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_____________________
* Corresponding author:
Sribalaji college of pharmacy,
Choppadandi,
Karimnagar, A.P. India
E-mail address: laxmideepak.pharma@gmail.com
Available Online at: www.ijrpp.com
ANTIPYRETIC ACTIVITY
CRISTATA WILLD. IN BREWER’S YEAST INDUC
RATS
*1
B.Deepak kumar, 2
Rajendar Rao.V,
Sri Balaji College Of Pharmacy,
________ ________________________________________________________________
ABSTRACT
The objective of the present work was to study the antipyretic activity of whole plant of
belongs to family Acantahaceae. The Petroleum ether extract was taken for the study and evaluated for antipyretic
activity using Brewer’s yeast induced pyrexia in Wister strain albino rats. The Petroleum ether extracts at a dose of
100mg/kg & 200mg/kg were evaluated for antipyretic activity. The extract of
significant (P < 0.01) dose dependent antipyreti
rats. The Petroleum ether extracts of Lepidagathis cristata
with the standard drug.
Keywords: Lepidagathis cristata, Antipyre
__ ______________________________________________________________________
INTRODUCTION
Pyrexia or fever is caused as a secondary impact of
infection, malignancy or other diseased states. It is the
body’s natural function to create an environment
where infectious agents or damaged tissues cannot
survive. Normally, the infected or damaged tissue
initiates the enhanced formation of pro
mediators (cytokines, such as interleukin 1
TNF- ), which increase the synthesis of prostaglandin
E2 (PgE2) near hypothalamic area and thereby trigger
the hypothalamus to elevate the body temperature.
When body temperature becomes high, the
temperature regulatory system, which is governed by a
nervous feedback mechanism, dilates the blood vessels
and increases sweating to reduce the temperature.
When the body temperature becomes low,
hypothalamus protects the internal temperature by
vasoconstriction. High fever often increases faster
disease progression by increasing tissue catabolism,
laxmideepak.pharma@gmail.com
Available Online at: www.ijrpp.com Print ISSN: 2278 - 2648
Online ISSN: 2278 - 2656
(Research article)
ANTIPYRETIC ACTIVITY OF WHOLE PLANT OF LEPIDAGATHIS
BREWER’S YEAST INDUCED HYPER
Rajendar Rao.V, 3
Mikkilineni Sindhu Devi, 4
Chandrashekar.B.
Sri Balaji College Of Pharmacy, Choppadandi, Karimnagar, A.P, India.
________________________________________________________________
The objective of the present work was to study the antipyretic activity of whole plant of Lepidagathis cristata
belongs to family Acantahaceae. The Petroleum ether extract was taken for the study and evaluated for antipyretic
yeast induced pyrexia in Wister strain albino rats. The Petroleum ether extracts at a dose of
100mg/kg & 200mg/kg were evaluated for antipyretic activity. The extract of Lepidagathis cristata
significant (P < 0.01) dose dependent antipyretic effect in yeast induced elevation of body temperature in experimental
Lepidagathis cristata plant have significant antipyretic activity when compared
, Antipyretic activity, Brewer’s yeast.
______________________________________________________________________
Pyrexia or fever is caused as a secondary impact of
infection, malignancy or other diseased states. It is the
function to create an environment
where infectious agents or damaged tissues cannot
survive. Normally, the infected or damaged tissue
initiates the enhanced formation of pro-inflammatory
(cytokines, such as interleukin 1, , , and
), which increase the synthesis of prostaglandin
E2 (PgE2) near hypothalamic area and thereby trigger
the hypothalamus to elevate the body temperature.
When body temperature becomes high, the
temperature regulatory system, which is governed by a
edback mechanism, dilates the blood vessels
and increases sweating to reduce the temperature.
When the body temperature becomes low,
hypothalamus protects the internal temperature by
vasoconstriction. High fever often increases faster
y increasing tissue catabolism,
dehydration, and existing complaints, COX
expression to reduce the elevated body temperature by
inhibiting PgE2 biosynthesis. These synthetic agents
irreversibly inhibit COX-2 with a high selectivity and
are toxic to the hepatic cells, glomeruli, cortex of brain,
and heart muscles. Natural COX
lower selectivity with fewer side effects [1,2]. A natural
antipyretic agent with reduced or no toxicity is
therefore, essential. Hence, the present study was
designed to determine the antipyretic effect of
petroleum ether extract of Lepidagathis cristata
Lepidagathis cristata Willd. (family: Acantahaceae)
Crested Lepidagathis is a perennial herb, with almost
no stem. Branches, 20 cm long, arise out of a globose
head on the ground, and spread out. Flowers also arise
stalk less from this globose head. Flowers are pale
pink, 2-lipped. The upper lip is notched, and the lower
lip is divided into 3 lobes.
