Antcins from Antrodia cinnamomea and Antrodia salmonea Inhibit Angiotensin-Converting Enzyme 2 (ACE2) in Epithelial Cells: Can Be Potential Candidates for the Development of SARS-CoV-2 Prophylactic Agents

Antcins are newly identified steroid-like compounds from Taiwan's endemic medicinal mushrooms and . Scientific studies of the past two decades confirmed that antcins have various pharmacological activities, including potent anti-oxidant and anti-inflammatory effects. The severe acute respirator...

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Published inPlants (Basel) Vol. 10; no. 8; p. 1736
Main Authors Senthil Kumar, K J, Gokila Vani, M, Hsieh, Han-Wen, Lin, Chin-Chung, Wang, Sheng-Yang
Format Journal Article
LanguageEnglish
Published Switzerland MDPI AG 23.08.2021
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Abstract Antcins are newly identified steroid-like compounds from Taiwan's endemic medicinal mushrooms and . Scientific studies of the past two decades confirmed that antcins have various pharmacological activities, including potent anti-oxidant and anti-inflammatory effects. The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) caused the coronavirus disease-2019 (COVID-19) pandemic and is characterized as a significant threat to global public health. It was recently identified that SARS-CoV-2 required angiotensin converting enzyme 2 (ACE2), a receptor which supports host cell entry and disease onset. Here, we report a novel function of antcins, in which antcins exhibit inhibitory effects on ACE2. Compared to the untreated control group, treatment with various antcins (antcin-A, antcin-B, antcin-C, antcin-H, antcin-I, and antcin-M) significantly inhibited ACE2 activity in cultured human epithelial cells. Indeed, among the investigated antcins, antcin-A, antcin-B, antcin-C, and antcin-I showed a pronounceable inhibition against ACE2. These findings suggest that antcins could be novel anti-ACE2 agents to prevent SARS-CoV-2 host cell entry and the following disease onset.
AbstractList Antcins are newly identified steroid-like compounds from Taiwan’s endemic medicinal mushrooms Antrodia cinnamomea and Antrodia salmonea. Scientific studies of the past two decades confirmed that antcins have various pharmacological activities, including potent anti-oxidant and anti-inflammatory effects. The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) caused the coronavirus disease-2019 (COVID-19) pandemic and is characterized as a significant threat to global public health. It was recently identified that SARS-CoV-2 required angiotensin converting enzyme 2 (ACE2), a receptor which supports host cell entry and disease onset. Here, we report a novel function of antcins, in which antcins exhibit inhibitory effects on ACE2. Compared to the untreated control group, treatment with various antcins (antcin-A, antcin-B, antcin-C, antcin-H, antcin-I, and antcin-M) significantly inhibited ACE2 activity in cultured human epithelial cells. Indeed, among the investigated antcins, antcin-A, antcin-B, antcin-C, and antcin-I showed a pronounceable inhibition against ACE2. These findings suggest that antcins could be novel anti-ACE2 agents to prevent SARS-CoV-2 host cell entry and the following disease onset.
Antcins are newly identified steroid-like compounds from Taiwan’s endemic medicinal mushrooms Antrodia cinnamomea and Antrodia salmonea . Scientific studies of the past two decades confirmed that antcins have various pharmacological activities, including potent anti-oxidant and anti-inflammatory effects. The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) caused the coronavirus disease-2019 (COVID-19) pandemic and is characterized as a significant threat to global public health. It was recently identified that SARS-CoV-2 required angiotensin converting enzyme 2 (ACE2), a receptor which supports host cell entry and disease onset. Here, we report a novel function of antcins, in which antcins exhibit inhibitory effects on ACE2. Compared to the untreated control group, treatment with various antcins (antcin-A, antcin-B, antcin-C, antcin-H, antcin-I, and antcin-M) significantly inhibited ACE2 activity in cultured human epithelial cells. Indeed, among the investigated antcins, antcin-A, antcin-B, antcin-C, and antcin-I showed a pronounceable inhibition against ACE2. These findings suggest that antcins could be novel anti-ACE2 agents to prevent SARS-CoV-2 host cell entry and the following disease onset.
