Loading…

Methanesulfonic acid sodium salt protects retina from acute light damage in mice

Background Methanesulfonic acid sodium salt (Dipyrone), an antipyretic and analgesic drug, has been demonstrated to improve cerebral ischemia through the inhibition of mitochondrial cell death cascades. The aim of this study was to evaluate the potential photoprotective activity of methanesulfonic a...

Full description

Saved in:
Bibliographic Details
Published in:Chinese medical journal 2012-07, Vol.125 (13), p.2310-2315
Main Authors: Wang, Hai-Yan, Gu, Qing, Xu, Xun
Format: Article
Language:English
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by
cites
container_end_page 2315
container_issue 13
container_start_page 2310
container_title Chinese medical journal
container_volume 125
creator Wang, Hai-Yan
Gu, Qing
Xu, Xun
description Background Methanesulfonic acid sodium salt (Dipyrone), an antipyretic and analgesic drug, has been demonstrated to improve cerebral ischemia through the inhibition of mitochondrial cell death cascades. The aim of this study was to evaluate the potential photoprotective activity of methanesulfonic acid sodium salt in a model of light-induced retinopathy. Methods One hundred mice were assigned randomly into vehicle (V), methanesulfonic acid sodium salt (D), light damage model plus vehicle (MV) and light damage model plus methanesulfonic acid sodium salt (MD) groups (n=25 each). In the MD group, methanesulfonic acid sodium salt (100 mg/kg) was administered by intraperitoneal injection 30 minutes before light exposure. Twenty-four hours after light exposure, hematoxylin and eosin staining and transmission electron microscopy (TEM) were used for histological evaluation. The thickness of the outer plus inner-segment and outer nuclear layer was measured on sections parallel to the vertical meridian of the eye at a distance of 1000 I~m from the optic nerve. Electroretinography (ERG) test was performed to assess the functional change. The morphology of mitochondria was also revealed by TEM. Finally, the expression of cytochrome c (CytC) and the relative apoptotic proteins were detected by Western blotting, and the interaction between mitochondrial proteins was investigated by co-immunoprecipitation. Results The photoreceptor inner and outer segments of the MV group were significantly disorganized than the MD group. The thicknesses of the outer plus inner-segment layers and the outer nuclear layer, and the amplitudes of the a and b waves of the scotopic ERG response markedly decreased in the MV group compared to those in the MD group (P 〈0.05). TEM examination revealed that the mitochondria of the MV group were distinctly swollen and contained disrupted cristae. In contrast, the morphology of mitochondria in the MD group was unaffected. Western blotting analysis showed that CytC, apoptosis proteinase activating factor-1 (Apaf-1), caspase 3, p53, p53-upregulated modulator of apoptosis (PUMA), Bax, and Bad were increased, whereas the anti-apoptotic proteins Bcl-2 and Bcl-XL were significantly decreased in the MV group than the MD group. Co-immunoprecipitation detection revealed that PUMA immunoreactivity precipitated by Bcl-XL decreased, whereas Bax immunoreactivity precipitated by Bcl-XL increased in the MD group compared to those in the MV group. Conclusion Methane
doi_str_mv 10.3760/cma.j.issn.0366-6999.2012.13.013
format article
fullrecord <record><control><sourceid>wanfang_jour_proqu</sourceid><recordid>TN_cdi_wanfang_journals_zhcmj201213013</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><cqvip_id>42476787</cqvip_id><wanfj_id>zhcmj201213013</wanfj_id><sourcerecordid>zhcmj201213013</sourcerecordid><originalsourceid>FETCH-LOGICAL-c268t-10b96921352307ca64093ee3413550f335317914f0b1a9e2d542ea425d7e6f93</originalsourceid><addsrcrecordid>eNo90E1LxDAQBuAgiq4ff0HiRby0JpkkbY6y-AWKHryXbJruZmnS3SZF9Ncb2dXTwPAww_sidENJCZUkt8brcl26GENJQMpCKqVKRigrKZSEwgGaMcFZISSnh2j2b07QaYxrQpgQlTxGJ4zVNasFn6H3V5tWOtg49d0QnMHauBbHoXWTx1H3CW_GIVmTIh5tckHjbhx8VlOyuHfLVcKt9nppsQvYO2PP0VGn-2gv9vMMfTzcf8yfipe3x-f53UthmKxTQclCScUoCAakMlpyosBa4HkjSAcggFaK8o4sqFaWtTmW1ZyJtrKyU3CGrndnP3XodFg262EaQ37YfK-MX_92QiE3kuHNDuYc28nG1HgXje37HHqYYkMJABdSAsv0ck-nhbdtsxmd1-NX89dWBlc7YFZDWG5dfvtnOOOVrOoKfgClYnnd</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1033456632</pqid></control><display><type>article</type><title>Methanesulfonic