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Haloalkane induced hepatic insult in murine model: amelioration by Oleander through antioxidant and anti-inflammatory activities, an in vitro and in vivo study
© The Author(s). 2016
Received: 28 January 2016
Accepted: 5 August 2016
Published: 11 August 2016
Nerium oleander L. (syn. Nerium indicum Mill, Nerium odorum Aiton) belongs to the family Apocynaceae. It is used for its anti-inflammatory, anti-diabetic, anti-cancer and hepatoprotective activities in traditional medicine. Previous pharmacognostic studies suggested that 70 % hydro-methanolic extracts of oleander possess potent free radical scavenging and anti-inflammatory activities, both of which are helpful against hepatotoxicity.
Hydro-methanolic extracts of oleander stem and root were evaluated for their hepatoprotective activities in acute CCl4 intoxicated mouse through in vitro and in vivo studies. Silymarin was used as positive reference. Antioxidant enzymes, pro-inflammatory markers and liver enzymatic and biochemical parameters were studied. The extracts were further chemically characterized using Fourier Transform Infrared (FTIR) spectroscopy and Gas chromatography-mass spectrometry (GC-MS).
CCl4 toxicity caused fatty liver formation by increase of relative liver weight (32.53 g) compared to control group (16.08 g). The elevated liver enzymatic and biochemical parameters due to CCl4 toxicity were considerably normalized by the extracts treatment under both in vivo and in vitro models. Oleander stem (NOSE) and root (NORE) extracts increased the reduced hepatic catalase activity 27.37 and 25.25 %, whereas peroxidase activity was increased 18.19 and 22.78 %, respectively. The extent of lipid peroxidation was significantly (p < 0.01) lowered 20.76 % (NOSE) and 21.12 % (NORE) compared to CCl4 group. The levels of pro-inflammatory tumor necrosis factor-α (TNF-α) was lowered 71.33 % (NOSE) and 61.60 % (NORE). Histopathological study demonstrated substantial reduction of hepatocellular necrosis, fatty infiltration, sinusoidal dilation, bile duct proliferation, vascular congestion, leukocyte infiltration in the silymarin and extract treated groups. Furthermore, various bioactive compounds were identified in the extracts such as apocynin, tocopherol, squalene, vanillin, isoeugenol, amyrin, lupeol etc.
The present study provided convincing evidence that oleander extracts possess potent hepatoprotective capacity which was primarily governed by its antioxidant and anti-inflammatory activities. The collegial bioactivities of the phytochemicals may be accredited behind the hepatoprotective activity of oleander.
KeywordsHepatoprotective Inflammation Liver Nerium Oxidative stress Xenobiotic
The liver is the largest organ of our body, contributing about 2 % of the total body weight. The liver is associated with most of the metabolic and physiological process including growth, immunity, nutrition, energy metabolism and reproduction . Production of different coagulation factors, antithrombin, thrombopoietin, angiotensinogen, insulin-like growth factor 1, albumin, catabolism of bilirubin and various hormones takes place in the hepatic system. Liver performs central role in the biotransformation and metabolism of xenobiotic compounds, which in some case results in liver damage . Though the liver possesses tremendous regenerative capacity, but very often subclinical live injury occurs due to toxic chemicals and their metabolic intermediates. Around the globe, drug induced hepatotoxicity has emerged as a serious medical concern where 10 % cases of acute liver failures are associated with idiosyncratic hepatotoxicity . Drug induced hepatotoxicity has now appeared as the leading cause behind acute liver failure among the US patients . The liver is one of the decisive organs of the body and therefore, requires safeguard from harmful chemicals.
Persistent exposure to xenobiotics, especially synthetic drugs and environmental chemicals cause serious liver damage due to its portal location in the circulation and central role in detoxification [5, 6]. Most xenobiotics are lipophilic in nature and thus, are poorly excreted by the kidney. The liver performs a critical role in biotransformation of such xenobiotics to more polar form in order to facilitate their excretion . Halogenated alkanes are organic xenobiotics which holds the potentiality to cause severe liver injury [2, 6]. CCl4 is a model haloalkane which is extensively used to study the pathophysiological implications of xenobiotic metabolism and hepatoprotective potentialities of natural compounds . Xenobiotic mediated liver damage like CCl4 toxicity, is primarily governed by free-radical mediated tissue injury and inflammatory damages. CCl4 cause hepatocellular ionic imbalance, oxidative stress, translational inhibition, Ca2+ shift, mitochondrial respiratory chain blockage and impairment of β-oxidation [9, 10]. Histopathological signs of CCl4 toxicity includes zonal haemorrhagic necrosis, fatty infiltration, sinusoidal dilation, calcification, vascular congestion, bile duct proliferation and leukocyte infiltration .
