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The in vitro antisickling and antioxidant effects of aqueous extracts Zanthoxyllum heitzii on sickle cell disorder
© Pauline et al.; licensee BioMed Central Ltd. 2013
Received: 26 February 2013
Accepted: 3 July 2013
Published: 6 July 2013
Several plant extracts from Rutaceae family are currently used to the management of sickle cell disorder (SCD) in the African. Few reports have shown that extracts from Zanthoxyllum or Fagara genus demonstrated anti-sickling property. This study investigates the in vitro antisickling and antioxidant properties of extracts from Zanthoxyllum heitzii.
The sickling of red blood cells (RBCs) was induced using sodium metabisulfite (2%) followed by treatment with extracts at different concentrations. The osmotic fragility tests permits to explore the effect of Z. heitzii extracts on haemoglobin S solubility and sickle cells membrane stability. For each extract, qualitative phytochemical tests were used to identify the presence of alkaloids, tannins, saponins, flavonoids, glycosides and phenols, while some quantitative methods such as Folin, Ferric Reducing Antioxidant Power (FRAP) and diphenyl 1, 2 picryl hydrazyl (DPPH) were used to determine the antioxidant potential of these extracts.
Sodium metabisulphite increased the sickling of RBCs from 29.62 to 55.46% during 2 h. Treatment of sickling cells with extracts at different concentrations showed that a decrease of the percentage of sickling cells was found in both induced and non induced sickling cells. The fruits extract of Z. heitzii demonstrated the best anti-sickling property. The same extract at 250 μg/mL showed the best membrane cell stability compared to others. All the extracts revealed an antioxidant and anti-radical activities although lesser compared to the standard.
The fruit extract of Z. Heitzii demonstrated the most significant antisickling effect with a potential for use in the clinical management of SCD.
KeywordsSickling cells Reversibility Antioxidant Hemolysis Zanthoxyllum heitzii
Sickle-cell disorder (SCD), or sickle-cell anaemia is an autosomal recessive genetic blood disorder with overdominance, characterized by red blood cells that assume an abnormal, rigid, sickle shape and known to be one of the diseases afflicting the population living mostly in Africa, South America and Asia. It also occurs in other ethnic groups, including people who are of Mediterranean and Middle Eastern descent. In Cameroon, the carrier (AS/AC) rate is estimated between 20-25% while the reported prevalence of SCD is between 2-3% , and the disease is tending to become a public health problem. As a genetic hereditary disease, no specific drugs are yet available; however several treatments have been investigated: (1) medullar transplantation is not only expensive but also faces incompatibility problems; (2) various proposed drugs (hydroxyurea, piracetam, calcium antagonists) tested against this disease for inhibition of hemoglobin S polymerization inside erythrocytes in order to increase the foetal hemoglobin rate (HbF) or decrease the sickling are toxic especially for a long time of use [2, 3]. Considering all genetic disorders, the debilitating effect, the cost of managing the SCD and the greater quantities of O2–, H2O2, •OH produced from sickle RBCs than do normal RBCs , research has been on-going to determine the efficacy of the use of natural products such as medicinal plants, nutritional complement against sickle cell disorder.
Some researchers have argued in favor of nutrition in the management of sickle cell disorder . The use of traditional medicine can’t fade out in the treatment and management of an array of diseases in the African continent. Several studies demonstrated the anti-sickling property of various extracts of Rutaceae family among them Zanthoxyllum macrophyla and Fagara zanthoxyloides. The roots of F. zanthoxyloides has been used in folk medicine during sickle cell crisis and also there is recent scientific reports its antisickling activity . Various molecules with anti-sickling property such as divanilloylquinic acids, vanillic acid, p-hydroxy benzoic acid, p-fluoro benzoic acid, 2-dihyroxymethyl benzoic acid have been isolated from these plants [8, 9].
Zanthoxylum heitzii (Aubrev. & Pellegr) or Fagara heitzii is a plant from Rutaceae family. The representatives of this family are distributed in 150 genera and 1500 species commonly found in tropical and warm temperate regions of the world [10, 11]. It is a family of great importance due to its uses in perfumery, food industry and management of diseases by the Traditional Health Practitioners. Zanthoxyllum heitzii is one of the cultivar of Fagara xanthozyloïdes found in the West region of Cameroon. Its fruits is used as a spice for the preparation of “nkui” and “Nah poh”, two dishes of Cameoon . It is also used as medicinal plant in central Africa for the treatment of many diseases such as cancer, syphilis, malaria, cardiac palpitations, uro-genital affections [13, 14]. Several molecules were isolated from the stem bark of Z. heitzii among them, two amides: heitziamide A and heitziamide B and two phenylethanoids: heitziethanoid A and heitziethanoid B and s trans-fagaramide, arnottianamide, iso-c fagarine, iso-skimmianine, arctigenin methyl ether, savinin, (+)-eudesmin, (+)-sesamin, lupeol, lupeone, b-sitosterol, stigmasterol and stigmasterol-3-O-β-D-glucopyranoside . The bark of Z. heitzii is used as insecticides and revealed some activities against cadiac affections . Fagaricine, an aqueous extract formulation from root of Z. heitzii was demonstrated as an immune-restorative phytomedicine to treat immunodeficiency .
