Evidence map›Paper›PMID 28369749›Full record

ArticleBritish journal of pharmacology2017

Olcegepant blocks neurogenic and non-neurogenic CGRPergic vasodepressor responses and facilitates noradrenergic vasopressor responses in pithed rats.

V H Avilés-Rosas, E Rivera-Mancilla, B A Marichal-Cancino, G Manrique-Maldonado, A H Altamirano-Espinoza, A Maassen Van Den Brink, C M Villalón

Open access · hybridAbstract read
In one paragraph

Article in British journal of pharmacology, 2017. 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
2.0field-weighted citation impact, top 15% 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, 23 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
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

7 authors at 2 institutions in 2 countries.

V H Avilés-RosasDepartamento de Farmacobiología, Cinvestav-Coapa, México D.F., Mexico.
E Rivera-MancillaDepartamento de Farmacobiología, Cinvestav-Coapa, México D.F., Mexico.
B A Marichal-CancinoDepartamento de Farmacobiología, Cinvestav-Coapa, México D.F., Mexico.
G Manrique-MaldonadoDepartamento de Farmacobiología, Cinvestav-Coapa, México D.F., Mexico.
A H Altamirano-EspinozaDepartamento de Farmacobiología, Cinvestav-Coapa, México D.F., Mexico.
A Maassen Van Den BrinkDepartment of Internal Medicine, Division of Pharmacology, Vascular and Metabolic Diseases, Erasmus MC, University Medical Center Rotterdam, Rotterdam, The Netherlands.
C M VillalónDepartamento de Farmacobiología, Cinvestav-Coapa, México D.F., Mexico.
Centro de Investigación y de Estudios Avanzados del Instituto Politécnico Nacional · MXErasmus MC · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background and purposeOlcegepant (BIBN4096BS) is a selective non-peptide CGRP receptor antagonist with acute antimigraine properties. Since systemic vascular tone is modulated by perivascular (primary sensory CGRPergic and sympathetic) nerves, this randomized study investigated in pithed rats the effect of acute i.v. treatment with olcegepant on the neurogenic and non-neurogenic: (i) CGRPergic vasodepressor responses; and (ii) noradrenergic vasopressor responses. The pithed rat is an experimental model predictive of systemic (cardio) vascular side effects. EXPERIMENTAL APPROACH: Seventy-five male Wistar rats (divided into 15 groups, n = 5 each) were pithed, artificially ventilated and prepared for: (i) spinal stimulation (T KEY

resultsOlcegepant (1000 and 3000 μg·kg CONCLUSIONS AND IMPLICATIONS: Olcegepant (i.v.) selectively blocked the neurogenic and non-neurogenic CGRPergic vasodepressor responses. This blockade by olcegepant potentiated the neurogenic and non-neurogenic noradrenergic vasopressor responses in pithed rats, an effect that might result in an increased vascular resistance and, consequently, in a prohypertensive action.

Indexed as

AnimalsCalcitonin Gene-Related PeptideDipeptidesDose-Response Relationship, DrugElectric StimulationMalePiperazinesQuinazolinesRatsRats, WistarStructure-Activity RelationshipVasoconstrictor AgentsCalcitonin Gene-Related PeptideDipeptidesolcegepantPiperazinesQuinazolinesVasoconstrictor Agents

Identifiers

PMID28369749
PMCPMC6398519
OpenAlexW2598229019

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.