Previously, we have demonstrated that the 70 % hydro-methanolic extracts of oleander possess potent antioxidant capacity . The extracts also demonstrated free radical scavenging activities against various reactive species associated with hepatotoxicity such as hydroxyl (OH●), superoxide (O2 ●−), peroxynitrite (ONOO−), singlet oxygen (1O2), hydrogen peroxide (H2O2) and nitric oxide (NO), in addition to potent iron (Fe2+) chelation activities, overload of which may lead to haemochromatic liver . It is interesting to note that, a recent in vivo preliminary study demonstrated that N. indicum leaf extract ameliorates haemochromatic conditions in mouse . Moreover, another recent study showed that N. indicum leaf extract attenuates CCl4 mediated hepatotoxicity in Swiss albino mouse . Simultaneously, the same 70 % hydro-methanolic extract of oleander leaf possess anti-inflammatory activities by modulation of Th1/Th2 cytokine balance, inhibition of cyclooxygenase, prostaglandin E2 (PGE2) and nitric oxide levels in mitogen induced splenic lymphocytes [15, 16]. Moreover, diverse pharmacognostic activities such as anti-diabetic, anti-microbial, antinociceptive, neuroprotective, anti-ulcer, anti-cancer etc. of oleander extracts and oleander derived bioactive components has also been demonstrated previously .
Oleander is extensively used as herbal medicine in different parts of the world . The pharmacognostic studies are mostly limited to the bioactivities of its leaf extracts. However, traditional therapies suggests extensive use of oleander stem and root to cure diverse ailments . Therefore, the present study was initiated to evaluate the proposed hepatoprotective potentiality of steam and root extracts of oleander against haloalkane induced hepatic injury in murine model. The study was supported by both in vitro and in vivo experiments. Further, phytochemical characterization were carried out using FTIR and GC-MS methods to reveal the bioactive constituents in the extracts and to correlate the individual bioactivities of the phytochemicals with the proposed hepatoprotective potentiality of oleander stem and root.
All the chemicals were procured from Sisco Research Laboratories Pvt. Ltd. (Mumbai, India) unless otherwise indicated. Silymarin was obtained from Sigma-Aldrich (USA). Fetal bovine serum (FBS), RPMI-1640, antibiotics and EZcount™ MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) Cell Assay Kit were purchased from HiMedia Laboratories Pvt. Ltd. (Mumbai, India). Albumin, γ-glutamyl transferase (GGT), lactate dehydrogenase (LDH), alkaline phosphatase (ALP), bilirubin, protein, aspartate transaminase (AST), acid phosphatase (ACP), alanine transaminase (ALT), glucose, urea and cholesterol estimation kits were obtained from Crest Biosystems (Goa, India). TNF-α ELISA kit was procured from Ray Bio (Georgia, United States) and Thiobarbituric acid reactive substances (TBARS) assay kit was purchased from Cayman chemical company (USA). Milli-Q ultrapure water from the departmental central facility was used in the experiments.
Preparation of plant extract
Stem and root samples of white flowered variety of oleander were collected from the garden of University of North Bengal (26.71°N, 88.35°S), India. The plant materials were identified by senior plant taxonomist Prof. Abhaya Prasad Das of Department of Botany, University of North Bengal. The voucher specimen was stored at the herbarium of Department of Botany, University of North Bengal with an accession number of 09618.
The stem and root samples were washed properly with double distilled water to remove any dust and foreign materials. The samples were then chopped to 0.5 cm pieces and shade dried at laboratory temperature (25 °C). After 20 days, 70 % hydro-methanolic extract of Oleander stem and root were prepared according to the previous method . A schematic representation of the extract preparation method is provided in the Additional file 1. The lyophilized extracts were stored at −20 °C until further use. The final yield of oleander stem (NOSE) and root (NORE) extracts were 11.82 and 15.22 % of dry weight (DW).
Swiss albino mice (6–8 weeks, 20–25 g) of both sex (3 male and 3 female per group) were maintained inside cage bins (Tarson, India) with rice husk bedding in the animal house of the Department of Zoology, University of North Bengal at a constant 12 h photoperiod (temperature 25 ± 2 °C; humidity 55 ± 5 %) with food and water ad libitum. All the experiments were approved by the ethical committee, University of North Bengal (No. 840/ac/04/CPCSEA) and conducted in accordance with the legislation for the protection of animals used for scientific purposes.
Acute toxicity study
OECD guidelines (test 423: Acute oral toxicity – Acute toxic class method, 2002) were followed to study the acute toxicity of the extracts . Mice were divided into eight groups (n = 6) and fasted overnight prior to the experiment. NOSE and NORE were administered orally at 250, 500, 1000 and 2000 mg/kg body weight (bw) dose. Each groups were carefully observed at 30 min and then 2, 4, 8, 24 and 48 h for development of any clinical or toxicological symptoms such as tremors, convulsions, salivation, diarrhoea, lethargy, sleep, coma and alteration in respiratory patterns, skin colour, behaviour pattern etc.
