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Glutathione S-transferase
activity of erythrocyte genotypes HbAA, HbAS and HbSS in
male volunteers administered with fansidar and quinine
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
18 May, 2009 |
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In vivo
investigations were carried out to ascertain the comparative
levels of erythrocyte GST activity between non-malarious and
malarious male subjects of HbAA, HbAS and HbSS erythrocyte
genotypes, administered with fansidar and quinine. The
incubation of human erythrocytes with
1-chloro-2,4-dinitrobenzene (CDNB) resulted in almost
quantitative conjugation of glutathione (GSH) to form
S-(2,4-dinitrophenyl) glutathione. Determination of GST
activity was carried out at 0, 3, 6 and 18 h, after two
antimalarial drugs (Fansidar and
quinine) were
adminis-tered to the volunteers. The control
values of non-malarious and malarious individuals
ranged between (3.27 to 12.50 iu/gHb) and (2.75
to 12.21 -iu/gHb) respectively. Erythrocyte GST
activity was significantly (p < 0.05) lower in P.
falciparum infected red cells compared to normal ones,
except parasitized male HbSS erythrocytes. Generally, the
pattern of in vivo erythrocyte GST activity in the
presence of the 2 antimalarial drugs showed 2 phase profile.
The first stage showed decreasing levels of relative GST
activity within approximate time range of 6 h after the
drugs were administered to the volunteers. The second phase
showed recovery of erythrocyte GST activity
(6 - 18 h approx.)
from the inhibitory effects of the drugs.
Key words:
Glutathione S-transferase (GST) activity, erythrocytes,
fansidar, quinine,
1-chloro-2, 4-dinitrobenzene (CDNB). |