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Journal of Applied Biomedicine

The Journal of University of South Bohemia

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Antiparasitic effects of Zingiber officinale (Ginger) extract against Toxoplasma gondii

1 / Jiang Meihua1 / Chu Jongphil1

1Department of Medical Zoology, Kyung Hee University School of Medicine, 1 Hoegi-dong, Dongdaemun-gu, Seoul 130-701, Republic of Korea; +82-2-961-0278; +82-10-2071-5679; +82-2-967-8401

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Citation Information: Journal of Applied Biomedicine. Volume 11, Issue 1, Pages 15–26, ISSN (Online) 1214-0287, ISSN (Print) 1214-021X, DOI: 10.2478/v10136-012-0014-y, January 2013

Publication History

Published Online:
2013-01-17

Summary

Zingiber officinale Roscoe, Ginger, has been used in folk medicine as a medicinal plant, as well as a spice and food in many countries. This research was carried out to evaluate the antiparasitic effect of ginger root extract (GE) and GE/F1 (fraction 1 obtained from GE) against Toxoplasma gondii (T. gondii) in vitro and invivo. The effects of GE and GE/F1 against the proliferation of T. gondii-infected C6 cells and T. gondii were evaluated by several indicators such as an MTT assay, nuclear staining, immunofluorescence staining, apoptotic proteins and animal testing. GE/F1 strongly inhibited the proliferation of T. gondii-infected C6 cells and T. gondii in a dose-dependent manner compared with sulfadiazine. After T. gondii invasion, C6 cells induced the activation of caspase-3, bax, p53 and p21 related to programmed cell death, and GE/F1 effectively suppressed the expression of caspase-3, bax, p53 and p21 causing cell death of the infected host cells. In addition, INF-γ, and IL-8 levels, and the viability of T. gondii-infected mice treated with GE/F1 (500 μg/ml) were not changed or increased during the period of the experiment. These results demonstrate that GE/F1 not only induces anti-T. gondii effects causing the inactivation of apoptotic proteins in infected host cells through the direct inhibition of T. gondii but also has antiparasitic properties which inhibit inflammatory cytokine secretion in vivo.

: Keywords apoptotic protein; C6 glioma cells; cytokine; p53; programmed cell death

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