Chattisgarh, they use this herb in treatment of
International Journal of
Research in Pharmacology and
Pharmacotherapeutics
14
(Research article)
LEPIDAGATHIS
ED HYPER PYREXIA
Chandrashekar.B.
________________________________________________________________
Lepidagathis cristata Willd,
belongs to family Acantahaceae. The Petroleum ether extract was taken for the study and evaluated for antipyretic
yeast induced pyrexia in Wister strain albino rats. The Petroleum ether extracts at a dose of
Lepidagathis cristata plant showed a
c effect in yeast induced elevation of body temperature in experimental
plant have significant antipyretic activity when compared
______________________________________________________________________
dehydration, and existing complaints, COX-2
expression to reduce the elevated body temperature by
inhibiting PgE2 biosynthesis. These synthetic agents
2 with a high selectivity and
hepatic cells, glomeruli, cortex of brain,
and heart muscles. Natural COX-2 inhibitors have
lower selectivity with fewer side effects [1,2]. A natural
antipyretic agent with reduced or no toxicity is
therefore, essential. Hence, the present study was
gned to determine the antipyretic effect of
Lepidagathis cristata.
Willd. (family: Acantahaceae)
Crested Lepidagathis is a perennial herb, with almost
no stem. Branches, 20 cm long, arise out of a globose
ad on the ground, and spread out. Flowers also arise
stalk less from this globose head. Flowers are pale
lipped. The upper lip is notched, and the lower
lip is divided into 3 lobes. Medicinal uses: In
Chattisgarh, they use this herb in treatment of fever
International Journal of
Research in Pharmacology and
Pharmacotherapeutics
15
B.Deepak Kumar et al / Int. Jour. of Res. in Pharmacology and Pharmacotherapeutics Vol-1 [1] 2012 [14-17]
www.ijrpp.com
particularly in treatment of Malarial fever. The
decoction of leaves is used internally for this purpose.
Its utility in treatment of fever has given it the name
Bukhar Jadi in reference literatures; the use of this
herb in treatment of itchy affections of skin has been
mentioned. The traditional healers of Chhattisgarh
Plains are aware of this use. In many parts of
Chhattisgarh, the cattle owners use the decoction of
this herb to wash the cattle in rainy season in order to
keep it free from flies [3]. Therefore, the main
objectives of present study were to investigate the
anti-pyretic activity of the Petroleum Ether Extract of
Lepidagathis cristata is being reported here.
MATERIALS AND METHODS
Plant material
The whole plant of Lepidagathis cristata was collected
from Tirumala hills, Tirupati, Andhra Pradesh. India. It
was identified and authenticated by Prof. Madhava
Chetty, K., Taxonomist, S.V. University, Tirupati,
Andhra Pradesh, India. A voucher specimen has been
kept in our laboratory for future reference.
Preparation of plant extract
The collected whole plant was dried at room
temperature, pulverized by a mechanical grinder,
sieved through 40mesh. About 100g of powdered
materials were extracted with petroleum ether (60°-
80°C) using soxhlet apparatus. The extraction was
carried out until the extractive becomes colourless.
The extract is then concentrated and dried under
reduced pressure. The solvent free semisolid mass
thus obtained is dissolved in tween 80 and used for
the experiment. The percentage yield of prepared
extracts was around 8.4%w/w.
Animals Used
Albino rats (180–200 g) of either sex were maintained
in a 12 h light/dark cycle at a constant temperature 25
◦C with free access to feed (Sai durga feeds and foods,
Bangalore) and water. All animals were fasted prior to
all assays and were allocated to different experimental
groups each of six rats. Moreover, the animals were
kept in specially constructed cages to prevent
coprophagia during the experiment. All experiments
were carried out according to the guidelines for care
and use of experimental animals and approved by
Committee for Control and Supervision of
Experiments on Animals (CPCSEA). Ethical committee
clearance was obtained from IAEC (Institutional Animal
Ethics Committee) of CPCSEA.
