ARTICLE INFO

Article Type

Original Research

Authors

Vafaeinejad   S. (1 )
Serki   E. (2)
Hassanpour Fard   M. (3 )
Hosseini   M. (* )






(* ) Experimental Medicine Research Center, Deputy of Research & Technology, Birjand University of Medical Sciences (BUMS), Birjand, Iran
(1 ) Anatomy Department, Medicine Faculty, Birjand University of Medical Sciences (BUMS), Birjand, Iran
(2) Biochemistry Department, Medicine Faculty, Birjand University of Medical Sciences (BUMS), Birjand, Iran
(3 ) Physiology & Pharmacology Department, , , , , Medicine Faculty, Birjand University of Medical Sciences (BUMS), Birjand, Iran

Correspondence

Address: Birjand University of Medical Sciences, Ghaffari Street, Birjand, Iran
Phone: +985632395360
Fax: +985632433001
mehranhosseiny@yahoo.co.in

Article History

Received:  September  30, 2014
Accepted:  February 18, 2015
ePublished:  April 16, 2015

BRIEF TEXT


… [1-7] Two common drugs to control and treat hyperlipidemia are statins and fibers that their mechanisms are reducing cholesterol biosynthesis, increasing lipolysis and eliminating of atherogenic particles in the plasma. Long-term treatments with these drugs cause many complications including liver poisoning and kidney disorder [8]. … [9-11] World Health Organization, also, emphasizes the identification and the use of native plants as complementary medicine in the treatment of diseases, especially in the developing countries [12]. … [13, 14] Among the useful medicinal plants that can reduce blood fat, Turnip (Brassica rapa) from the family of Brassicacea can be noted. The utilization of different parts of the plant (roots, leaves, seeds and flowers) is recommended in traditional medicine to treat various diseases including diabetes, obesity and hyperlipidemia [15]. Among the secondary compounds in turnip roots, Frolic acid and sinapic acid can be mentioned that substantially and exclusively are found in the root of the plant. ... [16]

The consumption of polyphenols and plant compounds rich in glycosides can reduce the risk of elevated blood lipids [17]. Frolic acid in oral doses up to 100 mg/kg of body weight in rats reduced their blood pressure [18, 19]. … [20] Frolic acid consumption of high-fat diet in exposed rats could be effective in lowering blood triglyceride and creating slow accumulation of fatty plaques in the aorta of the animals [21]. Synapic acid which is a phenolic compound has antioxidant properties that reduce blood lipids and inflammation [22].

The aim of this study was to investigate lipid-lowering effects of aqueous extract of the roots of turnips in the hyperlipidemia rats.

This is an experimental study.

Male Wistar rats weighing range 180-220 gr were studied in Experimental Medicine Research Center of Birjand University of Medical Sciences (Iran).

40 rats were studied.

In order to achieve the extract, 100g of turnip roots was solved in a liter (ratio of one to ten w / v) of distilled water kept 48 hours at room temperature in a magnetic shaker container. The solution initially was filtered with filters with decreasing porosity percentage, and finally it was filtered by whatman-filter-paper no. 14. The resulting solution was concentrated by rotary evaporator under vacuum at 45° C, and then, using a freeze dryer device (Dena FD-5005-BT; Iran), lyophilized powder was obtained. Alkaloid compounds, glycosides, flavonoids, saponins and tannins in the extract were qualitatively detected using Tiwari method. [23]. Polyphenols were determined quantitatively through the test repeated three times by spectrophotometric method according to the instruction by Živković et al. Notably, Galic acid was used as the standard for this test [24]. The animals were divided randomly into 5 groups: Group 1 (healthy control – receiving normal saline), group 2 (control hyperlipidemia- receiving normal saline), group 3 (positive control-10 mg /kg atorvastatin), Group 4 (200 mg/ kg turnip root aqueous extract) and 5 (400 mg/ kg turnip root aqueous extract). All the aforementioned groups received treatments orally for 10 days at a specified time. On the eleventh day after 18-hour fasting for all groups except control group, the groups were received 300 mg/ kg triton- WR1339 (Sigma Alderich; USA) intra-peritoneal injection [25-27]. The rats were kept in fasting and with only access to water. After 24 hours, blood was taken from their heart after anesthetizing with ether. To assess the levels of total cholesterol, triglyceride, HDL-cholesterol and LDL-cholesterol, tests were conducted by Auto-analyzer (Integra; Germany) and standard diagnostic kits (Roche; Germany). Data were statistically expressed as mean. The groups were compared using ANOVA, Tukey test and SPSS 18 software [28-39].

