Influence of sodium nitroprusside on human erythrocyte membrane water permeability: an NMR study
Sodium nitroprusside (SNP) is a nitric oxide (•NO) donor in vitro and in vivo. In this paper the time variation of the intracellular water proton nuclear magnetic resonance (NMR) effective relaxation time T'(2a) in SNP-treated human erythrocyte suspensions, containing 10 mM membrane impermeable...
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Veröffentlicht in: | General physiology and biophysics 2010-12, Vol.29 (4), p.373-380 |
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description | Sodium nitroprusside (SNP) is a nitric oxide (•NO) donor in vitro and in vivo. In this paper the time variation of the intracellular water proton nuclear magnetic resonance (NMR) effective relaxation time T'(2a) in SNP-treated human erythrocyte suspensions, containing 10 mM membrane impermeable paramagnetic MnCl2, has been measured. The observed T'(2a) time-course was analyzed in terms of the two mechanisms by which released •NO affects T'(2a). These are, respectively, enhancement of the intracellular water proton intrinsic NMR relaxation rate 1/T(2a) by paramagnetism of •NO subsequently bonded to iron atoms of intracellular deoxyhemoglobin, and suppression of diffusional water permeability P(d) as a consequence of nitrosylation of aquaporin-1 (AQP1) channel Cys189, either by direct reaction with •NO or with one of the •NO oxidation products, such as N2O3. The bound •NO on the Cys189 thiol residue appears to impose a less efficient barrier to water permeation through AQP1 than the larger carboxyphenylmercuryl residue from p-chloromercuribenzoate. The effect of •NO on P(d) is discussed in terms of NO-induced vasodilation. |
doi_str_mv | 10.4149/gpb_2010_04_373 |
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In this paper the time variation of the intracellular water proton nuclear magnetic resonance (NMR) effective relaxation time T'(2a) in SNP-treated human erythrocyte suspensions, containing 10 mM membrane impermeable paramagnetic MnCl2, has been measured. The observed T'(2a) time-course was analyzed in terms of the two mechanisms by which released •NO affects T'(2a). These are, respectively, enhancement of the intracellular water proton intrinsic NMR relaxation rate 1/T(2a) by paramagnetism of •NO subsequently bonded to iron atoms of intracellular deoxyhemoglobin, and suppression of diffusional water permeability P(d) as a consequence of nitrosylation of aquaporin-1 (AQP1) channel Cys189, either by direct reaction with •NO or with one of the •NO oxidation products, such as N2O3. The bound •NO on the Cys189 thiol residue appears to impose a less efficient barrier to water permeation through AQP1 than the larger carboxyphenylmercuryl residue from p-chloromercuribenzoate. 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In this paper the time variation of the intracellular water proton nuclear magnetic resonance (NMR) effective relaxation time T'(2a) in SNP-treated human erythrocyte suspensions, containing 10 mM membrane impermeable paramagnetic MnCl2, has been measured. The observed T'(2a) time-course was analyzed in terms of the two mechanisms by which released •NO affects T'(2a). These are, respectively, enhancement of the intracellular water proton intrinsic NMR relaxation rate 1/T(2a) by paramagnetism of •NO subsequently bonded to iron atoms of intracellular deoxyhemoglobin, and suppression of diffusional water permeability P(d) as a consequence of nitrosylation of aquaporin-1 (AQP1) channel Cys189, either by direct reaction with •NO or with one of the •NO oxidation products, such as N2O3. The bound •NO on the Cys189 thiol residue appears to impose a less efficient barrier to water permeation through AQP1 than the larger carboxyphenylmercuryl residue from p-chloromercuribenzoate. The effect of •NO on P(d) is discussed in terms of NO-induced vasodilation.