Background

Pesticides have been applied in agriculture and household to protect plants, animals and human from insects and vector diseases. The negligent and random uses of pesticides can cause environmental damage, food, water contamination, and health problems (e.g. cancer, nerve disease, birth defects). Cypermethrin (Cyp), a class II pyrethroid pesticide, first synthesized in 1974, widely used to control many pest species in agriculture, animal breeding and the household [1]. It has been reported that Cyp residues were found in the air, on walls and furniture after three months of household treatments [2]. Cyp was accumulated in adipose tissue, brain and liver of rats [3, 4] and has hepatotoxic potential in rodents [2, 5]. It crosses the blood–brain barrier and induces neurotoxicity and motor deficits [6]. However, due to the low toxicity of pyrethroids, persistence of these insecticides in mammalian tissues may be dangerous [3].

In fact, one possible mechanism of pesticide-induced toxicity is the production of reactive oxygen species (ROS) in the cell. ROS can alter oxidant/prooxidants statues and antioxidant defense system by increasing lipid peroxidation (LPO) and depleting the antioxidants in cell (enzymatic and non-enzymatic) which leading to a condition of oxidative stress [7]. It has been reported that ROS were involved in the toxicity of organophosphate insecticides (OPIs) such as chlorpyrifos [7] and pyrethroid insecticides such as prallethrin [8, 9] and a positive correlation with the liver damage has been reported. ROS, especially superoxide anion and hydrogen peroxide, are important signaling molecules in developing and proliferating cells, but also in the induction of programmed cell death [10]. ROS are transient species due to its high chemical reactivity that leads to the LPO and a massive protein oxidation and degradation [11, 12]. The author reported that ROS cause DNA damage and strand breaks as a result of modifying purines and pyrimidines bases by superoxide anion radical (O2•-), hydrogen peroxide (H2O2), and hydroxyl radical (HO•).

Cedrelopsis grevei is an endemic species in Madagascar. It was used in traditional medicine to treat malaria, fever and fatigue [13]. Our previous study [14] showed that sixty-four components were identified in C. grevei essential oil by GC-MS. The major constituents were: (E)-β-farnesene (27.61 %), δ-cadinene (14.48 %), α-copaene (7.65 %) and β -elemene (6.96 %). It exhibited antioxidant activities and concentration-dependent inhibitory effects on DPPH• and ABTS. Previous investigations of the trunk [15] and stem [16] bark of C. grevei showed that five coumarins i.e. norbraylin, methyl-O-cedrelopsin, cedrecoumarin A, scoparone and braylin were isolated. Atmaca et al. [17] showed that hepatoprotective effect of coumarins against oxidative stress and liver damage induced by carbon tetrachloride in male rats. In addition, phenolic compounds of C. grevei are playing an essential role in neutralizing free radical, quenching singlet and triplet oxygen, decomposing peroxides, stabilizing lipid peroxidation and protecting the cells against oxidative damage [18].

Currently, some synthetic antioxidant use to prevent free radical damage can induce side effects [19]. So, the dietary intake of natural products is considered very important for preventing a wide variety of diseases, including allergies, cardiovascular disease, certain forms of cancer, hepatic diseases, and inflammation, which involve free radical–mediated damage in pathologically generating processes [20]. Therefore, that is an essential research about suitable herbal drugs, that could replace the chemical ones [21]. However, the widespread use of C. grevei in traditional medicine stimulated us to explore its potential biological activity. To the best of our knowledge, no previous study of the antioxidant and hepatoprotective activities of C. grevei leaves extract have been reported. Therefore, the current study was designed to evaluate the antioxidant activity and hepatoprotective effect of C. grevei leaves against Cyp induced oxidative stress, lipid peroxidation and liver damage in male mice.

Materials and methods

Chemicals and reagents

The assay kits used for biochemical measurements of aspartate aminotransferases (AST; EC 2.6.1.1.), alanine aminotransferases (ALT; EC 2.6.1.2), alkaline phosphatase (ALP; EC 3.1.3.1), lactate dehydrogenase (LDH; EC 1.1.1.27), catalase (CAT; EC 1.11.1.6), superoxide dismutase (SOD; EC 1.15.1.1), glutathione-s-transferase (GST; EC 2.5.1.18), glutathione reduced (GSH), malondialdehyde (MDA) and total protein were purchased from Biodiagnostic Company, Dokki, Giza, Egypt. Cypermethrin (95.1 %) was obtained from Jiangsu Yangnong Chemical Co., Ltd, China. All other chemicals used were of analytical reagent grade. All reagents were purchased from Sigma–Aldrich–Fluka (Saint-Quentin France).

