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Comparative
osmotic fragility of three erythrocyte genotypes (HbAA, HbAS
and HbSS) of male participants administered with five antimalarial
drugs
P. C. Chikezie1, A. A.
Uwakwe2 and C.C. Monago2
1Department
of Biochemistry, Imo State University, Owerri, Imo State,
Nigeria.
2Department
of Biochemistry, University of Port-Harcourt, Port-Harcourt,
Rivers State, Nigeria.
*Corresponding author. E-mail:
p_chikezie@yahoo.com. Tel: +23408038935327.
Accepted 10 September, 2009 |
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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) before (control;
t = 0 h) and after (tests; that is, at t = 3, 6 and 18 h)
five (5) antimalarial drugs (FansidarTM, HalfanTM,
Quinine, CoartemTM, and Chloroquine phosphate)
were administered to male participants. Clinically confirmed
healthy non-malarious and malarious male participants
enrolled for this study. Erythrocytes obtained from these
individuals were suspended in two separate sets of Phosphate
Buffer Saline (PBS) solution 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<HbAS<HbSS irrespective of the malarial status of
participants. However, there was no significant difference (p
> 0.05) between the MCF values of HbAA and HbAS
erythrocytes. Comparatively, parasitized erythrocytes
exhibited significantly (p < 0.05) increased MCF
values. The five antimalarial drugs were agents of
erythrocyte destabilization in both categories of
participants. However, the overall capacities of the drugs
to perturb erythrocyte stability diminished as the
experimental time progressed.
Key words: Antimalarials, erythrocytes, mean corpuscular fragility,
genotypes, osmotic fragility. |