Evidence map›Paper›PMID 14724757›Full record

ArticleThe Journal of membrane biology2003

Differential expression of Kir6.1 and SUR2B mRNAs in the vasculature of various tissues in rats.

L Li, J Wu, C Jiang

Abstract readComparative Study
PubMed Publisher
In one paragraph

Article in The Journal of membrane biology, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

26 citing papers in PubMed, 64 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. The ATP sensitive potassium channel (KFrontiers in molecular neuroscience · 2023
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Tonic regulation of middle meningeal artery diameter by ATP-sensitive potassium channels.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2019
    Article
  12. KATP Channels in the Cardiovascular System.Physiological reviews · 2016
    Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
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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

3 authors at 1 institution in 1 country.

L LiDepartment of Biology, Georgia State University, 24 Peachtree Center Avenue, Atlanta, GA 30302-4010, USA.
J Wu
C Jiang
Georgia State University · US

Funding

Vascular KATP Channel Modulation in Hypercapnic AcidosisR01HL067890 · NHLBI · GEORGIA STATE UNIVERSITY · PI JIANG, CHUN · 2003 to 2006
$1.2M
KIR channel modulations in hypercapnic acidosisR01HL058410 · NHLBI · GEORGIA STATE UNIVERSITY · PI JIANG, CHUN · 1996 to 2004
$1.0M
NHLBI NIH HHS HL058410NHLBI NIH HHS HL067890NHLBI NIH HHS R01 HL058410NHLBI NIH HHS R01 HL067890
6 · The paper itself

Abstract

ATP-sensitive K(+) channels (K(ATP)) couple the intermediary metabolism to cellular excitability and play an important role in the cardio-protective effect of ischemic preconditioning and the activity-dependent autoregulation of cerebral circulation. Although previous studies using PCR and Northern blot suggest that the vascular isoform may consist of Kir6.1 and SUR2B, their expression and precise distribution in various vasculatures remain unknown. To illustrate their vascular expression, we performed this study using in situ hybridization histochemistry. Antisense riboprobes were synthesized by in vitro transcription and labeled with digoxigenin. Distributions of these mRNAs in the various blood vessels were revealed under a bright-field microscope. The expression of Kir6.1 and SUR2B mRNAs was observed in small and intermediate arteries as well as arterioles in several tissues, including basilar, vertebral, mesenteric, coronary and renal arteries. The transcripts were found in arterial smooth muscles. Also, we observed Kir6.1/SUR2B expression in capillary beds. The Kir6.1 and SUR2B expression pattern showed clear overlap, suggesting that they may form heteromeric K(ATP) channels in these tissues. The Kir6.1 and SUR2B stains were detected in aorta and renal tubular cells although their expression level was extremely low. In contrast, the Kir6.1 and SUR2B mRNAs were not seen in vena cava, other small veins, myocardium and skeletal muscles. With their strong expression in small arteries and capillaries, it is very likely that the Kir6.1 and SUR2B form the vascular isoform of K(ATP) channels in these vasculatures.

Indexed as

AnimalsArteriesATP-Binding Cassette TransportersBlood VesselsBrainCulture TechniquesGene Expression RegulationKidneyMuscle, SkeletalMuscle, Smooth, VascularMyocardiumOrgan SpecificityPotassium ChannelsPotassium Channels, Inwardly RectifyingRatsRats, Sprague-DawleyATP-Binding Cassette TransportersPotassium ChannelsPotassium Channels, Inwardly RectifyingReceptors, DrugRNA, MessengerSulfonylurea Receptors

Identifiers

PMID14724757
OpenAlexW1966152414

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.