Ameliorative effect of water spinach, Ipomea aquatica (Convolvulaceae), against experimentally induced arsenic toxicity
- Tarun K Dua†1,
- Saikat Dewanjee†1Email author,
- Moumita Gangopadhyay2,
- Ritu Khanra1,
- Muhammad Zia-Ul-Haq3 and
- Vincenzo De Feo4Email author
© Dua et al.; licensee BioMed Central. 2015
Received: 16 January 2015
Accepted: 6 February 2015
Published: 5 March 2015
Ipomea aquatica (Convolvulaceae) is traditionally used against Arsenic (As) poisoning in folk medicines in India. The present study was designed to explore the therapeutic role of aqueous extract of I. aquatica (AEIA) against As-intoxication.
AEIA was chemically standardized by spectroscopic and chromatographic analysis. The cytoprotective role of AEIA was measured on isolated murine hepatocytes. The effect on redox status were measured after incubating the hepatocytes with NaAsO2 (10 μM) + AEIA (400 μg/ml). The protective effect of AEIA (400 μg/ml) in expressions of apoptotic proteins were estimated in vitro. The protective role of AEIA was measured by in vivo assay in mice. Haematological, biochemical, As bioaccumulation and histological parameters were evaluated to ensure the protective role of AEIA (100 mg/kg) against NaAsO2 (10 mg/kg) intoxication.
Phytochemical analysis revealed presence of substantial quantities of phenolics, flavonoids, saponins and ascorbic acid in AEIA. Incubation of murine hepatocytes with AEIA (0–400 μg/ml) + NaAsO2 (10 μM) exerted a concentration dependent cytoprotective effect. Incubation of murine hepatocytes with NaAsO2 (10 μM, ~ IC50) induced apoptosis via augmenting oxidative stress. NaAsO2 treated hepatocytes exhibited significantly (p < 0.01) enhanced levels of ROS production, lipid peroxidation and protein carbonylation with concomitant depletion of antioxidant enzymes (p < 0.05-0.01) and GSH (p < 0.01) levels. However, AEIA (400 μg/ml) + NaAsO2 (10 μM) could significantly (p < 0.05-0.01) reinstate the aforementioned parameters to near-normal status. Besides, AEIA (400 μg/ml) could significantly counteract (p <0.05-0.01) ROS mediated alteration in the expressions of apoptotic proteins viz. Bcl-2, BAD, Cyt C, Apaf 1, caspases, Fas and Bid. In in vivo bioassay, NaAsO2 (10 mg/kg) treatment in mice caused significantly (p < 0.05-0.01) elevated As bioaccumulation, ATP levels, DNA fragmentations and oxidative stress in the liver, kidney, heart, brain and testes along with alteration in cytoarchitecture of these organs. In addition, the serum biochemical and haematological parameters were significantly (p < 0.05-0.01) altered in the NaAsO2-treated animals. However, concurrent administration of AEIA (100 mg/ml) could significantly reinstate the NaAsO2-induced pathogenesis.
Presence of substantial quantities of dietary antioxidants within AEIA would be responsible for overall protective effect.
