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Print version ISSN 0102-695X
Rev. bras. farmacogn. vol.22 no.3 Curitiba May/June 2012 Epub Jan 31, 2012
Anti-hyperlipidemic activity of oryzanol, isolated from crude rice bran oil, on Triton WR-1339-induced acute hyperlipidemia in rats
Somsuvra B. Ghatak; Shital J. Panchal
Department of Pharmacology, Institute of Pharmacy, Nirma University, India
Experimental studies carried out for evaluating the anti-hyperlipidemic properties of rice bran components have given interesting but often contrasting results. Therefore, the current study was initiated to investigate the anti-hyperlipidemic activity of oryzanol (OZ), a commercially-important bioactive phytochemical, isolated from crude rice bran oil (cRBO). OZ was isolated by a two-step solvent crystallization process from cRBO, which was extracted from fresh rice bran by hexane mediated soxhlet extraction. Subsequently, OZ (50 and 100 mg/kg, p.o.) was evaluated for anti-hyperlipidemic activity in Triton WR-1339-induced acute hyperlipidemic albino rats by estimating serum triacylglyceride (TG), total cholesterol (TC), very low density lipoprotein-cholesterol (VLDL-C), low-density lipoprotein-cholesterol (LDL-C) and high-density lipoprotein-cholesterol (HDL-C) levels with atorvastatin as the reference standard. The degree of protection was also assessed by measuring the levels of various hepatic anti-oxidant enzymes. OZ evoked a significant decrease in the levels of serum cholesterol, triacylglycerides, LDL, VLDL and a significant increase in the level of serum HDL and hepatic anti-oxidant enzymes. It also showed a significant ameliorative action on elevated atherogenic index (AI) and LDL/HDL-C ratios. These findings indicate that OZ possesses the potential to lower plasma lipid concentrations and might be of therapeutic benefit in hyperlipidemia and atherosclerosis.
Keywords: isolation, oryzanol, hyperlipidemia, rats, rice bran oil, Triton WR-1339.
Experimental and epidemiological studies have suggested that hyperlipidemia is a highly predictive risk factor for atherosclerosis, coronary artery disease (CAD), and cerebral vascular diseases, the primary causes of mortality in the developing countries like India (Ghatak & Asthana, 1995). The allopathic hypolipidemic drugs, although available at large in the market, their popularity has been marred by numerous side effects, severe contraindications and exuberant cost and this has further necessitated the search for alternatives (Speight, 1987). Furthermore, published reports have ascertained the isolation of certain nutrients that can be used as dietary supplements to meet up with the dietary imbalances in order to reduce the cardiovascular disease risk associated with hyperlipidemia (Cicero & Derosa, 2005). For instance, there are ample evidences elucidating the anti-hypercholesterolemic effect of fixed oils that are rich in polyunsaturated fatty acids, especially linolenic and linoleic acid.
It is in this context of developing alternative, effective and better anti-hyperlipidemic drugs for the prevention of cardiovascular diseases, that a global interest has been generated in recent years pertaining to the beneficial nutritive effects of bioactive phytochemicals like OZ, obtained from crude rice bran oil (cRBO) (Cicero & Gaddi, 2001).
RBO has been the focus of surmount attention because of its balanced fatty acid profile and rich source of bioactive phytoceuticals such as, OZ, tocopherols, phytic acid, lecithin, inositol, waxes etc. OZ is an important natural constituent of cRBO with its content ranging from 1.5 to 2.9% (Seetharamaiah & Prabhakar, 1986). Its fundamental molecular structure is the ferulic acid aromatic phenolic nucleus esterified to cyclopentanperihydrophenanthrene. OZ, although initially presumed to be a single component, it was shown to be a mixture of ferulic acid (4-hydroxo-3-methoxycinnamic acid) ester with phytosterol or triterpene alcohols. Major portions of OZ include cycloartenyl ferulate, 24-methylene cycloartanyl ferulate and campesteryl ferulate (Metwally et al., 1974). OZ is an anti-oxidant compound that has been associated with decreasing platelet aggregation, increasing the muscle mass and treating nerve imbalances and the disorders of menopause. It has also been shown to exhibit anti-aging effect similar to tocopherols, anti-dandruff and anti-itching properties and to cause an improvement of capillary action of blood vessels (Patel & Naik, 2004).
