Doxycycline reduces nitric oxide production in guinea pig inner ears
Abstract Objective Gentamicin application is an important therapeutic option to control vertigo spells in Ménière's disease. However, even in the case of low-dose intratympanic application, gentamicin might contribute to a pathological NO-increase leading to cochlear damage and hearing impairme...
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Veröffentlicht in: | Auris, nasus, larynx nasus, larynx, 2011-12, Vol.38 (6), p.671-677 |
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description | Abstract Objective Gentamicin application is an important therapeutic option to control vertigo spells in Ménière's disease. However, even in the case of low-dose intratympanic application, gentamicin might contribute to a pathological NO-increase leading to cochlear damage and hearing impairment. The study was performed to evaluate the nitric oxide (NO) reducing capacity of doxycycline in the inner ear after NO-induction by gentamicin. Methods In a prospective animal study, a single dose of gentamicin (10 mg/kg body weight) was injected intratympanically into male guinea pigs ( n = 48). The auditory brainstem responses (ABRs) were recorded prior to application and 3, 5 and 7 days afterwards. The organ of Corti and the lateral wall of 42 animals were isolated after 7 days and incubated separately for 6 h in cell culture medium. Doxycycline was adjusted to organ cultures of 5 animals. Two NOS inhibitors, NG -Nitro- l -arginine methyl ester ( l -NAME) and NG-monomethyl- l -arginine monoacetate ( l -NMMA), were applied in three different concentrations to the organ cultures of 30 animals in total (5 animals per concentration). As controls, seven animals received no further substance except gentamicin. The NO-production was quantified by chemiluminescence. Additional six gentamicin-treated animals were used for immunohistochemical studies. Results The ABRs declined continuously from the first to the seventh day after gentamicin application. Doxycycline reduced NO-production in the lateral wall by 54% ( p = .029) comparable to the effect of the applied nitric oxide inhibitors. In the organ of Corti, NO-production was reduced by about 41% showing no statistical significance in respect to great inter-animal variations. Conclusion The application of doxycycline might offer a new therapeutic approach to prevent NO-induced cochlea damage through ototoxic substances. |
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However, even in the case of low-dose intratympanic application, gentamicin might contribute to a pathological NO-increase leading to cochlear damage and hearing impairment. The study was performed to evaluate the nitric oxide (NO) reducing capacity of doxycycline in the inner ear after NO-induction by gentamicin. Methods In a prospective animal study, a single dose of gentamicin (10 mg/kg body weight) was injected intratympanically into male guinea pigs ( n = 48). The auditory brainstem responses (ABRs) were recorded prior to application and 3, 5 and 7 days afterwards. The organ of Corti and the lateral wall of 42 animals were isolated after 7 days and incubated separately for 6 h in cell culture medium. Doxycycline was adjusted to organ cultures of 5 animals. Two NOS inhibitors, NG -Nitro- l -arginine methyl ester ( l -NAME) and NG-monomethyl- l -arginine monoacetate ( l -NMMA), were applied in three different concentrations to the organ cultures of 30 animals in total (5 animals per concentration). As controls, seven animals received no further substance except gentamicin. The NO-production was quantified by chemiluminescence. Additional six gentamicin-treated animals were used for immunohistochemical studies. Results The ABRs declined continuously from the first to the seventh day after gentamicin application. Doxycycline reduced NO-production in the lateral wall by 54% ( p = .029) comparable to the effect of the applied nitric oxide inhibitors. In the organ of Corti, NO-production was reduced by about 41% showing no statistical significance in respect to great inter-animal variations. Conclusion The application of doxycycline might offer a new therapeutic approach to prevent NO-induced cochlea damage through ototoxic substances.