Cardioprotective role of leaves extracts of Carissa opaca against CCl4 induced toxicity in rats
© Sahreen et al.; licensee BioMed Central Ltd. 2014
Received: 6 February 2014
Accepted: 28 March 2014
Published: 9 April 2014
Carissa opaca are used traditionally in Pakistan for the treatment of various human ailments. Therefore, the study is arranged out to assess the cardio protective potential of different fractions of Carissa opaca leaves on CCl4-induced oxidative trauma in kidney.
The parameters studied in this respect were the cardiac function test (CK (U/l), CKMB (U/l), genotoxicity (% DNA fragmentation), characteristic morphological findings and antioxidant enzymatic level of cardiac tissue homogenate.
The protective effects of various fractions of Carissa opaca (C. opaca) leaves extract against CCl4 administration was reviewed by rat cardiac functions alterations. Chronic toxicity caused by eight week treatment of CCl4 to the rats significantly changed the cardiac function test, decreased the activities of antioxidant enzymes and glutathione contents whereas significant increase was found in lipid peroxidation comparative to control group. Administration of various fractions of C. opaca leaves extract with CCl4 showed protective ability against CCl4 intoxication by restoring the cardiac functions alterations, activities of antioxidant enzymes and lipid peroxidation in rat. CCl4 induction in rats also caused DNA fragmentation and histopathalogical abnormalities which were restored by co-admistration of various fraction of C. opaca leaves extract.
Results revealed that various fraction of C. opaca are helpful in cardiac dysfunctions.
Plants are used to extract pure compounds and development of new drugs, has supreme frankness of chemical diversity. Natural products derived from plant extracts/fractions are novel therapeutic agents for various infectious as well as degenerative diseases . People of developed countries have turned back their attention towards botanicals as medical care, but countries like Pakistan, China and India seek help from botanical healers since centuries to till date because they grant them substitutive health care services based on botanicals as an accessible and economical source in comparison to synthetic medicines . Hence, medicinal plants are considered as therapeutic agents against various diseases. No doubt indigenous use of plants is unlimited, but it is necessary to discover the pharmaceutically important agents responsible for protection against lethal diseases. It is anticipated that about one quarter of approved modern medicines has been derived from botanicals . Several anti-cancer drugs including, vinblastine and paclitaxel are exclusively derived from botanicals. Similarly, aspirin, a recognized pain killer, was actually a derivative of Salix and Spiraea species . Regarding the excessive use of botanicals as health care medicines, it has become an important step to screen the medicinal plants for bioactive compounds as a source of new antibiotic and cancer-related drugs. Carissa opaca Stapf ex Hanes is a 2–3 meter tall evergreen shrub containing glabrous or puberulous branches with opposite and ovate glabrous leaves, hard and sharp spines arising between the petiole. This plant is also reported in some areas of India, Burma and Sri Lanka . Jabeen et al.  reported the use of plant against worm infested sores of animals, asthma, stimulants and fly repellent. According to Saghir et al.  fruits and leaves are cardiac and stimulant. Abbasi et al.  described the traditional use of plant for the treatment of hepatitis and jaundice. Researchers have reported that plant is purgative, and give relief from cough, diarrhea and fever . Ahmad et al.  described the ethnobotanical use of stems, leaves and fruits of C. opaca in eye disorders and reported that mixture of C. opaca with roots of Mimosa pudica is used as aphrodisiac. Carbon tetrachloride (CCl4), a clear, colorless and nonflammable synthetic liquid, is a renowned model compound for producing chemical tissue toxicity by creation of free radicals in liver, kidney, heart, lung, testis, brain and blood [11, 12]. It is bio transformed by hepatic microsomal cytochrome P450 to trichloromethyl-free radical (CCl3 or CCl3OO) , which in turn, instigate lipid peroxidation process [14, 15]. The most widely established means of CCl4 induced cardiotoxicity is the creation of free radicals which is a rate limiting process in tissue peroxidative damage . The present study was conducted to examine the toxic upshots of CCl4 plus to compare the beneficial effects of plant extracts on heart tissue of various experimental groups.