Arsenic (As), a harmful metalloid, is one of the oldest known poison. It is a ubiquitous element with a ranking of 20 in the earth’s crust and 14 in sea water . Naturally occurring As compounds (arsenicals) principally exist in two forms: inorganic arsenic (in combination with oxygen, chlorine, sulfur etc.) and organic arsenic (in combination with carbon and hydrogen). However, inorganic arsenicals are considered to be the potential threat in arsenicosis. Trivalent inorganic arsenicals (arsenite) in underground water are major cause of arsenicosis affecting more than 140 million people in at least 70 countries like Afghanistan, Argentina, Bangladesh, Cambodia, Chile, China, India, Mexico, Mongolia, Myanmar, Nepal, Pakistan, Taiwan, Vietnam, sub-Shahran Africa and USA [2,3]. Following oral consumption of As contaminated drinking water, arsenites are absorbed through the gastrointestinal tract and distributed into various organs . However, arsenicals could also enter into the body via inhalation and dermal absorption. Following bioaccumulation, As participates in cellular redox events leading to generation of excessive reactive oxygen species (ROS). Besides, As has strong affinity toward thiol group, which is proposed to another pathway of developing oxidative stress during arsenicosis . The increasing oxidative stress and depletion of endogenous antioxidant system during As-intoxication trigger the apoptotic events. Oxidative stress also targets cellular macromolecules and causes oxidative damage of DNA, peroxidative damge of membrane lipids, and carbonylation of proteins and thereby participates in cellular pathophysiology . As affects almost all principle organs and tissues like liver, kidneys, lungs, heart, testes, brain and blood. Despite As toxicity as a global problem, there is no reliable, specific and safe treatment of arsenicosis. The primary treatment of As intoxication remains the chelation therapy with synthetic chelating agents like 2,3-dimercaprol, meso-2,3-dimercaptosuccinic acid and 2,3-dimercaptopropane-1-sulfonate [3,7]. However, many adverse effects including removal of essential metals and redistribution of As within tissues largely limited their clinical values [3,7,8]. On other hand, dietary antioxidants are known for long timr for their effectiveness against oxidative stress related complications without producing notable toxic manifestations. Considering the correlation between As toxicity and oxidative stress, researchers are looking forward for utilizing the dietary antioxidant/s to combat arsenicosis. In this issue, the World Health Organization (WHO) also recommended the ingestion of β-carotene, ascorbic acid, tocopherol and/or trace elements like Zn and Se to reverse symptoms of arsenicosis .
Materials and methods
Bovine serum albumin (BSA), Dulbecco’s modified Eagle’s medium (DMEM), fetal bovine serum (FBS), Bradford reagent, Collagenase type I, antibodies for immunoblotting were purchased from Sigma-Aldrich Chemical Company (St. Louis, MO), USA. Solvents (HPLC grade) were obtained from Merck, Mumbai, India. Kits for measurement of serum biochemical parameters were purchased from Span diagnostic Ltd., India. 1-Chloro-2,4-dinitrobenzene, ammonium sulphate, sodium arsenite (NaAsO2), 2,4-dinitrophenylhydrazine, ethylene diaminetetraacetic acid, 5,5-dithiobis(2-nitrobenzoic acid), N-ethylmaleimide, nitro blue tetrazolium, reduced nicotinamide adenine dinucleotide, potassium dihydrogen phosphate, phenazinemethosulphate, sodium pyrophosphate, reduced glutathione, sodium azide, thiobarbituric acid, 5-thio-2-nitrobenzoic acid and trichloro acetic acid were purchased from Sisco Research Laboratory, Mumbai, India.
Preparation of extract
Aerial parts of I. aquatica were collected in September, 2012 from West Bengal (22° 42′N, 87°32′E), India. The plant was authenticated by the Taxonomist, Botanical Survey of India, Shibpur, India and a voucher specimen (JU/PT/PC/07/12) has been deposited at the Advanced Pharmacognosy Research Laboratory, Department of Pharmaceutical Technology, Jadavpur University for future references. The plant material was dried under shade (<35°C, for 72 h), powdered and macerated with double distilled water containing 1% chloroform for 48 h (<35°C) with continuous stirring. The cellular debris were removed from extract by filtration and the resulting extract was lyophilized (Heto FD 3 Drywinner, USA) to get the crude extract AEIA (11.7%, w/w). The AEIA was suspended in tween 80 (1%) prior to each animal experiment, whereas for in vitro assay, AEIA was solubilized in DMSO (resultant ≤ 0.4% DMSO in contact to cells to avoid DMSO induced cytotoxicity).
