Comparative Study of Glutathione S-Transferase Activity of Three Human Erythrocyte Genotypes Infected With Plasmodium falciparum.
1Chikezie, P.C.; 1Chikezie, C.M; 2Uwakwe, A.A.; 2Monago, C.C.
1Department of Biochemistry, Imo State University, Owerri, Imo State, Nigeria.
Code Number: ja09032
Investigation to ascertain the levels of glutathione S-transferase (GST) activity of three human erythrocyte genotypes (HbAA, HbAS and HbSS) obtained from apparently healthy and clinically confirmed malarious subjects/volunteers was carried out. The incubation of human erythrocytes with 1-chloro-2,4dinitrobenzene (CDNB) resulted in almost quantitative conjugation of glutathione (GSH) to form S-(2,4dinitrophenyl) glutathione. The reaction formed the basis for the spectrophotometric determination of GST activity. The levels of GST activity of the red cell genotypes was in the order of HbAA
Four species of intracellular protozoa of the genus Plasmodium cause malaria. Plasmodium falciparum is the most dangerous and remains the world’s most common devastating human parasitic infection (AMR, 2003; Snow et al., 2005). This parasitic infection is affecting more than 500 million people and causing from 1.7 million to 2.5 million deaths each year of which children less than 5 years of age, pregnant women and non-immune individuals are preferentially affected (WHO, 1995). Human beings usually are affected by sporozoites by bite of infected female mosquitoes (genius Anopheles ); although malaria can be transmitted by transfusion of infected blood (Ali and Kadaru, 2005) and by sharing needles (Tracy and Webster, 2001). The parasites have a complicated life cycle that requires a vertebrate host for the asexual cycle and female Anopheles mosquitoes for completion of the sexual cycle. Marcus et al ., (1978), in their findings on the purification and characterization of glutathione-S transferase from human erythrocyte reported that the enzyme molecular weight of the enzyme is 47,500MW and is composed of two subunits. The enzyme was active with a variety of compound bearing an electrophilic centre. Although the physiological role of this enzyme is not fully known, it has been suggested that the location of the enzyme in erythrocytes is ideal for the removal of circulating xenobiotics (Marcus et al., 1978; Anosike et al ., 1991). Studies suggest that glutathione-S transferase occur in the erythrocytes primarily for the protection of erythrocytes against electrophilic compounds, rather than serving a general protective function in the body (Harvey and Beutler, 1982; Anosike et al. , 1991). Many studies of both humans and laboratory animals have documented strong associations between impaired or deficient GST activity and various diseases connected to oxidative stress injury. Such diseases include lung cancer, acute leukemia, and many others (Strange et al. , 1998; Ye and Song, 2005). Since malarial pathology progresses with increasing oxidative stress, the present study seeks to ascertain the influence of gender of human population on GST activity in malaria pathology. In addition, the study will investigate the influence of P. falciparum on metabolism of human three red blood cell genotypes (HbAA, HbAS and HbSS) with respect to levels of glutathione-S transferase activity. The findings may serve to provide reliable biochemical parameter for diagnosis in relation to the pathophysiology of malaria disease.
MATERIALS AND METHODS
Selection of Volunteers/ Experimental Design: Non-Malarious Subjects/Volunteers (Control Group): Seventy (70) male (61-73kg) subjects/volunteers of confirmed HbAA (25), HbAS (25) and HbSS (20) genotypes between the ages of 20-28years enrolled for this study. The female category was made up of forty-two (42) subjects/volunteers (55-69kg); HbAA (20), HbAS (20) and HbSS (12). Their age bracket was between 18-27years.
Malarious Subjects/Volunteers (Test Group): Sixty-one (61) male (59-79kg) subjects/volunteers – HbAA (24), HbAS (25) and HbSS (12) and fortythree (43) female (55-76kg) subjects/volunteers, HbAA (15), HbAS (15) and HbSS (13) enrolled for this study. The male and female subjects were between the age brackets of 21-34 and 20-25 years respectively.
Ethics: The institutional review board of the Department of Biochemistry, University of Port Harcourt, Port Harcourt, Nigeria, granted approval for this study and all subjects/ volunteers involved signed an informed consent form. This conducted study was in accordance with the ethical principles that have their origins in the Declaration of Helsinki. Individuals drawn were from Imo State University, Owerri, Nigeria and environs. The research protocols were in collaboration with registered and specialized clinics and medical laboratories.
