Evidence map›Paper›PMID 29675572›Full record

ArticleMolecular neurobiology2018

Baicalin Modulates APPL2/Glucocorticoid Receptor Signaling Cascade, Promotes Neurogenesis, and Attenuates Emotional and Olfactory Dysfunctions in Chronic Corticosterone-Induced Depression.

Chong Gao, Qiaohui Du, Wenting Li, Ruixia Deng, Qi Wang, Aimin Xu, Jiangang Shen

Abstract read
PubMed Publisher
In one paragraph

Article in Molecular neurobiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 2 pooled it
4.0field-weighted citation impact, top 6% 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

30 citing papers in PubMed, 2 syntheses or guidelines pooled it, 53 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

7 authors at 3 institutions in 2 countries.

Chong GaoSchool of Chinese Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, 10 Sasssoon Road, Hong Kong, Hong Kong SAR, China.
Qiaohui DuSchool of Chinese Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, 10 Sasssoon Road, Hong Kong, Hong Kong SAR, China.
Wenting LiSchool of Chinese Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, 10 Sasssoon Road, Hong Kong, Hong Kong SAR, China.
Ruixia DengSchool of Chinese Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, 10 Sasssoon Road, Hong Kong, Hong Kong SAR, China.
Qi WangInstitute of Clinical Pharmacology, Guangzhou University of Chinese Medicine, Guangzhou, Guangdong, China.
Aimin XuDepartment of Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, 21 Sasson Road, Hong Kong, Hong Kong SAR, China.
Jiangang ShenSchool of Chinese Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, 10 Sasssoon Road, Hong Kong, Hong Kong SAR, China. shenjg@hku.hk.ORCID http://orcid.org/0000-0002-4199-8095
Chinese University of Hong Kong · HKGuangzhou University of Chinese Medicine · CNUniversity of Hong Kong · HK

Funding

RGC GRF grants from Hong Kong Research Grants Council 777313M, 776512M, J.S.
6 · The paper itself

Abstract

Olfactory dysfunction is often accompanied with anxiety- and depressive-like behaviors in depressive patients. Impaired neurogenesis in hippocampus and subventricular zone (SVZ)-olfactory bulb (OB) contribute to anxiety- and depressive-like behaviors and olfactory dysfunctions. However, the underlying mechanisms of olfactory dysfunction remain unclear. Our previous study indicates that adaptor protein, phosphotyrosine interacting with PH domain and leucine zipper 2 (APPL2), could affect the activity and sensitivity of glucocorticoid receptor (GR) and mediate impaired hippocampal neurogenesis, which contribute the development of depression. In the present study, we further identified the roles of APPL2 in olfactory functions. APPL2 Tg mice displayed higher GR activity and less capacity of neurogenesis at olfactory system with less olfactory sensitivity than WT mice, indicating that APPL2 could be a potential therapeutic target for depression and olfactory deficits. We then studied the effects of baicalin, a medicinal herbal compound, on modulating APPL2/GR signaling pathway for promoting neurogenesis and antidepressant as well as improving olfactory functions. Baicalin treatment inhibited APPL2/GR signaling pathway and improved neurogenesis at SVZ, OB, and hippocampus in APPL2 Tg mice and chronic corticosterone-induced depression mouse model. Behavioral tests revealed that baicalin attenuated depressive- and anxiety-like behaviors and improve olfactory functions in the chronic depression mouse model and APPL2 Tg mice. Taken together, APPL2 could be a novel therapeutic target for improving depressant-related olfactory dysfunctions and baicalin could inhibit APPL2-mediated GR hyperactivity and promote adult neurogenesis, subsequently releasing depressive and anxiety symptoms and improving olfactory functions for antidepressant therapy.

Indexed as

EmotionsNeurogenesisSignal TransductionAdaptor Proteins, Signal TransducingAnimalsAnxietyBehavior, AnimalBrainCell Line, TumorCorticosteroneDepressionDisease Models, AnimalFlavonoidsHumansMaleMice, Inbred C57BLAdaptor Proteins, Signal TransducingbaicalinCorticosteroneDCC-interacting protein 13-beta, mouseFlavonoidsReceptors, GlucocorticoidAPPL2DepressionGlucocorticoid receptorHippocampusNeurogenesisOlfactory bulbOlfactory functionsSubventricular zone

Identifiers

PMID29675572
OpenAlexW2799756627

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.