Evidence map›Paper›PMID 33095440›Full record

ArticleNeurochemical research2020

Baicalein Ameliorates Epilepsy Symptoms in a Pilocarpine-Induced Rat Model by Regulation of IGF1R.

Pengfei Fu, Qiang Yuan, Yirui Sun, Xin Wu, Zhuoyin Du, Zhiqi Li, Jin Yu, Ke Lv, Jin Hu

Abstract read
PubMed Publisher
In one paragraph

Article in Neurochemical research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
0.7field-weighted citation impact, top 35% 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

21 citing papers in PubMed, 18 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.

Pengfei FuDepartment of Neurosurgery, Huashan Hospital, Fudan University, 12 Urumqi Middle Road, Shanghai, China. wscxzr@163.com.
Qiang YuanDepartment of Neurosurgery, Huashan Hospital, Fudan University, 12 Urumqi Middle Road, Shanghai, China. 297260090@qq.com.
Yirui SunDepartment of Neurosurgery, Huashan Hospital, Fudan University, 12 Urumqi Middle Road, Shanghai, China. cxshhsf@163.com.
Xin WuDepartment of Neurosurgery, Huashan Hospital, Fudan University, 12 Urumqi Middle Road, Shanghai, China.
Zhuoyin DuDepartment of Neurosurgery, Huashan Hospital, Fudan University, 12 Urumqi Middle Road, Shanghai, China.
Zhiqi LiDepartment of Neurosurgery, Huashan Hospital, Fudan University, 12 Urumqi Middle Road, Shanghai, China.
Jin YuDepartment of Integrative Medicine and Neurobiology, Shanghai Medical College, Fudan University, 130 Dongan Road, Shanghai, China.
Ke LvDepartment of Neurosurgery, Huashan Hospital, Fudan University, 12 Urumqi Middle Road, Shanghai, China.
Jin HuDepartment of Neurosurgery, Huashan Hospital, Fudan University, 12 Urumqi Middle Road, Shanghai, China. 17317821354@163.com.ORCID http://orcid.org/0000-0002-8070-239X
Fudan University · CNShanghai Medical College of Fudan University · CN

Funding

National Natural Science Foundation of China 81701206National Natural Science Foundation of China 81870968National Outstanding Youth Foundation of China 81671200Scientific and Innovative Action Plan of Shanghai 18441903300
6 · The paper itself

Abstract

Treatment for epilepsy, particularly temporal lobe epilepsy, is challenging. Baicalein has multiple effects, including anti-inflammatory action. However, little is known about its efficacy in treatment of epilepsy. In this study, we established a pilocarpine-induced rat model and used it for assessment of baicalein efficacy in vivo. We predicted the pharmacological mechanism of baicalein by network pharmacology and RNA sequencing analyses. Pilocarpine epileptic rats treated with baicalein exhibited improved average seizure severity, seizure frequency, seizure duration, and survival time. Network pharmacology and RNA sequencing identified the differentially expressed genes between the baicalein treatment and epileptic groups. Insulin-like growth factor 1 receptor (IGF1R) was chosen as the top candidate target because of its overlapping findings in RNA sequencing and network pharmacology data. Western blotting, immunofluorescence, and polymerase chain reaction analyses showed that baicalein inhibited microglial proliferation, IGF1R, and inflammatory cytokine expression. Moreover, baicalein improved epilepsy symptoms. Inhibition of IGF1R function by blocking with AXL1717 enhanced baicalein treatment efficacy both in vivo and in vitro. In conclusion, baicalein exerted antiepileptic effects by regulation of IGF1R in a pilocarpine-induced rat model.

Indexed as

AnimalsCell ProliferationEpilepsyFlavanonesHippocampusInflammationMaleMicrogliaPilocarpineRats, Sprague-DawleyReceptor, IGF Type 1baicaleinFlavanonesIgf1r protein, ratPilocarpineReceptor, IGF Type 1BaicaleinEpilepsyIGF1RInflammationMicrogliaNetwork pharmacology

Identifiers

PMID33095440
OpenAlexW3094443380

What OpenQuestion 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 OpenQuestion graph.