Neuroprotective effects of cutamesine, a ligand of the sigma-1 receptor chaperone, against noise-induced hearing loss
The sigma‐1 receptor, which is expressed throughout the brain, provides physiological benefits that include higher brain function. The sigma‐1 receptor functions as a chaperone in the endoplasmic reticulum and may control cell death and regeneration within the central nervous system. Cutamesine (1‐(...
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Veröffentlicht in: | Journal of neuroscience research 2015-05, Vol.93 (5), p.788-795 |
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creator | Yamashita, Daisuke Sun, Guang-wei Cui, Yong Mita, Shiro Otsuki, Naoki Kanzaki, Sho Nibu, Ken-ichi Ogawa, Kaoru Matsunaga, Tatsuo |
description | The sigma‐1 receptor, which is expressed throughout the brain, provides physiological benefits that include higher brain function. The sigma‐1 receptor functions as a chaperone in the endoplasmic reticulum and may control cell death and regeneration within the central nervous system. Cutamesine (1‐(3,4‐dimethoxyphenethyl)−4‐(3‐phenylpropyl) piperazine dihydrochloride) is a ligand selective for this receptor and may mediate neuroprotective effects in the context of neurodegenerative disease. We therefore assessed whether cutamesine protects the inner ear from noise‐induced or aging‐associated hearing loss. Immunohistochemistry and Western blotting revealed that the sigma‐1 receptor is present in adult cochlea. We treated mice with 0, 3, or 30 mg/kg cutamesine from 10 days before noise exposure until the end of the study. All subjects were exposed to a 120‐dB, 4‐kHz octave‐band noise for 2 hr. We assessed auditory thresholds by measuring the auditory‐evoked brainstem responses at 4, 8, and 16 kHz, prior to and 1 week, 1 month, or 3 months following noise exposure. For the aging study, measurements were made before treatment was initiated and after 3 or 9 months of cutamesine treatment. Damage to fibrocytes within the cochlear spiral limbus was assessed by quantitative histology. Cutamesine significantly reduced threshold shifts and cell death within the spiral limbus in response to intense noise. These effects were not dose or time dependent. Conversely, cutamesine did not prevent aging‐associated hearing loss. These results suggest that cutamesine reduces noise‐induced hearing loss and cochlear damage during the acute phase that follows exposure to an intense noise. © 2015 Wiley Periodicals, Inc. |
doi_str_mv | 10.1002/jnr.23543 |
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The sigma‐1 receptor functions as a chaperone in the endoplasmic reticulum and may control cell death and regeneration within the central nervous system. Cutamesine (1‐(3,4‐dimethoxyphenethyl)−4‐(3‐phenylpropyl) piperazine dihydrochloride) is a ligand selective for this receptor and may mediate neuroprotective effects in the context of neurodegenerative disease. We therefore assessed whether cutamesine protects the inner ear from noise‐induced or aging‐associated hearing loss. Immunohistochemistry and Western blotting revealed that the sigma‐1 receptor is present in adult cochlea. We treated mice with 0, 3, or 30 mg/kg cutamesine from 10 days before noise exposure until the end of the study. All subjects were exposed to a 120‐dB, 4‐kHz octave‐band noise for 2 hr. We assessed auditory thresholds by measuring the auditory‐evoked brainstem responses at 4, 8, and 16 kHz, prior to and 1 week, 1 month, or 3 months following noise exposure. For the aging study, measurements were made before treatment was initiated and after 3 or 9 months of cutamesine treatment. Damage to fibrocytes within the cochlear spiral limbus was assessed by quantitative histology. Cutamesine significantly reduced threshold shifts and cell death within the spiral limbus in response to intense noise. These effects were not dose or time dependent. Conversely, cutamesine did not prevent aging‐associated hearing loss. These results suggest that cutamesine reduces noise‐induced hearing loss and cochlear damage during the acute phase that follows exposure to an intense noise. © 2015 Wiley Periodicals, Inc.