Dipartimento di Malattie Infettive, Istituto Superiore di Sanità, Viale Regina Elena n. 299, 00161, Rome, Italy.
Department of Vector Biology, Max-Planck Institute for Infection Biology, Charitéplatz 1, 10117, Berlin, Germany.
Malar J. 2017 Sep 12;16(1):366. doi: 10.1186/s12936-017-2013-7.
Although malaria is a preventable and curable human disease, millions of people risk to be infected by the Plasmodium parasites and to develop this illness. Therefore, there is an urgent need to identify new anti-malarial drugs. Ca signalling regulates different processes in the life cycle of Plasmodium falciparum, representing a suitable target for the development of new drugs.
This study investigated for the first time the effect of a highly specific inhibitor of nicotinic acid adenine dinucleotide phosphate (NAADP)-induced Ca release (Ned-19) on P. falciparum, revealing the inhibitory effect of this compound on the blood stage development of this parasite. Ned-19 inhibits both the transition of the parasite from the early to the late trophozoite stage and the ability of the late trophozoite to develop to the multinucleated schizont stage. In addition, Ned-19 affects spontaneous intracellular Ca oscillations in ring and trophozoite stage parasites, suggesting that the observed inhibitory effects may be associated to regulation of intracellular Ca levels.
This study highlights the inhibitory effect of Ned-19 on progression of the asexual life cycle of P. falciparum. The observation that Ned-19 inhibits spontaneous Ca oscillations suggests a potential role of NAADP in regulating Ca signalling of P. falciparum.
尽管疟疾是一种可预防和可治愈的人类疾病,但仍有数百万人面临感染疟原虫并罹患该病的风险。因此,迫切需要寻找新的抗疟药物。钙信号转导调控疟原虫生命周期中的不同过程,是开发新药的合适靶点。
本研究首次调查了烟酰胺腺嘌呤二核苷酸磷酸(NAADP)诱导钙释放的高度特异性抑制剂 Ned-19 对恶性疟原虫的作用,揭示了该化合物对疟原虫红内期发育的抑制作用。Ned-19 抑制寄生虫从早期滋养体向晚期滋养体的转变,以及晚期滋养体向多核裂殖体的发育能力。此外,Ned-19 影响环和滋养体阶段寄生虫的自发细胞内钙振荡,表明观察到的抑制作用可能与细胞内钙水平的调节有关。
本研究强调了 Ned-19 对恶性疟原虫无性生殖周期进展的抑制作用。Ned-19 抑制自发钙振荡的观察结果表明 NAADP 在调节恶性疟原虫钙信号转导中可能具有重要作用。