C. opaca leaves were collected in June 2011 from the Quaid-i-Azam University Islamabad, Pakistan. The plants were recognized by their local names and then validated by Dr. Mir Ajab Khan, Department of Plant Sciences, Quaid-i-Azam University, Islamabad. A voucher specimen with Accession No. 24561 (C. opaca) was deposited at the Herbarium of Pakistan Quaid-i-Azam University, Islamabad Pakistan.
The collected plant samples were cleaned to get rid of dust particles and then dried under shade for one to two weeks. Willy Mill of 60-mesh size was used to prepare powder of dried samples and then each powdered plant sample was used for further solvent extraction. First of all, 5 kg of powdered sample was extracted twice with 10 L of 95% methanol at 25°C for 48 h. For filtration Whatman No. 1 filter paper was used and then filtrate was concentrated on rotary evaporator (Panchun Scientific Co., Kaohsiung, Taiwan) under reduced pressure at 40°C. In order to resolve the compounds with escalating polarity, a part of the extract was suspended in distilled water and subjected to liquid-liquid partition by using solvents in a sequence of n-hexane, ethyl acetate and methanol. After fractioning, the solvent of respective fractions was also evaporated by rotary evaporator. Extract was dried and then stored at 4°C for further in vivo investigation.
Six-week-old male Sprague Dawley rats weighing 180 ± 10 g were provided with food and water ad libitum and kept at 20–22°C on a 12-h light–dark cycle. All experimental procedures involving animals were conducted in accordance with the guidelines of National Institutes of Health (NIH guidelines). The study protocols were approved by Ethical committee of Quaid-i-Azam University Islamabad. The rats were acclimatized to laboratory condition for 7 days before commencement of experiment. For chronic toxicity eight week experiment was designed. 42 male albino rats were randomly divided into seven groups (6 rats of each group). Administration of CCl4 (0.5 ml/kg b.w., 20% CCl4/olive oil) was intraperitoneally (i.p.) twice a week for eight weeks. At the same time, the rats were administered individually silymarin (50 mg/kg b.w.) and extract (200 mg/kg b.w.) orally twice a week for eight weeks.
Following dosing plan was adapted for the study.
Group I. the normal control received only feed
Group II. Olive oil (0.5 ml/kg b.w. i.p.) + DMSO (0.5 ml/kg b.w. orally)
Group III. CCl4 twice a week (0.5 ml/kg b.w. i.p., 20% CCl4/olive oil)
Group IV. CCl4 twice a week (0.5 ml/kg b.w. i.p.) + sylimarin (50 mg/kg b.w. orally)
Group V. CCl4 twice a week (0.5 ml/kg b.w. i.p.) + HLC (200 mg/kg b.w., orally)
Group VI. CCl4 twice a week (0.5 ml/kg b.w. i.p.) + ELC (200 mg/kg b.w., orally)
Group VII. CCl4 twice a week (0.5 ml/kg b.w. i.p.) + MLC (200 mg/kg b.w., orally)
At the end of eight weeks, after 24 h of the last treatment, Urine was collected and stored at −70°C for further analysis, and then animals were given chloroform anesthesia and dissected from ventral side. Blood was drawn prior to the excision of tissues. The serum was separated and stored at −80°C after separation until it was assayed as described below. After taking blood the heart was removed and washed in ice cold saline. Subsequently, half of the organs were treated with liquid nitrogen and stored at −80°C for further enzymatic and DNA damage analysis while the other portion was processed for histology.
In order to evaluate the pharmacological effects of different fractions of C. opaca leaves extract against the toxicity induced with CCl4 in rats following assays had been carried out.
Biochemical analysis of serum
Estimation of serum marker enzymes viz; CK, CKMB was carried out by using standard AMP diagnostic kits.