In vitro studies

Plant material and extraction

The leaves of C. grevei was collected from Toliara, Madagascar and identified by Benja RAKOTONIRINA (Institut malgache de recherches appliquées (IMRA), Madagascar). A voucher specimen (No. TLR 07) was deposited at the Herbarium of IMRA, Madagascar. The leaves of C. grevei collected in Antananarivo, Madagascar were ground to fine powder and successively extracted with solvents of increasing polarity (cyclohexane, dichloromethane, ethyl acetate, ethanol and finally methanol). Thus, 200 g of leaves powder were placed in steeping with cyclohexane (2 L) for 4 h under frequent agitation at ambient temperature and pressure. The mixture was then filtrated using Wattman Paper (GF/A, 110 mm). The solvent was evaporated by rotary evaporation under vacuum at 30 °C. Then, the same powder extracted with cyclohexane was extracted again with the next solvent, dichloromethane, under the same conditions. The same protocol was applied for ethyl acetate, ethanol and methanol. Extracts were subsequently stored in sealed and amber vials at 4 °C for the following analysis.

Photochemical study

Determination of phenolic contents

The phenolic content of each extract was determined by Folin-Ciocalteu method [22]. Briefly, a mixture of diluted solution (20 μL) of each extract and 100 μL of Folin-Ciocalteu reagent (0.2 N) were prepared. The mixture was incubated for 5 min at room temperature and then 80 μL of sodium carbonate solution (75 g/L in water) was added. The absorbance was read at 765 nm, after 1 h against water blank. A standard calibration curve was plotted using gallic acid (0–300 mg/L). Results were expressed as g of gallic acid equivalents (GAE)/ Kg of dry mass.

Determination of flavonoids contents

The flavonoids were determined by Dowd method [22]. A mixture of diluted solution (100 μL) of each extract and 100 μL of aluminum trichloride (AlCl3) in methanol (2 %) were prepared. The absorbance of the mixture was measured at 415 nm, after 15 min. At the same time, a blank sample formed by methanol (100 μL) and extract (100 μL) without AlCl3. The results were expressed as g of quercetin equivalents (QE)/Kg of dry mass from calibration curve.

Determination of anthocyanin content

The absorbance of the extract was measured at 510 and 700 nm in buffers at pH 1.0 (hydrochloric acid–potassium chloride, 0.2 M) and 4.5 (acetic acid–sodium acetate, 1 M) [22] using 96-well plates. 20 μl extract solution was mixed with 180 μl of buffers and the wavelength reading was performed after 15 min of incubation. Anthocyanin contents were calculated using a molar extinction coefficient (ε) of 29600 (cyanidin-3-glucoside) and absorbance of A = [(A510 – A700) pH1.0 – (A510 – A700)pH4.5].

Determination of tannin content

Proanthocyanidins reactive to vanillin were analyzed by the vanillin method [22]. One milliliter of extract solution was placed in a test tube together with 2 mL of vanillin (1 % in 7 M H2SO4) in an ice bath and then incubated at 25 °C. After 15 min, the absorbance of the solution was read at 500 nm.

Antioxidant activity

The free radical scavenging activities by DPPH● and ABTS•+ assays were evaluated according to the method cited by Afoulous et al. [14]. Total reducing capacity of C. grevei extracts was determined according to the method of Oyaizu [23]. One mL of extract at different concentrations (250–1000 μg/ml) were mixed with 2.5 ml phosphate buffer (0.2 M, pH 6.6) and 2.5 mL potassium ferricyanide [K3 Fe (CN)6] (1 %). The mixture was incubated at 50 °C for 20 min, and then a portion (2.5 ml) of TCA (10 %) was added to the mixture, which was centrifuged for 10 min at 1000 x g. The upper layer of solution (2.5 ml) was mixed with distilled water (2.5 ml) and 0.5 mL FeCl3 (0.1 %). Then the absorbance was measured at 700 nm. Ascorbic acid (0.5-10 μg/ml) was used as the reference compound.

