Up- and down-modulation of liver cytochrome P450 activities and associated events in two murine malaria models
© De-Oliveira et al; licensee BioMed Central Ltd. 2010
Received: 29 December 2009
Accepted: 22 March 2010
Published: 22 March 2010
The mechanisms by which malaria up and down-regulates CYP activities are not understood yet. It is also unclear whether CYP activities are modulated during non-lethal malaria infections. This study was undertaken to evaluate the time course of CYP alterations in lethal (Plasmodium berghei ANKA) and non-lethal (Plasmodium chabaudi chabaudi) murine malaria. Additionally, hypotheses on the association of CYP depression with enhanced nitric oxide (NO) production, and of CYP2a5 induction with endoplasmic reticulum dysfunction, enhanced haem metabolism and oxidative stress were examined as well.
Female DBA-2 and C57BL/6 mice were infected with P.berghei ANKA or P. chabaudi and killed at different post-infection days. Infection was monitored by parasitaemia rates and clinical signs. NO levels were measured in the serum. Activities of CYP1a (ethoxyresorufin-O-deethylase), 2b (benzyloxyresorufin-O-debenzylase), 2a5 (coumarin-7-hydroxylase) and uridine-diphosphoglucuronyl-transferase (UGT) were determined in liver microsomes. Glutathione-S-transferase (GST) activity and concentrations of gluthatione (GSH) and thiobarbituric acid-reactive substances (TBARS) were determined in the liver. Levels of glucose-regulated protein 78 (GRP78) were evaluated by immunoblotting, while mRNAs of haemoxygenase-1 (HO-1) and inducible nitric oxide synthase (iNOS) were determined by quantitative RT-PCR.
Plasmodium berghei depressed CYP1a and 2b and induced 2a5 in DBA-2 mice. In P.berghei-infected C57BL/6 mice CYP activities remained unaltered. In both strains, GST and UGT were not affected by P.berghei. Plasmodium c. chabaudi depressed CYP1a and 2b and induced 2a5 activities on the day of peak parasitaemia or near this day. CYP2a5 induction was associated with over-expression of HO-1 and enhanced oxidative stress, but it was not associated with GRP78 induction, a marker of endoplasmic reticulum stress. Plasmodium chabaudi increased serum NO on days near the parasitaemia peak in both strains. Although not elevating serum NO, P.berghei enhanced iNOS mRNA expression in the liver.
Down-regulation of CYP1a and 2b and induction of 2a5 occurred in lethal and non-lethal infections when parasitaemia rates were high. A contribution of NO for depression of CYP2b cannot be ruled out. Results were consistent with the view that CYP2a5 and HO-1 are concurrently up-regulated and suggested that CYP2a5 induction may occur in the absence of enhanced endoplasmic reticulum stress.
Several studies have shown that stimulation of host defense mechanisms against infections, as well as treatment with pro-inflammatory cytokines, modulate the expression and activity of cytochrome P450 enzymes (CYP), thereby modifying the kinetics of drugs and toxicants [1, 2]. Along this line, it was reported that Plasmodium berghei infection depressed the total content of cytochrome P450s (CYPs) and the expression and activity of several CYP isoforms in the rodent liver [3–6]. Furthermore, it was recently shown that P.berghei ANKA malaria induced CYP2a5 activity . Since the aforementioned studies evaluated CYP changes only at a nearly terminal stage of lethal malaria, it remains unclear whether up- and down-modulation of CYPs occur at earlier stages of lethal infections and in non-lethal infections as well.
The mechanism by which murine CYP2a5 and its human orthologous 2A6 are up- or down-modulated by infections and inflammatory stimuli remains largely obscure. Kirby and coworkers suggested that inducers of CYP2a5 have in common the property of causing oxidative injury to endoplasmic reticulum (ER), thereby producing an overexpression of GRP78 in hepatocytes [8, 9]. Abu-Bakar et al, on the other side, suggested that CYP2a5 and 2A6 play a major role in the oxidative metabolism of bilirubin (BR), a breakdown product of haem. Since induction of HO-1 results in elevated levels of bilirubin, Abu-Bakar  advanced a hypothesis that a concurrent up-regulation of haem-oxygenase (HO) and CYP2a5 is critical for maintaining a balance between production and elimination of BR. In human Plasmodium falciparum and in rodent Plasmodium berghei malaria, intense haemolysis occurs and high levels of circulating haem may be present [11–13]. In human as well as in rodent cells, free haem excess up-regulates the expression of HO-1, the rate limiting enzyme in the process of converting potentially toxic free haem into equimolar amounts of carbon monoxide (CO), biliverdin and iron (Fe) [14, 15].