</description><identifier>ISSN: 0385-8146</identifier><identifier>EISSN: 1879-1476</identifier><identifier>DOI: 10.1016/j.anl.2011.02.013</identifier><identifier>PMID: 21616617</identifier><language>eng</language><publisher>Netherlands: Elsevier Ireland Ltd</publisher><subject>Animals ; Cytoprotection ; Cytoprotection - drug effects ; Doxycycline - pharmacology ; Ear, Inner - drug effects ; Ear, Inner - metabolism ; Evoked Potentials, Auditory, Brain Stem - drug effects ; Gentamicin ; Gentamicins - pharmacology ; Guinea Pigs ; Immunohistochemistry ; Lateral wall ; Luminescence ; Male ; NG-Nitroarginine Methyl Ester - pharmacology ; Nitric Oxide - biosynthesis ; omega-N-Methylarginine - pharmacology ; Organ culture ; Organ Culture Techniques ; Organ of Corti ; Organ of Corti - metabolism ; Otolaryngology ; Prospective Studies ; Tetracycline ; Up-Regulation</subject><ispartof>Auris, nasus, larynx, 2011-12, Vol.38 (6), p.671-677</ispartof><rights>Elsevier Ireland Ltd</rights><rights>2011 Elsevier Ireland Ltd</rights><rights>Copyright © 2011 Elsevier Ireland Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c431t-e50e72816392f7efb33bd55eb6ccea38b8a165098c9984b468d0a7796ab398073</citedby><cites>FETCH-LOGICAL-c431t-e50e72816392f7efb33bd55eb6ccea38b8a165098c9984b468d0a7796ab398073</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0385814611001489$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3536,27903,27904,65309</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21616617$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Helling, Kai</creatorcontrib><creatorcontrib>Wodarzcyk, Karl</creatorcontrib><creatorcontrib>Brieger, Jürgen</creatorcontrib><creatorcontrib>Schmidtmann, Irene</creatorcontrib><creatorcontrib>Li, Huige</creatorcontrib><creatorcontrib>Mann, Wolf J</creatorcontrib><creatorcontrib>Heinrich, Ulf-Rüdiger</creatorcontrib><title>Doxycycline reduces nitric oxide production in guinea pig inner ears</title><title>Auris, nasus, larynx</title><addtitle>Auris Nasus Larynx</addtitle><description>Abstract Objective Gentamicin application is an important therapeutic option to control vertigo spells in Ménière's disease. However, even in the case of low-dose intratympanic application, gentamicin might contribute to a pathological NO-increase leading to cochlear damage and hearing impairment. The study was performed to evaluate the nitric oxide (NO) reducing capacity of doxycycline in the inner ear after NO-induction by gentamicin. Methods In a prospective animal study, a single dose of gentamicin (10 mg/kg body weight) was injected intratympanically into male guinea pigs ( n = 48). The auditory brainstem responses (ABRs) were recorded prior to application and 3, 5 and 7 days afterwards. The organ of Corti and the lateral wall of 42 animals were isolated after 7 days and incubated separately for 6 h in cell culture medium. Doxycycline was adjusted to organ cultures of 5 animals. Two NOS inhibitors, NG -Nitro- l -arginine methyl ester ( l -NAME) and NG-monomethyl- l -arginine monoacetate ( l -NMMA), were applied in three different concentrations to the organ cultures of 30 animals in total (5 animals per concentration). As controls, seven animals received no further substance except gentamicin. The NO-production was quantified by chemiluminescence. Additional six gentamicin-treated animals were used for immunohistochemical studies. Results The ABRs declined continuously from the first to the seventh day after gentamicin application. Doxycycline reduced NO-production in the lateral wall by 54% ( p = .029) comparable to the effect of the applied nitric oxide inhibitors. In the organ of Corti, NO-production was reduced by about 41% showing no statistical significance in respect to great inter-animal variations. Conclusion The application of doxycycline might offer a new therapeutic approach to prevent NO-induced cochlea damage through ototoxic substances.