Quantitative analysis of phytoconstituents within AEIA was determined spectrophotometrically to evaluate total flavonoids , total phenolics , total saponins  and total carbohydrates . Dionex Ultimate 3000 HPLC (hi pressure liquid chromatography) system (Dionex, Germany), equipped with a reverse phase (RP) C-18 column (250 × 4.6 mm, particle size 5 μ) and an UV detector was used for identification of individual phenolic and flavonoid compounds. Briefly, the standard markers and AEIA were dissolved in methanol (HPLC grade) and filtered by cellulose nylon membrane filter (0.45 μm). The aliquots of the filtrate were eluted with isocratic solvent mixtures comprising methanol:acetonitrile:acetic acid:o-phosphoric acid:water (20:10:1:1:20) for flavonoids, methanol:water:acetic acid (75: 24:1) for phenolics and phosphate buffer (pH 3.0; 25 mM) for ascorbic acid with a flow rate of 1 ml/min and detected at 352, 254 and 230 nm, respectively. Ascorbic acid was quantified by RP-HPLC analysis.
Healthy male Swiss albino mice (25 ± 5 g) were obtained from the Ghosh Enterprise, Kolkata, India. The animals were kept in standard polypropylene cages and were fed standard diet and water ad libitum. Animals were kept under standard laboratory conditions of temperature (22 ± 2°C), humidity (40 ± 10%) and 12 h light–dark cycle. The principles of Laboratory Animals care  and the instructions given by our institutional animal ethical committee (Reg. no. 0367/01/C/CPCSEA) were followed throughout the experiment. The animals were acclimatized for a fortnight before starting experiment.
In vitro bioassay
Hepatocytes were isolated following the protocol of Sarkar and Sil  with little modification. Briefly, livers were separated aseptically from mice after CO2 euthanasia. The excised livers were washed with ice-cold PBS (pH 7.4) and hepatocytes were isolated by collagenase perfusion followed by mechanical disruption. Hepatocytes were passed through a wide bore syringe, filtered and centrifuged (500 rpm) for 5 min. The pellet was re-suspended in DMEM containing 10% FBS and incubated at 37°C and 5% CO2 tension.
Determination of cytotoxic effect of NaAsO2
Concentration dependent cytotoxic effect of NaAsO2 was determined by cell viability assay using MTT (3-(4, 5-dimethylthiazolyl-2)-2, 5-diphenyltetrazolium bromide) . Brifely, ~2 × 105 cells/well were seeded in tissue culture plates and incubated at 37°C and 5% CO2 tension. After seeding of 24 h, the cells were treated with NaAsO2 (0.5-10000 μM). After 2 h, the cells were treated with 40 μl of FBS-DMEM medium containing MTT (2 mg/ml) and incubated for 4 h. After 4 h of incubation period, the cells were treated with DMSO (150 μl), and readings were noted spectrophotometrically at 570 and 630 nm. The differences between these two absorbances and a percentage of the corresponding controls were used to express cell viability. The experiment was repeated thrice.
Determination of cytoprotective activity of AEIA
Time and dose dependent cytoprotective role of AEIA was measured by cell viability assessment. Briefly, ~2 × 105 cells/well were seeded in tissue culture plate and incubated at 37°C and 5% CO2. Twenty four h after seeding, the cells were incubated with NaAsO2 (10 μM) along with different doses of AEIA (0–400 μg/ml). The cell viabilities at different times (0.5-4 h) were determined by MTT assay . Three independent assays were carried out.
Hoechst staining was used to detect viable nuclei by evaluation of nuclear count and morphologies under fluorescence microscopy . Briefly, 2000 cells/well were seeded in tissue culture plates and incubated at 37°C and 5% CO2. Twenty four h after seeding, the cells were incubated with NaAsO2 (10 μM) + AEIA (400 μg/ml). After 2 h, the media was removed and the cells were washed with PBS. Then the cells were fixed in paraformaldehyde (4%) in PBS for 20 min. After 20 h, paraformaldehyde was removed and the cells were washed with PBS. The cells were incubated with Hoechst 33258 (5 μg/ml in PBS) for 20 min. Fluorescent nuclei were scored and categorized according to the condensation and staining characteristics of chromatin.
