Effect of acute and long-term administration of gold nanoparticles on biochemical parameters in rat brain.

Mater Sci Eng C Mater Biol Appl

Laboratório dos Processos Inflamatórios e Metabólicos, Programa de Pós-Graduação em Ciências da Saúde, Universidade do Sul de Santa Catarina, 88704-9000 Tubarão, SC, Brazil; Universidade Federal do Amazonas, Programa de Pós-graduação em Ciência e Engenharia de Materiais, Faculdade de Tecnologia, Manaus, AM, Brazil. Electronic address:

Published: October 2017

AI Article Synopsis

  • The study examined how gold nanoparticles (GNPs) affect oxidative stress and energy metabolism in rat brains.
  • Rats were given either one dose or daily doses of GNPs (10nm or 30nm) for either a short or long period, and various brain enzymes were analyzed after treatment.
  • Results showed that while some oxidative stress markers decreased and certain enzyme activities increased, there were notable changes in energy metabolism, indicating that oxidative stress might inhibit energy processes in the brain.

Article Abstract

The present study investigated stress oxidative parameters and activities of enzymes of the energy metabolism in various brain structures. Rats were subjected to acute and long-term administration of gold nanoparticles (GNPs) with mean diameters of 10nm and 30nm. Adult (60days old) male Wistar rats received a single intraperitoneal injection (acute administration; 70μg·kg) or repeated injections once daily for 28days (long-term administration; 70μg·kg) of saline solution or GNPs (10nm or 30nm). Twenty-four hours after administration of the final dose, the animals were killed and the cerebral structures were isolated for enzyme analysis. In this study, we observed that the thiobarbituric acid-reactive species and carbonyl protein levels were decreased after acute administration of GNPs, whereas the superoxide dismutase activity was increased after acute and long-term of GNPs. The catalase activity was affected by the administration of GNPs. Furthermore, we have not found change in the citrate synthase activity. The succinate dehydrogenase, malate dehydrogenase, complexes I, II, II-III and IV, and creatine kinase activities were altered. These results indicate that inhibition energy metabolism can be caused by oxidative stress.

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Source
http://dx.doi.org/10.1016/j.msec.2017.05.110DOI Listing

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