Hepatoprotective effect of methanol extracts of Zingiber officinale and Cichorium intybus

*Corresponding Author:

A. H. Atta
Department of Pharmacology, Faculty of Veterinary Medicine, Cairo University, Giza, Egypt
E-mail: attaattia52@yahoo.com

Abstract

The present work was carried out to investigate the hepatoprotective effect of ginger, chicory and their mixture against carbon tetrachloride intoxication in rats. Carbon tetrachloride treatment significantly elevated the alanine aminotransferase, aspartate aminotransferase, alkaline phosphatase and gamma glutamyltransferase activities and the serum triglycerides and cholesterol concentration as compared to control group. It also increased RBCs counts and Hb concentration, total or differential leucocytes counts. However it decreased platelet counts, platelet distribution width, mean platelet volume, platelet larger cell ratio. Methanol extract of ginger (250 and 500 mg/kg) and chicory (250 and 500 mg/kg) given alone or mixed (1:1 wt/wt) significantly restored the carbon tetrachloride-induced alterations in the biochemical and cellular constituents of blood. No toxic symptoms were reported in doses up to 5 g/kg. Alkaloids and/or nitrogenous bases, carbohydrates and/or glycosides, tannins, flavonoids, saponins and unsaturated sterols and/or triterpenes are the main active constituents of their methanol extract. The hepatoprotective effect of ginger and chicory was also confirmed by the histopathological examination of liver tissue.

Keywords

Carbon tetrachloride, chicory, cholesterol, creatinine, ginger, hepatotoprotective, histopathological, liver function, triglycerides

Liver dysfunction caused mostly due to exposure to toxic chemicals, certain drugs and environmental pollutants, has been on the increase for the past few decades. In many countries hepatopathy is increasingly being managed using herbal treatment [1]. Ginger (Zingiber officinale Roscoe, Zingiberaceae), a commonly used flavoring agent and cooking spice is added as a herbal supplement. It has a large variety of pharmacological activities such as antibacterial, antioxidant, and antiinflammatory effect as well as attenuation of lipid peroxidation and oxidative stress [2,3]. It has been reported to improve various gastrointestinal illnesses [4,5] and immunologic dysfunction [6]. It also has been reported to exert antidiabetic activity, reduce liver damage [7] and possess anticarcinogenic effect [8]. It also has been reported to be used in hypertension and for exerting cardioprotective and antioxidant property [4,9].

Chicory (Cichorium intybus, Asteraceae) is a root vegetable whose green leafy tops are also used in salads or as a coffee supplement. Recently pharmacological actions of chicory have attracted the attention of many researchers. It was reported to induce hypocholesterolemia [10], protect against hepatocellular damage [11,12] and inhibit lipid peroxidation [13,14]. It also has an antihyperglycaemic effect [15], regulate appetite and carbohydrate and lipid metabolism [16]. It was the aim of this work to explore the hepatoprotective effect of the methanol extract of ginger and chicory when given alone or in a mixture.

Materials and Methods

Zingiber officinale Roscoe, Zingiberaceae) rhizome and Cichorium intybus, Asteraceae) green plant were identified at the Herbarium of the department of Botany, Faculty of Science, Cairo University. A voucher sample was deposited in the department of Pharmacology, Faculty of Veterinary Medicine, Cairo University, Egypt. The air-dried plant material was moderately pulverized, and stored for further use. The powdered plant (200 g) was extracted and percolated in methanol 95% for 5 to 7 times till complete extraction. The methanol extracts was concentrated under reduced pressure using a rotary evaporator at temperature not more than 50°. The concentrated extract was kept at – 4° until used for phytochemical and pharmacological studies.

Animals

Sprague Dawley rats (150-170 g) and Swiss mice weighing 20±5 g of both sexes were obtained from Laboratory Animal Colony, Helwan, Egypt. Animals were maintained in the Animal House of Pharmacology Department, Faculty of Veterinary Medicine, Cairo University under controlled hygienic conditions. Animals were fed on locally manufactured pellets and water was provided ad libitum. Animals were allowed to acclimatize to the laboratory environment for 7 days before initiating experiments. Rats were used for evaluating hepatoprotective effect and mice were used for the acute toxicity testing of the plant extracts studied.

