Evidence map›Paper›PMID 31683684›Full record

ArticleMolecules (Basel, Switzerland)2019

Protective Effect and Mechanism of Boswellic Acid and Myrrha Sesquiterpenes with Different Proportions of Compatibility on Neuroinflammation by LPS-Induced BV2 Cells Combined with Network Pharmacology.

Xiao-Dong Miao, Li-Jie Zheng, Zi-Zhang Zhao, Shu-Lan Su, Yue Zhu, Jian-Ming Guo, Er-Xin Shang, Da-Wei Qian, Jin-Ao Duan

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

12 citing papers in PubMed, 32 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 2 institutions in 1 country.

Xiao-Dong MiaoJiangsu Key Laboratory for High Technology Research of TCM Formulae; Jiangsu Collaborative Innovation Center of Chinese Medicinal Resources Industrialization; National and Local Collaborative Engineering Center of Chinese Medicinal Resources Industrialization and Formulae Innovative Medicine, Nanjing University of Chinese Medicine, Nanjing 210023, China. miaoxiaodong94111@163.com.
Li-Jie ZhengJiangsu Key Laboratory of Research and Development in Marine Bio-resource Pharmaceutics, Nanjing University of Chinese Medicine, Nanjing 210023, China. 18851003108@163.com.
Zi-Zhang ZhaoJiangsu Key Laboratory for High Technology Research of TCM Formulae; Jiangsu Collaborative Innovation Center of Chinese Medicinal Resources Industrialization; National and Local Collaborative Engineering Center of Chinese Medicinal Resources Industrialization and Formulae Innovative Medicine, Nanjing University of Chinese Medicine, Nanjing 210023, China. 20181402@njucm.edu.cn.
Shu-Lan SuJiangsu Key Laboratory for High Technology Research of TCM Formulae; Jiangsu Collaborative Innovation Center of Chinese Medicinal Resources Industrialization; National and Local Collaborative Engineering Center of Chinese Medicinal Resources Industrialization and Formulae Innovative Medicine, Nanjing University of Chinese Medicine, Nanjing 210023, China. sushulan1974@163.com.
Yue ZhuJiangsu Key Laboratory for High Technology Research of TCM Formulae; Jiangsu Collaborative Innovation Center of Chinese Medicinal Resources Industrialization; National and Local Collaborative Engineering Center of Chinese Medicinal Resources Industrialization and Formulae Innovative Medicine, Nanjing University of Chinese Medicine, Nanjing 210023, China. zhuyue@njucm.edu.cn.
Jian-Ming GuoJiangsu Key Laboratory for High Technology Research of TCM Formulae; Jiangsu Collaborative Innovation Center of Chinese Medicinal Resources Industrialization; National and Local Collaborative Engineering Center of Chinese Medicinal Resources Industrialization and Formulae Innovative Medicine, Nanjing University of Chinese Medicine, Nanjing 210023, China. njuguo@njucm.edu.cn.
Er-Xin ShangJiangsu Key Laboratory for High Technology Research of TCM Formulae; Jiangsu Collaborative Innovation Center of Chinese Medicinal Resources Industrialization; National and Local Collaborative Engineering Center of Chinese Medicinal Resources Industrialization and Formulae Innovative Medicine, Nanjing University of Chinese Medicine, Nanjing 210023, China. shex@njucm.edu.cn.
Da-Wei QianJiangsu Key Laboratory for High Technology Research of TCM Formulae; Jiangsu Collaborative Innovation Center of Chinese Medicinal Resources Industrialization; National and Local Collaborative Engineering Center of Chinese Medicinal Resources Industrialization and Formulae Innovative Medicine, Nanjing University of Chinese Medicine, Nanjing 210023, China. qiandwnj@126.com.
Jin-Ao DuanJiangsu Key Laboratory for High Technology Research of TCM Formulae; Jiangsu Collaborative Innovation Center of Chinese Medicinal Resources Industrialization; National and Local Collaborative Engineering Center of Chinese Medicinal Resources Industrialization and Formulae Innovative Medicine, Nanjing University of Chinese Medicine, Nanjing 210023, China. duanja@163.com.
Center for High Pressure Science & Technology Advanced Research · CNNanjing University of Chinese Medicine · CN

Funding

Jiangsu Key Laboratory for High Technology Research of TCM Formulae Project No. FJGJS-2015-12
6 · The paper itself

Abstract

Frankincense and myrrha (FM), commonly used as a classical herbal pair, have a wide range of clinical applications and definite anti-inflammatory activity. However, anti-neuroinflammation effects and mechanisms are not clear. In this study, we adopted a lipopolysaccharide (LPS)-induced microglial (BV2) cell model and a network pharmacology method to reveal the anti-neuroinflammatory effects and mechanisms of boswellic acid (BA) and myrrha sesquiterpenes (MS) with different proportions of compatibility. The data showed that the different ratios of BA and MS had different degrees of inhibition of interleukin-1β (IL-1β), IL-6, and inducible nitric oxide synthase (iNOS) mRNA expression, down-regulated the phosphor-nuclear factor kappa B/nuclear factor kappa B (p-NF-ҡB)/(NF-ҡB), phosphorylated protein kinase b/protein kinase b (p-AKT/AKT), and Toll-like receptor 4 (TLR4) protein expression levels, and increased phospho-PI3 kinase (p-PI3K) protein expression levels. When the ratios of BA and MS were 10:1, 5:1, and 20:1, better effective efficacy was exhibited. According to the correlation analysis between the effect index and bioactive substances, it was suggested that 2-methoxy-5-acetoxy -fruranogermacr-1(10)-en-6-one (Compound 1), 3

Indexed as

AnimalsCell LineCell ShapeCell SurvivalCommiphoraGene Expression RegulationGene OntologyInflammationInterleukin-1betaInterleukin-6LipopolysaccharidesMiceMicrogliaNeuroprotective AgentsNF-kappa BNitric Oxide Synthase Type IIboswellic acidInterleukin-1betaInterleukin-6LipopolysaccharidesNeuroprotective AgentsNF-kappa BNitric Oxide Synthase Type IIProto-Oncogene Proteins c-aktRNA, MessengerSesquiterpenesToll-Like Receptor 4Triterpenesboswellic acidBV2 cellsdifferent proportions compatibilityfrankincensemyrrhamyrrha sesquiterpenesnetwork pharmacologyneuroinflammation

Identifiers

PMID31683684
PMCPMC6864549
OpenAlexW2982573488

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.