However, no studies have yet been carried out to investigate the antisickling and antioxidant properties of the various parts of this plant. The present study was performed with the aim to investigate the antioxidant property of Z. heitzii extracts, their effects on the sickling cells and on erythrocyte membrane stabilizing activities.
Plant materials and collection
Leaves, roots, fruits and stems barks of Zanthoxylum heitzii (Rutaceae) collected on the 30 June 2010 at Batchingou in the west of Cameroon and identified under the reference number 1441/H.N.C at the National Herbarium of Cameroon where the voucher specimen was deposited.
Extraction of the plant material
Air-dried leaves, fruits, roots and stems of Z. heitzii were ground and an aliquot (150 g) was extracted by maceration (72 h) in 1.5 L of water as solvent. The same procedure was repeated with residues and the mixture was filtered and concentrated to dryness. The extract was stored at 4°C in freeze - dried form and used for the study.
Collection of blood samples
The blood samples used in the evaluation of the anti-sickling activity of the plant extracts in this study were taken from patients between 19 and 31 years old known to have sickle cell disease, attending the Central hospital of Yaoundé . All these patients were confirmed regarding their SS status using the electrophoresis test. The blood samples were collected in the sodium EDTA tubes and stored for the experiment. A written informed consent was read and signed by all the patients participating in the study. All the research procedures have received the approval of Cameroon National Ethics Committee reference number 181/CNE/SE/2011 signed by Pr Lazare Kaptue, the president of the committee.
Erythrocyte membrane stability activity
The osmotic fragility of erythrocytes measures the membrane stabilizing effect of the extracts in osmotic stress/hypotonic lysis incubation. To 10 mL reaction vessel containing 4 mL of different concentrations (0.00 - 0.85%) of buffered saline with pH of 7.4, 1 ml of each extract (250 μg/mL) and 0.05 ml SS-RBC blood were added. The mixture was incubated at room temperature (25°C) for 24 h and then centrifuged at 3000 rpm for 15 min. The optical density of the supernatant was read at 540 nm against blank made of 0.85% buffered saline concentration . The mean corpuscular fragility (determined from the concentration of saline causing 50% haemolysis of the RBC) was obtained from a plot of lysis (%) versus NaCl concentration.
In vitro induction of sickling
Five milliliters blood samples obtained from patients were centrifuged at 5,000 rpm for 10 min in saline thrice to obtain the RBC which were then resuspended in normal saline and used for the analysis according to the method described . 100 μL of SS blood cell suspensions were mixed with 100 μL the presence of 2% sodium metabisulphite solution and incubated at 37°C. The time course of the sickling of SS erythrocytes was analyzed microscopically. The number of cell was counted every one hour and the percentage of sickling cells was calculated using the formula: (%) Sickling = Number of sickling cells × 100/total cells.
In vitro anti-sickling activity of the extracts
A serial of different concentrations of aqueous extracts Z. heitzii were prepared in the saline solution. For the assay 100 μL of SS-RBC pre-incubated with 2% Na2S2O5 was added to 100 μl of solution of different extracts for final concentration of 250, 500 and 1000 μg/mL. Each mixture was incubated at 37°C for 2 h (time necessary to obtain maximun sickling). After incubation, 10 μL of the mixture was diluted 100 times. A drop of each sample was examined under the oil immersion light microscope and both sickled cells and total cells were counted from five different fields of view across the slide. For the negative control, the solution containing the extract was replaced by the saline solution. The percentage of sickling was calculated using the formula: % of sickling = number of sickling cells × 100/total cells.
For the reversibility assay, freshly collected HbSS blood was diluted in 1:1 ratio with 0.9% normal saline (negative control) or test solution containing different extracts for final concentration of 250 μg/mL. The experiment was followed as mentioned above and the percentage of sickling cells was calculated.
