Oral exposure to cadmium and mercury alone and in combination causes damage to the lung tissue of Sprague-Dawley rats
•Oral exposure to cadmium and mercury causes changes to the lung architecture.•Changes in bronchiole morphology included an increase in smooth muscle mass.•Luminal epithelium degeneration, detachment and aggregation.•Prominent bronchiole-associated lymphoid tissue was present in Cd and Hg.•Ultrastru...
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description | •Oral exposure to cadmium and mercury causes changes to the lung architecture.•Changes in bronchiole morphology included an increase in smooth muscle mass.•Luminal epithelium degeneration, detachment and aggregation.•Prominent bronchiole-associated lymphoid tissue was present in Cd and Hg.•Ultrastructural examination confirmed the presence of fibrosis.
Environmental presence and human exposure to heavy metals in air and cigarette smoke has led to a worldwide increase in respiratory disease. The effects of oral exposure to heavy metals in liver and kidney structure and function have been widely investigated and the respiratory system as a target is often overlooked. The aim of the study was to investigate the possible structural changes in the lung tissue of Sprague-Dawley rats after oral exposure for 28 days to cadmium (Cd) and mercury (Hg), alone and in combination at 1000 times the World Health Organization’s limit for each metal in drinking water. Following exposure, the general morphology of the bronchiole and lungs as well as collagen and elastin distribution was evaluated using histological techniques and transmission electron microscopy. In the lungs, structural changes to the alveoli included collapsed alveolar spaces, presence of inflammatory cells and thickening of the alveolar walls. In addition, exposure to Cd and Hg caused degeneration of the alveolar structures resulting in confluent alveoli. Changes in bronchiole morphology included an increase in smooth muscle mass with luminal epithelium degeneration, detachment and aggregation. Prominent bronchiole-associated lymphoid tissue was present in the group exposed to Cd and Hg. Ultrastructural examination confirmed the presence of fibrosis where in the Cd exposed group, collagen fibrils arrangement was dense, while in the Hg exposed group, additional prominent elastin was present. This study identified the lungs as target of heavy metals toxicity following oral exposure resulting in cellular damage, inflammation and fibrosis and increased risk of respiratory disease where Hg showed the greatest fibrotic effect, which was further, aggravated in combination with Cd. |
doi_str_mv | 10.1016/j.etap.2019.03.021 |
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Environmental presence and human exposure to heavy metals in air and cigarette smoke has led to a worldwide increase in respiratory disease. The effects of oral exposure to heavy metals in liver and kidney structure and function have been widely investigated and the respiratory system as a target is often overlooked. The aim of the study was to investigate the possible structural changes in the lung tissue of Sprague-Dawley rats after oral exposure for 28 days to cadmium (Cd) and mercury (Hg), alone and in combination at 1000 times the World Health Organization’s limit for each metal in drinking water. Following exposure, the general morphology of the bronchiole and lungs as well as collagen and elastin distribution was evaluated using histological techniques and transmission electron microscopy. In the lungs, structural changes to the alveoli included collapsed alveolar spaces, presence of inflammatory cells and thickening of the alveolar walls. In addition, exposure to Cd and Hg caused degeneration of the alveolar structures resulting in confluent alveoli. Changes in bronchiole morphology included an increase in smooth muscle mass with luminal epithelium degeneration, detachment and aggregation. Prominent bronchiole-associated lymphoid tissue was present in the group exposed to Cd and Hg. Ultrastructural examination confirmed the presence of fibrosis where in the Cd exposed group, collagen fibrils arrangement was dense, while in the Hg exposed group, additional prominent elastin was present. This study identified the lungs as target of heavy metals toxicity following oral exposure resulting in cellular damage, inflammation and fibrosis and increased risk of respiratory disease where Hg showed the greatest fibrotic effect, which was further, aggravated in combination with Cd.