It has been noted that nitric oxide (NO) causes a concentration-dependent inhibition of CYP activities in liver microsomes in vitro [16, 17]. Based on these findings, and also on in vivo experiments in which iNOS inhibitors partially reversed LPS-induced decline of liver CYP activities, Khatsenko et al advanced a hypothesis that NO overproduction mediates the decrease in CYP activities induced by immunostimulation. Nonetheless, the idea that NO mediates a general depression of CYP activities caused by inflammatory and infectious stimuli remains controversial. Sewer et al reported that the down-modulation of murine CYP2c29, 2e1 and 3a11 by the Escherichia coli endotoxin in vivo occurs independently of NO production, a conclusion that is at variance with Khatsenko and coworkers' hypothesis. The same authors, however, observed a NO-dependent degradation of CYP2b proteins, a finding that reveals a possible mechanistic link between NO overproduction and inhibition of CYP2b during immunostimulation. In all aforementioned studies host defense responses were stimulated either by LPS or bacterial infections. So far no study has investigated whether depression of CYP1a and 2b activities correlates with periods of enhanced production of NO during the course of parasitic infections.
This study was undertaken to provide data on the time course of alterations of CYP2a5, 1a and 2b activities in the mouse liver during the evolution of lethal (P.berghei ANKA) and non-lethal (Plasmodium chabaudi chabaudi) malaria infections. Along this line, it was also examined whether down- modulation of CYP1a and 2b activities correlates with periods of NO overproduction during lethal and non-lethal infections. Additionally, the present study investigated whether the induction of CYP2a5 activity was associated with ER dysfunction (GRP78 protein overexpression), enhanced haem metabolism (HO-1 induction) and oxidative stress. The activity of uridine diphosphoglucuronyl transferase (UGT), an enzyme that plays a critical role in the elimination of bilirubin, was evaluated in P.berghei-infected mice as well .
Female DBA-2 and C57BL/6 mice, 7 to 10 weeks old, from the Oswaldo Cruz Foundation (FIOCRUZ) breeding stock were used. All mice were housed in standard plastic cages with stainless steel covers and white wood shavings as bedding. Temperature (23 ± 2°C), air relative humidity (approximately 70%) and photoperiod (lights on from 8:00 a.m. to 8:00 p.m.) were controlled in the animals' room. A commercial pellet diet (Nuvital CR1, Nuvilab®, Curitiba, PR, Brazil) and filtered tap water were provided ad libitum. The study protocol was approved by the Ethics Committee on the Use of Animals of the Oswaldo Cruz Foundation (CEUA-FIOCRUZ).
Substrates benzyloxy- and ethoxy-resorufin, coumarin, p-nitrophenol, 1-chloro-2,4-dinitrobenzene, uridine diphospho glucuronic acid (UDPGA), GSH, thiobarbituric acid (TBA), butylated hydroxytoluene (BHT), dithiothreitol (DTT), EDTA, pyrazole, Bradford reagent, BSA, sulphanylamide, naphtylenediamine dichlorhydrate (NEED), nitrate reductase, sodium nitrate, β-NADPH, β-NADP, glucose-6-phosphate, glucose-6-phosphate dehydrogenase, and E.coli LPS (type 0127:B8) were from Sigma Chemical Co (St. Louis, MO, USA). All other chemicals used in the experiments were of high analytical grade.
Parasites and infection
Parasites causing lethal (P.berghei ANKA strain) and non-lethal (P.chabaudi chabaudi AS strain) malaria infections in DBA-2 and C57BL/6 mice were used. Malaria-infected animals were inoculated by the i.p. route with 0.2 mL of PBS-diluted blood from a donor mouse containing either 106 (P.berghei) or 2 × 107 (P.chabaudi) parasitized erythrocytes (PE) per milliliter. The donor mice had been inoculated with a stabilate of the parasite kept at -80°C in Alsever's solution. For each malaria-infected mouse, an age-paired non-infected control animal of the same sex and strain was injected with 0.2 mL of PBS solution. After infection, mice were daily examined for clinical signs of illness and a small drop of blood was taken from the tail tip for determination of parasitaemia rates. The percentage of parasitized erythrocytes (% PE) was determined by examining thin blood smears stained by the Romanowski's method (Panótico Rápido, Laborclin®, Pinhais, PR, Brazil). Groups of infected mice and their matched non-infected controls were killed by cervical dislocation at different times after infection. After death, spleens and livers were removed as quickly as possible, freed from fat and extra tissue, weighed, frozen and kept at -80°C until further use.