Assessment of antioxidant enzymes
100 mg of heart tissue was homogenized in 10 volume of 100 mM KH2PO4 buffer containing 1 mM EDTA, pH 7.4 and centrifuged at 12,000 × g for 30 min at 4°C. The supernatant was collected and used for the following experiments.
Catalase assay (CAT)
CAT activity was determined by the modified protocol of Khan et al.. The reaction solution of CAT activities contained: 2.5 ml of 50 mM phosphate buffer (pH 5.0), 0.4 ml of 5.9 mM H2O2 and 0.1 ml enzyme extract. Changes in absorbance of the reaction solution at 240 nm were determined after one minute. One unit of CAT activity was defined as an absorbance change of 0.01 as units/min.
Peroxidase assay (POD)
Activities of POD were determined by the modified protocol of Khan et al.. The POD reaction solution contained: 2.5 ml of 50 mM phosphate buffer (pH 5.0), 0.1 ml of 20 mM guaiacol, 0.3 ml of 40 mM H2O2 and 0.1 ml enzyme extract. Changes in absorbance of the reaction solution at 470 nm were determined after one minute. One unit of POD activity was defined as an absorbance change of 0.01 units/min.
Superoxide dismutase assay (SOD)
SOD activity was estimated by the method of Kakkar et al. . Reaction mixture of this method contained: 0.1 ml of phenazine methosulphate (186 μM), 1.2 ml of sodium pyrophosphate buffer (0.052 mM; pH 7.0), 0.3 ml of supernatant after centrifugation (1500 × g for 10 min followed by 10000 × g for 15 min) of heart homogenate was added to the reaction mixture. Enzyme reaction was initiated by adding 0.2 ml of NADH (780 μM) and stopped after 1 min by adding 1 ml of glacial acetic acid. Amount of chromogen formed was measured by recording color intensity at 560 nm. Results are expressed in units/mg protein.
Glutathione-S-transferase assay (GST)
Glutathione-S-transferase activity was assayed by the method of Habig et al. . The reaction mixture consisted of 1.475 ml phosphate buffer (0.1 mol, pH 6.5), 0.2 ml reduced glutathione (1 mM), 0.025 ml (CDNB) (1 mM) and 0.3 ml of homogenate in a total volume of 2.0 ml. The changes in the absorbance were recorded at 340 nm and enzymes activity was calculated as nM CDNB conjugate formed/min/mg protein using a molar extinction coefficient of 9.6 × 103 M−1 cm−1.
Glutathione reductase assay (GR)
Glutathione reductase activity was determined by method of Carlberg and Mannervik . The reaction mixture consisted of 1.65 ml phosphate buffer: (0.1 mol; pH 7.6), 0.1 ml EDTA (0.5 mM), 0.05 ml oxidized glutathione (1 mM), 0.1 ml NADPH (0.1 mmol) and 0.1 ml of homogenate in a total volume of 2 ml. Enzyme activity was quantitated at 25°C by measuring disappearance of NADPH at 340 nm and was calculated as nM NADPH oxidized/min/mg protein using molar extinction coefficient of 6.22 × 103 M−1 cm−1.
Glutathione peroxidase assay (GPx)
Glutathione peroxidase activity was assayed by the modified method of Khan et al. . The reaction mixture consisted of 1.49 ml phosphate buffer (0.1 M; pH 7.4), 0.1 ml EDTA (1 mM), 0.1 ml sodium azide (1 mM), 0.05 ml glutathione reductase (1 IU/ml), 0.05 ml GSH (1 mM), 0.1 ml NADPH (0.2 mM), 0.01 ml H2O2 (0.25 mM) and 0.1 ml of homogenate in a total volume of 2 ml. The disappearance of NADPH at 340 nm was recorded at 25°C. Enzyme activity was calculated as nM NADPH oxidized/min/mg protein using molar extinction coefficient of 6.22 × 103 M−1 cm−1.
