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Exploring Anti-Nonalcoholic Fatty Liver Disease Mechanism of Gardeniae Fructus by Network Pharmacology, Molecular Docking, and Experiment Validation
[Image: see text] Gardeniae fructus (GF), the fruit from Gardenia jasminoides Ellis, is a traditional Chinese medicine used for the treatment of nonalcoholic fatty liver disease (NAFLD) in the clinic. To explore the hepatoprotective mechanism of GF for the treatment of NAFLD, we proposed a novel str...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9330257/ https://www.ncbi.nlm.nih.gov/pubmed/35910181 http://dx.doi.org/10.1021/acsomega.2c02629 |
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author | Tang, Zhongyan Li, Lin Xia, Zhengxiang |
author_facet | Tang, Zhongyan Li, Lin Xia, Zhengxiang |
author_sort | Tang, Zhongyan |
collection | PubMed |
description | [Image: see text] Gardeniae fructus (GF), the fruit from Gardenia jasminoides Ellis, is a traditional Chinese medicine used for the treatment of nonalcoholic fatty liver disease (NAFLD) in the clinic. To explore the hepatoprotective mechanism of GF for the treatment of NAFLD, we proposed a novel strategy that integrated in vivo efficacy evaluation, network pharmacology analysis, molecular docking, and experimental validation. A NAFLD animal model induced by high fat diet (HFD) feed was established, then orally administrated with or without GF. The results showed that GF significantly decreased the levels of serum total cholesterol (TC), lipoprotein cholesterol, triglyceride (TG), alanine aminotransferase, aspartate aminotransferase, lactate dehydrogenase, free fatty acids, glucose, and insulin and the levels of liver TG, TC, and malondialdehyde compared with the nontreated HFD group. Network pharmacology studies showed that quercetin, oleanolic acid, kaempferol, and geniposide were the main biocompounds in GF that targeted the PPARα and PPARγ genes through regulating the PPAR and AMPK signal pathways to protect against NAFLD. The interactions between bioactive compounds and their corresponding target proteins were analyzed by molecular docking and subsequently confirmed using the qRT-PCR assay. Collectively, GF was a therapeutic drug for the treatment of NAFLD. |
format | Online Article Text |
id | pubmed-9330257 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-93302572022-07-29 Exploring Anti-Nonalcoholic Fatty Liver Disease Mechanism of Gardeniae Fructus by Network Pharmacology, Molecular Docking, and Experiment Validation Tang, Zhongyan Li, Lin Xia, Zhengxiang ACS Omega [Image: see text] Gardeniae fructus (GF), the fruit from Gardenia jasminoides Ellis, is a traditional Chinese medicine used for the treatment of nonalcoholic fatty liver disease (NAFLD) in the clinic. To explore the hepatoprotective mechanism of GF for the treatment of NAFLD, we proposed a novel strategy that integrated in vivo efficacy evaluation, network pharmacology analysis, molecular docking, and experimental validation. A NAFLD animal model induced by high fat diet (HFD) feed was established, then orally administrated with or without GF. The results showed that GF significantly decreased the levels of serum total cholesterol (TC), lipoprotein cholesterol, triglyceride (TG), alanine aminotransferase, aspartate aminotransferase, lactate dehydrogenase, free fatty acids, glucose, and insulin and the levels of liver TG, TC, and malondialdehyde compared with the nontreated HFD group. Network pharmacology studies showed that quercetin, oleanolic acid, kaempferol, and geniposide were the main biocompounds in GF that targeted the PPARα and PPARγ genes through regulating the PPAR and AMPK signal pathways to protect against NAFLD. The interactions between bioactive compounds and their corresponding target proteins were analyzed by molecular docking and subsequently confirmed using the qRT-PCR assay. Collectively, GF was a therapeutic drug for the treatment of NAFLD. American Chemical Society 2022-07-12 /pmc/articles/PMC9330257/ /pubmed/35910181 http://dx.doi.org/10.1021/acsomega.2c02629 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Tang, Zhongyan Li, Lin Xia, Zhengxiang Exploring Anti-Nonalcoholic Fatty Liver Disease Mechanism of Gardeniae Fructus by Network Pharmacology, Molecular Docking, and Experiment Validation |
title | Exploring Anti-Nonalcoholic
Fatty Liver Disease Mechanism
of Gardeniae Fructus by Network Pharmacology, Molecular Docking, and
Experiment Validation |
title_full | Exploring Anti-Nonalcoholic
Fatty Liver Disease Mechanism
of Gardeniae Fructus by Network Pharmacology, Molecular Docking, and
Experiment Validation |
title_fullStr | Exploring Anti-Nonalcoholic
Fatty Liver Disease Mechanism
of Gardeniae Fructus by Network Pharmacology, Molecular Docking, and
Experiment Validation |
title_full_unstemmed | Exploring Anti-Nonalcoholic
Fatty Liver Disease Mechanism
of Gardeniae Fructus by Network Pharmacology, Molecular Docking, and
Experiment Validation |
title_short | Exploring Anti-Nonalcoholic
Fatty Liver Disease Mechanism
of Gardeniae Fructus by Network Pharmacology, Molecular Docking, and
Experiment Validation |
title_sort | exploring anti-nonalcoholic
fatty liver disease mechanism
of gardeniae fructus by network pharmacology, molecular docking, and
experiment validation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9330257/ https://www.ncbi.nlm.nih.gov/pubmed/35910181 http://dx.doi.org/10.1021/acsomega.2c02629 |
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