Research Journal of Medicine and Medical Sciences, 2(2): 58-61, 2007 2007, INSInet Publication

Antipyretic Activity of Roots of Laportea crenulata Gaud in Rabbit

Alam Khan, 2 Md. Abdullahil Baki, 1 M. Abdul Alim Al-Bari, 3 Sohel Hasan, 1 M Ashik Mosaddik, 1M. Motiur Rahman and 1M Ekramul Haque

Department of Pharmacy, University of Rajshahi, Rajshahi 6205, Bangladesh 2 Department of Zoology, University of Rajshahi, Rajshahi 6205, Bangladesh 3 Department of Biochemistry and Molecular Biology, University of Rajshahi, Rajshahi 6205, Bangladesh
Abstract: Antipyretic effect of petroleum ether and chloroform soluble fractions of ethanol extract of the roots of Laportea crenulata Gaud was investigated. Intraperitoneal administration of boiled milk at a dose 0.5 ml/kg body weight in albino rabbit leads to pyrexia. Intraperitoneal (i. p. route) administration of petroleum ether and chloroform soluble fractions of ethanol extract of the roots of L. crenulata at a dose 80 mg/kg body weight were shown significantly reduce the elevated body temperature of rabbit which was compared with standard aspirin (market product) and solvent used. Key words: Laportea crenulata, Antipyretic, Rabbit, Boiled milk, aspirin, petroleum ether fraction, chloroform faction. INTRODUCTION Laportea crenulata Gaud (syn. Urtica crenulata, Fam. Urticaceae), locally known as Agnichutra, is an evergreen shrub [2 ,3 ] that is widely distributed to Bangladesh, India, Srilanka and Malay island (2-4). The roots of the plant used traditionally for the treatment of bleeding from nose and/or mouth, excessive gas in the stomach, constipation, weakness, asthma, gout, mumps, whooping cough and chronic fever [1 , 3 , 4 ]. The roots of the plant also have stimulant, stomachic and diuretic properties [1 , 3 , 4 ]. A through literature survey reveals that the aqueous extract of related species, e.g Urtica macrorrhiza have shown analgesic and antipyretic activities [5 ], Urtica dioica have shown anti-inflammatory effect[6 ], cardiovascular effects [7 ], antioxidant, antimicrobial, antiulcer and analgesic activities [8 ] and lymphocyte proliferation and inhibition of nitric oxide production effect [9 ]. Although the plant is widely used for remission of several ailments related to fever, its antipyretic potential has not been explored yet. Therefore, in the present study an attempt was made to establish the antipyretic effect of petroleum ether and chloroform soluble fraction of ethanol extract of the roots of Laportea crenulata. Pyrexia or fever is caused as a secondary impact of infection, malignancy or other diseased states [1 0 ]. It is the bodys natural defence to create an environment where infectious agent or damaged tissue can not survive [1 0 ]. Normally the infected or damaged tissue initiates the enhanced formation of pro-inflammatory mediators (cytokines like interleukin 1, , and Corresponding author: TNF- ), which increase the synthesis of prostaglandin E2 (PGE2) near peptic hypothalamus area and thereby triggering the hypothalamus to elevate the body temperature [1 1 ]. As the temperature regulatory system is governed by a nervous feedback mechanism, so when body temperature becomes very high, it dilate the blood vessels and increase sweating to reduce the temperature; but when the body temperature become very low hypothalamus protect the internal temperature by vasoconstriction. High fever often increases faster disease progression by increasing tissue catabolism, dehydration and existing complaints, as found in HIV [1 2 ] . Most of the antipyretic drugs inhibit COX-2 expression to reduce the elevated body temperature by inhibiting PGE-2 biosynthesis [1 3 ]. Moreover, these synthetic agents irreversibly inhibit COX-2 with high selectivity but are toxic to the hepatic cells, golmeruli, cortex of brain and heart muscles, whereas natural COX-2 inhibitors have lower selectivity with fewer side effects [1 3 ] . A natural antipyretic agent with reduced or no toxicity is therefore, essential. As roots of L. crenulata is a old medicaments used in ailments that caused fever [1 ], so it will be a cost effective alternative approach to study this plant for the development of an effective antipyretic agent. M ATERIALS AND M ETHODS Plant M aterials: The roots of Laportea crenulata was collected from various part of Rangpur district of Bangladesh and identified by Prof. A.T.M .

