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Phylomedicine, Vol. 7(3), pp.

231-234
© Urban & Fischer Verlag 2000
hllp:l/www.urbanfischer.de/journals/phy1omed
Phytomedicine

Evaluation of anti-pyretic potential of Jussiaea


suffruticosa L. extract in rats
T. Murugesan, S. C. Mandal, T. Bhakta, J. Dasl, M. Pal and B. P. Saha
Department of Pharmaceutical Technology, Jadavpur University, Calcutta, India.
lDepartment of Pharmacology, Dr. B. C. Roy P. G. Institute of Basic Medical Sciences, University College of Medicine, Cal-
cutta, India.

Summary

A study was carried out to evaluate the anti-pyretic potential of the methanol extract of the aerial part
of]ussiaea suffruticosa Linn. (ME1S) on normal body temperature and yeast-induced pyrexia in albino
rats. Yeast suspension (10 ml/kg body wt.) increased rectal temperature after 19 hours of subcutaneous
injection. The ME1S, at doses of 100, 200 and 300 mg/kg body wt, p.o., showed significant reduction
in normal body temperature and yeast-provoked elevated temperature in a dose-dependent manner. The
effect also extended up to 5 hours after the drug administration. The anti-pyretic effect of ME1S was
comparable to that of paracetamol (150 mg/kg body wt, p.o.), a standard anti-pyretic agent.

Key words: Jussiaea suffruticosa; Ludwigia octovalvis; Oenothera octovalvis; ME]S; Anti-pyretic.

Introduction
The plant Jussiaea suffruticosa L. (Family: Onagra- Materials and methods
ceae) is well known as Banlunga (Hindi), Lalbunlunga
Plant material
(Bengali), Nirkkrambu, Kattukrambu (Tamil) in the
traditional medicine of India. The plant is semi-shrub- The plant Jussiaea suffruticosa Linn. was collected
by, erect, perennial, 60-90 em high, and distributed as from a cultivated paddy field near Thanjavur, Tamil-
a weed in cultivated paddy fields and wet fields nadu. The authentication of the plant was established
throughout India and Ceylon (Anonymous, 1966; by the Botanical Survey of India, Shibpur, Howrah and
Anonymous, 1986). The whole plant, reduced to pulp the voucher specimen (J.S.-l) has been deposited in our
and steeped in butter-milk, is useful in the treatment of Research laboratory for future reference. The whole
dysentery, mental illness and diarrhea. The decoction plants were dried under controlled temperature
of the plant is used as a vermifuge, astringent, carmina- (shade).
tive, and as a diuretic and anthelmintic (Anonymous,
1986; Kirtikar and Basu, 1935; Nadkarni et a!., 1992). Extraction procedure
It has come to our attention that the rural people of The dried and pulverized plants were extracted with
Tamilnadu, India, use the juice of the plant for the re- 90 % methanol in a Soxhlet apparatus. Solvent was re-
lief of fever. Based on the traditional use of the plant as moved in vacuo in a rotary evaporator to provide dry
an anti-pyretic agent, the present study was carried out extracts (yield 9.5% w/w, with respect to the dried
in an experimental animal model to substantiate the powder). The chemical constituents of the extract were
folklore claim. identified by qualitative analysis and confirmed by
thin-layer chromatography study (i. e., hRf values) for
the presence of flavanoids, steroids, alkaloids and tan-
nins. The methanol extract of Jussiaea suffruticosa
(ME]S) was stored in a dessicator and a weighed

0944-7113/00/07/03-135 $ 12.00/0
232 T. Murugesan et al.

Table 1. Effectof MEJS on normal body temperature.


