Hyperoxia, reactive oxygen species, and hyperventilation: oxygen sensitivity of brain stem neurons
Department of Anatomy and Physiology, Environmental and Hyperbaric Cell Biology Facility, Wright State University School of Medicine, College of Science and Mathematics, Dayton, Ohio 45435; and 1 Department of Military and Emergency Medicine, Uniformed Services University of the Health Sciences, Bet...
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Veröffentlicht in: | Journal of applied physiology (1985) 2004-02, Vol.96 (2), p.784-791 |
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creator | Dean, Jay B Mulkey, Daniel K Henderson, Richard A., III Potter, Stephanie J Putnam, Robert W |
description | Department of Anatomy and Physiology, Environmental and Hyperbaric Cell Biology Facility, Wright State University School of Medicine, College of Science and Mathematics, Dayton, Ohio 45435; and 1 Department of Military and Emergency Medicine, Uniformed Services University of the Health Sciences, Bethesda, Maryland 20814
Hyperoxia is a popular model of oxidative stress. However, hyperoxic gas mixtures are routinely used for chemical denervation of peripheral O 2 receptors in in vivo studies of respiratory control. The underlying assumption whenever using hyperoxia is that there are no direct effects of molecular O 2 and reactive O 2 species (ROS) on brain stem function. In addition, control superfusates used routinely for in vitro studies of neurons in brain slices are, in fact, hyperoxic. Again, the assumption is that there are no direct effects of O 2 and ROS on neuronal activity. Research contradicts this assumption by demonstrating that O 2 has central effects on the brain stem respiratory centers and several effects on neurons in respiratory control areas; these need to be considered whenever hyperoxia is used. This mini-review summarizes the long-recognized, but seldom acknowledged, paradox of respiratory control known as hyperoxic hyperventilation. Several proposed mechanisms are discussed, including the recent hypothesis that hyperoxic hyperventilation is initiated by increased production of ROS during hyperoxia, which directly stimulates central CO 2 chemoreceptors in the solitary complex. Hyperoxic hyperventilation may provide clues into the fundamental role of redox signaling and ROS in central control of breathing; moreover, oxidative stress may play a role in respiratory control dysfunction. The practical implications of brain stem O 2 and ROS sensitivity are also considered relative to the present uses of hyperoxia in respiratory control research in humans, animals, and brain stem tissues. Recommendations for future research are also proposed.
brain stem respiratory centers; central chemoreceptors; oxidative stress; hyperoxic hyperventilation
Address for reprint requests and other correspondence: J. B. Dean, Dept. of Anatomy and Physiology, 235C Bio. Sci. Bldg., 3640 Col. Glenn Hwy., Wright State Univ., Dayton, OH 45435 (E-mail: jay.dean{at}wright.edu ). |
doi_str_mv | 10.1152/japplphysiol.00892.2003 |
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Hyperoxia is a popular model of oxidative stress. However, hyperoxic gas mixtures are routinely used for chemical denervation of peripheral O 2 receptors in in vivo studies of respiratory control. The underlying assumption whenever using hyperoxia is that there are no direct effects of molecular O 2 and reactive O 2 species (ROS) on brain stem function. In addition, control superfusates used routinely for in vitro studies of neurons in brain slices are, in fact, hyperoxic. Again, the assumption is that there are no direct effects of O 2 and ROS on neuronal activity. Research contradicts this assumption by demonstrating that O 2 has central effects on the brain stem respiratory centers and several effects on neurons in respiratory control areas; these need to be considered whenever hyperoxia is used. This mini-review summarizes the long-recognized, but seldom acknowledged, paradox of respiratory control known as hyperoxic hyperventilation. Several proposed mechanisms are discussed, including the recent hypothesis that hyperoxic hyperventilation is initiated by increased production of ROS during hyperoxia, which directly stimulates central CO 2 chemoreceptors in the solitary complex. Hyperoxic hyperventilation may provide clues into the fundamental role of redox signaling and ROS in central control of breathing; moreover, oxidative stress may play a role in respiratory control dysfunction. The practical implications of brain stem O 2 and ROS sensitivity are also considered relative to the present uses of hyperoxia in respiratory control research in humans, animals, and brain stem tissues. Recommendations for future research are also proposed.