Alam Khan, Department of PharmacyUniversity of Rajshahi, Rajshahi- 6205, Bangladesh Fax: +880-721-750064. Tel: +880-721-750041/4110. E-mail address: [email protected] 58

Res. J. Medicine & Med. Sci., 2(2): 58-61, 2007 Naderuzzaman, Department of Botany, University of Rajshahi, Bangladesh where its voucher specimen (No. 1239) was deposited. The roots were cut, air-dried and ground into powder. Preparation of Petroleum Ether and Chloroform Fractions of Ethanol Extract: Powdered dried roots (900 g) of the plant were extracted (cold) with ethanol (5 L) in three flat bottom glass containers, through occasional shaking and stirring for 10 days [1 4 ]. The whole extract was filtered and the solvent were evaporated to dryness in vacuo with an Rotary Evaporator at 40-50C to afford a blackish green mass (45 g) which was further extracted with petroleum ether (3 x 50 ml), chloroform (3 x 50 ml) and methanol (3 x 50 ml) to afford petroleum ether, chloroform and methanol fractions, respectively[1 5 ,1 6 ]. The preliminary phytochemical screening of the different fractions was carried out by chemical tests and thin layer chromatographic methods [1 7 ]. Preparation of Sample and Standard Solutions: 2.5 percent ethanol in distilled water (autoclaved) was used as solvent to prepare sample and standard solutions. The sample solutions of petroleum ether and chloroform fractions were prepared by dissolving each dried fraction in the solvent to obtain 120 mg per 2 ml solution. To facilitate dissolution few drops of tween 80 was added. The each fraction was administrated at a dose of 80 mg/kg body weight[1 8 ]. Aspirin as Disprin soluble tablet was collected from local market of Reckitt Benckiser (Bangladesh) Ltd was used as known antipyretic agent. The standard solution was prepared by dissolving the tablet in the solvent to obtain 15 mg aspirin per 2 ml solution. The dose of aspirin was maintained 10 mg/kg body weight[1 9 ]. Animals: The experiment was carried out on albino rabbits. They were 13-15 months old of both sexes weighing between 1.5-1.6 kg [2 0 ]. They were collected from the International Center for Diarrhoeal Diseases and Research, Bangladesh (ICDDR,B). The rabbits were kept in iron cages [2 1 ] (considering group), were fed with cauliflower, cabbage, banana and tap water for 40 days before experiment to adjust with environment. Food and water were withdrawn 6 hours prior to the experiment [1 9 ]. The animals were grouped asa. Experimental groups- Two groups-one group receiving petroleum ether and other group receiving chloroform fraction. Control groups werei. Aspirin group (+Ve Control)- receiving standard antipyretic agent aspirin. ii. Solvent group (-Ve Control)- receiving solvent (used).

b.

Number of rabbits in each group was four. Acute Toxicity Study: Acute toxicity study was carried out by using graded doses of each fraction. Both petroleum ether and chloroform fractions were administered intraperitoneally in graded doses (200 to 1000 mg/kg body weight). They were observed continuously for the first 2 h for toxic symptoms and up to 24 h for mortality [2 2 ]. Treatment Protocol: Before experimentation rectal temperature of rabbits were recorded by inserting a well lubricated bulb of a thermometer in the rectum. Care was taken to insert it to the same depth each time (about 6 cm) [1 9 ]. Milk was collected from local cow had been boiled. W hen temperature of the boiled milk equilibrates to room temperature then rabbits were injected boiled milk at the dose of 0.5 ml/kg body weight, to induce pyrexia. Induction of fever was taken about one to two h [1 9 ].

Table 1: Effect of petroleum ether and chloroform fractions of Laportea crenulata Gaud on boiled m ilk induced pyrexia in rabbit. Rectal tem perature (F) Rectal tem p. after adm in. of fraction (F) --------------------------------------------------------------------------------------------------------------------------------Groups D ose N orm al(A) 3 h after boiled m ilk adm in. (B) 1 h (C 1 ) 2 h (C 2 ) 3 h (C 3 ) Solvent 2 m l /rabbit 101.40.2 104.00.23 103.90.23 103.90.23 103.70.31 (3.840.10) (3.840.10) (11.50.26) ---------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------Aspirin 10 m g/kg 101.40.1 104.10.11 103.70.23 101.50.10 101.50.10 (16.00.12) * (96.30.10)* (96.30.10)* ---------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------Pet. ether 80 m g/kg 101.40.1 104.10.08 103.90.28 101.70.13 101.70.13 (7.40.18) (88.90.23)* (88.90.23)* ---------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------80 m g/kg Chloroform 101.50.1 104.10.20 103.70.29 * 101.70.23 101.70.23 (40.00.10)* (92.30.20)* (92.30.20)* All values are expressed as m eanSE (n = 4), percentage reduction in rectal tem perature is given within parentheses. * P < 0.05 significant com pared to control (solvent). B - Cn --------- 100; where n = 1,2 and 3. B - A

