Evidence map›Paper›PMID 11060127›Full record

ArticleThe Journal of physiology2000

Patch-clamp characterisation of somatostatin-secreting -cells in intact mouse pancreatic islets.

S O Göpel, T Kanno, S Barg, P Rorsman

Open access · greenAbstract read
In one paragraph

Article in The Journal of physiology, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed
4.5field-weighted citation impact, top 5% 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

61 citing papers in PubMed, 142 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Metabolic Messengers: glucagon.Nature metabolism · 2023
    Review
  6. Regulation of α-cell glucagon secretion: The role of second messengers.Chronic diseases and translational medicine · 2022
    Review
  7. Ion Transport and Radioresistance.Reviews of physiology, biochemistry and pharmacology · 2022
    Review
  8. Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. The Difference δ-Cells Make in Glucose Control.Physiology (Bethesda, Md.) · 2018
    Review
  14. Article
  15. Review
  16. Article
  17. Review
  18. Article
  19. Article
  20. Paracrine regulation of glucagon secretion: the β/α/δ model.American journal of physiology. Endocrinology and metabolism · 2016
    Article

1 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

S O GöpelDepartment of Molecular and Cellular Physiology, Diabetes Research Unit, Institute of Physiological Sciences, Lund University, Solvegatan 19, S-223 62 Lund, Sweden.
T Kanno
S Barg
P Rorsman
Lund University · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The perforated patch whole-cell configuration of the patch-clamp technique was applied to superficial cells in intact mouse pancreatic islets. Three types of electrical activity were observed corresponding to alpha-, beta- and delta-cells. The delta-cells were electrically active in the presence of glucose but lacked the oscillatory pattern seen in the beta-cells. By contrast, the alpha-cells were electrically silent at high glucose concentrations but action potentials could be elicited by removal of the sugar. Both alpha- and beta-cells contained transient voltage-activated K+ currents. In the delta-cells, the K+ currents activated above -20 mV and were completely blocked by TEA (20 mM). The alpha-cells differed from the delta-cells in possessing a TEA-resistant K+ current activating already at -40 mV. Immunocytochemistry revealed the presence of Kv3.4 channels in delta-cells and TEA-resistant Kv4.3 channels in alpha-cells. Thus the presence of a transient TEA-resistant current can be used to functionally separate the delta- and alpha-cells. A TTX-sensitive Na+ current developed in delta-cells during depolarisations beyond -30 mV and reached a peak amplitude of 350 pA. Steady-state inactivation of this current was half-maximal at -28 mV. The delta-cells were also equipped with a sustained Ca2+ current that activated above -30 mV and reached a peak of 60 pA when measured at 2.6 mM extracellular Ca2+. A tolbutamide-sensitive KATP channel conductance was observed in delta-cells exposed to glucose-free medium. Addition of tolbutamide (0.1 mM) depolarised the delta-cell and evoked electrical activity. We propose that the KATP channels in delta-cells serve the same function as in the beta-cell and couple an elevation of the blood glucose concentration to stimulation of hormone release.

Indexed as

Potassium Channels, Voltage-GatedAdenosine TriphosphateAnimalsElectric ConductivityElectrophysiologyHomeostasisIn Vitro TechniquesIon Channel GatingIslets of LangerhansMiceMice, Inbred StrainsPatch-Clamp TechniquesPotassium ChannelsShal Potassium ChannelsShaw Potassium ChannelsSodium ChannelsAdenosine TriphosphateKcnc4 protein, mouseKcnd3 protein, mousePotassium ChannelsPotassium Channels, Voltage-GatedShal Potassium ChannelsShaw Potassium ChannelsSodium ChannelsSomatostatin

Identifiers

PMID11060127
PMCPMC2270149
OpenAlexW2149141875

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.