</description><subject>Animals</subject><subject>Cytoprotection</subject><subject>Cytoprotection - drug effects</subject><subject>Doxycycline - pharmacology</subject><subject>Ear, Inner - drug effects</subject><subject>Ear, Inner - metabolism</subject><subject>Evoked Potentials, Auditory, Brain Stem - drug effects</subject><subject>Gentamicin</subject><subject>Gentamicins - pharmacology</subject><subject>Guinea Pigs</subject><subject>Immunohistochemistry</subject><subject>Lateral wall</subject><subject>Luminescence</subject><subject>Male</subject><subject>NG-Nitroarginine Methyl Ester - pharmacology</subject><subject>Nitric Oxide - biosynthesis</subject><subject>omega-N-Methylarginine - pharmacology</subject><subject>Organ culture</subject><subject>Organ Culture Techniques</subject><subject>Organ of Corti</subject><subject>Organ of Corti - metabolism</subject><subject>Otolaryngology</subject><subject>Prospective Studies</subject><subject>Tetracycline</subject><subject>Up-Regulation</subject><issn>0385-8146</issn><issn>1879-1476</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kU1P3DAQhq2qVdnS_gAuKLeeks7EiT-EVKmCfiAh9QCcLceZRV6yzmIniP33OFrooQdOlq3nfeV5hrEThAoBxbdNZcNQ1YBYQV0B8ndshUrqEhsp3rMVcNWWChtxxD6ltAEALrn-yI5qFCgEyhW7uBif9m7vBh-oiNTPjlIR_BS9K8Yn31Oxi2N-nfwYCh-KuzmDttj5u3wLFAuyMX1mH9Z2SPTl5Txmt79-3pz_Ka_-_r48_3FVuobjVFILJGuFgut6LWndcd71bUudcI4sV52yKFrQymmtmq4RqgcrpRa241qB5Mfs66E3_-lhpjSZrU-OhsEGGudklGxlzRvOM4kH0sUxpUhrs4t-a-PeIJjFndmY7M4s7gzUJrvLmdOX9rnbUv8v8SorA2cHgPKMj56iSc5TcNT7SG4y_ejfrP_-X3qR7p0d7mlPaTPOMWR5Bk3KAXO9LG_ZHSIANkrzZ1szk1Y</recordid><startdate>20111201</startdate><enddate>20111201</enddate><creator>Helling, Kai</creator><creator>Wodarzcyk, Karl</creator><creator>Brieger, Jürgen</creator><creator>Schmidtmann, Irene</creator><creator>Li, Huige</creator><creator>Mann, Wolf J</creator><creator>Heinrich, Ulf-Rüdiger</creator><general>Elsevier Ireland Ltd</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>7X8</scope></search><sort><creationdate>20111201</creationdate><title>Doxycycline reduces nitric oxide production in guinea pig inner ears</title><author>Helling, Kai ; Wodarzcyk, Karl ; Brieger, Jürgen ; Schmidtmann, Irene ; Li, Huige ; Mann, Wolf J ; Heinrich, Ulf-Rüdiger</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c431t-e50e72816392f7efb33bd55eb6ccea38b8a165098c9984b468d0a7796ab398073</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Animals</topic><topic>Cytoprotection</topic><topic>Cytoprotection - drug effects</topic><topic>Doxycycline - pharmacology</topic><topic>Ear, Inner - drug effects</topic><topic>Ear, Inner - metabolism</topic><topic>Evoked Potentials, Auditory, Brain Stem - drug effects</topic><topic>Gentamicin</topic><topic>Gentamicins - pharmacology</topic><topic>Guinea Pigs</topic><topic>Immunohistochemistry</topic><topic>Lateral wall</topic><topic>Luminescence</topic><topic>Male</topic><topic>NG-Nitroarginine Methyl Ester - pharmacology</topic><topic>Nitric Oxide - biosynthesis</topic><topic>omega-N-Methylarginine - pharmacology</topic><topic>Organ culture</topic><topic>Organ Culture Techniques</topic><topic>Organ of Corti</topic><topic>Organ of Corti - metabolism</topic><topic>Otolaryngology</topic><topic>Prospective