Pabón Adriana, Deharo Eric, Zuluaga Lina, Maya Juan D, Saez Jairo, Blair Silvia
Grupo Malaria, Universidad de Antioquia, Medellín, Colombia.
Exp Parasitol. 2009 Aug;122(4):273-9. doi: 10.1016/j.exppara.2009.04.014. Epub 2009 May 12.
We studied the effects on total thiols glutathione (GSH) and cysteine contents in Plasmodium falciparum in vitro when treated with four steroid derivatives and a sapogenin (Diosgenone) extracted from Solanum nudum. We also determined their capacity to inhibit beta-hematin formation. We showed that SN-1 (16alpha-acetoxy-26-hydroxycholest-4-ene-3,22-dione) increased total glutathione and cysteine concentrations while SN-4 (26-O-beta-d-glucopyranosyloxy-16alpha-acetoxycholest-4-ene-3,22-dione) decreased the concentration of both thiols. Acetylation in C16 was crucial for the effect of SN-1 while type furostanol and terminal glucosidation were necessary for the inhibitory properties of SN-4. The combination of steroids and buthionine sulfoximine, a specific inhibitor of a step-limiting enzyme in GSH synthesis, did not modify the glutathione contents. Finally, we found that SN-1 inhibited more than 80% of beta-hematin formation at 5.0mM, while the other steroids did not show any effect.
我们研究了四种甾体衍生物和从野茄中提取的一种皂苷元(薯蓣皂苷元)在体外处理恶性疟原虫时,对其总硫醇(谷胱甘肽,GSH)和半胱氨酸含量的影响。我们还测定了它们抑制β-血红素形成的能力。我们发现,SN-1(16α-乙酰氧基-26-羟基胆甾-4-烯-3,22-二酮)可提高总谷胱甘肽和半胱氨酸浓度,而SN-4(26-O-β-D-吡喃葡萄糖氧基-16α-乙酰氧基胆甾-4-烯-3,22-二酮)则降低了两种硫醇的浓度。C16位的乙酰化对于SN-1的作用至关重要,而呋甾烷醇型和末端糖基化对于SN-4的抑制特性是必需的。甾体与丁硫氨酸亚砜胺(一种谷胱甘肽合成中限速酶的特异性抑制剂)的组合并未改变谷胱甘肽含量。最后,我们发现SN-1在5.0 mM时可抑制超过80%的β-血红素形成,而其他甾体则未显示出任何作用。