Evidence map›Paper›PMID 2454449›Full record

ArticlePflugers Archiv : European journal of physiology1988

Fast and slowly inactivating components of Ca-channel current and their sensitivities to nicardipine in isolated smooth muscle cells from rat vas deferens.

K Nakazawa, H Saito, N Matsuki

Abstract read
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In one paragraph

Article in Pflugers Archiv : European journal of physiology, 1988. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

18 citing papers in PubMed, 45 citations in OpenAlex.

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  18. Endothelin activates the dihydropyridine-sensitive, voltage-dependent Ca2+ channel in vascular smooth muscle.Proceedings of the National Academy of Sciences of the United States of America · 1989
    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 at 1 institution in 1 country.

K NakazawaDepartment of Chemical Pharmacology, Faculty of Pharmaceutical Sciences, University of Tokyo, Japan.
H Saito
N Matsuki
The University of Tokyo · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

(1) Fast and slowly inactivating components of Ca-channel current were compared to clarify whether more than one type of Ca-channel exists in smooth muscle cells from rat vas deferens using the whole cell variant of the patch clamp technique. The pipette was filled with 150 mM Cs solution to eliminate outward current and Ba was used as the charge carrier for Ca-channel current. (2) When activated by a 5 s test pulse to O mV from a holding potential of -60 mV, the inactivation process of Ba-current was well fitted by the sum of two exponentials. The time constant of the faster inactivating component was 100-300 s and that of the slower inactivating component was 1.5-3 s. Steady-state inactivation curves of the fast- and slow-components were very similar. (3) The inward current activated at O mV from -80 mV was inactivated faster than that from -30 mV. The voltage-dependencies of the peak current from holding potentials of -30 mV and -80 mV were similar. Both had voltage threshold at -30 mV and were maximal at +10 mV. (4) Low concentrations of nicardipine (10(-9) to 10(-7) M) preferentially inhibited the slow component while higher concentration (10(-6) to 10(-5) M) were required to block the fast component. The current activated from a holding potential of -30 mV was almost fully suppressed by 10(-7) M nicardipine whereas that from -80 mV was blocked only slightly.(ABSTRACT TRUNCATED AT 250 WORDS)

Indexed as

AnimalsBariumCalciumElectric ConductivityIon ChannelsMaleMuscle, SmoothNicardipineRatsVas DeferensBariumCalciumIon ChannelsNicardipine

Identifiers

PMID2454449
OpenAlexW1965721579

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.