Discovery of pulmonary fibrosis inhibitor targeting TGF-β RI in Polygonum cuspidatum by high resolution mass spectrometry with in silico strategy

Pulmonary fibrosis (PF) is an irreversible lung disease that is characterized by excessive scar tissue with a poor median survival rate of 2-3 years. The inhibition of transforming growth factor-β receptor type-I (TGF-β RI) by an appropriate drug may provide a promising strategy for the treatment of...

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Main Authors: Huarong Xu (Author), Jiameng Qu (Author), Jian Wang (Author), Kefei Han (Author), Qing Li (Author), Wenchuan Bi (Author), Ran Liu (Author)
Format: Book
Published: Elsevier, 2022-12-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Huarong Xu  |e author 
700 1 0 |a Jiameng Qu  |e author 
700 1 0 |a Jian Wang  |e author 
700 1 0 |a Kefei Han  |e author 
700 1 0 |a Qing Li  |e author 
700 1 0 |a Wenchuan Bi  |e author 
700 1 0 |a Ran Liu  |e author 
245 0 0 |a Discovery of pulmonary fibrosis inhibitor targeting TGF-β RI in Polygonum cuspidatum by high resolution mass spectrometry with in silico strategy 
260 |b Elsevier,   |c 2022-12-01T00:00:00Z. 
500 |a 2095-1779 
500 |a 10.1016/j.jpha.2020.05.007 
520 |a Pulmonary fibrosis (PF) is an irreversible lung disease that is characterized by excessive scar tissue with a poor median survival rate of 2-3 years. The inhibition of transforming growth factor-β receptor type-I (TGF-β RI) by an appropriate drug may provide a promising strategy for the treatment of this disease. Polygonum cuspidatum (PC) is a well-known traditional Chinese herbal medicine which has an anti-PF effect. Accordingly, a combination of high resolution mass spectrometry with an in silico strategy was developed as a new method to search for potential chemical ingredients of PC that target the TGF-β RI. Based on this strategy, a total of 24 ingredients were identified. Then, absorption, distribution, metabolism, and excretion (ADME)-related properties were subsequently predicted to exclude compounds with potentially undesirable pharmacokinetics behaviour. Molecular docking studies on TGF-β RI were adopted to discover new PF inhibitors. Eventually, a compound that exists in PC known as resveratrol was proven to have excellent biological activity on TGF-β RI, with an IC50 of 2.211 μM in vitro. Furthermore, the complex formed through molecular docking was tested via molecular dynamics simulations, which revealed that resveratrol had strong interactions with residues of TGF-β RI. This study revealed that resveratrol has significant potential as a treatment for PF due to its ability to target TGF-β RI. In addition, this research demonstrated the exploration of natural products with excellent biological activities toward specific targets via high resolution mass spectrometry in combination with in silico technology is a promising strategy for the discovery of novel drugs. 
546 |a EN 
690 |a Polygonum cuspidatum 
690 |a Pulmonary fibrosis 
690 |a TGF-β receptor type-I 
690 |a Resveratrol 
690 |a High resolution mass spectrometry 
690 |a Molecular docking 
690 |a Therapeutics. Pharmacology 
690 |a RM1-950 
655 7 |a article  |2 local 
786 0 |n Journal of Pharmaceutical Analysis, Vol 12, Iss 6, Pp 860-868 (2022) 
787 0 |n http://www.sciencedirect.com/science/article/pii/S2095177919308998 
787 0 |n https://doaj.org/toc/2095-1779 
856 4 1 |u https://doaj.org/article/bcbe2e9d8f5b4984937e1c538df6ea9d  |z Connect to this object online.