Evidence map›Paper›PMID 31141948›Full record

ArticleNutrients2019

Eunjin Sohn, Hye-Sun Lim, Yu Jin Kim, Bu-Yeo Kim, Joo-Hwan Kim, Soo-Jin Jeong

Abstract read
In one paragraph

Article in Nutrients, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Phylogenetic Analysis ofFrontiers in plant science · 2022
    Article
  11. Article
  12. Frontiers in pharmacology · 2021
    Article
  13. Catechol-Type Flavonoids from the Branches ofMolecules (Basel, Switzerland) · 2020
    Article
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

6 authors.

Eunjin SohnClinical Medicine Division, Korea Institute of Oriental Medicine, Daejeon 34054, South Korea. ssen4022@kiom.re.kr.
Hye-Sun LimClinical Medicine Division, Korea Institute of Oriental Medicine, Daejeon 34054, South Korea. qp1015@kiom.re.kr.
Yu Jin KimClinical Medicine Division, Korea Institute of Oriental Medicine, Daejeon 34054, South Korea. jinjin0228@kiom.re.kr.
Bu-Yeo KimClinical Medicine Division, Korea Institute of Oriental Medicine, Daejeon 34054, South Korea. buykim@kiom.re.kr.
Joo-Hwan KimDepartment of Life Science, Gachon University, Seongnam, Kyonggi-do 21936, South Korea. kimjh2009@gachon.ac.kr.
Soo-Jin JeongClinical Medicine Division, Korea Institute of Oriental Medicine, Daejeon 34054, South Korea. sjijeong@kiom.re.kr.

Funding

Korea Institute of Oriental Medicine KSN1515293
6 · The paper itself

Abstract

We aimed to investigate the therapeutic effects of an Elaeagnus glabra f. oxyphylla (EGFO) ethanol extract in mice with scopolamine-induced memory dysfunction. Fifty male mice were randomly divided into a normal control group, a scopolamine-treated group, a scopolamine and EGFO extract-treated group, and a scopolamine and tacrine-treated group. EGFO (50 or 100 mg/kg/day) was received for 21 days. Step-through passive avoidance and Y-maze tests were performed to examine the effects of treatment on learning and memory impairments. Acetylcholine (Ach) levels and acetylcholinesterase (AchE) activity were measured via an enzyme-linked immunosorbent assay (ELISA). Levels of choline acetyltransferase (ChAT), nerve growth factor (NGF), cAMP response element-binding protein (CREB), and apoptosis-related protein expression were determined via Western blot analysis. EGFO pretreatment significantly attenuated scopolamine-induced memory impairments, relative to findings observed in the scopolamine-treated group. Levels of cholinergic factors in the brain tissues were markedly attenuated in the scopolamine-treated group. EGFO treatment also attenuated neural apoptosis in scopolamine-treated mice by decreasing the expression of apoptosis-related proteins such as Bax, Bcl2, cleaved caspase-3, and TUNEL staining. These results suggest that EGFO improves memory and cognition in a mouse model of memory impairment by restoring cholinergic and anti-apoptotic activity, possibly via activation of CREB/NGF signaling.

Indexed as

ElaeagnaceaeAcetylcholineAcetylcholinesteraseAnimalsApoptosisApoptosis Regulatory ProteinsBehavior, AnimalBrainCholinergic FibersCognitionCyclic AMP Response Element-Binding ProteinDisease Models, AnimalGPI-Linked ProteinsMaleMemoryMemory DisordersAcetylcholineAcetylcholinesteraseAche protein, mouseApoptosis Regulatory ProteinsCreb1 protein, mouseCyclic AMP Response Element-Binding ProteinGPI-Linked ProteinsNerve Growth FactorPlant PreparationsScopolamineAlzheimer’s diseasecAMP response element-binding protein (CREB)cholinergic systemmemory dysfunctionnerve growth factor (NGF)scopolamine

Identifiers

PMID31141948
PMCPMC6627942

What OpenQuestion holds

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LicenceCC BY
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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.