</description><identifier>ISSN: 0360-4012</identifier><identifier>EISSN: 1097-4547</identifier><identifier>DOI: 10.1002/jnr.23543</identifier><identifier>PMID: 25612541</identifier><language>eng</language><publisher>United States: Blackwell Publishing Ltd</publisher><subject>Acoustic Stimulation - adverse effects ; Acoustics ; Age Factors ; Animals ; Animals, Newborn ; cell death ; cochlea ; Cochlea - drug effects ; Cochlea - growth & development ; Cochlea - metabolism ; cutamesine ; Disease Models, Animal ; Evoked Potentials, Auditory, Brain Stem - drug effects ; Follow-Up Studies ; Gene Expression Regulation - drug effects ; Hearing Loss, Noise-Induced - diagnosis ; Hearing Loss, Noise-Induced - drug therapy ; Male ; Mice ; Mice, Inbred C57BL ; Neuroprotective Agents - pharmacology ; Neuroprotective Agents - therapeutic use ; noise-induced hearing loss ; Organ of Corti - metabolism ; Organ of Corti - pathology ; Piperazines - pharmacology ; Piperazines - therapeutic use ; Receptors, sigma - agonists ; Sodium-Potassium-Exchanging ATPase - metabolism ; spiral limbus</subject><ispartof>Journal of neuroscience research, 2015-05, Vol.93 (5), p.788-795</ispartof><rights>2015 Wiley Periodicals, Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5953-792769d3942c2d0fb2c4996aa619df209b65da75c712e454262e4467b5436be73</citedby><cites>FETCH-LOGICAL-c5953-792769d3942c2d0fb2c4996aa619df209b65da75c712e454262e4467b5436be73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjnr.23543$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjnr.23543$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25612541$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yamashita, Daisuke</creatorcontrib><creatorcontrib>Sun, Guang-wei</creatorcontrib><creatorcontrib>Cui, Yong</creatorcontrib><creatorcontrib>Mita, Shiro</creatorcontrib><creatorcontrib>Otsuki, Naoki</creatorcontrib><creatorcontrib>Kanzaki, Sho</creatorcontrib><creatorcontrib>Nibu, Ken-ichi</creatorcontrib><creatorcontrib>Ogawa, Kaoru</creatorcontrib><creatorcontrib>Matsunaga, Tatsuo</creatorcontrib><title>Neuroprotective effects of cutamesine, a ligand of the sigma-1 receptor chaperone, against noise-induced hearing loss</title><title>Journal of neuroscience research</title><addtitle>Journal of Neuroscience Research</addtitle><description>The sigma‐1 receptor, which is expressed throughout the brain, provides physiological benefits that include higher brain function. The sigma‐1 receptor functions as a chaperone in the endoplasmic reticulum and may control cell death and regeneration within the central nervous system. Cutamesine (1‐(3,4‐dimethoxyphenethyl)−4‐(3‐phenylpropyl) piperazine dihydrochloride) is a ligand selective for this receptor and may mediate neuroprotective effects in the context of neurodegenerative disease. We therefore assessed whether cutamesine protects the inner ear from noise‐induced or aging‐associated hearing loss. Immunohistochemistry and Western blotting revealed that the sigma‐1 receptor is present in adult cochlea. We treated mice with 0, 3, or 30 mg/kg cutamesine from 10 days before noise exposure until the end of the study. All subjects were exposed to a 120‐dB, 4‐kHz octave‐band noise for 2 hr. We assessed auditory thresholds by measuring the auditory‐evoked brainstem responses at 4, 8, and 16 kHz, prior to and 1 week, 1 month, or 3 months following noise exposure. For the aging study, measurements were made before treatment was initiated and after 3 or 9 months of cutamesine treatment. Damage to fibrocytes within the cochlear spiral limbus was assessed by quantitative histology. Cutamesine significantly reduced threshold shifts and cell death within the spiral limbus in response to intense noise. These effects were not dose or time dependent. Conversely, cutamesine did not prevent aging‐associated hearing loss. These results suggest that cutamesine reduces noise‐induced hearing loss and cochlear damage during the acute phase that follows exposure to an intense noise. © 2015 Wiley Periodicals, Inc.