Evidence map›Paper›PMID 38070724›Full record

ArticleExperimental neurology2024

Enhancing cognitive function in chronic TBI: The Role of α7 nicotinic acetylcholine receptor modulation.

Dinesh K Sangadi, Akhila Sangadi, Fabiola Placeres-Uray, David J Titus, Timothy Johnstone, Derk Hogenkamp, Kelvin W Gee, Coleen M Atkins

Open access · greenAbstract read
In one paragraph

Article in Experimental neurology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.6field-weighted citation impact, top 29% 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

4 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. 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

8 authors at 5 institutions in 1 country.

Dinesh K SangadiThe Miami Project to Cure Paralysis, Department of Neurological Surgery, University of Miami Miller School of Medicine, 1095 NW 14th Terrace, Miami, FL 33136, USA.
Akhila SangadiThe Miami Project to Cure Paralysis, Department of Neurological Surgery, University of Miami Miller School of Medicine, 1095 NW 14th Terrace, Miami, FL 33136, USA.
Fabiola Placeres-UrayThe Miami Project to Cure Paralysis, Department of Neurological Surgery, University of Miami Miller School of Medicine, 1095 NW 14th Terrace, Miami, FL 33136, USA.
David J TitusDepartment of Psychiatry & Behavioral Sciences, University of Minnesota, Minneapolis, MN, USA.
Timothy JohnstoneDepartment of Pharmacology, College of Medicine, University of Arizona, Tucson, USA.
Derk HogenkampDepartment of Pharmaceutical Sciences, School of Medicine, University of California Irvine, Irvine, USA.
Kelvin W GeeDepartment of Pharmaceutical Sciences, School of Medicine, University of California Irvine, Irvine, USA.
Coleen M AtkinsThe Miami Project to Cure Paralysis, Department of Neurological Surgery, University of Miami Miller School of Medicine, 1095 NW 14th Terrace, Miami, FL 33136, USA. Electronic address: catkins@miami.edu.
Neurological Surgery · USUniversity of California, Irvine · USUniversity of Arizona · USUniversity of Miami · USUniversity of Minnesota · US

Funding

Rehabilitation Strategies for Memory Dysfunction After Traumatic Brain InjuryR01NS069721 · NINDS · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI ATKINS, COLEEN M. · 2010 to 2019
$3.7M
NINDS NIH HHS R01 NS069721
6 · The paper itself

Abstract

Traumatic brain injury (TBI) results in several pathological changes within the hippocampus that result in adverse effects on learning and memory. Therapeutic strategies to enhance learning and memory after TBI are still in the early stages of clinical development. One strategy is to target the α7 nicotinic acetylcholine receptor (nAChR), which is highly expressed in the hippocampus and contributes to the formation of long-term memory. In our previous study, we found that AVL-3288, a positive allosteric modulator of the α7 nAChR, improved cognitive recovery in rats after moderate fluid-percussion injury (FPI). However, whether AVL-3288 improved cognitive recovery specifically through the α7 nAChR was not definitively determined. In this study we utilized Chrna7 knockout mice and compared their recovery to wild-type mice treated with AVL-3288 after TBI. We hypothesized that AVL-3288 treatment would improve learning and memory in wild-type mice, but not Chrna7

Indexed as

alpha7 Nicotinic Acetylcholine ReceptorBrain Injuries, TraumaticAnimalsCognitionHippocampusMaleMiceMice, Inbred C57BLMice, KnockoutRatsalpha7 Nicotinic Acetylcholine ReceptorChrna7controlled cortical impacthippocampuslearning and memorytraumatic brain injuryα7 nicotinic acetylcholine receptor

Identifiers

PMID38070724
PMCPMC10843542
OpenAlexW4389463443

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.