Experimental design: in vivo
Animals were divided into 7 separate groups (n = 6) and following treatments were done once each day for 10 consecutive days: Control group received normal saline; CCl4 group received 1:1 (v/v) CCl4 in olive oil; Silymarin group received 1:1 (v/v) CCl4 in olive oil and 100 mg/kg bw silymarin; NOSE low group received 1:1 (v/v) CCl4 in olive oil and 50 mg/kg bw NOSE; NOSE high group received 1:1 (v/v) CCl4 in olive oil and 200 mg/kg bw NOSE; NORE low group received 1:1 (v/v) CCl4 in olive oil and 50 mg/kg bw NORE; NOSE high group received 1:1 (v/v) CCl4 in olive oil and 200 mg/kg bw NORE.
On 11th day i.e., 24 h after the last treatment, under anaesthesia (2 % ether), blood was collected from the treated animals by cardiac puncture and finally the animals were sacrificed. Blood was allowed to clot for 60 min at room temperature (25 °C) and then serum was collected by centrifuging at 1000 rpm for 5 min. The straw coloured serum was used to study liver marker enzymes. Liver samples were collected and washed with double distilled water to remove blood and used for antioxidant enzymatic assays. Liver tissue required for histological study were collected in Bouin’s solution.
Liver function test: in vivo
Serum samples from each group were used to study ACP, albumin, globulin, glucose, ALP, bilirubin, cholesterol, LDH, GGT, AST, ALT, total protein and urea levels using commercially available kits (Crest Biosystems).
Estimation of peroxidase and catalase activities
Peroxidase activity in the liver samples were estimated by measuring the oxidation of guiacol according to a standard method . Catalase activity was measured by degradation of substrate H2O2 by catalase in the liver tissue samples following the standard method described by Luck .
Experimental design: in vitro
The in vitro hepatoprotective capacity of NOSE and NORE were studied according to previously standardized methods with minor modifications [14, 21, 22]. Briefly, seven groups of primary explant culture of mice hepatocytes were prepared in RPMI-1640 medium (containing 50 U/ml penicillin, 50 U/ml streptomycin and 50 U/ml nystatin) supplemented with 10 % FBS. After 48 h of the culture, the following treatments were done: Control had no separate treatment; CCl4 group received 25 μl/ml CCl4; Silymarin group received 25 μl/ml CCl4 and 100 μg/ml silymarin; NOSE low group received 25 μl/ml CCl4 and 25 μg/ml NOSE; NOSE high group received 25 μl/ml CCl4 and 100 μg/ml NOSE; NORE low group received 25 μl/ml CCl4 and 25 μg/ml NORE and NORE high group received 25 μl/ml CCl4 and 100 μg/ml NORE.
The plates were incubated for 2 h and then culture supernatants were collected by centrifugation (5000 rpm for 10 min).
Liver function test: in vitro
Culture supernatants from each group were analysed for ACP, ALP, bilirubin, LDH, AST, ALT and total protein levels using commercially available kits (Crest Biosystems).
Measurement of lipid peroxidation
The extent of lipid peroxidation was measured in six sets using TBARS assay kit (Cayman) according to the manufacturer’s instructions. In brief, 100 μl serum samples of different groups were mixed with 100 μl sodium dodecyl sulphate (SDS) solution. The tubes were placed on boiling water bath after addition of 4 ml colour reagent. After 60 min incubation, the tubes were kept on ice for 10 min to stop the reaction. Then the solutions were centrifuged (1600 g) for 10 min at 4 °C and the absorbance of the supernatants were recorded at 340 nm.
Measurement of TNF-α
The amount of TNF-α released in culture supernatants were measured using TNF-α ELISA kit (Ray Bio) according to the manufacturer’s instructions. Absorbance was immediately measured at 450 nm using Bio-Rad iMark™ microplate absorbance reader. Standard was run in parallel to the samples.
Measurement of inhibition of NO
Culture supernatants were used to determine the NO level using the Griess reagent method  with some modifications. Briefly, culture supernatants (60 μl) from each group was mixed with 240 μl of Griess reagent (1 % sulfanilamide and 0.1 % N-(1-naphthyl) ethylenediamine hydrochloride in 2.5 % H3PO4) in a 96-well plate and incubated for 20 min at room temperature. The purple azo-dye formed, was detected at 540 nm.
Measurement of cell viability
Hepatocyte necrosis results due to CCl4 toxicity. Therefore, MTT assay was performed to measure the protection rendered by NOSE and NORE against CCl4 mediated toxicity. Hepatocytes were cultured as described under the in vitro experimental section. The cell viability assay was performed in six sets using EZcount™ MTT Cell Assay Kit (HiMedia) according to the manufacturer’s instructions.
