Temporal Changes in Rat Liver Gene Expression after Acute Cadmium and Chromium Exposure
U.S. Service Members and civilians are at risk of exposure to a variety of environmental health hazards throughout their normal duty activities and in industrial occupations. Metals are widely used in large quantities in a number of industrial processes and are a common environmental toxicant, which...
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creator | Madejczyk, Michael S Baer, Christine E Dennis, William E Minarchick, Valerie C Leonard, Stephen S Jackson, David A Stallings, Jonathan D Lewis, John A |
description | U.S. Service Members and civilians are at risk of exposure to a variety of environmental health hazards throughout their normal duty activities and in industrial occupations. Metals are widely used in large quantities in a number of industrial processes and are a common environmental toxicant, which increases the possibility of being exposed at toxic levels. While metal toxicity has been widely studied, the exact mechanisms of toxicity remain unclear. In order to further elucidate these mechanisms and identify candidate biomarkers, rats were exposed via a single intraperitoneal injection to three concentrations of CdCl2 and Na2Cr2O7, with livers harvested at 1, 3, or 7 days after exposure. Cd and Cr accumulated in the liver at 1 day post exposure. Cd levels remained elevated over the length of the experiment, while Cr levels declined. Metal exposures induced ROS, including hydroxyl radical (OH), resulting in DNA strand breaks and lipid peroxidation. Interestingly, ROS and cellular damage appeared to increase with time post-exposure in both metals, despite declines in Cr levels. Differentially expressed genes were identified via microarray analysis. Both met- als perturbed gene expression in pathways related to oxidative stress, metabolism, DNA damage, cell cycle, and inflammatory response. This work provides insight into the temporal effects and mechanistic pathways involved in acute metal intoxication, leading to the identification of candidate biomarkers.
Published in PLoS One, v10 n5 article e0127327 p1-27, 18 May 2015. |
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Published in PLoS One, v10 n5 article e0127327 p1-27, 18 May 2015.</description><subject>AMINO ACIDS</subject><subject>BIOMAKERS</subject><subject>CADMIUM</subject><subject>CELL CYCLES</subject><subject>CELLS(BIOLOGY)</subject><subject>CHROMIUM</subject><subject>CLINICAL MEDICINE</subject><subject>DEOXYRIBONUCLEIC ACIDS</subject><subject>DNA DAMAGE</subject><subject>EXPERIMENTAL DESIGN</subject><subject>EXPOSURE(PHYSIOLOGY)</subject><subject>GENE EXPRESSION</subject><subject>HYDROXYL RADICALS</subject><subject>INFLAMMATION</subject><subject>INTRAMUSCULAR INJECTIONS</subject><subject>LIVER</subject><subject>Medicine and Medical Research</subject><subject>METABOLISM</subject><subject>MICROARRAY ANALYSIS</subject><subject>OXIDATION</subject><subject>PERITONEUM</subject><subject>PERTURBATIONS</subject><subject>PHYSIOLOGICAL EFFECTS</subject><subject>RATS</subject><subject>RESPONSE(BIOLOGY)</subject><subject>RISK</subject><subject>Stress Physiology</subject><subject>TOXICITY</subject><subject>Toxicology</subject><subject>TRACER STUDIES</subject><fulltext>true</fulltext><rsrctype>report</rsrctype><creationdate>2015</creationdate><recordtype>report</recordtype><sourceid>1RU</sourceid><recordid>eNrjZAgPSc0tyC9KzFFwzkjMS08tVsjMUwhKLFHwySxLLVJwT81LVXCtKChKLS7OzM9TSEwrAYo6JpeWpCo4J6bkZpbmKiTmpQA1F-WDOUC1-cWlRak8DKxpiTnFqbxQmptBxs01xNlDN6UkMzm-uCQzL7Uk3tHF0czIyNTC2JiANAChIzYw</recordid><startdate>20150519</startdate><enddate>20150519</enddate><creator>Madejczyk, Michael S</creator><creator>Baer, Christine E</creator><creator>Dennis, William E</creator><creator>Minarchick, Valerie C</creator><creator>Leonard, Stephen S</creator><creator>Jackson, David A</creator><creator>Stallings, Jonathan D</creator><creator>Lewis, John A</creator><scope>1RU</scope><scope>BHM</scope></search><sort><creationdate>20150519</creationdate><title>Temporal Changes in Rat Liver Gene Expression after Acute Cadmium and Chromium Exposure</title><author>Madejczyk, Michael S ; Baer, Christine E ; Dennis, William E ; Minarchick, Valerie C ; Leonard, Stephen S ; Jackson, David A ; Stallings, Jonathan D ; Lewis, John