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Skeletal muscle contractions stimulate cGMP formation and attenuate vascular smooth muscle myosin phosphorylation via nitric oxide
Nitric oxide generated by neuronal nitric oxide synthase in contracting skeletal muscle fibers may regulate vascular relaxation via a cGMP-mediated pathway. Neuronal nitric oxide synthase content is greatly reduced in skeletal muscles from mdx mice. cGMP formation increased in contracting extensor d...
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Published in: | FEBS letters 1998-07, Vol.431 (1), p.71-74 |
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creator | Lau, Kim S. Grange, Robert W. Chang, Wen-Jinn Kamm, Kristine E. Sarelius, Ingrid Stull, James T. |
description | Nitric oxide generated by neuronal nitric oxide synthase in contracting skeletal muscle fibers may regulate vascular relaxation via a cGMP-mediated pathway. Neuronal nitric oxide synthase content is greatly reduced in skeletal muscles from
mdx mice. cGMP formation increased in contracting extensor digitorum longus muscles in vitro from C57 control, but not
mdx mice. The increase in cGMP content was abolished with
N
G-nitro-
l-arginine. Sodium nitroprusside treatment increased cGMP levels in muscles from both C57 and
mdx mice. Skeletal muscle contractions also inhibited phenylephrine-induced phosphorylation of smooth muscle myosin regulatory light chain. Arteriolar dilation was attenuated in contracting muscles from
mdx but not C57 mice. NO generated in contracting skeletal muscle may contribute to vasodilation in response to exercise. |
doi_str_mv | 10.1016/S0014-5793(98)00728-5 |
format | article |
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mdx mice. cGMP formation increased in contracting extensor digitorum longus muscles in vitro from C57 control, but not
mdx mice. The increase in cGMP content was abolished with
N
G-nitro-
l-arginine. Sodium nitroprusside treatment increased cGMP levels in muscles from both C57 and
mdx mice. Skeletal muscle contractions also inhibited phenylephrine-induced phosphorylation of smooth muscle myosin regulatory light chain. Arteriolar dilation was attenuated in contracting muscles from
mdx but not C57 mice. NO generated in contracting skeletal muscle may contribute to vasodilation in response to exercise.</description><identifier>ISSN: 0014-5793</identifier><identifier>EISSN: 1873-3468</identifier><identifier>DOI: 10.1016/S0014-5793(98)00728-5</identifier><identifier>PMID: 9684868</identifier><language>eng</language><publisher>England: Elsevier B.V</publisher><subject>[Ca2+]i, intracellular calcium ; Animals ; cGMP ; CHAPS, 3-[(3-chlolamido propyl)dimethyl-ammonia]-1-propane sulfonate ; Cyclic GMP - metabolism ; DMD, Duchenne's muscular dystrophy ; EDTA, ethylenediaminetetraacetic acid ; eNOS, endothelial nitric oxide synthase ; HRP, horse radish peroxidase ; Humans ; Hz, hertz ; In Vitro Techniques ; iNOS, inducible nitric oxide synthase ; L-NMMA, N G-monomethyl-l-arginine ; Male ; Mice ; Mice, Inbred C57BL ; Muscle Contraction ; Muscle, Skeletal - blood supply ; Muscle, Skeletal - metabolism ; Muscle, Skeletal - physiology ; Muscle, Smooth, Vascular - metabolism ; Muscular Dystrophies - metabolism ; Myosin Light Chains - metabolism ; Myosins - metabolism ; Nitric Oxide - metabolism ; Nitric oxide synthase ; NLA, N G-nitro-l-arginine ; nNOS, neuronal nitric oxide synthase ; NO, nitric oxide ; NOS, nitric oxide synthase ; Phosphorylation ; Physical Exertion ; PSS, physiological salt solution ; PVDF, polyvinylidene fluoride ; RLC, regulatory