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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
Main Authors: Lau, Kim S., Grange, Robert W., Chang, Wen-Jinn, Kamm, Kristine E., Sarelius, Ingrid, Stull, James T.
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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
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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. ; 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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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identifier ISSN: 0014-5793
ispartof FEBS letters, 1998-07, Vol.431 (1), p.71-74
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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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