In response to infection caused by Plasmodium parasites, the natural host defense mechanism is activated with involvement of phagocytes (macrophages and neutrophils). These, in turn, generate large amounts of ROS and RNS, causing an imbalance between the formation of oxidizing species and the activity of antioxidants. This imbalance is what triggers oxidative stress, which is an important mechanism of human hosts in response to infections and, in the case of malaria, can lead to the death of the parasites.
studies have demonstrated the ability of oxidative stress to promote the killing of parasites. Incubation of Plasmodium yoelii
species in the presence of glucose and glucose oxidase generated H2
, a reactive oxygen species, capable of killing the parasite. Likewise, when incubated in the presence of xanthine and xanthine oxidase, it generated free radical superoxide (O2•−
) and a subsequent burst of other oxidative products, with consequent destruction of parasites [32
Furthermore, oxidative stress markers in infected humans and rats are found in high levels compared to uninfected controls [21
]. In such cases oxidative stress seems to result from increased production of free radicals, a fact suggested by increased malondialdehyde (MDA), an important lipid peroxidation marker, and not from a decrease in levels of antioxidants, reinforcing the suggestion that oxidative stress is an important mechanism in parasite infection [24
Recent studies suggest that oxidative stress can take part in the pathogenesis of thrombocytopenia associated to malaria. Erel et al
] showed that the number of platelets and the activities of antioxidant enzymes—superoxide dismutase (SOD) and glutathione peroxidase (GSH-Px)—in patients with vivax
malaria were reduced while lipid peroxidation of platelets (estimated by measuring the MDA), was elevated in infected individuals, suggesting a negative correlation between platelet count and platelet level of lipid peroxidation. These data suggest that oxidative stress occupies an important role in the genesis of thrombocytopenia present in malaria through loss of elasticity of membranes and by increasing brittleness and causing dysfunction in receptors, resulting in considerable functional impairiment of thrombocytes.
Indeed, the importance of these radical species in the genesis of rheological changes in malaria patients has led us to believe that one should avoid iron replacement in infected individuals, despite the degree of anemia observed by the erythrocytes count [36
Along with the synthesis of radical species, organisms have developed different antioxidant defense mechanisms in response to increased oxidative stress. In fact, antioxidant defense is a natural physiological mechanism of organisms against damage caused by free radicals and it depends on the consumption of cellular and systemic antioxidant reserves. Endogenous synthesis of these antioxidant compounds typically consists of three interdependent systems: enzymatic, small molecules and metal chelation, which retards or prevents oxidation of biomolecules. The antioxidant defense system also avoids oxidative species generation by scavenging or by free radicals reduction, which by self-oxidation form less reactive compounds [38
Although several antioxidant enzymes are important in the defense system, the most important include GSH-Px, catalase and SOD. These enzymes act directly on some free radicals, making them less reactive. However, they are not able to act on the highly reactive free radicals that are chiefly responsible for oxidative pathological processes such as hydroxyl and perhydryl radicals or peroxynitrite.
As a result, our body uses small molecules that reduce the reactivity of various reactive radicals as an auxiliary antioxidant defense system. This group contains a large number of molecules, such as vitamins A, C and E, beta-carotene, uric acid and reduced glutathione molecule (GSH). In addition, our organism has proteins that bind to transition metals preventing them from catalyzing the Fenton and Haber-Weiss reactions, important sources of reactive species production. These metal chelators include ferritin, transferrin and lactoferrin (chelating iron), ceruloplasmin and albumin (copper chelators) and metallothioneins having thiol groups capable of binding several heavy metals [39
Among the antioxidant molecules, the GSH molecule stands out as being the most powerful protector of eukaryotic cells in the host defense against oxidative stress, acting upon several different mechanisms [40
]. In parallel, the secretion of tumor necrosis factor-alpha (TNF-α) appears to induce oxidative stress through modulation of GSH metabolism, playing an important role in malaria physiopathogenesis. In studies with rats, the administration of TNF-α induced decreased GSH levels, whereas in CD4+ and CD8+ splenic T cells, a significant increase occurred in oxidized glutathione (GSSG) [41
], thus both behaviors suggest oxidative stress increase. Several authors have reported decreased GSH in malaria patients [40
However, besides GSH, lower levels of various antioxidants are found in malaria patients caused by Plasmodium vivax
. These are: antioxidant enzymes and glutathione S
-transferase (GST) [21
], catalase, GSH-Px, SOD [11
], NADPH-methemoglobin reductase [11
]; heavy metal chelators desferrioxamine, salicylaldehyde isonicotinoyl [44
] and ferritin [42
]; small molecules such as vitamins A, E, C [45
]; the pro-vitamins α- and β-carotene, lycopene, lutein and zeaxanthin [45
], among others.