Acute toxicity study
The acute toxicity of Petroleum Ether extracts of
Lepidagathis cristata whole plant was determined as
per the OECD guideline no. 423 (Acute Toxic Class
Method) It was observed that the test extract was not
lethal to the rats even at 2000mg/kg 2000mg/kg
doses. Hence, 1/20th
(100mg/kg) and 1/10th
(200mg/kg)
of this dose was selected for further study [4].
Experimental Design
Group I: 2% v/v aqueous Tween 80 solutions (5 ml/kg
body wt., p.o)
[Control group]
Group II: Paracetamol (150 mg/kg body wt., p.o)
[Standard group]
Group III: 100 mg/kg PELC suspended in 2% v/v
aqueous Tween 80 solutions, p.o.
Group IV: 200 mg/kg PELC suspended in 2% v/v
aqueous Tween 80 solutions, p.o.
Induction of Brewer’s Yeast-Induced
Pyrexia
The rats were divided into four groups of six each. The
normal body temperature of each rat was measured
rectally at predetermined intervals and recorded
(Vogel, 2002). The rats were trained to remain quiet in
a restraint cage. A thermometer probe was inserted 3-4
cm deep into the rectum and fastened to the tail by
adhesive tape. Temperature was measured on a digital
thermometer. After measuring the basal rectal
temperature, the animals were injected subcutaneously
with 10 ml/kg body wt. of 15% w/v suspension of
brewer’s yeast, suspended in 0.5% w/v methylcellulose
solution [5]. The rats were then returned to their
housing cages. Nineteen hours after the yeast injection,
the animals were again restrained in individual cages
for rectal temperature recording.
Drug Administration
Nineteen hours after yeast injection, the PELC was
administered orally at doses of 100 and 200mg/kg
body wt. to two groups of animals, respectively. A
similar volume (5 ml/kg body wt.) of 2% aqueous
Tween 80 solutions was administered orally to the
control group. The fourth group of animals received
the standard drug, Paracetamol (150 mg/kg body wt.),
orally. The rats were restrained for rectal temperature
recording at the nineteenth hour, immediately before
PELC or 2% aqueous Tween 80 solution or paracetamol
administration, and again at one-hour intervals up to
the four hours after yeast injection [6].
16
B.Deepak Kumar et al / Int. Jour. of Res. in Pharmacology and Pharmacotherapeutics Vol-1 [1] 2012 [14-17]
www.ijrpp.com
Evaluation of parameters
Anti pyretic activity was evaluated by comparing initial
rectal temperature (°C) before yeast injection, with
rectal temperature (°C) after 18 hours of yeast injection
at different time intervals [7,8].
Statistical Analysis
All the values are expressed as mean ± S.E.M for 4
groups of six animals each. The data were analyzed for
significance using the unpaired two-tailed Student’s t-
test.
RESULTS AND DISCUSSION
The effect of PELC on yeast-induced pyrexia was
studied, and it was found that PELC at doses of 100
mg/kg and 200 mg/kg caused significant lowering of
body temperature up to fourth hour following its
administration. This effect was maximum at a dose of
200 mg/kg, in a dose-dependent manner, and caused
significant lowering of body temperature up to fourth
hour after its administration. The subcutaneous
injection of yeast suspension markedly elevated the
rectal temperature at the nineteenth hour after
administration. The results showed that the petroleum
ether extracts of Lepidagathis cristata L. possesses a
significant antipyretic effect in the yeast-provoked
elevation of body temperature in rats, and its effect is
comparable to that of Paracetamol (standard drug).
The antipyretic effect started as early as the first hour
after administration, and the effect was maintained for
four hours after its administration. The standard drug
paracetamol at the dose of 150 mg/kg significantly
reduced the yeast-provoked elevation of body
temperature [9]. The results obtained for both the
standard drug-treated and PELC treated rats were
compared with the control (2% aqueous Tween 80
solutions) group, and a significant reduction in the
yeast-elevated rectal temperature was observed in the
plant extract (Table 1).
Table:- 1 Antipyretic effect of Petroleum ether extracts of Lepidagathis cristata.