Studies</topic><topic>Tetracycline</topic><topic>Up-Regulation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Helling, Kai</creatorcontrib><creatorcontrib>Wodarzcyk, Karl</creatorcontrib><creatorcontrib>Brieger, Jürgen</creatorcontrib><creatorcontrib>Schmidtmann, Irene</creatorcontrib><creatorcontrib>Li, Huige</creatorcontrib><creatorcontrib>Mann, Wolf J</creatorcontrib><creatorcontrib>Heinrich, Ulf-Rüdiger</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Auris, nasus, larynx</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Helling, Kai</au><au>Wodarzcyk, Karl</au><au>Brieger, Jürgen</au><au>Schmidtmann, Irene</au><au>Li, Huige</au><au>Mann, Wolf J</au><au>Heinrich, Ulf-Rüdiger</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Doxycycline reduces nitric oxide production in guinea pig inner ears</atitle><jtitle>Auris, nasus, larynx</jtitle><addtitle>Auris Nasus Larynx</addtitle><date>2011-12-01</date><risdate>2011</risdate><volume>38</volume><issue>6</issue><spage>671</spage><epage>677</epage><pages>671-677</pages><issn>0385-8146</issn><eissn>1879-1476</eissn><abstract>Abstract Objective Gentamicin application is an important therapeutic option to control vertigo spells in Ménière's disease. However, even in the case of low-dose intratympanic application, gentamicin might contribute to a pathological NO-increase leading to cochlear damage and hearing impairment. The study was performed to evaluate the nitric oxide (NO) reducing capacity of doxycycline in the inner ear after NO-induction by gentamicin. Methods In a prospective animal study, a single dose of gentamicin (10 mg/kg body weight) was injected intratympanically into male guinea pigs ( n = 48). The auditory brainstem responses (ABRs) were recorded prior to application and 3, 5 and 7 days afterwards. The organ of Corti and the lateral wall of 42 animals were isolated after 7 days and incubated separately for 6 h in cell culture medium. Doxycycline was adjusted to organ cultures of 5 animals. Two NOS inhibitors, NG -Nitro- l -arginine methyl ester ( l -NAME) and NG-monomethyl- l -arginine monoacetate ( l -NMMA), were applied in three different concentrations to the organ cultures of 30 animals in total (5 animals per concentration). As controls, seven animals received no further substance except gentamicin. The NO-production was quantified by chemiluminescence. Additional six gentamicin-treated animals were used for immunohistochemical studies. Results The ABRs declined continuously from the first to the seventh day after gentamicin application. Doxycycline reduced NO-production in the lateral wall by 54% ( p = .029) comparable to the effect of the applied nitric oxide inhibitors. In the organ of Corti, NO-production was reduced by about 41% showing no statistical significance in respect to great inter-animal variations. Conclusion The application of doxycycline might offer a new therapeutic approach to prevent NO-induced cochlea damage through ototoxic substances.</abstract><cop>Netherlands</cop><pub>Elsevier Ireland Ltd</pub><pmid>21616617</pmid><doi>10.1016/j.anl.2011.02.013</doi><tpages>7</tpages></addata></record> |
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subjects | Animals Cytoprotection Cytoprotection - drug effects Doxycycline - pharmacology Ear, Inner - drug effects Ear, Inner - metabolism Evoked Potentials, Auditory, Brain Stem - drug effects Gentamicin Gentamicins - pharmacology Guinea Pigs Immunohistochemistry Lateral wall Luminescence Male NG-Nitroarginine Methyl Ester - pharmacology Nitric Oxide - biosynthesis omega-N-Methylarginine - pharmacology Organ culture Organ Culture Techniques Organ of Corti Organ of Corti - metabolism Otolaryngology Prospective Studies Tetracycline Up-Regulation |
title | Doxycycline reduces nitric oxide production in guinea pig inner ears |
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