The effect of stone-wool on rat lungs and on the primary culture of rat alveolar macrophages and type II pneumocytes

The effect of stone‐wool has been studied in both in vivo long term sequential and in vitro methods in male Sprague‐Dawley rats. Stone‐wool was administered by single intratracheal instillation and the lungs were examined after 1, 3 and 6 months of exposure by morphological methods. UICC crocidolite...

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Published inJournal of applied toxicology Vol. 26; no. 1; pp. 16 - 24
Main Authors Tátrai, Erzsébet, Brozik, Márta, Drahos, Ágnes, Kováčiková, Zuzana, Six, Éva, Csík, Márta, Dám, Annamária
Format Journal Article
LanguageEnglish
Published Chichester, UK John Wiley & Sons, Ltd 01.01.2006
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Abstract The effect of stone‐wool has been studied in both in vivo long term sequential and in vitro methods in male Sprague‐Dawley rats. Stone‐wool was administered by single intratracheal instillation and the lungs were examined after 1, 3 and 6 months of exposure by morphological methods. UICC crocidolite was applied as a positive control. In addition, the effects of both fibres were examined in primary cultures of alveolar macrophages (AM) and type II pneumocytes (T2) by morphological, biochemical and immunological methods. By the end of 6 months stone‐wool induced moderate pulmonary interstitial inflammation and fibrosis without progression, whereas crocidolite induced progressive interstitial inflammation and fibrosis as a function of time. Although stone‐wool inhibited phagocytosis, it did not induce serious membrane damage to the cells examined and did not destroy their ultrastructure. It significantly reduced the activity of Cu,Zn/superoxide dismutase (SOD) and alkaline phosphatase (AP) in alveolar macrophages and significantly decreased the activity of AP and γ‐glutamyl transpeptidase (GGT) in type II pneumocytes. Crocidolite, on the other hand, decreased the activity of all enzymes (glutathione peroxidase, GSH‐Px; glutathione reductase, GSH‐Rd) of glutathione metabolism as well as alkaline phosphatase in alveolar macrophages. It decreased the activity of all enzymes in type II pneumocytes, except for Cu,Zn/SOD. On exposure to stone‐wool, the production of inflammatory proteins, macrophage chemoattractant protein‐1 (MCP‐1) and macrophage inhibitory protein‐1α (MIP‐1α) increased in both cultured cells but did not reach the level induced by crocidolite. Our results suggested that stone‐wool is less toxic than crocidolite. Whether it is carcinogenic or not, is still an open question. Copyright © 2005 John Wiley & Sons, Ltd.
AbstractList The effect of stone-wool in both in vivo long term sequential and in vitro methods in male Sprague-Dawley rats is investigated. The stone-wool is administered by single intratracheal instillation and the lungs are examined after 1, 3 and 6 months of exposure by morphological methods. UICC crocidolite is applied as a positive control. The effects of both fibers are examined in primary cultures of alveolar macrophages (AM) and type II pneumocytes (T2) by morphological, biochemical and immunological methods. The stone-wool induced moderate pulmonary interstitial inflammation and fibrosis without progression, whereas crocidolite induced progressive interstitial inflammation and fibrosis as a function of time. It is found that the stone-wool is less toxic than crocidolite.
The effect of stone-wool has been studied in both in vivo long term sequential and in vitro methods in male Sprague-Dawley rats. Stone-wool was administered by single intratracheal instillation and the lungs were examined after 1, 3 and 6 months of exposure by morphological methods. UICC crocidolite was applied as a positive control. In addition, the effects of both fibres were examined in primary cultures of alveolar macrophages (AM) and type II pneumocytes (T2) by morphological, biochemical and immunological methods. By the end of 6 months stone-wool induced moderate pulmonary interstitial inflammation and fibrosis without progression, whereas crocidolite induced progressive interstitial inflammation and fibrosis as a function of time. Although stone-wool inhibited phagocytosis, it did not induce serious membrane damage to the cells examined and did not destroy their ultrastructure. It significantly reduced the activity of Cu,Zn/superoxide dismutase (SOD) and alkaline phosphatase (AP) in alveolar macrophages and significantly decreased the activity of AP and gamma-glutamyl transpeptidase (GGT) in type II pneumocytes. Crocidolite, on the other hand, decreased the activity of all enzymes (glutathione peroxidase, GSH-Px; glutathione reductase, GSH-Rd) of glutathione metabolism as well as alkaline phosphatase in alveolar macrophages. It decreased the activity of all enzymes in type II pneumocytes, except for Cu,Zn/SOD. On exposure to stone-wool, the production of inflammatory proteins, macrophage chemoattractant protein-1 (MCP-1) and macrophage inhibitory protein-1alpha (MIP-1alpha) increased in both cultured cells but did not reach the level induced by crocidolite. Our results suggested that stone-wool is less toxic than crocidolite. Whether it is carcinogenic or not, is still an open question.
