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Studies of single-walled carbon nanotubes-induced hepatotoxicity by NMR-based metabonomics of rat blood plasma and liver extracts

The toxicological effects of single-walled carbon nanotubes (SWCNTs) were investigated after intratracheal instillation in male Wistar rats over a 15-day period using metabonomic analysis of (1)H (nuclear magnetic resonance) NMR spectra of blood plasma and liver tissue extracts. Concurrent liver his...

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Autores principales: Lin, Bencheng, Zhang, Huashan, Lin, Zhiqing, Fang, Yanjun, Tian, Lei, Yang, Honglian, Yan, Jun, Liu, Huanliang, Zhang, Wei, Xi, Zhuge
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3664573/
https://www.ncbi.nlm.nih.gov/pubmed/23680025
http://dx.doi.org/10.1186/1556-276X-8-236
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author Lin, Bencheng
Zhang, Huashan
Lin, Zhiqing
Fang, Yanjun
Tian, Lei
Yang, Honglian
Yan, Jun
Liu, Huanliang
Zhang, Wei
Xi, Zhuge
author_facet Lin, Bencheng
Zhang, Huashan
Lin, Zhiqing
Fang, Yanjun
Tian, Lei
Yang, Honglian
Yan, Jun
Liu, Huanliang
Zhang, Wei
Xi, Zhuge
author_sort Lin, Bencheng
collection PubMed
description The toxicological effects of single-walled carbon nanotubes (SWCNTs) were investigated after intratracheal instillation in male Wistar rats over a 15-day period using metabonomic analysis of (1)H (nuclear magnetic resonance) NMR spectra of blood plasma and liver tissue extracts. Concurrent liver histopathology examinations and plasma clinical chemistry analyses were also performed. Significant changes were observed in clinical chemistry features, including alkaline phosphatase, total protein, and total cholesterol, and in liver pathology, suggesting that SWCNTs clearly have hepatotoxicity in the rat. (1)H NMR spectra and pattern recognition analyses from nanomaterial-treated rats showed remarkable differences in the excretion of lactate, trimethylamine oxide, bilineurin, phosphocholine, amylaceum, and glycogen. Indications of amino acid metabolism impairment were supported by increased lactate concentrations and decreased alanine concentrations in plasma. The rise in plasma and liver tissue extract concentrations of choline and phosphocholine, together with decreased lipids and lipoproteins, after SWCNTs treatment indicated a disruption of membrane fluidity caused by lipid peroxidation. Energy, amino acid, and fat metabolism appeared to be affected by SWCNTs exposure. Clinical chemistry and metabonomic approaches clearly indicated liver injury, which might have been associated with an indirect mechanism involving nanomaterial-induced oxidative stress.
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spelling pubmed-36645732013-06-03 Studies of single-walled carbon nanotubes-induced hepatotoxicity by NMR-based metabonomics of rat blood plasma and liver extracts Lin, Bencheng Zhang, Huashan Lin, Zhiqing Fang, Yanjun Tian, Lei Yang, Honglian Yan, Jun Liu, Huanliang Zhang, Wei Xi, Zhuge Nanoscale Res Lett Nano Express The toxicological effects of single-walled carbon nanotubes (SWCNTs) were investigated after intratracheal instillation in male Wistar rats over a 15-day period using metabonomic analysis of (1)H (nuclear magnetic resonance) NMR spectra of blood plasma and liver tissue extracts. Concurrent liver histopathology examinations and plasma clinical chemistry analyses were also performed. Significant changes were observed in clinical chemistry features, including alkaline phosphatase, total protein, and total cholesterol, and in liver pathology, suggesting that SWCNTs clearly have hepatotoxicity in the rat. (1)H NMR spectra and pattern recognition analyses from nanomaterial-treated rats showed remarkable differences in the excretion of lactate, trimethylamine oxide, bilineurin, phosphocholine, amylaceum, and glycogen. Indications of amino acid metabolism impairment were supported by increased lactate concentrations and decreased alanine concentrations in plasma. The rise in plasma and liver tissue extract concentrations of choline and phosphocholine, together with decreased lipids and lipoproteins, after SWCNTs treatment indicated a disruption of membrane fluidity caused by lipid peroxidation. Energy, amino acid, and fat metabolism appeared to be affected by SWCNTs exposure. Clinical chemistry and metabonomic approaches clearly indicated liver injury, which might have been associated with an indirect mechanism involving nanomaterial-induced oxidative stress. Springer 2013-05-16 /pmc/articles/PMC3664573/ /pubmed/23680025 http://dx.doi.org/10.1186/1556-276X-8-236 Text en Copyright ©2013 Lin et al.; licensee Springer. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Nano Express
Lin, Bencheng
Zhang, Huashan
Lin, Zhiqing
Fang, Yanjun
Tian, Lei
Yang, Honglian
Yan, Jun
Liu, Huanliang
Zhang, Wei
Xi, Zhuge
Studies of single-walled carbon nanotubes-induced hepatotoxicity by NMR-based metabonomics of rat blood plasma and liver extracts
title Studies of single-walled carbon nanotubes-induced hepatotoxicity by NMR-based metabonomics of rat blood plasma and liver extracts
title_full Studies of single-walled carbon nanotubes-induced hepatotoxicity by NMR-based metabonomics of rat blood plasma and liver extracts
title_fullStr Studies of single-walled carbon nanotubes-induced hepatotoxicity by NMR-based metabonomics of rat blood plasma and liver extracts
title_full_unstemmed Studies of single-walled carbon nanotubes-induced hepatotoxicity by NMR-based metabonomics of rat blood plasma and liver extracts
title_short Studies of single-walled carbon nanotubes-induced hepatotoxicity by NMR-based metabonomics of rat blood plasma and liver extracts
title_sort studies of single-walled carbon nanotubes-induced hepatotoxicity by nmr-based metabonomics of rat blood plasma and liver extracts
topic Nano Express
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3664573/
https://www.ncbi.nlm.nih.gov/pubmed/23680025
http://dx.doi.org/10.1186/1556-276X-8-236
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