Compararive osmotic fragility of erythrocyte genotypes (HBAA, HBAS and HBSS) of male subjects administered antimalarial drugs

PAUL CHIDOKA CHIKEZIE, A. Uwakwe, C. Monago
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Abstract

In vivo study was carried out to ascertain the mean corpuscular fragility (MCF) index and corresponding stability of three erythrocyte genotypes (HbAA, HbAS and HbSS) in male volunteers, before (control; t=0 hour) and after (tests; i.e. at t=3, 6 and 18 hours) of administration of five (5) antimalarial drugs (FansidarTM, HalfanTM, quinine, CoartemTM, and chloroquine phosphate). Clinically confirmed healthy non-malarious and malarious male subjects/volunteers enrolled for this study. Erythrocytes obtained from these individuals were suspended in two separate sets of phosphate buffer saline (PBS) solutions of decreasing concentrations in the following order: 0.9, 0.7, 0.6, 0.4, 0.3 and 0.2 g/100 ml. Spectrophotometric method was used to determine the level of erythrocyte osmotic fragility. The mean (± S.D) MCF values of the three genotypes were in the order: HbAA there was no significant difference (p>0.05) between the MCF values of HbAA and HbAS erythrocytes. Comparatively, parasitized erythrocytes exhibited significantly (p redox equilibrium of the red cells are agents of membrane  destabilization.
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服用抗疟药物的男性受试者红细胞基因型(HBAA、HBAS和HBSS)的渗透脆弱性比较
通过体内研究,确定男性志愿者三种红细胞基因型(HbAA、HbAS和HbSS)在对照前的平均红细胞脆性(MCF)指数和相应的稳定性;T =0小时)和之后(试验;即在t= 3,6和18小时)服用五(5)种抗疟药物(FansidarTM、HalfanTM、奎宁、CoartemTM和磷酸氯喹)。临床确认的健康非疟疾和疟疾男性受试者/志愿者参加了这项研究。将这些人的红细胞分别悬浮在两组浓度递减的磷酸缓冲盐水(PBS)溶液中,浓度依次为:0.9、0.7、0.6、0.4、0.3和0.2 g/100 ml。用分光光度法测定红细胞渗透脆性水平。三种基因型的平均(±S.D) MCF值依次为:HbAA。HbAA与HbAS红细胞的MCF值无显著差异(p < 0.05)。相比之下,寄生红细胞表现出明显的氧化还原平衡,红细胞是膜不稳定的因素。
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