</description><subject>Cell Membrane Permeability - drug effects</subject><subject>Diffusion</subject><subject>Erythrocyte Membrane - drug effects</subject><subject>Erythrocyte Membrane - metabolism</subject><subject>Humans</subject><subject>Intracellular Space - drug effects</subject><subject>Intracellular Space - metabolism</subject><subject>Kinetics</subject><subject>Magnetic Resonance Spectroscopy - methods</subject><subject>Male</subject><subject>Nitric Oxide Donors - pharmacology</subject><subject>Nitroprusside - pharmacology</subject><subject>Water - metabolism</subject><issn>0231-5882</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkDtPwzAURj2AaFU6syFvTKF-xjEbqnhUKiAhmIPjODQoToIfQvn3GLUwcJcrfTr309UB4AyjS4aZXL2PVUkQRiViJRX0CMwRoTjjRUFmYOn9B0rDhSQEnYAZwZiLFMzB26Zvumh6beDQQD_UbbSwb4MbRhe9b-uU93AXreqhcVPYuUFPwUBrbOVUb-CXCsbB0ThrVNV2bZiuYGIfH56hD7GeTsFxozpvloe9AK-3Ny_r-2z7dLdZX28zTakImazqWnCGdJETQxRtCNJSSVkgkv5kikiiK0pEzbDkucyR4JznjEpBKikKSRfgYt87uuEzGh9K23ptui49OURfFrhgiBApErnak9oN3jvTlKNrrXJTmfT9yCz_yUwX54fuWFlT__G_Guk3ruxx2g</recordid><startdate>201012</startdate><enddate>201012</enddate><creator>Lahajnar, Gojmir</creator><creator>Sobotič, Barbara</creator><creator>Sepe, Ana</creator><creator>Jazbinšek, Vojko</creator><creator>Pečar, Slavko</creator><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>201012</creationdate><title>Influence of sodium nitroprusside on human erythrocyte membrane water permeability: an NMR study</title><author>Lahajnar, Gojmir ; Sobotič, Barbara ; Sepe, Ana ; Jazbinšek, Vojko ; Pečar, Slavko</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c337t-9bdd7540c862e2a3f20c9a998020004a292cb327d419569607555643972b97893</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Cell Membrane Permeability - drug effects</topic><topic>Diffusion</topic><topic>Erythrocyte Membrane - drug effects</topic><topic>Erythrocyte Membrane - metabolism</topic><topic>Humans</topic><topic>Intracellular Space - drug effects</topic><topic>Intracellular Space - metabolism</topic><topic>Kinetics</topic><topic>Magnetic Resonance Spectroscopy - methods</topic><topic>Male</topic><topic>Nitric Oxide Donors - pharmacology</topic><topic>Nitroprusside - pharmacology</topic><topic>Water - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lahajnar, Gojmir</creatorcontrib><creatorcontrib>Sobotič, Barbara</creatorcontrib><creatorcontrib>Sepe, Ana</creatorcontrib><creatorcontrib>Jazbinšek, Vojko</creatorcontrib><creatorcontrib>Pečar, Slavko</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>General physiology and biophysics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lahajnar, Gojmir</au><au>Sobotič, Barbara</au><au>Sepe, Ana</au><au>Jazbinšek, Vojko</au><au>Pečar, Slavko</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Influence of sodium nitroprusside on human erythrocyte membrane water permeability: an NMR study</atitle><jtitle>General physiology and biophysics</jtitle><addtitle>Gen Physiol Biophys</addtitle><date>2010-12</date><risdate>2010</risdate><volume>29</volume><issue>4</issue><spage>373</spage><epage>380</epage><pages>373-380</pages><issn>0231-5882</issn><abstract>Sodium nitroprusside (SNP) is a nitric oxide (•NO) donor in vitro and in vivo. In this paper the time variation of the intracellular water proton nuclear magnetic resonance (NMR) effective relaxation time T'(2a) in SNP-treated human erythrocyte suspensions, containing 10 mM membrane impermeable paramagnetic MnCl2, has been measured. The observed T'(2a) time-course was analyzed in terms of the two mechanisms by which released •NO affects T'(2a). These are, respectively, enhancement of the intracellular water proton intrinsic NMR relaxation rate 1/T(2a) by paramagnetism of •NO subsequently bonded to iron atoms of intracellular deoxyhemoglobin, and suppression of diffusional water permeability P(d) as a consequence of nitrosylation of aquaporin-1 (AQP1) channel Cys189, either by direct reaction with •NO or with one of the •NO oxidation products, such as N2O3. The bound •NO on the Cys189 thiol residue appears to impose a less efficient barrier to water permeation through AQP1 than the larger carboxyphenylmercuryl residue from p-chloromercuribenzoate. The effect of •NO on P(d) is discussed in terms of NO-induced vasodilation.</abstract><cop>Slovakia</cop><pmid>21157000</pmid><doi>10.4149/gpb_2010_04_373</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Cell Membrane Permeability - drug effects Diffusion Erythrocyte Membrane - drug effects Erythrocyte Membrane - metabolism Humans Intracellular Space - drug effects Intracellular Space - metabolism Kinetics Magnetic Resonance Spectroscopy - methods Male Nitric Oxide Donors - pharmacology Nitroprusside - pharmacology Water - metabolism |
title | Influence of sodium nitroprusside on human erythrocyte membrane water permeability: an NMR study |
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