Evidence map›Paper›PMID 9032690›Full record

ArticleThe Journal of physiology1997

An ATP-gated cation channel with some P2Z-like characteristics in gastric smooth muscle cells of toad.

M Ugur, R M Drummond, H Zou, P Sheng, J J Singer, J V Walsh

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In one paragraph

Article in The Journal of physiology, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.0field-weighted citation impact, top 15% 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

7 citing papers in PubMed, 33 citations in OpenAlex.

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  6. Single channel properties of P2X2 purinoceptors.The Journal of general physiology · 1999
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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

6 authors at 1 institution in 1 country.

M UgurDepartment of Physiology, University of Massachusetts Medical School, Worcester 01655, USA.
R M Drummond
H Zou
P Sheng
J J Singer
J V Walsh
University of Massachusetts Chan Medical School · US

Funding

IONIC CHANNELS IN DISSOCIATED SMOOTH MUSCLE CELLSR01DK031620 · NIDDK · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI WALSH, JOHN V · 1986 to 2000
$412k
SMOOTH MUSCLE FUNCTION--CELLULAR &MOLECULAR MECHANISMSP01HL047530 · NHLBI · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI FOGARTY, KEVIN E · 1993 to 1997
–
NHLBI NIH HHS HL-47530NIDDK NIH HHS DK-31620
6 · The paper itself

Abstract

1. Whole-cell and single-channel currents elicited by extracellular ATP were studied in freshly dissociated smooth muscle cells from the stomach of the toad Bufo marinus using standard patch clamp and microfluorimetric techniques. 2. This ATP-gated cation channel shares a number of pharmacological and functional properties with native rat myometrium receptors, certain native P2Z purinoceptors and the recently cloned P2X7 purinoceptor. But, unlike the last two, the ATP-gated channel does not mediate the formation of large non-specific pores. Thus, it may represent a novel member of the P2X or P2Z class. 3. Extracellular application of ATP (> or = 150 microM) elicited an inward whole-cell current at negative holding potentials that was inwardly rectifying and showed no sign of desensitization. Na+, Cs+ and, to a lesser degree, the organic cation choline served as charge carriers, but Cl- did not. Ratiometric fura-2 measurements indicated that the current is carried in part by Ca2+. The EC50 for ATP was 700 microM in solutions with a low divalent cation concentration. 4. ATP (> or = 100 microM) at the extracellular surface of cell-attached or excised patches elicited inwardly rectifying single-channel currents with a 22 pS conductance. Cl- did not serve as a charge carrier but both Na+ and Cs+ did, as did choline to a lesser extent. The mean open time of the channel was quite long, with a range in hundreds of milliseconds at a holding potential of -70 mV. 5. Mg2+ and Ca2+ decreased the magnitude of the ATP-induced whole-cell currents. Mg2+ decreased both the amplitude and the activity of ATP-activated single-channel currents. 6. ADP, UTP, P1, P5-di-adenosine pentaphosphate (AP5A), adenosine and alpha, beta-methylene ATP (alpha, beta-Me-ATP) did not induce significant whole-cell current. ATP-gamma-S and 2-methylthio ATP (2-Me-S-ATP) were significantly less effective than ATP in inducing whole-cell currents, whereas benzoylbenzoyl ATP (BzATP) was more effective. BzATP, alpha, beta-Me-ATP, ATP-gamma-S and 2-Me-S-ATP induced single-channel currents, but a higher concentration of alpha, beta-Me-ATP was required. 7. BzATP did not induce the formation of large non-specific pores, as assayed using mag-fura-2 as a high molecular mass probe.

Indexed as

Adenosine TriphosphateAnimalsBufo marinusCalciumCations, DivalentCell Membrane PermeabilityElectric StimulationElectrophysiologyGTP-Binding ProteinsIn Vitro TechniquesIon Channel GatingMembrane PotentialsMuscle, SmoothPatch-Clamp TechniquesRatsReceptors, Purinergic P2Adenosine TriphosphateCalciumCations, DivalentGTP-Binding ProteinsReceptors, Purinergic P2

Identifiers

PMID9032690
PMCPMC1159212
OpenAlexW1964157039

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.