In the last couple of decades, numerous studies have been carried out to elucidate the effect of RBO and OZ activity on lipid metabolism and oxidation in rats, rabbits, hamsters, monkeys and humans. While most of these studies have confirmed the OZ component of RBO to be responsible for the cholesterol lowering property in chronic hyperlipidemia models using high fat diet, the studies carried out on the rats have yielded interesting but often contrasting results (Cicero & Derosa, 2005). Furthermore, there is paucity of reports on the potential effects of OZ on acute hyperlipidemia using Triton WR-1339, a non-ionic detergent (oxyethylated tertiary octyl phenol formaldehyde polymer) that has been widely used to produce acute hyperlipidemia in animal models in order to screen natural or chemical drugs and to study cholesterol and triacylglycerol metabolism (Zeniya & Reuben, 1988).
In light of the above perspective, the current investigation was carried to assess the anti-hyperlipidemic activity of OZ in triton WR-1339-induced acute hyperlipidemia in rats.
Materials and methods
Drugs and chemicals
Rice bran was procured from Suryodaya Rice Mills, Ahmedabad, Gujarat through their milling process. Triton WR-1339 was purchased from Sigma-Aldrich Chemie GMBH. Atorvastatin calcium was obtained as a gift sample from Troikaa Pharmaceuticals Limited, India. Thiobarbituric acid was purchased from Spectrochem Pvt. Ltd., India. All diagnostic kits were purchased from Lab Care Diagnostics Pvt. Ltd., India. All solvents and reagents were either of HPLC grade or of analytical reagent grade and were obtained from commercial sources.
Extraction of RBO
Fresh rice bran obtained from the local rice mill was stored in a refrigerator before use. Crude RBO was extracted from rice bran (50 g) by soxhlet extraction for 3 h using hexane as the solvent. The extracted crude oil was stored at -5 ºC and subsequently analyzed for the various physicochemical parameters, such as organoleptic characters, specific gravity, viscosity, moisture content, saponification value, unsaponifiable matter, wax content, iodine value, acetyl value, acid value, hydroxyl value, ester value and peroxide value using various standard official methods, the results of which have already been published previously (Ghatak & Panchal, 2010).
Isolation of OZ from cRBO
The isolation of OZ from cRBO was achieved by a two-step crystallization process previously described by Zullaikah et al. (2009) with some modifications. In the first step of isolation, the OZ-rich product was concentrated in the liquid phase by solvent crystallization using methanol/acetone (7:3, v/v). In the second step, the OZ-rich product was kept at ambient temperature for 24 h. After that, hexane was added as an anti-solvent and kept at 5±1 ºC for 48 h. Under optimal operational conditions, supplemented by considerable savings of both time and solvents, white OZ crystals with a purity of 94.07% and recovery of 55.61% were obtained.
Adult wistar rats of either sex weighing 250-300 g were procured from the central animal facility of the Institute of Pharmacy, Nirma University, Ahmedabad. The animals were maintained at controlled temperature as well as humidity and fed with standard diet and water provided ad libitum. The experimental protocol was approved by Institutional Animal Ethics Committee (IAEC) of Institute of Pharmacy, Nirma University, as per the guidance of committee for the purpose of Control and Supervision of Experiments on Animals (CPCSEA), Ministry of Social Justice and Empowerment, Government of India. Test doses of OZ were selected for rats (50 and 100 mg/kg b. w., p.o.) based on the published literature reports (Sakamoto et al., 1987; Nakayama et al., 1987).
Rats (n=36) were randomized into the following groups:
1) Normal Control (NC): Received no treatment.
2) Vehicle Control (VC): Administered with 4% Tween-80 solution per day for 21 days.
3) Triton WR 1339 treated group (TRIT-C): 4% Tween-80 solution per day for 21 days and on the 21st day intra-peritoneal injection of Triton WR 1339 (400 mg/kg in saline) was given.
4) Oryzanol 50 mg/kg+Triton WR 1339 (OZ-50): Oryzanol 50 mg/kg/day, p.o in 4% Tween-80 solution was administered for 21 days and on the 21st day intra-peritoneal injection of triton WR 1339 (400 mg/kg in saline) in saline was given.
5) Oryzanol 100 mg/kg+Triton WR 1339 (OZ-100): Oryzanol 100 mg/kg/day, p.o in 4% Tween-80 solution was administered for 21 days and on the 21st day intra-peritoneal injection of triton WR 1339 (400 mg/kg in saline) in saline was given.
6) Atorvastatin 2 mg/kg+Triton WR 1339 (Ator): Atorvastatin (2 mg/kg/day, orally in 0.5% CMC) was administered for 21 days and on 21st day intra-peritoneal injection of triton WR 1339 (400 mg/kg in saline) was given.
After 24 h of triton injection or in case of control after 24 h of vehicle or drug treatment, blood samples were collected from the retro-orbital plexus of rat.
