A mushroom-derived amino acid, ergothioneine, is a potential inhibitor of inflammation-related DNA halogenation

Myeloperoxidase (MPO)-generated halogenating molecules, such as hypochlorous acid and hypobromous acid (HOBr), in inflammatory regions are postulated to contribute to disease progression. In this study, we showed that ergothioneine (EGT), derived from an edible mushroom, inhibited MPO activity as we...

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Published inBioscience, biotechnology, and biochemistry Vol. 80; no. 2; pp. 313 - 317
Main Authors Asahi, Takashi, Wu, Xiaohong, Shimoda, Hiroshi, Hisaka, Shinsuke, Harada, Etsuko, Kanno, Tomomi, Nakamura, Yoshimasa, Kato, Yoji, Osawa, Toshihiko
Format Journal Article
LanguageEnglish
Published England Taylor & Francis 01.02.2016
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Abstract Myeloperoxidase (MPO)-generated halogenating molecules, such as hypochlorous acid and hypobromous acid (HOBr), in inflammatory regions are postulated to contribute to disease progression. In this study, we showed that ergothioneine (EGT), derived from an edible mushroom, inhibited MPO activity as well as the formation of 8-bromo-2′-deoxyguanosine in vitro. The HOBr scavenging effect of EGT is higher than those of ascorbic acid and glutathione. We initially observed that the administration of Coprinus comatus, an edible mushroom containing a high amount of EGT, inhibited the UV-B-induced inflammatory responses and DNA halogenation, suggesting that EGT is a promising anti-inflammatory agent from mushrooms. The ergothioneine-rich Coprinus extract inhibited both MPO activity and HOBr-induced DNA damage in addition to inhibition of UV-B-induced inflammatory responses.
AbstractList Myeloperoxidase (MPO)-generated halogenating molecules, such as hypochlorous acid and hypobromous acid (HOBr), in inflammatory regions are postulated to contribute to disease progression. In this study, we showed that ergothioneine (EGT), derived from an edible mushroom, inhibited MPO activity as well as the formation of 8-bromo-2′-deoxyguanosine in vitro. The HOBr scavenging effect of EGT is higher than those of ascorbic acid and glutathione. We initially observed that the administration of Coprinus comatus, an edible mushroom containing a high amount of EGT, inhibited the UV-B-induced inflammatory responses and DNA halogenation, suggesting that EGT is a promising anti-inflammatory agent from mushrooms. The ergothioneine-rich Coprinus extract inhibited both MPO activity and HOBr-induced DNA damage in addition to inhibition of UV-B-induced inflammatory responses.
Myeloperoxidase (MPO)-generated halogenating molecules, such as hypochlorous acid and hypobromous acid (HOBr), in inflammatory regions are postulated to contribute to disease progression. In this study, we showed that ergothioneine (EGT), derived from an edible mushroom, inhibited MPO activity as well as the formation of 8-bromo-2'-deoxyguanosine in vitro. The HOBr scavenging effect of EGT is higher than those of ascorbic acid and glutathione. We initially observed that the administration of Coprinus comatus, an edible mushroom containing a high amount of EGT, inhibited the UV-B-induced inflammatory responses and DNA halogenation, suggesting that EGT is a promising anti-inflammatory agent from mushrooms.
Author Asahi, Takashi
Hisaka, Shinsuke
Kanno, Tomomi
Osawa, Toshihiko
Harada, Etsuko
Wu, Xiaohong
Kato, Yoji
Nakamura, Yoshimasa
Shimoda, Hiroshi
Author_xml – sequence: 1
  givenname: Takashi
  surname: Asahi
  fullname: Asahi, Takashi
  organization: Graduate School of Bioagricultural Sciences, Nagoya University
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  givenname: Xiaohong
  surname: Wu
  fullname: Wu, Xiaohong
  organization: HealthCare Systems Co., Ltd
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  givenname: Hiroshi
  surname: Shimoda
  fullname: Shimoda, Hiroshi
  organization: Oryza Oil & Fat Chemical Co., Ltd
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  givenname: Shinsuke
  surname: Hisaka
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  organization: Faculty of Pharmacy, Department of Pharmacy, Meijo University
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  surname: Harada
  fullname: Harada, Etsuko
  organization: Iwade Research Institute of Mycology
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  surname: Kanno
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  organization: Hokkaido University of Education
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  organization: Graduate School of Environmental and Life Science, Okayama University
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  surname: Kato
  fullname: Kato, Yoji
  organization: School of Human Science and Environment, University of Hyogo
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  givenname: Toshihiko
  surname: Osawa
  fullname: Osawa, Toshihiko
  organization: Faculty of Psychological and Physical Science, Aichi Gakuin University
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Keywords ergothioneine
hypobromous acid
myeloperoxidase
mushroom
anti-inflammatory agent
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Snippet Myeloperoxidase (MPO)-generated halogenating molecules, such as hypochlorous acid and hypobromous acid (HOBr), in inflammatory regions are postulated to...
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SubjectTerms Agaricales - chemistry
amino acids
Animals
anti-inflammatory agent
anti-inflammatory agents
Anti-Inflammatory Agents - isolation & purification
Anti-Inflammatory Agents - pharmacology
ascorbic acid
Ascorbic Acid - pharmacology
biotechnology
Bromates - antagonists & inhibitors
Bromates - metabolism
Coprinus comatus
Deoxyguanosine - analogs & derivatives
Deoxyguanosine - antagonists & inhibitors
Deoxyguanosine - biosynthesis
disease progression
DNA
DNA - antagonists & inhibitors
DNA - metabolism
ergothioneine
Ergothioneine - isolation & purification
Ergothioneine - pharmacology
glutathione
Glutathione - pharmacology
Halogenation - drug effects
hypobromous acid
Hypochlorous Acid - antagonists & inhibitors
Hypochlorous Acid - metabolism
Inflammation - drug therapy
Inflammation - etiology
Inflammation - metabolism
Inflammation - pathology
Male
Mice
Mice, Hairless
mushroom
mushrooms
myeloperoxidase
Peroxidase - antagonists & inhibitors
Peroxidase - metabolism
Ultraviolet Rays - adverse effects
Title A mushroom-derived amino acid, ergothioneine, is a potential inhibitor of inflammation-related DNA halogenation
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