The Mechanisms of the Herbal Components of CRSAS on HK-2 Cells in a Hypoxia/Reoxygenation Model Based on Network Pharmacology

Background. Acute kidney injury is a global problem, which brings a great burden to the society and family. The component of rhubarb, Salvia miltiorrhiza, Astragalus membranaceus, and safflower (CRSAS) has been proved as an useful agent to treat acute kidney injury (AKI) patients in China. Objective...

Full description

Bibliographic Details
Main Authors: Naijing Ye, Dengpiao Xie, Bing Yang, Mingquan Li
Format: Article
Language:English
Published: Hindawi Limited 2020-01-01
Series:Evidence-Based Complementary and Alternative Medicine
Online Access:http://dx.doi.org/10.1155/2020/5352490
id doaj-102a2d176c7346da8c9a9ff734f8e106
record_format Article
spelling doaj-102a2d176c7346da8c9a9ff734f8e1062020-11-25T03:02:56ZengHindawi LimitedEvidence-Based Complementary and Alternative Medicine1741-427X1741-42882020-01-01202010.1155/2020/53524905352490The Mechanisms of the Herbal Components of CRSAS on HK-2 Cells in a Hypoxia/Reoxygenation Model Based on Network PharmacologyNaijing Ye0Dengpiao Xie1Bing Yang2Mingquan Li3Hospital of Chengdu University of Traditional Chinese Medicine, Chengdu, Sichuan, ChinaHospital of Chengdu University of Traditional Chinese Medicine, Chengdu, Sichuan, ChinaSichuan 2nd Hospital of Traditional Chinese Medicine, Chengdu, Sichuan, ChinaHospital of Chengdu University of Traditional Chinese Medicine, Chengdu, Sichuan, ChinaBackground. Acute kidney injury is a global problem, which brings a great burden to the society and family. The component of rhubarb, Salvia miltiorrhiza, Astragalus membranaceus, and safflower (CRSAS) has been proved as an useful agent to treat acute kidney injury (AKI) patients in China. Objective. To assess the effect of CRSAS on human renal tubular epithelial cells (HK-2) after the hypoxia/reoxygenation (H/R) and investigate the potential mechanisms. Methods. Network pharmacology was used to predict the potential pathways shared by CRSAS and AKI. Cell counting kit-8 (CCK-8) was used to assess the HK-2 vitality. Apoptosis of HK-2 cells was detected by carboxyfluorescein succinimidyl ester/propidium iodide (CFSF/PI) staining. Expression of GRP78, CHOP, caspase-3, and Bax was detected by western blot and quantitative real-time RT-PCR. Result. CRSAS and AKI shared the endoplasmic reticulum stress (ERS) pathway based on network pharmacology analysis. CRSAS increases the vitality of HK-2 cells and reduces the apoptosis of HK-2 cells induced by H/R injury. The expression of GRP78 and CHOP in CRSAS groups was lower than that of control groups. Conclusions. H/R can induce HK-2 cell apoptosis and ERS. CRSAS can reduce HK-2 cell apoptosis by inhibiting the ERS. Therefore, CRSAS might be able to treat kidney disease due to I/R injury. Animal experiment should be done to further prove our finding.http://dx.doi.org/10.1155/2020/5352490
collection DOAJ
language English
format Article
sources DOAJ
author Naijing Ye
Dengpiao Xie
Bing Yang
Mingquan Li
spellingShingle Naijing Ye
Dengpiao Xie
Bing Yang
Mingquan Li
The Mechanisms of the Herbal Components of CRSAS on HK-2 Cells in a Hypoxia/Reoxygenation Model Based on Network Pharmacology
Evidence-Based Complementary and Alternative Medicine
author_facet Naijing Ye
Dengpiao Xie
Bing Yang
Mingquan Li
author_sort Naijing Ye
