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THE EFFECT OF ASTURTIUM OFFICIALE O BLOOD GLUCOSE LEVEL I DIABETIC RATS Hassan Fallah Hoseini 1, Ahmad R. Gohari 2, Soodabeh Saeidnia 2 *, aghi Shahabi Majd 3, Abbass Hadjiakhoondi 2 1- Department of Pharmacology, Institute of Medicinal Plants ACECR, Tehran, Iran 2- Medicinal Plants Research Center, Tehran University of Medical Sciences, Tehran, Iran, P. O. Box 14155-6451, Tel & Fax: +98-21-64122330, saeidnia_s@tums.ac.ir 3- Physiology and Pharmacology Department, School of Medicine, Medical Sciences University of Mazandaran, Sari, Iran. Summary In this article, the effect of asturtium officinale (watercress, belonging to Brassicaceae) extracts on the blood glucose level was evaluated in diabetic rats. After inducing diabetes via streptozotocin injection, the animals were orally received various concentrations of. officinale extracts (ethyl acetate, methanol and aqueous) for short (one week) and long (two months) periods. Only 800 and 00 mg/kg of the methanol extract of. officinale caused a significant decrease in the blood glucose level after one week treatment. At the end of two months treatment with ethyl acetate extract, the blood glucose level reduced and this reduction was significant statistically in the group, received of the extract. The decreasing of blood glucose was comparable with glybenclamide as an anti-diabetic drug. Long period treatment of the animals with methanol and aqueous extracts were not effective. Keywords: asturtium officinale, Brassicaceae, streptozotocin, blood glucose Introduction asturtium officinale R. Br. (watercress) is an aquatic herb belonging to Brassicaceae family and frequently found in association with Veronica anagallis-aquatica. There is apparently no relation between them except they both prefer the same habitat.. officinale, named Alafe-Cheshmeh in Persian language, has the white flowers (1).. officinale is used to palliate abdominal pain and eaten as a vegetable or salads. This herb is used to treat, bronchitis, and diuresis, as anti-ulcerogenic, in the treatment of scurvy, tuberculosis, influenza, asthma, nutritional supplement and also seems to have antimicrobial and anticarcinogenic (2-5).. officinale, which contains a glucosinolate named gluconasturtiin, has been traditionally used for treatment of diabetes, an endocrinal chronic disease caused by altered carbohydrate metabolism and characterized by elevated blood glucose levels (6,7).. officinale extracts showed an antioxidant activity via reducing cellular lipid peroxidation, reducing power, free radical and superoxide anion radical scavenging activities (2). Regarding to the potential use of antioxidant treatment in this disease, watercress could be a choice of more investigation for diabetes treatment (8). 866

The present paper reports the effect of. officinale, which has been used in the Eastern traditional medicine for anti-diabetic activity, on the blood glucose level in streptozotocin diabetic rats. Material and methods Plant material Aerial parts of asturtium officinale were collected in April 2008 from southern parts of Qazvin province in Iran during the full flowering stage. A voucher specimen was preserved for further reference at the Herbarium of Institute of Medicinal Plants ACECR, Tehran, Iran. Preparation of the extracts Air-dried aerial parts of the plant (3 kg) were cut in to small pieces then powdered and percolated consequently with ethyl acetate, methanol and water. After filtering, the solutions were concentrated under reduced pressure to gain ethyl acetate (63 g), methanol (405 g) and aqueous (930 g) extracts. Animals Wistar rats weighting 200-250 g (prepared from Seromsazi-Razi Institute, Iran) were kept in the animal house under standard condition in 12h / 12h light dark cycle (23 ± 3 C). The animals received standard pellet diet and water ad libitum. Animal handling was performed as per Good Laboratory Practice. Research proposal was prepared based on the CPCSEA (Committee for the Perpose of Control and Supervision of Experiments on Animal) and approved by IAEC (Institutional Animal Ethical Committee) of Tehran University of Medical Sciences. In order to induce the diabetes, the animals were injected by streptozotocin at the dose of of the body weight intraperitoneally. Diabetic animals and non-diabetic control group were kept in metabolic cages individually, separately and under feeding and metabolism control. Glucose in the blood of diabetic rats exceeded that of the nondiabetic control ones. Food and water consumption were measured in terms of gram and milliliter respectively. Urine volume was measured in terms of milliliter on a daily basis. Glucose in blood serum was also measured, so that chemical diabetes was verified in rats with fasting blood sugar more than 200 mg/dl (9). Administration of the extracts The rats were randomly selected and divided in to several groups of -12 in each. The normal group was non diabetic animals. The positive control rats were received glybenclamide mg/kg/day. Other groups were treated orally (via gavage) the different doses of the methanol and aqueous extracts (, 50, 0, 200, 400, 600, 800 and 00 mg/kg) and ethyl acetate extract (5,, 50, 0 and ) for short (one week) and long (8 weeks) period study. In all animals, blood glucose was measured. Statistical analysis The data were expressed as Mean ± SD. One-way AOVA was used for comparison of the data followed by Duncan's Multiple Range Test and P values less than 0.05 were considered significant. 867

