Evidence map›Paper›PMID 32133639›Full record

ArticleBritish journal of pharmacology2020

The effect of maslinic acid on cognitive dysfunction induced by cholinergic blockade in mice.

Ho Jung Bae, Jihyun Kim, Jaehoon Kim, Nayeon Goo, Mudan Cai, Kyungnam Cho, Seo Yun Jung, Huiyoung Kwon, Dong Hyun Kim, Dae Sik Jang and 1 more

Open access · greenAbstract read
In one paragraph

Article in British journal of pharmacology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

16 citing papers in PubMed, 31 citations in OpenAlex.

  1. Review
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  7. Neurotrophic Natural Products.Progress in the chemistry of organic natural products · 2024
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  10. Review
  11. Pharmaceuticals (Basel, Switzerland) · 2022
    Article
  12. Review
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  14. Review
  15. Article
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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

11 authors at 2 institutions in 1 country.

Ho Jung BaeDepartment of Life and Nanopharmaceutical Science, Kyung Hee University, Seoul, Republic of Korea.
Jihyun KimDepartment of Life and Nanopharmaceutical Science, Kyung Hee University, Seoul, Republic of Korea.
Jaehoon KimDepartment of Life and Nanopharmaceutical Science, Kyung Hee University, Seoul, Republic of Korea.
Nayeon GooDepartment of Life and Nanopharmaceutical Science, Kyung Hee University, Seoul, Republic of Korea.
Mudan CaiDepartment of Life and Nanopharmaceutical Science, Kyung Hee University, Seoul, Republic of Korea.
Kyungnam ChoDepartment of Life and Nanopharmaceutical Science, Kyung Hee University, Seoul, Republic of Korea.
Seo Yun JungDepartment of Life and Nanopharmaceutical Science, Kyung Hee University, Seoul, Republic of Korea.
Huiyoung KwonDepartment of Medicinal Biotechnology, College of Health Sciences, Dong-A University, Busan, Republic of Korea.
Dong Hyun KimDepartment of Medicinal Biotechnology, College of Health Sciences, Dong-A University, Busan, Republic of Korea.
Dae Sik JangDepartment of Life and Nanopharmaceutical Science, Kyung Hee University, Seoul, Republic of Korea.
Jong Hoon RyuDepartment of Life and Nanopharmaceutical Science, Kyung Hee University, Seoul, Republic of Korea.
Kyung Hee University · KRDong-A University · KR

Funding

Ministry of Education, Science and Technology 2018R1A2A2A05023165Ministry of Science and ICT, South Korea NRF-2017R1A5A2014768
6 · The paper itself

Abstract

background and purposeAlzheimer's disease (AD) is the most prevalent disease associated with cognitive dysfunction. Current AD therapeutic agents have several gastrointestinal or psychological adverse effects and therefore, novel therapeutic agents with fewer adverse effects must be developed. Previously, we demonstrated that oleanolic acid, which is similar in chemical structure to maslinic acid, ameliorates cognitive impairment through the activation of tropomyosin receptor kinase (TrkB)-ERK-cAMP response element-binding protein (CREB) phosphorylation and increased levels of brain-derived neurotrophic factor (BDNF). In the present study, we investigate the effect of maslinic acid on cholinergic blockade-induced memory impairment in mice. METHODS AND KEY

resultsMaslinic acid reversed scopolamine-induced memory impairment, as determined by the Y-maze, passive avoidance and Morris water maze tests. In addition, we also observed that ERK-CREB, PI3K and PKB (Akt) phosphorylation levels were increased by maslinic acid administration in the mouse hippocampus. Moreover, we determined that the effects of maslinic acid on scopolamine-induced memory impairment in the passive avoidance test were abolished by a specific TrkB receptor antagonist (ANA-12). Additionally, we observed similar temporal changes in the expression levels between BDNF and tissue plasminogen activator in the hippocampus. CONCLUSION AND IMPLICATIONS: These findings suggest that maslinic acid enhances cognitive function through the activation of BDNF and its downstream pathway signalling in the hippocampus and that it might be a potential therapeutic agent for cognitive decline, such as that observed in AD.

Indexed as

Cognitive DysfunctionTissue Plasminogen ActivatorAnimalsBrain-Derived Neurotrophic FactorCholinergic AgentsCyclic AMP Response Element-Binding ProteinHippocampusMaze LearningMiceOleanolic AcidScopolamineTriterpenesBrain-Derived Neurotrophic FactorCholinergic AgentsCyclic AMP Response Element-Binding Proteinmaslinic acidOleanolic AcidScopolamineTissue Plasminogen ActivatorTriterpenes

Identifiers

PMID32133639
PMCPMC7312314
OpenAlexW3009809162

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.