Increased Cholesterol is one of the main culprits responsible for cardiovascular diseases. The present study was designed to evaluate the effect of ethanolic extract of Cleome brachycarpa on cholesterol and hepatic parameters and to evaluate whether its use can be helpful in treatment of hepatic and cardiovascular diseases.

The study was conducted on albino rabbits weighing 1000gms-1600gms. The animals were administered 300mg/kg of ethanolic extract of Cleome brachycarpa that was further diluted in Dimethyl sulfoxide and dose was adjusted in ml based on weight of animals. After 7 days dosing animals blood was drawn by cardiac puncture and Lipid profile and Liver function tests were done.

Our study showed that Ethanolic extract of Cleome brachycarpa possess significant hypolipidemic effects.It also lowers Total and Direct Bilirubin and Alkaline Phosphatase but elevates SGPT, SGOT and Gamma-GT. Cleome brachycarpa can be used in hyperlipidemia but monitoring of liver enzymes may be required during therapy.

Keywords: Alkaline Phosphatase; Bilirubin; Cholestrol; Cleome brachycarpa; Gamma-GT; Hyperlipidemia

ALP: Alkaline Phosphate; SGOT: Serum Glutamic Oxaloacetic Transaminases; SGPT: Serum Glutamic Pyruvic Transaminase; GGT: Gamma Glutamyl Transferase; TB: Total Bilirubin; LDL: Low- Density Lipoprotein; HDL: High- Density Lipoprotein; LCF: Lipid Clearing Factor; DMSO: Dimethyl Sulfoxide; VLDL: Very Low- Density Lipoprotein; GPT: Glutamic-Pyruvic Transaminase

Hyperlipidemia is defined as abnormal increased levels of lipoproteins or lipids in the blood [1]. Hyperlipidemia can lead to number of cardiovascular disorders mostly due to artherosclerosis. Cardiovascular diseases are the most prevalent cause of death all around the world [2]. Since the beginning of human civilization, plants have been used for treatment of different ailments. Phytochemicals are synthesized by plants which are chemical compounds [3]. Plants which contain phytochemicals when consumed by humans as a source of food are helpful in treating different diseases [4].

Plants had been used for healthcare and medicinal purposes long before it was recorded in history. As early as 3000 BC Egyptian papyrus and ancient Chinese writing describe medicinal uses of plant [5]. The use of herbs to treat different diseases is very common in under developed third world countries because it is cheaper and safer than modern allopathic medicine. According to survey conducted by World Health Organization 80% of the population of some African and Asian countries still prefer to use herbal medicine [6].

Cleome includes species which have ecological, ethno botanical and medicinal value. Cleome belongs to a small family of flowering plants and is the largest genus comprising of about 180-200 species [7]. Cleome comprises of herbaceous annual or perennial plants and shrubs. Genus Cleome was classified under family Capparidaceae however recently on the basis of DNA studies it has been placed under family Cleomaceae [8].
Traditionally leaf paste of cleome has been effective in headache. Cleome gynandra’s leaf juice is effective in earache and skin diseases [9]. Boiled leaves of Cleome serrulata are used in black paint preparation. Rubifacient and counter-irritant properties are found in species like Cleome viscose, Cleome gynandra and Cleome chelidonii. They are also used for rheumatism [10].

Cleome brachycarpa is mostly distributed in tropical and subtropical regions [11]. Through spectroscopic analysis of Cleome brachycarpa,Cabralealactone, Ursolic acid and new trinortriterpenoid dilactone deacetoxybrachycarpone has been isolated [12]. A new triterpenoid Cleocarbpone was also isolated from Cleome brachycarpa which has double oxygen function at C-24 and belongs to dammarane series [13]. Cleome brachycarpa has shown to possess numerous beneficial effects. The plant possesses anti-bacterial and anti-fungal properties and is thought to be useful appetizer and effective in abdominal discomfort [14]. The ethanolic extract of Cleome brachycarpa possesses anxiolytic properties [15] and also has positive effect on memory [16]. The leaves also possess anti-inflammatory properties, useful in rheumatism and are also effective in leucoderma and scabies [17]. The objective of the above study was to evaluate the effect of ethanolic extract of Cleome brachycarpa on lipid profile and on hepatic parameters in healthy rabbits.

The plant Cleome brachycarpa was provided by Dr. Iqbal Azhar from Department of Pharmacognosy University of Karachi.

Extraction of plant

The plant was first washed with water to reduce microbial load. The whole plant of Cleome brachycarpa was cut into small pieces and dried at 50°C, and then it was powdered. Next this powdered material was macerated with 95% ethanol for 3 days. It was then filtered and reduced to dryness under pressure. The process of maceration was repeated twice and then dried using (vacuum) evaporator.

Animals selected

For biochemical screening albino rabbits of either sex weighing 1000- 1600 grams were selected. Biochemical variations produced in rabbits and humans are comparatively similar therefore rabbits were selected for these tests [18]. The rabbits were equally divided into 2 groups, each containing 10 animals. First group served as Control, second was given Cleome brachycarpa. Animals were handled as per specifications provided in Helsinki Resolution 1964 and study was approved by our Board of Advanced Studies and Research vide Resol.No,09 Dated:20-04-2011& 22-04-2011.

Dosing regimen

First group was taken as control and given DMSO( Dimethyl sulfoxide) (same calculated ml as other groups) orally. Second group was given 300mg/kg Cleome brachycarpa, the dose was adjusted based on weight of rabbits. Standard solution of 1500mg/10ml was prepared in DMSO and it was administered orally in ml by serial dilution method once daily for 7 days.

