Eugenol mitigated acute lung but not spermatic toxicity of C60 fullerene emulsion in mice

C60 fullerene (C60) is a nano-pollutant that can damage the respiratory system. Eugenol exhibits significant anti-inflammatory and antioxidant properties. We aimed to investigate the time course of C60 emulsion-induced pulmonary and spermatic harms, as well as the effect of eugenol on C60 emulsion t...

Full description

Autores:
Gomes Pinheiro, Felipe
Moreira-Gomes, Maria Diana
Nascimento Machado, Mariana
dos Santos Almeida, Tailane
da Penha Apolinario Barboza, Priscila
Silva Oliveira, Luis Felipe
Sales Avila Cavalcante, Francisco
Henrique Leal-Cardoso, Jose
Soares Fortunato, Rodrigo
Araujo Zin, Walter
Tipo de recurso:
http://purl.org/coar/resource_type/c_816b
Fecha de publicación:
2020
Institución:
Corporación Universidad de la Costa
Repositorio:
REDICUC - Repositorio CUC
Idioma:
eng
OAI Identifier:
oai:repositorio.cuc.edu.co:11323/7566
Acceso en línea:
https://hdl.handle.net/11323/7566
https://doi.org/10.1016/j.envpol.2020.116188
https://repositorio.cuc.edu.co/
Palabra clave:
Lung mechanics
Inflammation
Oxidative stress
Sperm vitality
C60 toxicity
Rights
openAccess
License
CC0 1.0 Universal
Description
Summary:C60 fullerene (C60) is a nano-pollutant that can damage the respiratory system. Eugenol exhibits significant anti-inflammatory and antioxidant properties. We aimed to investigate the time course of C60 emulsion-induced pulmonary and spermatic harms, as well as the effect of eugenol on C60 emulsion toxicity. The first group of mice (protocol 1) received intratracheally C60 emulsion (1.0 mg/kg BW) or vehicle and were tested at 12, 24, 72 and 96 h (F groups) thereafter. The second group of mice (protocol 2) received intratracheally C60 emulsion or vehicle, 1 h later were gavaged with eugenol (150 mg/kg) or vehicle, and experiments were done 24 h after instillation. Lung mechanics, morphology, redox markers, cytokines and epididymal spermatozoa were analyzed. Protocol 1: Tissue damping (G) and elastance (H) were significantly higher in F24 than in others groups, except for H in F72. Morphological and inflammatory parameters were worst at 24 h and subsequently declined until 96 h, whereas redox and spermatic parameters worsened over the whole period. Eugenol eliminated the increase in G, H, cellularity, and cytokines, attenuated oxidative stress induced by C60 exposure, but had no effect on sperm. Hence, exposure to C60 emulsion deteriorated lung morphofunctional, redox and inflammatory characteristics and increased the risk of infertility. Furthermore, eugenol avoided those changes, but did not prevent sperm damage.