Effect of α-tocopheryloxy acetic acid, a vitamin E derivative mitocan, on the experimental infection of mice with Plasmodium yoelii

Abstract Background Malaria parasites are known to be vulnerable to oxidative stress. In this study, the effects of the administration of α-tocopheryloxy acetic acid (α-TEA), which is a vitamin E analogue mitocan, on Plasmodium yoelii infection in mice were examined. Methods Alpha-TEA was mixed with...

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Published in:Malaria Journal
Main Authors: Kasumi Kawamura, Aiko Kume, Rika Umemiya-Shirafuji, Shunji Kasai, Hiroshi Suzuki
Format: Article in Journal/Newspaper
Language:English
Published: BMC 2021
Subjects:
Online Access:https://doi.org/10.1186/s12936-021-03817-9
https://doaj.org/article/3680af0046f4496f824c5cad9fcc45b6
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spelling ftdoajarticles:oai:doaj.org/article:3680af0046f4496f824c5cad9fcc45b6 2023-05-15T15:18:14+02:00 Effect of α-tocopheryloxy acetic acid, a vitamin E derivative mitocan, on the experimental infection of mice with Plasmodium yoelii Kasumi Kawamura Aiko Kume Rika Umemiya-Shirafuji Shunji Kasai Hiroshi Suzuki 2021-06-01T00:00:00Z https://doi.org/10.1186/s12936-021-03817-9 https://doaj.org/article/3680af0046f4496f824c5cad9fcc45b6 EN eng BMC https://doi.org/10.1186/s12936-021-03817-9 https://doaj.org/toc/1475-2875 doi:10.1186/s12936-021-03817-9 1475-2875 https://doaj.org/article/3680af0046f4496f824c5cad9fcc45b6 Malaria Journal, Vol 20, Iss 1, Pp 1-9 (2021) α-tocopheryloxy acetic acid Mice Plasmodium yoelii Reactive oxygen species Arctic medicine. Tropical medicine RC955-962 Infectious and parasitic diseases RC109-216 article 2021 ftdoajarticles https://doi.org/10.1186/s12936-021-03817-9 2022-12-31T11:25:25Z Abstract Background Malaria parasites are known to be vulnerable to oxidative stress. In this study, the effects of the administration of α-tocopheryloxy acetic acid (α-TEA), which is a vitamin E analogue mitocan, on Plasmodium yoelii infection in mice were examined. Methods Alpha-TEA was mixed with diet and fed to C57BL/6J mice before and/or after infection. For parasite infection, 4 × 104 red blood cells infected with P. yoelii (strain 17XL) were inoculated by intraperitoneal injection. In another series of experiment, the effect of the oral administration of α-TEA on P. yoelii 17XL infection in mice was examined. Finally, the combined effect of α-TEA and dihydroartemisinin or chloroquine on P. yoelii 17XL infection was examined. Results When 0.25% α-TEA was mixed with the diet for 7 days before infection and 14 days after infection (in total for 21 days), for 14 days after infection, and for 11 days from the third day after infection, all P. yoelii 17XL-infected mice survived during the observation period. However, all control mice died within 12 days after infection. These results indicated that α-TEA functions effectively even when administered post-infection. The oral administration of α-TEA for P. yoelii 17XL infection was also significant. Although the infected mice in the solvent control died within 10 days after infection, 90% of the mice infected with P. yoelii 17XL survived during the observation period when treated with 10 mg/head/day of α-TEA for 3 days from day 3 after infection. Although the combined effect of α-TEA and dihydroartemisinin (DHA) or chloroquine on P. yoelii 17XL infection was significant, no synergistic or additive effects were observed from the survival curve. Conclusions This study showed the beneficial effects of α-TEA on the experimental infection of mice with P. yoelii 17XL. The stimulatory action of α-TEA on mitochondria and the accompanying reactions, such as reactive oxygen species production, and induction of apoptosis might have some effect on malarial infection. Article in Journal/Newspaper Arctic Directory of Open Access Journals: DOAJ Articles Arctic Malaria Journal 20 1
institution Open Polar
collection Directory of Open Access Journals: DOAJ Articles
op_collection_id ftdoajarticles
language English
topic α-tocopheryloxy acetic acid
Mice
Plasmodium yoelii
Reactive oxygen species
Arctic medicine. Tropical medicine
RC955-962
Infectious and parasitic diseases
RC109-216
spellingShingle α-tocopheryloxy acetic acid
Mice
