Evidence map›Paper›PMID 38689378›Full record

ArticleBritish journal of pharmacology2024

Activation of M

Roberto Cadeddu, Giulia Braccagni, Caterina Branca, Easton R van Luik, Christopher Pittenger, Morten Skøtt Thomsen, Marco Bortolato

Abstract read
In one paragraph

Article in British journal of pharmacology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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.

Roberto CadedduDepartment of Pharmacology and Toxicology, College of Pharmacy, University of Utah, Salt Lake City, Utah, USA.
Giulia BraccagniDepartment of Pharmacology and Toxicology, College of Pharmacy, University of Utah, Salt Lake City, Utah, USA.
Caterina BrancaDepartment of Pharmacology and Toxicology, College of Pharmacy, University of Utah, Salt Lake City, Utah, USA.
Easton R van LuikDepartment of Pharmacology and Toxicology, College of Pharmacy, University of Utah, Salt Lake City, Utah, USA.
Christopher PittengerDepartment of Psychiatry, School of Medicine, Yale University, New Haven, Connecticut, USA.ORCID https://orcid.org/0000-0003-2117-9321
Morten Skøtt ThomsenNeuroscience Research, H. Lundbeck A/S, Valby, Copenhagen, Denmark.
Marco BortolatoDepartment of Pharmacology and Toxicology, College of Pharmacy, University of Utah, Salt Lake City, Utah, USA.ORCID https://orcid.org/0000-0002-4498-9637

Funding

Exploring the role of neurosteroids in tic modulationR21NS108722 · NINDS · UNIVERSITY OF UTAH · PI BORTOLATO, MARCO, PITTENGER, CHRISTOPHER JOHN · 2018 to 2019
$428k
Exploring the role of the protocadherin CELSR3 in Tourette syndromeR21NS125519 · NINDS · UNIVERSITY OF UTAH · PI BORTOLATO, MARCO · 2022 to 2023
$419k
NINDS NIH HHS NS108722NINDS NIH HHS NS125519NINDS NIH HHS R21 NS108722NINDS NIH HHS R21 NS125519
6 · The paper itself

Abstract

background and purposeCurrent pharmacotherapies for Tourette syndrome (TS) are often unsatisfactory and poorly tolerated, underscoring the need for novel treatments. Insufficient striatal acetylcholine has been suggested to contribute to tic ontogeny. Thus, we tested whether activating M EXPERIMENTAL APPROACH: Studies were conducted using CIN-d and D1CT-7 mice, two TS models characterized by early-life depletion of striatal cholinergic interneurons and cortical neuropotentiation, respectively. First, we tested the effects of systemic and intrastriatal xanomeline, a selective M KEY

resultsSystemic and intrastriatal xanomeline reduced TS-related behaviours in CIN-d and D1CT-7 mice. Most effects were blocked by M CONCLUSION AND IMPLICATIONS: Activation of striatal M

Indexed as

Corpus StriatumDisease Models, AnimalMuscarinic AgonistsReceptor, Muscarinic M4Tourette SyndromeAnimalsBehavior, AnimalDioxolesMaleMiceMice, Inbred C57BLPyridinesReceptor, Muscarinic M1ThiadiazolesThiophenesTicsDioxolesMuscarinic AgonistsPyridinesReceptor, Muscarinic M1Receptor, Muscarinic M4ThiadiazolesThiophenesxanomelineanimal modelsmuscarinic receptorstriatumtic disordersxanomeline

Identifiers

PMID38689378
PMCPMC13403342

What OpenQuestion holds

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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.