In vivo studies

Animals and treatments

Healthy adult male mice weighing 22.5 ± 1.0 g were obtained from the Animal Breeding House of the National Research Centre (NRC), Dokki, Giza, Egypt. Animals were housed in clean plastic cages in the laboratory animal room (23 ± 2 °C) on the standard pellet diet and tap water ad-libitum, a minimum relative humidity of 40 % and a 12 h dark/light cycle. Mice were allowed to acclimate to laboratory conditions for 7 days prior to dosing. The experimental work on mice was performed with the approval of the Animal Care & Experimental Committee, National Research Centre, Giza, Egypt, and international guidelines for the care and use of laboratory animals.

Animals were randomly divided into six groups (six mice each), control, Cyp, extract (150 and 300 mg/kg. b.wt), Cyp plus extract (150 or 300 mg/kg. b.wt) groups. Cyp and C. grevei extracts were administered by gavages in a fixed volume of 0.1 ml/mice daily for 28 days. Cyp was dissolved in corn oil and given via oral route at dose 13.8 mg/kg b.wt 1/10 LD50 [24]. C. grevei extracts were dissolved in water and given via oral route at dose 150 and 300 mg/kg b.wt. Dosages were freshly prepared, adjusted weekly for body weight changes, while a control group was received corn oil.

Sample collections

At the end of the experiment, blood samples were drawn from the retro-orbital venous plexus of the animals in glass tubes. Within 20 min of blood collection, the sera were drawn after centrifugation at 3500 rpm for 10 min at 4 °C. The sera were kept in a deep freezer (−20 °C) for biochemical analysis. Portions of liver from all animals in each group were homogenized in 50 mM Tris–HCl buffer (pH 7.4) containing 1.15 % potassium chloride. The homogenates were centrifuged at 10,000 g for 15 min at 4 °C. The collected supernatants were used for the estimation of the activities of CAT, SOD, GST enzymes and the contents of GSH and LPO.

Body weights and relative liver weights

During the experimental period, body weight changes of male mice were recorded weekly. At the end of treatments, the mice were sacrificed by cervical dislocation. Liver of mice was quickly removed, cleaned, weighed and used for biochemical and histological studies. Then, relative weight of liver was calculated.

Biochemical measurements

All biochemical measurements (AST, ALT, ALP, LDH, SOD, CAT, GST, MDA, and GSH) were determined using commercial kits in accordance with manufacturers’ instructions using a spectrophotometer (Shimadzu UV–VIS Recording 2401, PC, Japan).

Histological study

Small pieces of liver samples from each group were dissected and fixed in 10 % neutral formalin, dehydrated in ascending grades of alcohol and embedded in paraffin wax. Paraffin sections (5 μm thick) were stained for routine histological study using haematoxylin and eosin (H&E). Two slides were prepared for each mice; each slid content two sections. Ten field areas for each section were selected and examined for histopathological changes (x160) under light microscope. According to Michael [25], the liver fields were scored as follows: normal appearance (−), minimal cellular disruption in less than 1 % of field area (+), mild cellular disruption of 1-30 % of field area (++), moderate cellular disruption of 31-60 % of field area (+++), severe cell disruption of 61-90 % of field area (++++) and very severe cellular disruption of 91-100 % of field area (++++).

Statistical analysis

The results were expressed as means ± S.D. All data were done with the Statistical Package for Social Sciences (SPSS 17.0 for windows). The results were analyzed using one way analysis of variance (ANOVA) followed by Duncan’s test for comparison between different treatment groups. Statistical significance was set at P ≤ 0.05.

Results

The highest yield of C. grevei was obtained with the dichloromethane extract (4.6 %) of the plant material. While, the low yield was observed with the ethyl acetate extract (0.44 %). This variation in the yields of different extracts can be explained by the difference of polarity for compounds present in the plant (Table 1). Methanolic and ethanolic extracts of C. grevei were found to have high total phenolic content, 41.67 ± 0.19 and 39.12 ± 0.44 g GAE/Kg ES, respectively (Table 2). So, in the present study, the polar extracts containing the highest amount of phenolic (EtOH and MeOH) were selected for the further analysis. The ethanol extract is the richest by tannins with 22.14 ± 1.03 g EC/kg ES, followed by methanol extract with 12.69 ± 0.63 g EC/Kg ES. The ethanolic and methanol extracts have obtained intermediate values for anthocyanins (respectively 1.86 ± 0.13 and 1.35 ± 0.08 g C3GE/Kg ES) (Table 2), while flavonoids not detected.