brain stem respiratory centers; central chemoreceptors; oxidative stress; hyperoxic hyperventilation
Address for reprint requests and other correspondence: J. B. Dean, Dept. of Anatomy and Physiology, 235C Bio. Sci. Bldg., 3640 Col. Glenn Hwy., Wright State Univ., Dayton, OH 45435 (E-mail: jay.dean{at}wright.edu ).</description><identifier>ISSN: 8750-7587</identifier><identifier>EISSN: 1522-1601</identifier><identifier>DOI: 10.1152/japplphysiol.00892.2003</identifier><identifier>PMID: 14715688</identifier><language>eng</language><publisher>United States: Am Physiological Soc</publisher><subject>Animals ; Brain ; Brain Stem - cytology ; Brain Stem - metabolism ; Brain Stem - physiology ; Humans ; Hyperoxia - metabolism ; Hyperoxia - physiopathology ; Hyperventilation - metabolism ; Hyperventilation - physiopathology ; Neurons ; Neurons - physiology ; Oxygen ; Oxygen - metabolism ; Reactive Oxygen Species - metabolism ; Respiratory system</subject><ispartof>Journal of applied physiology (1985), 2004-02, Vol.96 (2), p.784-791</ispartof><rights>Copyright American Physiological Society Feb 2004</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c461t-9ab44cadb9f059c5cf4fca84ca6f3d83e5bc5016fd0e12661b47359afea5f2663</citedby><cites>FETCH-LOGICAL-c461t-9ab44cadb9f059c5cf4fca84ca6f3d83e5bc5016fd0e12661b47359afea5f2663</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,3026,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/14715688$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Dean, Jay B</creatorcontrib><creatorcontrib>Mulkey, Daniel K</creatorcontrib><creatorcontrib>Henderson, Richard A., III</creatorcontrib><creatorcontrib>Potter, Stephanie J</creatorcontrib><creatorcontrib>Putnam, Robert W</creatorcontrib><title>Hyperoxia, reactive oxygen species, and hyperventilation: oxygen sensitivity of brain stem neurons</title><title>Journal of applied physiology (1985)</title><addtitle>J Appl Physiol (1985)</addtitle><description>Department of Anatomy and Physiology, Environmental and Hyperbaric Cell Biology Facility, Wright State University School of Medicine, College of Science and Mathematics, Dayton, Ohio 45435; and 1 Department of Military and Emergency Medicine, Uniformed Services University of the Health Sciences, Bethesda, Maryland 20814
Hyperoxia is a popular model of oxidative stress. However, hyperoxic gas mixtures are routinely used for chemical denervation of peripheral O 2 receptors in in vivo studies of respiratory control. The underlying assumption whenever using hyperoxia is that there are no direct effects of molecular O 2 and reactive O 2 species (ROS) on brain stem function. In addition, control superfusates used routinely for in vitro studies of neurons in brain slices are, in fact, hyperoxic. Again, the assumption is that there are no direct effects of O 2 and ROS on neuronal activity. Research contradicts this assumption by demonstrating that O 2 has central effects on the brain stem respiratory centers and several effects on neurons in respiratory control areas; these need to be considered whenever hyperoxia is used. This mini-review summarizes the long-recognized, but seldom acknowledged, paradox of respiratory control known as hyperoxic hyperventilation. Several proposed mechanisms are discussed, including the recent hypothesis that hyperoxic hyperventilation is initiated by increased production of ROS during hyperoxia, which directly stimulates central CO 2 chemoreceptors in the solitary complex. Hyperoxic hyperventilation may provide clues into the fundamental role of redox signaling and ROS in central control of breathing; moreover, oxidative stress may play a role in respiratory control dysfunction. The practical implications of brain stem O 2 and ROS sensitivity are also considered relative to the present uses of hyperoxia in respiratory control research in humans, animals, and brain stem tissues. Recommendations for future research are also proposed.
