Evidence map›Paper›PMID 41378220›Full record

ArticleFrontiers in pharmacology2025

Allocryptopine, tetrahydropalmatine, and tetrahydroberberine N-oxide alkaloids alleviate cellular stress by modulating calcium homeostasis and the MAPK and akt/GSK-3β/tau signaling pathways.

Serap Nigdelioglu Dolanbay, Belma Aslim

Abstract read
In one paragraph

Article in Frontiers in pharmacology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Review
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

2 authors.

Serap Nigdelioglu DolanbayDepartment of Biology, Faculty of Science, Gazi University, Ankara, Türkiye.
Belma AslimDepartment of Biology, Faculty of Science, Gazi University, Ankara, Türkiye.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Methods: The plant was collected, identified, and the GGAE was prepared by macerating dried, pulverized material in chloroform. The GGAE's neuroprotective properties were assessed using the rat pheochromocytoma (PC12) cell line. Intracellular calcium levels were analyzed via flow cytometry; gene expression of L-type voltage-gated calcium channel subtypes was evaluated with qRT-PCR; and the phosphorylation status of key proteins (p-ERK1/2, p-JNK, p-p38, p-Akt, p-GSK-3β, and p-Tau) was determined using Western blotting. The binding energies and contact residues of alkaloids (allocryptopine, tetrahydropalmatine, and tetrahydroberberine N-oxide) found in the GGAE were determined to target proteins (AKT1, CACNA1C, CACNA1D, ERK1/2, GSK3β, JNK, P38, and TAU). Results: The results suggest that the GGAE helps maintain intracellular calcium homeostasis and functions as an L-type Ca Discussion: These findings suggest that the GGAE exerts a comprehensive neuroprotective effect, positioning it as a promising therapeutic candidate for the treatment of NDs.

Indexed as

Akt/GSK-3β/tau signaling pathwayalkaloidGlaucium grandiflorumintracellular Ca2+ homeostasisMAPK signaling pathways

Identifiers

PMID41378220
PMCPMC12685886

What OpenQuestion holds

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Registered trials

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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.