Evidence map›Paper›PMID 19327362›Full record

ArticleInternational journal for parasitology2009

Identification of an Ascaris G protein-coupled acetylcholine receptor with atypical muscarinic pharmacology.

Michael J Kimber, Laura Sayegh, Fouad El-Shehabi, Chuanzhe Song, Mostafa Zamanian, Debra J Woods, Tim A Day, Paula Ribeiro

Abstract read
In one paragraph

Article in International journal for parasitology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
3.9field-weighted citation impact, top 7% 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

13 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Cholinergic receptors on intestine cells of Ascaris suum and activation of nAChRs by levamisole.International journal for parasitology. Drugs and drug resistance · 2020
    Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Parasite neuropeptide biology: Seeding rational drug target selection?International journal for parasitology. Drugs and drug resistance · 2012
    Review
  11. Review
  12. Article
  13. Ion channels and receptor as targets for the control of parasitic nematodes.International journal for parasitology. Drugs and drug resistance · 2011
    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 3 institutions in 2 countries.

Michael J KimberDepartment of Biomedical Sciences, Iowa State University, Ames, IA 50011, USA.
Laura Sayegh
Fouad El-Shehabi
Chuanzhe Song
Mostafa Zamanian
Debra J Woods
Tim A Day
Paula Ribeiro
Iowa State University · USMcGill University · CAPfizer (United States) · US

Funding

STRUCTURE AND FUNCTION OF SCHISTOSOME NEUROPEPTIDE FR01AI049162 · NIAID · IOWA STATE UNIVERSITY · PI DAY, TIMOTHY A · 2000 to 2009
$2.4M
NIAID NIH HHS R01 AI049162
6 · The paper itself

Abstract

Acetylcholine (ACh) is a neurotransmitter/neuromodulator in the nematode nervous system and induces its effects through interaction with both ligand-gated ion channels (LGICs) and G protein-coupled receptors (GPCRs). The structure, pharmacology and physiological importance of LGICs have been appreciably elucidated in model nematodes, including parasitic species where they are targets for anthelmintic drugs. Significantly less, however, is understood about nematode ACh GPCRs, termed GARs (G protein-linked ACh receptors). What is known comes from the free-living Caenorhabditis elegans as no GARs have been characterized from parasitic species. Here we clone a putative GAR from the pig gastrointestinal nematode Ascaris suum with high structural homology to the C. elegans receptor GAR-1. Our GPCR, dubbed AsGAR-1, is alternatively spliced and expressed in the head and tail of adult worms but not in dorsal or ventral body wall muscle, or the ovijector. ACh activated AsGAR-1 in a concentration-dependent manner but the receptor was not activated by other small neurotransmitters. The classical muscarinic agonists carbachol, arecoline, oxotremorine M and bethanechol were also AsGAR-1 agonists but pilocarpine was ineffective. AsGAR-1 activation by ACh was partially antagonized by the muscarinic blocker atropine but pirenzepine and scopolamine were largely ineffective. Certain biogenic amine GPCR antagonists were also found to block AsGAR-1. Our conclusion is that Ascaris possesses G protein-coupled ACh receptors that are homologous in structure to those present in C. elegans, and that although they have some sequence homology to vertebrate muscarinic receptors, their pharmacology is atypically muscarinic.

Indexed as

AcetylcholineAnimalsAscaris suumCaenorhabditis elegansDose-Response Relationship, DrugExpressed Sequence TagsFemaleMolecular Sequence DataMuscarinic AgonistsPolymerase Chain ReactionProtein IsoformsReceptors, G-Protein-CoupledReceptors, MuscarinicSequence HomologySwineAcetylcholineMuscarinic AgonistsProtein IsoformsReceptors, G-Protein-CoupledReceptors, Muscarinic

Identifiers

PMID19327362
PMCPMC2713365
OpenAlexW2083457557

What OpenQuestion holds

Textmetadata
LicenceTDM
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.