Evidence map›Paper›PMID 39462270›Full record

ArticleJournal of cellular and molecular medicine2024

Puerarin alleviates apoptosis and inflammation in kidney stone cells via the PI3K/AKT pathway: Network pharmacology and experimental verification.

Yuexian Xu, Hu Liang, Xike Mao, Zhenyu Song, Xudong Shen, Defeng Ge, Yang Chen, Bingbing Hou, Zongyao Hao

Erratum issuedAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Yuexian XuDepartment of Urology, The First Affiliated Hospital of Anhui Medical University, Hefei, China.ORCID 0000-0003-0986-5505
Hu LiangDepartment of Urology, The First Affiliated Hospital of Anhui Medical University, Hefei, China.
Xike MaoDepartment of Urology, The First Affiliated Hospital of Anhui Medical University, Hefei, China.
Zhenyu SongDepartment of Urology, The First Affiliated Hospital of Anhui Medical University, Hefei, China.
Xudong ShenDepartment of Urology, The First Affiliated Hospital of Anhui Medical University, Hefei, China.
Defeng GeDepartment of Urology, The First Affiliated Hospital of Anhui Medical University, Hefei, China.
Yang ChenDepartment of Urology, The First Affiliated Hospital of Anhui Medical University, Hefei, China.
Bingbing HouDepartment of Urology, The First Affiliated Hospital of Anhui Medical University, Hefei, China.
Zongyao HaoDepartment of Urology, The First Affiliated Hospital of Anhui Medical University, Hefei, China.

Funding

National Natural Science Foundation of China 82070724National Natural Science Foundation of China 82370768
6 · The paper itself

Abstract

Puerarin(PUE), an isoflavonoid extracted from Pueraria root, has anti-apoptotic effects. The objective of this research is to examine the impact of PUE on renal apoptosis and inflammation resulting from renal calculi and to elucidate its mechanism. The approach of network pharmacology and molecular docking was employed to discover potential targets and pathways of PUE. An animal model of calcium oxalate crystal deposition by intraperitoneal injection of glyoxylate and a model of COM-induced human renal tubular epithelial cells (HK2) were used to investigate the pharmacological mechanisms of PUE against apoptosis and inflammation. We used haematoxylin-eosin (H&E) and Periodic Acid-Schiff staining (PAS) to assess the effect of PUE on crystal deposition and damage. The mechanism of PUE was elucidated and validated using Western blotting, histology and immunohistochemical staining. Network pharmacology findings indicated that the PI3K/AKT pathway plays a crucial role in PUE. We experimentally demonstrate that PUE alleviated COM-induced changes in apoptotic proteins, increased inflammatory indicators and changes in oxidative stress-related indicators in HK2 cells by activating the PI3K/AKT pathway, reduced serum creatinine and urea nitrogen levels in mice caused by CaOx, alleviated crystal deposition and damage, and alleviated apoptosis, oxidative stress and inflammation. Puerarin attenuates renal apoptosis and inflammation caused by kidney stones through the PI3K/AKT pathway.

Indexed as

ApoptosisInflammationIsoflavonesKidney CalculiNetwork PharmacologyPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktSignal TransductionAnimalsCalcium OxalateCell LineDisease Models, AnimalEpithelial CellsHumansKidney TubulesMaleCalcium OxalateIsoflavonesPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktpuerarinapoptosiskidney stonenetwork pharmacologypuerarin

Identifiers

PMID39462270
PMCPMC11512754

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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.