Preparation of subcellular fractions for phase I and II enzyme assays
Microsomal fraction I
Liver microsomal fraction I (MF I) was prepared as described previously , except for the use of 100 mM Tris 150 mM KCl buffer solution pH 7.4 instead of the sucrose solution. Aliquots of MF I were stored at -80°C until further use. MF I was used for the monooxygenase and UGT activities.
Microsomal fraction II
Liver microsomal fraction II (MF II) was used for determination of microsomal glutathione S-transferase (mGST) activity. It was prepared essentially as described for MF I, except for using 150 mM Tris pH 8.0 buffer solution to avoid cytosolic contamination . Aliquots of MF II were stored at -80°C until further use.
Liver cytosolic fraction (CF) was prepared as recommended by Abel et al. Briefly, liver was homogeneized in 10 mM Tris 250 mM sucrose 0.2 mM DTT 1 mM EDTA buffer solution pH 7.4 and centrifuged at 10 000 × g for 10 min at 4°C. The supernatant was then centrifuged at 15 000 × g for 20 min at 4°C, filtered in gauze and centrifuged at 105 000 × g for 1 h at 4°C. Aliquots of CF were stored at -80°C until further assay of the cytosolic GST (cGST) activity.
Total protein determination
Protein concentration in MF I, MF II and in CF was determined using Bradford reagent and BSA as the standard . The method was adapted to a microplate and absorbance was read at 595 nm in a spectrophotometer Spectramax Plus® (Molecular Devices, USA).
Benzyloxy-(BROD) and ethoxy- (EROD) resorufin-O-dealkylases were determined in 96-well microplates as described by Kennedy and Jones , with some modifications . Substrate final concentration was 5 μM and 0.025 mg of microsomal protein was added to each well (MF I). After a 10-min incubation period at 37°C, 100 μL of acetonitrile was added to each well and the amount of resorufin was measured in a fluorescence plate reader (Spectramax Gemini XS®, Molecular Devices, USA) with excitation and emission wavelengths set at 530 and 590 nm, respectively.
Coumarin hydroxylase (COH) activity
COH activity was assayed as reported by Iersel et al with a few adaptations. 50 mM Tris buffer pH 7.4, 10 μM coumarin and 0.4 mg (DBA-2) or 0.8 mg (C57BL/6) of protein was added to reaction tubes for a final volume of 0.5 mL. After a 3 min pre-incubation period, reaction was initiated by addition of a NADPH regenerating system (0.5 mM β-NADP, 10 mM glucose 6-phosphate, 0.5 U/mL glucose 6-phosphate dehydrogenase and 10 mM magnesium chloride). The reaction took place for 10 min at 37°C with shaking and was stopped by addition of HCl 2N. The reaction product (umbelliferone or 7-hydroxycoumarin) was extracted with chloroform and taken to tubes containing 1.6 M glycine-NaOH solution pH 10.4. The amount of umbelliferone was measured by using a spectrofluorimeter Shimadzu RF5301 PC® with excitation and emission wavelengths set at 355 nm and 460 nm, respectively, and a 3 nm band slit width.
UGT activity was determined as reported by Bock et al. 100 mM Tris pH 7.4, 0.25% triton X-100, 5 mM p-nitrophenol, 50 mM MgCl2 and 0.1 mg of protein (MF I) were added to reaction tubes to a final volume of 0.5 mL. After a 2 min pre-incubation period, UDPGA (3 mM) was added to start the reaction. After 30 min, trichloroacetic acid 5% was added to stop the reaction and the samples were centrifuged at 2 300 rpm in a bench centrifuge. 1 mL of supernatant was added to a cuvette that received 250 μL of 2 N NaOH. Samples were carried to a spectrophotometer Shimadzu UV 1601® set at 405 nm and the enzyme activity was calculated using the molar extinction coefficient of 14.9 mM-1 cm-1 settled by Martin and Black .