Table 1 Solvents extract and yield of Cedrelpsis grevei
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Table 2 Chemical composition of C. grevei leaves extracts
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Figure 1 illustrates a decrease in the concentration of DPPH radical due to the scavenging ability of C. grevei extracts. On DPPH radical, EtOH and MeOH had scavenging effects with increasing concentration in the range of 95–400 μg/mL, and the scavenging effect of EtOH was lower than MeOH. The IC50 value of ascorbic acid was 4.7 μg/mL. MeOH extract (400 μg/mL) exhibited the highest inhibition of about 69.45 %, but this is lower in EtOH extract whose percentage of inhibition is 61.27 %. ABTS assay is shown in Fig. 2. C. grevei extracts (100 μg/mL) exhibited the highest inhibition of 76.81 % and 78.35 % of MeOH and EtOH extracts. As illustrated in Fig. 3, Fe3+ was transformed to Fe2+ in the presence of MeOH and EtOH extracts of C. grevei to measure the reductive capability. C. grevei extracts had significant inhibition of reducing power with increasing concentration in the range of 0.10-0.125 mg/mL.

Fig. 1
figure 1

DPPH radical scavenging activity (%) of MeOH and EthOH extracts of C. grevei. Bars represent the mean ± SD

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Fig. 2
figure 2

ABTS•+ Scavenging activity (%) of MeOH and EthOH extracts of C. grevei. Bars represent the mean ± SD

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Fig. 3
figure 3

Reducing power (absorbance at 700 nm) of MeOH and EthOH extracts of C. grevei. Values are mean ± SD

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In the present study, the body weight loss was markedly observed of mice treated with Cyp compared to the control group (Fig. 4A). The difference between the two groups was statistically significant (30.38 g vs. 32.82 g, P ≤ 0.05). Co- administration of C. grevei (MeOH extract) at 300 mg/kg b.wt. to mice of Cyp group restored body weight to normal range (33.81 g vs. 32.82 g). As shown in Fig. 4B, significant decrease in relative liver weight was observed after treatment of mice with Cyp compared to control group (5.44 % g vs. 4.88 % g). Co-administration of C. grevei at 150 & 300 mg/kg b.wt. with Cyp modulated significantly relative live weight to the normal control value (4.98 %, 4.91 % vs. 4.88 %).

Fig. 4
figure 4

Body (a) and relative liver (b) weights of rats exposed to cypermethrin (Cyp) and the protective effect of C. grevei (MeOH extract). Bars represent the mean of 6 mice ± SD; values are not sharing superscripts letters (a, b, c, d, e) differ significantly at P ≤ 0.05. Relative liver weight (%) = (liver weight/body weight) X 100. Con: control; Cyp: cypermethrin; Ext 150: 150 mg/kg b.wt of C. grevei extract; Ext 300: 300 mg/kg b.wt of C. grevei extract (MeOH extract)

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The oral administration of the two tested doses of C. grevei extract (150 & 300 mg/kg/day) to normal mice produced no changes in all serum biochemical parameters of liver compared to the normal control mice (Table 3). In contrast, male mice exposed to Cyp (13.80 mg/kg/day) induced a severe hepatic damage in serum enzyme activities of ALT, AST and ALP levels comparable to control (Table 3). Also in Cyp-treated mice, serum LDH activity was increased by 37.53 %, while it was decreased by −27.84 % in the liver homogenate. However, co-administration of C. grevei extract to Cyp-treated mice resulted in a partial recovery in the above-mentioned parameters (AST, ALT, ALP and LDH) in a dose dependent manner. The high dose of C. grevei extract (300 mg/kg) was more effective than low dose (150 mg/kg) to attenuate the perturbations in the tested enzymes (Table 3).

Table 3 Effect of C. grevei MeOH extract on SOD, CAT, GST, LPO and GSH in liver of mice exposed to cypermethrin
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In the liver homogenates of Cyp-treated mice, the activities of SOD, CAT, GST and the level of GSH decreased significantly (P ≤ 0.05) by 20.5 %, 38.5 %, 18.6 % and 30.1 %, respectively, while the level of MDA increased significantly (P ≤ 0.05) by 51.0 % when compared to the corresponding controls (Table 4). In this study, MDA level increased in mice exposed to Cyp. Co-administration of C. grevei extract to Cyp-treated mice resulted in a partial recovery in the above-mentioned parameters in a dose dependent manner. The high dose of C. grevei extract (300 mg/kg) was more effective than low dose (150 mg/kg) to attenuate the perturbations in the tested enzymes (Table 4).