Antioxidant and phytochemical screening
The antiradical activity of the plant extract was examined based on the scavenging effect of the stable DPPH and hydroxyl free radical activity as well as the determination of power reducing and antioxidant capacity antivities.
Scavenging Activity of DPPH Radical
The DPPH free radical scavenging assay was carried out for the evaluation of the antioxidant activity . Briefly, in 3 mL of each diluted extract, 1 ml of methanol solution of DPPH 0.1 mM was added. The mixture was kept in the dark at room temperature for 30 min and the absorbance was measured at 517 nm against a blank. The following equation was used to determine the percentage of the radical scavenging activity of each extract.
Percentage of radical scavenging activity = [(OD control - OD sample)/OD control] × 100 The IC50 value (μg/mL) is the effective concentration at which DPPH radicals were scavenged. by 50% and the value was obtained by interpolation from linear regression analysis.
Hydroxyl radical scavenging activity
The scavenging activity of the extract on hydroxyl radical was measured according to a previously described method . In 1.5 mL of each diluted extract, 60 μL of FeCl3 (1 mM), 90 μL of 1,10- Phenanthroline (1 mM), 2.4 ml of 0.2 M phosphate buffer, pH 7.8 and 150 μL of H2O2 (0.17 M) were added respectively. The mixture was then homogenized and incubated at room temperature for 5 min. The absorbance was read at 560 nm against the blank. The percentage of the radical scavenging activity of each extract was calculated from the equation below:
Percentage of radical scavenging activity = [(OD control - OD sample)/OD control] × 100. The extract concentration providing 50% inhibition (IC50) was calculated and obtained by interpolation from linear regression analysis.
Reducing power assay
One milliliter of different concentration of extract (20-80-120-240 μg/mL) diluted in distilled water was mixed with 2.5 mL of phosphate buffer (0.2 M, pH 6.6) and 2.5 mL of potassium ferrocyanide (1%). The mixture was incubated at 50°C for 20 min. Aliquot (2.5 mL) of trichloroacetic acid (10%) was added to the mixture and centrifuged at 3000 rpm for 10 min. The upper layer of the solution (2.5 mL) was mixed with 2.5 mL of distilled water and 0.5 mL of FeCl3 (0.1%). The increased absorbance was measured at 700 nm against the blank indicates the increasing of the reducing power .
Total antioxidant activity by ferric reducing antioxidant power assay (FRAP)
The FRAP method was used to determine the total antioxidant activity which measures the reduction of ferric ion to the ferrous form in the presence of antioxidant compounds . The fresh FRAP reagent consist of 500 mL of acetate buffer (300 mM pH 3, 6), 50 mL of 2, 4, 6- Tri (2- pyridyl)-s-triazin (TPTZ) (10 mM), and 50 mL of FeCl3 · 6H2O (50 mM). For the assay, 75 μL of each extract were mixed with 2 ml of FRAP reagent and the optical density was read after 2 min at 593 nm against the blank.
The standard procedure was used for screening Z. heitzii extract for the presence of alkaloids, tannins, saponins, flavonoids, glycosides and phenols .
Each test was performed in triplicate and the results were expressed as mean ± standard deviation. The Kruskal-Wallis non parametric test followed by a post hoc Dunnet T3 (p < 0.05) was used to analyze the antioxidant capacity, total phenols content as well as the radical scavenging activity of each extract. The correlation between antioxidant capacity and total phenols content was established using the Pearson product moment correlation. The IC 50 was determined with the multiple regression analysis. The software SPSS version 10.1 for Windows was used for statistical analysis.
Antioxidant and antiradical properties of the plant extract of Z. heitzii
Part of plant studied
Extraction yield (%)
In vitro antiradical and antioxidant of the extract
Antioxidant Properties (at 500 μg/mL of extract)
Reducing power (Optical density at 700 nm)
Antioxidant potential (mgEqBHT/g of extract)
8.17 ± 1.3
2.77 ± 0.4
0.12 ± 0.01
120 ± 2.4
32.25 ± 0.9
2.09 ± 0.7
0.11 ± 0.02
135 ± 1.5
8.8 ± 1.8
2.58 ± 0.3
0.12 ± 0.00
137 ± 3.5
6.60 ± 0.5
2.15 ± 0.9
0.12 ± 0.05
140 ± 5.3
12.61 ± 1.3
5.03 ± 0.3
0.23 ± 0.04
210 ± 1.9
The anti-radical and antioxidant activities of the extracts using different methods showed that these activities vary depending on the part of the plant. The IC50 of the extracts on DPPH and hydroxyl radicals varied from 6.60 to 32.25 μg/mL and from 9.2 to 3.5 μg/mL respectively (Table 1). All the extracts have significantly inhibited the hydroxyl radicals with IC50 less than 3 μg/ml except the control. The noticeable of the reducing power activity and the antioxidant properties of this plant could serve as a significant indicator of the antioxidant potential. The results of reducing power activity showed that at 50 μg/mL all the extracts demonstrated a weak activity (Table 1). The phytochemical screening of these extracts revealed the presence of alkaloids, phenols, mucilage and saponins. However, tannins and lipids were not detected in these extracts. Flavonoids are found in all extracts apart from that of the root.