GST activities in microsomal (MF II) and cytosolic (CF) fractions were determined as described in details by Habig et al. Briefly, 100 mM K2HPO4 buffer solution pH 6.5, 1 mM 1-chloro-2,4-dinitrobenzene, 1 mM glutathione, 5 μg (CF) or 50 μg (MF II) of protein and 0.1% Triton X-100 (MF II only) were added to the cuvette (final volume of 1 mL) where the reaction took place. The differential absorbance was recorded using a spectrophotometer Shimadzu UV 1601® (set at 340 nm) and the amount of conjugate formed was calculated using the molar extinction coefficient of 9.6 mM-1 cm-1.
Measurement of GSH levels
After mouse death, the liver was removed as quickly as possible, washed in iced PBS, dried and homogenized in 100 mM NaPO4 5 mM EDTA buffer solution . The hepatic homogenate was centrifuged at 10 000 × g at 4°C for 15 min and the supernatant was frozen and kept at -70°C until further use. After thawing, the supernatant (10 μL) was incubated with 12.5 μL of 25% phosphoric acid and 37 μL of 0.1 mM NaPO4 5 mM EDTA buffer solution pH 8.0 for 10 min at 4°C. It was centrifuged again at 13 000 × g for 10 min at 4°C, and the newly obtained supernatant was incubated with 0.1% o-phthaldialdehyde methanol solution and the same basic buffer solution for additional 15 min at room temperature. GSH concentration was then measured using a spectrofluorimeter (Shimadzu RF 5301 PC®) with wavelength parameters set at 350 nm (excitation), 420 nm (emission) and 3 nm (band slit width) and GSH standard curve [30, 31].
Thiobarbituric acid reactive substances (TBARS) assay
TBARS were measured as described by Hermes-Lima et al. Livers were homogenized in a 0.2% phosphoric acid solution (1:5, w/v) and in another volume of a 2.0% phosphoric acid solution. 0.4 mL aliquots of homogenized tissue received the same volume of either 10 μM butylated hydroxytoluene (BHT) 1% thiobarbituric acid (TBA) - samples - or 3 mM HCl - blanks (each sample having its own blank). Both tubes received 0.2 mL of 7% phosphoric acid and were heated in boiling water for 15 min. After cooling at room temperature, the tubes received 1.5 mL of butanol, were vortex vigorously for 40 sec and centrifuged for 10 min. Two distinct phases appeared, an organic phase on the top (TBA-MDA complex) and an aqueous phase on the bottom. The absorbance of organic phase supernatant was read at 532 nm and 600 nm while blanks were scanned between 400 and 600 nm. To calculate malondialdehyde (MDA) concentration, absorbance at 600 nm was subtracted from that at 532 nm and a molar absorption coefficient of 156 mM-1cm-1 was used .
Nitric oxide (NO) levels in blood serum
NO production was evaluated by measuring total nitrite in serum as described in details elsewhere . Briefly, nitrate was reduced to nitrite by incubating the serum sample with a nitrate reductase and the total amount of nitrite was then determined by the Griess method. Results are expressed as μM concentration of NO2-.
Reverse transcriptase-polymerase chain reaction (RT-PCR) analysis (iNOS, HO-1)
Levels of mRNA in the liver and spleen were determined by real time RT-PCR as follows. RNA was extracted using Trizol® reagent, quantified in a Nanodrop® spectrophotometer, used (3 μg) as template to cDNA synthesis. The cDNA synthesis reaction was conducted in a Mastercycler Gradient thermocycler (Eppendorff®) using Superscript II® system (Invitrogen®) and oligo DT primers (Promega®). Relative expressions of iNOS and HO-1 were determined using Taqman® assays (Applied Biosystems®). Assays Mm00440485_m1 and Mm00516007_m1 were used for iNOS and HO-1 respectively, and the assay 4352341E was used for β-actin (endogenous control). Real time reactions were conducted in a 7500 Fast real time thermocycler (Applied Biosystems®). The relative quantification of the target genes was made using the ΔΔCt method.