Assay of antioxidant markers
Different sets of hepatocytes, each containing 1 ml of suspension (~2 × 106 cells/ml) were used in experiments. The prophylactic role of AEIA against NaAsO2-intoxication was analyzed by incubating hepatocytes with extracts (400 μg/ml) and NaAsO2 (10 μM) together for 2 h at 37°C. One set of hepatocytes incubated with NaAsO2 (10 μM) and one set without any treatment were kept as toxic and normal control, respectively. Generation of intracellular ROS has been quantified by the slightly modified method of LeBel and Bondy  and 2′, 7′-dichlorofluorescein (DCF) formation was measured by using a fluorescence microscopy. The degree of lipid peroxidation was measured by estimating thiobarbituric acid reactive substances (TBARS) following the protocol of Ohkawa et al. . The level of protein carbonylation was determined in accordance to Uchida and Stadtman . A previously reported method of Ghosh et al.  was used to assess the level of intracellular antioxidant enzymes like catalase (CAT), superoxide dismutase (SOD), glutathione peroxidase (GPx), glutathione reductase (GR) and glutathione-S-transferase (GST), while, non-enzymatic antioxidant viz. reduced glutathione (GSH) level was measured by the method of Hissin and Hilf .
Immunoblotting of signaling proteins
Cells under different treatments were separated by centrifugation (800 g, for 5 min). The isolated cells were treated with 30 μl of lysis buffer and incubated within ice for 30 min followed by centrifugation (14000 g, for 10 min) to remove cellular debris and to isolate proteins as supernatant. Samples containing proteins (20 μg) were subjected to SDS-PAGE (10%) and transferred to a nitrocellulose membrane following standard dry transfer protocol. Membranes were blocked (4°C; 1 h) using Tris-buffered saline with 0.1% Tween 20 (TBST) containing non-fat dry milk (5%) to prevent non-specific binding with gentle shaking. The membranes were washed with TBST (pH 7.6) for three times (5 min, each) with gentle shaking. Then the membranes were incubated with primary antibodies viz. anti-caspase 3 and 9 (1:2000), anti-caspase 8 (1:1000), anti-Bad (1:3000), anti-Bcl-2 (1:3000), anti-Fas and anti-Bid (1: 1000), anti-cytochrome (Cyt) C and anti-Apaf (apoptotic protease activating factor) 1 (1: 2000) in TBST containing 5% of BSA at 4°C overnight with gentle shaking. The membranes were washed with TBST (pH 7.6) for three times (5 min, each) with gentle shaking and incubated with appropriate HRP conjugated secondary antibody (1:3000 dilution) in TBST containing non-fat dry milk (5%) for 1 h at room temperature and finally developed by the HRP substrate 3, 3′-diaminobenzidine tetrahydrochloride system (Bangalore Genei, India). The Western blot analysis and densitometry studies were performed using Image Lab 5.2 software (Bio-Rad, CA, USA).
In vivo bioassay
Group I: Normal control, animals received only 1% tween 80 (p.o., once daily) for 15 days;
Group II: Toxic control, mice treated with NaAsO2 (10 mg/kg body weight, p.o., once daily) for 10 days
Group III: Animals were treated with AEIA (100 mg/kg body weight, p.o., once daily) for 15 days, prior to NaAsO2 (10 mg/kg body weight, p.o., once daily) for 10 days .
Based on in vitro data and previous observations, an optimum dose of AEIA of 100 mg/kg body weight was used in vivo study as per the recommendation of Institutional animal ethical committee.
On day 16, the treated mice were subjected to CO2 euthanasia and sacrificed by cervical dislocation. For haematological assays, blood samples were collected from retro-orbital venous plexus in Eppendorf tubes rinsed with anticoagulant before sacrificing. The organs (liver, kidney, brain, heart and testes) were excised, cleaned and washed three times with PBS to remove adherent blood. The organs were homogenized in 0.1 M Tris–HCl-0.001 M EDTA buffer (pH 7.4) and centrifuged (12,000 g; 30 min) at 4°C. The supernatant were collected and used for assaying biochemical parameters.
Haematological and serum biochemical parameters
Total erythrocyte count and haemoglobin content were determined by using standard laboratory procedures. Serum biochemical parameters viz. alanine aminotransferase (ALT), aspartate aminotransferase (AST), creatinine kinase (CK), cholesterol, lactate dehydrogenase (LDH), urea, and triglycerides were estimated by commercially available kits (Span Diagnostic Limited, India).
