Evidence map›Paper›PMID 36018506›Full record

ArticleNeurotoxicity research2022

Calpain Inhibitor Calpeptin Improves Alzheimer's Disease-Like Cognitive Impairments and Pathologies in a Diabetes Mellitus Rat Model.

Min Li, Siqi Zhou, Gege Wang, Luyao Qiao, Shouqin Yi, Tianpei Li, Xin Pan, Xu Liu, Zhenyu Tang

Abstract read
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Article in Neurotoxicity research, 2022. 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
0.8field-weighted citation impact, top 33% 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.

Min Li *Department of Neurology, The Second Affiliated Hospital of Nanchang University, Nanchang, 330006, China.
Siqi Zhou *Department of Neurology, The Second Affiliated Hospital of Nanchang University, Nanchang, 330006, China.
Gege WangDepartment of Neurology, The Second Affiliated Hospital of Nanchang University, Nanchang, 330006, China.
Luyao QiaoDepartment of Neurology, The Second Affiliated Hospital of Nanchang University, Nanchang, 330006, China.
Shouqin YiDepartment of Neurology, The Second Affiliated Hospital of Nanchang University, Nanchang, 330006, China.
Tianpei LiDepartment of Neurology, The Second Affiliated Hospital of Nanchang University, Nanchang, 330006, China.
Xin PanDepartment of Neurology, The Second Affiliated Hospital of Nanchang University, Nanchang, 330006, China.
Xu LiuDepartment of Neurology, The Second Affiliated Hospital of Nanchang University, Nanchang, 330006, China.
Zhenyu TangDepartment of Neurology, The Second Affiliated Hospital of Nanchang University, Nanchang, 330006, China. tangzyjr@163.com.
Nanchang University · CNSecond Affiliated Hospital of Nanchang University · CN

Funding

National Natural Science Foundation of China 82060214
6 · The paper itself

Abstract

Diabetes mellitus (DM) has been considered an accelerator of Alzheimer's disease (AD), but the cellular and molecular mechanisms underlying this effect are not fully understood. Here, we attempted to determine the role and regulatory mechanism of calpain in the AD-like cognitive decline and pathological changes in rats caused by DM. In the initial stages, our results verified that DM model rats showed cognitive impairment, as well as a loss of neurons, decreased pericyte marker (PDGFR-β and α-SMA), and calpain-2 expression and amyloid-β (Aβ) deposition in the hippocampal tissues. In high glucose-induced primary pericytes, the cell apoptotic rate was increased, and cell proliferation was inhibited in a time-dependent manner. The protein level of calpain-2 was also upregulated by HG induction, but the level of calpain-1 did not change with HG treatment, which was also observed in DM model rats. Subsequently, some DM model rats were administered calpeptin, an inhibitor of calpain. Our data revealed that calpeptin treatment significantly suppressed calpain-1 and calpain-2 expression in the hippocampal tissues and effectively improved the cognitive impairments of DM model rats. Neuronal loss, Aβ accumulation, pericyte loss, inflammation, and oxidative stress injury in the hippocampal tissues of DM model rats were also partly rescued by calpeptin administration. Our work demonstrated that the calpain inhibitor calpeptin could alleviate DM-induced AD-like cognitive impairments and pathological changes in rats, and this effect may be associated with pericytes. Calpeptin may become a promising drug to treat the AD-like complications of DM.

Indexed as

Alzheimer DiseaseCognitive DysfunctionDiabetes MellitusAmyloid beta-PeptidesAnimalsCalpainDipeptidesGlucoseGlycoproteinsRatsAmyloid beta-PeptidesCalpaincalpain inhibitorscalpeptinDipeptidesGlucoseGlycoproteinsAlzheimer’s diseaseCalpainCognitive impairmentsDiabetes mellitusPericytes

Identifiers

PMID36018506
OpenAlexW4293194395

What Socratic holds

Textmetadata
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.