Similarly, Plasmodium falciparum
malaria patients presented lower levels of antioxidants, such as ascorbate, which correlated with disease severity, in contrast to elevated levels of urate and ceruloplasmin [48
]. Accordingly, the increase in levels of urate may indicate the presence of ischemia-reperfusion syndrome (IRS) responsible for free radical production in ischemic conditions or even in hypoxia [49
] due to parasite-induced hemolysis and cytoadherence.
Likewise, decreased GST activity is directly related to the severity of the parasitemia, since the production of this enzyme reduces complications of malaria and occurrence of severe malaria [21
]. In this sense, the assessment of GST levels, lipid peroxidation and catalase, may be considered as potential biochemical markers of disease severity.
In children, all acute phase proteins (APP) are useful markers of the type and severity of inflammation in malaria, since all APP, except for α1-antichymotrypsin, were significantly correlated with splenomegaly, while α1-acid glycoprotein (AGP) and C-reactive protein (CRP) indicated chronic inflammation [50
]. Likewise, concentrations of albumin, apolipoprotein A1 (apoA1), transferrin, zinc, vitamin A, immunoglobulins G and M, interleukin 10 (IL-10), tumor necrosis factor-alpha (TNF-α) and interferon-gamma (IFN-γ) were verified. Children with malaria had decreased levels of apoA1 and albumin, but high levels of IL-10 when compared to children without malaria. All antioxidants studied showed lower levels in patients with the disease [51
In another study, mice infected with Plasmodium berghei
showed significantly increased lactate and alanine concentrations in the final stage of cerebral malaria, additionally, glutamine and essential amino acids levels were slightly elevated in the brain [52
Mice infected with P. vinckei vinckei
exhibit erythrocytic protection against reactive oxygen species by the enzymes superoxide dismutase, catalase, glutathione peroxidase, glutathione reductase, NADPH and NADH-methemoglobin reductase in red blood cells [34
In cultured endothelial cells incubated with heme, an aggravation of oxidative stress mediated by polymorphonuclear leukocytes was observed, which may probably be reversed by heme-oxygenase and ferritin mRNA induction, additionally to the administration of antioxidants such as catalase, reduced glutathione and superoxide dismutase [42
Another possibility of damage reversion consists in the administration of iron chelators, which inhibits the growth of P. falciparum in vitro
, such as hydrophilic desferrioxamine (DFO). Related factors to the use of these substances showed greater efficiency of anti-malarial drug action [44
infection in mice induces liver injury, increases mRNA expression of interleukin-12 (IL-12), protein 40 (p40) as well as IFN-γ, interleukin-4 (IL-4) and IL-10, with consequent increase in NO synthesis. Treatment with anti-IL-12 provides an indirect reduction of free radical production, thus prolonging survival, reducing liver damage and weight loss, but without alteration of the parasitemia [53
A study conducted with 273 children between the ages of 1–10 with acute uncomplicated P. falciparum
malaria in Kampala, Uganda, verified the antioxidant status in the pathogenesis of the disease. Children with acute malaria had low antioxidant plasma concentrations. On the other hand, in children with higher plasma lycopene levels, there was fast parasitemia clearance [45
In addition to lycopene, other antioxidant substances are known to act as an adjunct in drug therapy such as riboflavin, a reducing agent that acts in the parasite food vacuole and hemozoin formation [54
], which, as allicin, is an inhibitor of cysteine protease found in garlic extracts and acts by inhibiting circumsporozoite protein (CSP) processing, essential for the invasion of host cells [55
Oxidative stress is commonly observed to arise from five sources during disease physio-pathogeny: 1, Inflammatory process initiated in the host in response to infection; 2, transition metal catalysis, since in feeding on hemoglobin, the parasite releases significant amounts of free iron; 3, the occurrence of ischemia-reperfusion syndrome, resulting from cytoadherence processes and anemia triggered by infection; 4, direct reactive species production by the parasite; and 5, action of antimalarial drugs.