The effect of stone-wool has been studied in both in vivo long term sequential and in vitro methods in male Sprague-Dawley rats. Stone-wool was administered by single intratracheal instillation and the lungs were examined after 1, 3 and 6 months of exposure by morphological methods. UICC crocidolite was applied as a positive control. In addition, the effects of both fibres were examined in primary cultures of alveolar macrophages (AM) and type II pneumocytes (T2) by morphological, biochemical and immunological methods. By the end of 6 months stone-wool induced moderate pulmonary interstitial inflammation and fibrosis without progression, whereas crocidolite induced progressive interstitial inflammation and fibrosis as a function of time. Although stone-wool inhibited phagocytosis, it did not induce serious membrane damage to the cells examined and did not destroy their ultrastructure. It significantly reduced the activity of Cu,Zn/eroxide dismutase (SOD) and alkaline phosphatase (AP) in alveolar macrophages and significantly decreased the activity of AP and -glutamyl transpeptidase (GGT) in type II pneumocytes. Crocidolite, on the other hand, decreased the activity of all enzymes (glutathione peroxidase, GSH-Px; glutathione reductase, GSH-Rd) of glutathione metabolism as well as alkaline phosphatase in alveolar macrophages. It decreased the activity of all enzymes in type II pneumocytes, except for Cu,Zn/SOD. On exposure to stone-wool, the production of inflammatory proteins, macrophage chemoattractant protein-1 (MCP-1) and macrophage inhibitory protein-1 (MIP-1) increased in both cultured cells but did not reach the level induced by crocidolite. Our results suggested that stone-wool is less toxic than crocidolite. Whether it is carcinogenic or not, is still an open question.
The effect of stone‐wool has been studied in both in vivo long term sequential and in vitro methods in male Sprague‐Dawley rats. Stone‐wool was administered by single intratracheal instillation and the lungs were examined after 1, 3 and 6 months of exposure by morphological methods. UICC crocidolite was applied as a positive control. In addition, the effects of both fibres were examined in primary cultures of alveolar macrophages (AM) and type II pneumocytes (T2) by morphological, biochemical and immunological methods. By the end of 6 months stone‐wool induced moderate pulmonary interstitial inflammation and fibrosis without progression, whereas crocidolite induced progressive interstitial inflammation and fibrosis as a function of time. Although stone‐wool inhibited phagocytosis, it did not induce serious membrane damage to the cells examined and did not destroy their ultrastructure. It significantly reduced the activity of Cu,Zn/superoxide dismutase (SOD) and alkaline phosphatase (AP) in alveolar macrophages and significantly decreased the activity of AP and γ‐glutamyl transpeptidase (GGT) in type II pneumocytes. Crocidolite, on the other hand, decreased the activity of all enzymes (glutathione peroxidase, GSH‐Px; glutathione reductase, GSH‐Rd) of glutathione metabolism as well as alkaline phosphatase in alveolar macrophages. It decreased the activity of all enzymes in type II pneumocytes, except for Cu,Zn/SOD. On exposure to stone‐wool, the production of inflammatory proteins, macrophage chemoattractant protein‐1 (MCP‐1) and macrophage inhibitory protein‐1α (MIP‐1α) increased in both cultured cells but did not reach the level induced by crocidolite. Our results suggested that stone‐wool is less toxic than crocidolite. Whether it is carcinogenic or not, is still an open question. Copyright © 2005 John Wiley & Sons, Ltd.
Author Brozik, Márta
Kováčiková, Zuzana
Csík, Márta
Tátrai, Erzsébet
Six, Éva
Dám, Annamária
Drahos, Ágnes
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Issue 1
Keywords Lung disease
Lectin
MCP-1
Rat
Respiratory disease
antioxidant system
stone-wool
Rodentia
alveolar macrophages
lectins
EDXA
Antioxidant
Mineral fiber
Respiratory system
In vitro
Vertebrata
Mammalia
Pulmonary fibrosis
Animal
MIP-1α
Primary culture
Macrophage
pneumocytes
Language English
License CC BY 4.0
2005 John Wiley & Sons, Ltd.
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Snippet The effect of stone‐wool has been studied in both in vivo long term sequential and in vitro methods in male Sprague‐Dawley rats. Stone‐wool was administered by...
The effect of stone-wool has been studied in both in vivo long term sequential and in vitro methods in male Sprague-Dawley rats. Stone-wool was administered by...
The effect of stone-wool in both in vivo long term sequential and in vitro methods in male Sprague-Dawley rats is investigated. The stone-wool is administered...
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StartPage 16
SubjectTerms alveolar macrophages
Animals
antioxidant system
Biological and medical sciences
Cell Membrane - drug effects
Cell Membrane - pathology
Chemokine CCL2 - metabolism
Chemokine CCL3
Chemokine CCL4
EDXA
lectins
Lung - drug effects
Lung - enzymology
Lung - pathology
Lung - ultrastructure
Lymph Nodes - drug effects
Lymph Nodes - ultrastructure
Macrophage Inflammatory Proteins - metabolism
Macrophages, Alveolar - drug effects
Macrophages, Alveolar - enzymology
Macrophages, Alveolar - ultrastructure
Male
MCP-1
Medical sciences
Microscopy, Electron, Scanning
Microscopy, Electron, Transmission
Mineral Fibers - toxicity
MIP-1α
pneumocytes
Pneumology
pulmonary fibrosis
Pulmonary Fibrosis - chemically induced
Pulmonary Fibrosis - pathology
Rats
Rats, Sprague-Dawley
Respiratory system : syndromes and miscellaneous diseases
stone-wool
Toxicology
Title The effect of stone-wool on rat lungs and on the primary culture of rat alveolar macrophages and type II pneumocytes
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Volume 26
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