In the initial evaluation of the aqueous extract of the roots of turnips, there were flavonoid and tannin in the extract, while the quality tests indicated the absence of saponins, glycosides and alkaloids, in this extract. The amount of phenolic compounds in the turnip extract in Folin-Ciocalteu test repeated three times was 3.8± 0.42 mg/gr of Gallic acid. Triton led to a significant increase in the levels of total cholesterol, triglyceride and LDL-cholesterol, as well as a significant decrease in the level of HDL-cholesterol compared to the control group. 200 mg /kg turnip root aqueous extract could control the increase of total cholesterol and keep it in the normal range. Although the extract of turnip in both doses controlled both LDL- cholesterol and triglyceride increases, it could not keep the values in the normal range. 10 mg/kg atorvastatin could control LDL-cholesterol increase. Nevertheless, it could not keep the cholesterol and triglyceride factors in the normal range. The effect of atorvastatin on triglyceride level control is greater than turnip extracts (both doses), although no one could keep triglyceride levels in the normal range. HDL-cholesterol levels showed that none of the extract and atorvastatin groups could prevent its decrease.

Levels of total cholesterol, triglyceride and LDL cholesterol increased with a very high slope with Triton administration, and HDL-cholesterol levels were significantly decreased by a lower intensity. 200 mg/kg turnips aqueous extract could increase the total cholesterol caused by triton injection keeping it in the normal range. In addition, it could control triglyceride and LDL cholesterol increase, although their rates were beyond the normal range. Turnip root extract could better control the level of total cholesterol compared to atorvastatin, while it showed a weaker effect of other factors. Receiving turnip extract for a month can increase total cholesterol, triglyceride and LDL cholesterol in the alloxan diabetic rats and increase HDL cholesterol [40]. Significant reduction of total cholesterol and triglyceride levels has been observed in rats with dyslipidemia caused by 2-week treatment fructose diet with 400 mg /kg turnip root alcoholic extract for [41]. 5-week turnip root alcoholic extract can significantly reduce the cholesterol and triglyceride levels in rats affected by congenital type 2 diabetes [42].

To explain mechanism for lowering blood lipids, HMG-CoA reductase enzyme measurement by liver, as well as intestinal phospholipases, should be considered.

Failure to measure reductase liver HMG-CoA enzyme and intestinal phospholipases were the limitations of this study.

Turnip root extract due to the presence of phenolic compounds effective on fat control can effectively inhibit the increase of cholesterol and triglyceride levels in rats with intense hyperlipidemia with reverse and dose-dependent effect.

Researchers thank Dr. Malakaneh for providing Triton –WR1339.

Non-declared

Methods were approved by Ethics Committee of Research and Technology Deputy of Birjand University of Medical Sciences.

The study was funded by Research Deputy of Birjand University of Medical Sciences.

