New series of imidazoles showed promising growth inhibitory and curative potential against trypanosoma infection

Oluyomi Stephen Adeyemi, Nthatisi Innocentia Molefe-Nyembe, Abiodun Omokehinde Eseola, Winfried Plass, Oluwatosin Kudirat Shittu, Ibrahim Olatunji Yunusa, Olubunmi Atolani, Ikponmwosa Owen Evbuomwan, Oluwakemi J. Awakan, Keisuke Suganuma, Kentaro Kato

研究成果: Article査読

抄録

The Trypanosoma spp. cause animal and human trypanosomiasis characterized with appreciable health and economic burden mostly in developing nations. There is currently no effective therapy for this parasitic disease, due to poor drug efficacy, drug resistance, and unwanted toxicity, etc. Therefore, new anti-Trypanosoma agents are urgently needed. This study explored new series of imidazoles for antiTrypanosoma properties in vitro and in vivo. The imidazoles showed moderate to strong and specific action against growth of T. congolense. For example, the efficacy of the imidazole compounds to restrict Trypanosoma growth in vitro was ≥ 12-fold specific towards T. congolense relative to the mammalian cells. Additionally, the in vivo study revealed that the imidazoles exhibited promising anti-Trypanosoma efficacy corroborating the in vitro anti-parasite capacity. In particular, three imidazole compounds (C1, C6, and C8) not only cleared the systemic parasite burden but cured infected rats after no death was recorded. On the other hand, the remaining five imidazole compounds (C2, C3, C4, C5, and C7) drastically reduced the systemic parasite load while extending survival time of the infected rats by 14 days as compared with control. Untreated control died 3 days post-infection, while the rats treated with diminazene aceturate were cured comparable to the results obtained for C1, C6, and C8. In conclusion, this is the first study demonstrating the potential of these new series of imidazoles to clear the systemic parasite burden in infected rats. Furthermore, a high selectivity index of imidazoles towards T. congolense in vitro and the oral LD50 in rats support anti-parasite specific action. Together, findings support the anti-parasitic prospects of the new series of imidazole derivatives.

本文言語English
ページ(範囲)199-207
ページ数9
ジャーナルYale Journal of Biology and Medicine
94
2
出版ステータスPublished - 2021 6

ASJC Scopus subject areas

  • 生化学、遺伝学、分子生物学(全般)

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