title The Mechanisms of the Herbal Components of CRSAS on HK-2 Cells in a Hypoxia/Reoxygenation Model Based on Network Pharmacology
title_short The Mechanisms of the Herbal Components of CRSAS on HK-2 Cells in a Hypoxia/Reoxygenation Model Based on Network Pharmacology
title_full The Mechanisms of the Herbal Components of CRSAS on HK-2 Cells in a Hypoxia/Reoxygenation Model Based on Network Pharmacology
title_fullStr The Mechanisms of the Herbal Components of CRSAS on HK-2 Cells in a Hypoxia/Reoxygenation Model Based on Network Pharmacology
title_full_unstemmed The Mechanisms of the Herbal Components of CRSAS on HK-2 Cells in a Hypoxia/Reoxygenation Model Based on Network Pharmacology
title_sort mechanisms of the herbal components of crsas on hk-2 cells in a hypoxia/reoxygenation model based on network pharmacology
publisher Hindawi Limited
series Evidence-Based Complementary and Alternative Medicine
issn 1741-427X
1741-4288
publishDate 2020-01-01
description Background. Acute kidney injury is a global problem, which brings a great burden to the society and family. The component of rhubarb, Salvia miltiorrhiza, Astragalus membranaceus, and safflower (CRSAS) has been proved as an useful agent to treat acute kidney injury (AKI) patients in China. Objective. To assess the effect of CRSAS on human renal tubular epithelial cells (HK-2) after the hypoxia/reoxygenation (H/R) and investigate the potential mechanisms. Methods. Network pharmacology was used to predict the potential pathways shared by CRSAS and AKI. Cell counting kit-8 (CCK-8) was used to assess the HK-2 vitality. Apoptosis of HK-2 cells was detected by carboxyfluorescein succinimidyl ester/propidium iodide (CFSF/PI) staining. Expression of GRP78, CHOP, caspase-3, and Bax was detected by western blot and quantitative real-time RT-PCR. Result. CRSAS and AKI shared the endoplasmic reticulum stress (ERS) pathway based on network pharmacology analysis. CRSAS increases the vitality of HK-2 cells and reduces the apoptosis of HK-2 cells induced by H/R injury. The expression of GRP78 and CHOP in CRSAS groups was lower than that of control groups. Conclusions. H/R can induce HK-2 cell apoptosis and ERS. CRSAS can reduce HK-2 cell apoptosis by inhibiting the ERS. Therefore, CRSAS might be able to treat kidney disease due to I/R injury. Animal experiment should be done to further prove our finding.
url http://dx.doi.org/10.1155/2020/5352490
work_keys_str_mv AT naijingye themechanismsoftheherbalcomponentsofcrsasonhk2cellsinahypoxiareoxygenationmodelbasedonnetworkpharmacology
AT dengpiaoxie themechanismsoftheherbalcomponentsofcrsasonhk2cellsinahypoxiareoxygenationmodelbasedonnetworkpharmacology
AT bingyang themechanismsoftheherbalcomponentsofcrsasonhk2cellsinahypoxiareoxygenationmodelbasedonnetworkpharmacology
AT mingquanli themechanismsoftheherbalcomponentsofcrsasonhk2cellsinahypoxiareoxygenationmodelbasedonnetworkpharmacology
AT naijingye mechanismsoftheherbalcomponentsofcrsasonhk2cellsinahypoxiareoxygenationmodelbasedonnetworkpharmacology
AT dengpiaoxie mechanismsoftheherbalcomponentsofcrsasonhk2cellsinahypoxiareoxygenationmodelbasedonnetworkpharmacology
AT bingyang mechanismsoftheherbalcomponentsofcrsasonhk2cellsinahypoxiareoxygenationmodelbasedonnetworkpharmacology
AT mingquanli mechanismsoftheherbalcomponentsofcrsasonhk2cellsinahypoxiareoxygenationmodelbasedonnetworkpharmacology
_version_ 1715319069020782592