acid sodium salt protects retina from acute light damage in mice</title><source>HEAL-Link subscriptions: Lippincott Williams &amp; Wilkins</source><creator>Wang, Hai-Yan ; Gu, Qing ; Xu, Xun</creator><creatorcontrib>Wang, Hai-Yan ; Gu, Qing ; Xu, Xun</creatorcontrib><description>Background Methanesulfonic acid sodium salt (Dipyrone), an antipyretic and analgesic drug, has been demonstrated to improve cerebral ischemia through the inhibition of mitochondrial cell death cascades. The aim of this study was to evaluate the potential photoprotective activity of methanesulfonic acid sodium salt in a model of light-induced retinopathy. Methods One hundred mice were assigned randomly into vehicle (V), methanesulfonic acid sodium salt (D), light damage model plus vehicle (MV) and light damage model plus methanesulfonic acid sodium salt (MD) groups (n=25 each). In the MD group, methanesulfonic acid sodium salt (100 mg/kg) was administered by intraperitoneal injection 30 minutes before light exposure. Twenty-four hours after light exposure, hematoxylin and eosin staining and transmission electron microscopy (TEM) were used for histological evaluation. The thickness of the outer plus inner-segment and outer nuclear layer was measured on sections parallel to the vertical meridian of the eye at a distance of 1000 I~m from the optic nerve. Electroretinography (ERG) test was performed to assess the functional change. The morphology of mitochondria was also revealed by TEM. Finally, the expression of cytochrome c (CytC) and the relative apoptotic proteins were detected by Western blotting, and the interaction between mitochondrial proteins was investigated by co-immunoprecipitation. Results The photoreceptor inner and outer segments of the MV group were significantly disorganized than the MD group. The thicknesses of the outer plus inner-segment layers and the outer nuclear layer, and the amplitudes of the a and b waves of the scotopic ERG response markedly decreased in the MV group compared to those in the MD group (P 〈0.05). TEM examination revealed that the mitochondria of the MV group were distinctly swollen and contained disrupted cristae. In contrast, the morphology of mitochondria in the MD group was unaffected. Western blotting analysis showed that CytC, apoptosis proteinase activating factor-1 (Apaf-1), caspase 3, p53, p53-upregulated modulator of apoptosis (PUMA), Bax, and Bad were increased, whereas the anti-apoptotic proteins Bcl-2 and Bcl-XL were significantly decreased in the MV group than the MD group. Co-immunoprecipitation detection revealed that PUMA immunoreactivity precipitated by Bcl-XL decreased, whereas Bax immunoreactivity precipitated by Bcl-XL increased in the MD group compared to those in the MV group. Conclusion Methanesulfonic acid sodium salt is an effective photoprotective agent against light-induced retinopathy through the inhibition of CytC-mediated mitochondrial impairment.</description><identifier>ISSN: 0366-6999</identifier><identifier>EISSN: 2542-5641</identifier><identifier>DOI: 10.3760/cma.j.issn.0366-6999.2012.13.013</identifier><identifier>PMID: 22882854</identifier><language>eng</language><publisher>China: Department of Ophthalmology, Shanghai First People's Hospital,Affiliate of Shanghai Jiao Tong University, Shanghai 200080,China</publisher><subject>Animals ; Apoptosis - drug effects ; Apoptosis - radiation effects ; BCL-XL ; Blotting, Western ; Electroretinography ; Immunoprecipitation ; Light - adverse effects ; Male ; Mesylates - therapeutic use ; Mice ; Microscopy, Electron, Transmission ; Mitochondrial Proteins - metabolism ; Random Allocation ; Retina - drug effects ; Retina - radiation effects ; Retina - ultrastructure ; Tumor Suppressor Protein p53 - metabolism ; 光保护剂 ; 光损伤 ; 小鼠 ; 