Collection of Blood Samples/Preparation of Erythrocyte Haemolysate: Five milliliters (5.0ml) of venous blood obtained from the volunteers by venipuncture was stored in EDTA anticoagulant tubes. Blood of HbSS genotype and malarious blood samples were from patients attending clinics at the Federal Medical Center (FMC), Imo State University Teaching Hospital (IMSUTH), Orlu, St.John Clinic / Medical Diagnostic Laboratories, Avigram Medical Diagnostic Laboratories, and Qualitech Medical Diagnostic Laboratories. These centers are located in Owerri, Imo State, Nigeria. The erythrocytes were washed by methods as described by Tsakiris et al.,(2005). Within 2hours of collection of blood samples, portions of 1.0ml of the samples were introduced into centrifuge test tubes containing 3.0ml of buffer solution pH=7.4: 250mM tris (hydroxyl methyl) amino ethane–HCl(Tris-HCl)/140mMNaCl/I.0mMMgCl2/10mMglucose). The erythrocytes were separated from plasma by centrifugation at 1200g for 10minutes, washed three times by three similar centrifugations with the buffer solution. The erythrocytes re-suspended in 1.0ml of this buffer were stored at 40C. The washed erythrocytes were lysed by freezing/thawing as described by Galbraith and Watts, (1980) and Kamber et al., (1984). The erythrocyte haemolysate was used for the determination of GST activity.
Determination of Erythrocytes Haemolysate Haemoglobin Concentration: A modified method (Baure, 1980), based on cyanomethaemoglobin reaction was used for the determination of haemolysate haemoglobin concentration. The expressed values were in grams per deciliter (g/dl). A 0.05ml portion of human red blood cell haemolysate was added to 4.95ml of Drabkin reagent. The mixture was left to stand for 10minutes and absorbance read at λmax =540nm against a blank (Drabkin reagent only). The absorbance was used to evaluate for haemolysate haemoglobin concentration by comparing the values with the standards.
Determination of Erythrocyte Haemolysate Glutathione S-transferase Activity: GST activity was assayed spectrophotometrically by monitoring the conjugation of 1-chloro-2,4dinitro benzene (CDNB) with glutathione (GSH) at λmax=340nm at 37oC. (Habig et al., 1974).
CDNB + GSH → CDNB – S – glutathione. The enzyme assay was according to methods of Habig et al., (1974) with minor modifications (Anosike et al.,1991).The 1.0ml in 2% ethanol enzyme assay mixture contained 0.5mMCDNB (0.02ml),1.0mMGSH(0.05ml),0.68ml of distilled water and 100mMPhosphate buffer (K2HPO4/KH2PO4; pH=6.5) (0.2ml). The CDNB was pre mixed with the Phosphate buffer before use. The Phosphate buffer-CDNB mixture was pre-incubated for 10 minutes at 37oC and the reaction started by adding GSH, followed immediately by an aliquot (0.05ml) of the haemolysate. The rate of increase in absorbance at λmax = 340nm was measured for 10minutes at 37oC against a blank solution containing the reaction mixture, in which; the haemolysate was substituted with distilled water.
Statistical Analyses: The experiments were designed in a completely randomized method and data collected were analyzed by the analysis of variance procedure while treatment means were separated by the Least Significance Difference (LSD) incorporated in the Statistical Analysis System (SAS) package of 9.1 version.(2006).
Calculation of Enzyme Activity: The expression below was used to evaluate erythrocyte GST activity in international unit per gram haemoglobin (iu/gHb).
EMBED IMAGE HERE
EA = Enzyme activity in iu/gHb [Hb] = Haemolysate haemoglobin concentration (g/dl)
RESULTS AND DISCUSSION
The mean (+S.D) activity of glutathione S-transferase (GST) of three erythrocyte genotypes (HbAA, HbAS and HbSS) of blood samples obtained from nonmalarious and malarious human subjects/volunteers is presented in Table 1 below.