Quinone reductase assay (QR)
The activity of quinone reductase was determined by the method of Benson et al. . The 3.0 ml reaction mixture consisted of 2.13 ml Tris–HCl buffer (25 mM; pH 7.4), 0.7 ml BSA, 0.1 ml FAD, 0.02 ml NADPH (0.1 mM), and 0.l ml of homogenate. The reduction of dichlorophenolindophenol (DCPIP) was recorded at 600 nm and enzyme activity was calculated as nM of DCPIP reduced/min/mg protein using molar extinction coefficient of 2.1 × 104 M−1 cm−1.
Reduced glutathione assay (GSH)
Reduced glutathione was estimated by the method of Jollow et al. . 1.0 ml sample of homogenate was precipitated with 1.0 ml of (4%) sulfosalicylic acid. The samples were kept at 4°C for 1 h and then centrifuged at 1200 × g for 20 min at 4°C. The total volume of 3.0 ml assay mixture contained 0.1 ml filtered aliquot, 2.7 ml phosphate buffer (0.1 M; pH 7.4) and 0.2 ml DTNB (100 mM). The yellow color developed was read immediately at 412 nm on a SmartSpecTM plus Spectrophotometer. It was expressed as μM GSH/g tissue.
Estimation of lipid peroxidation assay
The assay for lipid peroxidation was carried out following the modified method of Iqbal et al. . The reaction mixture in a total volume of 1.0 ml contained 0.58 ml phosphate buffer (0.1 M; pH 7.4), 0.2 ml homogenate sample, 0.2 ml ascorbic acid (100 mM), and 0.02 ml ferric chloride (100 mM). The reaction mixture was incubated at 37°C in a shaking water bath for 1 h. The reaction was stopped by addition of 1.0 ml 10% trichloroacetic acid. Following addition of 1.0 ml 0.67% thiobarbituric acid, all the tubes were placed in boiling water bath for 20 min and then shifted to crushed ice-bath before centrifuging at 2500 × g for 10 min. The amount of TBARS formed in each of the samples was assessed by measuring optical density of the supernatant at 535 nm using spectrophotometer against a reagent blank. The results were expressed as nM TBARS/min/mg tissue at 37°C using molar extinction coefficient of 1.56 × 105 M−1 cm−1.
Hydrogen peroxide assay (H2O2)
Hydrogen peroxide (H2O2) was assayed by H2O2-mediated horseradish peroxidase-dependent oxidation of phenol red by the method of Pick and Keisari . 2.0 ml of homogenate sample was suspended in 1.0 ml of solution containing phenol red (0.28 nM), horse radish peroxidase (8.5 units), dextrose (5.5 nM) and phosphate buffer (0.05 M; pH 7.0) and were incubated at 37°C for 60 min. The reaction was stopped by the addition of 0.01 ml of NaOH (10 N) and then centrifuged at 800 × g for 5 min. The absorbance of the supernatant was recorded at 610 nm against a reagent blank. The quantity of H2O2 produced was expressed as nM H2O2/min/mg tissue based on the standard curve of H2O2 oxidized phenol red.
DNA had been isolated and its fragmentation percent was quantified in molecular studies of in vivo toxicity.
DNA fragmentation assay with diphenylamine reaction
DNA fragmentation from tissue extract was determined using the procedure of Wu et al. . 100 mg tissue was homogenized in TTE solution. 0.1 ml of homogenate was labeled B, centrifuged at 200 × g at 4°C for 10 min, got supernatant labeled S. S tubes were centrifuged at 20,000 × g for 10 min at 4°C to separate intact chromatin, was labeled T. 1.0 ml of 25% TCA was added in all tubes T, B, S and incubated over night at 4°C. After incubation precipitated DNA was recovered by pelleting for 10 min at 18,000 × g at 4°C. 160 μl of 5% TCA was added to each pellet and heated for 15 min at 90°C then 320 μl of freshly prepared DPA solution was added, vortexed and incubated for 4 hr 37°C. Optical density was read at 600 nm with a spectrophotometer (Smart spec TM Plus, catalog # 170–2525).
