Evidence map›Paper›PMID 10098975›Full record

ArticleMolecular and cellular biochemistry1999

Ca2+ -induced Ca2+ desensitization of myosin light chain phosphorylation and contraction in phasic smooth muscle.

T Murahashi, A Fujita, T Kitazawa

Abstract read
PubMed
In one paragraph

Article in Molecular and cellular biochemistry, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.4field-weighted citation impact, top 39% of its field
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

8 citing papers in PubMed, 11 citations in OpenAlex.

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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 at 1 institution in 1 country.

T MurahashiDepartment of Physiology and Biophysics, Georgetown University School of Medicine, Washington, DC 20007, USA.
A Fujita
T Kitazawa
Georgetown University · US

Funding

G PROTEIN-MEDIATED CA++ SENSITIZATION IN SMOOTH MUSCLER01HL051824 · NHLBI · GEORGETOWN UNIVERSITY · PI KITAZAWA, TOSHIO · 1993 to 2002
$952k
NHLBI NIH HHS R01 HL51824
6 · The paper itself

Abstract

The temporal relationship between Ca2+ -induced contraction and phosphorylation of 20 kDa myosin light chain (MLC) during a step increase in Ca2+ was investigated using permeabilized phasic smooth muscle from rabbit portal vein and guinea-pig ileum at 25 degrees C. We describe here a Ca2+ -induced Ca2+ desensitization phenomenon in which a transient rise in MLC phosphorylation is followed by a transient rise in contractile force. During and after the peak contraction, the force to phosphorylation ratio remained constant. Further treatment with cytochalasin D, an actin fragmenting agent, did not affect the transient increase in phosphorylation, but blocked force development. Together, these results indicate that the transient phosphorylation causes the transient contraction and that neither inhomogeneous contractility nor reduced thin filament integrity effects the transient phosphorylation. Lastly, we show that known inhibitors to MLC kinase kinases and to a Ca2+ -dependent protein phosphatase did not eliminate the desensitized contractile force. This study suggests that the Ca2+ -induced Ca2+ desensitization phenomenon in phasic smooth muscle does not result from any of the known intrinsic mechanisms involved with other aspects of smooth muscle contractility.

Indexed as

AnimalsCalcineurin InhibitorsCalciumCytochalasin DEnzyme ActivationGuinea PigsIn Vitro TechniquesMaleMuscle ContractionMuscle, SmoothMyosin-Light-Chain KinaseMyosin-Light-Chain PhosphataseMyosin Light ChainsPhosphoprotein PhosphatasesPhosphorylationRabbitsCalcineurin InhibitorsCalciumCytochalasin DMyosin-Light-Chain KinaseMyosin-Light-Chain PhosphataseMyosin Light ChainsPhosphoprotein Phosphatases

Identifiers

PMID10098975
OpenAlexW1487435899

What OpenQuestion holds

Texttitle and abstract
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.