</description><identifier>ISSN: 1382-6689</identifier><identifier>EISSN: 1872-7077</identifier><identifier>DOI: 10.1016/j.etap.2019.03.021</identifier><identifier>PMID: 30981014</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Alveoli ; Animal tissues ; Cadmium ; Cigarette smoke ; Collagen ; Degeneration ; Drinking water ; Elastin ; Epithelium ; Exposure ; Fibrils ; Fibrosis ; Health risks ; Heavy metals ; Inflammation ; Kidneys ; Lungs ; Lymphoid tissue ; Mercury ; Mercury (metal) ; Metals ; Morphology ; Muscles ; Reactive oxygen species ; Respiratory diseases ; Respiratory system ; Rodents ; Smoke ; Smooth muscle ; Structure-function relationships ; Target recognition ; Thickening ; Toxicity ; Transmission electron microscopy</subject><ispartof>Environmental toxicology and pharmacology, 2019-07, Vol.69, p.86-94</ispartof><rights>2019 Elsevier B.V.</rights><rights>Copyright © 2019 Elsevier B.V. All rights reserved.</rights><rights>Copyright Elsevier Science Ltd. Jul 2019</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c384t-af5a3ff81640ef06afd0f9535f5e9268195006d069fd7047577692832d79f0263</citedby><cites>FETCH-LOGICAL-c384t-af5a3ff81640ef06afd0f9535f5e9268195006d069fd7047577692832d79f0263</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.etap.2019.03.021$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,777,781,3537,27905,27906,45976</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30981014$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Koopsamy Naidoo, Sirasha Venketsamy</creatorcontrib><creatorcontrib>Bester, Megan Jean</creatorcontrib><creatorcontrib>Arbi, Sandra</creatorcontrib><creatorcontrib>Venter, Chantelle</creatorcontrib><creatorcontrib>Dhanraj, Priyanka</creatorcontrib><creatorcontrib>Oberholzer, Hester Magdalena</creatorcontrib><title>Oral exposure to cadmium and mercury alone and in combination causes damage to the lung tissue of Sprague-Dawley rats</title><title>Environmental toxicology and pharmacology</title><addtitle>Environ Toxicol Pharmacol</addtitle><description>•Oral exposure to cadmium and mercury causes changes to the lung architecture.•Changes in bronchiole morphology included an increase in smooth muscle mass.•Luminal epithelium degeneration, detachment and aggregation.•Prominent bronchiole-associated lymphoid tissue was present in Cd and Hg.•Ultrastructural examination confirmed the presence of fibrosis.
Environmental presence and human exposure to heavy metals in air and cigarette smoke has led to a worldwide increase in respiratory disease. The effects of oral exposure to heavy metals in liver and kidney structure and function have been widely investigated and the respiratory system as a target is often overlooked. The aim of the study was to investigate the possible structural changes in the lung tissue of Sprague-Dawley rats after oral exposure for 28 days to cadmium (Cd) and mercury (Hg), alone and in combination at 1000 times the World Health Organization’s limit for each metal in drinking water. Following exposure, the general morphology of the bronchiole and lungs as well as collagen and elastin distribution was evaluated using histological techniques and transmission electron microscopy. In the lungs, structural changes to the alveoli included collapsed alveolar spaces, presence of inflammatory cells and thickening of the alveolar walls. In addition, exposure to Cd and Hg caused degeneration of the alveolar structures resulting in confluent alveoli. Changes in bronchiole morphology included an increase in smooth muscle mass with luminal epithelium degeneration, detachment and aggregation. Prominent bronchiole-associated lymphoid tissue was present in the group exposed to Cd and Hg. Ultrastructural examination confirmed the presence of fibrosis where in the Cd exposed group, collagen fibrils arrangement was dense, while in the Hg exposed group, additional prominent elastin was present. This study identified the lungs as target of heavy metals toxicity following oral exposure resulting in cellular damage, inflammation and fibrosis and increased risk of respiratory disease where Hg showed the greatest fibrotic effect, which was further, aggravated in combination with Cd.