Evidence map›Paper›PMID 16685563›Full record

ArticlePflugers Archiv : European journal of physiology2006

Nonmuscle myosin, force maintenance, and the tonic contractile phenotype in smooth muscle.

Albert Y Rhee, Ozgur Ogut, Frank V Brozovich

Abstract read
PubMed Publisher
In one paragraph

Article in Pflugers Archiv : European journal of physiology, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

21 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Signaling and metabolic properties of fast and slow smooth muscle types from mice.Pflugers Archiv : European journal of physiology · 2018
    Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Transgenic overexpression of ribonucleotide reductase improves cardiac performance.Proceedings of the National Academy of Sciences of the United States of America · 2013
    Article
  12. Article
  13. Article
  14. Article
  15. Biochemistry of smooth muscle myosin light chain kinase.Archives of biochemistry and biophysics · 2011
    Review
  16. Article
  17. Review
  18. Nonmuscle myosin is regulated during smooth muscle contraction.American journal of physiology. Heart and circulatory physiology · 2009
    Article
  19. Review
  20. Load-dependent mechanism of nonmuscle myosin 2.Proceedings of the National Academy of Sciences of the United States of America · 2007
    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

3 authors.

Albert Y RheeDepartment of Physiology, University of Maryland, Baltimore, MD, USA.
Ozgur Ogut
Frank V Brozovich

Funding

REGULATION OF VASCULAR SMOOTH MUSCLE CONTRACTIONR01HL044181 · NHLBI · MAYO CLINIC · PI BROZOVICH, FRANK V · 1997 to 2005
$2.0M
REGULATION OF VASCULAR SMOOTH MUSCLE CONTRACTIONR29HL044181 · NHLBI · GRADUATE HOSPITAL (PHILADELPHIA) · PI BROZOVICH, FRANK V · 1990 to 1994
–
NHLBI NIH HHS HL 44181
6 · The paper itself

Abstract

Recent studies have demonstrated that nonmuscle (NM) myosin II forms filaments and can generate and maintain force in smooth muscle tissue [Lofgren et al. (2003) J Gen Physiol 121:301-310; Morano et al. (2000) Nat Cell Biol 2:371-375]. To further investigate the mechanical contribution of NM myosin to force maintenance during smooth muscle contraction, we utilized a selective inhibitor of the NM myosin ATPase, blebbistatin [Straight et al. (2003) Science 299:1743-1747]. Force and myosin light chain (MLC(20)) phosphorylation were measured during KCl stimulation of small strips of intact mouse bladder and aorta at 22 degrees C. The bladder strips contracted with a typical phasic force response, characterized by a large, rapid, transient increase in force followed by a decline to a lower, steady-state level. The addition of blebbistatin did not alter the peak force, but decreased force maintenance. KCl depolarization of aortic strips resulted in a tonic contraction; force increased to a sustained steady state. Similar to the bladder tissue, blebbistatin substantially decreased the steady-state force in the aorta. Blebbistatin did not influence the MLC(20) phosphorylation transient in either tissue type. Additionally, blebbistatin did not change the maximum shortening velocity (V (max)) during KCl depolarization of the aorta. Our results also suggest that NMIIA and NMIIB isoforms are differentially expressed. The expression of NMIIA is more prominent in the bladder, while NMIIB expression is predominant in the aorta. These results suggest that NM myosin contributes to the mechanism of force maintenance in smooth muscle, and could suggest that the expression of NMIIB is a factor for determining the tonic contractile phenotype.

Indexed as

AnimalsAorta, ThoracicDose-Response Relationship, DrugHeterocyclic Compounds, 4 or More RingsHydroxymethylglutaryl-CoA Reductase InhibitorsImmunohistochemistryKineticsMaleMiceMice, Inbred C57BLMuscle ContractionMuscle, SmoothMuscle TonusMyosin Light ChainsMyosinsPhenotypeblebbistatinHeterocyclic Compounds, 4 or More RingsHydroxymethylglutaryl-CoA Reductase InhibitorsMyosin Light ChainsMyosinsPotassium Chloride

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.