Evidence map›Paper›PMID 36080202›Full record

ArticleMolecules (Basel, Switzerland)2022

Bioinformatics-Guided Identification of Ethyl Acetate Extract of Citri Reticulatae Pericarpium as a Functional Food Ingredient with Anti-Inflammatory Potential.

Enyao Ma, Lu Jin, Chunguo Qian, Chong Feng, Zhimin Zhao, Hongru Tian, Depo Yang

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.0field-weighted citation impact, top 27% 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

7 citing papers in PubMed, 11 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 1 institution in 1 country.

Enyao MaGuangdong Hanchao Traditional Chinese Medicine Technology Co., Ltd., Guangzhou 510163, China.
Lu JinSchool of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou 510006, China.
Chunguo QianSchool of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou 510006, China.
Chong FengGuangzhou Caizhilin Pharmaceutical Co., Ltd., Guangzhou 510360, China.
Zhimin ZhaoSchool of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou 510006, China.ORCID 0000-0002-3384-2365
Hongru TianSchool of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou 510006, China.
Depo YangSchool of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou 510006, China.
Sun Yat-sen University · CN

Funding

Guangdong Science and Technology Department 2020B020221002Guangdong Science and Technology Department 2021KJ142Guangdong Science and Technology Department 2021KJ268Ministry of Science and Technology of the People´s Republic of China 2017YFC1701100
6 · The paper itself

Abstract

Citri Reticulatae Pericarpium (CRP) is one of the most commonly used food supplements and folk medicines worldwide, and possesses cardiovascular, digestive, and respiratory protective effects partially through its antioxidant and anti-inflammatory functions. The unique aromatic flavor and mild side effects make CRP a promising candidate for the development of anti-inflammatory functional food. However, recent studies show that the crude alcoholic extract and some isolated compounds of CRP show compromised anti-inflammatory activity, which became the main factor hindering its further development. To identify the bioactive compounds with anti-inflammatory potential, and improve the anti-inflammatory effects of the extract, a bioinformatics-guided extraction protocol was employed in this study. The potential bioactive candidates were identified by combing network pharmacology analysis, molecular docking, principal components analysis, k-means clustering, and in vitro testing of reference compounds. Our results demonstrated that 66 compounds in CRP could be grouped into four clusters according to their docking score profile against 24 receptors, while the cluster containing flavonoids and phenols might possess a more promising anti-inflammatory function. In addition, in vitro anti-inflammatory tests of the seven reference compounds demonstrated that hesperitin, naringenin, and gardenin B, which were grouped into a cluster containing flavonoids and phenols, significantly decreased LPS-induced NO, TNF-α, and IL-6 production of macrophages. While the compounds outside of that cluster, such as neohesperidin, naringin, hesperidin, and sinensetin showed little effect on alleviating LPS-induced NO and proinflammatory cytokine production. Based on the chemical properties of selected compounds, ethyl acetate (EtOAc) was selected as the solvent for extraction, because of its promising solubility of flavonoids and phenols. Furthermore, the ethanol alcoholic extract was used as a reference. The chemical profiling of EtOAc and crude alcoholic extract by HPLC/MS/MS also demonstrated the decreased abundance of flavonoid glycosides in EtOAc extract but increased abundance of phenols, phenolic acid, and aglycones. In accordance with the prediction, the EtOAc extract of CRP, but not the crude alcoholic extract, significantly decreased the NO, IL-6, and TNF-α production. Taken together, the results suggested selective extraction of phenols and flavonoids rich extract was able to increase the anti-inflammatory potential of CRP partially because of the synergistic effects between flavonoids, phenols, and enriched polymethoxyflavones. Our study might pave the road for the development of ethyl acetate extract of CRP as a novel functional food with anti-inflammatory function.

Indexed as

CitrusFood IngredientsAcetatesAnti-Inflammatory AgentsComputational BiologyFlavonoidsFunctional FoodInterleukin-6LipopolysaccharidesMolecular Docking SimulationPhenolsPlant ExtractsTandem Mass SpectrometryTumor Necrosis Factor-alphaAcetatesAnti-Inflammatory Agentsethyl acetateFlavonoidsFood IngredientsInterleukin-6LipopolysaccharidesPhenolsPlant ExtractsTumor Necrosis Factor-alphaanti-inflammatory functional foodCitri Reticulatae PericarpiumHPLC/MS/MS-based chemical profilingmolecular dockingnetwork pharmacology analysis

Identifiers

PMID36080202
PMCPMC9457579
OpenAlexW4293217968

What OpenQuestion holds

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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.