TABLES and CHARTS

Show attach file


CITIATION LINKS

[1]Jellinger PS, Smith DA, Mehta AE, Ganda O, Handelsman Y, Rodbard HW, et al. American association of clinical endocrinologists' guidelines for management of dyslipidemia and prevention of atherosclerosis. Endocr Pract. 2012;18(2):269-93.
[2]Miller M. Dyslipidemia and cardiovascular risk: The importance of early prevention. QJM. 2009;102(9):657- 67.
[3]Anandhi R, Annadurai T, Anitha TS, Muralidharan AR, Najmunnisha K, Nachiappan V, et al. Antihypercholesterolemic and antioxidative effects of an extract of the oyster mushroom, pleurotus ostreatus, and its major constituent, chrysin, in triton WR-1339- induced hypercholesterolemic rats. J physiol Biochem. 2013;69(2):313-23.
[4]Katz J, Chaushu G, Sharabi Y. On the association between hypercholesterolemia, cardiovascular disease and severe periodontal disease. J Clin Periodontol. 2001;28(9):865-8.
[5]Roger VL, Go AS, Lloyd-Jones DM, Adams RJ, Berry JD, Brown TM, et al. Heart disease and stroke statistics-- 2011 update: A report from the American Heart Association. Circulation. 2011;123(4):e18-e209.
[6]Chen ZY, Ma KY, Liang Y, Peng Ch, Zuo Y. Role and classification of cholesterol-lowering functional foods. J Functional Foods. 2011;3(2):61-9.
[7]Rye KA, Bursill CA, Lambert G, Tabet F, Barter PJ. The metabolism and anti-atherogenic properties of HDL. J Lipid Res. 2009;50Suppl:S195-200.
[8]Duriez P. Mechanisms of actions of statins and fibrates. Therapie. 2003;58(1):5-14. [French]
[9]Lei YF, Chen JL, Wei H, Xiong CM, Zhang YH, Ruan JL. Hypolipidemic and anti-inflammatory properties of Abacopterin A from Abacopteris penangiana in high-fat diet-induced hyperlipidemia mice. Food and Chem Toxicol. 2011;49(12):3206-10.
[10]Li SY, Chang CQ, Ma FY, Yu CL. Modulating effects of chlorogenic acid on lipids and glucose metabolism and expression of hepatic peroxisome proliferator-activated receptor-α in golden hamsters fed on high fat diet. Biomed Environ Sci. 2009;22(2):122-9.
[11]Yang X, Yang L, Zheng H. Hypolipidemic and antioxidant effects of mulberry (Morus alba L.) fruit in hyperlipidaemia rats. Food Chem Toxicol. 2010;48(8- 9):2374-9.
[12]Who launches the first global strategy on traditional and alternative medicine. Cent Eur J Public Health. 2002;10(4):145-56.
[13]Chansouria JPN, Ray AB, Hemalatha S. Medicinal plants: Hypolipidemic, hypocholesterolemic, and antiatherosclerotic properties. Lucknow: International Book Distributing Co; 2006.
[14]Russo VM. Vegetable brassicas and related crucifers. Crop production science in horticulture 14. Int J Veg Sci. 2008;14(1):93.
[15]Shukia R, Sharma SB, Puri D, Prabhu KM, Murthy PS. Medicinal plants for treatment of diabetes mellitus. Indian J Cli Biochem. 2000;15(Suppl 1):169-77.
[16]Fernandes F, Valentão P, Sousa C, Pereira JA, Seabra RM, Andrade PB. Chemical and antioxidative assessment of dietary turnip (Brassica rapa var. rapa L.). Food Chem. 2007;105(3):1003-10.
[17]Prassas I, Diamandis EP. Novel therapeutic applications of cardiac glycosides. Nat Rev Drug Discov. 2008;7(11):926-35.
[18]Alam MA, Sernia C, Brown L. Ferulic acid improves cardiovascular and kidney structure and function in hypertensive rats. J Cardiovasc Pharmacol. 2013;61(3):240-9.
