Evidence map›Paper›PMID 41751415›Full record

ArticleCurrent issues in molecular biology2026

A Water Extract of Mixed Mushroom Mycelia Mitigates Cognitive Deficit and Oxidative Stress After Global Cerebral Ischemia-Reperfusion Injury.

Hyeon-Jeong Noh, Ji-Hyun Moon, Hye Jeong Ahn, Ah La Choi, Nam Seob Lee, Young Gil Jeong, Sang Seop Lee, Yung Choon Yoo, Ji-Min Lee, Do-Eun Kim and 5 more

Abstract read
In one paragraph

Article in Current issues in molecular biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

15 authors.

Hyeon-Jeong NohDepartment of Biomedical Materials, Konyang University, Daejeon 35365, Republic of Korea.ORCID 0000-0001-8892-538X
Ji-Hyun MoonDepartment of Anatomy, College of Medicine, Konyang University, Daejeon 35365, Republic of Korea.
Hye Jeong AhnDepartment of Anatomy, College of Medicine, Konyang University, Daejeon 35365, Republic of Korea.ORCID 0009-0004-2786-8982
Ah La ChoiDepartment of Anatomy, College of Medicine, Konyang University, Daejeon 35365, Republic of Korea.
Nam Seob LeeDepartment of Anatomy, College of Medicine, Konyang University, Daejeon 35365, Republic of Korea.
Young Gil JeongDepartment of Anatomy, College of Medicine, Konyang University, Daejeon 35365, Republic of Korea.
Sang Seop LeeDepartment of Microbiology, College of Medicine, Konyang University, Daejeon 35365, Republic of Korea.ORCID 0009-0008-2767-2065
Yung Choon YooDepartment of Microbiology, College of Medicine, Konyang University, Daejeon 35365, Republic of Korea.ORCID 0000-0001-8905-6104
Ji-Min LeeDepartment of Medicine, Konyang University, Daejeon 35365, Republic of Korea.
Do-Eun KimDepartment of Medicine, Konyang University, Daejeon 35365, Republic of Korea.
Jaeku KangDepartment of Pharmacology, College of Medicine, Konyang University, Daejeon 35365, Republic of Korea.ORCID 0000-0002-8660-7940
Jong Yea ParkGiunchan Co., Ltd., Cheonan 31035, Republic of Korea.
Hyun Min KimGiunchan Co., Ltd., Cheonan 31035, Republic of Korea.
Sung Baek KimDepartment of Biomedical Materials, Konyang University, Daejeon 35365, Republic of Korea.ORCID 0000-0001-8672-4760
Seung Yun HanDepartment of Anatomy, College of Medicine, Konyang University, Daejeon 35365, Republic of Korea.ORCID 0000-0002-7055-6341

Funding

National Research Foundation #RS-2023-00251456Regional Innovation System & Education(RISE) program through the Daejeon RISE Center #2025-RISE-06-001
6 · The paper itself

Abstract

backgroundGMK is a bioactive material newly identified from a water extract of mixed mushroom mycelia (

methodsGCIRI was induced in male Sprague-Dawley rats by bilateral common carotid artery occlusion with hypovolemia (BCCAO/H). GMK (30 or 90 mg/kg, p.o.) was administered once daily for 14 days before surgery. Cognitive functions were evaluated using the Y-maze, Barnes maze, and passive avoidance tests. Hippocampal CA1 neuronal survival and glial activation were analyzed by cresyl violet staining and Iba1/GFAP immunohistochemistry. In parallel, PC12 cells were pretreated with GMK (100 or 200 μg/mL, 24 h) before oxygen-glucose deprivation and reoxygenation (OGD/R), and apoptosis (TUNEL, Bax/Bcl-2), oxidative stress markers (ROS, MDA, and NO), antioxidant enzymes including glutathione peroxidase (GPX) and catalase (CAT), and signaling proteins (p-ERK/ERK, iNOS) were examined.

resultsGMK significantly ameliorated GCIRI-induced learning and memory impairments, protected CA1 pyramidal neurons, and reduced microglial and astrocytic activation. In OGD/R-challenged PC12 cells, GMK attenuated apoptosis, suppressed ROS, MDA, and NO production, normalized GPX and CAT activities, and favorably regulated p-ERK and iNOS pathways.

conclusionsThese findings suggest that GMK confers dose-dependent behavioral and histopathological protection against GCIRI, potentially by modulating redox- and apoptosis-related signaling (Bax/Bcl-2, GPX/CAT, and ERK/iNOS pathways), with more consistent effects at a higher dose.

Indexed as

anti-apoptoticBCCAO/H modelcognitive impairmentglobal cerebral ischemia–reperfusion injuryGMKhippocampal CA1oxidative stressPC12 cells

Identifiers

PMID41751415
PMCPMC12939780

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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.