</description><subject>Acoustic Stimulation - adverse effects</subject><subject>Acoustics</subject><subject>Age Factors</subject><subject>Animals</subject><subject>Animals, Newborn</subject><subject>cell death</subject><subject>cochlea</subject><subject>Cochlea - drug effects</subject><subject>Cochlea - growth & development</subject><subject>Cochlea - metabolism</subject><subject>cutamesine</subject><subject>Disease Models, Animal</subject><subject>Evoked Potentials, Auditory, Brain Stem - drug effects</subject><subject>Follow-Up Studies</subject><subject>Gene Expression Regulation - drug effects</subject><subject>Hearing Loss, Noise-Induced - diagnosis</subject><subject>Hearing Loss, Noise-Induced - drug therapy</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Neuroprotective Agents - pharmacology</subject><subject>Neuroprotective Agents - therapeutic use</subject><subject>noise-induced hearing loss</subject><subject>Organ of Corti - metabolism</subject><subject>Organ of Corti - pathology</subject><subject>Piperazines - pharmacology</subject><subject>Piperazines - therapeutic use</subject><subject>Receptors, sigma - agonists</subject><subject>Sodium-Potassium-Exchanging ATPase - metabolism</subject><subject>spiral limbus</subject><issn>0360-4012</issn><issn>1097-4547</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkU9rFEEQxRtRzCZ68AtIgxcFJ-n_bR9l0dUYRhRF8NL09NTs9jozvXbPRPPt7c0mOQiCpyqKXz3q1UPoCSWnlBB2th3TKeNS8HtoQYnRlZBC30cLwhWpBKHsCB3nvCWEGCP5Q3TEpKJMCrpAcw1zirsUJ_BTuAQMXVe6jGOH_Ty5AXIY4SV2uA9rN7b7-bQBnMN6cBXFCTzsppiw37gdpHjNrl0Y84THGDJUYWxnDy3egEthXOM-5vwIPehcn-HxTT1BX9---bJ8V118XL1fvr6ovCyHVtowrUzLjWCetaRrmBfGKOcUNW3HiGmUbJ2WXlMGxTNTpQilm_IK1YDmJ-j5QbcY_DlDnuwQsoe-dyPEOVuq1CsmiaLif1CupNSGFPTZX-g2zmksRvYU46JAslAvDpRPxXGCzu5SGFy6spTYfWy2xGavYyvs0xvFuRmgvSNvcyrA2QH4FXq4-reSPa8_30pWh42QJ_h9t-HSD6s019J-q1d2df59-Ul8qG3N_wAg369U</recordid><startdate>201505</startdate><enddate>201505</enddate><creator>Yamashita, Daisuke</creator><creator>Sun, Guang-wei</creator><creator>Cui, Yong</creator><creator>Mita, Shiro</creator><creator>Otsuki, Naoki</creator><creator>Kanzaki, Sho</creator><creator>Nibu, Ken-ichi</creator><creator>Ogawa, Kaoru</creator><creator>Matsunaga, Tatsuo</creator><general>Blackwell Publishing Ltd</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><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>7QG</scope><scope>7QP</scope><scope>7QR</scope><scope>7TK</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>201505</creationdate><title>Neuroprotective effects of cutamesine, a ligand of the sigma-1 receptor chaperone, against noise-induced hearing loss</title><author>Yamashita, Daisuke ; Sun, Guang-wei ; Cui, Yong ; Mita, Shiro ; Otsuki, Naoki ; Kanzaki, Sho ; Nibu, Ken-ichi ; Ogawa, Kaoru ; Matsunaga, Tatsuo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5953-792769d3942c2d0fb2c4996aa619df209b65da75c712e454262e4467b5436be73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Acoustic Stimulation - adverse effects</topic><topic>Acoustics</topic><topic>Age Factors</topic><topic>Animals</topic><topic>Animals, Newborn</topic><topic>cell death</topic><topic>cochlea</topic><topic>Cochlea - drug effects</topic><topic>Cochlea - growth & development</topic><topic>Cochlea - metabolism</topic><topic>cutamesine</topic><topic>Disease Models, Animal</topic><topic>Evoked Potentials, Auditory, Brain Stem - drug effects</topic><topic>Follow-Up Studies</topic><topic>Gene Expression Regulation - drug effects</topic><topic>Hearing Loss, Noise-Induced - diagnosis</topic><topic>Hearing Loss, Noise-Induced - drug therapy</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Neuroprotective Agents - pharmacology</topic><topic>Neuroprotective Agents - therapeutic use</topic><topic>noise-induced hearing loss</topic><topic>Organ of Corti - metabolism</topic><topic>Organ of Corti - pathology</topic><topic>Piperazines - pharmacology</topic><topic>Piperazines - therapeutic use</topic><topic>Receptors, sigma - agonists</topic><topic>Sodium-Potassium-Exchanging ATPase - metabolism</topic><topic>spiral