首页> 美国卫生研究院文献>British Journal of Industrial Medicine >Pulmonary toxicity of components of textile paint linked to the Ardystil syndrome: intratracheal administration in hamsters.
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Pulmonary toxicity of components of textile paint linked to the Ardystil syndrome: intratracheal administration in hamsters.

机译:与Ardystil综合征有关的纺织涂料成分的肺毒性:仓鼠气管内给药。

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摘要

OBJECTIVES: It was hypothesised from an epidemiological investigation that a formula change from Acramin FWR (a polyurea) to Acramin FWN (a polyamide-amine) had led to severe pulmonary disease in textile printing sprayers in SPAIN AND ALGERIA. To verify this, the pulmonary toxicity of the components of the paint systems involved was assessed in experimental animals. METHODS: Individual components and relevant mixtures, diluted in phosphate buttered saline, were given by intratracheal instillation of 2 ml/kg to hamsters. Pulmonary toxicity was assessed on days 3, 7, 14, 28, and 92 after a single intratracheal instillation, by histology and by measuring wet and dry lung weight, protein concentration, the activities of lactate dehydrogenase, alkaline phosphatase, beta-N-acetyl-glucosaminidase, and gamma-glutamyltransferase, inflammatory cell number and distribution in bronchoalveolar lavage fluid (BALF), and hydroxyproline content in dried lung tissue. RESULTS: Based on the doses that killed 50% of the animals (LD50s), the various components were found to be 10 to 1250 times more toxic when given intratracheally than when given orally (according to reported oral LD50s in rats). Acramin FWN, Acramin FWR, Acrafix FHN, or their mixtures caused lung damage. Protein concentration, enzyme activities, total cell number, and percentage of polymorphonuclear neutrophils were increased in BALF during the first week after intratracheal instillation. Lung weights remained high for at least a month. Histology showed inflammatory cell infiltration and subsequent fibrosis with collagen deposition. This finding was confirmed by an increased hydroxyproline content in dried lung tissue. Acramoll W did not show toxic effects. CONCLUSIONS: The study suggests that there is no major difference, in hamsters, between the acute intratracheal toxicity of Acramin FWR and that of Acramin FWN. Consequently, there is no simple toxicological explanation for the epidemiological hypothesis. However, the pulmonary toxicity of these non-irritant polymeric compounds is surprisingly high. The Ardystil disaster and these results should serve as a strong warning that conventional toxicity testing of chemicals does not necessarily protect workers against respiratory toxicity.
机译:目的:根据一项流行病学调查假设,在西班牙和阿尔及利亚的纺织品印花喷雾机中,从Acramin FWR(聚脲)到Acramin FWN(聚酰胺-胺)的配方变化已导致严重的肺部疾病。为了证实这一点,在实验动物中评估了所涉及的涂料体系的组分的肺毒性。方法:将2 ml / kg的气管内滴入仓鼠中,将其各自的成分和相关混合物稀释于磷酸黄油中,并进行稀释。在一次气管内滴注后第3、7、14、28和92天评估肺部毒性,方法是通过组织学,测量肺干湿重,蛋白质浓度,乳酸脱氢酶,碱性磷酸酶,β-N-乙酰基的活性-氨基葡萄糖苷酶和γ-谷氨酰转移酶,支气管肺泡灌洗液(BALF)中的炎症细胞数量和分布以及干燥的肺组织中的羟脯氨酸含量。结果:根据杀死50%动物的剂量(LD50),发现气管内给予的各种成分的毒性比口服给予的高10到1250倍(根据报告的大鼠口服LD50)。 Acramin FWN,Acramin FWR,Acrafix FHN或它们的混合物引起肺损伤。气管内滴注后第一周,BALF中的蛋白质浓度,酶活性,总细胞数和多形核中性粒细胞百分比增加。肺部重量一直保持高位至少一个月。组织学显示炎性细胞浸润和随后的纤维化以及胶原沉积。干燥的肺组织中羟脯氨酸含量增加证实了这一发现。 Acramoll W没有显示毒性作用。结论:该研究表明,在仓鼠中,Acramin FWR和Acramin FWN的急性气管内毒性之间没有重大差异。因此,没有流行病学假设的简单毒理学解释。但是,这些非刺激性高分子化合物的肺毒性令人惊讶地高。 Ardystil灾难和这些结果应作为一个强有力的警告,即化学药品的常规毒性测试不一定能保护工人免受呼吸道毒性。

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