Hepatoprotective effect

The model described by Chakraborti and Handa [17] was used. Rats were divided into eight equal groups of six rats each. All groups received the administered doses orally by using stomach tube. Rats of group I (normal control) were given 2.5 ml/ kg corn oil daily for 5 days and this group served as an environmental control. Rats of the 2nd group were used as positive control and were given 2.5 ml/kg carbon tetrachloride (50 % CCl₄ in corn oil). Rats of the 3rd and 4th groups were administered ginger extract at a dose of 250 and 500 mg/kg, respectively, while those of the 5th and 6th group were administered chicory extract in a dose of 250 and 500 mg/kg. The 7th group received 250 mg/ kg of a 1:1 w/w mixture of ginger and chicory extracts. Doses were calculated depending on the yield of the methanol extract of an amount of the plants equivalent to human consumption. Rats of the 8th group were used as a standard treated group and received orally 25 mg/kg silymarin for the same period. All groups, except normal control group received 2.5 ml/kg CCl₄ (50% of CCl₄ in corn oil) on the 2nd and 3rd day. On the fifth day, blood samples were collected from the orbital plexus of all rats. Serum samples were separated and used for determination of different biochemical parameters. After collection of the blood samples, all rats were sacrificed to collect the liver for histopathological examination. Animals were handled according to the local rules and regulation of Experimental Animals, Cairo University.

Blood samples

Blood samples were collected 24 h after CCl₄ administration through retro-orbital puncture. Blood samples were allowed to clot and centrifuged to separate clear serum. The activities of alanine aminotransferases (ALT), aspartate aminotransferase (AST), alkaline phosphatase (AP) [18], gamma glutamyltransferase (GGT) [19] and the level of glucose [20], triglyceride [21], total proteins, albumin and bilirubin [22], were determined using kits obtained from bioMérieux, France; while creatinine [23] and cholesterol [24] levels were determined using kits obtained from Diamond, Cairo, Egypt.

Pathological studies

Liver tissue specimens were collected from all groups’ immediately after sacrifice of rats and fixed in 10% formol saline. Paraffin sections of 5 μ thickness were prepared, stained by Hematoxylene and Eosin (H & E) and examined microscopically.

Acute toxicity study in mice

The acute toxicity of plant extract was tested as described by Tanira et al. [25], using three doses (0.4, 1 and 2.5 g/kg orally). Control rats were kept under the same conditions without any treatments. Observation period extended up to 72 h post administration. In addition, the general behavior of animals, signs of discomfort, or any nervous manifestations were observed. The large dose was selected to represent the maximum dose in relation to the extract-dry plant yield.

Phytochemical screening

The extracts were screened for the presence of tannins, saponins, sterols and or triterpenes, alkaloids, anthraquinones, flavonoids, lactones/esters, protein and or amino acids and carbohydrates and or glycosides with thin layer chromatography (TLC) as described by Stahl [26]. Thin layer plates precoated with Silica gel G (Merck, 0.25 mm thickness) were used. Development was carried out with different solvent systems, ethyl acetate:methanol:water (100:13.5:10 v/v), ethyl acetate:formic acid:acetic acid:water (100:11:11:27 v/v), chloroform:methanol:water (64:50:10 v/v), benzene:ethyl acetate (86:14 v/v) and ethyl acetate:methanol:water:acetic acid (65:15:15:10 v/v/v/v).

After development in the solvents the plates were dried and sprayed with Dragendorrf’s, AlCl₃, Hydroxylamine-ferric chloride, and ninhydrin and antimony trichloride for the detection of alkaloids, flavonoids, lactones/ esters, protein/amino acids and sterols/triterpenes. Detection of anthraquinones, saponins, tannins glycosides/ carbohydrate was carried out using KOH, anisaldehyde-sulphuric acid reagents, ferric chloride and naphthoresorcinol reagents respectively [27]. Detection was carried out by visualization in visible light and under UV light (λ366 nm).

Statistical analysis

Results are expressed as mean±standard deviation (SD). Differences between means in different groups were tested for significance using a one-way analysis of variance (ANOVA) followed by Duncan’s test and P value of 0.05 or less was considered significant.

Results

Toxicity testing

Oral administration of methanol extracts of either ginger or chicory in doses up to 5 g/kg revealed no symptoms of morbidity or mortality were reported. Therefore LD₅₀ is more than 5 mg/kg indicating that the tested plants are safe for use.

Phytochemical study

Preliminary phytochemical screening of the tested extracts revealed the presence of alkaloids and/or nitrogenous bases, carbohydrates and/or glycosides, tannins, flavonoides, saponins and unsaturated sterols and/or triterpenes in both ginger and chicory. Resins are reported only in ginger methanol extract.

