Evidence map›Paper›PMID 39416424›Full record

ArticleDrug design, development and therapy2024

Jujuboside A Regulates Calcium Homeostasis and Structural Plasticity to Alleviate Depression-Like Behavior via Shh Signaling in Immature Neurons.

Ziyan Zhong, Jian Liu, Yan Luo, Mei Wu, Feng Qiu, Hongqing Zhao, Yang Liu, Yajing Wang, Hongping Long, Lei Zhao and 3 more

Abstract read
In one paragraph

Article in Drug design, development and therapy, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

6 citing papers in PubMed.

  1. 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

13 authors.

Ziyan Zhong *Science & Technology Innovation Center, Hunan University of Chinese Medicine, Changsha, Hunan, 410208, People's Republic of China.
Jian Liu *The First Hospital, Hunan University of Chinese Medicine, Changsha, Hunan, 410007, People's Republic of China.
Yan LuoScience & Technology Innovation Center, Hunan University of Chinese Medicine, Changsha, Hunan, 410208, People's Republic of China.
Mei WuScience & Technology Innovation Center, Hunan University of Chinese Medicine, Changsha, Hunan, 410208, People's Republic of China.
Feng QiuScience & Technology Innovation Center, Hunan University of Chinese Medicine, Changsha, Hunan, 410208, People's Republic of China.
Hongqing ZhaoScience & Technology Innovation Center, Hunan University of Chinese Medicine, Changsha, Hunan, 410208, People's Republic of China.
Yang LiuScience & Technology Innovation Center, Hunan University of Chinese Medicine, Changsha, Hunan, 410208, People's Republic of China.
Yajing WangOffice of Science & Technology, Hunan University of Chinese Medicine, Changsha, Hunan, 410208, People's Republic of China.
Hongping LongThe First Hospital, Hunan University of Chinese Medicine, Changsha, Hunan, 410007, People's Republic of China.ORCID 0000-0001-8891-5851
Lei ZhaoSchool of Integrated Chinese and Western Medicine, Hunan University of Chinese Medicine, Changsha, Hunan, 410208, People's Republic of China.
Yuhong WangScience & Technology Innovation Center, Hunan University of Chinese Medicine, Changsha, Hunan, 410208, People's Republic of China.
Yuanshan HanThe First Hospital, Hunan University of Chinese Medicine, Changsha, Hunan, 410007, People's Republic of China.
Pan MengScience & Technology Innovation Center, Hunan University of Chinese Medicine, Changsha, Hunan, 410208, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Depression, a leading cause of disability worldwide, is characterized by dysfunction of immature neurons, resulting in dysregulated calcium homeostasis and impaired structural plasticity. Jujuboside A (JuA), a biologically active compound derived from Methods: Sprague-Dawley rats were subjected to chronic unpredictable mild stress (CUMS) to induce a depression model. JuA (12.5 mg/kg, 25 mg/kg, 50 mg/kg) was administered orally for 4 weeks. Emotional and cognitive function were assessed. Monoamine neurotransmitter levels were measured using enzyme-linked immunosorbent assay (ELISA). The number of immature neurons and calcium homeostasis were evaluated by immunofluorescence. Western blotting and immunofluorescence were employed to detect the expression of Sonic hedgehog (Shh) signaling proteins. Additionally, lentiviral vector expressing Shh shRNA (LV-Shh-RNAi) were infused intracerebrally to investigate the role of Shh in JuA's antidepressant effects. Results: JuA significantly ameliorated depressive-like behavior and cognitive dysfunction in CUMS rats, increased monoamine neurotransmitter levels in serum and hippocampal tissue, reduced the number of BrdU/DCX (bromodeoxyuridine/doublecortin)-positive immature neurons, and attenuated calcium ion (Ca Conclusion: These findings collectively suggest that JuA improves depressive-like behavior in CUMS rats by modulating calcium homeostasis and synaptic structural plasticity in immature neurons through the Shh signaling pathway.

Indexed as

CalciumDepressionHedgehog ProteinsHomeostasisSaponinsSignal TransductionAnimalsAntidepressive AgentsDisease Models, AnimalDose-Response Relationship, DrugMaleNeuronal PlasticityNeuronsRatsRats, Sprague-DawleyAntidepressive AgentsCalciumHedgehog Proteinsjujuboside ASaponinsShh protein, ratCalcium homeostasisDepressionImmature neuronJujuboside ASonic hedgehog

Identifiers

PMID39416424
PMCPMC11482263

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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.