Evidence map›Paper›PMID 10432349›Full record

ArticleThe Journal of physiology1999

Nitric oxide synthase inhibitors reduce sarcomere addition in rat skeletal muscle.

T J Koh, J G Tidball

Abstract read
In one paragraph

Article in The Journal of physiology, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

17 citing papers in PubMed.

  1. Effect of perindopril on physical function in elderly people with functional impairment: a randomized controlled trial.CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne · 2007
    Trial
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Exercise training modulates the nitric oxide synthase profile in skeletal muscle from old rats.The journals of gerontology. Series A, Biological sciences and medical sciences · 2009
    Article
  10. Article
  11. Review
  12. Mechanotransduction in skeletal muscle.Frontiers in bioscience : a journal and virtual library · 2007
    Review
  13. Article
  14. Reactive oxygen species and redox-regulation of skeletal muscle adaptations to exercise.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2005
    Review
  15. Signaling from novel splice variants of hormone receptors in cancer.International journal of gastrointestinal cancer · 2002
    Review
  16. Review
  17. Effect of NO on satellite cell proliferation during functional unloading and muscle stretching.Doklady biological sciences : proceedings of the Academy of Sciences of the USSR, Biological sciences sections
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

T J KohDepartment of Physiological Science, University of California, Los Angeles, CA 90095-1527, USA.
J G Tidball

Funding

REGULATION OF MYOTENDINOUS JUNCTION STRUCTURER01AR040343 · NIAMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI TIDBALL, JAMES G · 1989 to 2001
$485k
CALPAIN ACTIVITY REGULATION IN MODIFIED MUSCLE LOADINGF32AR008479 · NIAMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI KOH, TIMOTHY J · 1997 to 1998
–
NIAMS NIH HHS AR08479NIAMS NIH HHS AR40343NIAMS NIH HHS F32 AR008479
6 · The paper itself

Abstract

1. Mechanical stimuli are thought to modulate the number of sarcomeres in series (sarcomere number) in skeletal muscle fibres. However, the mechanisms by which muscle cells transduce mechanical signals into serial sarcomere addition have not been explored. In this study, we test the hypothesis that nitric oxide positively modulates sarcomere addition. 2. The soleus muscle was cast-immobilized in a shortened position in 3-week-old female Wistar rats. After 4 weeks, the casts were removed, creating a period of rapid sarcomere addition. During the remobilization period, nitric oxide synthase (NOS) inhibitors or substrate were administered. 3. Rats treated with the non-isoform-specific NOS inhibitor L-nitro-arginine methyl ester during 3 weeks of remobilization had smaller soleus sarcomere numbers than control rats. Rats treated with 1-(2-trifluoromethyl-phenyl)-imidazole, which has greater specificity for the neuronal isoform than for the endothelial isoform of NOS, also had smaller soleus sarcomere numbers than control rats. These results suggest that inhibition of the neuronal isoform of NOS reduces sarcomere addition during remobilization. 4. Rats treated with L-arginine, the substrate for NOS, during 1 week of remobilization had soleus sarcomere numbers for the immobilized-remobilized muscle which were closer to that for the contralateral, non-immobilized muscle than did rats that were not treated with L-arginine. 5. These results support the hypothesis that nitric oxide derived from the neuronal isoform of NOS positively modulates sarcomere addition.

Indexed as

AnimalsBody WeightEnzyme InhibitorsFemaleHydroxyprolineImmobilizationMotor ActivityMuscle, SkeletalNG-Nitroarginine Methyl EsterNitric Oxide SynthaseOrgan SizeRatsRats, WistarSarcomeresEnzyme InhibitorsHydroxyprolineNG-Nitroarginine Methyl EsterNitric Oxide SynthaseNon-programmatic

Identifiers

PMID10432349
PMCPMC2269494

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.