Effects of intranasal exposure to spores of Stachybotrys atra in mice

The effects of highly toxic and nontoxic spores of Stachybotrys atra were investigated in mice after six intranasal administrations of 1 x 10(5) and 1 x 10(3) spores in phosphate-buffered saline during a 3-week period. Toxic spores contained the trichothecene mycotoxins, satratoxins G and H, as well...

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Veröffentlicht in:Fundamental and applied toxicology 1997-02, Vol.35 (2), p.182-188
Hauptverfasser: NIKULIN, M, REIJULA, K, JARVIS, B. B, VEIJALAINEN, P, HINTIKKA, E.-L
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container_issue 2
container_start_page 182
container_title Fundamental and applied toxicology
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creator NIKULIN, M
REIJULA, K
JARVIS, B. B
VEIJALAINEN, P
HINTIKKA, E.-L
description The effects of highly toxic and nontoxic spores of Stachybotrys atra were investigated in mice after six intranasal administrations of 1 x 10(5) and 1 x 10(3) spores in phosphate-buffered saline during a 3-week period. Toxic spores contained the trichothecene mycotoxins, satratoxins G and H, as well as the immunosuppressant stachybotrylactones and -lactams. No trichothecenes were detected in the nontoxic spores, and they contained only minor amounts of stachybotrylactones and -lactams. In mice injected with toxic and nontoxic spores, the platelet count was decreased and leucocyte and erythrocyte counts, hemoglobin concentration, and hematocrit were increased. No IgG antibodies to S. atra were detected in sera of mice exposed intranasally to spores. No histological changes were detected in spleen, thymus, or intestines of mice. The mice receiving 1 x 10(5) toxic spores intranasally developed severe inflammatory changes within both bronchioles and alveoli. Hemorrhage was detected in alveoli. The mice receiving 1 x 10(5) nontoxic spores also developed inflammatory changes in the lungs, but these changes were significantly milder than those in mice receiving toxic spores. The mice receiving 1 x 10(3) toxic spores developed inflammatory changes in the lungs that were less severe than those in the mice receiving 1 x 10(5) toxic spores. No inflammatory changes were detected in the mice receiving 1 x 10(3) of nontoxic spores. The present findings indicate that exposure to S. atra spores containing toxins (satratoxins) can be a significant health risk.
doi_str_mv 10.1006/faat.1996.2274
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No histological changes were detected in spleen, thymus, or intestines of mice. The mice receiving 1 x 10(5) toxic spores intranasally developed severe inflammatory changes within both bronchioles and alveoli. Hemorrhage was detected in alveoli. The mice receiving 1 x 10(5) nontoxic spores also developed inflammatory changes in the lungs, but these changes were significantly milder than those in mice receiving toxic spores. The mice receiving 1 x 10(3) toxic spores developed inflammatory changes in the lungs that were less severe than those in the mice receiving 1 x 10(5) toxic spores. No inflammatory changes were detected in the mice receiving 1 x 10(3) of nontoxic spores. The present findings indicate that exposure to S. atra spores containing toxins (satratoxins) can be a significant health risk.</description><identifier>ISSN: 0272-0590</identifier><identifier>EISSN: 1095-6832</identifier><identifier>DOI: 10.1006/faat.1996.2274</identifier><identifier>PMID: 9038239</identifier><identifier>CODEN: FAATDF</identifier><language>eng</language><publisher>Boston, MA: Academic Press</publisher><subject>Administration, Intranasal ; Animals ; Antigens, Fungal - immunology ; Biological and medical sciences ; Blood Cell Count - drug effects ; Experimental and animal immunopathology. 