Evidence map›Paper›PMID 32580575›Full record

ArticleCephalalgia : an international journal of headache2020

Evaluation of LY573144 (lasmiditan) in a preclinical model of medication overuse headache.

Jill C Rau, Edita Navratilova, Janice Oyarzo, Kirk W Johnson, Sheena K Aurora, Todd J Schwedt, David W Dodick, Frank Porreca

Open access · hybridAbstract read
In one paragraph

Article in Cephalalgia : an international journal of headache, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.3field-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

17 citing papers in PubMed, 36 citations in OpenAlex.

  1. Review
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  8. The 5-HTNature reviews. Neurology · 2023
    Review
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  12. A prolactin-dependent sexually dimorphic mechanism of migraine chronification.Cephalalgia : an international journal of headache · 2022
    Article
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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 1 country.

Jill C RauMayo Clinic, Scottsdale, AZ, USA.
Edita NavratilovaDepartment of Pharmacology, Arizona Health Sciences Center, University of Arizona, Tucson, AZ, USA.ORCID 0000-0002-1497-125X
Janice OyarzoMayo Clinic, Scottsdale, AZ, USA.
Kirk W JohnsonEli Lilly, Indianapolis, IN, USA.
Sheena K AuroraEli Lilly, Indianapolis, IN, USA.
Todd J SchwedtMayo Clinic, Scottsdale, AZ, USA.
David W DodickMayo Clinic, Scottsdale, AZ, USA.
Frank PorrecaMayo Clinic, Scottsdale, AZ, USA.
Mayo Clinic in Arizona · USEli Lilly (United States) · USUniversity of Arizona · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMedication overuse is a significant issue that complicates the treatment of headache disorders. The most effective medications for the acute treatment of migraine all have the capacity to induce medication overuse headache (MOH). Novel acute migraine-specific treatments are being developed. However, because the mechanism(s) underlying medication overuse headache are not well understood, it is difficult to predict whether any particular acute medication will induce MOH in susceptible individuals. LY573144 (lasmiditan), a 5-HT

methodsSprague Dawley rats were administered six doses of lasmiditan (10 mg/kg), sumatriptan (10 mg/kg), or sterile water orally over 2 weeks and cutaneous allodynia was evaluated regularly in the periorbital and hindpaw regions using von Frey filaments. Testing continued until mechanosensitivity returned to baseline levels. Rats were then submitted to bright light stress (BLS) or nitric oxide (NO) donor administration and were again evaluated for cutaneous allodynia in the periorbital and hindpaw regions hourly for 5 hours.

resultsBoth lasmiditan and sumatriptan exhibited comparable levels of drug-induced cutaneous allodynia in both the periorbital and hindpaw regions, which resolved after cessation of drug administration. Both lasmiditan and sumatriptan pre-treatment resulted in cutaneous allodynia that was evoked by either BLS or NO donor.

conclusionsIn a pre-clinical rat model of MOH, oral lasmiditan, like sumatriptan, induced acute transient cutaneous allodynia in the periorbital and hindpaw regions that after resolution could be re-evoked by putative migraine triggers. These results suggest that lasmiditan has the capacity to induce MOH through persistent latent peripheral and central sensitization mechanisms.

Indexed as

AnalgesicsAnimalsBenzamidesCentral Nervous System SensitizationDisease Models, AnimalHeadache Disorders, SecondaryHyperalgesiaPiperidinesPyridinesRatsRats, Sprague-DawleySerotonin Receptor AgonistsSumatriptanAnalgesicsBenzamideslasmiditanPiperidinesPyridinesSerotonin Receptor AgonistsSumatriptanallodynialasmiditanmigrainePainstresssumatriptan

Identifiers

PMID32580575
PMCPMC7412873
OpenAlexW3037986320

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.