2.1. Oxidative Stress as Host Defense Mechanism against Plasmodium Infection
It has been shown that oxidative stress is related to a protective role in malaria patients, as possible agents capable of destroying the Plasmodium
. Thus, H2
can operate independently as cytotoxic agents or form other toxic molecules, including radical OH•
, hypochlorous acid (HOCl) and peroxynitrite (ONOO−
) in the presence of NO [22
The increased production of ROS by phagocytes, as part of the host defense, is a primary event. ROS generated by macrophages are known as non-specific effectors molecules in the host’s defense arsenal, which can contribute to oxidative damage in the parasite as well as parasitized erythrocytes, once ROS are able to diffuse through the membrane of red blood cells [56
]. Likewise, neutrophils secrete proteolytic enzymes and ROS, which in low concentrations can trigger apoptosis of endothelial cells and necrosis in high concentrations [57
In fact, it is generally accepted that ROS, including O2•−
, can destroy the parasite intraerythrocytically [35
]. Therefore, severe malaria caused by Plasmodium falciparum
is associated with activation of neutrophils and monocytes, elevated levels of cytokines and endothelial injury. Thus, activated neutrophils and their secreted products can exert not only anti-parasitic, but also endothelial injury, which can lead to organic failure in severe malaria [57
The inflammatory process mediated by effector immune response mechanisms is required as the homeostasis of the organism is modified. However, in some cases, such as in malaria, these mechanisms are not sufficient to eliminate some Plasmodium species and to some extent, may act in a manner that further harms the host cell.
With regard to malaria, the immune mechanisms are not fully understood yet, but it is known that the cytokine profile, which is proven effective in tackling the infection, is the mechanism that involves cellular response by helper T lymphocytes (Th) 1, with prevalence of TNF-α, IFN and IL-12. On the other hand, the Th2 profile (IL-4, IL-5, IL-10 and Transforming Growth Factor beta—TGF-β) are considered to aggravate severe conditions of the disease. However, there is no consensus on these profiles [56
], because different cellular responses act efficiently in different stages of parasite elimination: the first, essential at the initial process of infection, allows the host to mount an adaptive immune response against the parasite, but on becoming exaggerated or chronic, may favor severe anemia processes; the second promotes the clearance of the initial response (Th1) to be replaced by the adaptive action response. Obviously, if such responses are not properly activated, the parasite will tend to resist host defense [58
Nevertheless, we know the importance of ROS/RNS participation in the parasitemia elimination process as the main mechanism through which most anti-malaria drugs act. These substances are also known to regulate immune responses by stimulating or inhibiting production of a certain cytokine, transcription factor and even regulating cell death processes [59
Apoptosis is a natural process of cell death induced by intracellular mechanisms without the release of intracellular contents in the extracellular matrix. Such a mechanism is particularly interesting, since toxic substances from intracellular apoptotic cells do not harm surrounding cells, unlike necrosis. Cytochrome c, a mitochondrial protein, is among the substances known to regulate this process, which under normal conditions, linked to phospholipid (cardiolipin), participates in the electron transport chain [60
]. However, under stressful conditions, cardiolipin is oxidized, releasing cytochrome c, which upon reaching the cytosol, forms complexes with activating proteins of the apoptotic process.
The oxidation process of fatty acids, termed lipid peroxidation, appears to originate from the cardiolipin oxidation in the apoptosis context. Dey et al
] attribute the hydroxyl radical with the function of triggering the process in hepatocytes.