Estimation of biochemical parameters
Collection of serum
The blood samples were withdrawn from retro-orbital plexus under light ether anesthesia without any anticoagulant and allowed to clot for 10 min at room temperature. It was centrifuged at 2500 x g for 20 min. The serum obtained was kept at 4 °C until used.
Isolation of liver
All the animals were euthanasiously sacrificed by cervical dislocation. Liver was collected and was blotted free of blood and tissue fluids. Then it was weighed on balance and the relative weight was calculated.
Preparation of the tissue homogenate for enzyme assay
Liver, kept in cold conditions (pre-cooled in inverted petridish on ice) was removed. It was cross chopped with surgical scalpel into fine slices and was chilled in the cold 0.25 M sucrose, quickly blotted on a filter paper. The tissue was minced and homogenized in 10 mM Tris-HCl buffer, pH 7.4 (10% w/v) with 25 strokes of tight teflon pestle of glass homogenizer at a speed of 2500 x g. The clear supernatant was used for other enzymes assays.
Parameters assessed in serum
In vitro quantitative determinations of the activity of TC, TG, LDL-C, HDL-C concentration in serum were carried out using standard enzymatic kits (Lab Care Diagnostics, India). The concentration of VLDL-C was estimated as per the method proposed by Russell et al. (1990). Various other coronary disease risk factors such as atherogenic index (A.I.), HDL ratio and LDL-C/HDL-C ratio were also evaluated as per previously reported methods (Sheela & Augusti; 1995; Sharma et al., 1995).
Parameters assessed in the liver homogenate
The activities of anti-oxidant enzymes like reduced glutathione and the extent of lipid peroxidation were assayed in the liver homogenate as per previously established methods (Moron et al., 1979; Ohkawa et al., 1979; Lowry et al., 1951).
All the values are expressed as mean±SEM. Statistics was applied using Graph Pad Prism version 5.0 for Windows, Graph Pad software, San Diego, California, USA. One way ANOVA followed by Tukeys multiple comparison test was used to determine the statistical significance between various groups. Differences were considered to be statistically significant when p<0.05.
Effects on serum lipid profile
The normal control and vehicle control animals showed nearly similar lipid profile. Treatment with triton WR 1339 showed a significant increase in serum TC, LDL-C, TG and VLDL-C when compared to the normal control animals. A significant decrease in HDL-C was observed in the triton WR 1339 control animals. A dose dependant reduction in the levels of TC, TG, LDL-C and VLDL-C was observed with 50 mg/kg and 100 mg/kg dose of OZ. A significant increase in HDL-C levels was seen in the animals pretreated with 100 mg/kg/day of OZ (Figure 1).
Effects on atherogenic index, HDL-C ratio and LDL-C/HDL-C ratio (Coronary disease risk factors)
Atherogenic index (A.I.), an indicator of the deposition of foam cells or plaque or fatty infiltration or lipids in aorta and liver, was found to be higher in the Triton WR 1339 group as compared to the normal and vehicle control group. Other coronary disease risk predictor indices such as HDL ratio and LDL-C/HDL-C in the Triton WR 1339 group were also higher as compared to the groups pre-treated with OZ (Table 1).
Effects on lipid peroxidation and anti-oxidant enzyme level
Malondialdehyde level was measured as an index of lipid peroxidation in the liver homogenate. Triton WR 1339 controlled animals showed a malondialdehyde (MDA) level (nmol/mg protein) significantly higher than that observed in normal and vehicle control groups. Atorvastatin 2 mg/kg and OZ 50 and 100 mg/kg significantly reduced the MDA level. A remarkable depression was seen in the levels of antioxidant enzyme- reduced glutathione (μg/mg protein) in the triton WR 1339 treated group as compared to the normal control. Pre-treatment with OZ 50 mg/kg and 100 mg/kg showed a significant dose-dependent increase in the levels of reduced glutathione (Figure 2).
There are ample scientific evidences to demonstrate the hypocholesterolemic effects of rice bran in experimental animals and humans in long term experimental models of hyperlipidemia, induced by high fat diet. Such effects may be attributed to the unsaponifiable fraction of rice bran oil, primarily phytosterol, tocols (tocopherols and tocotrienols), OZ, triterpene alcohol and other minor compounds (Sharma & Rukmini, 1986). Although the exact mechanism of action of rice bran and the derived oil on lipid metabolism is not completely evident as yet, the possible fundamental anti-atherosclerotic role rests on OZ (Kanbara et al., 1992).
The reduction of TC by OZ was associated with a decrease in its LDL fraction, which is a potentially modifiable risk factor of cardiovascular diseases and the target of several hypocholesterolemic therapies. The findings of the present study suggest that cholesterol-lowering activity of OZ can result from the enhanced catabolism of LDL-C through hepatic receptors for final elimination in the form of bile acids (Khanna et al., 2002).