Results In this study, we evaluated the effect of the watercress extracts on the blood glucose of the diabetic rats. The results of short period (one week) consumption of watercress ethyl acetate, methanol and aqueous extracts have been summarized in the tables 1-3. Also, the results of two months study on the ethyl acetate extract have been shown in table 4. Table 1. Blood glucose evaluation of the short period treated rats with ethyl acetate extract of asturtium officinale compared to control. control 5 mg/kg mg/kg Blood glucose 275.7000 296.6000 278.3000 254.0000 255.2000 198.0000 122.44913 167.31288 86.37650 122.84227 119.63909 69.02978 * The mean difference is significant at the 0.05 level (P < 0.05); Control: The diabetic rats which received no drug or treatment; Treated rats: The diabetic rats which received different doses of the ethyl acetate extract of. officinale. Table2. Blood glucose evaluation of the short period treated rats with methanol extract of asturtium officinale compared to control. control mg/kg 400 mg/kg 600 mg/kg 800 mg/kg 00 mg/kg 12 6 Blood glucose 266.5000 167.3000 179.8000 2.0000 165.8000 144.8000 145.8000 132.5000 * 125.5000 * 116.76044 36.43884 43.38151 112.05713 49.42289 129.05021 66.59963 36.63408 31.08501 * The mean difference is significant at the 0.05 level (P < 0.05); Control: The diabetic rats which received no drug or treatment; Treated rats: The diabetic rats which received different doses of the methanol extract of. officinale.. 868

Table 3. Blood glucose evaluation of the short period treated rats with aqueous extract of asturtium officinale compared to control. control mg/kg 400 mg/kg 600 mg/kg 800 mg/kg 00 mg/kg Blood glucose 185.4000 176.2000 166.0000 179.5000 175.9000 155.2000 142.9000 179.6000 173.3000 75.46773 48.12668 63.51378 41.29366 45.84382 48.571 28.25853 56.81197 52.46597 * The mean difference is significant at the 0.05 level (P < 0.05); Control: The diabetic rats which received no drug or treatment; Treated rats: The diabetic rats which received different doses of the aqueous extract of. officinale. Table 4. Blood glucose evaluation of the long period (2 month) treated rats with ethyl acetate extract of asturtium officinale compared to control. In the beginning of treatment After 2 month treatment Control Glybenclamide Control Glybenclamide 12 9 12 9 Blood glucose 266.5000 250.7000 264.4444 255.2000 198.0000 269.0000 141.4000 * 160.5556 142.5000 * 183.0000 116.76044 130.46247 125.49613 119.63909 69.02978 158.80577 57.31783 80.59174 35.55668 57.31783 * The mean difference is significant at the 0.05 level (P < 0.05); Control: The diabetic rats which received no drug or treatment; Treated rats: The diabetic rats which received different doses of the Morus nigra extract. 869