</description><subject>Alveoli</subject><subject>Animal tissues</subject><subject>Cadmium</subject><subject>Cigarette smoke</subject><subject>Collagen</subject><subject>Degeneration</subject><subject>Drinking water</subject><subject>Elastin</subject><subject>Epithelium</subject><subject>Exposure</subject><subject>Fibrils</subject><subject>Fibrosis</subject><subject>Health risks</subject><subject>Heavy metals</subject><subject>Inflammation</subject><subject>Kidneys</subject><subject>Lungs</subject><subject>Lymphoid tissue</subject><subject>Mercury</subject><subject>Mercury (metal)</subject><subject>Metals</subject><subject>Morphology</subject><subject>Muscles</subject><subject>Reactive oxygen species</subject><subject>Respiratory diseases</subject><subject>Respiratory system</subject><subject>Rodents</subject><subject>Smoke</subject><subject>Smooth muscle</subject><subject>Structure-function relationships</subject><subject>Target recognition</subject><subject>Thickening</subject><subject>Toxicity</subject><subject>Transmission electron microscopy</subject><issn>1382-6689</issn><issn>1872-7077</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNp9kEuP1DAQhC0EYh_wBzggS5wT2nZixxIXtMtLWmkPwNnyxu3BoyQOdrww_x7PzsKRU5daVdXqj5BXDFoGTL7dt7jZteXAdAuiBc6ekHM2KN4oUOpp1WLgjZSDPiMXOe8BWC_E8JycCdBDrejOSblNdqL4e425JKRbpKN1cygztYujM6axpAO1U1zwYRMWOsb5Lix2C7FqWzJm6uxsdw_p7QfSqSw7uoWcC9Lo6dc12V3B5tr-mvBAk93yC_LM2ynjy8d5Sb5__PDt6nNzc_vpy9X7m2YUQ7c11vdWeD8w2QF6kNY78LoXve9Rczkw3QNIB1J7p6BTvVJS80Fwp7QHLsUleXPqXVP8WTBvZh9LWupJw3mnleg6xauLn1xjijkn9GZNYbbpYBiYI2mzN0fS5kjagDCVdA29fqwudzO6f5G_aKvh3cmA9cH7gMnkMeAyogsJx824GP7X_wevE48Z</recordid><startdate>20190701</startdate><enddate>20190701</enddate><creator>Koopsamy Naidoo, Sirasha Venketsamy</creator><creator>Bester, Megan Jean</creator><creator>Arbi, Sandra</creator><creator>Venter, Chantelle</creator><creator>Dhanraj, Priyanka</creator><creator>Oberholzer, Hester Magdalena</creator><general>Elsevier B.V</general><general>Elsevier Science Ltd</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>7ST</scope><scope>7TK</scope><scope>7U7</scope><scope>C1K</scope><scope>SOI</scope></search><sort><creationdate>20190701</creationdate><title>Oral exposure to cadmium and mercury alone and in combination causes damage to the lung tissue of Sprague-Dawley rats</title><author>Koopsamy Naidoo, Sirasha Venketsamy ; Bester, Megan Jean ; Arbi, Sandra ; Venter, Chantelle ; Dhanraj, Priyanka ; Oberholzer, Hester Magdalena</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c384t-af5a3ff81640ef06afd0f9535f5e9268195006d069fd7047577692832d79f0263</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Alveoli</topic><topic>Animal tissues</topic><topic>Cadmium</topic><topic>Cigarette smoke</topic><topic>Collagen</topic><topic>Degeneration</topic><topic>Drinking water</topic><topic>Elastin</topic><topic>Epithelium</topic><topic>Exposure</topic><topic>Fibrils</topic><topic>Fibrosis</topic><topic>Health risks</topic><topic>Heavy metals</topic><topic>Inflammation</topic><topic>Kidneys</topic><topic>Lungs</topic><topic>Lymphoid tissue</topic><topic>Mercury</topic><topic>Mercury (metal)</topic><topic>Metals</topic><topic>Morphology</topic><topic>Muscles</topic><topic>Reactive oxygen species</topic><topic>Respiratory diseases</topic><topic>Respiratory system</topic><topic>Rodents</topic><topic>Smoke</topic><topic>Smooth muscle</topic><topic>Structure-function relationships</topic><topic>Target recognition</topic><topic>Thickening</topic><topic>Toxicity</topic><topic>Transmission electron microscopy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Koopsamy Naidoo, Sirasha