brain stem respiratory centers; central chemoreceptors; oxidative stress; hyperoxic hyperventilation
Address for reprint requests and other correspondence: J. B. Dean, Dept. of Anatomy and Physiology, 235C Bio. Sci. Bldg., 3640 Col. Glenn Hwy., Wright State Univ., Dayton, OH 45435 (E-mail: jay.dean{at}wright.edu ).</description><subject>Animals</subject><subject>Brain</subject><subject>Brain Stem - cytology</subject><subject>Brain Stem - metabolism</subject><subject>Brain Stem - physiology</subject><subject>Humans</subject><subject>Hyperoxia - metabolism</subject><subject>Hyperoxia - physiopathology</subject><subject>Hyperventilation - metabolism</subject><subject>Hyperventilation - physiopathology</subject><subject>Neurons</subject><subject>Neurons - physiology</subject><subject>Oxygen</subject><subject>Oxygen - metabolism</subject><subject>Reactive Oxygen Species - metabolism</subject><subject>Respiratory system</subject><issn>8750-7587</issn><issn>1522-1601</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kVFv2yAUhdG0as26_YXV2kP7Umdgg437NlXtWqlSX7JnhPElIXLABTuL_31xkm1VpfKCuHzn6OochM4JnhPCsh9r2XVttxqDce0cY15l8wzj_AOaxd8sJQUmH9GMlwynJePlKfocwhpjQikjn9ApoSVhBeczVN-PHXi3M_Iq8SBVb7aQuN24BJuEDpSBcJVI2ySriduC7U0re-Ps9T8KbDBRZvoxcTqpvTRx2MMmsTB4Z8MXdKJlG-Dr8T5Dv-9uFzf36ePTr4ebn4-pogXp00rWlCrZ1JXGrFJMaaqV5HFU6LzhObBaMUwK3WAgWVGQmpY5q6QGyXR852fo4uDbefc8QOjFxgQFbSstuCEIvs-JVBH8_gZcu8HbuJvI4iExSR6h8gAp70LwoEXnzUb6URAspg7E6w7E3ltMHUTlt6P9UG-g-a87hh6BywOwMsvVH-NBHF3ccpxcRVWITJScRjJ_n7wb2nYBu36S_FWIrtH5C_CiqfQ</recordid><startdate>20040201</startdate><enddate>20040201</enddate><creator>Dean, Jay B</creator><creator>Mulkey, Daniel K</creator><creator>Henderson, Richard A., III</creator><creator>Potter, Stephanie J</creator><creator>Putnam, Robert W</creator><general>Am Physiological Soc</general><general>American Physiological Society</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>7QP</scope><scope>7QR</scope><scope>7TK</scope><scope>7TS</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20040201</creationdate><title>Hyperoxia, reactive oxygen species, and hyperventilation: oxygen sensitivity of brain stem neurons</title><author>Dean, Jay B ; Mulkey, Daniel K ; Henderson, Richard A., III ; Potter, Stephanie J ; Putnam, Robert W</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c461t-9ab44cadb9f059c5cf4fca84ca6f3d83e5bc5016fd0e12661b47359afea5f2663</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Animals</topic><topic>Brain</topic><topic>Brain Stem - cytology</topic><topic>Brain Stem - metabolism</topic><topic>Brain Stem - physiology</topic><topic>Humans</topic><topic>Hyperoxia - metabolism</topic><topic>Hyperoxia - physiopathology</topic><topic>Hyperventilation - metabolism</topic><topic>Hyperventilation - physiopathology</topic><topic>Neurons</topic><topic>Neurons - physiology</topic><topic>Oxygen</topic><topic>Oxygen - metabolism</topic><topic>Reactive Oxygen Species - metabolism</topic><topic>Respiratory system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dean, Jay B</creatorcontrib><creatorcontrib>Mulkey, Daniel K</creatorcontrib><creatorcontrib>Henderson, Richard A., III</creatorcontrib><creatorcontrib>Potter, Stephanie J</creatorcontrib><creatorcontrib>Putnam, Robert W</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Physical Education Index</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of applied physiology (1985)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dean, Jay B</au><au>Mulkey, Daniel