Evidence map›Paper›PMID 39050707›Full record

ArticleTurkish journal of biology = Turk biyoloji dergisi2024

O-demethyl galantamine alters protein expression in cerebellum of 5xFAD mice.

İrem Kiriş, Merve Karayel Başar, Büşra Gürel, Tomasz Mroczek, Ahmet Tarık Baykal

Abstract read
In one paragraph

Article in Turkish journal of biology = Turk biyoloji dergisi, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

İrem KirişDepartment of Biochemistry and Molecular Biology, Institute of Health Sciences, Acıbadem Mehmet Ali Aydınlar University, İstanbul, Turkiye.ORCID https://orcid.org/0000-0003-0958-114X
Merve Karayel BaşarDepartment of Biochemistry and Molecular Biology, Institute of Health Sciences, Acıbadem Mehmet Ali Aydınlar University, İstanbul, Turkiye.ORCID https://orcid.org/0000-0001-6460-4151
Büşra GürelNanotechnology Research and Application Center, SUNUM, Sabancı University, İstanbul, Turkiye.ORCID https://orcid.org/0000-0001-9779-1467
Tomasz MroczekChair and Department of Pharmacognosy, Medical University of Lublin, Lublin, Poland.ORCID https://orcid.org/0000-0002-5267-7182
Ahmet Tarık BaykalDepartment of Medical Biochemistry, Faculty of Medicine, Acıbadem Mehmet Ali Aydınlar University, İstanbul, Turkiye.ORCID https://orcid.org/0000-0002-8814-7351

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background/aim: Alzheimer's disease (AD), one of the most common health issues, is characterized by memory loss, severe behavioral disorders, and eventually death. Despite many studies, there are still no drugs that can treat AD or stop it from progressing. Previous in vitro tests showed that O-demethyl galantamine (ODG) might have therapeutic potential owing to its 10 times higher acetylcholinesterase inhibitory activity than galantamine (GAL). Materials and methods: We aimed to assess the effect of ODG at the molecular level in a 12-month-old 5xFAD Alzheimer's mouse model. To this end, following the administrations of ODG and GAL (used as a positive control), protein alterations were investigated in the cortex, hippocampus, and cerebellum regions of the brain. Surprisingly, GAL altered proteins prominently in the cortex, while ODG exclusively exerted its effect on the cerebellum. Results: GNB1, GNB2, NDUFS6, PAK2, and RhoA proteins were identified as the top 5 hub proteins in the cerebellum of ODG-treated mice. Reregulation of these proteins through Ras signaling and retrograde endocannabinoid signaling pathways, which were found to be enriched, might contribute to reversing AD-induced molecular changes. Conclusion: We suggest that, since it targets specifically the cerebellum, ODG may be further evaluated for combination therapies for AD.

Indexed as

5xFADAlzheimer’s diseaselabel-free proteomicsneurodegenerationo-demethyl galantaminesanguinine

Identifiers

PMID39050707
PMCPMC11265889

What Socratic holds

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Registered trials

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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.