light chain ; sGC, soluble guanylyl cyclase ; Skeletal muscle ; SNP, sodium nitroprusside ; Space life sciences ; TLCK, N-α-p-tosyl-l-lysine chloromethyl ketone ; Vascular smooth muscle ; Vasodilation</subject><ispartof>FEBS letters, 1998-07, Vol.431 (1), p.71-74</ispartof><rights>1998 Federation of European Biochemical Societies</rights><rights>FEBS Letters 431 (1998) 1873-3468 © 2015 Federation of European Biochemical Societies</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5385-efc496c4bd020b41b4f95aacf06b58d5edd2930d7c8439486fdf285f21368d7b3</citedby><cites>FETCH-LOGICAL-c5385-efc496c4bd020b41b4f95aacf06b58d5edd2930d7c8439486fdf285f21368d7b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0014579398007285$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,777,781,3536,27905,27906,45761</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9684868$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lau, Kim S.</creatorcontrib><creatorcontrib>Grange, Robert W.</creatorcontrib><creatorcontrib>Chang, Wen-Jinn</creatorcontrib><creatorcontrib>Kamm, Kristine E.</creatorcontrib><creatorcontrib>Sarelius, Ingrid</creatorcontrib><creatorcontrib>Stull, James T.</creatorcontrib><title>Skeletal muscle contractions stimulate cGMP formation and attenuate vascular smooth muscle myosin phosphorylation via nitric oxide</title><title>FEBS letters</title><addtitle>FEBS Lett</addtitle><description>Nitric oxide generated by neuronal nitric oxide synthase in contracting skeletal muscle fibers may regulate vascular relaxation via a cGMP-mediated pathway. Neuronal nitric oxide synthase content is greatly reduced in skeletal muscles from
mdx mice. cGMP formation increased in contracting extensor digitorum longus muscles in vitro from C57 control, but not
mdx mice. The increase in cGMP content was abolished with
N
G-nitro-
l-arginine. Sodium nitroprusside treatment increased cGMP levels in muscles from both C57 and
mdx mice. Skeletal muscle contractions also inhibited phenylephrine-induced phosphorylation of smooth muscle myosin regulatory light chain. Arteriolar dilation was attenuated in contracting muscles from
mdx but not C57 mice. NO generated in contracting skeletal muscle may contribute to vasodilation in response to exercise.</description><subject>[Ca2+]i, intracellular calcium</subject><subject>Animals</subject><subject>cGMP</subject><subject>CHAPS, 3-[(3-chlolamido propyl)dimethyl-ammonia]-1-propane sulfonate</subject><subject>Cyclic GMP - metabolism</subject><subject>DMD, Duchenne's muscular dystrophy</subject><subject>EDTA, ethylenediaminetetraacetic acid</subject><subject>eNOS, endothelial nitric oxide synthase</subject><subject>HRP, horse radish peroxidase</subject><subject>Humans</subject><subject>Hz, hertz</subject><subject>In Vitro Techniques</subject><subject>iNOS, inducible nitric oxide synthase</subject><subject>L-NMMA, N G-monomethyl-l-arginine</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Muscle Contraction</subject><subject>Muscle, Skeletal - blood supply</subject><subject>Muscle, Skeletal - metabolism</subject><subject>Muscle, Skeletal - physiology</subject><subject>Muscle, Smooth, Vascular - metabolism</subject><subject>Muscular Dystrophies - metabolism</subject><subject>Myosin Light Chains - metabolism</subject><subject>Myosins - metabolism</subject><subject>Nitric Oxide - metabolism</subject><subject>Nitric oxide synthase</subject><subject>NLA, N G-nitro-l-arginine</subject><subject>nNOS, neuronal nitric oxide synthase</subject><subject>NO, nitric oxide</subject><subject>NOS, nitric oxide