Gel electrophoresis (SDS-PAGE) and immunoblotting analysis (GRP78 protein)
SDS-PAGE was performed using 8% polyacrilamide resolving gel as described by Laemmli . Microsomal proteins were separated by applying a constant current (30 mA) onto the gel (Hoefer miniVE system, GE Healthcare®). After separation, microsomal proteins were transferred into nitrocellulose membranes (Hybond ECL, GE Healthcare®) using the Hoefer miniVE semi-dry system (GE Healthcare®). Primary antibody was a rabbit polyclonal IgG (SC 13968, Santa Cruz Biotechnologies®, lot # F2206) against an epitope corresponding to amino acids 525-653 mapping at the C-terminus of the 78 kDa glucose-regulated protein (GRP78) of human origin. The blots were developed using a commercially available alkaline phosphatase kit (BIORAD® AP conjugate substrate kit).
Modulation of liver CYP activities during P. berghei (lethal) infection
Alterations of liver monooxygenase activities during P.berghei infection are also shown in Figures 1 (DBA-2) and 2 (C57BL/6). The effects of P.berghei infection on DBA-2 liver enzymes were not examined beyond PID20 because mortality was high after this day. As shown in Figure 1, activities of CYP2a5 and 1a were up and down-regulated, respectively, only at the terminal stage of infection (EROD: PID20; COH: PID16 and 20). The activity of CYP2b, however, showed a progressive depression - from PID8 on - as infection evolved to a more severe stage (Figure 1B).
Changes of CYP activities in P. chabaudi- infected mice (non-lethal malaria)
In the DBA-2 strain of mice, an induction of CYP2a5 activity (COH) was found on the day of peak parasitaemia (PID5) only, while activities of CYP1a (EROD) and 2b (BROD) remained unaltered at all times after infection (Figure 4B). In C57BL/6 mice infected with P.chabaudi, however, the activity of CYP2a5 (COH) was not altered during the whole course of the infection, although the activities of CYP1a (EROD) and 2b (BROD) were depressed around the day of peak parasitaemia, PIDs 2-6 and PID5, respectively (Figure 5B).
Nitric oxide (NO) production during the course of P. berghei and P. chabaudi infections
Activity of GST and UGT, and levels of GSH and TBARS in the liver of P. berghei-infected mice
Phase-II enzyme activity, glutathione and TBARS in the liver of P.berghei-infected mice
80.4 ± 4.5
700 ± 100
8.4 ± 3.2
86.0 ± 8.0
13.5 ± 3.9
91.0 ± 5.4
800 ± 100
9.0 ± 3.0
76.9 ± 9.0
39.0 ± 5.5*
85.6 ± 6.1
1 400 ± 100
7.4 ± 3.7
35.0 ± 9.8
19.5 ± 2.7
95.9 ± 2.7
1 500 ± 100
5.5 ± 3.0
16.9 ± 8.6*
23.6 ± 12.3
Effect of P. berghei infection on the expression of inducible haem oxygenase (HO-1) in the liver of DBA-2 mice
Effect of P. berghei infection on the level of glucose-regulated protein 78 (GRP78) in the mouse liver
Data provided by this study confirmed that P.berghei infection induces CYP2a5 (COH) and depresses CYP1a (EROD) and 2b (BROD) activities in the liver of DBA-2 mice . Furthermore, it was also shown that non-lethal (P.c.chabaudi) infection up- (CYP2a5) and down- (CYP1a and 2b) modulates CYP activities in the liver of DBA-2 and C57BL/6 mice on the day, and/or shortly before or after the day on which parasitaemia peak was recorded. It is of note that CYP activities remained almost unaltered in C57BL/6 mice infected with P.berghei, most of which developed severe neurological symptoms compatible with cerebral malaria. Compared to P.berghei-infected DBA-2, however, C57BL/6 mice presented lower parasitaemia rates before dying with cerebral malaria symptoms. Modulation of CYP activities by malaria, therefore, is not necessarily associated with a terminal stage of an invariably lethal infection, because, on one side, it was not observed in mice (C57BL/6) developing a severe and deadly cerebral malaria, and, on the other side, it occurred near the parasitaemia peak in animals with non-lethal infections. Taken together, findings presented here suggested that high parasitaemia rate was a major clinical feature associated with infection-produced alterations of liver CYP activities regardless of whether infection further progressed toward the death (P.berghei) or cure (P.chabaudi) of malarious mice. Additionally, necropsy data showed that livers of P.chabaudi-infected mice, due to a continuous accumulation of malaria pigment (haemozoin), became even darker and more enlarged after the day of parasitaemia peak, when CYP activities had returned to the levels recorded in non-infected controls. The foregoing observation suggested that up- (CYP2a5) and down- (CYP1a and 2b) regulations of liver CYP activities during malaria infections do not seem to be associated with accumulation of haemozoin in the hepatic tissue.
