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Toxic effects of excess exposure to boric acid on serum biochemical aspect, hematology and histological alterations and ameliorative potential role of melatonin in rats.过量接触硼酸对大鼠血清生化指标、血液学及组织学改变的毒性作用以及褪黑素的改善作用
Saudi J Biol Sci. 2022 Oct;29(10):103425. doi: 10.1016/j.sjbs.2022.103425. Epub 2022 Aug 22.

本文引用的文献

1
The urinary excretion of boric acid preparations following oral administration and topical applications to intact and damaged skin of rabbits.口服硼酸制剂以及将其局部应用于家兔完整皮肤和破损皮肤后,硼酸制剂的尿排泄情况。
Toxicol Appl Pharmacol. 1959 May;1(3):267-76. doi: 10.1016/0041-008x(59)90111-5.
2
Inabsorbability of boric acid in infant powder.婴儿爽身粉中硼酸的不可吸收性。
AMA Am J Dis Child. 1954 Jul;88(1):72-80. doi: 10.1001/archpedi.1954.02050100074009.
3
The toxicity of boric acid and the clinical implications of the use of borated baby powders.硼酸的毒性及含硼爽身粉使用的临床意义。
Bulletin NY Med Coll. 1953;16:92-101.
4
Boric acid poisoning; report of four cases and a review of 109 cases from the world literature.硼酸中毒:4例报告及对世界文献中109例病例的综述
J Pediatr. 1953 Dec;43(6):631-43. doi: 10.1016/s0022-3476(53)80304-5.
5
Statistical issues in the design, analysis and interpretation of animal carcinogenicity studies.动物致癌性研究的设计、分析与解读中的统计学问题。
Environ Health Perspect. 1984 Dec;58:385-92. doi: 10.1289/ehp.8458385.
6
Salmonella mutagenicity test results for 250 chemicals.250种化学物质的沙门氏菌致突变性测试结果。
Environ Mutagen. 1983;5 Suppl 1:1-142.
7
[Toxicity of boric acid].[硼酸的毒性]
Dermatologica. 1971;143(4):227-34.
8
Toxicologic studies on borax and boric acid.硼砂和硼酸的毒理学研究。
Toxicol Appl Pharmacol. 1972 Nov;23(3):351-64. doi: 10.1016/0041-008x(72)90037-3.
9
Boric acid treatment of vulvovaginal candidiasis.硼酸治疗外阴阴道念珠菌病。
Obstet Gynecol. 1974 Jun;43(6):893-5.
10
Toxic and gonadotropic effects of cadmium and boron relative to standards for these substances in drinking water.相对于饮用水中这些物质的标准,镉和硼的毒性及促性腺作用。
Environ Health Perspect. 1976 Feb;13:69-75. doi: 10.1289/ehp.761369.

硼酸对雄性和雌性B6C3F1小鼠的毒性和致癌性研究。

Toxicity and carcinogenicity studies of boric acid in male and female B6C3F1 mice.

作者信息

Dieter M P

机构信息

National Institute of Environmental Health Sciences, Research Triangle Park, NC 27709.

出版信息

Environ Health Perspect. 1994 Nov;102 Suppl 7(Suppl 7):93-7. doi: 10.1289/ehp.94102s793.

DOI:10.1289/ehp.94102s793
PMID:7889889
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1566652/
Abstract

Toxicity and potential carcinogenicity studies of boric acid were investigated in mice to verify in a second rodent species that this was a noncarcinogenic chemical. Earlier chronic studies in rats indicated boric acid was not a carcinogen. The chemical is nominated for testing because over 200 tons are produced annually, there are multiple uses for the product, and there is potential for widespread human exposure, both orally and dermally. Both sexes of B6C3F1 mice were offered diets mixed with boric acid for 14 days, 13 weeks, or 2 years. Dietary doses used in the acute, 14-day study were 0, 0.62, 1.25, 2.5, 5, and 10%; those in the subchronic, 13-week study were 0, 0.12, 0.25, 0.50, 1, and 2%; and doses in the 2-year, chronic study were 0, 0.25, and 0.50% in the diet. Mortality, clinical signs of toxicity, estimates of food consumption, body weight gain, and histopathologic examination of selected tissues constituted the variables measured. In the 14-day study mortality was proportional to dose and time of exposure in both sexes, occurring in dose groups as low as 2.5% and as early as 7 days of exposure. Body weights were depressed more than 10% below controls in the higher dose groups of both sexes. Mortality in the 13-week study was confined to the two highest dose groups in male mice and to the 2%-dose group in females. Body weight depression from 8 to 23% below those of controls occurred in the 0.50% and higher dose groups of both sexes.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在小鼠身上进行了硼酸的毒性和潜在致癌性研究,以在第二种啮齿动物物种中验证其为非致癌化学物质。早期对大鼠的慢性研究表明硼酸不是致癌物。该化学品被指定进行测试,因为其年产量超过200吨,有多种用途,且存在通过口服和皮肤广泛接触人类的可能性。给B6C3F1小鼠的雌雄两性提供含硼酸的饲料,喂养14天、13周或2年。急性14天研究中使用的饲料剂量为0%、0.62%、1.25%、2.5%、5%和10%;亚慢性13周研究中使用的剂量为0%、0.12%、0.25%、0.50%、1%和2%;2年慢性研究中饲料中的剂量为0%、0.25%和0.50%。测量的变量包括死亡率、毒性临床体征、食物消耗量估计、体重增加以及对选定组织的组织病理学检查。在14天研究中,死亡率与剂量和暴露时间成正比,在雌雄两性中,低至2.5%的剂量组以及早在暴露7天时就出现死亡。在雌雄两性的高剂量组中,体重比对照组低10%以上。在13周研究中,死亡率仅限于雄性小鼠的两个最高剂量组和雌性小鼠的2%剂量组。在雌雄两性中,0.50%及以上剂量组的体重比对照组低8%至23%。(摘要截短至250字)