Evidence map›Paper›PMID 27822668›Full record

ArticleNeurochemical research2017

Chronic Intermittent Hypobaric Hypoxia Pretreatment Ameliorates Ischemia-Induced Cognitive Dysfunction Through Activation of ERK1/2-CREB-BDNF Pathway in Anesthetized Mice.

Jintian Wang, Shixiao Zhang, Huijuan Ma, Shijie Yang, Zhao Liu, Xiaolei Wu, Sheng Wang, Yi Zhang, Yixian Liu

Abstract read
PubMed Publisher
In one paragraph

Article in Neurochemical research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.2field-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

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

15 citing papers in PubMed, 33 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 1 institution in 1 country.

Jintian WangDepartment of Physiology, Hebei Medical University, 361 Zhongshan East Road, Shijiazhuang, 050017, China.
Shixiao ZhangDepartment of Physiology, Hebei Medical University, 361 Zhongshan East Road, Shijiazhuang, 050017, China.
Huijuan MaDepartment of Physiology, Hebei Medical University, 361 Zhongshan East Road, Shijiazhuang, 050017, China.
Shijie YangDepartment of Urology, Third Hospital of Hebei Medical University, Shijiazhuang, 050051, China.
Zhao LiuDepartment of Physiology, Hebei Medical University, 361 Zhongshan East Road, Shijiazhuang, 050017, China.
Xiaolei WuDepartment of Physiology, Hebei Medical University, 361 Zhongshan East Road, Shijiazhuang, 050017, China.
Sheng WangDepartment of Physiology, Hebei Medical University, 361 Zhongshan East Road, Shijiazhuang, 050017, China.
Yi ZhangDepartment of Physiology, Hebei Medical University, 361 Zhongshan East Road, Shijiazhuang, 050017, China.
Yixian LiuDepartment of Physiology, Hebei Medical University, 361 Zhongshan East Road, Shijiazhuang, 050017, China. phylyx2004@126.com.
Hebei Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chronic intermittent hypobaric hypoxia (CIHH) has protective effects on heart and brain against ischemia injury through mobilizing endogenous adaptive mechanisms. However, whether CIHH prevents against cognitive impairment was not elucidated. The present study aimed to investigate the effect and mechanism of CIHH treatment on ischemia/reperfusion (IR)-induced cognitive dysfunction. Mice were randomly divided into 8 groups: Control, Sham, CIHH (simulating 5000 m high-altitude for 28 days, 6 h per day), IR (three 16-min occlusions of bilateral common carotid arteries interrupted by two 10-min intervals), CIHH + IR, PD98059 (inhibitor of MEK1/2) + CIHH + IR, PD98059 + Sham and PD98059 + IR group. Morris water maze and step-down passive avoidance tests were performed to evaluate the capability of learning and memory 1 month after ischemia. Thionine dyeing was to examine histological manifestations of pyramidal neurons in hippocampus CA1 region. Western blotting assay was for measurement of the protein expressions in ERK1/2-CREB-BDNF signaling pathway. There were a shorter escape latency and a longer percentage of time retaining in the target quadrant in Morris water maze test, fewer times of errors in the step-down avoidance test and a higher neuronal density of the hippocampal CA1 subfield in CIHH + IR group than in IR group. CIHH upregulated the expressions of BDNF, phosphorylated CREB, ERK1/2 and TrkB with or without ischemia. The protective effects of CIHH were abolished by PD98059 administration 15 min before ischemia. CIHH ameliorated ischemia-induced cognitive dysfunction through activation of ERK1/2-CREB-BDNF signaling pathway.

Indexed as

AnimalsBrain-Derived Neurotrophic FactorBrain IschemiaCognitive DysfunctionCyclic AMP Response Element-Binding ProteinHypoxiaMaleMAP Kinase Signaling SystemMaze LearningMiceMice, Inbred ICRRandom AllocationTreatment OutcomeBrain-Derived Neurotrophic FactorCreb1 protein, mouseCyclic AMP Response Element-Binding ProteinBrain-derived neurotrophic factorChronic intermittent hypobaric hypoxiaCognitive dysfunctionExtracellular signal-regulated kinasesIschemia/reperfusionMouse

Identifiers

PMID27822668
OpenAlexW2549454969

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.