% reduction =

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Res. J. Medicine & Med. Sci., 2(2): 58-61, 2007 Then solvent (2 ml) was given on negative control group, known antipyretic agent aspirin solution (2 ml) was given on positive control group and two sample solutions (each 2 ml) were given to two experimental groups (Table 1). Intraperitoneal route was used to administer boiled milk, aspirin solution, solvent and sample solution. Finally, rectal temperatures were recorded 1 h intervals up to 3 h. RESULTS AND DISCUSSIONS The preliminary phytochemical screening of the petroleum ether and chloroform fraction showed the presence of steroids, tannins and flavonoids. In acute toxicity study, both fractions were found to be safe and no mortality was observed to a dose as high as 800 mg/kg. The results of effect of two fractions of roots of L. crenulata on boiled milk induced pyrexia in rabbits are depicted in Table 1. Both petroleum ether and chloroform fractions produced significant (P<0.05) antipyretic effect. At a dose of 80 mg/kg body weight, chloroform fraction reduced (92.30.20) % of elevated rectal temperate compared to aspirin (96.30.10) % followed by petroleum ether fraction (88.90.23) % after 3 hours. It was also observed that solvent have no effect on the reduction of pyrexia of rabbit. Search for safe herbal remedies with potent antipyretic activity received momentum recently as the available antipyretic, such as paracetamol, aspirin, nimusulide etc. have toxic effect to the various organs of the body [2 3 ]. The acute toxicity result reveals that this plant might be considered as a broad non-toxic one. T he antipyretic activity exhibited that the both petroleum ether and chloroform fraction of ethanol extract of roots possess a significant antipyretic effect in maintaining normal body temperature and reducing boiled milk induced elevated rectal temperature in rabbits and their effect are comparable to that of standard antipyretic drug aspirin. Such reduction of rectal temperature of tested animals by the both fractions at 80 mg/kg appears to be due to the presence of a single bioactive principles or mixture of compounds in them. The phytochemical analysis of the petroleum ether and chloroform fractions showed the presence of steroids, tannins and flavonoids. The antipyretic activity observed can be attributed to the presence of steroids [1 0 ]. Moreover, in many studies, flavonoids have been reported to exhibit antipyretic effect[2 4 , 2 5]. Recently, related species of L. crenulata (syn. Urtica crenulata), e.g aqueous extract of Untica macrorrhiza suppressed yeast induced fever in rats at a dose of 200 to 400 mg/kg body weight[5 ]. It was also evident from the study that the antipyretic activity of chloroform fraction at 80 mg/kg Bhattacharya, S., 1990. Chrinjib Banoushadi. 3 rd ed., Vol. 2, Anand Publishing Ltd., Calcutta-9, pp: 236-237. 2. Hooker, J.D., 1879. Flora of British India. 1 st ed., Vol-5, Reeve, London, pp: 550. 3. Kirtikar, K.R. and B.D. Basu, 1993. Indian M edicinal Plants. 2 n d ed., Vol. 3, Delhi, India, pp: 2343. 4. Hasan, A. and A.M. Haque, 1993. Amadar Bonoohshodi Sompod. 1 st ed., Hasan book house, Dhaka, Bangladesh, pp: 59. 5. Yongna, Z., R. W antana, B. Pisit, L. Zhongkun and Z. Rongping, 2005. Analgesic and antipyretic activities of aqueous extract of Urtica macrorrhiza in experimental animals. Fitoterapia, 76: 91-95. 6. Obertreis, B., K. Giller, T. Teucher, B. Behnke and H. Schmitz, 1996. Antiinflammatory effect of Urtica dioica extract in comparison to caffeic malic acid. Arzneimittelforschung, 46: 52-56. 7. Legssyer, A., A. Ziyyat, H. Mekhfi, M. Bnouham, A. Tahri, M. Serhrouchni, J. Hoerter and R. Fischmeister, 2002. Cardiovascular effects of Urtica dioica L in isolated rat heart and aorta. Phytotherapy Research, 16: 503-307. 8. Gulcin, I., O.I. Kufrevioglu, M. Oktay and M .E . B uyuko kuroglu, 20 0 4 . A n tio x i d a n t , antimicrobial, antiulcer and alalgesic activities of ne ttle (U r tic a d io ic a L .). Jo urna l o f Ethnopharmacology, 90: 205-215. 9. Harput, U.S., I. Saracoglu and Y. Ogihara, 2005. Stimulation of lymphocyte proliferation and inhibition of nitric oxide production by aqueous Urtica dioica extract. Phytotherapy Research, 19: 346-348. 10. Chattopadhyay, D., G. Arunachalam, L. Ghosh, K. Rajendran, A.B. M andal and S.K. Bhattacharya, 2005. Antipyretic activity of Alstonia macrophylla W all ex A. DC: An ethnomedicine of Andaman Islands. Journal of Pharmacy and Pharmaceutical Science, 8: 558-564. 11. Spacer, C.B. and C.D. Breder, 1994. The neurologic basis of fever. New England Journal of Medicine, 330: 1880-1886. 1. body weight is almost similar to the standard aspirin group and more than the petroleum ether fraction. The present study, therefore, supports the claims of traditional medicine practitioners as an antipyretic remedy. However, to know the exact mechanism of action of L. crenulata root extract further study with purified fractions/ bioactive compounds are warranted. REFERENCES

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