Further to lipid peroxidation, it is known that NO can play a key role in eliminating the parasite. According to Jaramil et al
], despite the contribution of NO as a free radical in the destruction of Plasmodium
, too much NO causes immune-suppression and leads to the development of cerebral malaria. Some parasitic molecules are well known for inducing NO, but there is a direct contribution of malarial pigment—hemozoin, which, associated with the IFN mediator of mRNA synthesis by the enzyme nitric oxide synthase (iNOS), is a potent inducer of NO generation in macrophages via extracellular signal regulated by kinase (ERK) and nuclear factor κB (NF-κB). It is also known that at the hepatic stage, defense mechanisms are strictly related to the production of IFN by Natural Killer cells (NK), with subsequent NO synthesis [63
It has also been observed that in addition to inducing NO, hemozoin is responsible for macrophage activation through mechanisms partially dependent on NO [15
] and, according to Brinkmann et al
], on other ROS/RNS such as the superoxide radical and hydrogen peroxide. Similarly, increased levels of iNOS in human monocytes are not associated with the worsening of malaria in patients infected with P. falciparum
Syarifah et al
] studying mice susceptible and resistant to cerebral malaria infected with Plasmodium berghei
, observed that the expression of cytokines (except for IL-4 and RANTES) as well as the expression of NO tested on mice spleen cells was enhanced in cells of resistant animals when compared to cells of susceptible animals. It is important to emphasize the high production of TNF-α in resistant mice, suggesting that activation of macrophages is significantly higher in these animals. Corroborating these findings, Kumaratilake et al
], using radiometric assays that quantify the antiplasmodial effect of phagocytes, verified in humans infected by P. falciparum
that TNF-α increased the release of toxic reactive oxygen intermediates on neutrophils, which contributed to the elimination of the parasite.
Additionally, it has been demonstrated that the free heme can stimulate both neutrophil migration and ROS/RNS production by a G protein-coupled receptor, more specifically the inhibitory Gα receptor, which in turn activates protein kinase C, increasing the inflammatory response [68
] and delaying apoptosis [59
], thereby most probably contributing to the immune-suppression induced by malaria [69
Among several cytokines already studied, an increase in the Granulocyte-Macrophage Colony-Stimulating Factor (GM-CSF) appears to correlate with the reduction of parasitemia and, in this context, with oxidative stress. GM-CSF is a cytokine with stimulatory action on granulocytes and macrophages and promotes an increase in the number and activity of these cells, acting effectively in cellular immunity against malaria. Several studies have shown that previous administration of GM-CSF, alone or associated with other factors, protected experimental animals from infection by various parasites [70
Similarly, animals deficient in GM-CSF synthesis had an impaired immune response against parasite infection [72
]. There seems to be a relation between GM-CSF and oxidative stress: GM-CSF and IL-4 receptors may be modified by lipid peroxidation products originating from hemozoin released by rupture of parasitized erythrocytes, such as 4-hydroxynonenal (4-HNE). GM-CSF and IL-4 are stimulators of the differentiation of hemozoin-loaded monocytes in dendritic cells. This differentiation can be inhibited by the 4-HNE and play an important role in immune suppression present in malaria [73
Moreover, this mechanism appears to be associated with the expression of peroxisome proliferator-activated receptor gamma (PPAR-γ) in immature dendritic cells loaded with hemozoin following administration of (15) S
-hydroxyeicosatetraenoic acid—a PPARγ ligand produced by hemozoin via peroxidation induced by the heme—which inhibits the differentiation process of these cells [74
There is also a relationship between GM-CSF and NO, as shown by Kaur et al
], demonstrating that pre-treatment with GM-CSF and methionine encephalin (TGG) protects mice from malaria. However, when animals were pre-treated with inhibitors of inducible form and both forms of NOS, the mortality rate of the animals increased significantly, suggesting that the protection exerted by GM-CSF/TGG was, at least partially, due to NO.
2.1.1. The Role of NO in the Physiopathology of Malaria
NO is one of the smallest and simplest biosynthesized molecules [75
]. It is an inorganic, colorless, free radical gas, with seven nitrogen and eight oxygen electrons [76
] and presents a sometimes beneficial, sometimes harmful dubious role in the body [77
]. It has been shown to be involved in many important biological functions, such as vasodilatation, blood pressure regulation, inflammation and unspecific immunity, neuronal plasticity, as well as to act as a neurotransmitter in the brain and peripheral nervous system. This molecule is also capable of lysing tumor cells [78
It is produced from the l
-arginine substrate by nitric oxide synthase (NOS). Nitric oxide is produced in significant quantities during the inflammatory response by macrophages and other immune cells, which express the inducible isoform of nitric oxide synthase (iNOS). Nitric oxide produced in these circumstances causes lethal oxidative damage to target cells, such as bacteria and other micro-organisms [80
Despite being an important cytotoxic mediator of immune activated cells, capable of destroying pathogens and tumor cells, NO is potentially toxic, mainly in situations of oxidative stress, which leads to the generation of reactive oxygen intermediates and an antioxidant system deficiency [77
Nitric oxide plays an important role in physiological functions and, consequently, many diseases may be related to a high or low NO level in the body. The role of nitric oxide in blood-stage malaria remains unknown.
