Evidence map›Paper›PMID 37621124›Full record

ArticleJournal of cellular and molecular medicine2023

AR/PCC herb pair inhibits osteoblast pyroptosis to alleviate diabetes-related osteoporosis by activating Nrf2/Keap1 pathway.

Fangda Fu, Huan Luo, Yu Du, Yuying Chen, Kun Tian, Jin Pan, Jian Li, Nani Wang, Ronghua Bao, Hongting Jin and 3 more

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
4.5field-weighted citation impact, top 5% 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

22 citing papers in PubMed, 1 synthesis or guideline pooled it, 29 citations in OpenAlex.

  1. Pooled it
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  17. AugmentedJournal of inflammation research · 2024
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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

13 authors at 5 institutions in 1 country.

Fangda FuInstitute of Orthopaedics and Traumatology, The First Affiliated Hospital of Zhejiang Chinese Medical University (Zhejiang Provincial Hospital of Traditional Chinese Medicine), Hangzhou, China.
Huan LuoDepartment of Pharmacy, The Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
Yu DuThe First Affiliated Hospital of Zhejiang Chinese Medical University, Hangzhou, China.
Yuying ChenThe Fourth Clinical Medical College of Zhejiang Chinese Medical University, Hangzhou, China.
Kun TianDepartment of Orthopaedics, The First Affiliated Hospital of Zhejiang Chinese Medical University, Hangzhou, China.
Jin PanDepartment of Architecture, School of Architecture, China Academy of Art, Hangzhou, China.
Jian LiDepartment of Orthopaedics, Hangzhou Ninth People's Hospital, Hangzhou, China.
Nani WangDepartment of Medicine, Zhejiang Academy of Traditional Chinese Medicine, Hangzhou, China.
Ronghua BaoHangzhou Fuyang Hospital of TCM Orthopedics and Traumatology, Hangzhou, China.
Hongting JinInstitute of Orthopaedics and Traumatology, The First Affiliated Hospital of Zhejiang Chinese Medical University (Zhejiang Provincial Hospital of Traditional Chinese Medicine), Hangzhou, China.
Peijian TongInstitute of Orthopaedics and Traumatology, The First Affiliated Hospital of Zhejiang Chinese Medical University (Zhejiang Provincial Hospital of Traditional Chinese Medicine), Hangzhou, China.
Hongfeng RuanInstitute of Orthopaedics and Traumatology, The First Affiliated Hospital of Zhejiang Chinese Medical University (Zhejiang Provincial Hospital of Traditional Chinese Medicine), Hangzhou, China.ORCID 0000-0001-8868-9313
Chengliang WuInstitute of Orthopaedics and Traumatology, The First Affiliated Hospital of Zhejiang Chinese Medical University (Zhejiang Provincial Hospital of Traditional Chinese Medicine), Hangzhou, China.
Zhejiang Chinese Medical University · CN117th Hospital of People's Liberation Army · CNChina Academy of Art · CNHangzhou Hospital of Traditional Chinese Medicine · CNSecond Affiliated Hospital of Zhejiang University · CN

Funding

National Natural Science Foundation of China 81973870National Natural Science Foundation of China 81973881National Natural Science Foundation of China 82174140National Natural Science Foundation of China 82174401Natural Science Foundation of Zhejiang Province LBY22H270008Natural Science Foundation of Zhejiang Province LQ23H270003Natural Science Foundation of Zhejiang Province LY22H270003Research Project of Zhejiang Chinese Medical University 2021JKZDZC02Research Project of Zhejiang Chinese Medical University 2021JKZKTS036AResearch Project of Zhejiang Chinese Medical University Affiliated Hospital 2022FSYYZQ02Research Project of Zhejiang Chinese Medical University Affiliated Hospital 2022FSYYZZ05Traditional Chinese Medical Administration of Zhejiang Province 2021ZB090Traditional Chinese Medical Administration of Zhejiang Province 2022ZB119Traditional Chinese Medical Administration of Zhejiang Province 2022ZX005Traditional Chinese Medical Administration of Zhejiang Province 2023ZL128Traditional Chinese Medical Administration of Zhejiang Province 2023ZR019Zhejiang Chinese Medical University Schoo-level Education and Teaching Reform Project CY22001Zhejiang Medical and Health Science and Technology Project 2021KY22Zhejiang Medical and Health Science and Technology Project 2023RC194
6 · The paper itself

Abstract

Osteoporosis is a prevalent complication of diabetes, characterized by systemic metabolic impairment of bone mass and microarchitecture, particularly in the spine. Anemarrhenae Rhizoma/Phellodendri Chinensis Cortex (AR/PCC) herb pair has been extensively employed in Traditional Chinese Medicine to manage diabetes; however, its potential to ameliorate diabetic osteoporosis (DOP) has remained obscure. Herein, we explored the protective efficacy of AR/PCC herb pair against DOP using a streptozotocin (STZ)-induced rat diabetic model. Our data showed that AR/PCC could effectively reduce the elevated fasting blood glucose and reverse the osteoporotic phenotype of diabetic rats, resulting in significant improvements in vertebral trabecular area percentage, trabecular thickness and trabecular number, while reducing trabecular separation. Specifically, AR/PCC herb pair improved impaired osteogenesis, nerve ingrowth and angiogenesis. More importantly, it could mitigate the aberrant activation of osteoblast pyroptosis in the vertebral bodies of diabetic rats by reducing increased expressions of Nlrp3, Asc, Caspase1, Gsdmd and IL-1β. Mechanistically, AR/PCC activated antioxidant pathway through the upregulation of the antioxidant response protein Nrf2, while concurrently decreasing its negative feedback regulator Keap1. Collectively, our in vivo findings demonstrate that AR/PCC can inhibit osteoblast pyroptosis and alleviate STZ-induced rat DOP, suggesting its potential as a therapeutic agent for mitigating DOP.

Indexed as

AnemarrhenaDiabetes Mellitus, ExperimentalOsteoporosisAnimalsAntioxidantsKelch-Like ECH-Associated Protein 1NF-E2-Related Factor 2NLR Family, Pyrin Domain-Containing 3 ProteinOsteoblastsPyroptosisRatsAntioxidantsKelch-Like ECH-Associated Protein 1NF-E2-Related Factor 2NLR Family, Pyrin Domain-Containing 3 ProteinAnemarrhenae Rhizoma/Phellodendri Chinensis Cortex herb pairdiabetesNrf2/Keap1 signallingosteoporosispyroptosis

Identifiers

PMID37621124
PMCPMC10660633
OpenAlexW4386153724

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.