Liver samples were removed from the animals of the in vivo experiments after collection of blood and were fixed overnight in 10 % buffered formalin. The samples were subjected to dehydration and then embedded in paraffin blocks. Thick sections (4 μm) of the paraffin embedded livers were cut in a microtome and then dewaxed in xylene, rehydrated in a series of different grades of alcohol and then washed with distilled water for 5 min. Subsequently, the sections were stained with haematoxylin for 40 s and counterstained with eosin for 20 s. The sections were dehydrated in graded alcohol series and washed in xylene. The slides were observed (100× and 400×) for signs hepatic injury using Nikon ECLIPS E200 microscope.
Fourier Transform Infrared (FTIR) spectroscopy analysis
FTIR spectrophotometry was used to identify the characteristic functional groups in NOSE and NORE. Small quantity (<10 mg) of dried extracts were taken in CaF2 vessel and placed in the sample cup of a diffuse reflectance accessory. The IR spectrum was obtained using Shimadzu 8300 FTIR spectrophotometer at ambient temperature. Background correction was made by taking IR spectrum of de-ionized water as the reference in identical condition. The sample was scanned from 400 to 4000 cm−1 for 16 times to increase the signal to noise ratio.
NOSE and NORE were initially bi-fractionated by dissolving in dichloromethane and n-hexane separately. The mixtures were centrifuged thrice (12,000 rpm) for 15 min. The clear supernatant was used for GC-MS analysis using Agilent 5975C GC-MS system (Agilent Technologies, USA) attached with HP-5 ms Capillary Column (30 m × 0.25 mm i.d. × 0.25 μm film thickness). The machine was equipped with inert MSD triple axis mass detector conditioned at ion trap 200 °C, transfer line 280 °C, electron energy 70 eV (vacuum pressure- 2.21e–0.5 torr) was used for analysis. Helium was used as carrier gas (1 ml/min). Sample volume was 2 μl and injected in a splitless mode. The column temperature was kept at 60 °C for 1 min followed by 5 °C/min up to 250 °C. The major and essential compounds present in samples were identified by their retention times and mass fragmentation patterns using Agilent Chem Station Integrator and the database of National Institute Standard and Technology (NIST) with a MS library version 2010.
All data are reported as mean ± SD of six measurements. Statistical analysis was performed and graphs were prepared using KyPlot Data Analysis and Visualization software version 5.0.2 (32 bit). Comparison between groups were performed using one-way analysis of variance (ANOVA). p < 0.05 was considered significant.
Acute toxicity study
NOSE and NORE were administered to experimental animals up to 2000 mg/kg dose for evaluation of toxicity and selection of experimental doses. However, up to the highest dose, no signs of mortality or physiological discomfort were observed in the animals. Therefore, 1/40th (50 mg/kg) and 1/10th (200 mg/kg) of the highest dose were selected for the in vivo hepatoprotective experiments.
Body and liver weight
Changes of the body weight (g) and liver weight (g) in different experimental groups. Data represented as mean ± SD of six observations
Initial body weight
Final body weight
% body weight change
Relative liver weight
22.17 ± 0.70
24.23 ± 0.99*
9.26 ± 1.18 ▲
4.37 ± 0.21
18.04 ± 0.13
21.10 ± 0.34
17.49 ± 0.27***
17.07 ± 2.56 ▼
5.32 ± 0.18**
32.53 ± 3.03
21.64 ± 0.19
23.43 ± 0.25***
8.29 ± 1.39 ▲
4.30 ± 0.09NS
18.37 ± 0.22
21.71 ± 0.49
22.36 ± 0.67NS
3.96 ± 3.90 ▲
4.59 ± 0.16NS
20.56 ± 1.36
22.25 ± 0.38