A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-dtic_stinet_ADA6225833</frbrgroupid><rsrctype>reports</rsrctype><prefilter>reports</prefilter><language>eng</language><creationdate>2015</creationdate><topic>AMINO ACIDS</topic><topic>BIOMAKERS</topic><topic>CADMIUM</topic><topic>CELL CYCLES</topic><topic>CELLS(BIOLOGY)</topic><topic>CHROMIUM</topic><topic>CLINICAL MEDICINE</topic><topic>DEOXYRIBONUCLEIC ACIDS</topic><topic>DNA DAMAGE</topic><topic>EXPERIMENTAL DESIGN</topic><topic>EXPOSURE(PHYSIOLOGY)</topic><topic>GENE EXPRESSION</topic><topic>HYDROXYL RADICALS</topic><topic>INFLAMMATION</topic><topic>INTRAMUSCULAR INJECTIONS</topic><topic>LIVER</topic><topic>Medicine and Medical Research</topic><topic>METABOLISM</topic><topic>MICROARRAY ANALYSIS</topic><topic>OXIDATION</topic><topic>PERITONEUM</topic><topic>PERTURBATIONS</topic><topic>PHYSIOLOGICAL EFFECTS</topic><topic>RATS</topic><topic>RESPONSE(BIOLOGY)</topic><topic>RISK</topic><topic>Stress Physiology</topic><topic>TOXICITY</topic><topic>Toxicology</topic><topic>TRACER STUDIES</topic><toplevel>online_resources</toplevel><creatorcontrib>Madejczyk, Michael S</creatorcontrib><creatorcontrib>Baer, Christine E</creatorcontrib><creatorcontrib>Dennis, William E</creatorcontrib><creatorcontrib>Minarchick, Valerie C</creatorcontrib><creatorcontrib>Leonard, Stephen S</creatorcontrib><creatorcontrib>Jackson, David A</creatorcontrib><creatorcontrib>Stallings, Jonathan D</creatorcontrib><creatorcontrib>Lewis, John A</creatorcontrib><creatorcontrib>ARMY CENTER FOR ENVIRONMENTAL HEALTH RESEARCH FORT DETRICK MD</creatorcontrib><collection>DTIC Technical Reports</collection><collection>DTIC STINET</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Madejczyk, Michael S</au><au>Baer, Christine E</au><au>Dennis, William E</au><au>Minarchick, Valerie C</au><au>Leonard, Stephen S</au><au>Jackson, David A</au><au>Stallings, Jonathan D</au><au>Lewis, John A</au><aucorp>ARMY CENTER FOR ENVIRONMENTAL HEALTH RESEARCH FORT DETRICK MD</aucorp><format>book</format><genre>unknown</genre><ristype>RPRT</ristype><btitle>Temporal Changes in Rat Liver Gene Expression after Acute Cadmium and Chromium Exposure</btitle><date>2015-05-19</date><risdate>2015</risdate><abstract>U.S. Service Members and civilians are at risk of exposure to a variety of environmental health hazards throughout their normal duty activities and in industrial occupations. Metals are widely used in large quantities in a number of industrial processes and are a common environmental toxicant, which increases the possibility of being exposed at toxic levels. While metal toxicity has been widely studied, the exact mechanisms of toxicity remain unclear. In order to further elucidate these mechanisms and identify candidate biomarkers, rats were exposed via a single intraperitoneal injection to three concentrations of CdCl2 and Na2Cr2O7, with livers harvested at 1, 3, or 7 days after exposure. Cd and Cr accumulated in the liver at 1 day post exposure. Cd levels remained elevated over the length of the experiment, while Cr levels declined. Metal exposures induced ROS, including hydroxyl radical (OH), resulting in DNA strand breaks and lipid peroxidation. Interestingly, ROS and cellular damage appeared to increase with time post-exposure in both metals, despite declines in Cr levels. Differentially expressed genes were identified via microarray analysis. Both met- als perturbed gene expression in pathways related to oxidative stress, metabolism, DNA damage, cell cycle, and inflammatory response. This work provides insight into the temporal effects and mechanistic pathways involved in acute metal intoxication, leading to the identification of candidate biomarkers.
Published in PLoS One, v10 n5 article e0127327 p1-27, 18 May 2015.</abstract><oa>free_for_read</oa></addata></record> |
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subjects | AMINO ACIDS BIOMAKERS CADMIUM CELL CYCLES CELLS(BIOLOGY) CHROMIUM CLINICAL MEDICINE DEOXYRIBONUCLEIC ACIDS DNA DAMAGE EXPERIMENTAL DESIGN EXPOSURE(PHYSIOLOGY) GENE EXPRESSION HYDROXYL RADICALS INFLAMMATION INTRAMUSCULAR INJECTIONS LIVER Medicine and Medical Research METABOLISM MICROARRAY ANALYSIS OXIDATION PERITONEUM PERTURBATIONS PHYSIOLOGICAL EFFECTS RATS RESPONSE(BIOLOGY) RISK Stress Physiology TOXICITY Toxicology TRACER STUDIES |
title | Temporal Changes in Rat Liver Gene Expression after Acute Cadmium and Chromium Exposure |
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