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The present findings indicate that exposure to S. atra spores containing toxins (satratoxins) can be a significant health risk.</description><subject>Administration, Intranasal</subject><subject>Animals</subject><subject>Antigens, Fungal - immunology</subject><subject>Biological and medical sciences</subject><subject>Blood Cell Count - drug effects</subject><subject>Experimental and animal immunopathology. Animal models</subject><subject>Female</subject><subject>Immunization</subject><subject>Immunoglobulin G - immunology</subject><subject>Immunopathology</subject><subject>Inflammation - chemically induced</subject><subject>Inflammation - pathology</subject><subject>Lung - pathology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mycotoxins - chemistry</subject><subject>Mycotoxins - toxicity</subject><subject>Protein Synthesis Inhibitors - chemistry</subject><subject>Protein Synthesis Inhibitors - toxicity</subject><subject>Spores, Fungal - immunology</subject><subject>Stachybotrys - immunology</subject><subject>Stachybotrys atra</subject><subject>Trichothecenes - chemistry</subject><subject>Trichothecenes - toxicity</subject><subject>Weight Gain - drug effects</subject><issn>0272-0590</issn><issn>1095-6832</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9j71PwzAUxC0EKqWwsiF5QGwp_ogdvxFV5UOqxADM0bNji6CkCbEj0f--EURMb7jf3b0j5JqzNWdM3wfEtOYAei1EkZ-QJWegMm2kOCVLJgqRMQXsnFzE-MUY5ypnC7IAJo2QsCTbbQjepUi7QOt9GnCPERvqf_oujoOnqaOx7wb_C7wldJ8H26XhEClO8GShbe38JTkL2ER_Nd8V-Xjcvm-es93r08vmYZf1UuqUWTQChAINgKwCJlzwJjfCgeTaWh6EkyZHWRiN1fR15by3wVtuNC8Ko-SK3P3l9kP3PfqYyraOzjcN7n03xpIr4BJUMYE3Mzja1ldlP9QtDody3j3pt7OO0WETpt2ujv-YUKaAqe8I_jZmow</recordid><startdate>19970201</startdate><enddate>19970201</enddate><creator>NIKULIN, M</creator><creator>REIJULA, K</creator><creator>JARVIS, B. 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Animal models</topic><topic>Female</topic><topic>Immunization</topic><topic>Immunoglobulin G - immunology</topic><topic>Immunopathology</topic><topic>Inflammation - chemically induced</topic><topic>Inflammation - pathology</topic><topic>Lung - pathology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mycotoxins - chemistry</topic><topic>Mycotoxins - toxicity</topic><topic>Protein Synthesis Inhibitors - chemistry</topic><topic>Protein Synthesis Inhibitors - toxicity</topic><topic>Spores, Fungal - immunology</topic><topic>Stachybotrys - immunology</topic><topic>Stachybotrys atra</topic><topic>Trichothecenes - chemistry</topic><topic>Trichothecenes - toxicity</topic><topic>Weight Gain - drug effects</topic><toplevel>online_resources</toplevel><creatorcontrib>NIKULIN, M</creatorcontrib><creatorcontrib>REIJULA, K</creatorcontrib><creatorcontrib>JARVIS, B. 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identifier ISSN: 0272-0590
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source MEDLINE; Oxford University Press Journals All Titles (1996-Current); Alma/SFX Local Collection
subjects Administration, Intranasal
Animals
Antigens, Fungal - immunology
Biological and medical sciences
Blood Cell Count - drug effects
Experimental and animal immunopathology. Animal models
Female
Immunization
Immunoglobulin G - immunology
Immunopathology
Inflammation - chemically induced
Inflammation - pathology
Lung - pathology
Male
Medical sciences
Mice
Mycotoxins - chemistry
Mycotoxins - toxicity
Protein Synthesis Inhibitors - chemistry
Protein Synthesis Inhibitors - toxicity
Spores, Fungal - immunology
Stachybotrys - immunology
Stachybotrys atra
Trichothecenes - chemistry
Trichothecenes - toxicity
Weight Gain - drug effects
title Effects of intranasal exposure to spores of Stachybotrys atra in mice
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