Sample Collection: 7ml of blood samples were drawn from rabbits after 7 day dosing by cardiac puncture. 5ml blood is taken in gel tube for lipid profile and other biochemical analysis.

Estimation of lipid profile

Clotted blood samples were centrifuged for 15 minutes at 3000rpm to separate serum using Humalyzer 3000, semi-automatic chemistry analyzer model # 16700 (Human Germany). The parameters were analyzed within 3 hours of sample collection using standard kits supplied by Human.

Estimation of cholesterol

Cholesterol oxidase/peroxidase aminophenazone(CHOD-PAP method) which involves enzymatic colorimetric test for cholesterol with lipid clearing factor (LCF) was used to determine cholesterol in serum [19].

Estimation of HDL and LDL-cholesterol

Mostly laboratories use selective precipitation for removing VLDL and LDL, whereas supernatant fraction contains HDL which is enzymatically measured [20]. We used Human cholesterol test kit with precipitant, standard and HDL- cholesterol using Friedwald Method. LDL was also determined using Friedwald Method [21].

Estimation of liver function test

Using standard reagent kits of Human Germany, liver enzymes (SGPT and SGOT) were measured after centrifugation and obtaining serum.

Estimation of SGPT and SGOT

For GPT estimation liquid UV test method Alanine aminotransferase was used [22].
By Glutamic Oxaloacetic Transaminase (GOT) Aspartate amino Transferase (ASAT) International Federation of Clinical Chemistry (IFCC) mod liquid UV test the SGOT test was performed [22].

Estimation of alkaline phosphatase (ALP)

Using standard kits supplied by Human (HUMALYZER 3000) ALP was analyzed [23].

Estimation of gamma- glutamyl transferase (γ-GT)

Using colorimetric method γ-GT was estimated in the serum based on Szasz Method [24].

Estimation of Bilirubin

By photometric test total bilirubin and Direct Bilirubin was measured in serum [25].

By taking mean of all the values they are compared with means of control and Cleome brachycarpa and by student significance T –test the significance of difference between means are determined. A value of p< 0.05 is considered significant, p<0.001 as more significant and p<0.0001 as highly significant. By Alcarz and Jimenez method all statistical procedures have been performed [26].

Herbal preparations have been used since ancient times as a source of medicinal agent because of their therapeutic efficacy, low cost and safety. Cleome brachycarpa belonging to family Cleomaceae has not been vastly investigated although it has been shown to possess a number of therapeutic effects.

The major contributing factors in the pathogenesis of atherosclerosis and resulting cardiovascular diseases are increased plasma lipids [27]. Cholesterol is main reason of unanticipated progression and development of atheroma plaque [28]. Past studies indicate that high cholesterol prompts atherosclerosis and heart diseases as well as diabetes mellitus and cancerous development. Lowering the cholesterol level has an impact on prostrate tumors i.e it impedes their development [29].

There are also reports that LDL and HDL levels are more particular and sensitive biochemical markers of cardiovascular disease and HDL also serves to protect against advancement of atherosclerosis [30]. Table 1 & 2 shows effect of ethanolic extract of Cleome brachycarpa on lipid profile. Our results show highly significant decrease in cholesterol and LDL cholesterol p<0.0001 while there was no significant effect on HDL cholesterol p= IS. Saponins have been shown to possess hypocholesterolemic properties [31]. They act by decreasing the intestinal absorption of cholesterol; they are also thought to interfere with the cholesterol metabolism by interfering with circulating bile acids [32]. Ursolic acid present in cleome also possesses lipid lowering and cardio-protective properties [33].

Liver is the focus of biotransformation and metabolism of huge number of drugs and foreign agents thus hepatic damage is potential effect of many drugs [34]. Genuine underlying ailments can be found by rise of hepatic enzymes for example alanine transaminase and aspartate transaminase [35]. ALT is likewise signified as serum glutamate pyruvate transaminase and AST can be additionally called as serum glutamate oxaloacetate transaminase.

Hepatocytes contain the enzyme SGPT. This enzyme is leaked into the blood when these cells are damaged, where it is measured. SGPT is extremely elevated in acute liver diseases. SGOT is comparable to SGPT since it is also present in hepatocytes. It is elevated in acute liver damage, additionally it is present in erythrocytes, cardiac and skeletal muscle and not particular to liver [36]. Alkaline phosphatase is specific in cells lining biliary duct. ALP levels elevate in infiltrative diseases of liver. Gamma GT is present in cell membranes of many tissues of bile duct, gall bladder, heart, brain and kidney etc [37].

Normal heme catabolism results in yellow breakdown product called Bilirubin. It has been found in plants too. It is excreted in bile and urine [38]. Total or direct bilirubin is usually estimated to monitor gall bladder or liver problems [39]. Cleome brachycarpa highly significantly increases SGPT, SGOT and γ-GT levels p<0.0001 showing liver damage or hepatotoxic effects. It highly significantly reduces p <0.0001 total and direct bilirubin and has no effect on alkaline phosphatase as such. The hepatotoxic effect may be due to deacetoxybrachycarpone or cabralealactone but further work needs to be done to evaluate its effects.

On the basis of our study we can conclude that Cleome brachycarpa possesses hypolipidemic effects and could be beneficial in patients suffering from cardiovascular disease as but dose reduction needs to be done along with monitoring of liver parameters to avoid hepatotoxic effects.

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