Many authors believe that NO is not capable of killing parasites at in the blood-stage of malaria. They have reached this conclusion by comparing serum nitric oxide levels in Plasmodium
infected mice and humans against control levels in mice and human individuals. These studies conclude that nitrite and nitrate levels (NN—stable metabolites of NO) in infected individuals do not differ from control levels, and even with an increased NN serum concentration during the blood-stage of malaria, parasitemia is not different compared to control values [26
Sobolewski et al
] also questioned the role of NO in the progression of malaria parasitemia, stating that intraerythrocytic Plasmodia
are protected from reactive oxygen species by hemoglobin, occurring naturally in high concentrations within red blood cells (RBC), requiring levels of reactive oxygen species that surpass hemoglobin protection. In their experiments, NO was not able to fight the parasite until levels close to saturation. Other studies with iNOS−/− knockout mice found parasitemia levels similar to that of control animals [82
However, some researchers like Stevenson et al
] and Böhlke [89
] suggest that NO has a protective role against blood-stage malaria and claim that NO is an essential factor for malaria resolution by P. Falciparum
. They believe that elevated serum nitric oxide levels are toxic to the parasite [90
In our personal experience, despite decreasing parasitemia in infected mice by P. berghei
, inhibition of NOS enzymes favors the development of severe forms of the disease, notably cerebral malaria, suggesting that NO is a protective factor preventing aggravation of the disease [91
The chief answer to this impasse is that NO can act both directly and indirectly on malaria resolution. It may have a direct action as a parasiticide explained by the action of peroxynitrite, resulting from the reaction of NO with O2•−. Although indirectly, nitric oxide contributes to parasiticidal activity. This can occur through increased immune activity, absence of IL-4, the relationship between NO and GM-CSF/PPAR-γ, or the relationship between NO and increased ROS/RNS.
Nevertheless, we also agree that NO has a parasiticidal role in malaria, since high serum levels of it favor parasitemia resolution without harming the host. This gas, previously seen as a toxic agent, is considered today as a way to resolve this disease, since it may directly act on the inflammatory process and indirectly enable the necessary cytokines to activate the immune system.
NOS enzymes are dimeric flavoproteins containing tetrahydrobiopterin homologous to cytochrome P450. There is a classification type that differentiates enzymes according to their physiological function, and names them by inducible NOS (iNOS) and constitutive NOS (cNOS). The other classification type for NOS enzymes is based on the type of cell in which they are present. These are named: NOS1 (present in the cytosol of neurons) [92
], NOS2 (present in immune system cells) [93
], and NOS3 (present in endothelial cells) [95
Studies indicate that NO produced by iNOS activation plays an important role in killing several pathogens, including Plasmodium
]. However, recent studies in animal models have shown that NOS deficiency or inhibition is not enough for protection against P. berghei
] but hemozoin induces NO formation via iNOS [20
] and the increase in monocyte count may be associated with high levels of mRNA of this enzyme [65
In contrast, NO produced by endothelial NOS on all tissues acts as blood flow regulator, causing vasodilatation, preventing platelet aggregation and inhibiting adhesion of lymphocytes and monocytes to to endothelium [77
], which prevents local ischemia. These effects are crucial in preventing cerebral malaria, and the administration of exogenous NO, or substances that release NO, has been investigated as adjunctive treatment for malaria, with great results in improving microcirculation, reducing brain inflammation and protecting the blood-brain barrier [24
], thus decreasing oxidative stress. Exogenous NO is also indicated in the prophylaxis of lung damage of malaria patients [102
Infection with the malaria parasite in the Anopheles stephensi
mosquito induces the expression of nitric oxide synthase. This induction results in the synthesis of inflammatory levels of NO in the host circulation, causing an impact on parasite development. It has also been demonstrated that glycosylphosphatidylinositol can induce the expression of NOS [103
An important fact is that livers from immunized mice express mRNA for iNOS between 12 and 24 h after the arrival of sporozoites in the liver, and these animals, even when treated with a NOS inhibitor, are completely protected against the parasite at the erythrocyte stage of malaria [104
Other studies have correlated the incidence of malaria to changes in the promoters of genes encoding the enzymes iNOS and G6PD [105
2.1.2. Hemolysis as an Oxidative Stress Induction Factor in Malaria
During the erythrocytic phase of malaria, red blood cell lysis and the release of hemozoin occurs, which consists primarily of ferriprotoporphyrin IX dimers and monomers (FP) and methemoglobin in plasmodial proteins. Hemozoin is able to induce cytokine release (TNF-α and IL-1) through cells of the monocyte/macrophages system. Free heme is a powerful free radical generator, which can cause serious molecular damage to both host and parasite; the heme group contains Fe2+ atoms that can catalyze Fenton and Haber-Weiss reactions, generating free radicals. This is why certain drugs, such as chloroquine, have an active mechanism to prevent hemozoin formation, promoting accumulation of free heme. Thus, chloroquine increases the availability of intracellular heme by disrupting the plasma membrane structure and increasing oxidative stress in Plasmodium.