Assessment of antioxidant markers related to organ dysfunction
Distribution of As in tissues was measured by flame atomic absorption spectroscopy . The antioxidant enzymes, intercellular ROS, lipid peroxidation, protein carbonylation, and non-enzymatic antioxidant were assayed following standard assay protocols mentioned earlier. Co-enzymes Q (Q9 and Q10) were isolated and estimated by HPLC a previously described method of Zhang et al. . Intracellular ATP concentrations were assessed by commercial kits (Abcam, Cambridge, USA) following manufacturer protocol.
The mice organs’ from different groups were fixed in buffered formalin (10%) and were processed for paraffin sectioning. Organ sections (5 μm) were stained with hematoxylin and eosin to study the histology of organs .
Data were statistically analyzed by one way ANOVA and represented as mean ± SE followed by Dunnett’s t-test using GRAPHPAD INSTAT version 3.05 (GraphPad software, CA, U.S.A). The values were considered significant when p < 0.05. The graphs were drawn using GRAPHPAD PRISM version 6 (GraphPad software, CA, U.S.A).
Quantitative phytochemical analysis revealed substantial quantities of flavonoids (~37.9 mg/gDW), phenolics (~22.7 mg/gDW), saponins (~51.2 mg/gDW), carbohydrates (~132.7 mg/gDW) and ascorbic acid (~3.1 mg/gDW). The identification of phenolics and flavonoids were done by comparing retention time (Rt) and UV spectra with standard flavonoids and phenolic compounds by using RP-HPLC analysis. The results revealed presence of flavonoids namely myricetin, quercetin and apigenin in AEIA (Additional file 1: Figure S1, Panel A). In search of phenolics, AEIA revealed presence of gallic acid and chlorogenic acid (Additional file 1: Figure 1, Panel B). HPLC analysis of ascorbic acid has been depicted in Additional file 1: Figure S1, Panel C.
Effect of AEIA against NaAsO2-intoxication in vitro
Dose dependent effect of NaAsO2 induced cytotoxicity
Dose dependent cytoprotective role of AEIA against NaAsO2 induced cytotoxicity
Results of the dose dependent protective role of AEIA (50–400 μg/ml) in NaAsO2 (10 μM) induced cytotoxicity in hepatocytes have been depicted in Figure 2B. NaAsO2 (10 μM, ~ IC50) exposure caused significant reduction in cell viability up to 4 h. Simultaneous treatment of hepatocytes with AEIA (50–400 μg/ml) and NaAsO2 (10 μM) prevented the reduction in cell viability in a concentration dependant manner. However, after 2 h the cytoprotective effect appeared to be optimum. Based on this observation, the concentration of AEIA, and incubation time have been calibrated as 400 μg/ml and 2 h, respectively, for subsequent in vitro study.
Effect on Hoechst staining
The anti-cytotoxic effect of AEIA was estimated by fluorescence microcopy after Hoechst staining (Figure 2C) of hepatocytes under different treatments. NaAsO2 (10 μM) treated hepatocytes showed significantly less number of visible nuclei; however, the visible nuclei exhibited specific pattern of morphological changes, condensation, fragmentation of the nuclei and chromatin condensation. Simultaneous incubation of hepatocytes with AEIA (400 μg/ml) and NaAsO2 (10 μM) could significantly counteract the cytotoxic effect of NaAsO2 (10 μM) and restore nuclear morphology near to normalcy.
