Evidence map›Paper›PMID 22441675›Full record

ArticleMolecules and cells2012

Neurotensin modulates pacemaker activity in interstitial cells of Cajal from the mouse small intestine.

Jun Lee, Young Dae Kim, Chan Guk Park, Man Yoo Kim, In Yeoub Chang, Dong Chuan Zuo, Pawan Kumar Shahi, Seok Choi, Cheol Ho Yeum, Jae Yeoul Jun

Open access · hybridAbstract read
In one paragraph

Article in Molecules and cells, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.0field-weighted citation impact, top 23% 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

6 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Flufenamic acid as an ion channel modulator.Pharmacology & therapeutics · 2013
    Review
  6. HIZ's relation to axial load and low back pain: investigated with axial loaded MRI and pressure controlled discography.European spine journal : official publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society · 2013
    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

10 authors at 1 institution in 1 country.

Jun LeeDepartment of Internal Medicine, College of Medicine, Chosun University, Gwangju 501-759, Korea.
Young Dae Kim
Chan Guk Park
Man Yoo Kim
In Yeoub Chang
Dong Chuan Zuo
Pawan Kumar Shahi
Seok Choi
Cheol Ho Yeum
Jae Yeoul Jun
Chosun University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neurotensin, a tridecapeptide localized in the gut to discrete enteroendocrine cells of the small bowel mucosa, is a hormone that plays an important role in gastrointestinal secretion, growth, and motility. Neurotensin has inhibitory and excitatory effects on peristaltic activity and produces contractile and relaxant responses in intestinal smooth muscle. Our objective in this study is to investigate the effects of neurotensin in small intestinal interstitial cells of Cajal (ICC) and elucidate the mechanism. To determine the electrophysiological effects of neurotensin on ICC, whole-cell patch clamp recordings were performed in cultured ICC from the small intestine. Exposure to neurotensin depolarized the membrane of pacemaker cells and produced tonic inward pacemaker currents. Only neurotensin receptor1 was identified when RT-PCR and immunocytochemistry were performed with mRNA isolated from small intestinal ICC and c-Kit positive cells. Neurotensin-induced tonic inward pacemaker currents were blocked by external Na⁺-free solution and in the presence of flufenamic acid, an inhibitor of non-selective cation channels. Furthermore, neurotensin-induced action is blocked either by treatment with U73122, a phospholipase C inhibitor, or thapsigargin, a Ca²⁺-ATPase inhibitor in ICC. We found that neurotensin increased spontaneous intracellular Ca²⁺ oscillations as seen with fluo4/AM recording. These results suggest that neurotensin modulates pacemaker currents via the activation of non-selective cation channels by intracellular Ca²⁺-release through neurotensin receptor1.

Indexed as

AnimalsCalciumCalcium-Transporting ATPasesCells, CulturedEndoplasmic ReticulumFemaleInterstitial Cells of CajalIntestine, SmallIn Vitro TechniquesIon ChannelsMaleMembrane PotentialsMiceMice, Inbred BALB CMuscle, SmoothNeurotensinCalciumCalcium-Transporting ATPasesIon ChannelsNeurotensinneurotensin type 1 receptorReceptors, NeurotensinSodiumType C Phospholipases

Identifiers

PMID22441675
PMCPMC3887726
OpenAlexW2032832507

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.