As a result of oxidative stress, lipid peroxidation occurs, promoting functional and structural changes of the plasma membrane that lead to hemolysis, which has always been linked to increased levels of thiobarbituric acid reactive substances (TBARS), markers of lipid peroxidation. The high levels of lipid peroxidation products, such as TBARS, have already been seen in erythrocytes parasitized by P. falciparum
, P. vinckei
, P. berghei
, and P. chabaudi
Hemolysis or extensive cell damage can lead to increased concentrations of free heme, causing oxidative stress and inflammation. Whereas heme induces neutrophil chemotaxis, Porto et al
] reported that several heme analogs are able to induce neutrophil migration in vitro
and in vivo
, and that mesoporphyrins, molecules lacking vinyl groups in their rings, were not chemotactic for neutrophils and selectively inhibited heme-induced migration. The authors conclude that heme activates neutrophils through chemoattractant signaling and that mesoporphyrins may be important in the treatment of inflammatory consequences such as bleeding and hemolytic disorders.
Additionally, the cellular response to hemozoin entails cytokine release [15
] and generation of reactive oxygen species such as NO [106
]. Research on oxidative stress induced by hemozoin/heme is exciting the scientific community because supports the development of new drugs, as is the case with the potential antimalarial [(aryl)arysulfanylmethyl] Pyridine (AASMP) [108
2.1.3. Oxidative Stress and the Membrane of Infected-Erythrocyte
During the development of the blood esquizogeny, P. falciparum
trophozoites increase the viscosity of red blood cells by causing changes in the parasitized cell surface permitting its adhesion to the endothelial wall of capillaries, which seems to be a defense mechanism of the parasite, preventing the passage of parasitized red blood cells through the spleen and their consequent destruction [109
]. However, the increased viscosity of the cells appears to be primarily responsible for the blocking of blood vessels, especially of kidney capillaries, pulmonary capillaries and brain capillaries, and cerebral malaria is the most common reason for coma and death in infected children [110
Among the changes that take place on the surface of red blood cells is the phenomenon of lipid peroxidation. In this sense, the parasitized erythrocytes are known to contain large amounts of monohydroxy derivatives of polyenoic fatty acids (OH-PUFA) in their lipids, suggesting the occurrence of lipid peroxidation due to the release of heme iron from non-enzymatic breakdown [112
]. One of the common OH-PUFA found and already described as toxic is the 12- and 15-hydroxy-arachidonic acid (HETE). It is known that the concentrations of OH-PUFA increase according to the evolutionary stage of the parasite. However, low concentrations of HETE were found after phagocytosis of parasitized RBCs, suggesting that other lipid peroxidation products also may play a key role in this process [112
Additionally, oxidative changes in P. falciparum
-infected red blood cells seem to be associated with the accelerated aging of these cells and contribute to the development of anemia presented by these subjects [10
]. The development of anemia can promote changes in the circulatory physiology, leading to the existence of moments of hypoxia alternating with the maintenance of tissue oxygenation at basal levels, favoring the participation of ischemia and reperfusion syndrome (IRS) responsible for an additional production of free radicals [39
Indeed, increased lipid peroxidation and oxidative stress reported in human malaria can affect the membrane of infected erythrocytes, also promoting the reduction of the deformity of these cells, which has been linked to increased mortality of adults and children with malaria. The deleterious consequences of increased cell rigidity include microcirculatory obstruction (exacerbating tissue hypoperfusion) and cell stiffness with subsequent removal by the spleen, which increases anemia [11
However, in P. falciparum