synthase</subject><subject>Phosphorylation</subject><subject>Physical Exertion</subject><subject>PSS, physiological salt solution</subject><subject>PVDF, polyvinylidene fluoride</subject><subject>RLC, regulatory light chain</subject><subject>sGC, soluble guanylyl cyclase</subject><subject>Skeletal muscle</subject><subject>SNP, sodium nitroprusside</subject><subject>Space life sciences</subject><subject>TLCK, N-α-p-tosyl-l-lysine chloromethyl ketone</subject><subject>Vascular smooth muscle</subject><subject>Vasodilation</subject><issn>0014-5793</issn><issn>1873-3468</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><recordid>eNqNkE2P1SAYhYnRjNfRnzAJK6OLKpTSwso4k_kwGaPJ6JpQeMmgbbkCvXq3_nLp7XW2uiAEnnPOCwehM0reUELbt3eE0KbinWSvpHhNSFeLij9CGyo6VrGmFY_R5kHyFD1L6RspZ0HlCTqRrWhEKzbo9913GCDrAY9zMgNgE6Yctck-TAmn7Md50LlcX3_8jF2Io14I1pPFOmeY5gXudDJFFnEaQ8j3f6PGfUh-wtv7kMqK-2H17rzGk8_RGxx-eQvP0ROnhwQvjvsp-np1-eXiprr9dP3h4v1tZTgTvAJnGtmaprekJn1D-8ZJrrVxpO25sBysrSUjtjOiYbL8zllXC-5qylphu56dopdr7jaGHzOkrEafDAyDniDMSQlCio-yIuSr0MSQUgSnttGPOu4VJWrpXh26V0uxSgp16F7x4js7Dpj7EeyD61h24Tcr_-kH2P9fqLq6PK8PZAFSHK6XUe_WKCiF7TxElYyHyYD1EUxWNvh_PPYPvWGrtg</recordid><startdate>19980710</startdate><enddate>19980710</enddate><creator>Lau, Kim S.</creator><creator>Grange, Robert W.</creator><creator>Chang, Wen-Jinn</creator><creator>Kamm, Kristine E.</creator><creator>Sarelius, Ingrid</creator><creator>Stull, James T.</creator><general>Elsevier B.V</general><scope>6I.</scope><scope>AAFTH</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>7X8</scope></search><sort><creationdate>19980710</creationdate><title>Skeletal muscle contractions stimulate cGMP formation and attenuate vascular smooth muscle myosin phosphorylation via nitric oxide</title><author>Lau, Kim S. ; Grange, Robert W. ; Chang, Wen-Jinn ; Kamm, Kristine E. ; Sarelius, Ingrid ; Stull, James T.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5385-efc496c4bd020b41b4f95aacf06b58d5edd2930d7c8439486fdf285f21368d7b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>[Ca2+]i, intracellular calcium</topic><topic>Animals</topic><topic>cGMP</topic><topic>CHAPS, 3-[(3-chlolamido propyl)dimethyl-ammonia]-1-propane sulfonate</topic><topic>Cyclic GMP - metabolism</topic><topic>DMD, Duchenne's muscular dystrophy</topic><topic>EDTA, ethylenediaminetetraacetic acid</topic><topic>eNOS, endothelial nitric oxide synthase</topic><topic>HRP, horse radish peroxidase</topic><topic>Humans</topic><topic>Hz, hertz</topic><topic>In Vitro Techniques</topic><topic>iNOS, inducible nitric oxide synthase</topic><topic>L-NMMA, N G-monomethyl-l-arginine</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Muscle Contraction</topic><topic>Muscle, Skeletal - blood supply</topic><topic>Muscle, Skeletal - metabolism</topic><topic>Muscle, Skeletal - physiology</topic><topic>Muscle, Smooth, Vascular - metabolism</topic><topic>Muscular Dystrophies - metabolism</topic><topic>Myosin Light Chains - metabolism</topic><topic>Myosins - metabolism</topic><topic>Nitric Oxide - metabolism</topic><topic>Nitric oxide synthase</topic><topic>NLA, N G-nitro-l-arginine</topic><topic>nNOS, neuronal nitric oxide synthase</topic><topic>NO, nitric oxide</topic><topic>NOS, nitric oxide synthase</topic><topic>Phosphorylation</topic><topic>Physical Exertion</topic><topic>PSS, physiological salt solution</topic><topic>PVDF, polyvinylidene fluoride</topic><topic>RLC, regulatory light chain</topic><topic>sGC, soluble guanylyl cyclase</topic><topic>Skeletal muscle</topic><topic>SNP, sodium nitroprusside</topic><topic>Space life sciences</topic><topic>TLCK, N-α-p-tosyl-l-lysine chloromethyl ketone</topic><topic>Vascular smooth muscle</topic><topic>Vasodilation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lau, Kim S.