DNA Isolations and ladder assay
DNA was isolated by using the methods of Wu et al. . 100 mg of tissue in a petri dish was washed with DNA Buffer and homogenized in 1 ml lysis buffer. 100 μl of proteinase K (10 mg/ml) and 240 μl 10% SDS, shaked gently, and incubate overnight at 45°C in a water bath then 0.4 ml of phenol, was added shaked for 5–10 min, and centrifuge at 3000 rpm for 5 min at 10°C. Supernatant was mixed with 1.2 ml phenol, 1.2 ml Chloroform/isoamyl alcohol (24:1); shaked for 5–10 min, and centrifuged at 3000 rpm for 5 min at 10°C. 25 μl of 3 M sodium acetate (pH 5.2) and 5 ml ethanol was added with supernatant, shake until DNA was precipitated. DNA was washed with 70% ethanol, dried, dissolved in TE buffer and its concentration checked at 260 and 280 nm.5 μg of total DNA and 0.5 μg DNA standard per well were loaded on 1.5% agarose gel containing ethidium bromide. Electrophoresis was performed for 45 min with 100 V batteries, and DNA was observed under digital gel doc system and photographed.
Histopathological study of tissue
After weighting the portion specifies for histology small pieces of tissue was fixed for 3–4 h in fixative sera followed by dehydration with ascending grades of alcohol (80%, 90%, and 100%) and transferred in cedar wood oil. When tissue becomes clear then all tissues were embedded in paraplast and prepared blocks for further microtomy. 3–4 μm thin slides were prepared with microtome; wax was removed, stained with hemotoxilin-eosin and photographed under light microscope at 10x and 40x.
To find the different treatment effects of in vivo studies one way analysis of variance was carried by computer software SPSS 13.0. Level of significance among the various treatments was determined by LSD at 0.05% level of probability.
Effects of C. opaca leaves against CCl4 induced cardio toxicity in rat
In order to evaluate the protective of different fractions of C. opaca leaves against CCl4-induced cardiac injuries, the level of antioxidant enzymes, an indicator of oxidative damage, was monitored. Cardiac function test and histology of the organ was also inspected to estimate the effects of different fractions of C. opaca leaves.
Effects of C. opaca leave on cardiac function tests of rats
Effects of various fractions of C. opaca leaves on heart function tests
94.36 ± 3.48e
118.97 ± 5.42d
Oil + DMSO
100.13 ± 5.44e
111.41 ± 3.09d
910.46 ± 9.66a
259.23 ± 3.55a
Sily + CCl4
295.78 ± 8.37d
156.28 ± 3.00c
HLC + CCl4
630.66 ± 9.56b
239.68 ± 3.37b
ELC + CCl4
398.10 ± 8.29c
190.01 ± 4.17c
MLC + CCl4
311.66 ± 9.09d
158.68 ± 4.40c
Effects of C. opaca leave on cardiac enzymatic antioxidant levels
Effects of various fractions of C . opaca leaves on tissue proteins and antioxidant enzyme levels
SOD (U/mg protein)
TBARS (nM/min/mg protein)
4.21 ± 0.19c
9.05 ± 0.30c
3.00 ± 0.27c
2.87 ± 0.36c
1.432 ± 0.011e
Oil + DMSO
4.13 ± 0.26c
8.84 ± 0.27c
3.12 ± 0.21c
2.67 ± 0.33c
1.480 ± 0.016e
2.47 ± 0.34a
5.03 ± 0.71a
1.05 ± 0.10a
4.11 ± 0.08a
2.524 ± 0.077a
Sily + CCl4
3.66 ± 0.20b
8.24 ± 0.78c
2.63 ± 0.14b
3.47 ± 0.14b
1.548 ± 0.027d
HLC + CCl4
3.34 ± 0.16b
5.56 ± 0.39a
1.11 ± 0.23a
4.03 ± 0.13a
2.272 ± 0.078b
ELC + CCl4
3.32 ± 0.22b
7.80 ± 0.68b
1.95 ± 0.27b
3.36 ± 0.06b
1.744 ± 0.072c
MLC + CCl4