22.67 ± 0.18NS
1.89 ± 2.38 ▲
4.55 ± 0.29NS
20.05 ± 1.18
22.14 ± 0.38
22.59 ± 0.21NS
2.25 ± 2.02 ▲
4.41 ± 0.16NS
19.50 ± 0.58
22.20 ± 0.57
22.33 ± 0.46NS
1.48 ± 0.26 ▲
4.24 ± 0.10NS
19.00 ± 0.52
Liver marker enzymes and biochemical parameters (in vivo)
Changes in the levels of various enzymatic and biochemical parameters of the serum samples of seven experimental groups. Data represented as mean ± SD of six observations
3.61 ± 0.31
10.94 ± 1.04***
5.76 ± 0.43** b
10.01 ± 0.61*** d
8.75 ± 0.44*** c
9.64 ± 0.31*** d
8.55 ± 0.32*** c
10.86 ± 1.29
28.44 ± 1.25***
12.93 ± 0.80NS a
24.92 ± 2.27*** d
22.21 ± 2.45** a
24.56 ± 0.95*** c
22.10 ± 1.45*** b
65.88 ± 3.74
137.28 ± 2.95***
74.01 ± 0.16NS a
121.27 ± 2.89*** a
99.19 ± 5.48*** b
117.93 ± 6.30*** b
110.25 ± 5.00*** b
42.63 ± 1.4
126.26 ± 4.88***
53.81 ± 3.15** a
109.27 ± 4.21*** c
81.27 ± 7.66** d
119.23 ± 6.40*** d
95.94 ± 10.39*** c
2.51 ± 0.36
6.06 ± 0.23***
3.35 ± 0.12* a
5.48 ± 0.33*** d
4.9 ± 0.36** c
5.5 ± 0.25*** c
4.48 ± 0.24** b
53.53 ± 1.28
80.38 ± 1.55***
55.23 ± 3.48NS a
76.40 ± 4.71** d
63.39 ± 1.42*** a
74.96 ± 2.95*** c
65.86 ± 3.43** b
4.77 ± 0.29
3.10 ± 0.23**
4.94 ± 0.05NS a
3.29 ± 0.21** d
4.19 ± 0.24NS b
3.62 ± 0.13** c
3.88 ± 0.07** b
3.18 ± 0.07
1.42 ± 0.13***
2.86 ± 0.17* a
1.53 ± 0.27*** d
1.96 ± 0.22*** a
1.55 ± 0.09*** NS
1.71 ± 0.26*** NS
1.59 ± 0.30
1.68 ± 0.12NS
2.11 ± 0.17NS c
1.76 ± 0.28NS d
2.23 ± 0.03* b
2.06 ± 0.12NS c
2.17 ± 0.20NS c
0.41 ± 0.03
1.15 ± 0.04***
0.51 ± 0.02* a
1.01 ± 0.03*** b
0.91 ± 0.06*** b
1.11 ± 0.07*** d
1.01 ± 0.02*** b
20.58 ± 2.39
111.84 ± 3.54***
35.25 ± 6.78* a
106.83 ± 3.23*** d
75.67 ± 5.59*** a
89.96 ± 3.77*** b
67.71 ± 7.43*** a
219.16 ± 7.19
526.97 ± 7.97***
288.44 ± 10.99*** a
511.31 ± 6.73*** d
433.8 ± 17.47*** b
495.13 ± 12.21*** c
472.24 ± 12.07*** b
78.86 ± 3.49
134.52 ± 0.78***
105.62 ± 3.36*** a
122.00 ± 5.39*** a
114.62 ± 5.39*** b
124.96 ± 5.38 *** d
113.48 ± 6.80** b
Estimation of hepatic anti-oxidative enzymes: catalase and peroxidase
Liver marker enzymes and biochemical parameters (in vitro)
Changes in the levels of various enzymatic and biochemical parameters of the culture supernatants of the experimental groups. Data represented as mean ± SD of six observations
0.71 ± 0.10
1.74 ± 0.11***
1.17 ± 0.16* b
1.58 ± 0.12*** d
1.48 ± 0.08*** c
1.61 ± 0.15** d
1.40 ± 0.16** c
3.09 ± 0.11
7.51 ± 0.33***
4.13 ± 0.25** a
6.79 ± 0.24*** c
5.91 ± 0.27*** b
6.99 ± 0.37*** d
6.09 ± 0.50*** c
14.87 ± 0.72
44.49 ± 0.75***
16.39 ± 1.41NS a
43.86 ± 2.60*** d
36.32 ± 1.21*** a
38.06 ± 3.76*** c
29.53 ± 3.22** b
5.81 ± 0.15
27.55 ± 0.52***
10.57 ± 0.29*** a
26.33 ± 1.29*** d
22.17 ± 2.40*** c
24.47 ± 1.82*** c
20.77 ± 1.63*** b
0.59 ± 0.04
0.78 ± 0.02**
0.58 ± 0.01NS a
0.77 ± 0.01** d
0.71 ± 0.03* d
0.74 ± 0.00** d
0.72 ± 0.01** c
0.13 ± 0.00
0.53 ± 0.05***
0.17 ± 0.00** a
0.56 ± 0.14** b
0.40 ± 0.02*** b
0.465 ± 0.02*** d
0.43 ± 0.02** d
6.48 ± 0.75
5.3 ± 0.26NS
5.7 ± 0.42 NS d
5.61 ± 0.23 NS d
6.05 ± 0.15 NS c
5.77 ± 0.12NS c
6.02 ± 0.21NS c
35.94 ± 29.66
181.33 ± 11.24**
94.16 ± 7.34* a
138.59 ± 14.05** c
105.00 ± 10.02* a
144.40 ± 11.49** c
114.87 ± 10.53* b
Lipid peroxidation (MDA content)
CCl4 mediated direct cellular damage (Fig. 2b) was represented by significant (p < 0.001) difference (61.92 %) in cell viability between control and CCl4 group. However, the cell viability was improved by subsequent treatment with silymarin (p < 0.001) and the oleander extracts (p < 0.01). The extent of improvement of cell viability were 106.95, 47.32 and 51.60 %, respectively for in silymarin, NOSE high and NORE groups.
