Fullerene and fullerene whisker are not carcinogenic to the lungs and pleura in rat long-term study after 2-week intra-tracheal intrapulmonary administration.
Asraful Nahar SheemaAya Naiki-ItoAnna KakehashiOmnia Hosny Mohamed AhmedDavid B AlexanderWilliam T AlexanderTakamasa NumanoHiroyuki KatoYuko GotoHiroshi TakaseAkihiko HiroseTakatsugu WakaharaKun'ichi MiyazawaSatoru TakahashiHiroyuki TsudaPublished in: Archives of toxicology (2024)
Fullerene whiskers (FLW)s are thin rod-like structures composed of C 60 and C 70 fullerene (FL). The shape of FLWs suggests potential toxic effects including carcinogenicity to the lung and pleura, similar to effects elicited by asbestos and multi-walled carbon nanotubes (MWCNT)s. However, no long-term carcinogenic studies of FL or FLW have been conducted. In the present study we investigated the pulmonary and pleural carcinogenicity of FL and FLW. Twelve-week-old male F344 rats were administered 0.25 or 0.5 mg FL, FLW, MWCNT-7, and MWCNT-N by intra-tracheal intra-pulmonary spraying (TIPS). Acute lung lesions and carcinogenicity were analyzed at 1 and 104 weeks after 8 doses/15 days TIPS administration. At week 1, FLW, MWCNT-7, and MWCNT-N significantly increased alveolar macrophage infiltration. Expression of Ccl2 and Ccl3, reactive oxygen species production, and cell proliferation were significantly increased by administration of MWCNT-7 and MWCNT-N but not FL or FLW. At week 104, the incidence of bronchiolo-alveolar adenoma plus adenocarcinoma was significantly increased in the MWCNT-7 and MWCNT-N groups, and the incidence of mesothelioma was significantly increased in the MWCNT-7 group. No significant induction of pulmonary or pleural tumorigenesis was observed in the FL or FLW groups. The number of 8-OHdG-positive cells in the alveolar epithelium was significantly increased in the MWCNT-7 and MWCNT-N groups but not in the FL or FLW groups. FL and FLW did not exert pulmonary or pleural carcinogenicity in our study. In addition, oxidative DNA damage was implicated in MWCNT-induced lung carcinogenesis, suggesting that it may be a useful initial marker of carcinogenicity.
Keyphrases
- pulmonary hypertension
- dna damage
- cell proliferation
- reactive oxygen species
- oxidative stress
- risk factors
- high resolution
- radiation therapy
- poor prognosis
- drug induced
- induced apoptosis
- risk assessment
- signaling pathway
- liver injury
- clinical trial
- walled carbon nanotubes
- binding protein
- cell death
- cell cycle
- mass spectrometry
- study protocol
- mechanical ventilation
- human health
- stress induced
- high speed