limbus</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yamashita, Daisuke</creatorcontrib><creatorcontrib>Sun, Guang-wei</creatorcontrib><creatorcontrib>Cui, Yong</creatorcontrib><creatorcontrib>Mita, Shiro</creatorcontrib><creatorcontrib>Otsuki, Naoki</creatorcontrib><creatorcontrib>Kanzaki, Sho</creatorcontrib><creatorcontrib>Nibu, Ken-ichi</creatorcontrib><creatorcontrib>Ogawa, Kaoru</creatorcontrib><creatorcontrib>Matsunaga, Tatsuo</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Animal Behavior Abstracts</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of neuroscience research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yamashita, Daisuke</au><au>Sun, Guang-wei</au><au>Cui, Yong</au><au>Mita, Shiro</au><au>Otsuki, Naoki</au><au>Kanzaki, Sho</au><au>Nibu, Ken-ichi</au><au>Ogawa, Kaoru</au><au>Matsunaga, Tatsuo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Neuroprotective effects of cutamesine, a ligand of the sigma-1 receptor chaperone, against noise-induced hearing loss</atitle><jtitle>Journal of neuroscience research</jtitle><addtitle>Journal of Neuroscience Research</addtitle><date>2015-05</date><risdate>2015</risdate><volume>93</volume><issue>5</issue><spage>788</spage><epage>795</epage><pages>788-795</pages><issn>0360-4012</issn><eissn>1097-4547</eissn><abstract>The sigma‐1 receptor, which is expressed throughout the brain, provides physiological benefits that include higher brain function. The sigma‐1 receptor functions as a chaperone in the endoplasmic reticulum and may control cell death and regeneration within the central nervous system. Cutamesine (1‐(3,4‐dimethoxyphenethyl)−4‐(3‐phenylpropyl) piperazine dihydrochloride) is a ligand selective for this receptor and may mediate neuroprotective effects in the context of neurodegenerative disease. We therefore assessed whether cutamesine protects the inner ear from noise‐induced or aging‐associated hearing loss. Immunohistochemistry and Western blotting revealed that the sigma‐1 receptor is present in adult cochlea. We treated mice with 0, 3, or 30 mg/kg cutamesine from 10 days before noise exposure until the end of the study. All subjects were exposed to a 120‐dB, 4‐kHz octave‐band noise for 2 hr. We assessed auditory thresholds by measuring the auditory‐evoked brainstem responses at 4, 8, and 16 kHz, prior to and 1 week, 1 month, or 3 months following noise exposure. For the aging study, measurements were made before treatment was initiated and after 3 or 9 months of cutamesine treatment. Damage to fibrocytes within the cochlear spiral limbus was assessed by quantitative histology. Cutamesine significantly reduced threshold shifts and cell death within the spiral limbus in response to intense noise. These effects were not dose or time dependent. Conversely, cutamesine did not prevent aging‐associated hearing loss. These results suggest that cutamesine reduces noise‐induced hearing loss and cochlear damage during the acute phase that follows exposure to an intense noise. © 2015 Wiley Periodicals, Inc.</abstract><cop>United States</cop><pub>Blackwell Publishing Ltd</pub><pmid>25612541</pmid><doi>10.1002/jnr.23543</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Acoustic Stimulation - adverse effects Acoustics Age Factors Animals Animals, Newborn cell death cochlea Cochlea - drug effects Cochlea - growth & development Cochlea - metabolism cutamesine Disease Models, Animal Evoked Potentials, Auditory, Brain Stem - drug effects Follow-Up Studies Gene Expression Regulation - drug effects Hearing Loss, Noise-Induced - diagnosis Hearing Loss, Noise-Induced - drug therapy Male Mice Mice, Inbred C57BL Neuroprotective Agents - pharmacology Neuroprotective Agents - therapeutic use noise-induced hearing loss Organ of Corti - metabolism Organ of Corti - pathology Piperazines - pharmacology Piperazines - therapeutic use Receptors, sigma - agonists Sodium-Potassium-Exchanging ATPase - metabolism spiral limbus |
title | Neuroprotective effects of cutamesine, a ligand of the sigma-1 receptor chaperone, against noise-induced hearing loss |
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