CYP2a5 is induced by phenobarbital, pyrazole, virus and bacterial hepatitis as well as by liver fluke (Fasciola hepatica and Opisthorchis viverrini) infections [39–41]. Recently, it was described that CYP2a5 is induced in DBA-2 and C57BL/6 mice infected with P. berghei ANKA. All aforementioned infections and the prototypical CYP2a5-inducer pyrazole - but not phenobarbital - produced extensive liver injury and a marked rise in serum levels of ALT and AST as well . The expression of CYP2a5 in a glucose-6-phosphate dehydrogenase (G6PD)-deficient mouse model of oxidative stress was studied by Nichols and Kirby . The G6PD-deficient mouse exhibits increased susceptibility to oxidative stress and the authors found that treatment of wild type and G6PD-deficient mice with pyrazole for 72 hours led to a greater degree of induction of CYP2a5 in the deficient animals. TBARS and other markers of oxidative stress, however, were not altered by pyrazole either in wild or in G6PD-deficient mice. On the other side, oxidative stress markers were enhanced, whereas CYP2a5 was not induced by treatment of wild type or G6PD-deficient mice with menadione, a pro-oxidant agent. Nichols and Kirby  also noted that pyrazole produced a greater increase in GRP78 protein in G6PD-deficient mice than in wild type mice, and that menadione did not alter GRP78 levels either in wild type or in G6PD-deficient animals. Based on these findings, the authors suggested that generalized cellular oxidative stress does not play a key role in the up-regulation of CYP2a5 and that other factors related to G6PD-deficiency such as ER stress may be involved.
Results from the present study indicated that levels of the putative oxidative stress marker TBARS were increased, while expression of GRP78 remained unchanged in the liver of P.berghei-infected DBA-2 mice. The effects of malaria on TBARS and GRP78 expression were similar to the effects of menadione, a pro-oxidant agent non-inducer of CYP2a5, and contrasted with the effects of pyrazole, a prototypical inducer of CYP2a5. Therefore, it seems difficult reconciling all aforementioned studies findings through a common hypothesis on the role of oxidative stress and ER stress on CYP2a5 induction by chemicals and infections. Nonetheless, it should be borne in mind that lack of GRP78 induction does not necessarily imply that malaria elicited no ER stress. Although being considered a marker of ER stress, GRP78 over-expression is in fact a homeostatic response that protects the cell against damage caused by ER dysfunction or stress. If GRP78 were not up-regulated, ER stress would result in more marked ER accumulation of unfolded proteins and more severe hepatocellular injury. This interpretation is consistent with elevated serum ALT and AST levels noted in P.berghei-infected DBA-2 mice , an indication that enhanced oxidative stress during malaria may have caused liver cell injury.
HO-1 is an inducible and rate-limiting enzyme of haem catabolic pathway. It catalyzes the opening of porphyrin ring to form biliverdin that is subsequently converted to bilirubin by biliverdin reductase. Circulating free haem is a potent oxidant and cytotoxic agent and thus up-regulation of HO-1 expression by oxidative stress, heavy metals and a variety of other inducers is regarded as a protective response. Although being a protective antioxidant compound, bilirubin is very hydrophobic and may also cause toxicity when it is accumulated in tissues due to impaired conjugation and excretion (e.g. neurotoxicity in neonatal jaundice and cholestatic diseases). The main route of bilirubin elimination involves glucuronidation mediated by UGT1A1 and excretion of conjugated metabolites into the bile. Nonetheless, it has been suggested that oxidative metabolism of bilirubin would be an important alternative route of elimination when glucuronidation is impaired . Based on the observation that CYP2a5 is induced by substances known to affect haem balance, including metals and porphyrinogenic agents , Abu Bakar et al suggested that CYP2a5 plays a role in the oxidative metabolism of bilirubin. Moreover, the authors pointed out that the foregoing CYP2a5 inducers also up-regulated HO-1, and that CYP2a5 over-expression is often associated with a decrease of total CYP content, which in turn has been shown to be associated with HO-1 induction as well. A hypothesis was advanced that a coordinated regulation of CYP2a5 and HO-1 expressions contributes to achieving a balance between bilirubin production and elimination. The concurrent induction of CYP2a5 and HO-1 in the liver of P. berghei-infected DBA-2 mice is consistent with this view .