The mean (+S.D) activity of glutathione S-transferase (GST) in the three genotypes was in the order: HbAA
Previous investigations by Sarini et al., (1993), reported that increased parasitaemia accompanied decrease in the activities of enzymes of the glutathione system, namely glutathione peroxidase (GPx), glutathione reductase (GRx) and glutathione S-transferase (GST) in the red blood cells (RBC) lysates. In the present study, GST activity was significantly (p<0.05) decreased in P. falciparum infected erythrocytes, compared to red cells obtained from apparently healthy non-malarious individuals (Table 1). This observation was in concordance with the reports of Sohail et al., (2007). In their views, decreasing GST activity might play important role in host defense mechanisms against malarial infection by up-regulating oxidative defense mechanisms. They further suggested that GST activity evaluation might be a reliable biochemical marker and possess promising rational for diagnostic and therapeutic potential in malaria. In the same vein, previous reports have shown that antioxidants such as glutathione (GSH), catalase and α-tocopherol were lower in patients with malaria (Becker et al., 2004; Kavishe et al., 2006) and visceral Leishmaniasis (Neupane et al., 2008) than the control groups. Therefore, inoculation of the malarial parasites usually accompanies production of reactive oxygen species (ROS) such as superoxide anions, hydrogen peroxide, hydroxyl radicals and nitric oxide as a host defense mechanism (Becker et al., 2004). The accumulated ROS because of decreased antioxidant scavenging activities engenders vast membrane lipid peroxidation with concomitant membrane damage and oxidation of haemoglobin to methaemoglobin (Nuepane et al., 2008). Since there was no significant difference (p>0.05) in erythrocyte GST activity between non-malarious and malarious male subjects/volunteers of HbSS genotype (Table 1), it is probable the host erythrocytes did not deploy oxidative up-regulatory mechanism as a means for parasitic control and elimination. The available high oxidative potentials of these erythrocytes as earlier reported by Anosike et al., (1991) must have fulfilled the antifecundity property of this erythrocyte genotype.
Another plausible reason for decreased GST activity of erythrocytes obtained from malarious human subjects; hinged on the pathophysiology of malaria disease have been described (Dubios et al., 1995, Liebau et al., 2002). Consequent upon ingestion and digestion of large quantities of erythrocyte haemoglobin by the parasite, it subsequently has to handle and deal with high amount of potentially parasitotoxic ferroprotoporhyrin IX (FPIX) - haemin. As mentioned earlier, P. falciparum GST (pfGST) are able to bind efficiently to FPIX (Harwaldt et al., 2002). The uncompetitive interaction inhibits GST activity preferentially by binding to preformed GST-GSH complex (Hiller et al., 2006). The significantly higher erythrocyte GST activity of malarious female erythrocytes (HbAA, HbAS and HbSS) compared to malarious male red cells (Table 1) seem to suggest the influence of sex hormones on in vivo enzyme activity. Reports indicate that mammalian GSTs are involved in intracellular transport of varieties of endogenous metabolites including sex hormones by their ability to bind to these compounds (Abramovitz et al., 2006; Listowsky et al., 1998). This interaction often impairs the catalytic activity of the enzyme (Salinas and Wong 1999: Sheeham et al., 2001: Deponte and Becker, 2005). For instance, it has been demonstrated that testosterone and progesterone have varied capacities to bind to mammalian GSTs with moderate (10-6 < Kd <10-4 M) or high (Kd < 10-6 M) affinity respectively (Listowsky et al., 1998). Previous studies have also showed specific binding of testosterone to parasitic Schistosoma haematobium GST protein (Sh28GST) exhibited high affinity (Kd =2.57 x 10-7 M) (Remoue et al., 2002). This mechanism was closely associated with the reduction of Schistosoma fecundity in male individuals. Therefore, in human schistosomiasis, this GSTdependent effect of sexual steroids could have an influence on the age- and sex-dependent level of infection. Indeed, observations showed genderdependent pattern of prevalence and intensity of infection after puberty for several parasitic species (Bundy, 1988). Since variability in erythrocyte GST activity of malarious human subjects/volunteers was gender dependent, the findings of the present study suggest sex hormones might have contributed to the significant difference (p<0.05) in GST activity between the two sexes infected with P. falciparum . Therefore, gender-dependent level of malarial infection showed similar patterns as described in human infection of Schistosoma haematobium. On the contrary, with respect to HbAA and HbAS erythrocytes of non-malarious individuals, there was no significant difference (p<0.05) between levels of male and female GST activity. In agreement with this observation, Zhang et al., (2006) and Anosike et al., (1991) stated that gender did not significantly influence GST activity of apparently healthy Chinese and Nigerian subjects respectively. Comparative studies of human erythrocyte GST showed a variable activity in the order HbAA
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