Evidence map›Paper›PMID 35875675›Full record

ArticleDrug design, development and therapy2022

Magnesium Lithospermate B Protects Against Cisplatin-Induced Acute Kidney Injury via Alleviating Mitochondrial Dysfunction.

Daoqi Shen, Man Guo, Xuemei Geng, Jinbo Yu, Zhen Zhang, Jing Lin, Pan Lin, Xiaoqiang Ding, Xialian Xu

Open access · goldAbstract read
In one paragraph

Article in Drug design, development and therapy, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

9 citing papers in PubMed, 13 citations in OpenAlex.

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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

9 authors at 5 institutions in 1 country.

Daoqi ShenDepartment of Nephrology, Zhongshan Hospital, Fudan University, Shanghai, People's Republic of China.
Man GuoDepartment of Nephrology, Zhongshan Hospital, Fudan University, Shanghai, People's Republic of China.
Xuemei GengDepartment of Nephrology, Zhongshan Hospital, Fudan University, Shanghai, People's Republic of China.
Jinbo YuDepartment of Nephrology, Zhongshan Hospital, Fudan University, Shanghai, People's Republic of China.
Zhen ZhangDepartment of Nephrology, Zhongshan Hospital, Fudan University, Shanghai, People's Republic of China.
Jing LinDepartment of Nephrology, Zhongshan Hospital, Fudan University, Shanghai, People's Republic of China.
Pan LinDepartment of Nephrology, Zhongshan Hospital, Fudan University, Shanghai, People's Republic of China.
Xiaoqiang DingDepartment of Nephrology, Zhongshan Hospital, Fudan University, Shanghai, People's Republic of China.
Xialian XuDepartment of Nephrology, Zhongshan Hospital, Fudan University, Shanghai, People's Republic of China.
Fudan University · CNShanghai Medical Information Center · CNSun Yat-sen University · CNThe First Affiliated Hospital, Sun Yat-sen University · CNZhongshan Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Apoptosis plays a critical role in cisplatin-induced acute kidney injury (AKI) and is related to mitochondrial dysfunction. Magnesium lithospermate B (Mlb), one of the most important components of Methods: Renal injury induced by cisplatin in mouse renal tubular epithelial cells (mTECs) was measured by quantifying serum creatinine levels, mitochondrial morphology, cell viability, apoptosis, Dynamin-related protein 1(Drp1) expression, etc. The cells were then administered Mlb to determine its protective effects against cisplatin-induced AKI. Results: Mlb treatment significantly reduced serum creatinine levels and pathological injury of renal, inhibited the production of malondialdehyde, and reduced the depletion of superoxide dismutase. In addition, Mlb reduced Bax/Bcl2, cleaved caspase-3/caspase-3, and maintained mitochondrial integrity after AKI. Mlb administration also improved cell viability and reduced the percentage of apoptotic cells in vitro. Furthermore, Mlb reduced mitochondrial reactive oxygen species, improved mitochondrial membrane potential, and ameliorated mitochondrial morphological abnormalities by downregulating Drp1 expression. Conclusion: These results indicated that Mlb could protect the kidneys against cisplatin-induced apoptosis by alleviating mitochondrial dysfunction.

Indexed as

Acute Kidney InjuryCisplatinAnimalsApoptosisCaspase 3CreatinineDrugs, Chinese HerbalMiceMitochondriaRatsRats, Sprague-DawleyCaspase 3CisplatinCreatinineDrugs, Chinese Herballithospermate Bacute renal injuryapoptosiscisplatin-induced nephrotoxicitymitochondria homeostasisSalvia miltiorrhiza Bunge

Identifiers

PMID35875675
PMCPMC9296868
OpenAlexW4285404402

What Socratic holds

Textmetadata
LicenceCC BY-NC
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 Socratic graph.