Venketsamy</creatorcontrib><creatorcontrib>Bester, Megan Jean</creatorcontrib><creatorcontrib>Arbi, Sandra</creatorcontrib><creatorcontrib>Venter, Chantelle</creatorcontrib><creatorcontrib>Dhanraj, Priyanka</creatorcontrib><creatorcontrib>Oberholzer, Hester Magdalena</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Environment Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Environment Abstracts</collection><jtitle>Environmental toxicology and pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Koopsamy Naidoo, Sirasha Venketsamy</au><au>Bester, Megan Jean</au><au>Arbi, Sandra</au><au>Venter, Chantelle</au><au>Dhanraj, Priyanka</au><au>Oberholzer, Hester Magdalena</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Oral exposure to cadmium and mercury alone and in combination causes damage to the lung tissue of Sprague-Dawley rats</atitle><jtitle>Environmental toxicology and pharmacology</jtitle><addtitle>Environ Toxicol Pharmacol</addtitle><date>2019-07-01</date><risdate>2019</risdate><volume>69</volume><spage>86</spage><epage>94</epage><pages>86-94</pages><issn>1382-6689</issn><eissn>1872-7077</eissn><abstract>•Oral exposure to cadmium and mercury causes changes to the lung architecture.•Changes in bronchiole morphology included an increase in smooth muscle mass.•Luminal epithelium degeneration, detachment and aggregation.•Prominent bronchiole-associated lymphoid tissue was present in Cd and Hg.•Ultrastructural examination confirmed the presence of fibrosis.
Environmental presence and human exposure to heavy metals in air and cigarette smoke has led to a worldwide increase in respiratory disease. The effects of oral exposure to heavy metals in liver and kidney structure and function have been widely investigated and the respiratory system as a target is often overlooked. The aim of the study was to investigate the possible structural changes in the lung tissue of Sprague-Dawley rats after oral exposure for 28 days to cadmium (Cd) and mercury (Hg), alone and in combination at 1000 times the World Health Organization’s limit for each metal in drinking water. Following exposure, the general morphology of the bronchiole and lungs as well as collagen and elastin distribution was evaluated using histological techniques and transmission electron microscopy. In the lungs, structural changes to the alveoli included collapsed alveolar spaces, presence of inflammatory cells and thickening of the alveolar walls. In addition, exposure to Cd and Hg caused degeneration of the alveolar structures resulting in confluent alveoli. Changes in bronchiole morphology included an increase in smooth muscle mass with luminal epithelium degeneration, detachment and aggregation. Prominent bronchiole-associated lymphoid tissue was present in the group exposed to Cd and Hg. Ultrastructural examination confirmed the presence of fibrosis where in the Cd exposed group, collagen fibrils arrangement was dense, while in the Hg exposed group, additional prominent elastin was present. This study identified the lungs as target of heavy metals toxicity following oral exposure resulting in cellular damage, inflammation and fibrosis and increased risk of respiratory disease where Hg showed the greatest fibrotic effect, which was further, aggravated in combination with Cd.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>30981014</pmid><doi>10.1016/j.etap.2019.03.021</doi><tpages>9</tpages></addata></record> |
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subjects | Alveoli Animal tissues Cadmium Cigarette smoke Collagen Degeneration Drinking water Elastin Epithelium Exposure Fibrils Fibrosis Health risks Heavy metals Inflammation Kidneys Lungs Lymphoid tissue Mercury Mercury (metal) Metals Morphology Muscles Reactive oxygen species Respiratory diseases Respiratory system Rodents Smoke Smooth muscle Structure-function relationships Target recognition Thickening Toxicity Transmission electron microscopy |
title | Oral exposure to cadmium and mercury alone and in combination causes damage to the lung tissue of Sprague-Dawley rats |
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