Discussion Diabetes mellitus is an important chronic disease related to serious complications. Research documents have suggested that enhanced oxidation is responsible for some of the complications of diabetes. The information about the benefit of antioxidants, vitamins and supplementations is conflicting because some trials have demonstrated adverse effects of excessive consumption of vitamin supplements (). asturtium officinale, which has been used in folk medicine by the people of south eastern region of Iran, has a high hypolipidaemic activity and this may be attributed to its antioxidative potential (11). Based on unpublished data, the aqueous extract of this plant could reduce the plasma glucose level. There fore, in this article we examined the effect of several extraxts of. officinale on the blood glucose level in the streptozotocin diabetic rats. Streptozotocin or streptozocin is an antibiotic which cause pancreatic -cell destruction and widely used for inducing insulin-dependent diabetes mellitus in the animal models. (12). As it can be seen in the table 1 and 3 regarding to short period study, none of the doses of ethyl acetate and aqueous extracts for. officinale caused a significant reduction in the plasma glucose level compare to control. Only 800 and 00 mg/kg of the methanol extract of. officinale caused a significant decrease in the blood glucose level (see table 2). The data of the long period investigation (2 months) were not significant for methanol and aqueous extracts. When two months treatment of the diabetic rats with ethyl acetate extract was carried out, the blood glucose reduced and this reduction was significant in the group, received of the extract. The decreasing of blood glucose is comparable with glybenclamide as a well-known anti-diabetic drug. In conclusion, it seems that the. officinale (watercress) is a potential source of antihyperglycemic compounds and we suggest continuing the phytochemical study to find out its pharmacologically active component(s). Acknowledgments This research has been supported by Tehran University of Medical Sciences and Health Services grant (o.6626). References 1. http://www.wnmu.edu/academic/nspages2/gilaflora/nasturtium_officinale.html 2. Ozen T, Investigation of antioxidant properties of asturtium officinale (watercress) leaf extracts. Acta Polon Pharm- Drug Res 2009; 66: 187-193. 3. Palaniswamy UR, McAvoy RJ, Bible BB, Stuart JD. Ontogenic variations of ascorbic acid and phenathyl isothiocyanate concentration in watercress (asturtium officinale R. Br) leaves. J Agric Food Chem 2003; 51: 5504-5509. 870

4. Chen L, Mohr S, Yang CS. Decrease of plasma and urinary oxidative metabolites of acetaminophen after consumption of watercress by human volunteers. Clin Pharm Ther 1996; 60: 651-660. 5. Mozaffarian V. A Dictionary of Iranian Plant ames. Tehran, Farhang Moaser Publication, 1996: 422. 6. Engelen-Eigles G, Holden G, Cohen JD, Gardner G. The effect of temperature, photoperiod, and light quality on gluconasturtiin concentration in watercress (asturtium officinale R. Br.). J Agric Food Chem 2006; 54: 328-334. 7. Zargari A. Medicinal Plants. 4th edn., Vol. 1, Tehran, Tehran University Publication, 1985: 198-201. 8. Schultz Johansen J, Harris A, Rychly DJ, Ergul A.Oxidative stress and the use of antioxidants in diabetes: Linking basic science to clinical practice. Cardiovasc Diabetol 2005; 4: 5. 9. Karunanayake EH, Hearse D J, Mellows G. The metabolic fate and elimination of streptozocin. Biochem Soc Trans 1975; 3: 4-14.. Hasanain B and Mooradian AD. Antioxidant vitamins and their influence in diabetes mellitus. Curr Diabetes Rep 2002; 2: 1534-4827. 11. Yazdanparast R, Bahramikia S, Ardestani A. asturtium officinale reduces oxidative stress and enhances antioxidant capacity in hypercholesterolaemic rats. Chem Biol Interact 2008; 172: 176 184. 12. Kenneth KW, Youming H. Streptozotocin Induced Diabetic Models in Mice and Rats. Current Protocols in Pharmacology 2008, DOI:.02/0471141755.ph0547s40. 871