3.75 ± 0.15b
8.07 ± 0.52b
2.21 ± 0.36b
3.32 ± 0.10b
1.617 ± 0.092c
Effects of various fractions of C . opaca leaves on phase II antioxidant enzymes and DNA fragmentation
GST (nM/min/mg protein)
GPx (nM/min/mg protein)
GR (nM/min/mg protein)
GSH (μM/g tissue)
QR (nM/min/mg protein)
DNA damages %
146.34 ± 5.62d
100.5 ± 4.38c
164.37 ± 6.31e
18.15 ± 1.36c
97.70 ± 4.12d
10.47 ± 2.46d
Oil + DMSO
139.19 ± 4.17d
105.91 ± 4.72c
158.81 ± 5.96e
19.04 ± 1.50c
102.13 ± 3.26d
11.23 ± 3.94d
105.50 ± 4.23a
78.64 ± 2.38a
104.33 ± 3.33a
11.26 ± 0.65a
63.30 ± 2.36a
43.37 ± 3.66a
Sily + CCl4
130.53 ± 3.13c
90.56 ± 1.81b
147.18 ± 2.49d
15.28 ± 1.40b
89.14 ± 2.71c
16.40 ± 1.34c
HLC + CCl4
105.48 ± 2.14a
78.76 ± 1.06a
110.43 ± 3.65a
13.17 ± 0.47b
65.09 ± 2.18a
32.30 ± 3.71b
ELC + CCl4
114.73 ± 2.94b
84.06 ± 1.47b
133.23 ± 3.62d
14.25 ± 0.47b
75.14 ± 2.21b
15.22 ± 3.23c
MLC + CCl4
122.08 ± 3.49c
87.09 ± 2.02b
142.51 ± 2.20d
14.17 ± 1.16b
80.42 ± 4.08b
14.17 ± 3.02c
Effects of C. opaca leaves on DNA damages (ladder assay)
Effects of C. opaca leaves on cardiac histoarchitecture
In the literature it has been studied that CCl4 can generate oxidative stress in tissues other than liver, such as kidneys, heart, lung, testis, brain and blood [27, 28]. Thus, oxidative insults induced by CCl4 resulted in degenerative processes of various tissues. As cardiac tissue has affinity for CCl4 due to cytochrome P450. So, oxidative damage to lipids and proteins of heart tissues probably occurred due to CCl4 intoxication. In view of that, natural resources are being soughed for their potential tissue protective effects. An approach for detection of cardiac injury, tissue ischemia and myocardial infarction involves measurements of the well known cardiac marker enzymes for example, creatine kinase (CK), cardiac creatine kinase-MB fraction (CK-MB), AST, ALT, ALP, LDH, and cholesterol in serum [29, 30]. The important point is that all of the above discussed enzymes are not restricted to cardiac tissue except CK and CKMB, their increased activity in serum is responsible for in non-cardiac tissue injuries like liver. CKMB, a myocardial enzyme determines the degree of myocyte injury that’s why WHO accepted it as gold standard indicator of myocardial injury . The integrity of cardiac cell membrane gets disturbed as a consequence of peroxidation of membrane by oxygen-derived free radicals  causing leakage of enzymes. This accounts for the decreased activities of these enzymes in heart tissue because these enzymes enter into the plasma thus increasing their concentration in the serum as an indicator of myocyte injury . CCl4 intoxication was responsible for excess release of CK and CKMB in the serum of rats and this study correlates with the commonly reported study that Dox-induced free radical generation activates cardiac myocytes disruption and peroxidation of membrane, which boosted the CKMB level of serum [34, 35]. A marked reduction in the levels of CK and CK-MB, being marker parameters of heart damage in experimental groups treated with various fractions of tested samples proves improved cardiac function in CCl4-treated group. These serological studies have a superb correlation with histological examination of cardiac tissue of rats.