Plasmodium yoelii
Reactive oxygen species
Arctic medicine. Tropical medicine
RC955-962
Infectious and parasitic diseases
RC109-216
Kasumi Kawamura
Aiko Kume
Rika Umemiya-Shirafuji
Shunji Kasai
Hiroshi Suzuki
Effect of α-tocopheryloxy acetic acid, a vitamin E derivative mitocan, on the experimental infection of mice with Plasmodium yoelii
topic_facet α-tocopheryloxy acetic acid
Mice
Plasmodium yoelii
Reactive oxygen species
Arctic medicine. Tropical medicine
RC955-962
Infectious and parasitic diseases
RC109-216
description Abstract Background Malaria parasites are known to be vulnerable to oxidative stress. In this study, the effects of the administration of α-tocopheryloxy acetic acid (α-TEA), which is a vitamin E analogue mitocan, on Plasmodium yoelii infection in mice were examined. Methods Alpha-TEA was mixed with diet and fed to C57BL/6J mice before and/or after infection. For parasite infection, 4 × 104 red blood cells infected with P. yoelii (strain 17XL) were inoculated by intraperitoneal injection. In another series of experiment, the effect of the oral administration of α-TEA on P. yoelii 17XL infection in mice was examined. Finally, the combined effect of α-TEA and dihydroartemisinin or chloroquine on P. yoelii 17XL infection was examined. Results When 0.25% α-TEA was mixed with the diet for 7 days before infection and 14 days after infection (in total for 21 days), for 14 days after infection, and for 11 days from the third day after infection, all P. yoelii 17XL-infected mice survived during the observation period. However, all control mice died within 12 days after infection. These results indicated that α-TEA functions effectively even when administered post-infection. The oral administration of α-TEA for P. yoelii 17XL infection was also significant. Although the infected mice in the solvent control died within 10 days after infection, 90% of the mice infected with P. yoelii 17XL survived during the observation period when treated with 10 mg/head/day of α-TEA for 3 days from day 3 after infection. Although the combined effect of α-TEA and dihydroartemisinin (DHA) or chloroquine on P. yoelii 17XL infection was significant, no synergistic or additive effects were observed from the survival curve. Conclusions This study showed the beneficial effects of α-TEA on the experimental infection of mice with P. yoelii 17XL. The stimulatory action of α-TEA on mitochondria and the accompanying reactions, such as reactive oxygen species production, and induction of apoptosis might have some effect on malarial infection.
format Article in Journal/Newspaper
author Kasumi Kawamura
Aiko Kume
Rika Umemiya-Shirafuji
Shunji Kasai
Hiroshi Suzuki
author_facet Kasumi Kawamura
Aiko Kume
Rika Umemiya-Shirafuji
Shunji Kasai
Hiroshi Suzuki
author_sort Kasumi Kawamura
title Effect of α-tocopheryloxy acetic acid, a vitamin E derivative mitocan, on the experimental infection of mice with Plasmodium yoelii
title_short Effect of α-tocopheryloxy acetic acid, a vitamin E derivative mitocan, on the experimental infection of mice with Plasmodium yoelii
title_full Effect of α-tocopheryloxy acetic acid, a vitamin E derivative mitocan, on the experimental infection of mice with Plasmodium yoelii
title_fullStr Effect of α-tocopheryloxy acetic acid, a vitamin E derivative mitocan, on the experimental infection of mice with Plasmodium yoelii
title_full_unstemmed Effect of α-tocopheryloxy acetic acid, a vitamin E derivative mitocan, on the experimental infection of mice with Plasmodium yoelii
title_sort effect of α-tocopheryloxy acetic acid, a vitamin e derivative mitocan, on the experimental infection of mice with plasmodium yoelii
publisher BMC
publishDate 2021
url https://doi.org/10.1186/s12936-021-03817-9
https://doaj.org/article/3680af0046f4496f824c5cad9fcc45b6
geographic Arctic
geographic_facet Arctic
genre Arctic
genre_facet Arctic
op_source Malaria Journal, Vol 20, Iss 1, Pp 1-9 (2021)
op_relation https://doi.org/10.1186/s12936-021-03817-9
https://doaj.org/toc/1475-2875
doi:10.1186/s12936-021-03817-9
1475-2875
https://doaj.org/article/3680af0046f4496f824c5cad9fcc45b6
op_doi https://doi.org/10.1186/s12936-021-03817-9
container_title Malaria Journal
container_volume 20
container_issue 1
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