Evidence map›Paper›PMID 28317098›Full record

ArticleBritish journal of pharmacology2017

CGRP receptor activity in mice with global expression of human receptor activity modifying protein 1.

Keegan J Bohn, Baolin Li, Xiaofang Huang, Bianca N Mason, Anne-Sophie Wattiez, Adisa Kuburas, Christopher S Walker, Peiyi Yang, Jianliang Yu, Beverly A Heinz and 2 more

Open access · bronzeAbstract 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 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 18% 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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 19 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. PACAP Induces Light Aversion in Mice by an Inheritable Mechanism Independent of CGRP.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2021
    Article
  10. Cross-talk signaling in the trigeminal ganglion: role of neuropeptides and other mediators.Journal of neural transmission (Vienna, Austria : 1996) · 2020
    Review
  11. Current understanding of trigeminal ganglion structure and function in headache.Cephalalgia : an international journal of headache · 2019
    Review
  12. Article
  13. Increased receptor activity-modifying protein 1 in the nervous system is sufficient to protect against autonomic dysregulation and hypertension.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2019
    Article
  14. Article
  15. CGRP in Animal Models of Migraine.Handbook of experimental pharmacology · 2019
    Review
  16. Targeted CGRP Small Molecule Antagonists for Acute Migraine Therapy.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2018
    Review
  17. 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

12 authors at 4 institutions in 2 countries.

Keegan J BohnDepartment of Molecular Physiology and Biophysics, University of Iowa, Iowa City, IA, USA.
Baolin LiNeuroscience Research Division, Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN, USA.
Xiaofang HuangNeuroscience Research Division, Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN, USA.
Bianca N MasonMolecular and Cellular Biology Program, University of Iowa, Iowa City, IA, USA.
Anne-Sophie WattiezDepartment of Molecular Physiology and Biophysics, University of Iowa, Iowa City, IA, USA.
Adisa KuburasDepartment of Molecular Physiology and Biophysics, University of Iowa, Iowa City, IA, USA.
Christopher S WalkerMaurice Wilkins Centre and Centre for Brain Research, School of Biological Sciences, University of Auckland, Auckland, New Zealand.
Peiyi YangQuantitative Biology, Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN, USA.
Jianliang YuQuantitative Biology, Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN, USA.
Beverly A HeinzQuantitative Biology, Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN, USA.
Kirk W JohnsonNeuroscience Research Division, Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN, USA.
Andrew F RussoDepartment of Molecular Physiology and Biophysics, University of Iowa, Iowa City, IA, USA.
Eli Lilly (United States) · USUniversity of Iowa · USMaurice Wilkins Centre · NZVeterans Health Administration · US

Funding

Perivascular mechanisms of CGRP-induced migraine symptomsR01NS075599 · NINDS · UNIVERSITY OF IOWA · PI RUSSO, ANDREW F · 2011 to 2023
$5.0M
Photosensitivity as a preclinical assessment for treatment of post-traumatic headacheI01RX002101 · VA · IOWA CITY VA MEDICAL CENTER · PI PIEPER, ANDREW A, RUSSO, ANDREW F · 2016 to 2020
–
NINDS NIH HHS R01 NS075599RRD VA I01 RX002101
6 · The paper itself

Abstract

background and purposeCGRP is a potent vasodilator and nociceptive neuropeptide linked to migraine. CGRP receptors are heterodimers of receptor activity modifying protein 1 (RAMP1) and either calcitonin receptor-like receptor (CLR; forms canonical CGRP receptor) or calcitonin receptor (CT receptor; forms AMY EXPERIMENTAL APPROACH: cAMP production was measured in primary cultures of aortic smooth muscle and trigeminal ganglia neurons from global hRAMP1 mice and non-transgenic littermates. Functional activity and inhibition were compared with clonal cell lines expressing combinations of CLR or CT receptors with RAMP1. KEY

resultsCultured smooth muscle from global hRAMP1 mice had a 10-fold greater CGRP-induced cAMP maximal response (Rmax) than non-transgenic littermates, with similar EC CONCLUSIONS AND IMPLICATIONS: Overexpression of hRAMP1 increases CGRP signalling by changing the maximal response or ligand sensitivity, depending on tissue type. Furthermore, telcagepant inhibited transgenic hRAMP1 CGRP receptors, but the degree of inhibition suggests that the transgenic mice are only partially humanized or both canonical CGRP and AMY

Indexed as

AnimalsAzepinesCalcitonin Gene-Related Peptide Receptor AntagonistsCells, CulturedCHO CellsCricetulusDose-Response Relationship, DrugFemaleGene Expression ProfilingHumansImidazolesMaleMiceMice, TransgenicReceptor Activity-Modifying Protein 1Receptors, Calcitonin Gene-Related PeptideAzepinesCalcitonin Gene-Related Peptide Receptor AntagonistsImidazolesReceptor Activity-Modifying Protein 1Receptors, Calcitonin Gene-Related Peptidetelcagepant

Identifiers

PMID28317098
PMCPMC5446571
OpenAlexW2603213603

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.