There is considerable evidence that induction of CAT, POD, SOD and phase-II detoxifying enzymes, including GPx, GR and GST can adjust the verge for chemical carcinogenesis by increasing resistance against toxic substances. Cellular antioxidant enzymes like SOD, GPx, CAT and GST are important cellular guards due to detoxifying ability against free radicals. Numerous diverse results have been reported for the variation of these antioxidant enzyme activities in rat model against CCl4 challenges . In cellular defense system, GSH has the conjugating aptitude with metabolites/free radicals, thus stabilizing the membranes from detrimental effects of lipid peroxides. Depletion in GSH content indicates the condition of oxidative stress caused by adriamycin administration . It also has been reported that cellular GSH depletion is closely related with lipid peroxidation induced by toxic agents . Lipid peroxidation is also involved in pathogenesis of adriamycin-induced cardiomyopathy. The present remarks are in conformity with previous reports, which showed that myocardial antioxidant defense mechanism was working at a lower rate regardless of higher degree of oxidative trauma in CCl4-induced cardiomyopathy state. In the present investigation, rats treated with various fractions of tested samples practiced abridged lipid peroxidation with enhanced GSH level and GPx, GST and GR activities. It appears therefore that various fractions of tested samples protects the cardiac tissue against CCl4-induced lipid peroxidation and has the antioxidant propensity.
ROS have an immense damage to DNA, causing DNA mutations responsible for various degenerative diseases. Several specific and unspecific repair enzymes remove oxidative DNA modifications. Since oxidative DNA damage is continuously induced and repaired, a steady-state level of oxidative DNA damage is expected under normal conditions. Oxidative stress causes an increase in oxidative DNA damage . Regarding to present findings CCl4 cause the degradation of DNA by generating free radicals. Similar finding have also been described by Manierea et al.  that the chemicals such as CCl4, and other xenobiotic compounds induce the production of reactive free radicals which cause the oxidative damage to DNA, with formation of DNA adducts and genetic mutations. The DNA damage in various tissues like brain, testis, adrenal and liver was reported but data for DNA damage is scanty for cardiac tissue. Administration of various fractions of tested samples in experimental groups to CCl4 intoxicated rats confined the cardiac tissues and there was a marked decline in percentage of fragmented DNA that was further confirmed by DNA ladder assay.
The microscopic structural changes in the heart tissues of CCl4 intoxicated rats had similarity with previous report of Jayakumar et al. . Co-treatment with various fractions of tested samples in experimental groups showed substantial avoidance in the structural alterations. This indicates that administration of various fractions of tested samples scavenged the free radicals to stop cellular damages. Previous reports have also confirmed the beneficial effects of supplementation of antioxidants in adriamycin induced myocardial injury. Histopatholgical studies revealed myocardial atrophy, nuclear pyknosis, and cytoplasmic vacuoles in the CCl4 treated hearts. Similar observations have also been made in earlier studies on acute doxorubicin induced cardiotoxicity [42, 43]. Regarding the comparative studies of CCl4 with other toxic chemicals on cardiac tissue, similar toxic effects were reported by with other chemicals . In the present study the main effects of CCl4 was the prominent fatty change congestion in the blood vessel clearing of cytoplasm with foamy appearance and nuclear degeneration in some area was observed which was significantly recovered by various fractions of tested samples that may be attributed to the individuals or combined action of bioactive compounds present in respective fraction. Similar results were reported by the study of Khan et al.  and Eshaghi et al. extract ameliorated the CCl4-induced cardiotoxicity of male albino rats.
The protective effect observed in this study provide some mechanistic evidence for why indigenous people of Pakistan and other Asian countries found it useful for the cariadic ailments as well as food additive.
We are very thankful to Higher Education Commission (HEC) Pakistan for provision research funds.
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