Table 4 Effect of C. grevei MeOH extract on the activity of ALT, AST, ALP and LDH in serum and LDH in liver homogenate of mice exposed to cypermethrin
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The representative picutures of histopathological examination of the liver tissue are shown in Fig. 5 (A-D) and the semi quantitative histological scoring of liver damage is presented in Table 5. Liver sections from the control group mice showed normal hepatic cytoarchitecture. They formed of hepatocytes radiating from central vein to the periphery of the lobules (Fig. 5A). Liver lobules of Cyp-treated mice showed severe degeneration in hepatocytes, necroses, dilation of portal vein with inflammatory cell infiltration in the portal area (Fig. 5B). Liver sections of mice treated with Cyp + Ext 150 (Fig. 5C) showed mild to moderate dilatation of central vein and ballooning degeneration in surrounding hepatocytes. Whereas, in cypermethrin + Ext 300 treated mice (Fig. 5C) showed only moderate dilatation of portal vein.

Fig. 5
figure 5

Paraffin sections of liver stained by haematoxylin and eosin (H&E) for histopathological changes. Control group and extract groups [A] showing the normal histological structure of the central vein (CV) and surrounding hepatocytes (H) (x40). Cypermethrin group showing [B] degeneration in hepatocytes and dilation of portal vein with inflammatory cells infiltration (m) in the portal area (x80). Cypermethrin plus extract at 150 mg/kg. b.wt. [C] showing dilatation of central vein (CV) ballooning degeneration (h) in surrounding hepatocytes (x80). Cypermethrin plus extract at 300 mg/kg. b.wt. [D] showing dilatation of portal vein (x80)

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Table 5 The severity of the reaction in liver tissue of different groups according to the histopathological alterations.
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Discussion

The natural antioxidants present in many plants reduce oxidative damage and help prevent mutagenesis, carcinogenesis and aging due to their radical scavenging activities [8, 20]. Therefore, phenolic compounds of plants are very important because their hydroxyl groups confer antioxidant activity. Results of the present study showed that phenolics content of methanol and ethanol extract of C. grevei were similar quantities. However, no work in the literature cited the quantification of phenolic compound of that family. We have not detected flavonoids. These results are contradictory to those presented by the study of Paris and Debray [26], which showed that the leaves of C. grevei contain 2 % flavonoids as glycosides of flavonols. The ethanol extract is the richest by tannins, followed by methanol extract. In addition, the ethanolic and methanol extracts have obtained intermediate values for anthocyanins [26].

Free radicals are continuously produced in body and cause the oxidation of biomolecules (e.g., protein, amino acids, lipid and DNA) which leads to cell injury and death. Our results revealed that EtOH and MeOH extract of C. grevei had DPPH scavenging activity in a concentration depending manner. C. grevei extracts (100 μg/mL) exhibited the highest inhibition of ABTS. In reducing power assay, Fe3+ was transformed to Fe2+ in the presence of MeOH and EtOH extracts of C. grevei to measure the reductive capability. C. grevei extracts had significant inhibition of reducing power with increasing concentration in the range of 0.10-0.125 mg/mL. The result obtained by this method confirms those of tests DPPH and ABTS.

In toxicological studies, changes in the body weight and relative organs weights are important criteria for evaluation of organ toxicity and were used as a valuable index of insecticide-related organ damage [8]. Liver is the first organ to face any foreign molecule that is carried through portal circulation and it is subjected to most damage. It has been previously reported that during liver damage there was an observed decrease in antioxidant defenses in the liver [26]. In the present study, the body weights of mice treated with Cyp was markedly less while relative liver weight was increased compared to the control group. Administration of C. grevei extract at 300 mg/kg b.wt. to Cyp-intoxicated mice restored body weight to normal range and modulated significantly relative live weight to the normal control value. The decrease in body weight of Cyp treated mice was considered the result of direct toxicity and/or indirect toxicity related to the liver damage [27–29]. It may be attributed to the effect of insecticides on gastrointestinal tract resulting in decreased appetite and absorption of nutrients from gut [30]. Other investigations have reported the reduction in body weight and change in relative organs weights in Cyp-treated rats [31, 32] and in rabbits [33]

Cyp treatment induced a severe hepatic damage in serum enzyme activities of ALT, AST, ALP and LDH of male mice. The increase in serum AST, ALT and ALP enzymes may be due to liver dysfunction and disturbance in the biosynthesis of these enzymes with alteration in the permeability of the liver membrane takes place [34]. The increase in serum LDH activity may be due to the hepatocellular necrosis leading to leakage of the enzyme into the blood stream [35]. However, co-administration of C. grevei extract to Cyp-treated mice resulted in a partial recovery in the above-mentioned parameters (AST, ALT, ALP and LDH). The high dose of C. grevei extract (300 mg/kg) was more effective than low dose (150 mg/kg) to attenuate the perturbations in the tested enzymes.

