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Ocular injury by transient formaldehyde exposure in a rabbit eye model
Formaldehyde (FA) is frequently used in sterilizing surgical instruments and materials. Exposure to FA is highly concerned for eye tissues. Rabbit corneal epithelial cells were examined for changes after FA exposure. Our results showed that cell survival decreased 7 days after transient 3 min exposu...
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Published in: | PloS one 2013-06, Vol.8 (6), p.e66649 |
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description | Formaldehyde (FA) is frequently used in sterilizing surgical instruments and materials. Exposure to FA is highly concerned for eye tissues. Rabbit corneal epithelial cells were examined for changes after FA exposure. Our results showed that cell survival decreased 7 days after transient 3 min exposure to more than 100 ppm FA by trypan blue staining while MTT assay detected significant decrease at 20 ppm at 24 hours observation. The decrease of cell survival rate was concentration (up to 600 ppm)- and observation time (1-7 day)- dependent. The cell number decreased after 100 ppm FA exposure for more than 10 min at 7-day observation. The FA treated cells showed increased apoptosis/necrosis and cell cycle accumulation at sub G1 phase as well as mitochondria clustering around nucleus. The in vivo rabbit eye exposure for tear production by Schirmer's test revealed that the FA-induced overproduction of tear also exhibited observation time (1-10 day)- and FA concentration (20-300 ppm for 5 min exposure)-dependent. Activated extracellular signal-regulated kinase (pERK2) in cornea explants by western blotting was reduced and increased c-Jun amino - terminal kinase (JNK) activation (pJNK) in cornea and conjunctiva was evident at 2 month after exposure to 50-200 ppm FA for 5 min. In conclusion, injury to the eye with transient exposure of up to 100 ppm FA for 3 min decreased corneal cell survival while a more sensitive MTT test detected the cell decrease at 20 ppm FA exposure. Morphology changes can be observed even at 5 ppm FA exposure for 3 min at 7 days after. The FA exposure also increased apoptotic/necrotic cells and sub-G1 phase in cell cycle. Long term effect (2 months after exposure) on the eye tissues even after the removal of FA can be observed with persistent JNK activation in cornea and conjunctiva. |
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Exposure to FA is highly concerned for eye tissues. Rabbit corneal epithelial cells were examined for changes after FA exposure. Our results showed that cell survival decreased 7 days after transient 3 min exposure to more than 100 ppm FA by trypan blue staining while MTT assay detected significant decrease at 20 ppm at 24 hours observation. The decrease of cell survival rate was concentration (up to 600 ppm)- and observation time (1-7 day)- dependent. The cell number decreased after 100 ppm FA exposure for more than 10 min at 7-day observation. The FA treated cells showed increased apoptosis/necrosis and cell cycle accumulation at sub G1 phase as well as mitochondria clustering around nucleus. The in vivo rabbit eye exposure for tear production by Schirmer's test revealed that the FA-induced overproduction of tear also exhibited observation time (1-10 day)- and FA concentration (20-300 ppm for 5 min exposure)-dependent. Activated extracellular signal-regulated kinase (pERK2) in cornea explants by western blotting was reduced and increased c-Jun amino - terminal kinase (JNK) activation (pJNK) in cornea and conjunctiva was evident at 2 month after exposure to 50-200 ppm FA for 5 min. In conclusion, injury to the eye with transient exposure of up to 100 ppm FA for 3 min decreased corneal cell survival while a more sensitive MTT test detected the cell decrease at 20 ppm FA exposure. Morphology changes can be observed even at 5 ppm FA exposure for 3 min at 7 days after. The FA exposure also increased apoptotic/necrotic cells and sub-G1 phase in cell cycle. Long term effect (2 months after exposure) on the eye tissues even after the removal of FA can be observed with persistent JNK activation in cornea and conjunctiva.