Evidence map›Paper›PMID 31070533›Full record

ArticlePharmaceutical biology2018

In vivo protective effects of chlorogenic acid against triptolide-induced hepatotoxicity and its mechanism.

Jun-Ming Wang, Rong-Xing Chen, Lu-Lu Zhang, Ning-Ning Ding, Chen Liu, Ying Cui, Yong-Xian Cheng

Open access · goldAbstract read
In one paragraph

Article in Pharmaceutical biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 33 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

7 authors at 2 institutions in 1 country.

Jun-Ming Wanga College of Pharmacy , Henan University of Chinese Medicine , Zhengzhou , China.
Rong-Xing Chena College of Pharmacy , Henan University of Chinese Medicine , Zhengzhou , China.
Lu-Lu Zhanga College of Pharmacy , Henan University of Chinese Medicine , Zhengzhou , China.
Ning-Ning Dinga College of Pharmacy , Henan University of Chinese Medicine , Zhengzhou , China.
Chen Liua College of Pharmacy , Henan University of Chinese Medicine , Zhengzhou , China.
Ying Cuia College of Pharmacy , Henan University of Chinese Medicine , Zhengzhou , China.
Yong-Xian Chengc Health Science Center , Shenzhen University , Shenzhen , China.
First Affiliated Hospital of Henan University · CNShenzhen University Health Science Center · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

contextTriptolide (TP) has outstanding biological activities, but it induces toxicities, particular hepatotoxicity, severely limiting its clinical application. Chlorogenic acid (CGA) has prominently medicinal and nutritional values. However, until now, it is not known whether CGA could mitigate TP-induced hepatotoxicity.

objectiveThis study explored the possible protection of CGA against TP-induced hepatotoxicity and its potential mechanisms, for the first time. MATERIAL AND

methodsKM mice were treated orally with TP at a single dose of 1 mg/kg at 4 h after being treated with CGA (10, 20 and 40 mg/kg) for seven continuous days. Blood samples were collected at 24 h after TP administration for measurement of serum biomarkers, and hepatic tissues for analysis of potential mechanisms.

resultsTP treatment-induced acute hepatotoxicity manifested by the significant elevation in serum alanine transaminase (93.9 U/L), aspartate transaminase (185.8 U/L) and hepatic malondialdehyde (0.637 μmol/mg protein), and the remarkable reduction in hepatic glutathione (1.425 μg/mg protein), glutathione S-transferase, glutathione peroxidase, superoxide dismutase and catalase (91.7, 320.7, 360.6 and 140.7 U/mg protein, respectively). In contrast, pretreatment with CGA for 7 days effectively attenuated acute liver injury and oxidative stress caused by TP with each ED DISCUSSION AND

conclusionsCombined CGA medication may probably reduce the risk of TP poisoning, and in-depth mechanisms can be developed around the signal molecules of Nrf2.

Indexed as

AnimalsAntineoplastic Agents, AlkylatingChemical and Drug Induced Liver InjuryChlorogenic AcidDiterpenesDose-Response Relationship, DrugEpoxy CompoundsMaleMiceOxidative StressPhenanthrenesProtective AgentsAntineoplastic Agents, AlkylatingChlorogenic AcidDiterpenesEpoxy CompoundsPhenanthrenesProtective Agentstriptolideantioxidant defencehepatoprotectionNrf2Oxidative stress

Identifiers

PMID31070533
PMCPMC6300082
OpenAlexW2905106196

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.