甲磺酸 ; 线粒体蛋白质 ; 视网膜电图 ; 钠盐</subject><ispartof>Chinese medical journal, 2012-07, Vol.125 (13), p.2310-2315</ispartof><rights>Copyright © Wanfang Data Co. Ltd. All Rights Reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://image.cqvip.com/vip1000/qk/85656X/85656X.jpg</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22882854$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, Hai-Yan</creatorcontrib><creatorcontrib>Gu, Qing</creatorcontrib><creatorcontrib>Xu, Xun</creatorcontrib><title>Methanesulfonic acid sodium salt protects retina from acute light damage in mice</title><title>Chinese medical journal</title><addtitle>Chinese Medical Journal</addtitle><description>Background Methanesulfonic acid sodium salt (Dipyrone), an antipyretic and analgesic drug, has been demonstrated to improve cerebral ischemia through the inhibition of mitochondrial cell death cascades. The aim of this study was to evaluate the potential photoprotective activity of methanesulfonic acid sodium salt in a model of light-induced retinopathy. Methods One hundred mice were assigned randomly into vehicle (V), methanesulfonic acid sodium salt (D), light damage model plus vehicle (MV) and light damage model plus methanesulfonic acid sodium salt (MD) groups (n=25 each). In the MD group, methanesulfonic acid sodium salt (100 mg/kg) was administered by intraperitoneal injection 30 minutes before light exposure. Twenty-four hours after light exposure, hematoxylin and eosin staining and transmission electron microscopy (TEM) were used for histological evaluation. The thickness of the outer plus inner-segment and outer nuclear layer was measured on sections parallel to the vertical meridian of the eye at a distance of 1000 I~m from the optic nerve. Electroretinography (ERG) test was performed to assess the functional change. The morphology of mitochondria was also revealed by TEM. Finally, the expression of cytochrome c (CytC) and the relative apoptotic proteins were detected by Western blotting, and the interaction between mitochondrial proteins was investigated by co-immunoprecipitation. Results The photoreceptor inner and outer segments of the MV group were significantly disorganized than the MD group. The thicknesses of the outer plus inner-segment layers and the outer nuclear layer, and the amplitudes of the a and b waves of the scotopic ERG response markedly decreased in the MV group compared to those in the MD group (P 〈0.05). TEM examination revealed that the mitochondria of the MV group were distinctly swollen and contained disrupted cristae. In contrast, the morphology of mitochondria in the MD group was unaffected. Western blotting analysis showed that CytC, apoptosis proteinase activating factor-1 (Apaf-1), caspase 3, p53, p53-upregulated modulator of apoptosis (PUMA), Bax, and Bad were increased, whereas the anti-apoptotic proteins Bcl-2 and Bcl-XL were significantly decreased in the MV group than the MD group. Co-immunoprecipitation detection revealed that PUMA immunoreactivity precipitated by Bcl-XL decreased, whereas Bax immunoreactivity precipitated by Bcl-XL increased in the MD group compared to those in the MV group. Conclusion Methanesulfonic acid sodium salt is an effective photoprotective agent against light-induced retinopathy through the inhibition of CytC-mediated mitochondrial impairment.</description><subject>Animals</subject><subject>Apoptosis - drug effects</subject><subject>Apoptosis - radiation effects</subject><subject>BCL-XL</subject><subject>Blotting, Western</subject><subject>Electroretinography</subject><subject>Immunoprecipitation</subject><subject>Light - adverse effects</subject><subject>Male</subject><subject>Mesylates - therapeutic use</subject><subject>Mice</subject><subject>Microscopy, Electron, Transmission</subject><subject>Mitochondrial Proteins - metabolism</subject><subject>Random Allocation</subject><subject>Retina - drug effects</subject><subject>Retina - radiation effects</subject><subject>Retina - ultrastructure</subject><subject>Tumor Suppressor Protein p53 - metabolism</subject><subject>光保护剂</subject><subject>光损伤</subject><subject>小鼠</subject><subject>甲磺酸</subject><subject>线粒体蛋白质</subject><subject>视网膜电图</subject><subject>钠盐</subject><issn>0366-6999</issn><issn>2542-5641</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNo90E1LxDAQBuAgiq4ff0HiRby0JpkkbY6y-AWKHryXbJruZmnS3SZF9Ncb2dXTwPAww_sidENJCZUkt8brcl26GENJQMpCKqVKRigrKZSEwgGaMcFZISSnh2j2b07QaYxrQpgQlTxGJ4zVNasFn6H3V5tWOtg49d0QnMHauBbHoXWTx1H3CW_GIVmTIh5tckHjbhx8VlOyuHfLVcKt9nppsQvYO2PP0VGn-2gv9vMMfTzcf8yfipe3x-f53UthmKxTQclCScUoCAakMlpyosBa4HkjSAcggFaK8o4sqFaWtTmW1ZyJtrKyU3CGrndnP3XodFg262EaQ37YfK-MX_92QiE3kuHNDuYc28nG1HgXje37HHqYYkMJABdSAsv0ck-nhbdtsxmd1-NX89dWBlc7YFZDWG5dfvtnOOOVrOoKfgClYnnd</recordid><startdate>20120705</startdate><enddate>20120705</enddate><creator>Wang, Hai-Yan</creator><creator>Gu, Qing</creator><creator>Xu, Xun</creator><general>Department of Ophthalmology, Shanghai First People's Hospital,Affiliate of Shanghai Jiao Tong University, Shanghai 200080,China</general><scope>2RA</scope><scope>92L</scope><scope>CQIGP</scope><scope>W91</scope><scope>~WA</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope><scope>2B.</scope><scope>4A8</scope><scope>92I</scope><scope>93N</scope><scope>PSX</scope><scope>TCJ</scope></search><sort><creationdate>20120705</creationdate><title>Methanesulfonic acid sodium salt protects retina from acute light damage in mice</title><author>Wang, Hai-Yan ; Gu, Qing ; Xu, Xun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c268t-10b96921352307ca64093ee3413550f335317914f0b1a9e2d542ea425d7e6f93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Animals</topic><topic>Apoptosis - drug effects</topic><topic>Apoptosis - radiation effects</topic><topic>BCL-XL</topic><topic>Blotting, Western</topic><topic>Electroretinography</topic><topic>Immunoprecipitation</topic><topic>Light - adverse effects</topic><topic>Male</topic><topic>Mesylates - therapeutic use</topic><topic>Mice</topic><topic>Microscopy, Electron, Transmission</topic><topic>Mitochondrial Proteins - metabolism</topic><topic>Random Allocation</topic><topic>Retina - drug effects</topic><topic>Retina - radiation effects</topic><topic>Retina - ultrastructure</topic><topic>Tumor Suppressor Protein p53 - metabolism</topic><topic>光保护剂</topic><topic>光损伤</topic><topic>小鼠</topic><topic>甲磺酸</topic><topic>线粒体蛋白质</topic><topic>视网膜电图</topic><topic>钠盐</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Hai-Yan</creatorcontrib><creatorcontrib>Gu, Qing</creatorcontrib><creatorcontrib>Xu, Xun</creatorcontrib><collection>维普_期刊</collection><collection>中文科技期刊数据库-CALIS站点</collection><collection>维普中文期刊数据库</collection><collection>中文科技期刊数据库-医药卫生</collection><collection>中文科技期刊数据库- 镜像站点</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><collection>Wanfang Data Journals - Hong Kong</collection><collection>WANFANG Data Centre</collection><collection>Wanfang Data Journals</collection><collection>万方数据期刊 - 香港版</collection><collection>China Online Journals (COJ)</collection><collection>China Online Journals (COJ)</collection><jtitle>Chinese medical journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Hai-Yan</au><au>Gu, Qing</au><au>Xu, Xun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Methanesulfonic acid sodium salt protects retina from acute light damage in mice</atitle><jtitle>Chinese medical journal</jtitle><addtitle>Chinese Medical Journal</addtitle><date>2012-07-05</date><risdate>2012</risdate><volume>125</volume><issue>13</issue><spage>2310</spage><epage>2315</epage><pages>2310-2315</pages><issn>0366-6999</issn><eissn>2542-5641</eissn><abstract>Background Methanesulfonic acid sodium salt (Dipyrone), an antipyretic and analgesic drug, has been demonstrated to improve cerebral ischemia through the inhibition of mitochondrial cell death cascades. The aim of this study was to evaluate the potential photoprotective activity of methanesulfonic acid sodium salt in a model of light-induced retinopathy. Methods One hundred mice were assigned randomly into vehicle (V), methanesulfonic acid sodium salt (D), light damage model plus vehicle (MV) and light damage model