infections, red blood cells infected by mature trophozoites and schizonts are sequestered in the capillaries of various organs, which prevents their removal by the spleen. The adhesion of these cells to the vascular endothelium (cytoadherence phenomenon) can be related to a large number of antigenic variants encoded on the parasite’s surface that bind to endothelial receptors [113
This cytoadherence phenomenon is mediated by parasite proteins expressed via stimulation of the var
gene on the surface of infected red blood cells, such as P. falciparum
erythrocyte membrane protein 1 (PfEMP1). The expression of such proteins allows these parasitized erythrocytes to connect to different host molecules located in the vascular endothelium, such as intercellular adhesion molecule type 1 (ICAM-1), platelet endothelial cell adhesion molecule (PECAM), vascular cell adhesion molecule (VECAM), hyaluronic acid, heparin sulfate and others, interrupting blood flow and causing the impairment of tissues irrigated by clogged vessels [113
Other parasite proteins that promote increased membrane stiffness of infected erythrocytes are histidine-rich protein associated with deformity (KAHRP) and 3 erythrocyte membrane protein of P. falciparum
(PfEMP3). Studies have shown that in the absence of both proteins, membranes showed low levels of rigidity, and that KAHRP had a greater effect on the stiffness than PfEMP3, suggesting that these parasite proteins contribute to the rigidity of red blood cells [115
2.1.4. Ischemia and Reperfusion Syndrome as Oxidative Stress Induction Factors in Malaria
IRS occurs in malaria during sequestration of parasitized erythrocytes in certain tissues as a result of disrupting large amounts of erythrocytes promoted by Plasmodium during malarial paroxysm and of cytoadherence of erythrocytes to blood vessels.
In this syndrome, restriction of blood flow leads to O2
concentrations lower than normal [39
], resulting in the uncoupling of mitochondrial oxidative phosphorylation leading to a decrease in adenosine triphosphate (ATP) production. This is followed by the consumption of stored cellular ATP, which is further degraded to adenosine diphosphate (ADP) and adenosine monophosphate (AMP) and finally to adenosine. Should irrigation be restored at this stage, adenosine may be re-phosphorylated to ATP. However, if hypoxia persists, adenosine will be irreversibly metabolized to inosine and hypoxanthine. During ischemia, ATP shortage would cause failure of sodium-potassium dependent ATPase, with consequent accumulation of intracellular Na+
and extracellular K+
. These alterations could trigger the occurrence of cellular edema by causing increased osmotic pressure and cytoplasmic decompartmentalization.
The phenomenon of cytoplasmic decompartmentalization can be seen as a cellular distress condition, in which ions kept in watertight compartments flood into the cytoplasm, causing activation of enzymes that should be inactive, triggering communication processes at the intracellular level, or promoting free radical production. In this mechanism, Ca2+ ions and ferrous ions (Fe2+) are quite important. The free Ca2+ in the cytosol activates the protease calpain, which in turn promotes the breakage of a peptide bond of the enzyme xanthine dehydrogenase (XD), changing its activity to xanthine oxidase (XO).
Unlike XD, XO needs oxygen to convert hypoxanthine into xanthine. Thus, during ischemia three crucial phenomena occur with merely preparatory effects: The production of hypoxanthine from ATP, the conversion of XD in XO, and cytoplasmic decompartmentalization (which also releases iron from ferritin into the cytoplasm).
On the other hand, with reperfusion, the renewed oxygen supply catalyzes the metabolism of hypoxanthine by XO. This reaction leads to the production of xanthine, uric acid, O2•− and H2O2. It should be noted that ROS and RNS production only occurs during reperfusion. In turn with the ROS/RNS produced in reperfusion, O2•− and H2O2 can react together in the presence of iron (Haber-Weiss reaction) to yield the OH• radical and trigger the magnification and propagation of oxidative damage.