TY - JOUR
T1 - Zinc oxide nanoparticles induce an adverse effect on blood glucose levels depending on the dose and route of administration in healthy and diabetic rats
AU - Virgen-Ortiz, Adolfo
AU - Apolinar-Iribe, Alejandro
AU - Díaz-Reval, Irene
AU - Parra-Delgado, Hortensia
AU - Limón-Miranda, Saraí
AU - Sánchez-Pastor, Enrique Alejandro
AU - Castro-Sánchez, Luis
AU - Castillo, Santos Jesús
AU - Dagnino-Acosta, Adan
AU - Bonales-Alatorre, Edgar
AU - Rodriguez-Hernández, Alejandrina
N1 - Publisher Copyright:
© 2020 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2020/10
Y1 - 2020/10
N2 - 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.
AB - 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.
KW - Diabetes
KW - Hyperglycemic response
KW - Nanomedicine
KW - Nanoparticle toxicology
KW - Zinc
KW - Zinc oxide nanoparticles
UR - http://www.scopus.com/inward/record.url?scp=85092492423&partnerID=8YFLogxK
U2 - 10.3390/nano10102005
DO - 10.3390/nano10102005
M3 - Artículo
C2 - 33053624
AN - SCOPUS:85092492423
VL - 10
SP - 1
EP - 10
JO - Nanomaterials
JF - Nanomaterials
SN - 2079-4991
IS - 10
M1 - 2005
ER -