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 in | Bioscience, biotechnology, and biochemistry Vol. 80; no. 2; pp. 313 - 317 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
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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. |
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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 – sequence: 2 givenname: Xiaohong surname: Wu fullname: Wu, Xiaohong organization: HealthCare Systems Co., Ltd – sequence: 3 givenname: Hiroshi surname: Shimoda fullname: Shimoda, Hiroshi organization: Oryza Oil & Fat Chemical Co., Ltd – sequence: 4 givenname: Shinsuke surname: Hisaka fullname: Hisaka, Shinsuke organization: Faculty of Pharmacy, Department of Pharmacy, Meijo University – sequence: 5 givenname: Etsuko surname: Harada fullname: Harada, Etsuko organization: Iwade Research Institute of Mycology – sequence: 6 givenname: Tomomi surname: Kanno fullname: Kanno, Tomomi organization: Hokkaido University of Education – sequence: 7 givenname: Yoshimasa surname: Nakamura fullname: Nakamura, Yoshimasa email: yossan@cc.okayama-u.ac.jp organization: Graduate School of Environmental and Life Science, Okayama University – sequence: 8 givenname: Yoji surname: Kato fullname: Kato, Yoji organization: School of Human Science and Environment, University of Hyogo – sequence: 9 givenname: Toshihiko surname: Osawa fullname: Osawa, Toshihiko organization: Faculty of Psychological and Physical Science, Aichi Gakuin University |
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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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