Evidence map›Paper›PMID 27999666›Full record

ArticleTranslational neurodegeneration2016

Beclin-1- mediated autophagy may be involved in the elderly cognitive and affective disorders in streptozotocin-induced diabetic mice.

Zhu-Fei Guan, Xiu-Ling Zhou, Xiao-Ming Zhang, Yu Zhang, Yan-Mei Wang, Qi-Lin Guo, Gang Ji, Guo-Feng Wu, Na-Na Wang, Hao Yang and 4 more

Open access · goldAbstract read
In one paragraph

Article in Translational neurodegeneration, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.9field-weighted citation impact, top 13% 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

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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

26 citing papers in PubMed, 68 citations in OpenAlex.

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  11. The Contribution of Type 2 Diabetes to Parkinson's Disease Aetiology.International journal of molecular sciences · 2024
    Review
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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

14 authors at 6 institutions in 1 country.

Zhu-Fei GuanDepartment of Geriatric Neurology, Huashan Hospital, Fudan University; National Clinical Medicine Research Center for Age-related Diseases, 12 Middle WuLuMuQi Rd, Shanghai, 200040 China ; State Key Laboratory of Medical Neurobiology, Department of Neurobiology, School of Basic Medical Neurobiology, Department of Neurobiology School of Basic Medical Science, Shanghai Medical College, Fudan University, 131 DongAn Rd, Shanghai, 200032 China.
Xiu-Ling ZhouDepartment of Ultrasonics, Huashan Hospital, Fudan University, Shanghai, 200040 China.
Xiao-Ming ZhangDepartment of Geriatric Neurology, Huashan Hospital, Fudan University; National Clinical Medicine Research Center for Age-related Diseases, 12 Middle WuLuMuQi Rd, Shanghai, 200040 China.
Yu ZhangDepartment of Geriatric Neurology, Huashan Hospital, Fudan University; National Clinical Medicine Research Center for Age-related Diseases, 12 Middle WuLuMuQi Rd, Shanghai, 200040 China.
Yan-Mei WangDepartment of Geriatric Neurology, Huashan Hospital, Fudan University; National Clinical Medicine Research Center for Age-related Diseases, 12 Middle WuLuMuQi Rd, Shanghai, 200040 China.
Qi-Lin GuoState Key Laboratory of Medical Neurobiology, Department of Neurobiology, School of Basic Medical Neurobiology, Department of Neurobiology School of Basic Medical Science, Shanghai Medical College, Fudan University, 131 DongAn Rd, Shanghai, 200032 China.
Gang JiState Key Laboratory of Medical Neurobiology, Department of Neurobiology, School of Basic Medical Neurobiology, Department of Neurobiology School of Basic Medical Science, Shanghai Medical College, Fudan University, 131 DongAn Rd, Shanghai, 200032 China.
Guo-Feng WuDepartment of EmergencyNeurology, Guiyang Medical University, Guiyang, 550004 China.
Na-Na WangDepartment of Geriatric Neurology, Huashan Hospital, Fudan University; National Clinical Medicine Research Center for Age-related Diseases, 12 Middle WuLuMuQi Rd, Shanghai, 200040 China.
Hao YangDepartment of Geriatric Neurology, Huashan Hospital, Fudan University; National Clinical Medicine Research Center for Age-related Diseases, 12 Middle WuLuMuQi Rd, Shanghai, 200040 China.
Zhong-Yu YuDepartment of Geriatric Neurology, Huashan Hospital, Fudan University; National Clinical Medicine Research Center for Age-related Diseases, 12 Middle WuLuMuQi Rd, Shanghai, 200040 China.
Hou-Guang ZhouDepartment of Geriatric Neurology, Huashan Hospital, Fudan University; National Clinical Medicine Research Center for Age-related Diseases, 12 Middle WuLuMuQi Rd, Shanghai, 200040 China.
Jing-Chun GuoState Key Laboratory of Medical Neurobiology, Department of Neurobiology, School of Basic Medical Neurobiology, Department of Neurobiology School of Basic Medical Science, Shanghai Medical College, Fudan University, 131 DongAn Rd, Shanghai, 200032 China.
Ying-Chao LiuDepartment of Neurosurgery, Shandong Provincial Hospital, 5 Latitude and 7 longitude Rd, Jinan, 250021 China.
National Clinical Research Center for Digestive Diseases · CNFudan University · CNState Key Laboratory of Medical NeurobiologyGuiyang Medical University · CNHuashan Hospital · CNShandong Provincial Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDiabetes is the most common metabolic disease with many chronic complications, and cognitive disorders are one of the common complications in patients with diabetes. Previous studies have showed that autophagy played important roles in the progression of metabolic syndrome, diabetes and other diseases. So we investigated whether aged diabetic mice are prone to be associated with the cognitive and affective disorders and whether Beclin-1-mediated autophagy might be involved in thepahological process.

methodsHigh-fat diet/streptozotocin (STZ) injection-induced diabetic C57 mice were adopted in this study. Cognitive disorders were detected by Morris water maze and fear conditional test. Affective disorders were detected by tail suspension test and forced swimming test. Magnetic resonance imaging was applied to observe changes of morphology and metabolism in the brain. The 18 F-fluorodeoxyglucose positron emission tomography (FDG-PET) was used to assess metabolism changes in the brain of aged diabetic mice. Autophagy were evaluated by Beclin- 1, LC3II/I and P62, which were detected by western blot analysis and observed by electron microscopy.

results1. Compared with control group, diabetes mice showed significantly decreasing abilities in spatial memory and conditioned fear memory (all

conclusionCompared with normal aged mice, diabetic aged mice were apt to cerebral small vessel disease and associated with cognitive and affective disorders, which may be related to the significantly reduced glucose metabolism in hippocampus and amygdala. Beclin1 mediated autophagy in hippocampus probably played an important role in cognitive and affective disorders of STZ-induced aged diabetic mice.

Identifiers

PMID27999666
PMCPMC5154026
OpenAlexW2563195238

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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.