Treatment Rectal temperature (0C) before and after treatment
Oh 1h 2h 3h 4h 5h
Control
5 mllkg
body wt. 37.4 ± 0.2 37.2 ± 0.1 37.4 ± 0.3 37.3 ± 0.2 37.3 ± 0.1 37.0 ± 0.2
MEJS
100 mglkg
body wt. 37.2 ± 0.1 36.7 ± O.3 c 36.6 ± 0.2b 36.5 ± O.3 b 36.7 ± 0.2b 36.8 ± 0.3
MEJS
200mglkg
body wt, 37.3 ± 0.2 36.2 ± 0.1" 36.2 ± 0.2a 36.3 ± 0.2b 36.7 ± 0.2b 36.7 ± 0.2b
MEJS
300 rng/kg
body wt, 37.1 ± 0.2 35.8 ± 0.2a 35.8 ± 0.2a 35.8 ± 0.1" 35.9 ± 0.2a 36.0 ± 0.2b
Each value representsmean ± SEof 6 rats.
Control =2 % aqueous tragacanth solution.
a p < 0.001, b P < 0.01, P < 0,05, as compared to the control values of corresponding hour.
C

MEJS - Methanol extract of Jussiaea suffruticosa Linn.

amount was suspended in 2 % tragacanth solution for turned to their housing cages. After 19 h of yeast injec-
the present study. tion, the animals were again restrained in individual
cages for the recording of their rectal temperatures as
described previously.
Animals used
Adult albino rats (Wistar strain) of either sex weighing
180-200 g each were used. The animals were main- Drug administration
tained under suitable nutritional and environmental After 19 h of yeast injection, the MEJS was adminis-
conditions throughout the experiment. tered orally at doses of 100, 200 and 300 mg/kg body
wt. to three groups of animals, respectively. A similar
volume (5 ml/kg body wt.) of 2 % aqueous tragacanth
Study on normal body temperature
solution was administered orally to the control group
Rats of either sex were divided into four groups, com-
of animals. The fifth group of animals received the
prising six in each group for this experiment. The body
standard drug, paracetamol (150 mg/kg body wt.)
temperature of each rat was measured rectally at pre-
orally. Rats were restrained for recording of their rectal
determined intervals before and for 5 h after adminis-
temperatures at the nineteenth, immediately before
tration of either 2 % aqueous tragacanth solution (con-
MEJS or saline or paracetamol administration, and
trol) or MEJS at doses of 100, 200 and 300 mg/kg
again at one hour's interval up to the twenty-third h,
body wt. orally.
after yeast injection.

Induction of yeast-induced pyrexia


Rats were divided into five groups of six rats each. The
Statistical analysis
normal body temperature of each rat was measured
rectally at predetermined intervals and recorded. Fever The data were analyzed for significance using the un-
was induced as per the method described by Smith and paired two-tailed student's t-test (Woodson, 1987).
Hambourger (1935). The rats were trained to remain
quiet in a restraint cage. A thermister probe was insert-
ed 3-4 em deep into the rectum and fastened to the tail Results
by adhesive tape. The temperature was measured on a
thermometer. After measuring the basal rectal tempera- Effect of the MEJS on normal body temperature in rats
ture, animals were given a subcutaneous injection of 10 is presented in Table 1. It was found that the MEJS at
mllkg body wt. of 15% w/v yeast suspended in doses of 100 mg/kg body wt, caused significant lower-
0.5% w/v methylcellulose solution. Rats were then re- ing of body temperature up to 4 h following its admin-
Eva lua tion of th e anti-pyretic potential of Jussiaea suffruticosa L. ex tract in rat s 233

Table 2. Effect of MEJS on yeast-induced pyrexia in rats.


Treatment Rectal temperatur e (0C) after yeast injection at
Dh 19 h 20 h 21 h 22 h 23 h
Control
5mllkg
body w t, 37.6 ± 0.02 39.6 ± 0.02 39.5 ± 0.03 39.3 ± 0.07 39.1 ± 0.03 39.04 ± 0.03
Paracetamol
150 mg/kg
body wt. 37.8 ± 0.01 39.7 ± 0.03 38.4 ± 0.01" 38.0 ± 0.01" 37.8 ± O.osa 37.7 ± 0.03a
MEJS
100 mg/kg
body wt, 37.5 ± 0.04 39.7 ± 0.01 39.0 ± o.oi- 38.5 ± 0.02b 38.3 ± O.OSb 37.9 ± 0.09 a
MEJS
200 mg/kg
body wt. 37.4 ± 0.01 39.7 ± 0.01 38.8 ± 0.04" 38.3 ± 0.05a 37.9 ± 0.08 a 37.7 ± 0.06a
MEJS
300 mg/kg
body wt , 37.6 ± 0.07 39.7 ± 0.07a 38.5 ± 0.01" 37.8 ± 0.03a 37.5 ± 0.01" 37.5 ± 0.05 a
Each value represents mean ± SE of 6 rats.
Control =2 % aqueous tragacanth solution.
a p < 0,001, b P < 0.01 as compared to the control values of corresponding hour.
MEJS - Methanol extract of [ussiaea suffruticosa Linn.

