Evidence map›Paper›PMID 20847183›Full record

ArticleHuman reproduction (Oxford, England)2010

Human oocytes express ATP-sensitive K(+) channels.

Qingyou Du, Sofija Jovanović, Andriy Sukhodub, Evelyn Barratt, Ellen Drew, Katherine M Whalley, Vanessa Kay, Marie McLaughlin, Evelyn E Telfer, Christopher L R Barratt and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Human reproduction (Oxford, England), 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.1field-weighted citation impact, top 21% 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

9 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
  2. Electrophysiology of Human Gametes: A Systematic Review.The world journal of men's health · 2022
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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

11 authors at 3 institutions in 1 country.

Qingyou DuDivision of Medical Sciences/MACHS, Ninewells Hospital and Medical School, University of Dundee, Dundee, UK.
Sofija Jovanović
Andriy Sukhodub
Evelyn Barratt
Ellen Drew
Katherine M Whalley
Vanessa Kay
Marie McLaughlin
Evelyn E Telfer
Christopher L R Barratt
Aleksandar Jovanović
Ninewells Hospital · GBUniversity of Dundee · GBUniversity of Edinburgh · GB

Funding

Biotechnology and Biological Sciences Research Council S18744Medical Research Council G0901839Wellcome Trust
6 · The paper itself

Abstract

backgroundATP-sensitive K(+) (K(ATP)) channels link intracellular metabolism with membrane excitability and play crucial roles in cellular physiology and protection. The K(ATP) channel protein complex is composed of pore forming, Kir6.x (Kir6.1 or Kir6.2) and regulatory, SURx (SUR2A, SUR2B or SUR1), subunits that associate in different combinations. The objective of this study was to determine whether mammalian oocytes (human, bovine, porcine) express K(ATP) channels.

methodsSupernumerary human oocytes at different stages of maturation were obtained from patients undergoing assisted conception treatments. Bovine and porcine oocytes in the germinal vesicle (GV) stage were obtained by aspirating antral follicles from abattoir-derived ovaries. The presence of mRNA for K(ATP) channel subunits was determined using real-time RT-PCR with primers specific for Kir6.2, Kir6.1, SUR1, SUR2A and SUR2B. To assess whether functional K(ATP) channels are present in human oocytes, traditional and perforated patch whole cell electrophysiology and immunoprecipitation/western blotting were used.

resultsReal-time PCR revealed that mRNA for Kir6.1, Kir6.2, SUR2A and SUR2B, but not SUR1, were present in human oocytes of different stages. Only SUR2B and Kir6.2 mRNAs were detected in GV stage bovine and porcine oocytes. Immunoprecipitation with SUR2 antibody and western blotting with Kir6.1 antibody identified bands corresponding to these subunits in human oocytes. In human oocytes, 2,4-dinitrophenol (400 µM), a metabolic inhibitor known to decrease intracellular ATP and activate K(ATP) channels, increased whole cell K(+) current. On the other hand, K(+) current induced by low intracellular ATP was inhibited by extracellular glibenclamide (30 µM), an oral antidiabetic known to block the opening of K(ATP) channels.

conclusionsIn conclusion, mammalian oocytes express K(ATP) channels. This opens a new avenue of research into the complex relationship between metabolism and membrane excitability in oocytes under different conditions, including conception.

Indexed as

2,4-DinitrophenolAdenosine TriphosphateAnimalsATP-Binding Cassette TransportersCattleGlyburideHumansKATP ChannelsOocytesPatch-Clamp TechniquesPotassium Channels, Inwardly RectifyingReceptors, DrugSulfonylurea ReceptorsSwine2,4-DinitrophenolABCC8 protein, humanABCC9 protein, humanAdenosine TriphosphateATP-Binding Cassette TransportersGlyburideKATP ChannelsPotassium Channels, Inwardly RectifyingReceptors, DrugSulfonylurea ReceptorsuK-ATP-1 potassium channel

Identifiers

PMID20847183
PMCPMC2955558
OpenAlexW2154081746

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.