Evidence map›Paper›PMID 37482752›Full record

ArticleBMB reports2023

Characterization of age- and stage-dependent impaired adult subventricular neurogenesis in 5XFAD mouse model of Alzheimer's disease.

Hyun Ha Park, Byeong-Hyeon Kim, Seol Hwa Leem, Yong Ho Park, Hyang-Sook Hoe, Yunkwon Nam, Sujin Kim, Soo Jung Shin, Minho Moon

Open access · goldAbstract readNews
In one paragraph

Article in BMB reports, 2023. 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
1.4field-weighted citation impact, top 20% 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, 7 citations in OpenAlex.

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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

9 authors at 2 institutions in 1 country.

Hyun Ha ParkDepartment of Biochemistry, College of Medicine, Konyang University, Daejeon 35365, Korea.
Byeong-Hyeon KimDepartment of Biochemistry, College of Medicine, Konyang University, Daejeon 35365, Korea.
Seol Hwa LeemDepartment of Biochemistry, College of Medicine, Konyang University, Daejeon 35365, Korea.
Yong Ho ParkDepartment of Biochemistry, College of Medicine, Konyang University, Daejeon 35365, Korea.
Hyang-Sook HoeDepartment of Neural Development and Disease, Korea Brain Research Institute (KBRI), Daegu 41068; Department of Brain & Cognitive Sciences, Daegu Gyeongbuk Institute of Science & Technology (DGIST), Daegu 42988, Korea.
Yunkwon NamDepartment of Biochemistry, College of Medicine, Konyang University, Daejeon 35365, Korea.
Sujin KimDepartment of Biochemistry, College of Medicine, Konyang University, Daejeon 35365; Research Institute for Dementia Science, Konyang University, Daejeon 35365, Korea.
Soo Jung ShinDepartment of Biochemistry, College of Medicine, Konyang University, Daejeon 35365, Korea.
Minho MoonDepartment of Biochemistry, College of Medicine, Konyang University, Daejeon 35365; Research Institute for Dementia Science, Konyang University, Daejeon 35365, Korea.
Konyang University · KRDaegu Gyeongbuk Institute of Science and Technology · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alzheimer's disease (AD) is a progressive neurodegenerative disease characterized by cognitive decline. Several recent studies demonstrated that impaired adult neurogenesis could contribute to AD-related cognitive impairment. Adult subventricular zone (SVZ) neurogenesis, which occurs in the lateral ventricles, plays a crucial role in structural plasticity and neural circuit maintenance. Alterations in adult SVZ neurogenesis are early events in AD, and impaired adult neurogenesis is influenced by the accumulation of intracellular Aβ. Although Aβ-overexpressing transgenic 5XFAD mice are an AD animal model well representative of Aβ-related pathologies in the brain, the characterization of altered adult SVZ neurogenesis following AD progression in 5XFAD mice has not been thoroughly examined. Therefore, we validated the characterization of adult SVZ neurogenesis changes with AD progression in 2-, 4-, 8-, and 11-monthold male 5XFAD mice. We first investigated the Aβ accumulation in the SVZ using the 4G8 antibody. We observed intracellular Aβ accumulation in the SVZ of 2-month-old 5XFAD mice. In addition, 5XFAD mice exhibited significantly increased Aβ deposition in the SVZ with age. Next, we performed a histological analysis to investigate changes in various phases of adult neurogenesis, such as quiescence, proliferation, and differentiation, in SVZ. Compared to age-matched wild-type (WT) mice, quiescent neural stem cells were reduced in 5XFAD mice from 2-11 months of age. Moreover, proliferative neural stem cells were decreased in 5XFAD mice from 2 to 8 months of age. Furthermore, differentiations of neuroblasts were diminished in 5XFAD mice from 2-11 months of age. Intriguingly, we found that adult SVZ neurogenesis was reduced with aging in healthy mice. Taken together, our results revealed that impairment of adult SVZ neurogenesis appears with aging or AD progression. [BMB Reports 2023; 56(9): 520-525].

Indexed as

Alzheimer DiseaseNeural Stem CellsNeurodegenerative DiseasesAmyloid beta-PeptidesAnimalsDisease Models, AnimalMaleMiceMice, TransgenicNeurogenesisAmyloid beta-Peptides

Identifiers

PMID37482752
PMCPMC10547970
OpenAlexW4383225882

What OpenQuestion holds

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LicenceCC BY-NC
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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 OpenQuestion graph.