Evidence map›Paper›PMID 32284524›Full record

ArticleMedical science monitor : international medical journal of experimental and clinical research2020

CYP2A13 Acts as the Main Metabolic CYP450s Enzyme for Activating Leonurine in Human Bronchial Epithelial Cells.

Ting Xu, Xuxu Li, Tian Leng, Tianchi Zhuang, Yan Sun, Yajun Tang, Li Wang, Muyi Yang, Minghui Ji

Open access · hybridAbstract read
In one paragraph

Article in Medical science monitor : international medical journal of experimental and clinical research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.3field-weighted citation impact, top 47% 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

4 citing papers in PubMed, 5 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 1 institution in 1 country.

Ting XuSchool of Nursing, Nanjing Medical University, Nanjing, Jiangsu, China (mainland).
Xuxu LiSchool of Nursing, Nanjing Medical University, Nanjing, Jiangsu, China (mainland).
Tian LengSchool of Nursing, Nanjing Medical University, Nanjing, Jiangsu, China (mainland).
Tianchi ZhuangSchool of Nursing, Nanjing Medical University, Nanjing, Jiangsu, China (mainland).
Yan SunSchool of Nursing, Nanjing Medical University, Nanjing, Jiangsu, China (mainland).
Yajun TangSchool of Nursing, Nanjing Medical University, Nanjing, Jiangsu, China (mainland).
Li WangSchool of Public Health, Nanjing Medical University, Nanjing, Jiangsu, China (mainland).
Muyi YangDepartment of Obstetrics, Nanjing First Hospital, Nanjing Medical University, Nanjing, Jiangsu, China (mainland).
Minghui JiSchool of Nursing, Nanjing Medical University, Nanjing, Jiangsu, China (mainland).
Nanjing Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND Leonurine is an active component of the traditional Chinese medicine Leonurus japonicus. This study aimed to investigate the effects of overexpressed CYP450s on the metabolic activity of leonurine. MATERIAL AND METHODS BEAS-2B cells stably expressing CYP1A1, 1A2, 2A13, 2B6, and 3A4 were constructed. CYP450s expression was identified using reverse-transcription PCR and Western blot assay. CCK-8 assay was used to evaluate the effect of leonurine on cell activity. Leonurine was incubated in vitro with CYP1A1, 1A2, 2A13, 2B6, and 3A4 metabolic enzymes to evaluate the clearance rate of CYP450 enzymes for leonurine. UPLC-MS was used to detect changes of drug concentration and discover the main metabolic enzymes affecting leonurine. RESULTS BEAS-2B cells stably expressing CYP1A1, 1A2, 2A13, 2B6, and 3A4 were successfully constructed. According to primary mass spectra and secondary mass spectra of leonurine, the main metabolic enzymes were 312.1550 [H+] and 181.0484. Compared to the control group, residue of leonurine in CYP2A13 group was significantly reduced (F=5.307, p=0.024). Compared to the 0-min group, the clearance rate of leonurine in the CYP2A13-treated group was significantly decreased at 120 min after treatment (F=7.273, p=0.007). CCK-8 results also showed that activity of BEAS-2B cells that overexpress CYP2A13 gradually decreased with increased concentration of leonurine. Although CYP2A13 demonstrated good metabolic activity for leonurine, we found that CYP1A1, 1A2, 2B6, and 3A4 had no metabolic effects on leonurine. CONCLUSIONS Leonurine can be effectively activated through CYP2A13 enzyme metabolism, and further inhibits activity of human lung epithelial cells (BEAS-2B). Therefore, CYP2A13 is a main metabolic enzyme for leonurine in BEAS-2B cells.

Indexed as

Aryl Hydrocarbon HydroxylasesBronchiCell LineEpithelial CellsGallic AcidHumansInactivation, MetabolicAryl Hydrocarbon HydroxylasesCYP2A13 protein, humanGallic Acidleonurine

Identifiers

PMID32284524
PMCPMC7174896
OpenAlexW3006772712

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.