K</au><au>Henderson, Richard A., III</au><au>Potter, Stephanie J</au><au>Putnam, Robert W</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hyperoxia, reactive oxygen species, and hyperventilation: oxygen sensitivity of brain stem neurons</atitle><jtitle>Journal of applied physiology (1985)</jtitle><addtitle>J Appl Physiol (1985)</addtitle><date>2004-02-01</date><risdate>2004</risdate><volume>96</volume><issue>2</issue><spage>784</spage><epage>791</epage><pages>784-791</pages><issn>8750-7587</issn><eissn>1522-1601</eissn><abstract>Department of Anatomy and Physiology, Environmental and Hyperbaric Cell Biology Facility, Wright State University School of Medicine, College of Science and Mathematics, Dayton, Ohio 45435; and 1 Department of Military and Emergency Medicine, Uniformed Services University of the Health Sciences, Bethesda, Maryland 20814
Hyperoxia is a popular model of oxidative stress. However, hyperoxic gas mixtures are routinely used for chemical denervation of peripheral O 2 receptors in in vivo studies of respiratory control. The underlying assumption whenever using hyperoxia is that there are no direct effects of molecular O 2 and reactive O 2 species (ROS) on brain stem function. In addition, control superfusates used routinely for in vitro studies of neurons in brain slices are, in fact, hyperoxic. Again, the assumption is that there are no direct effects of O 2 and ROS on neuronal activity. Research contradicts this assumption by demonstrating that O 2 has central effects on the brain stem respiratory centers and several effects on neurons in respiratory control areas; these need to be considered whenever hyperoxia is used. This mini-review summarizes the long-recognized, but seldom acknowledged, paradox of respiratory control known as hyperoxic hyperventilation. Several proposed mechanisms are discussed, including the recent hypothesis that hyperoxic hyperventilation is initiated by increased production of ROS during hyperoxia, which directly stimulates central CO 2 chemoreceptors in the solitary complex. Hyperoxic hyperventilation may provide clues into the fundamental role of redox signaling and ROS in central control of breathing; moreover, oxidative stress may play a role in respiratory control dysfunction. The practical implications of brain stem O 2 and ROS sensitivity are also considered relative to the present uses of hyperoxia in respiratory control research in humans, animals, and brain stem tissues. Recommendations for future research are also proposed.
brain stem respiratory centers; central chemoreceptors; oxidative stress; hyperoxic hyperventilation
Address for reprint requests and other correspondence: J. B. Dean, Dept. of Anatomy and Physiology, 235C Bio. Sci. Bldg., 3640 Col. Glenn Hwy., Wright State Univ., Dayton, OH 45435 (E-mail: jay.dean{at}wright.edu ).</abstract><cop>United States</cop><pub>Am Physiological Soc</pub><pmid>14715688</pmid><doi>10.1152/japplphysiol.00892.2003</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Brain Brain Stem - cytology Brain Stem - metabolism Brain Stem - physiology Humans Hyperoxia - metabolism Hyperoxia - physiopathology Hyperventilation - metabolism Hyperventilation - physiopathology Neurons Neurons - physiology Oxygen Oxygen - metabolism Reactive Oxygen Species - metabolism Respiratory system |
title | Hyperoxia, reactive oxygen species, and hyperventilation: oxygen sensitivity of brain stem neurons |
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