Increased levels of HDL after administration of OZ indicated its potent protective action against atherogenesis since an independent inverse relationship between blood HDL-C levels and cardiovascular risk incidence has been documented widely (Malloy & Kan, 1994). The underlying mechanism may be attributed to the enhancement of lecithin cholesteryl acyl transferase (LCAT), which plays a key role in incorporating the free cholesterol into HDL and transferring back to VLDL or Intermediate Density Lipoproteins (IDL), which is taken back by the liver cells (Devi & Sharma, 2004). Additional mechanism may involve an inhibition of hepatic triglyceride lipase (HTL) on HDL which may lead to a rapid catabolism of blood lipids through extrahepatic tissues (Anila &Vijayalakshmi, 2002).
Moreover, OZ at the dose of 100 mg/kg/day; p.o. significantly suppressed the elevated levels of TG, thereby suggesting that OZ is able to restore, at least partially, the catabolism of triacylglycerides.
Administration of OZ provides a beneficial effect on lipid metabolism in regard to the reduction of AI. In fact, the AI was decreased in all the treated groups, with a significant reduction being observed in the OZ 100 mg/kg/day, p.o. and atorvastatin 2 mg/kg, p.o. treated group. Similar results have been reported while investigating the hypolipidemic effect of other natural products (Cherng & Shih, 2005). Such an ameliorative action may be attributed to the lipid-lowering property of OZ.
Furthermore, there exists a positive correlation between an increased LDL-C/HDL-C ratio and the development of atherosclerosis. Again, the administration of OZ 100 mg/kg/day, p.o. and atorvastatin 2 mg/kg, p.o. significantly suppressed the higher values of LDL-C/HDL-C ratio elucidating the beneficial effect of OZ in preventing atherosclerosis incidence.
Oxidative stress is one of the prominent causative factors for hyperlipidemia (Lee et al., 2002). Increased lipid peroxidation is thought to be a consequence of oxidative stress due to impairment in the dynamic balance between pro-oxidant and antioxidant mechanism, resulting in the formation of free radicals, the natural by-products of many oxidative metabolic processes within cells causing damage to cell walls, certain cell structures and genetic material within the cells. Our study indicated that circulating concentration of MDA in the triton induced group was significantly higher than the control as well as the vehicle control group, indicating increasing oxidative stress with hyperlipidemia. These increased levels could be attributed to increased reactive oxygen species (ROS) production and/or deficiency of antioxidant defense system. Similarly, decreased activities of reduced glutathione, one of the first lines of cellular defense against oxidative injury, had been observed in the triton induced group. Thus, insufficient detoxification of these reactive oxygen species by antioxidant enzymes may lead to an occurrence of imbalance between antioxidant and oxidant systems. Low reduced glutathione activity could also attribute to enzyme inactivation by ROS bringing about damage to proteins. Interestingly, pre-treatment with OZ at 50 mg/kg and 100 mg/kg doses reduced the level of lipid peroxides (MDA) and increased the levels of reduced glutathione, indicating an effective anti-oxidant property of the test drug. The findings are in concordance to that reported in the literature, which indicates OZ to be an effective scavenger of free radicals (Xu & Godber, 2001).
It is possible that OZs antihypercholesterolemic effect is partially due to its sterol moiety, which is partly split off from the ferulic acid structure in the small intestine by cholesterol esterase (Swell et al., 1954). The antiatherogenic action of OZ could also be based on the inhibition of the accumulation of cholesterol-esters within the macrophages or by the modulation of cholesterol acid esterase and acyl-CoA-cholesterol-acyltransferase (Rukmini & Raghuram, 1991).
Therefore, the findings obtained from the current study reinforce the potential anti-hyperlipidemic activity of OZ in an acute hyperlipidemia model in rats, which may be attributed partially to its anti-oxidant activity. The findings are encouraging for further assessment to elucidate a more detailed mechanism(s) of action on a cellular and molecular level for the anti-hyperlipidemic activity of OZ.
The authors wish to thank the Department of Science & Technology, New Delhi, India for providing financial assistance (INSPIRE Fellowship: JRF Professional) for carrying out this work.
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Shital J. Panchal
Department of Pharmacology, Institute of Pharmacy, Nirma University, Sarkhej-Gandhinagar Highway, Ahmedabad-382 481, Gujarat, India
Tel: +91 9687626589
Fax: +91 79 2717 241917
Received 15 Jul 2011
Accepted 1 Nov 2011