Contrasting with the up- and down-modulation of CYPs, activities of liver conjugation enzymes (UGT and microsomal and cytosolic GST) remained unchanged in P.berghei-infected mice. Carvalho et al also found that UGT activity was unaltered in liver microsomes of Swiss Webster mice infected with P. berghei. Murdoch et al, however, evaluated phenol conjugation in perfused rat livers and noted that P.berghei infection decreased phenol glucuronide formation. Along the same line, Ismail et al described that malaria impaired glucuronidation of paracetamol in rats in vivo. In both cases, ex vivo and in vivo reductions in phenol and paracetamol glucuronidations may have been due to a lower availability of the co-substrate uridine diphosphoglucuronic acid (UDPGA) in the liver of infected rats. As pointed out by Murdoch et al, UDPGA availability depends on hepatic glycogen stores, which were partially depleted in malarious rats. Therefore, even if expression and catalytic activity of UGT remains unaltered, a lower availability of the co-substrate UDPGA in the liver of malarious individuals may eventually reduce the rate of glucuronidation reactions.
There are few data on the effects of rodent malaria on the expression and activity of GSTs in the host liver. Results from this study with P.berghei ANKA infections are at variance with those reported by Ahmad and Srivastava  for mice infected with Plasmodium yoelii nigeriensis. The authors found a decline of microsomal and cytosolic GST activities in the liver and spleen of infected mice that were to some extent reversed by treatment with mefloquine and menadione. The differences between results from this study and those reported by Ahmad and Srivastava  are possibly explained by differences regarding parasite species, murine strains and severities of malaria infection.
During malaria infection both hosts and parasites are under oxidative stress and reactive oxygen species (ROS, e.g., superoxide anions and hydroxyl radicals) are produced by host's activated neutrophils and by the degradation of haemoglobin by parasites as well. Although killing the parasite, enhanced ROS production also contributes to pathological changes in the host including red blood cell sequestration, cerebral pathology, anemia, and respiratory distress. Data from this study showed that levels of TBARS - a marker for lipid peroxidation and oxidative stress - were enhanced in the liver of DBA-2 mice infected with P.berghei, thereby supporting the view that hepatic tissue is under oxidative stress during severe malaria infection. No alteration of TBARS levels was found in the liver of infected C57BL/6 mice. On the day of sacrifice, however, infected C57BL/6 mice exhibited lower parasitaemia rates and less darkened and enlarged livers than infected DBA-2 mice. Levels of GSH in the liver, on the other side, were reduced by infection in C57BL/6 but not in DBA-2. It is of note that background levels (i.e., non-infected control levels) of GSH in the DBA-2 strain were higher than in the C57BL/6 strain. It is not clear why hepatic GSH levels were depleted by malaria in C57BL/6 mice but not in DBA-2 mice. A number of factors can affect the availability of GSH (a powerful antioxidant) in the liver and owing to this fact a decline of the ratio between reduced (GSH) and oxidized (GSSG) glutathione is a more reliable indicator of imbalance between pro-oxidant and antioxidant mechanisms (oxidative stress) than a decrease of GSH levels.
Nonetheless, data from this study strongly suggest that, owing to their lower levels of GSH, infected C57BL/6 mice are more vulnerable to hepatic injury (including DNA damage) caused by electrophiles than non-infected mice.