Effect on serum biochemical constituents

The CCl₄ intoxication significantly elevated the ALT, AST, ALP and GGT activity as compared to control group. Ginger methanol extract in small or large dose decreased only the activity of ALP and GGT, however it did not significantly affect the level of ALT or AST. Methanol extract of chicory in both doses and mixture of both chicory and ginger (1:1; w/w) significantly decreased serum ALT, AST and ALP. Oral administration of silymarine (25 mg/kg) did not significantly alter the elevated serum liver enzymatic activity (fig. 1).

CCl₄ significantly increased serum trigycerides and cholesterol concentration. Methanol extract of chicory and ginger in both doses as well as their mixture (1:1; wt/wt) significantly decreased serum trigycerides and cholesterol concentration. Their lowering effect was more potent than that of silymarine. There was no significant effect on serum total bilirubin, total protein level or albumen concentration after administration of methanol extract of ginger, chicory in both doses as well as their mixture (Table 1).These results revealed that the CCl₄ treatment at a dose of 2.5 ml /kg did not affect the serum glucose, urea or creatinine level compared to control group. Neither silymarine nor ginger and small dose of chicory affected serum glucose, urea or creatinine. Only large dose of chicory and mixture of both of ginger and chicory significantly decreased serum urea level (fig. 2).

Table 1: Effect Of Methanol Extracts Of Ginger And Chicory On Serum Biochemical Constituents In Carbon Tetrachloride–Induced Hepatotoxicity

Effect on RBCs and related indices

CCl₄ significantly increased RBC counts and Hb concentration. Chicory in both doses and also the mixture of both ginger and chicory significantly increased the RBCs count, Hb and haematocrite concentration when compared to control or carbon tetrachloride- intoxicated group. Ginger did not affect any of the blood parameters (Table 2).

Table 2: Effect Of Methanol Extract Of Ginger, Chicory And Mixture Of Both On Some Hematological Indices

Effect on total and differential leucocytic counts

CCl₄ did not significantly affect total or differential leucocytes counts. There was no significant difference in the total WBCs count between any of plant extract or silymarine- and CCl₄ alone-treated groups. Lymphocytes and eosinophiles percent were significantly decreased. Monocyte percent was significantly increased in ginger treated rats. On the other hand monocytes were significantly increased and the eosinophile count was significantly decreased in chicory-, mixture of ginger and chicory-, and silymarine-treated rats. Basophiles percent were significantly decreased in mixture of ginger and chicory- and silymarine-treated rats (Table 3).

Table 3: Effect Of Methanol Extract Of Ginger, Chicory And Mixture Of Both On Total And Differential Leucocytes Count

Effect on blood platelets

Results indicated that platelet counts (PLT)×10³ / μl in control group was 751.5±78.87. In CCl₄-intoxicated rats, platelet counts, platelet distribution width (PDW), mean platelet volume (MPV), platelet larger cell ratio (P-LCR) was significantly (P>0.05) decreased in comparison to normal control. Ginger in the large dose, chicory in both doses and mixture of both ginger and chicory as well as silymarine significantly increased platelets counts, platelet distribution width (PDW), mean platelet volume (MPV), platelet larger cell ratio (P-LCR) to levels nearly similar to that of normal control (Table 4).

Table 4: Effect Of Methanol Extract Of Ginger, Chicory And Mixture Of Both On Plt, Mpv, P-Lcr

Pathological examination

Macroscopically, the livers in CCl₄-treated group were enlarged, friable and pale in color. The livers of ginger-treated rats was slightly enlarged, moderate friable and mottled in appearance. Liver from rats treated with chicory was apparently normal in texture. Histopathological observation of CCl₄- treated group showed very severe hepatotoxicity as evidenced by the appearance of centrilobular necrosis, ballooning degeneration in hepatocytes, congestion in the central vein and sinusoids, proliferation of Kupffer cells and mononuclear leucocytes inflammatory cells infiltration mainly surrounding the central vein (fig. 3b) compared to normal non treated rats (fig. 3a). In ginger and chicory-treated groups, moderate to mild degenerated and necrobiotic changes (centrolobular) in the hepatocytes were observed (fig. 3c and d, respectively). Similar picture was observed in silymarine- and mixture of ginger and chicory-treated groups (picture not shown).

