Bioenergetic failure correlates with autophagy and apoptosis in rat liver following silver nanoparticle intraperitoneal administration

• Published in: Particle and fibre toxicology Vol. 10; no. 1; p. 40
• Main Authors: Lee, Tzu-Ying, Liu, Maw-Shung, Huang, Li-Ju, Lue, Sheng-I, Lin, Lung-Chang, Kwan, Aij-Lie, Yang, Rei-Cheng
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 19-08-2013; BioMed Central
• Subjects: Adenosine Triphosphate - metabolism; Animals; Apoptosis; Apoptosis - drug effects; Autophagy; Autophagy (Cytology); Autophagy - drug effects; Caspase 3 - metabolism; Chemical and Drug Induced Liver Injury - etiology; Chemical and Drug Induced Liver Injury - metabolism; Chemical and Drug Induced Liver Injury - pathology; Energy conservation; Energy Metabolism - drug effects; In Situ Nick-End Labeling; Injections, Intraperitoneal; Japan; Liver; Liver - drug effects; Liver - metabolism; Liver - ultrastructure; Liver Function Tests; Male; Medicine; Microscopy; Microscopy, Electron, Transmission; Microtubule-Associated Proteins - metabolism; Nanoparticles; Nanoparticles - administration & dosage; Nanoparticles - toxicity; Pediatrics; Physiological aspects; Proteins; Rats, Sprague-Dawley; Rodents; Silver; Silver - administration & dosage; Silver - blood; Silver - toxicity; Taiwan; Time Factors; Japan; Taiwan
• ISSN: 1743-8977; 1743-8977
• DOI: 10.1186/1743-8977-10-40

Deposition and accumulation of silver nanoparticles (Ag-nps) in the liver have been shown to induce hepatotoxicity in animal studies. The hepatotoxicity may include oxidative stress, abnormalities in energy metabolism, and cell death. Studies have indicated that autophagy is an intracellular event involving balance of energy, nutrients, and turnover of subcellular organelles. The present study was undertaken to test the hypothesis that autophagy plays a role in mediating hepatotoxicity in animal after exposure to Ag-nps. Focus was placed on interrelationship between energy metabolism, autophagy, apoptosis and hepatic dysfunction.
Sprague Dawley rats were intraperitoneally injected with Ag-nps (10-30 nm in diameter) at concentration of 500 mg kg(-1). All animals were sacrificed on days 1, 4, 7, 10 and 30 after exposure and blood and liver tissues were collected for further studies.
Uptake of Ag-nps was quite prompt and not proportional to the blood Ag concentration. Declination of ATP (-64% in days 1) and autophagy (determined by LC3-II protein expression and morphological evaluation) increased and peaked on the first day. The ATP content remained at low level even though the autophagy has been activated. Apoptosis (based on caspase-3 protein expression and TUNEL-positive cells staining) began to rise sigmoidally at days 1 and 4, reached a peak level at day 7, and remained at the same levels during days 7-30 post exposure. Meanwhile, autophagy exhibited a gradual decrease from days 1-10 and the decrease at day 30 was statistically significant as compared to day 0 (sham group). Inflammatory reaction (histopathological evaluation) was found at day 10 and preceded to an advanced degree at day 30 when liver function was impaired.
These results indicate that following Ag-nps administration, autophagy was induced; however, failure to preserve autophagy compounded with energy reduction led to apoptosis and the eventual impairment of liver function. The study provides an in-vivo evidence of hepatotoxicity by continuous exposure of Ag-nps in rats.