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1.
Folia Histochem Cytobiol ; 53(4): 294-306, 2015.
Artículo en Inglés | MEDLINE | ID: mdl-26615817

RESUMEN

INTRODUCTION: Exposure to Asian sand dust (ASD) is associated with enhanced pulmonary morbidity and mortality, and the reporting of such cases has rapidly increased in East Asia since 2000. The purpose of the study was to assess chronic lung toxicity induced by ASD. MATERIAL AND METHODS: A total of 174 ICR mice were randomly divided into 5 control and 17 exposure groups. Suspensions of low dose (0.2, 0.4 mg) and high dose (3.0 mg) of ASD particles in saline were intratracheally instilled into ICR mice, followed by sacrifice at 24 hours, 1 week, and 1, 2, 3 and 4 months after instillation. Paraffin sections of lung tissues were stained with hematoxylin and eosin and by immunohistochemistry to detect α-smooth muscle actin, collagen III, matrix metalloproteinase-9 (MMP-9), tissue inhibitor of metalloproteinases-1 (TIMP-1), CD3, CD20, immunoglobulin G, interleukin-1ß and inducible nitric oxide synthase. RESULTS: A lung histological examination revealed similar patterns in the lesions of the groups treated with high (3.0 mg) or low dose (0.4 mg) of ASD. Acute inflammation was observed 24 h after treatment and subsided after 1 week; persistent granulomatous changes were observed at 2 months, focal lymphocytic infiltration at 3 months, and granuloma formation at 4 months. An increase in the size of granulomatous lesions was observed over time and was accompanied by collagen deposition in the lesions. The cytoplasm of macrophages in inflammatory lesions showed positive immunolabeling for MMP-9 at 24 h, 1 and 2 months after instillation of 3.0 mg of ASD. Positive immunolabeling for TIMP-1 was demonstrated in the cytoplasm of macrophages at 2 and 4 months after instillation of 3.0 mg of ASD. These findings suggest association between the expression of MMP-9 and TIMP-1 with the development of lung granulomatous lesions. CONCLUSIONS: These findings suggest that collagen deposition resulting from the altered regulation of extracellular matrix is associated with granuloma formation in the lungs of mice treated with ASD.


Asunto(s)
Polvo , Fibrosis Pulmonar/inducido químicamente , Fibrosis Pulmonar/patología , Dióxido de Silicio/toxicidad , Animales , Granuloma/inducido químicamente , Inflamación/inducido químicamente , Pulmón/efectos de los fármacos , Pulmón/metabolismo , Pulmón/patología , Metaloproteinasa 9 de la Matriz/metabolismo , Ratones , Ratones Endogámicos ICR , Fibrosis Pulmonar/diagnóstico , Inhibidor Tisular de Metaloproteinasa-1/metabolismo , Tráquea
2.
Toxicol Pathol ; 41(1): 48-62, 2013 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-22744225

RESUMEN

Asian sand dust (ASD) events are associated with an increase in pulmonary morbidity and mortality. The number of ASD events has increased rapidly in the east Asian region since 2000. To study the chronic lung toxicity of ASD, saline suspensions of low doses (200 and 400 µg) and high doses (800 and 3,000 µg) of ASD were intratracheally instilled into ICR mice. Animals were sacrificed at 24 hr, 1 week, or 1, 2, or 3 months after instillation. Histopathological examination revealed that ASD induced acute inflammation at 24 hr after instillation. The acute inflammation was transient and subsided at 1 week and 1 month after instillation. At 2 and 3 months after instillation, focal infiltration of lymphocytes with accumulation of epithelioid macrophages, which is a suggestive finding of transformation to granuloma, and granuloma formation were occasionally observed. Aggregation of macrophages containing particles was observed in the pulmonary lymph nodes at 3 months after instillation in high-dose groups. Prolonged inflammatory foci (granuloma) and presence of ASD particles in pulmonary lymph nodes would have a chance to induce immunological modulation leading to adverse health effects in the exposed animals.


Asunto(s)
Polvo , Pulmón/efectos de los fármacos , Pulmón/patología , Neumonía/inducido químicamente , Neumonía/patología , Dióxido de Silicio/toxicidad , Actinas/metabolismo , Animales , Antígenos CD20/metabolismo , Líquido del Lavado Bronquioalveolar/química , Líquido del Lavado Bronquioalveolar/citología , Complejo CD3/metabolismo , Granuloma/inducido químicamente , Granuloma/patología , Histocitoquímica , Exposición por Inhalación , Masculino , Ratones , Ratones Endogámicos ICR , Modelos Inmunológicos , Infiltración Neutrófila , Dióxido de Silicio/administración & dosificación , Pruebas de Toxicidad Crónica , Factor de Necrosis Tumoral alfa/metabolismo
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