It is well known that NO production in response to secretion of pro-inflammatory cytokines during infection and inflammation is mediated by an up-regulation of iNOS . In human malaria, NO has been suggested to have a dual role. In P. falciparum malaria, despite mediating the intra-hepatic killing of the parasite, NO is thought to contribute to the pathogenesis of the disease . In rodent malaria, however, the role of NO is still unclear. Despite the general idea that it depends on the parasite-host relationship, iNOS mRNA induction in rodent malaria may vary according to the stage of infection, the degree of parasitaemia, the species and strain of Plasmodium and the target organ or tissue examined . In this study, no enhancement of serum NO was found in P.berghei-infected mice while slight increases of serum levels of NO were observed near the day of parasitaemia peak in P.chabaudi-infected animals. Nonetheless, levels of iNOS mRNA in the liver of P.berghei-infected mice were higher than levels in non-infected controls, thereby indicating that iNOS expression was up-regulated by lethal malaria. A possible explanation for unchanged serum levels of NO, in the presence of over-expression of iNOS in hepatic and splenic tissues, is an increase in NO scavenging by free haemoglobin in the blood of infected mice. Nitric oxide binds avidly to haem iron, and haemoglobin (Hb) is released into the circulation when red blood cells (RBC) are disrupted during parasite schizogony. Along this line, Sobolewski et al found that plasma levels of free Hb were rather high in P.berghei-infected mice (e.g. on PID6), and additionally demonstrated in vitro that cell free Hb is at least 1 000 times more efficient in scavenging NO than the intracellular Hb. It should be pointed out that intravenous infusions of cell free haemoglobin and chronic haemolysis due to sickle-cell disease limit NO bioavailability as well . The induction of iNOS mRNA expression in P.berghei-infected mice strongly suggested that malaria infection elicited NO production in the hepatic tissue. The idea that NO is a mediator of the down-modulation of CYP expression by inflammatory stimuli is plausible because NO binds haem proteins and inhibits catalytic activities of CYPs in in vitro test systems [16, 17]. Nonetheless, Khatsenko and coworkers' hypothesis has not been supported by data provided by other authors. Sewer et al, for instance, reported that LPS depressed the expression of CYP2c29, 2e1 and 3a11 in iNOS knockout mice. More recently, however, Morgan and coworkers [2, 51] showed that NO over-production caused a selective depression of CYP2b rather than an unspecific down-regulation of CYPs. Furthermore, Lee et al showed that CYP2b underwent a post-transcriptional NO-dependent ubiquitination and proteosomal degradation and suggested that these events are triggered by a modification of aminoacid residues of CYP2b proteins by reactive nitrogen species. If this view holds true, it seems fair to think that NO overproduction arising from iNOS up-regulation in the hepatic tissue is the mechanism, or one of the mechanisms, by which malaria depressed CYP2b activity in the mouse liver.
The mechanism by which malaria down-modulates the expression and activity of other CYP isoforms is still unclear. Gu et al suggested that NFκB activation could play a role in the down-modulation of CYPs by inflammatory and infectious diseases and malaria was reported to enhance TLR-mediated pro-inflammatory responses . Therefore, the idea that NFκB activation mediates the down-modulation of liver CYPs by blood stage malaria seems plausible.
Finally, it should be borne in mind that there are differences in the pathology produced by P. berghei and P.chabaudi in murine hosts and that caused by P. falciparum and Plasmodium vivax in humans. Results from this study showed that up- and down-regulation of CYP activities during P.berghei and P.chabaudi infections occurred when parasitaemia rates were high. Compared to the hyperparasitaemia noted in murine infections, parasitaemia rates in human P.falciparum infection are low due to the adherence of trophozoite/schizont-infected erythrocytes to the endothelium of capillaries and venules. Nonetheless, it was reported that, in patients with P.falciparum malaria, clearance rates of quinine  and caffeine  were slower thereby suggesting that drug metabolism is depressed during human malaria as well. There are only a few studies on the influence of malaria on drug metabolism in humans and more data are needed on the alterations of drug kinetics in P.falciparum and also in P.vivax malaria. At any rate, data presented here demonstrated that liver CYP activities are modulated during murine lethal and non-lethal infections and it seems fair to think that this modulation of enzymes involved in drug metabolism also occurs in human falciparum malaria.
In conclusion, results from this study showed that down-regulation of CYP1a and 2b, as well as up-regulation of CYP2a5 occur in both lethal and non-lethal murine malaria. It was also demonstrated that alterations of CYP activities in murine malaria occurred only when parasitaemia rates were high, and apparently were not associated with liver enlargement and haemozoin accumulation. Since iNOS was induced in the liver of P.berghei-infected mice, a contribution of NO for depression of CYP2b activity cannot be ruled out. No induction of GRP78 was found in P.berghei-infected mice, a finding that suggests that CYP2a5 up-modulation may occur in the absence of ER stress. Finally, results from this study are consistent with the view that HO-1 and CYP2a5 are concurrently up-regulated in the mouse liver.
The authors are indebted to Prof. Dr. Graziela Zanini (Evandro Chagas Hospital, FIOCRUZ, Rio de Janeiro, Brazil) for assistance with mouse infections and parasitaemia analysis. This study was financed by a grant from the National Research Council - Brazil (CNPq). LSG, CMS and FJR were recipients of fellowships from CNPq.
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