[19]Ardiansyah, Ohsaki Y, Shirakawa H, Koseki T, Komai M. Novel effects of a single administration of ferulic acid on the regulation of blood pressure and the hepatic lipid metabolic profile in stroke-prone spontaneously hypertensive rats. J Agric Food Chem. 2008;56(8):2825- 30.
[20]Suzuki A, Kagawa D, Fujii A, Ochiai R, Tokimitsu I, Saito I. Short- and long-term effects of ferulic acid on blood pressure in spontaneously hypertensive rats. Am J Hypertens. 2002;15(4Pt1):351-7.
[21]Wang B, Ouyang J, Liu Y, Yang J, Wei L, Li K, et al. Sodium ferulate inhibits atherosclerogenesis in hyperlipidemia rabbits. Journal Cardiovasc Pharmacol. 2004;43(4):549-54.
[22]Silambarasan T, Manivannan J, Priya MK, Suganya N, Chatterjee S, Raja B. Sinapic acid protects heart against ischemia/reperfusion injury and H9c2 cardiomyoblast cells against oxidative stress. Biochem Biophys Res Commun. 2015;456(4):853-9.
[23]Tiwari P, Kumar B, Kaur M, Kaur G, Kaur H. Phytochemical screening and extraction: A review. Internationale Pharmaceutica Sciencia. 2011;1(1):98- 106.
[24]Živković J, Mujić I, Nikolić G, Vidović S, Mujić A. Extraction and analysis of condensed tannins in Castanea Sativa Mill. J Cent Eur Agric. 2009;10(3):283-8.
[25]Chen J, Li X. Hypolipidemic effect of flavonoids from mulberry leaves in triton WR-1339 induced hyperlipidemic mice. Asia Pac J Clin Nutr. 2007;16(Suppl 1):290-4.
[26]Da Rocha JT, Sperança A, Nogueira CW, Zeni G. Hypolipidaemic activity of orally administered diphenyl diselenide in Triton WR-1339-induced hyperlipidaemia in mice. J Pharm Pharmacol. 2009;61(12):1673-9.
[27]Ferreira JM, Sousa DF, Dantas MB, Fonseca SG, Menezes DB, Martins AM, et al. Effects of Bixa orellana L. seeds on hyperlipidemia. Phytother Res. 2013;27(1):144-7.
[28]Harnafi H, Serghini Caid H, Bouanani NH, Aziz M, Amrani S. Hypolipemic activity of polyphenol-rich extracts from Ocimum basilicum in Triton WR-1339- induced hyperlipidemic mice. Food Chem. 2008;108(1):205-12.
[29]Kourounakis AP, Victoratos P, Peroulis N, Stefanou N, Yiangou M, Hadjipetrou L, et al. Experimental hyperlipidemia and the effect of NSAIDs. Exp Mol Pathol. 2002;73(2):135-8.
[30]Kremmer T, Holczinger L. Effect of vincristine on triton WR-1339 induced hyperlipidemia in mice. Biochem Pharmacol. 1974;23(23):3317-21.
[31]Pérez C, Canal JR, Romero A, Torres MD. Experimental hypertriglyceridaemia and hypercholesterolaemia in rats. Acta Physiologica Hungarica. 1999; 86(1): 57-68.
[32]Sharma RD. Effect of various isoflavones on lipid levels in triton-treated rats. Atheroscler. 1979;33(3):371-5.
[33]Shattat G, Al-Qirim R, Al-Hiari Y, Sheikha GA, Al- Qirim T, El-Huneidi W, et al. Synthesis and antihyperlipidemic evaluation of N-(benzoylphenyl)-5- fluoro-1H-indole-2-carboxamide derivatives in triton WR-1339-induced hyperlipidemic rats. Mol. 2010;15(9):5840-9.
[34]Friedman M, Byers SO. The mechanism responsible for the hypercholesteremia induced by triton WR-1339. J Exp Med. 1953;97(1):117-30.
[35]Hayashi H, Niinobe S, Matsumoto Y, Suga T. Effects of triton WR-1339 on lipoprotein lipolytic activity and lipid content of rat liver lysosomes. J Biochem. 1981;89(2):573-9.