Discussion

Results of this study revealed that there were no symptoms of morbidity or mortality reported 48 h after oral administration of tested methanol extracts of both ginger and chicory in doses up to 5000 mg/ kg in mice. These results indicated that both tested extracts were safe to be used and they are nontoxic. In this respect [28] reported that plants with LD₅₀ more than 5000 mg/kg is considered nontoxic. A toxicological evaluation of a chicory root extract was also done by Schmidt et al. [29]. They reported that there were no observed adverse effects of chicory extract in their studies. The NOAEL (no observable effective level) for the extract is 1000 mg/kg when administered orally for 28 days. Moreover, the extract was nontoxic up to a dose of 1500 mg/kg [30].

Estimation of the activity of ALT, AST and GGT are good marker of assessment liver function. These enzymes are normally located in the cytosol of hepatocytes. When liver cells are damaged, these enzymes are released in the plasma and increased their activity in plasma is a useful marker of the extent and type hepatocellular damage [1]. Carbon tetrachloride administration to experimental animals induced acute pathological changes in the liver. This finding correlates with the marked increase in serum ALT, AST and GGT activities. Moreover, the increased triglyceride content in the blood is in correlation with the fatty degeneration of the liver induced by CCl₄ [31]. Biochemical mechanism for CCl₄ toxicity based on mitochondrial damage was previously described [32].

The present results clearly demonstrate the marked antihepatotoxic effects of methanol extract of ginger, chicory and their mixture (1:1 wt/wt) as compared to the reference drug, silymarine. This fact is based on the tendency of liver enzymes, glucose and triglycerides to return towards their respective levels in the normal control group. Previous studies have demonstrated that both ginger [7,33], or chicory [11,12] exhibited hepatoprotective effect. In this study additional evidence that not only methanol extract of ginger or chicory but also a mixture of both (1:1 wt/wt) exhibited a hepatoprotective effect which was more effective in reducing serum liver enzymes towards or even below the normal values than ginger or chicory alone. The decreased liver enzymes below the carbon tetrachloride-treated or normal rats are probably due to a membrane stabilizing effect.

Although the active compounds of the tested plants have not been well identified in the present study, preliminary phytochemical study revealed the presence of alkaloids and/or nitrogenous bases, carbohydrates and/or glycosides, tannins, flavonoids, saponins and unsaturated sterols and/or triterpenes as major active constituents. Saponins, flavonoids, and alkaloids have been previously reported in the crude extract of ginger [4]. The reduced lipid peroxidation in rat liver homogenates were reported to be due to total phenolics or flavonoids contents of some medicinal plants [13]. Therefore the protective effect of plant extract against CCl₄ hepatotoxicity may be attributed to the presence of triterpenoids and steroids [16].

Many compounds known to be beneficial against CCl₄-mediated liver injury exert their protective action by toxin-mediated lipid peroxidation either via decreased production of carbon tetrachloride derived free radicals or through the antioxidant activity of the protective agents themselves [34]. Phenolic compounds were also separated from ginger [5] and chicory [14]. These constituents were reported to exhibit strong antioxidant properties and cytoprotective actions in rats [5]. Therefore it may be suggested that the hepatoprotective effect of the tested plants is due at least partially to their content of flavonoids and or triterpenoids.

The triglyceride and cholesterol lowering effect could be related to the total lipid lowering effect by ginger [2,35]. The blood glucose lowering effect may be due to the presence of inulin and oligofructose [16,36].

Although no available literature could be obtained concerning the effect of the tested methanol extracts on blood cellular elements, however the increased RBCs count and Hb and HCT in chicory and mixture treated rats could be attributed to its protective effect on bone marrow [30,37]. The increased monocyte counts in blood of rats treated with methanol extract of ginger and /or chicory may be related to the antiinflammatory effect of their active constituents [38,39] and to their immunoprotectant effect [36,40]. The present data clearly demonstrate that oral administration of methanol extract of ginger or chicory has restored the platelets counts which were decreased after CCl₄ -induced intoxication.

Oral administration of the tested methanol extracts revealed that administration of mixture of both ginger and chicory improved of the degenerative histopathological changes induced by CCl₄ intoxication in liver. In this concern, it is reported that cichorium root extract therapy leads to normalization of some morphofunctional liver features (decreases glycogen content and cell necrosis) in rats with CCl₄-induced hepatitis [12,41]. The antihepatotoxic activity of ginger extract may be due to its direct radical scavenging activity [33]. In conclusion, ginger or chicory were effective as antihepatotoxic and can be considered as good natural sources of hepatoprotective constituents.

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