Niu Guodong, Kalani Komal, Wang Xiaohong, Li Jun
Department of Biological Sciences, Florida International University, Miami, FL 33199, USA.
Biomolecular Sciences Institute, Florida International University, Miami, FL 33199, USA.
Pharmaceuticals (Basel). 2021 Nov 29;14(12):1238. doi: 10.3390/ph14121238.
As part of our drug discovery program against malaria, the extract was discovered to inhibit proliferation in blood and transmission to mosquitoes. Bioactivity-guided fractionation of extraction was carried out using chromatographic techniques. We determined the activities of fractions against asexual stage parasite proliferation in culture and sexual stage parasite transmission to mosquitoes using standard membrane feeding assays (SMFA). One active compound was isolated. Based on mass spectrometry and nuclear magnetic resonance profiles, the compound was structurally determined to be sterigmatocystin. Sterigmatocystin inhibited proliferation in the blood with an IC of 34 µM and limited the sexual parasites to infect mosquitoes with an IC of 48 µM. Meanwhile, sterigmatocystin did not show any acute toxicity to human kidney cells at a concentration of 64 µM or lower. Sterigmatocystin can be used as a drug lead for malaria control and as a probe to understand molecular mechanisms of malaria transmission.
作为我们抗疟疾药物研发计划的一部分,发现该提取物可抑制血液中的增殖以及向蚊子的传播。使用色谱技术对提取物进行生物活性导向分级分离。我们使用标准膜饲法(SMFA)测定了各馏分对培养物中无性阶段寄生虫增殖和有性阶段寄生虫向蚊子传播的活性。分离出一种活性化合物。根据质谱和核磁共振谱图,确定该化合物结构为柄曲霉素。柄曲霉素抑制血液中增殖的IC50为34 μM,并以48 μM的IC50限制有性寄生虫感染蚊子。同时,柄曲霉素在浓度为64 μM或更低时对人肾细胞未显示任何急性毒性。柄曲霉素可作为控制疟疾的药物先导物以及了解疟疾传播分子机制的探针。