Network Pharmacology-Based Analysis of Pogostemon cablin (Blanco) Benth Beneficial Effects to Alleviate Nonalcoholic Fatty Liver Disease in Mice

Nonalcoholic fatty liver disease (NAFLD) is the most common cause of chronic liver disease and is associated with high morbidity and mortality. Pogostemon cablin (Blanco) Benth/Huo Xiang (HX) is a perennial herb with unique anti-oxidant and anti-inflammatory properties, and thus, can positively affe...

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Autores principales: Yizhe Cui, Qiuju Wang, Renxu Chang, Ahmad Aboragah, Juan J. Loor, Chuang Xu
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Publicado: Frontiers Media S.A. 2021
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spelling oai:doaj.org-article:6256fc54d82242abac7e8f9ae26e1dac2021-11-30T17:59:10ZNetwork Pharmacology-Based Analysis of Pogostemon cablin (Blanco) Benth Beneficial Effects to Alleviate Nonalcoholic Fatty Liver Disease in Mice1663-981210.3389/fphar.2021.789430https://doaj.org/article/6256fc54d82242abac7e8f9ae26e1dac2021-11-01T00:00:00Zhttps://www.frontiersin.org/articles/10.3389/fphar.2021.789430/fullhttps://doaj.org/toc/1663-9812Nonalcoholic fatty liver disease (NAFLD) is the most common cause of chronic liver disease and is associated with high morbidity and mortality. Pogostemon cablin (Blanco) Benth/Huo Xiang (HX) is a perennial herb with unique anti-oxidant and anti-inflammatory properties, and thus, can positively affect liver function. In this study, we used network pharmacology to predict the potential mechanism of HX on NAFLD. Pharmacological experiments were used to verify the effect of HX on the functions of NAFLD. Network pharmacology identified nine components that interacted with 82 NAFLD-related targets, revealing four target genes: TNF, IL6, TP53, and AKT1. HX prevents the development and progression of NAFLD through different pathways and targets with quercetin-regulated lipid metabolism, anti-inflammatory, and anti-oxidant pathways playing an essential role in the treatment of NAFLD. Compared with feeding HFD, HX significantly attenuated lipid accumulation in vivo with mice and also in vitro with mouse liver cells. A high dose of HX decreased hepatocyte lipid accumulation and the abundance of SREBF1 and FASN. Validation experiments revealed that HX inhibited the activation of NF-κB/IκB signaling and decreased the release and levels of pro-inflammatory factors (TNF-α and IL-6). These data suggest that HX can attenuate abnormal lipid metabolic responses and enhance antioxidant mechanisms. Thus, the pharmacological effects from plants used in traditional Chinese medicine are achievde through a multi-level response.Yizhe CuiYizhe CuiQiuju WangRenxu ChangAhmad AboragahJuan J. LoorChuang XuChuang XuFrontiers Media S.A.articlenetwork pharmacologyPogostemon cablin (Blanco) BenthmiceAML12 cellsmulti-targetsNAFLDTherapeutics. PharmacologyRM1-950ENFrontiers in Pharmacology, Vol 12 (2021)
institution DOAJ
collection DOAJ
language EN
topic network pharmacology
Pogostemon cablin (Blanco) Benth
mice
AML12 cells
multi-targets
NAFLD
Therapeutics. Pharmacology
RM1-950
spellingShingle network pharmacology
Pogostemon cablin (Blanco) Benth
mice
AML12 cells
multi-targets
NAFLD
Therapeutics. Pharmacology
RM1-950
Yizhe Cui
Yizhe Cui
Qiuju Wang
Renxu Chang
Ahmad Aboragah
Juan J. Loor
Chuang Xu
Chuang Xu
Network Pharmacology-Based Analysis of Pogostemon cablin (Blanco) Benth Beneficial Effects to Alleviate Nonalcoholic Fatty Liver Disease in Mice
description Nonalcoholic fatty liver disease (NAFLD) is the most common cause of chronic liver disease and is associated with high morbidity and mortality. Pogostemon cablin (Blanco) Benth/Huo Xiang (HX) is a perennial herb with unique anti-oxidant and anti-inflammatory properties, and thus, can positively affect liver function. In this study, we used network pharmacology to predict the potential mechanism of HX on NAFLD. Pharmacological experiments were used to verify the effect of HX on the functions of NAFLD. Network pharmacology identified nine components that interacted with 82 NAFLD-related targets, revealing four target genes: TNF, IL6, TP53, and AKT1. HX prevents the development and progression of NAFLD through different pathways and targets with quercetin-regulated lipid metabolism, anti-inflammatory, and anti-oxidant pathways playing an essential role in the treatment of NAFLD. Compared with feeding HFD, HX significantly attenuated lipid accumulation in vivo with mice and also in vitro with mouse liver cells. A high dose of HX decreased hepatocyte lipid accumulation and the abundance of SREBF1 and FASN. Validation experiments revealed that HX inhibited the activation of NF-κB/IκB signaling and decreased the release and levels of pro-inflammatory factors (TNF-α and IL-6). These data suggest that HX can attenuate abnormal lipid metabolic responses and enhance antioxidant mechanisms. Thus, the pharmacological effects from plants used in traditional Chinese medicine are achievde through a multi-level response.
format article
author Yizhe Cui
Yizhe Cui
Qiuju Wang
Renxu Chang
Ahmad Aboragah
Juan J. Loor
Chuang Xu
Chuang Xu
author_facet Yizhe Cui
Yizhe Cui
Qiuju Wang
Renxu Chang
Ahmad Aboragah
Juan J. Loor
Chuang Xu
Chuang Xu
author_sort Yizhe Cui
title Network Pharmacology-Based Analysis of Pogostemon cablin (Blanco) Benth Beneficial Effects to Alleviate Nonalcoholic Fatty Liver Disease in Mice
title_short Network Pharmacology-Based Analysis of Pogostemon cablin (Blanco) Benth Beneficial Effects to Alleviate Nonalcoholic Fatty Liver Disease in Mice
title_full Network Pharmacology-Based Analysis of Pogostemon cablin (Blanco) Benth Beneficial Effects to Alleviate Nonalcoholic Fatty Liver Disease in Mice
title_fullStr Network Pharmacology-Based Analysis of Pogostemon cablin (Blanco) Benth Beneficial Effects to Alleviate Nonalcoholic Fatty Liver Disease in Mice
title_full_unstemmed Network Pharmacology-Based Analysis of Pogostemon cablin (Blanco) Benth Beneficial Effects to Alleviate Nonalcoholic Fatty Liver Disease in Mice
title_sort network pharmacology-based analysis of pogostemon cablin (blanco) benth beneficial effects to alleviate nonalcoholic fatty liver disease in mice
publisher Frontiers Media S.A.
publishDate 2021
url https://doaj.org/article/6256fc54d82242abac7e8f9ae26e1dac
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