Ergothioneine Prevents Neuronal Cell Death Caused by the Neurotoxin 6-Hydroxydopamine

Author:

Yuzawa Saho1,Nakashio Motonari1,Ichimura Suzuna1,Shimoda Mikako1,Nakashima Ayaka2,Marukawa-Hashimoto Yuka2,Kawano Yusuke2,Suzuki Kengo2,Yoshitomi Kenichi3,Kawahara Masahiro1ORCID,Tanaka Ken-ichiro1ORCID

Affiliation:

1. Laboratory of Bio-Analytical Chemistry, Research Institute of Pharmaceutical Sciences, Faculty of Pharmacy, Musashino University, 1-1-20 Shinmachi, Nishitokyo, Tokyo 202-8585, Japan

2. Euglena, Co., Ltd., 5-29-11 G-BASE Tamachi 2nd Floor Shiba, Minato-ku, Tokyo 108-0014, Japan

3. Sakichi, Co., Ltd., 5-531 Kuromaru-Machi, Omura, Nagasaki 856-0808, Japan

Abstract

Neuronal cell death is a key mechanism involved in the development and exacerbation of Parkinson’s disease (PD). The excessive production of reactive oxygen species (ROS) is a major cause leading to neuronal death; therefore, compounds that prevent oxidative stress-dependent neuronal death may be promising as a preventive method for PD. Ergothioneine is a natural amino acid with antioxidant properties, and its protective functions in the body are attracting attention. However, there has been no investigation into the protective functions of ergothioneine using in vivo and in vitro PD models. Thus, in this study, we analyzed the efficacy of ergothioneine against 6-hydroxydopamine (6-OHDA)-dependent neuronal cell death using immortalized hypothalamic neurons (GT1-7 cells). First, we found that ergothioneine prevents 6-OHDA-dependent neuronal cell death by suppressing ROS overproduction in GT1-7 cells. The cytoprotective effect of ergothioneine was partially abolished by verapamil, an inhibitor of OCTN1, which is involved in ergothioneine uptake. Furthermore, ergothioneine-rich Rice-koji (Ergo-koji) showed cytoprotective and antioxidant effects similar to those of ergothioneine. Taken together, these results suggest that ergothioneine or foods containing ergothioneine may be an effective method for preventing the development and progression of PD.

Funder

Euglena, Co., Ltd.

Japan Society for the Promotion of Science

Publisher

MDPI AG

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