Effect on redox status
Effect on intrinsic and extrinsic pathways of cell death
Effect of AEIA against NaAsO2-intoxication in vivo
Effect on haematological and serum biochemical parameters
Effect on haematological and serum biochemical parameters in absence (NaAsO 2 ) and presence of AEIA (AEIA + NaAsO 2 ) in mouse
Total erythrocyte count (x10 6/ mm 3 )
Lactate dehydrogenase (U/l)
Creatinine kinase (IU/ mg protein)
6.05 ± 0.28
9.12 ± 0.79
72.21 ± 4.11
53.33 ± 3.44
24.17 ± 2.25
32.48 ± 2.11
205.56 ± 12.33
132.45 ± 7.11
122.41 ± 7.12
3.25 ± 0.22#
5.24 ± 0.76#
154.22 ± 7.43#
78.35 ± 4.72#
58.11 ± 3.41#
64.04 ± 3.50#
284.67 ± 16.17$
191.14 ± 7.22#
238.33 ± 10.94#
4.98 ± 0.27**
8.17 ± 0.54**
105.23 ± 5.02*
59.67 ± 3.92**
42.14 ± 2.01**
54.92 ± 3.88*
231.71 ± 17.92*
161.45 ± 6.25*
168.85 ± 9.15**
The haematological parameters exhibited significant (p < 0.01) reduction in total erythrocyte counts and haemoglobin content in NaAsO2 (10 mg/kg) treated mice (group II). However, simultaneous administration of AEIA (100 mg/kg) along with NaAsO2 (10 mg/kg) could significantly reinstate the erythrocyte counts (p < 0.01) and haemoglobin content (p < 0.01) to near-normal status. NaAsO2 (10 mg/kg) treated mice exhibited a significant (p < 0.01) increase in AST, ALT, urea, lactate dehydrogenase, creatinine kinase, cholesterol and triglyceride levels. However, concurrent administration of AEIA (100 mg/kg) along with NaAsO2 (10 mg/kg) could significantly reinstate the serum biochemical parameters near to normalcy.
Effect on ss bioaccumulation
Effect on DNA fragmentation and ATP level
The percentages of DNA fragmentation in brain, kidney, heart, liver and testes of the experimental mice have been depicted in Figure 6B. Daily administration of NaAsO2 (10 mg/kg, up to 10 days) significantly increased (p < 0.01) the DNA fragmentation in the hepatic, renal, cardiac, cerebral and testicular tissues amounting ~ 148%, 152%, 138% and 130 and 135%, respectively. However, concurrent administration of AEIA (100 mg/kg) along with NaAsO2 (10 mg/kg) could significantly (p < 0.01) inhibit DNA fragmentation in aforementioned tissues. Intercellular ATP level within the tissues is an indicative of pathophysiological events. In this study, intracellular ATP level in the selected tissues was investigated (Figure 6C). It was observed that, NaAsO2 caused significant (p < 0.01) increment in intracellular ATP levels in mice tissues. Concurrent administration of AEIA (100 mg/kg) along with NaAsO2 (10 mg/kg) could significantly (p < 0.01) reinstate the ATP level near to normalcy.
Effect on redox status
Effect on histology of organs
As, a toxic element, exerts toxic manifestations in different organs. Generation of excessive ROS viz. super oxide radical, hydrogen peroxide and hydroxyl radical, is proposed to be the principle mechanism in As-intoxication . ROS is not only responsible to induce peroxidative alteration of cellular lipids, carbonylation of proteins, fragmentation of DNA, reduction of cellular antioxidant molecules in the biological systems, but also affect the cell proliferation index by altering the signal transduction, cell cycle control, cellular differentiation and apoptosis . The present study describes the protective role of AEIA against As toxicity employing suitable in vitro and in vivo preclinical assays. In this study, NaAsO2 (10 μM) exerted a significant reduction of the viability of murine hepatocytes in vitro. Hoechst staining of As-intoxicated hepatocytes confirmed the observation of cell viability assay and induction of apoptosis. Moreover, a distinct pattern of visible nuclei with chromatin condensation were noticed in Hoechst staining of NaAsO2-intoxicated hepatocytes. However, simultaneous incubation of hepatocytes with AEIA (400 μM) + NaAsO2 (10 μM) could reinstate the viability of cells, apparent from both cell viability and image assay.
