Evidence map›Paper›PMID 37686275›Full record

ArticleInternational journal of molecular sciences2023

The Anti-Calcitonin Gene-Related Peptide (Anti-CGRP) Antibody Fremanezumab Reduces Trigeminal Neurons Immunoreactive to CGRP and CGRP Receptor Components in Rats.

Birgit Vogler, Annette Kuhn, Kimberly D Mackenzie, Jennifer Stratton, Mária Dux, Karl Messlinger

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.7field-weighted citation impact, top 31% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Review
  2. Article
  3. 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

6 authors at 3 institutions in 3 countries.

Birgit VoglerInstitute of Physiology and Pathophysiology, Friedrich-Alexander-University, D-91054 Erlangen, Germany.
Annette KuhnInstitute of Physiology and Pathophysiology, Friedrich-Alexander-University, D-91054 Erlangen, Germany.
Kimberly D MackenzieTeva Pharmaceuticals, Redwood City, CA 94063, USA.
Jennifer StrattonTeva Pharmaceuticals, Redwood City, CA 94063, USA.
Mária DuxDepartment of Physiology, University of Szeged, H-6720 Szeged, Hungary.ORCID 0000-0002-9941-8188
Karl MesslingerInstitute of Physiology and Pathophysiology, Friedrich-Alexander-University, D-91054 Erlangen, Germany.ORCID 0000-0002-8099-3860
Friedrich-Alexander-Universität Erlangen-Nürnberg · DETeva Pharmaceuticals (United States) · USUniversity of Szeged · HU

Funding

Alexander von Humboldt Foundation Research Group Linkage Program between the Institutes of Physiology of the FAU Erlan-gen-Nürnberg and the University of SzegedTeva Pharmaceuticals none
6 · The paper itself

Abstract

Treatment with the anti-CGRP antibody fremanezumab is successful in the prevention of chronic and frequent episodic migraine. In preclinical rat experiments, fremanezumab has been shown to reduce calcitonin gene-related peptide (CGRP) release from trigeminal tissues and aversive behaviour to noxious facial stimuli, which are characteristic pathophysiological changes accompanying severe primary headaches. To further decipher the effects of fremanezumab that underlie these antinociceptive effects in rats, immunohistochemistry and ELISA techniques were used to analyse the content and concentration of CGRP in the trigeminal ganglion, as well as the ratio of trigeminal ganglion neurons which are immunoreactive to CGRP and CGRP receptor components, 1-10 days after subcutaneous injection of fremanezumab (30 mg/kg) compared to an isotype control antibody. After fremanezumab treatment, the fraction of trigeminal ganglion neurons which were immunoreactive to CGRP and the CGRP receptor components calcitonin receptor-like receptor (CLR) and receptor activity modifying protein 1 (RAMP1) was significantly lowered compared to the control. The content and concentration of CGRP in trigeminal ganglia were not significantly changed. A long-lasting reduction in CGRP receptors expressed in trigeminal afferents may contribute to the attenuation of CGRP signalling and antinociceptive effects of monoclonal anti-CGRP antibodies in rats.

Indexed as

Calcitonin Gene-Related PeptideReceptors, Calcitonin Gene-Related PeptideAnalgesicsAnimalsAntibodies, MonoclonalNeuronsRatsAnalgesicsAntibodies, MonoclonalCalcitonin Gene-Related PeptidefremanezumabReceptors, Calcitonin Gene-Related Peptidecalcitonin gene-related peptideCGRP releasefremanezumabmigraine painmonoclonal antibodyrattrigeminal ganglion

Identifiers

PMID37686275
PMCPMC10487893
OpenAlexW4386284363

What OpenQuestion holds

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LicenceCC BY
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.