</creatorcontrib><creatorcontrib>Grange, Robert W.</creatorcontrib><creatorcontrib>Chang, Wen-Jinn</creatorcontrib><creatorcontrib>Kamm, Kristine E.</creatorcontrib><creatorcontrib>Sarelius, Ingrid</creatorcontrib><creatorcontrib>Stull, James T.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><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>FEBS letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lau, Kim S.</au><au>Grange, Robert W.</au><au>Chang, Wen-Jinn</au><au>Kamm, Kristine E.</au><au>Sarelius, Ingrid</au><au>Stull, James T.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Skeletal muscle contractions stimulate cGMP formation and attenuate vascular smooth muscle myosin phosphorylation via nitric oxide</atitle><jtitle>FEBS letters</jtitle><addtitle>FEBS Lett</addtitle><date>1998-07-10</date><risdate>1998</risdate><volume>431</volume><issue>1</issue><spage>71</spage><epage>74</epage><pages>71-74</pages><issn>0014-5793</issn><eissn>1873-3468</eissn><abstract>Nitric oxide generated by neuronal nitric oxide synthase in contracting skeletal muscle fibers may regulate vascular relaxation via a cGMP-mediated pathway. Neuronal nitric oxide synthase content is greatly reduced in skeletal muscles from
mdx mice. cGMP formation increased in contracting extensor digitorum longus muscles in vitro from C57 control, but not
mdx mice. The increase in cGMP content was abolished with
N
G-nitro-
l-arginine. Sodium nitroprusside treatment increased cGMP levels in muscles from both C57 and
mdx mice. Skeletal muscle contractions also inhibited phenylephrine-induced phosphorylation of smooth muscle myosin regulatory light chain. Arteriolar dilation was attenuated in contracting muscles from
mdx but not C57 mice. NO generated in contracting skeletal muscle may contribute to vasodilation in response to exercise.</abstract><cop>England</cop><pub>Elsevier B.V</pub><pmid>9684868</pmid><doi>10.1016/S0014-5793(98)00728-5</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
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language | eng |
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source | Wiley; ScienceDirect Journals |
subjects | [Ca2+]i, intracellular calcium Animals cGMP CHAPS, 3-[(3-chlolamido propyl)dimethyl-ammonia]-1-propane sulfonate Cyclic GMP - metabolism DMD, Duchenne's muscular dystrophy EDTA, ethylenediaminetetraacetic acid eNOS, endothelial nitric oxide synthase HRP, horse radish peroxidase Humans Hz, hertz In Vitro Techniques iNOS, inducible nitric oxide synthase L-NMMA, N G-monomethyl-l-arginine Male Mice Mice, Inbred C57BL Muscle Contraction Muscle, Skeletal - blood supply Muscle, Skeletal - metabolism Muscle, Skeletal - physiology Muscle, Smooth, Vascular - metabolism Muscular Dystrophies - metabolism Myosin Light Chains - metabolism Myosins - metabolism Nitric Oxide - metabolism Nitric oxide synthase NLA, N G-nitro-l-arginine nNOS, neuronal nitric oxide synthase NO, nitric oxide NOS, nitric oxide synthase Phosphorylation Physical Exertion PSS, physiological salt solution PVDF, polyvinylidene fluoride RLC, regulatory light chain sGC, soluble guanylyl cyclase Skeletal muscle SNP, sodium nitroprusside Space life sciences TLCK, N-α-p-tosyl-l-lysine chloromethyl ketone Vascular smooth muscle Vasodilation |
title | Skeletal muscle contractions stimulate cGMP formation and attenuate vascular smooth muscle myosin phosphorylation via nitric oxide |
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