[36]Roitelman J, Olender EH, Bar-Nun S, Dunn WA Jr, Simoni RD. Immunological evidence for eight spans in the membrane domain of 3-hydroxy-3-methylglutaryl coenzyme A reductase: Implications for enzyme degradation in the endoplasmic reticulum. J Cell Biol. 1992;117(5):959-73.
[37]Bertges LC, Mourão Jr CA, Souza JB, Cardoso VAC. Hyperlipidemia induced by Triton WR1339 (Tyloxapol) in wistar rats. Rev Bras Cien Med Saúde. 2011;1(1):32–4.
[38]Rony KA, Ajith TA, Nima N, Janardhanan KK. Hypolipidemic activity of Phellinus rimosus against triton WR-1339 and high cholesterol diet induced hyperlipidemic rats. Environ Toxicol Pharmacol. 2014;37(2):482-92.
[39]Schurr PE, Schultz JR, Parkinson TM. Triton-induced hyperlipidemia in rats as an animal model for screening hypolipidemic drugs. Lipids. 1972;7(1):68-74.
[40]Akbari F, Ansari Samani R, Karimi A, Mortazaei S, Shahinfard N, Rafieian M. Effect of turnip on glucose and lipid profiles of alloxan-induced diabetic rats. Iranian J Endocrinol Metabol. 2013;14(5):492-7. [Persian]
[41]Abo-youssef AM, Mohammed R. Effects of brassica rapa on fructose-induced metabolic syndrome in rats: A comparative study. Int J Pharm Sci Rev Res. 2013;21(1):1-5.
[42]Jung UJ, Baek NI, Chung HG, Bang MH, Jeong TS, Lee KT, et al. Effects of the ethanol extract of the roots of Brassica rapa on glucose and lipid metabolism in C57BL/KsJ-db/db mice. Clin Nut. 2008;27(1):158-67.
[43]Kim EO, Min KJ, Kwon TK, Um BH, Moreau RA, Choi SW. Anti-inflammatory activity of hydroxycinnamic acid derivatives isolated from corn bran in lipopolysaccharide-stimulated Raw 264.7 macrophages. Food Chem Toxicol. 2012;50(5):1309-16.
[44]Max B, Torrado AM, Moldes AB, Converti A, Domínguez JM. Ferulic acid and p-coumaric acid solubilization by alkaline hydrolysis of the solid residue obtained after acid prehydrolysis of vine shoot prunings: Effect of the hydroxide and pH. Biochem Eng J. 2009;43(2):129-34.
[45]Ou S, Kwok KCh. Ferulic acid: pharmaceutical functions, preparation and applications in foods. J Sci Food Agric. 2004;84(11):1261-9.
[46]Ou Sh, Luo Y, Xue F, Huang C, Zhang N, Liu Z. Seperation and purification of ferulic acid in alkalinehydrolysate from sugarcane bagasse by activated charcoal adsorption/anion macroporous resin exchange chromatography. J Food Eng. 2007;78(4):1298-304.
[47]Zhao Z, Egashira Y, Sanada H. Ferulic acid is quickly absorbed from rat stomach as the free form and then conjugated mainly in liver. J Nut. 2004;134(11):3083-8.
[48]Son MJ, Rico CW, Nam SH, Kang MY. Influence of oryzanol and ferulic acid on the lipid metabolism and antioxidative status in high fat-fed mice. J Clin Biochem Nut. 2010;46(2):150-6.
[49]Adam A, Crespy V, Levrat-Verny MA, Leenhardt F, Leuillet M, Demigné C, et al. The bioavailability of ferulic acid is governed primarily by the food matrix rather than its metabolism in intestine and liver in rats. J Nut. 2002;132(7):1962-8.
[50]Kanchana G, Shyni WJ, Rajadurai M, Periasamy R. Evaluation of antihyperglycemic effect of sinapic Acid in normal and streptozotocin-induced diabetes in albino rats. Global J Pharmacol. 2011;5(1):33-9.
[51]Roy SJ, Mainzen Prince PS. Protective effects of sinapic acid on cardiac hypertrophy, dyslipidaemia and altered electrocardiogram in isoproterenol-induced myocardial infarcted rats. Eur J Pharmacol. 2013;699(1– 3):213-8.