plus methanesulfonic acid sodium salt (MD) groups (n=25 each). In the MD group, methanesulfonic acid sodium salt (100 mg/kg) was administered by intraperitoneal injection 30 minutes before light exposure. Twenty-four hours after light exposure, hematoxylin and eosin staining and transmission electron microscopy (TEM) were used for histological evaluation. The thickness of the outer plus inner-segment and outer nuclear layer was measured on sections parallel to the vertical meridian of the eye at a distance of 1000 I~m from the optic nerve. Electroretinography (ERG) test was performed to assess the functional change. The morphology of mitochondria was also revealed by TEM. Finally, the expression of cytochrome c (CytC) and the relative apoptotic proteins were detected by Western blotting, and the interaction between mitochondrial proteins was investigated by co-immunoprecipitation. Results The photoreceptor inner and outer segments of the MV group were significantly disorganized than the MD group. The thicknesses of the outer plus inner-segment layers and the outer nuclear layer, and the amplitudes of the a and b waves of the scotopic ERG response markedly decreased in the MV group compared to those in the MD group (P 〈0.05). TEM examination revealed that the mitochondria of the MV group were distinctly swollen and contained disrupted cristae. In contrast, the morphology of mitochondria in the MD group was unaffected. Western blotting analysis showed that CytC, apoptosis proteinase activating factor-1 (Apaf-1), caspase 3, p53, p53-upregulated modulator of apoptosis (PUMA), Bax, and Bad were increased, whereas the anti-apoptotic proteins Bcl-2 and Bcl-XL were significantly decreased in the MV group than the MD group. Co-immunoprecipitation detection revealed that PUMA immunoreactivity precipitated by Bcl-XL decreased, whereas Bax immunoreactivity precipitated by Bcl-XL increased in the MD group compared to those in the MV group. Conclusion Methanesulfonic acid sodium salt is an effective photoprotective agent against light-induced retinopathy through the inhibition of CytC-mediated mitochondrial impairment.</abstract><cop>China</cop><pub>Department of Ophthalmology, Shanghai First People's Hospital,Affiliate of Shanghai Jiao Tong University, Shanghai 200080,China</pub><pmid>22882854</pmid><doi>10.3760/cma.j.issn.0366-6999.2012.13.013</doi><tpages>6</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0366-6999
ispartof Chinese medical journal, 2012-07, Vol.125 (13), p.2310-2315
issn 0366-6999
2542-5641
language eng
recordid cdi_wanfang_journals_zhcmj201213013
source HEAL-Link subscriptions: Lippincott Williams & Wilkins
subjects Animals
Apoptosis - drug effects
Apoptosis - radiation effects
BCL-XL
Blotting, Western
Electroretinography
Immunoprecipitation
Light - adverse effects
Male
Mesylates - therapeutic use
Mice
Microscopy, Electron, Transmission
Mitochondrial Proteins - metabolism
Random Allocation
Retina - drug effects
Retina - radiation effects
Retina - ultrastructure
Tumor Suppressor Protein p53 - metabolism
光保护剂
光损伤
小鼠
甲磺酸
线粒体蛋白质
视网膜电图
钠盐
title Methanesulfonic acid sodium salt protects retina from acute light damage in mice
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-06T10%3A06%3A46IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-wanfang_jour_proqu&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Methanesulfonic%20acid%20sodium%20salt%20protects%20retina%20from%20acute%20light%20damage%20in%20mice&rft.jtitle=Chinese%20medical%20journal&rft.au=Wang,%20Hai-Yan&rft.date=2012-07-05&rft.volume=125&rft.issue=13&rft.spage=2310&rft.epage=2315&rft.pages=2310-2315&rft.issn=0366-6999&rft.eissn=2542-5641&rft_id=info:doi/10.3760/cma.j.issn.0366-6999.2012.13.013&rft_dat=%3Cwanfang_jour_proqu%3Ezhcmj201213013%3C/wanfang_jour_proqu%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c268t-10b96921352307ca64093ee3413550f335317914f0b1a9e2d542ea425d7e6f93%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1033456632&rft_id=info:pmid/22882854&rft_cqvip_id=42476787&rft_wanfj_id=zhcmj201213013&rfr_iscdi=true