Effects of the intranasal application of gold nanoparticles on the pulmonary tissue after acute exposure to industrial cigarette smoke.
Germano Duarte PortoDaniela Pacheco Dos Santos HaupenthalPriscila Soares SouzaGustavo de Bem SilveiraRenata Tiscoski NesiPaulo Emílio FeuserJonathann Corrêa PossatoVanessa Moraes de AndradeRicardo Aurino PinhoPaulo Cesar Lock SilveiraPublished in: Journal of biomedical materials research. Part B, Applied biomaterials (2021)
Inhalation of harmful particles appears as a primary factor for the onset and establishment of chronic obstructive pulmonary disease (COPD). Cigarette smoke acutely promotes an exacerbated inflammatory response with oxidative stress induction with DNA damage. Administration of Gold Nanoparticles (GNPs) with 20 nm in different concentrations can revert damages caused by external aggravations. The effects of GNPs in a COPD process have not been observed until now. The objective of this work was to evaluate the therapeutic effects of intranasal administration of different doses of GNPs after acute exposure to industrial cigarette smoke. Thirty male Swiss mice were randomly divided into five groups: Sham; cigarette smoke (CS); CS + GNPs 2.5 mg/L; CS + GNPs 7.5 mg/L and CS + GNPs 22.5 mg/L. The animals were exposed to the commercial cigarette with filter in an acrylic inhalation chamber and treated with intranasal GNPs for five consecutive days. The results demonstrate that exposure to CS causes an increase in inflammatory cytokines, histological changes, oxidative and nitrosive damage in the lung, as well as increased damage to the DNA of liver cells, blood plasma and lung. Among the three doses of GNPs (2.5, 7.5, and 22.5 mg/L) used, the highest dose had better anti-inflammatory effects. However, GNPs at a dose of 7.5 mg/L showed better efficacies in reducing ROS formation, alveolar diameter, and the number of inflammatory cells in histology, in addition to significantly reduced rate of DNA damage in lung cells without additional systemic genotoxicity already caused by cigarette smoke.
Keyphrases
- oxidative stress
- dna damage
- induced apoptosis
- gold nanoparticles
- inflammatory response
- cell cycle arrest
- chronic obstructive pulmonary disease
- endoplasmic reticulum stress
- dna repair
- cell death
- type diabetes
- ischemia reperfusion injury
- pulmonary hypertension
- wastewater treatment
- clinical trial
- signaling pathway
- metabolic syndrome
- lung function
- risk assessment
- reduced graphene oxide
- photodynamic therapy
- insulin resistance
- optical coherence tomography