Induction of mesothelioma by a single intrascrotal administration of multi-wall carbon nanotube in intact male Fischer 344 rats

被引:219
作者
Sakamoto, Yoshimitsu [1 ]
Nakae, Dai [1 ,2 ]
Fukumori, Nobutaka [1 ]
Tayama, Kuniaki [1 ]
Maekawa, Akihiko [2 ,3 ]
Imai, Kiyoshi [4 ]
Hirose, Akihiko [5 ]
Nishimura, Tetsuji [6 ]
Ohashi, Norio [1 ]
Ogata, Akio [1 ]
机构
[1] Tokyo Metropolitan Inst Publ Hlth, Dept Environm Hlth & Toxicol, Shinjuku Ku, Tokyo 1690073, Japan
[2] Tokyo Univ Agr, Setagaya Ku, Tokyo 1568502, Japan
[3] Natl Inst Technol & Evaluat, Chem Management Ctr, Safety Assessment Div, Shibuya Ku, Tokyo 1510066, Japan
[4] Biosafety Res Ctr Foods Drugs & Pesticides, Shizuoka 4371213, Japan
[5] Natl Inst Hlth Sci, Biol Safety Res Ctr, Div Risk Assessment, Setagaya Ku, Tokyo 1588501, Japan
[6] Natl Inst Hlth Sci, Div Environm Chem, Setagaya Ku, Tokyo 1588501, Japan
关键词
Multi-wall carbon nanotube; Mesothelioma; Nanomaterial; Carcinogenicity; Hazard identification; Rat; ASBESTOS-INDUCED DISEASES; PERITONEAL-CAVITY; FIBERS; INTRAPERITONEAL; CARCINOGENICITY; PATHOGENICITY; PATHOGENESIS; TOXICITY; HEALTH; NANOTECHNOLOGY;
D O I
10.2131/jts.34.65
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
The present study assessed a carcinogenic hazard of multi-wall carbon nanotube (MWCNT) in intact (not genetically modified) rodents. MWCNT (1 mg/kg body weight, 7 animals), crocidolite (2 mg/kg body weight, 10 animals) or vehicle (2% carboxymethyl Cellulose, 5 animals) was administered to male Fischer 344 rats (12 weeks old) by a single intrascrotal injection. Rats were autopsied immediately after death, when becoming moribund or at the end of the maximal observation period scheduled to be 52 weeks. After 37-40 weeks, however, 6 MWCNT-treated animals died or became moribund due to intraperitoneally disseminated mesothelioma (6/7, 85.7%) with bloody ascites. Peritoneal mesothelium was generally hypertrophic, and numerous nodular or papillary lesions of mesothelioma and mesothelial hyperplasia were developed. While mesothelioid cells were predominant in relatively early stage tumors, advanced stage mesotheliomas were constituted by 2 portions occupied by mesothelioid cells on the surface and spindle-shaped sarcomatous cells in the depth. In the latter, the histological transition was apparently observed between these 2 portions. Mesotheliomas were invasive to adjacent organs and tissues, and frequently metastasized into the pleura. Only I rat survived for 52 weeks ill the MWCNT-treated group, and similar findings except mesothelioma were observed. All 10 crocidolite-treated and 5 vehicle-treated rats survived for 52 weeks without any particular changes except deposition of asbestos in the former case. It is thus indicated that MWCNT possesses carcinogenicity causing mesothelioma at a high rate in intact male rats under the present experimental conditions. The present data identifies a carcinogenic hazard of MWCNT and will serve as one of the indispensable evidences to be used for the risk assessment crucial for not only protection and improvement Of human health and welfare, but also safe and acceptable development and prevalence of this and similar upcoming materials.
引用
收藏
页码:65 / 76
页数:12
相关论文
共 39 条
[1]   A trial on the quantitative risk assessment of man-made mineral fibers by the rat intraperitoneal administration assay using the JFM standard fibrous samples [J].
Adachi, S ;
Kawamura, K ;
Takemoto, K .
INDUSTRIAL HEALTH, 2001, 39 (02) :168-174
[2]  
BERNSTEIN DM, 1999, TOXICOLOGY CHEMICALS, P44
[3]  
BLOBEL GA, 1985, AM J PATHOL, V121, P235
[4]   Tumorigenicity of cellulose fibers injected into the rat peritoneal cavity [J].
Cullen, RT ;
Miller, BG ;
Clark, S ;
Davis, JMG .
INHALATION TOXICOLOGY, 2002, 14 (07) :685-703
[5]  
Davis J M, 1989, IARC Sci Publ, P33
[6]  
DAVIS JMG, 1976, ANN ANAT PATHOL, V21, P199
[7]  
DAVIS JMG, 1986, BRIT J EXP PATHOL, V67, P415
[8]  
DAVIS JMG, 1988, BRIT J EXP PATHOL, V69, P717
[9]   Carbon nanotubes: A review of their properties in relation to pulmonary toxicology and workplace safety [J].
Donaldson, Ken ;
Aitken, Robert ;
Tran, Lang ;
Stone, Vicki ;
Duffin, Rodger ;
Forrest, Gavin ;
Alexander, Andrew .
TOXICOLOGICAL SCIENCES, 2006, 92 (01) :5-22
[10]  
Donaldson K, 2008, J TOXICOL SCI, V33, P385, DOI 10.2131/jts.33.385