Evidence map›Paper›PMID 21566016›Full record

ArticleAmerican journal of physiology. Gastrointestinal and liver physiology2011

Basally activated nonselective cation currents regulate the resting membrane potential in human and monkey colonic smooth muscle.

Laura Dwyer, Poong-Lyul Rhee, Vanessa Lowe, Haifeng Zheng, Lauren Peri, Seungil Ro, Kenton M Sanders, Sang Don Koh

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Gastrointestinal and liver physiology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.9field-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

23 citing papers in PubMed, 36 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Modelling Human Colonic Smooth Muscle Cell Electrophysiology.Cellular and molecular bioengineering · 2017
    Article
  12. Article
  13. The role of K⁺ conductances in regulating membrane excitability in human gastric corpus smooth muscle.American journal of physiology. Gastrointestinal and liver physiology · 2015
    Article
  14. Article
  15. The TRPM4 channel inhibitor 9-phenanthrol.British journal of pharmacology · 2014
    Review
  16. TRPM4 channels in smooth muscle function.Pflugers Archiv : European journal of physiology · 2013
    Review
  17. Review
  18. TRPM4 channel: a new player in urinary bladder smooth muscle function in rats.American journal of physiology. Renal physiology · 2013
    Article
  19. Article
  20. Regulation of gastrointestinal motility--insights from smooth muscle biology.Nature reviews. Gastroenterology & hepatology · 2012
    Review
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

8 authors at 2 institutions in 2 countries.

Laura DwyerDepartment of Physiology and Cell Biology, University of Nevada School of Medicine, Reno, 89557, USA. skoh@medicine.nevada.edu
Poong-Lyul Rhee
Vanessa Lowe
Haifeng Zheng
Lauren Peri
Seungil Ro
Kenton M Sanders
Sang Don Koh
University of Nevada, Reno · USSamsung Medical Center · KR

Funding

Tissue, Cell and Tissue Culture CoreP01DK041315 · NIDDK · UNIVERSITY OF NEVADA RENO · PI KEEF, KATHLEEN D · 1989 to 2018
$26.3M
NIDDK NIH HHS DK 41315NIDDK NIH HHS P01 DK041315
6 · The paper itself

Abstract

Resting membrane potential (RMP) plays an important role in determining the basal excitability of gastrointestinal smooth muscle. The RMP in colonic muscles is significantly less negative than the equilibrium potential of K(+), suggesting that it is regulated not only by K(+) conductances but by inward conductances such as Na(+) and/or Ca(2+). We investigated the contribution of nonselective cation channels (NSCC) to the RMP in human and monkey colonic smooth muscle cells (SMC) using voltage- and current-clamp techniques. Qualitative reverse transcriptase-polymerase chain reaction was performed to examine potential molecular candidates for these channels among the transient receptor potential (TRP) channel superfamily. Spontaneous transient inward currents and holding currents were recorded in human and monkey SMC. Replacement of extracellular Na(+) with equimolar tetraethylammonium or Ca(2+) with Mn(2+) inhibited basally activated nonselective cation currents. Trivalent cations inhibited these channels. Under current clamp, replacement of extracellular Na(+) with N-methyl-D-glucamine or addition of trivalent cations caused hyperpolarization. Three unitary conductances of NSCC were observed in human and monkey colonic SMC. Molecular candidates for basally active NSCC were TRPC1, C3, C4, C7, M2, M4, M6, M7, V1, and V2 in human and monkey SMC. Comparison of the biophysical properties of these TRP channels with basally active NSCC (bI(NSCC)) suggests that TRPM4 and specific TRPC heteromultimer combinations may underlie the three single-channel conductances of bI(NSCC). In conclusion, these findings suggest that basally activated NSCC contribute to the RMP in human and monkey colonic SMC and therefore may play an important role in determining basal excitability of colonic smooth muscle.

Indexed as

AdultAgedAnimalsCationsColonFemaleGastrointestinal MotilityHumansIn Vitro TechniquesMacaca fascicularisMaleMembrane PotentialsMiddle AgedMuscle, SmoothPatch-Clamp TechniquesReverse Transcriptase Polymerase Chain ReactionCationsSodiumTRPC Cation ChannelsTRPM4 protein, humanTRPM Cation Channels

Identifiers

PMID21566016
PMCPMC3154607
OpenAlexW2083806469

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.