istra tion, This effect was maxim al at doses of 200 an d paracetamol do not infl uence body tempe ra tur e when
30 0 mg/kg bod y w t , in a dose-dependent manner and it it is elevated by factors such as exe rcise or increases in
ca used significant lowering of bod y temperature up to ambient tem perature (Goodman and Gilma n, 1996).
5 h after its ad ministration. T he subcutaneous injectio n T he present results show th at th e methano l extract of
of yeast suspe nsion mark edly elevated th e rectal tem- Jussiaea suffruticosa (MElS) possesses a significa nt an -
pera ture after 19 h of administration. Tre atment w ith tipyretic effect in yeas t-provoked eleva tio n of body
th e MElS at the doses of 100, 200 and 300 mg/kg body tem perature in rats, and its effect is comparable to th at
wt, decreased the rectal temp erature of the rats in a of paracetamol (standar d d ru g). Furtherm ore, th e
dose-d ependent manner. The anti pyretic effect started MElS also significantly reduced the normal body tem-
as early as 1 h, and the effect was ma intained for 4 h, pera ture, and this is to be studied fur ther for the exact
after its administration. T he standard drug paraceta- mechani sm of action.
mol at 150 mg/kg body wt. dose significa ntly reduced
the yeas t-provoked elevat ion of body temperature. The Acknowledgement
results ob ta ined fro m bo th th e standard-d rug- treated The authors are grateful to CSIR, New Delhi, for financial
an d M El S-treated rats were co mpared with th e control support to T. Murugesan for this project. We owe our thanks
(2 % aqueous tr agacanth so lution) group an d we ob- to Sri Vasavi Soft Drinks Pvt.Ltd., Mysore, for free samples of
serve d a significant reduction in the yeast-elevated rec- yeast and Dr. Pulok K. Murk herjee,J.S.S. Collegeof Pharma-
tal temperature (Table 2) . cy, Ooty, for his technical assistance.

Discussion
References
Fever may be a result of infection o r one of the seque-
lae of tissu e dam age, inflammation, graft rejection, or Anonymous: The Wealth of India, Vol. I. Publication and In-
formation Directorate, CSIR, New Delhi, p. 311, 1966.
other disease states. Antipyretics are drugs which re -
Anonymous: The Useful Plants of India. Publication and In-
du ce eleva ted body temperature. Regulation of body formation Directorate, CSIR, New Delhi, p. 305, 1986.
temperatu re requires a delicate balan ce between th e Goodman and Gilman: The Pharmacological Basisof Thera-
pr oduction and loss of heat, and the hypothalamus reg- peutics, Ninth Ed. McGraw-Hili, Professions division,
ulates th e set point at which bo dy temperatur e is main- New York, pp. 959-975, 1996.
tained. In fever this set point is eleva ted and drugs like Kritikar, K. R., Basu, B. D. in: E Blatter, J. F. Caius, Mhaskar
234 T. Murugesan et al.

[Eds.). Indian Medicinal Plants. Bishen Sing and Mahendra Address


Pal sing, Dehradun, pp. 2020-202 1, 1935.
Na dkarni, K. M., N adkarni, A. K.: Indian Materia Medica, B. P. Saha, Department of Pharmaceutical Technology,
Vol. I. Popular Parka shan , Bombay, p. 731, 1992. Jadavpur University, Calcutta 700032, India.
Smith , P. K., Hambourger, W. E.: ]. Pharmacal. Exp. Ther.
54: 346, 1935.
Woodson, R. E: Statistical Methods for the Analysis of Bio-
medical data (Wiley series in Probability and Mathematical
Statistics), Wiley, New York, pp. 315-3 16, 1987.

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