Haematological and serum biochemical parameters stay earlier indicators of any pathophysiological state. In this study, a considerable reduction in total erythrocyte count and haemoglobin content was observed in NaAsO2-intoxicated mice, which is in accordance to the observation by Kavita et al. . Cell viability and membrane integrity are directly related to each other. The increased concentrations of tissue specific enzymes in serum are the indications of membrane leakage. LDH and CK are the intracellular enzymes having high tissue specificity [31,34]. Increased levels of serum LAD and CK in NaAsO2 (10 μM) intoxicated mice supported the membrane damage and concomitant reduction of cell viability. As undergoes biotransformation in the liver where it binds with the thiol group of proteins and enzymes, thereby, interferes the integrity of plasma membrane of hepatocytes leading to leakage of AST and ALT in serum [34,35]. As-intoxication significantly increased serum level of urea, which may be indicative of protein catabolism and renal dysfunction . In this study, NaAsO2-intoxicated mice exhibited hyperlipidemia evidenced by significantly higher cholesterol and triglycerides levels in serum, which is in accordance to the observation by Das et al. . Increased synthesis or decreased removal of lipoproteins can be the possible reason of As-mediated hyperlipidemia. Concurrent treatment with AEIA along with NaAsO2 could significantly reinstate the haematological and serum biochemical parameters to near-normal status, which is an indicative of therapeutic potential of AEIA against As-intoxication.
NaAsO2-induced toxicity is associated with ROS generation which exerts direct toxic effect on critical tissues and attributes in apoptotic cell death. In this study, a significant increase in the accumulation of intercellular ROS was observed in both in vitro and in vivo assays. The inexorable generation of ROS during As-intoxication could be associated with elevated levels of lipid peroxidation and protein carbonylation. Both are principally involved in oxidative modifications of structural lipids and proteins of cell membrane leading to cell membrane damage . However, co-administration of AEIA along with NaAsO2 could significantly inhibit lipid peroxidation and protein carbonylation via direct scavenging/quenching free radicals (ROS) produced during As-intoxication.
Ubiquinols (co-enzymes Q) functions as cellular electron transporters, thereby, act as antioxidants through scavenging ROS . Co-enzymes Q are distributed within all major organales of cells including mitochondria, Golgi apparatus, endoplasmic reticulum, lysosomes, peroxysomes etc. A significant reduction of co-enzymes Q (Q9 and Q10) levels indicated the redox stress during As-intoxication. The accumulation of intracellular As may interfere with the activity of the enzyme viz. cytosolic NADPH-CoQ reductase accountable for the reduction of ubiquinone to ubiquinols . Simultaneous administration of AEIA along with NaAsO2 could significantly reinstate co-enzymes Q levels in the tissues. The extracts might exert this effect through promoting clearance of As from the system.
The intra-cellular antioxidant system comprises antioxidant enzymes along with some non-enzymatic antioxidants. SOD and catalase are important radical scavenging enzymes. SOD acts by quenching the superoxide radicals leading to the formation of hydrogen peroxide and molecular oxygen, while, CAT is well known to detoxify hydrogen peroxide . GPx coupled with GR accelerates reduction of lipid peroxide by the reaction with GSH . GST protects cells against oxidants by removing free radicals. Significant reduction of these antioxidant enzymes during As-intoxication may be due to an enhanced production of ROS and/or down-regulation in the synthesis of antioxidant enzymes by persistent toxic effect of NaAsO2 . Thiol-based antioxidant system, GSH, helps to protect cells from ROS . The metabolism and excretion of As is dependent on GSH. In liver, As is metabolized into soluble mono-, di- or tri hydroxyl arsenic acid in presence of GSH . As has strong affinity toward thiol group resulting depletion of GSH level in the tissues of NaAsO2-intoxicated mice confirmed this fact. Significant reduction of GR and GPx levels may be accountable to reduction of GSH in the tissue of As-intoxicated mice.
Intracellular As accumulation is thought to be major concern in chronic arsenicosis. The cellular uptake of arsenic has been investigated. In this study, NaAsO2-intoxication caused significantly high levels of bioaccumulation of As within the tissues. Increment of As burden within the tissues directly proportional to the redox stress via excessive generation of ROS. ROS down-regulates GSH and glutathione dependent enzymes which participate in As clearance via transforming into soluble methylated arsenic acid . However, concurrent treatment with AEIA along with NaAsO2 could significantly reduce As accumulation within the tissues. The AEIA could exert this effect either by inhibiting ROS and restoring glutathione system to promote As clearance via bio-transformtion into soluble methylated arsenic acid and/or by promoting the clearance of intercellular As via chemo-transformation into soluble chelate with As. Presence of substantial quantities of dietary antioxidants (flavonoids, phenolics and ascorbic acid) and metal chelating metabolites (flavonoids and saponins) within the test extract would be accountable for As-clearance [36,41,42].
