Mercado-Feliciano Minerva, Herbert Ronald A, Wyde Michael E, Gerken Diane K, Hejtmancik Milton R, Hooth Michelle J
National Toxicology Program, National Institute of Environmental Health Sciences, National Institutes of Health, Research Triangle Park, NC 27709, USA.
Cutan Ocul Toxicol. 2013 Sep;32(3):234-40. doi: 10.3109/15569527.2012.746358. Epub 2012 Dec 11.
Pyrogallol (CAS No. 87-66-1), a benzenetriol used historically as a hair dye and currently in a number of industrial applications, was nominated to the National Toxicology Program (NTP) for testing based on the lack of toxicity and carcinogenicity data. Three-month and two-year toxicity studies to determine the toxicity and carcinogenicity of pyrogallol when applied to naïve skin (i.e. dermal administration) were conducted in both sexes of F344/N rats and B6C3F1/N mice. In the three-month studies, adult rodents were administered pyrogallol in 95% ethanol five days per week for 3 months at doses of up to 150 mg/kg body weight (rats) or 600 mg/kg (mice). Based on the subchronic studies, the doses for the two-year studies in rats and mice were 5, 20 and 75 mg/kg of pyrogallol. All mice and most rats survived until the end of the three-month study and body weights were comparable to controls. During the two-year study, survival of dosed rats and male mice was comparable to controls; however survival of 75 mg/kg female mice significantly decreased compared to controls. The incidences of microscopic non-neoplastic lesions at the site of application were significantly higher in all dosed groups of rats and mice and in both the 3-months and two-year studies. In the two-year study, hyperplasia, hyperkeratosis and inflammation tended to be more severe in mice than in rats, and in the mice they tended to be more severe in females than in males. The incidence of squamous cell carcinoma at the site of application (SOA) in 75 mg/kg female mice and SOA squamous cell papillomas in 75 mg/kg male mice were greater than controls. Pyrogallol was carcinogenic in female mice and may have caused tumors in male mice.
连苯三酚(化学物质登记号:87 - 66 - 1),一种历史上用作染发剂且目前用于多种工业用途的苯三酚,由于缺乏毒性和致癌性数据而被提交至美国国家毒理学计划(NTP)进行测试。在F344/N大鼠和B6C3F1/N小鼠的雌雄两性中开展了为期三个月和两年的毒性研究,以确定连苯三酚经皮肤给药(即涂抹于未接触过该物质的皮肤)时的毒性和致癌性。在为期三个月的研究中,成年啮齿动物每周五天接受溶于95%乙醇的连苯三酚,持续3个月,大鼠的剂量最高达150毫克/千克体重,小鼠的剂量最高达600毫克/千克。基于亚慢性研究,大鼠和小鼠两年研究的剂量分别为5、20和75毫克/千克连苯三酚。所有小鼠和大多数大鼠存活至三个月研究结束,体重与对照组相当。在两年研究期间,给药大鼠和雄性小鼠的存活率与对照组相当;然而,75毫克/千克雌性小鼠的存活率与对照组相比显著降低。在大鼠和小鼠的所有给药组以及三个月和两年研究中,给药部位的微观非肿瘤性病变发生率均显著更高。在两年研究中,增生、角化过度和炎症在小鼠中往往比在大鼠中更严重,并且在小鼠中雌性比雄性更严重。75毫克/千克雌性小鼠给药部位的鳞状细胞癌发生率以及75毫克/千克雄性小鼠给药部位的鳞状细胞乳头状瘤发生率均高于对照组。连苯三酚对雌性小鼠具有致癌性,并且可能在雄性小鼠中引发了肿瘤。