Evidence map›Paper›PMID 7690256›Full record

ArticleBiophysical journal1993

Restricted ion flow at the nuclear envelope of cardiac myocytes.

J O Bustamante

Open access · greenAbstract read
In one paragraph

Article in Biophysical journal, 1993. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

13 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Article
  3. Dendrimer-assisted patch-clamp sizing of nuclear pores.Pflugers Archiv : European journal of physiology · 2000
    Article
  4. Calcium, ATP and nuclear pore channel gating.Pflugers Archiv : European journal of physiology · 2000
    Article
  5. Nuclear hourglass technique: an approach that detects electrically open nuclear pores in Xenopus laevis oocyte.Proceedings of the National Academy of Sciences of the United States of America · 1999
    Article
  6. Article
  7. Article
  8. Article
  9. The ion channel behavior of the nuclear pore complex.The Journal of membrane biology · 1995
    Article
  10. Article
  11. Imaging nuclear pores of aldosterone-sensitive kidney cells by atomic force microscopy.Proceedings of the National Academy of Sciences of the United States of America · 1994
    Article
  12. Nuclear electrophysiology.The Journal of membrane biology · 1994
    Review
  13. 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

1 author at 1 institution in 1 country.

J O BustamanteUniversity of Maryland School of Medicine, Department of Physiology, Baltimore 21201.
University of Maryland, Baltimore · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Flow of small ions across the nuclear envelope (NE) is thought to occur without restriction through large diameter nuclear pore complexes (NPCs). However, investigations with electron and fluorescence microscopy, and with patch-clamp and microelectrode electrophysiology, suggest that in many animal and plant cell types small ions move through a barrier having the signature of large conductance nuclear ion channels (NICs). As nucleocytoplasmic transport and gene activity are regulated by cytoplasmic signals and as it has recently been shown by this investigator that cardiac NICs are sensitive to cAMP-dependent processes (1), it was considered relevant to further investigate the effects of various cytosolic signals on NIC activity. Ion species substitution demonstrated that K+ is the major species responsible for NIC currents. The Na-channel blocker tetrodotoxin (TTX, 100 microM) and the Ca-channel blocker diltiazem (100 microM) had no effect, indicating no relation of NICs to Na- or Ca-channels in transit to the cell surface membrane. Zn2+ (100 microM) blocked NIC activity, suggesting a dual role in nucleocytoplasmic transport and gene function. GTP did not produce measurable effect. However, its nonhydrolyzable analogue GTP-gamma-S (10 microM) suppressed NIC activity, suggesting a role for GTP hydrolysis in NIC function. Deoxynucleotides (dNTPs, 200 microM) produced a transient increase in NIC activity, pointing to a modulation of NIC function by nucleic acid substrates. These results indicate a role for NICs in mediating: (a) control of gene activity by transduction and other cytosolic signals, and (b) nuclear demands and response to such signals.

Indexed as

AnimalsCell NucleusCells, CulturedDeoxyribonucleotidesDiltiazemDNAElectric StimulationGuanosine 5'-O-(3-Thiotriphosphate)HeartIon ChannelsMaleMembrane PotentialsMiceMicroscopy, FluorescenceMyocardiumNuclear EnvelopeDeoxyribonucleotidesDiltiazemDNAGuanosine 5'-O-(3-Thiotriphosphate)Ion ChannelsTetrodotoxinZinc

Identifiers

PMID7690256
PMCPMC1262508
OpenAlexW2100971576

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.