Measurement of TNF-α
The levels of TNF-α in different groups are demonstrated in Fig. 2c. The level of TNF-α in control was 58 ± 20.22 pg/ml, which was 18.54 fold increased to 1075.66 ± 61.53 pg/ml due to CCl4 toxicity. However, the TNF-α level was subsequently lowered to 43.19, 71.33 and 61.60 % in silymarin, NOSE high and NORE high groups respectively, compared to CCl4 group. All the extract treated groups demonstrated higher TNF-α inhibitory activities than the silymarin group.
Inhibition of nitric oxide
CCl4 toxicity resulted in 3.22 fold increase in NO release compared to control (Fig. 2d). However, significant (p < 0.001) lowering of NO level was observed in the treated groups. The NO level in silymarin, NOSE high and NORE high groups were 111.88 ± 8.60, 142.89 ± 8.72 and 161.24 ± 7.39 % respectively, when NO release of control was considered as 100 %. This resulted in 0.34, 0.44 and 0.50 fold lowering of NO level.
FTIR and GC-MS analysis
The toxicity profile of CCl4 has been thoroughly studied and is well established [25–27]. CCl4 has a rich history of environmental toxicity and occupational hazard due to its extensive use in industrial sectors. This had led to an awareness in the industrial and domestic use of CCl4 from the early 70’s, leading to a ban on production and import of CCl4 in 1996 . However, CCl4 continues to play an essential role as a model haloalkane xenobiotic in the pharmaco-toxicological studies. CCl4 induced liver damage is primarily initiated by the formation of trichloromethyle radical (CCl3 ●) due to cytochrome P450 mediated reductive dehalogenation of CCl4 [8, 29]. Persistent formation of the highly reactive CCl3 ● in the liver cause steatosis, lipid peroxidation leading to hepatocarcinoma . Additionally, fusion of CCl3 ● with diatomic oxygen generates highly reactive trichloromethylperoxy radical (CCl3OO●) which further causes damage to mitochondria, endoplasmic reticulum and plasma membrane permeability, resulting in loss of cytosolic Ca2+ sequestration and homeostasis . The present study demonstrated that, antioxidant rich oleander extracts hold the potentiality to ameliorate CCl4 induced hepatotoxicity in murine model. The data were further supported by the identification of several phytochemical constituents with well-established hepatoprotective potentialities.
CCl4 toxicity caused significant (p < 0.001) loss of body weight as well as highest relative liver weight in the animals. Compared to control and silymarin group, the final body weight change in the extract treated groups were much less. This may presumably indicate the potentiality of oleander extracts to restrict body weight increase through anti-hyperlipidemic activity as demonstrated previously by body weight lowering capability of oleander . Compared to control, 1.80 fold higher relative liver weight in the CCl4 group reflected formation of fatty liver which was further supported by increased blood cholesterol level and extensive steatosis throughout the CCl4 intoxicated liver samples. However, comparatively lower relative liver weight associated with insignificant total body weight change demonstrated the potentiality of oleander extracts to prevent severe physiological consequences due to CCl4 poisoning.
The altered levels of hepatobillary enzymes transaminase and phosphatase along with other enzymatic and biochemical parameters serve as biomarkers of hepatotoxicity whereas, normalization of the parameters represents improvement of normal liver functions [31–33]. N. indicum leaf extract has previously been shown to normalize similar liver biomarkers under CCl4 toxicity . Moreover, oleander floral extracts normalized the elevated AST, GGT, ALT, LDH, ALP and creatinine levels in blood under isoproterenol-induced oxidative stress in rats . Furthermore, the anti-hyperlipidemic activities were evident through lowering of cholesterol levels and associated lowering of fatty infiltrations and steatosis under the histopathological studies, which were further supported by the previous studied of Gayathri et al. . The blood glucose level lowering capacity of the oleander extracts is also supported by its ethnopharmacological claim of hypoglycaemic activities as well as a recent study that demonstrated anti-diabetic activities of oleander leaf under alloxan induced diabetes in mouse . CCl4 toxicity in the present study, resulted in significant (p < 0.001) elevation of ACP, ALP, AST, ALT, GGT, LDH, glucose, urea, globulin, bilirubin and cholesterol levels, signifying liver injury. Only the protein and albumin levels were decreased compared to control. The parameters were subsequently normalized up to certain extent due to silymarin and oleander extract treatments.