Intercellular redox stress plays an important role in DNA damage. The most reactive hydroxyl radical reacts with pyrimidine bases principally thiamine and remove a hydrogen atom from methyl group and -C-H bond of deoxyribose . As a result, DNA strands are broken and/or DNAs are cross-linked. The DNA fragmentation plays a pivotal role in cell-death process in diabetic pathophysiology. In this study, significant DNA fragmentation was notices in the tissues of NaAsO2 intoxicated mice. However, AEIA could significantly counteract with DNA fragmentation probably by scavenging ROS and reducing oxidative stress.
Apoptosis, a self-destructive mechanism, is accomplished by mitochondrion-dependent (intrinsic) and/or independent (extrinsic) pathways. Redox stress attributes a principle role in initiation and execution of apoptotic pathway. A significant increase in the intracellular ATP concentration supported the incidence of apoptosis. Apoptosis is primarily executed by up-regulation of some pro-apoptotic and down-regulation of anti-apoptotic transcription proteins. Bcl 2, a member of anti-apoptotic protein, acts on the mitochondria to regulate the release of cytochrome c and initiate the caspases dependent apoptotic pathway. Bad, a pro-apoptotic protein, can modulate the pro-apoptotic processes by inhibiting Bcl 2 proteins . Cyt C promotes ATP dependant formation of apoptosome by the aggregation of caspase 9 together with Apaf1 resulting in caspase 9 activation . Caspase 9 then activates the rest of the caspase cascade by triggering the caspase 3 leading to apoptosis. The death receptor, Fas, Bid and caspase 8 comprise the extrinsic receptor mediated pathway. The Fas system activates caspase 8 which interacts with the intrinsic apoptotic pathway through activation of Bid, a pro-apoptotic protein . In the present study, immunoblot analyses confirmed the involvement of both intrinsic and extrinsic pathways of apoptotic cell death in NaAsO2-intoxicated hepatocytes. However, AEIA could significantly reinstate these changes in transcription levels of apoptotic proteins near to normal status. Radical scavenging activity of AEIA would be accountable to anti-apoptotic activity of extract.
Finally, histological assessments showed that NaAsO2 caused abnormal histological changes within the tissues. However, pre-treatment with the extract could attenuate these histological changes and restore cyto-architecture near to the normal status.
In this study, we observed presence of phenolics (gallic acid and chlorogenic acid) and flavonoids (myricetin, quercetin and apigenin) in AEIA. Phenolics and flavonoids are potent antioxidants , which prevent apoptosis caused by oxidants . Phenolics have been reported to exhibit anti-apoptotic potential through a Bcl-2 independent mechanism [48,49], while, anti-apoptotic activity of flavonoids is thought to be mediated at the mitochondria (intrinsic) levels . Earlier investigation revealed the prophylactic effect of ascorbic acid against As-toxicity through antioxidant mechanism . Presence of substantial quantity of ascorbic acid in AEIA would play crucial role in overall protective effect against As-toxicity. On other hand, phenolics and saponins have been reported to exhibit chelating properties to mop up arsenites from the body [42,51]. Therefore, phenolics, flavonoids, ascorbic acid and saponins within AEIA would offer a cumulative effect to ensure the protection against As-intoxication.
The financial support of the Council for Scientific and Industrial Research, New Delhi, India is gratefully acknowledged through Senior Research Fellowship to Mr. Tarun K. Dua [CSIR- SRF Ref. No.: 09/096(773)/2013-EMR-I dated 15th March, 2013]. Authors are grateful to Jadavpur University, Kolkata, India for providing necessary facilities for this study. Finally, the authors would like to say thanks to the reviewers for their time and valuable comments to improve the quality of this manuscript.
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