas, Universidad de Colima, Colima C.P. 28045, Mexico
Hortensia Parra-Delgado
Facultad de Ciencias Químicas, Universidad de Colima, Coquimatlán, Colima C.P. 28400, Mexico
Saraí Limón-Miranda
Departamento de Ciencias Químico Biológicas y Agropecuarias, URS, Universidad de Sonora, Navojoa, Sonora C.P. 85880, Mexico
Enrique Alejandro Sánchez-Pastor
Centro Universitario de Investigaciones Biomédicas, Universidad de Colima, Colima C.P. 28045, Mexico
Luis Castro-Sánchez
Centro Universitario de Investigaciones Biomédicas, CONACYT-Universidad de Colima, Universidad de Colima, Colima C.P. 28045, Mexico
Santos Jesús Castillo
Departamento de Investigación en Física, A.P. 5-088, Hermosillo, Sonora C.P. 83000, Mexico
Adan Dagnino-Acosta
Centro Universitario de Investigaciones Biomédicas, CONACYT-Universidad de Colima, Universidad de Colima, Colima C.P. 28045, Mexico
Edgar Bonales-Alatorre
Centro Universitario de Investigaciones Biomédicas, Universidad de Colima, Colima C.P. 28045, Mexico
Alejandrina Rodríguez-Hernández
Facultad de Medicina, Universidad de Colima, Colima C.P. 28040, Mexico
Different studies in experimental diabetes models suggest that zinc oxide nanoparticles (ZnONPs) are useful as antidiabetic agents. However, this evidence was performed and measured in long-term treatments and with repeated doses of ZnONPs. This work aimed to evaluate the ZnONPs acute effects on glycemia during the next six h after an oral or intraperitoneal administration of the treatment in healthy and diabetic rats. In this study, the streptozotocin-nicotinamide intraperitoneal administration in male Wistar rats were used as a diabetes model. 10 mg/kg ZnONPs did not modify the baseline glucose in any group. Nevertheless, the ZnONPs short-term administration (100 mg/kg) induced a hyperglycemic response in a dose and route-dependent administration in healthy (130 ± 2 and 165 ± 10 mg/dL with oral and intraperitoneal, respectively) and diabetic rats (155 ± 2 and 240 ± 20 mg/dL with oral, and intraperitoneal, respectively). The diabetic rats were 1.5 fold more sensitive to ZnONPs effect by the intraperitoneal route. In conclusion, this study provides new information about the acute response of ZnONPs on fasting glycemia in diabetic and healthy rat models; these data are essential for possible future clinical approaches.