Oleander extracts were further evaluated through primary culture to ameliorate CCl4 induced toxicity in mouse hepatocytes in vitro. Cultured liver cells are biochemically prototypical to intact hepatic system and therefore, serves as a model for evaluation of in vitro hepatotoxicity . The results of in vitro studies demonstrated hepatoprotective potentialities of the extracts by normalization of the liver enzymatic and biochemical parameters as well. Liver, in spite of having the highest regenerative capacity, persistent exposure to cytochrome P450 activated organic xenobiotics and their reactive metabolic intermediates  cause tremendous hepatocellular necrosis. Necrotic hepatocytes with fragmented nucleus and distorted cellular margins were clearly evident through histopathological observations. Zonal haemorrhagic necrosis around portal veins in the CCl4 group signified that the hepatocellular injury had exceeded the regenerative power of the liver. This was further confirmed through MTT cell viability assay which showed 61.92 % loss of cell viability due to direct CCl4 exposure in the culture medium. However, subsequent treatment with silymarin and oleander extracts prevented further hepatocellular damage resulting in significantly (p < 0.001) increase in viable cells compared to CCl4 group.
Xenobiotic intoxicated liver encounters a plethora of free radicals and reactive metabolic intermediates which results in great damage to cellular components and the extent of free radical medicated damage is proportional to the extent of lipid peroxidation [37–39]. The resultant oxidative stress further deactivates the cellular antioxidative enzymes . Peroxidase and catalase are two major antioxidative enzymes responsible for the neutralization of free radicals. Peroxidase reduces and converts hydroperoxides and lipid peroxides into non-reactive species, whereas catalase prevents the formation of highly reactive OH● by scavenging H2O2 which participates in the Fenton reaction. Inhibition of both enzymatic activities accumulates O2 ●− and H2O2 which accentuate a cascade of free radical formation. CCl4 derived trichloromethylperoxy radical (CCl3OO●) abstracts proton from polyunsaturated fatty acids in the biological membranes and cause lipid peroxidation . The reactive carbonyl compound MDA is a biomarker for oxidative damage and subsequent lipid peroxidation. The 70 % hydro-methanolic extracts of oleander previously demonstrated potent free radical scavenging activities by inhibiting some of the most harmful free radicals such as OH●, O2 ●−, NO, ONOO−, H2O2 and 1O2 . The study further showed that oleander extracts hold the ability to prevent Fenton reaction by means of neutralization of hydroperoxides and also inhibit lipid peroxidation by scavenging OH● directly. Lipid membranes are vulnerable to oxidative and nitrosative stress due to high amount of polyunsaturated fatty acids and transition metals. Transition metals such as iron are capable of damaging nuclear proteins, DNA, inhibit enzymes and degrade lipid membrane through oxidative Haber-Weiss reaction [41–43]. Our previous study showed potent iron chelation ability by the oleander extracts . Recent studies also showed that 70 % hydro-methanolic extract of N. indicum leaf could ameliorate hemochromatosis and fibrosis in liver due to its potent antioxidant and iron chelation activities [13, 14]. Thus, the present study corroborates the previous findings of the antioxidative protection by oleander extracts. Lowering of liver antioxidative enzymes due to CCl4 toxicity marked increased oxidative stress, resulting in the elevation of lipid peroxidation. However, the diminished catalase and peroxidase levels and elevated MDA level were subsequently normalized by NOSE and NORE administration. The present observations thus, remains in accordance with the previous reports showing improvement of in-house antioxidative enzymes by oleander leaf and flower extracts under oxidative stress [34, 44].
Liver diseases are accompanied by inflammatory conditions which accentuate the progression of liver failure. TNF-α and NO play a major role as pro-inflammatory mediators during CCl4 mediated liver injury which leads towards apoptotic cell death and fibrosis [8, 45]. Under such xenobiotic induced hepatotoxic conditions, activated Kupffer cells secret a vast array of cytokines (TNF-α, IL-1, IL-8, IL-6), chemokines (KC/GRO, IP-109, MIP-2, MCP-1) and pro-inflammatory mediators such as NO, which initiate hepatic inflammation and induce toxicity either by direct cellular damage or by chemoacttracting neutrophils and lymphocytes . TNF-α initiates hepatotoxicity and fibrogenesis and overproduction of NO results in endotoxin shock and inflammatory hepatic injury [45, 47, 48]. Inducible nitric oxide synthase (iNOS) in liver parenchymal and non-parenchymal cells are induced by TNF-α resulting in nitrosative stress. In liver mitochondria, O2 ●− couples with an excess of NO to generate the highly reactive ONOO−. Interestingly, the anti-inflammatory activity of oleander extract is well known in traditional medicine and the extracts are also used in the treatment of diverse inflammatory disorders [17, 49]. In a preliminary study, Erdemoglu et al.  demonstrated anti-inflammatory activities of ethanolic and aqueous extracts of oleander leaves. Moreover, the 70 % hydro-methanolic extract of oleander leaves were demonstrated to possess anti-inflammatory activities by modulation of Th1/Th2 cytokine levels accompanied by inhibition of NO, COX and PGE2 levels in concanavalin A activated murine splenic lymphocytes [15, 16]. In the present study, CCl4 toxicity resulted significant (p < 0.001) increase in TNF-α and NO levels, which were subsequently lowered by the oleander extracts. This exhibited potent anti-inflammatory activities of oleander extracts through suppression of pro-inflammatory mediators of chronic hepatotoxicity.
