Literature DB >> 7806639

Comparison of the effects of 2,3-butanedione monoxime on force production, myosin light chain phosphorylation and chemical energy usage in intact and permeabilized smooth and skeletal muscles.

M J Siegman1, S U Mooers, T B Warren, D M Warshaw, M Ikebe, T M Butler.   

Abstract

The primary goal of this study was to determine the utility of 2,3-butanedione monoxime as a tool for determining and separating the chemical energy usage associated with force production from that of force-independent, or 'activation' processes in smooth and skeletal muscles. We determined the effects of 2,3-butanedione monoxime on force production, myosin light chain phosphorylation and high energy phosphate usage in intact and permeabilized smooth (rabbit taenia coli) and skeletal (mouse extensor digitorum longus) muscles. In the intact taenia coli, 2,3-butanedione monoxime depressed the tonic phase of the tetanus, contractures evoked by high potassium (90 mM) and by carbachol (10(-5) M) and the small force response evoked by these agonists after treatment with D-600 (10(-5) M). In the electrically stimulated intact taenia coli 2,3-butanedione monoxime (0-20 mM) caused a proportional inhibition of tetanic force output, myosin light chain phosphorylation and high energy phosphate usage (ED50 approximately 7 mM for all these parameters). At 20 mM 2,3-butanedione monoxime, force and energy usage fell to near zero and the degree of myosin light chain phosphorylation decreased to resting values, indicating a shut-down of both force-dependent and force-independent energy usage at high concentrations of 2,3-butanedione monoxime. In permeabilized taenia coli, 2,3-butanedione monoxime had little or no depressant effects on force production, ATPase activity or calcium sensitivity. 2,3-butanedione monoxime had a very modest inhibitory effect on the in vitro motility of unregulated actin filaments interacting with thiophosphorylated myosin. In solution, 2,3-butanedione monoxime inhibited myosin light chain kinase, but not the phosphatase (SMP-IV). These results suggest that the major effect of 2,3-butanedione monoxime is not on the contractile proteins themselves, but rather on calcium delivery during excitation, thereby reducing the degree of activation of myosin light chain kinase and subsequent activation of myosin by light chain phosphorylation. Thus, 2,3-butanedione monoxime is not useful for the determination of the energetics of activation processes in smooth muscle because of its inhibition of both force-dependent and force-independent processes. In contrast, in the intact mouse extensor digitorum longus, 2,3-butanedione monoxime inhibits tetanic force production (ED50 approximately 2 mM) to a much greater extent than myosin light chain phosphorylation. When 2,3-butanedione monoxime was used to manipulate force production in muscles at L(o), it was found that approximately 60% of the total energy usage was force-independent and the remainder was force-dependent.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1994        PMID: 7806639     DOI: 10.1007/bf00122119

Source DB:  PubMed          Journal:  J Muscle Res Cell Motil        ISSN: 0142-4319            Impact factor:   2.698


  53 in total

1.  Substrate based inhibitors of smooth muscle myosin light chain kinase.

Authors:  S Moreland; M Ikebe; J T Hunt; R S Moreland
Journal:  Biochem Biophys Res Commun       Date:  1992-05-29       Impact factor: 3.575

2.  The estimation of creatine and of diacetyl.

Authors:  P Eggleton; S R Elsden; N Gough
Journal:  Biochem J       Date:  1943       Impact factor: 3.857

3.  The effects of a calcium dependent protease on the ultrastructure and contractile mechanics of skinned uterine smooth muscle.

Authors:  J R Haeberle; S A Coolican; A Evan; D R Hathaway
Journal:  J Muscle Res Cell Motil       Date:  1985-06       Impact factor: 2.698

4.  Perfusion cuvette for the simultaneous measurement of mechanical, optical and energetic parameters of skinned muscle fibres.

Authors:  K Güth; R Wojciechowski
Journal:  Pflugers Arch       Date:  1986-11       Impact factor: 3.657

5.  Ca2+ can affect Vmax without changes in myosin light chain phosphorylation in smooth muscle.

Authors:  M J Siegman; T M Butler; S U Mooers; A Michalek
Journal:  Pflugers Arch       Date:  1984-08       Impact factor: 3.657

6.  Phosphorylation of the 20,000-dalton light chain of smooth muscle myosin by the calcium-activated, phospholipid-dependent protein kinase. Phosphorylation sites and effects of phosphorylation.

