Evidence map›Paper›PMID 21913893›Full record

ArticleBritish journal of pharmacology2012

What makes the α(1A)-adrenoceptor gene express the α(1L)-adrenoceptor functional phenotype?

Sabatino Ventura

Abstract readComment
In one paragraph

Article in British journal of pharmacology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. What makes the αBritish journal of pharmacology · 2019
    Review
  2. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

1 author.

Sabatino VenturaMedicinal Chemistry and Drug Action, Monash Institute of Pharmaceutical Sciences, Monash University, Parkville, Vic., Australia. sab.ventura@monash.edu

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The α(1A)-adrenoceptor is therapeutically exploited because of its prevalence in the lower urinary tract. The pharmacology shown by this lower urinary tract α(1A)-adrenoceptor is different from that shown by other α(1A)-adrenoceptors, which has led to it being subclassified as an α(1L)-adrenoceptor. Only in the last few years was it shown that this pharmacologically distinct α(1L)-adrenoceptor is a product of the α(1A)-adrenoceptor gene. In this issue of the BJP, Nishimune et al. review the literature on α(1L)-adrenoceptor pharmacology and discuss the possible molecular mechanisms by which the α(1A)-adrenoceptor gene is able to produce two pharmacologically distinct adrenoceptor subtypes. Based primarily from their own research using cell lines transfected with α(1A)-adrenoceptors, they conclude that a protein that interacts with the receptor is the most plausible explanation. The challenge remains to identify any such interacting protein and show how it is able to change the pharmacology of the receptor for different ligands.

Indexed as

Adrenergic alpha-1 Receptor AntagonistsAnimalsHumansPrazosinReceptors, Adrenergic, alpha-1Urinary TractAdrenergic alpha-1 Receptor AntagonistsPrazosinReceptors, Adrenergic, alpha-1

Identifiers

PMID21913893
PMCPMC3372710

What OpenQuestion holds

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Registered trials

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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.