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0066649</identifier><identifier>PMID: 23818956</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Activation ; Animals ; Apoptosis ; Apoptosis - drug effects ; Biology ; Blotting, Western ; Cell cycle ; Cell number ; Cell survival ; Cell Survival - drug effects ; Clustering ; Conjunctiva ; Conjunctiva - drug effects ; Conjunctiva - metabolism ; Conjunctiva - pathology ; Cornea ; Cornea - drug effects ; Cornea - metabolism ; Cornea - pathology ; Cytology ; Disinfectants - toxicity ; Dose-Response Relationship, Drug ; Epithelial cells ; Epithelial Cells - drug effects ; Epithelial Cells - metabolism ; Epithelial Cells - pathology ; Explants ; Exposure ; Extracellular signal-regulated kinase ; Eye ; Eye injuries ; Eye Injuries - chemically induced ; Eye Injuries - metabolism ; Formaldehyde ; Formaldehyde - toxicity ; G1 phase ; G1 Phase Cell Cycle Checkpoints - drug effects ; In vivo methods and tests ; JNK Mitogen-Activated Protein Kinases - metabolism ; JNK protein ; Kinases ; Laboratory animals ; Medical instruments ; Medical laboratories ; Medicine ; Mitochondria ; Mitogen-Activated Protein Kinase 1 - metabolism ; Morphology ; Nuclei ; Penicillin ; Proteins ; Rabbits ; Surgery ; Surgical equipment ; Surgical instruments ; Survival ; Tao Yuan ; Tearing ; Tears - drug effects ; Time Factors ; Tissues ; Transcription factors ; Western blotting</subject><ispartof>PloS one, 2013-06, Vol.8 (6), p.e66649</ispartof><rights>COPYRIGHT 2013 Public Library of Science</rights><rights>2013 Lai et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. 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Exposure to FA is highly concerned for eye tissues. Rabbit corneal epithelial cells were examined for changes after FA exposure. Our results showed that cell survival decreased 7 days after transient 3 min exposure to more than 100 ppm FA by trypan blue staining while MTT assay detected significant decrease at 20 ppm at 24 hours observation. The decrease of cell survival rate was concentration (up to 600 ppm)- and observation time (1-7 day)- dependent. The cell number decreased after 100 ppm FA exposure for more than 10 min at 7-day observation. The FA treated cells showed increased apoptosis/necrosis and cell cycle accumulation at sub G1 phase as well as mitochondria clustering around nucleus. The in vivo rabbit eye exposure for tear production by Schirmer's test revealed that the FA-induced overproduction of tear also exhibited observation time (1-10 day)- and FA concentration (20-300 ppm for 5 min exposure)-dependent. Activated extracellular signal-regulated kinase (pERK2) in cornea explants by western blotting was reduced and increased c-Jun amino - terminal kinase (JNK) activation (pJNK) in cornea and conjunctiva was evident at 2 month after exposure to 50-200 ppm FA for 5 min. In conclusion, injury to the eye with transient exposure of up to 100 ppm FA for 3 min decreased corneal cell survival while a more sensitive MTT test detected the cell decrease at 20 ppm FA exposure. Morphology changes can be observed even at 5 ppm FA exposure for 3 min at 7 days after. The FA exposure also increased apoptotic/necrotic cells and sub-G1 phase in cell cycle. Long term effect (2 months after exposure) on the eye tissues even after the removal of FA can be observed with persistent JNK activation in cornea and conjunctiva.