Authors:  M Ikebe; D J Hartshorne; M Elzinga
Journal:  J Biol Chem       Date:  1987-07-15       Impact factor: 5.157

7.  The effects of 2,3-butanedione monoxime on initial heat, tension, and aequorin light output of ferret papillary muscles.

Authors:  E M Blanchard; G L Smith; D G Allen; N R Alpert
Journal:  Pflugers Arch       Date:  1990-04       Impact factor: 3.657

8.  Effects of 2,3-butanedione monoxime on contraction of frog skeletal muscles: an X-ray diffraction study.

Authors:  N Yagi; S Takemori; M Watanabe; K Horiuti; Y Amemiya
Journal:  J Muscle Res Cell Motil       Date:  1992-04       Impact factor: 2.698

9.  Mechanism of action of 2, 3-butanedione 2-monoxime on contraction of frog skeletal muscle fibres.

Authors:  K Horiuti; H Higuchi; Y Umazume; M Konishi; O Okazaki; S Kurihara
Journal:  J Muscle Res Cell Motil       Date:  1988-04       Impact factor: 2.698

10.  Butanedione monoxime suppresses contraction and ATPase activity of rabbit skeletal muscle.

Authors:  H Higuchi; S Takemori
Journal:  J Biochem       Date:  1989-04       Impact factor: 3.387

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  10 in total

1.  Effects of vanadate, phosphate and 2,3-butanedione monoxime (BDM) on skinned molluscan catch muscle.

Authors:  Stefan Galler; Marion Christine Höpflinger; Oleg Andruchov; Olena Andruchova; Herbert Grassberger
Journal:  Pflugers Arch       Date:  2004-10-15       Impact factor: 3.657

2.  Force-dependent and force-independent heat production in single slow- and fast-twitch muscle fibres from Xenopus laevis.

Authors:  H P Buschman; W J van der Laarse; G J Stienen; G Elzinga
Journal:  J Physiol       Date:  1996-10-15       Impact factor: 5.182

3.  Redundant mechanisms for anaphase chromosome movements: crane-fly spermatocyte spindles normally use actin filaments but also can function without them.

Authors:  Lacramioara Fabian; Arthur Forer
Journal:  Protoplasma       Date:  2005-10-05       Impact factor: 3.356

Review 4.  Energy turnover for Ca2+ cycling in skeletal muscle.

Authors:  C J Barclay; R C Woledge; N A Curtin
Journal:  J Muscle Res Cell Motil       Date:  2007-09-20       Impact factor: 2.698

5.  The scaffolding protein ZO-1 coordinates actomyosin and epithelial apical specializations in vitro and in vivo.

Authors:  Matthew A Odenwald; Wangsun Choi; Wei-Ting Kuo; Gurminder Singh; Anne Sailer; Yitang Wang; Le Shen; Alan S Fanning; Jerrold R Turner
Journal:  J Biol Chem       Date:  2018-09-21       Impact factor: 5.157

6.  2,3-butanedione monoxime (BDM), a potent inhibitor of actin-myosin interaction, induces ion and fluid transport in MDCK monolayers.

Authors:  Aida M Castillo; José Luis Reyes; Elsa Sánchez; Ricardo Mondragón; Isaura Meza
Journal:  J Muscle Res Cell Motil       Date:  2002       Impact factor: 2.698

7.  Rho-stimulated contractility drives the formation of stress fibers and focal adhesions.

Authors:  M Chrzanowska-Wodnicka; K Burridge
Journal:  J Cell Biol       Date:  1996-06       Impact factor: 10.539

Review 8.  Small-molecule inhibitors of myosin proteins.

Authors:  Lisa M Bond; David A Tumbarello; John Kendrick-Jones; Folma Buss
Journal:  Future Med Chem       Date:  2013-01       Impact factor: 3.808

9.  2,3-Butanedione monoxime (BDM) as a myosin inhibitor.

Authors:  E Michael Ostap
Journal:  J Muscle Res Cell Motil       Date:  2002       Impact factor: 3.352

10.  Myosin is involved in postmitotic cell spreading.

Authors:  L P Cramer; T J Mitchison
Journal:  J Cell Biol       Date:  1995-10       Impact factor: 10.539

  10 in total

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