Antcins are newly identified steroid-like compounds from Taiwan's endemic medicinal mushrooms and . Scientific studies of the past two decades confirmed that antcins have various pharmacological activities, including potent anti-oxidant and anti-inflammatory effects. The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) caused the coronavirus disease-2019 (COVID-19) pandemic and is characterized as a significant threat to global public health. It was recently identified that SARS-CoV-2 required angiotensin converting enzyme 2 (ACE2), a receptor which supports host cell entry and disease onset. Here, we report a novel function of antcins, in which antcins exhibit inhibitory effects on ACE2. Compared to the untreated control group, treatment with various antcins (antcin-A, antcin-B, antcin-C, antcin-H, antcin-I, and antcin-M) significantly inhibited ACE2 activity in cultured human epithelial cells. Indeed, among the investigated antcins, antcin-A, antcin-B, antcin-C, and antcin-I showed a pronounceable inhibition against ACE2. These findings suggest that antcins could be novel anti-ACE2 agents to prevent SARS-CoV-2 host cell entry and the following disease onset.
Author Gokila Vani, M
Lin, Chin-Chung
Wang, Sheng-Yang
Hsieh, Han-Wen
Senthil Kumar, K J
AuthorAffiliation 1 Bachelor Program of Biotechnology, National Chung Hsing University, Taichung 402, Taiwan; zenkumar@dragon.nchu.edu.tw
2 Department of Forestry, National Chung Hsing University, Taichung 402, Taiwan; mgvani2009@gmail.com
3 Taiwan Leader Biotech Company, Taipei 103, Taiwan; ck_hsieh@twleaderlife.com (H.-W.H.); johnson@twleaderlifw.com (C.-C.L.)
4 Agricultural Biotechnology Research Center, Academia Sinica, Taipei 11529, Taiwan
AuthorAffiliation_xml – name: 4 Agricultural Biotechnology Research Center, Academia Sinica, Taipei 11529, Taiwan
– name: 1 Bachelor Program of Biotechnology, National Chung Hsing University, Taichung 402, Taiwan; zenkumar@dragon.nchu.edu.tw
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– name: 2 Department of Forestry, National Chung Hsing University, Taichung 402, Taiwan; mgvani2009@gmail.com
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BackLink https://www.ncbi.nlm.nih.gov/pubmed/34451782$$D View this record in MEDLINE/PubMed
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Keywords COVID-19
ACE2
SARS-CoV-2
antcin
Antrodia cinnamomea
Antrodia salmonea
Language English
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Snippet Antcins are newly identified steroid-like compounds from Taiwan's endemic medicinal mushrooms and . Scientific studies of the past two decades confirmed that...
Antcins are newly identified steroid-like compounds from Taiwan’s endemic medicinal mushrooms Antrodia cinnamomea and Antrodia salmonea. Scientific studies of...
Antcins are newly identified steroid-like compounds from Taiwan's endemic medicinal mushrooms Antrodia cinnamomea and Antrodia salmonea. Scientific studies of...
Antcins are newly identified steroid-like compounds from Taiwan’s endemic medicinal mushrooms Antrodia cinnamomea and Antrodia salmonea . Scientific studies of...
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SubjectTerms ACE2
Angiotensin
Angiotensin-converting enzyme 2
antcin
Antioxidants
Antrodia cinnamomea
Antrodia salmonea
Brief Report
Colon
Conversion
Coronaviruses
COVID-19
COVID-19 vaccines
Cytotoxicity
Diabetes
Disease prevention
Disease transmission
Drug dosages
Enzymes
Epithelial cells
Epithelium
Glycoproteins
Infections
Inflammation
Investigations
Oxidants
Oxidizing agents
Pandemics
Peptidyl-dipeptidase A
Proteins
Public health
Respiratory diseases
RNA polymerase
SARS-CoV-2
Severe acute respiratory syndrome
Severe acute respiratory syndrome coronavirus 2
Steroids
Viral diseases
Viral infections
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Title Antcins from Antrodia cinnamomea and Antrodia salmonea Inhibit Angiotensin-Converting Enzyme 2 (ACE2) in Epithelial Cells: Can Be Potential Candidates for the Development of SARS-CoV-2 Prophylactic Agents
URI https://www.ncbi.nlm.nih.gov/pubmed/34451782
https://www.proquest.com/docview/2565518910/abstract/
https://search.proquest.com/docview/2566045661
https://pubmed.ncbi.nlm.nih.gov/PMC8399673
https://doaj.org/article/302ee522506449fc8fc773b5c2e78468
Volume 10
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