The hepatoprotective potentiality of oleander extracts were further established through detailed histopathological studies. The results clearly demonstrated that deformed hepatic architecture due to CCL4 toxicity was subsequently attenuated by oleander extracts. CCl4 toxicity initiated tremendous hepatocellular degeneration as evident by scattered hepatocellular necrosis and in some cases with central haemorrhagic necrosis. Deformed nucleus containing overlapping hepatocytes with irregular cellular margins were characteristics of CCl4 group which highly contrasted the prominent nucleus containing healthy hepatocytes with conspicuous cellular boundaries in the control. Loss of cellular integrity in the CCl4 group were visible in terms of disorganized arrangement of the hepatocytes. Interestingly, liver samples of the CCl4 group exhibited an extensive, yet typical signs of inflammation by means of infiltration of leukocytes from the portal regions extended towards the hepatocyte rich central zones, which were comparatively less in the silymarin and extract treated groups. Extensive fatty infiltration throughout the CCl4 group liver samples signified initiation of macrovascular steatosis and adipose degeneration that were less in the NOSE and NORE groups. Moreover, the deformity of the hepatic nodules associated vascular congestions with occasional bile duct proliferations were also lowered in the silymarin and extract treated groups. Overall, the deformed hepatocellular architecture of the CCl4 group were significantly normalized by oleander extracts.
NOSE and NORE were further analysed using FTIR and GC-MS method to reveal the phytochemical constituents responsible for the potent hepatoprotective potentiality. Different functional groups were identified through FTIR analysis, which correlating with the compounds identified in the GC-MS study. Alkanes like tetradecane and hexadecane resulted in = C-H bending. The C-O stretching of carboxylic moiety resulted due to the presence of linoleic acid, n-hexadecanoic acid, benzoic acid, eicosenoic acid, oleic acid etc. The O-H stretching of the alcohol/phenolic species were supported by the presence of lupeol, amyrin, isoeugenol, vanillin and other phenolic phytochemicals. In GC-MS analysis, both the fractions of the extracts revealed the presence of several bioactive constituents which corroborates a previous report of a preliminary phytochemical analysis of oleander . The 70 % hydro-methanolic extracts of oleander leaf, steam and root possessed high amount of phenolic and flavonoid contents, contributing to its antioxidant and free radical scavenging activities . A detailed account of related bioactivities of individual phytocompounds are enlisted in Additional file 5, which supports the view that the hepatoprotective activity of oleander extract resulted due to additive and synergistic activities of the component phytochemicals.
ACP, acid phosphatase; ALP, alkaline phosphatase; ALT, alanine transaminase; AST, aspartate transaminase; CCl4, carbon tetrachloride; DW, dry weight; FTIR, Fourier Transform Infrared; GC-MS, Gas chromatography-mass spectrometry; GGT, gamma-glutamyl transferase; LDH, lactate dehydrogenase; MDA, malondialdehyde; MTT, 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide; NO, nitric oxide; NORE, Nerium oleander root extract; NOSE, Nerium oleander stem extract; SDS, sodium dodecyl sulphate; TBARS, thiobarbituric acid reactive substances; TNF-α, tumor necrosis factor-α.
The authors are grateful to Mr. Bijoy Mahanta for his assistance in animal maintenance.
The present study was not supported by any external funding agencies.
Availability of data and materials
The supporting materials can be obtained upon request via email to the corresponsing author.
PD performed the in vitro and in vivo experiments, statistical analysis and drafted the manuscript. SD assisted in the in vivo experiments and performed the histopathological study. ABR performed the GC-MS analysis. MPS supervised the phytochemical analysis, analysed the GC-MS data and drafted the phytochemical part of the manuscript. TKC designed, supervised and coordinated the study and drafted the manuscript. All authors have read and approved the final version of the manuscript.
The authors declare that they have no competing interests.
Consent for publication
This section is not applicable for the study.
Ethics approval and consent to participate
All the experiments were approved by the ethical committee, University of North Bengal (No. 840/ac/04/CPCSEA) and conducted in accordance with the legislation for the protection of animals used for scientific purposes. The study does not include human subjects.
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