For the pharmacological discovery of novel drugs, the primary essential information regarding the chemical constituents are generally provided by the qualitative phytochemical screening of plant extracts. In the present study, qualitative tests for different extracts of Z. heitzii showed the presence of several groups of bioactives molecules such as phenolics and alkaloids. Since the structure and chemical composition of plant parts affect the ability of permeability, infiltration and solubilization of groups of the bioactives compounds by the solvent, in the same way, the quantitative and qualitative differences between the phytochemical compounds in the extracts influence their biological activities. The treatment of erythrocytes with metabisulphite (2%) showed a significant augmentation of sickling. Thus sodium metabisulphite creates hypoxic conditions for red blood cells leading to the loss of the morphology and sickled erythrocytes. In vitro deoxygenation of RBC by sodium metabisulphite caused progressive aggregation and polymerization of the individual hemoglobin molecules . The process of gelation (polymerization) of hemoglobin molecules increases the formation of sickling cells. The sickle cell hemoglobin (HbS) is a product of a defective genetic code of hemoglobin molecule. The sickling cells treated with extracts at different concentrations decreased as well as the naïve red blood cells used in the reversibility study when treated at 250 μg/mL. The activity of the extracts could be due to the presence of some bioactive compounds they possess. The phytochemical screening of these extracts revealed compounds such as phenols, flavonoids, alkaloids, saponins. The anti-sickling activity could be linked to their ability either to inhibit in vitro polymerization of haemoglobin or to some structural modification linked to the environment of haemoglobin by the extracts .
Several researches have established that the capability of a biomolecule to avoid in vitro polymerization depends on one or combinations of the following options: (a) The tendency and efficiency to bind to the complimentary contact region/site of deoxyHbS monomers [25, 26]; (b) Modification of amino acid residues that contribute to the three-dimensional structures of HbS contact region and other critical sites ; (c) Stabilization of the R (relaxed) state of HbS molecule [3, 24, 27]. For sickle cell disorder, the study of antioxidants especially in various antisickling agents has a great importance because different antisickling agents have different degrees of effect.
Studies demonstrated that antioxidant molecules were found to be potent inhibitors of sickle cell haemoglobin polymerization, and equally improved the oxidant status of sickle erythrocytes [28–30]. This difference between the anti-sickling activities noted in our study could be attributed to different concentrations of the antioxidant molecules such as polyphenol, flavonoids identified in the different parts Z. heitzii. Also, the affinity of the molecule with haemoglobin binding site would determine the degree of the active anti-sickling agents. Like many proven anti-sickling agents, the most probable site for binding is the heme pocket and the erythrocyte membrane. The relation between antiradical and antioxidant activities of the extracts and their antisickling activity could be explained by the ability of these extracts to give hydrogen or electron atom to the iron molecule of haemoglobin . Antioxidants (scavengers of free radicals) are believed to be major components of the anti-sickling properties . Plants which demonstrated antioxidant property can be therapeutically useful . Thus, it is believed that the higher the antioxidant property of an antisickling agent, the higher its possible anti-sickling effect, as this enables it reduce oxidative stress that contributes to sickle cell crisis and increase the membrane protection of the cells. Since the sickle cell anemic individual undergoes oxidative stress at the onset of crises, these plants can be used to mop up any free radical released and so contribute to the effective management of the disorder. The antioxidant properties of phenolics are important in scavenging and neutralization of free radicals which can cause damage to cells if left in the system. Thus the increased intake of dietary antioxidants from Z. heitzii fruits may help to maintain an adequate antioxidant defense status and consequently contribute to the management of SCD.
The fruit extract of Z. heitzii demonstrated significant antisickling and antioxidant properties. Therefore further studies are indicated to establish these data in transgenic mice models for human SCD. In addition, the toxicity profiles and bioguided fractionation studies need to be undertaken.
The authors would like to thank all the authorities of the Central Hospital of Yaoundé and all the patients who accepted to provide their blood to conduct this study. The financial contribution of the authors helps to fund this research no other funding grants was obtained elsewhere.
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