</description><subject>Activation</subject><subject>Animals</subject><subject>Apoptosis</subject><subject>Apoptosis - drug effects</subject><subject>Biology</subject><subject>Blotting, Western</subject><subject>Cell cycle</subject><subject>Cell number</subject><subject>Cell survival</subject><subject>Cell Survival - drug effects</subject><subject>Clustering</subject><subject>Conjunctiva</subject><subject>Conjunctiva - drug effects</subject><subject>Conjunctiva - metabolism</subject><subject>Conjunctiva - pathology</subject><subject>Cornea</subject><subject>Cornea - drug effects</subject><subject>Cornea - metabolism</subject><subject>Cornea - pathology</subject><subject>Cytology</subject><subject>Disinfectants - toxicity</subject><subject>Dose-Response Relationship, Drug</subject><subject>Epithelial cells</subject><subject>Epithelial Cells - drug effects</subject><subject>Epithelial Cells - metabolism</subject><subject>Epithelial Cells - pathology</subject><subject>Explants</subject><subject>Exposure</subject><subject>Extracellular signal-regulated kinase</subject><subject>Eye</subject><subject>Eye injuries</subject><subject>Eye Injuries - chemically induced</subject><subject>Eye Injuries - metabolism</subject><subject>Formaldehyde</subject><subject>Formaldehyde - toxicity</subject><subject>G1 phase</subject><subject>G1 Phase Cell Cycle Checkpoints - drug effects</subject><subject>In vivo methods and tests</subject><subject>JNK Mitogen-Activated Protein Kinases - metabolism</subject><subject>JNK protein</subject><subject>Kinases</subject><subject>Laboratory animals</subject><subject>Medical instruments</subject><subject>Medical laboratories</subject><subject>Medicine</subject><subject>Mitochondria</subject><subject>Mitogen-Activated Protein Kinase 1 - metabolism</subject><subject>Morphology</subject><subject>Nuclei</subject><subject>Penicillin</subject><subject>Proteins</subject><subject>Rabbits</subject><subject>Surgery</subject><subject>Surgical equipment</subject><subject>Surgical instruments</subject><subject>Survival</subject><subject>Tao Yuan</subject><subject>Tearing</subject><subject>Tears - drug effects</subject><subject>Time Factors</subject><subject>Tissues</subject><subject>Transcription factors</subject><subject>Western blotting</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNqNkl1r2zAUhs3YWLtu_2BshkFhF8n0ZUW6GZTSboFCYF-34lg-ThRsK5Ps0fz7KYtbYthg6ELi6Dmvjl7eLHtNyZzyBf2w9UPooJnvfIdzQqSUQj_JzqnmbCYZ4U9PzmfZixi3hBRcSfk8O2NcUaULeZ7druzQQMhdtx3CPi_3eR-giw67Pq99aKGpcLOvMMf7nY9DwETmkAcoS9fnuMe89RU2L7NnNTQRX437Rfb99ubb9efZ3erT8vrqbmalZv0MBK2RlJICL0WlKCzqhbSqWGiOomCqEHXBkFRYIdGK11xZJQVlCsrEKMovsrdH3V3joxktiCYZQqjiSrNELI9E5WFrdsG1EPbGgzN_Cj6sDYTe2QYNgVKWjGqUSIXWCJXVZVETTlmasOBJ6-P42lC2WNlkSoBmIjq96dzGrP0vw6VShRZJ4N0oEPzPAWP_j5FHag1pKtfVPonZ1kVrrsRCUc0EO2jN_0KlVWHrbApB7VJ90vB-0pCYHu_7NQwxmuXXL__Prn5M2csTdoPQ9Jvom6F3votTUBxBG3yMAetH5yg5_J8-uGEOGTZjhlPbm1PXH5seQst_A1-160A</recordid><startdate>20130620</startdate><enddate>20130620</enddate><creator>Lai, Li-Ju</creator><creator>Hsu, Wei-Hsiu</creator><creator>Wu, Albert M</creator><creator>Wu, June H</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>IOV</scope><scope>ISR</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20130620</creationdate><title>Ocular injury by transient formaldehyde exposure in a rabbit eye model</title><author>Lai, Li-Ju ; Hsu, Wei-Hsiu ; Wu, Albert M ; Wu, June H</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c692t-a41fe0b61a3b4d81a7f76c85793e452854f52e0dede0983f38c864128ab579813</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Activation</topic><topic>Animals</topic><topic>Apoptosis</topic><topic>Apoptosis - drug effects</topic><topic>Biology</topic><topic>Blotting, Western</topic><topic>Cell cycle</topic><topic>Cell number</topic><topic>Cell survival</topic><topic>Cell Survival - drug effects</topic><topic>Clustering</topic><topic>Conjunctiva</topic><topic>Conjunctiva - drug effects</topic><topic>Conjunctiva - metabolism</topic><topic>Conjunctiva - pathology</topic><topic>Cornea</topic><topic>Cornea - drug effects</topic><topic>Cornea - metabolism</topic><topic>Cornea - pathology</topic><topic>Cytology</topic><topic>Disinfectants - toxicity</topic><topic>Dose-Response Relationship, Drug</topic><topic>Epithelial cells</topic><topic>Epithelial Cells - drug effects</topic><topic>Epithelial Cells - metabolism</topic><topic>Epithelial Cells - pathology</topic><topic>Explants</topic><topic>Exposure</topic><topic>Extracellular signal-regulated kinase</topic><topic>Eye</topic><topic>Eye injuries</topic><topic>Eye Injuries - chemically induced</topic><topic>Eye Injuries - metabolism</topic><topic>Formaldehyde</topic><topic>Formaldehyde - 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Exposure to FA is highly concerned for eye tissues. Rabbit corneal epithelial cells were examined for changes after FA exposure. Our results showed that cell survival decreased 7 days after transient 3 min exposure to more than 100 ppm FA by trypan blue staining while MTT assay detected significant decrease at 20 ppm at 24 hours observation. The decrease of cell survival rate was concentration (up to 600 ppm)- and observation time (1-7 day)- dependent. The cell number decreased after 100 ppm FA exposure for more than 10 min at 7-day observation. The FA treated cells showed increased apoptosis/necrosis and cell cycle accumulation at sub G1 phase as well as mitochondria clustering around nucleus. The in vivo rabbit eye exposure for tear production by Schirmer's test revealed that the FA-induced overproduction of tear also exhibited observation time (1-10 day)- and FA concentration (20-300 ppm for 5 min exposure)-dependent. Activated extracellular signal-regulated kinase (pERK2) in cornea explants by western blotting was reduced and increased c-Jun amino - terminal kinase (JNK) activation (pJNK) in cornea and conjunctiva was evident at 2 month after exposure to 50-200 ppm FA for 5 min. In conclusion, injury to the eye with transient exposure of up to 100 ppm FA for 3 min decreased corneal cell survival while a more sensitive MTT test detected the cell decrease at 20 ppm FA exposure. Morphology changes can be observed even at 5 ppm FA exposure for 3 min at 7 days after. The FA exposure also increased apoptotic/necrotic cells and sub-G1 phase in cell cycle. Long term effect (2 months after exposure) on the eye tissues even after the removal of FA can be observed with persistent JNK activation in cornea and conjunctiva.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>23818956</pmid><doi>10.1371/journal.pone.0066649</doi><tpages>e66649</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Activation Animals Apoptosis Apoptosis - drug effects Biology Blotting, Western Cell cycle Cell number Cell survival Cell Survival - drug effects Clustering Conjunctiva Conjunctiva - drug effects Conjunctiva - metabolism Conjunctiva - pathology Cornea Cornea - drug effects Cornea - metabolism Cornea - pathology Cytology Disinfectants - toxicity Dose-Response Relationship, Drug Epithelial cells Epithelial Cells - drug effects Epithelial Cells - metabolism Epithelial Cells - pathology Explants Exposure Extracellular signal-regulated kinase Eye Eye injuries Eye Injuries - chemically induced Eye Injuries - metabolism Formaldehyde Formaldehyde - toxicity G1 phase G1 Phase Cell Cycle Checkpoints - drug effects In vivo methods and tests JNK Mitogen-Activated Protein Kinases - metabolism JNK protein Kinases Laboratory animals Medical instruments Medical laboratories Medicine Mitochondria Mitogen-Activated Protein Kinase 1 - metabolism Morphology Nuclei Penicillin Proteins Rabbits Surgery Surgical equipment Surgical instruments Survival Tao Yuan Tearing Tears - drug effects Time Factors Tissues Transcription factors Western blotting |
title | Ocular injury by transient formaldehyde exposure in a rabbit eye model |
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