SOD and CAT are known to play an important role in scavenging ROS. SOD catalyzes the destruction of the superoxide radicals to H2O2, while CAT reduces the H2O2 into water and oxygen to prevent oxidative stress and in maintaining cell homeostasis. In addition, GST play essential role in the detoxification process. In the liver homogenates of Cyp-treated mice, the activities of SOD, CAT, GST and the level of GSH decreased significantly, while the level of LPO increased significantly. The change in SOD and CAT might be in response to increased oxidative stress. Considering that GST are detoxifying enzymes that catalyze the conjugation of a variety of electrophilic substrates to the thiol group of GSH, producing less toxic forms [36], the significant decrease of GST activity may indicate insufficient detoxification of Cyp in intoxicated mice.

Malondialdehyde (MDA) is a major oxidation product of peroxidized polyunsaturated fatty acids and increased MDA content is an important indicator of lipid peroxidation (LPO) [37]. In the present study, MDA level increased in mice exposed to Cyp. However, when a condition of oxidative stress strongly establishes, the defense capacities against ROS becomes insufficient, in turn ROS also affect the antioxidant defense mechanisms, reduces the intracellular concentration of GSH, alters the activity of antioxidant enzymes e.g., SOD & CAT and increase MDA. These indirectly suggest an increased production of oxygen free radicals in mice. Highly reactive oxygen metabolites, especially hydroxyl radicals, act on unsaturated fatty acids of phospholipid components of membranes to produce malondialdehyde, an LPO product [38]. However, co-administration of C. grevei extract to Cyp-treated mice resulted in a partial recovery in the above-mentioned parameters in a dose dependent manner.

The histopathological changes in liver showed that exposure of mice to Cyp resulted in degenerative changes in the liver, including degeneration, necrosis, and inflammatory cells in the portal area. The biomarkers of liver dysfunction corroborated with the histopathological lesions observed in the current study. These observations indicated marked changes in the overall histoarchitecture of liver in response to Cyp, which could be due to its toxic effects primarily by the generation of reactive oxygen species causing damage to the various membrane components of the cell. Co-administration of C. grevei extract showed marked improvement in its histological structure in comparison to Cyp-treated group alone and represented by nil to moderate degree in inflammatory cell infiltration in portal area, degeneration in hepatocytes and congestion in the portal vein and central vein.

The present study has demonstrated that C. grevei exert have a hepatoprotective effect against Cyp-induced oxidative damage and hepatotoxicity in mice. Normalized antioxidant enzymes and reduction in MDA level are likely to be the major mechanisms by which C. grevei prevented development of the liver damage. Supporting this hypothesis, we observed significant increases in SOD, CAT, and GST enzyme activity and decreases in the levels of MDA in liver tissue concomitant with insignificant changes in liver serum dysfunction biomarkers (AST, ALT, ALP and LDH) of Cyp-treated mice by the administration of C grevei especially at high dose (300 mg/kg/day). This might be due to the antioxidant activity and hydroxyl radical scavenging effect of C. grevei, which sported by DPPH, ABTS scavenging activity and reducing power measurements. However, the antioxidant activity of an antioxidant compound have been attributed to various mechanisms, among which are prevention of chain initiation, binding of transition metal ion catalysts, decomposition of peroxides, prevention of continued hydrogen abstraction, reductive capacity and radical scavenging [38].

Conclusion

In view of the data of the present study, it can deduce that Cyp caused oxidative damage and liver dysfunction in male mice. C. grevei extract has protective effects on Cyp-induced lipid peroxidation, oxidative stress and liver damage. C. grevei was found to be an effective antioxidant in many in vitro assays such as DPPH, ABTS and reducing power. These results indicated that administration of C. grevei is useful, easy, and economical to protect humans against pesticides toxicity. The results presented here can be considered as the first information on the hepatoprotective and antioxidant properties of C. grevei extracts.