Treatment/Dose
Initial rectal
Temp. in °C
before yeast
injection
Rectal temp. in °C after 18 hours of yeast injection
(Mean±Sem)
0 hr 1 hr 2 hr 3 hr 4 hr
Group I
(2% aqueous Tween 80 solution,
5ml/kg, p.o)
37.05±0.02
39.16 ±
0.05
39.20 ±
0.04
39.42 ±
0.05
39.69 ±
0.04
39.95 ±
0.06
Group II
(Paracetamol,
150mg/kg, p.o)
37.14±0.01
39.09 ±
0.03
38.44 ±
0.01a
38.16 ±
0.01 a
37.68 ±
0.05 a
37.21 ±
0.03 a
Group III
(PELC,
100mg/kg, p.o)
37.09±0.03
39.98 ±
0.01
39.50 ±
0.01b
39.34 ±
0.02 b
38.13 ±
0.05 b
37.51 ±
0.08 a
Group IV
(PELC,
200mg/kg, p.o)
37.10±0.07
40.12 ±
0.07
39.25 ±
0.01a
38.20 ±
0.03 a
37.65 ±
0.01 a
37.18 ±
0.05 a
Each value represents mean ± SEM (n=6); a
p<0.001,b
p<0.01, as compared to control.
17
B.Deepak Kumar et al / Int. Jour. of Res. in Pharmacology and Pharmacotherapeutics Vol-1 [1] 2012 [14-17]
www.ijrpp.com
REFERENCES
1. Spacer CB, Breder CD. The neurologic basis of
fever. N Engl J Med., 330, 1994, 1880-1886.
2. Cheng L, Ming-liang H, Lars B et al. Is COX-2 a
perpetrator or a protector? Selective COX-2
inhibitors remain controversial. Acta
Pharmacologica Sinica, 26, 2005, 926-933.
3. Madhava Chetty K. Lepidagathis cristata
Willd. Chittoor medicinal plants, Himalaya
Book Publications, Tirupati, 2005, pp 544.
4. OECD, 2002. Acute oral toxicity. Acute oral
toxic class method guideline 423 adopted
23.03.1996. In: Eleventh Addendum to the,
OECD, guidelines for the testing of chemicals
organisation for economical co-operation and
development, Paris, June, 2000.
5. Vogel HG. Drug Discovery and Evaluation
Pharmacological Assays, 2nd edition,
Springer, New York, 2002,716.
6. Turner RA. Screening method in
Pharmacology, Academic Press, New York &
London, 1965, 268.
7. Ghosh MN. Fundamentals of experimental
pharmacology, 2nd edition, Scientific book
Agency, Calcutta, 2005,156-157.
8. Kulkarni SK. Hand Book of Experimental
Pharmacology, 3rd revised edition, Vallabh
Prakashan, New Delhi, 2006, 178-180.
9. Rajnarayana K, Reddy MS. Chaluvadi MR.
Bioflavonoids classification, pharmacological,
biochemical effects and therapeutical
potential. Indian J. of Pharmaceutical
Sciences, 2006, 68(3), 380-384.

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  • 1. _____________________ * Corresponding author: Sribalaji college of pharmacy, Choppadandi, Karimnagar, A.P. India E-mail address: laxmideepak.pharma@gmail.com Available Online at: www.ijrpp.com ANTIPYRETIC ACTIVITY CRISTATA WILLD. IN BREWER’S YEAST INDUC RATS *1 B.Deepak kumar, 2 Rajendar Rao.V, Sri Balaji College Of Pharmacy, ________ ________________________________________________________________ ABSTRACT The objective of the present work was to study the antipyretic activity of whole plant of belongs to family Acantahaceae. The Petroleum ether extract was taken for the study and evaluated for antipyretic activity using Brewer’s yeast induced pyrexia in Wister strain albino rats. The Petroleum ether extracts at a dose of 100mg/kg & 200mg/kg were evaluated for antipyretic activity. The extract of significant (P < 0.01) dose dependent antipyreti rats. The Petroleum ether extracts of Lepidagathis cristata with the standard drug. Keywords: Lepidagathis cristata, Antipyre __ ______________________________________________________________________ INTRODUCTION Pyrexia or fever is caused as a secondary impact of infection, malignancy or other diseased states. It is the body’s natural function to create an environment where infectious agents or damaged tissues cannot survive. Normally, the infected or damaged tissue initiates the enhanced formation of pro mediators (cytokines, such as interleukin 1 TNF- ), which increase the synthesis of prostaglandin E2 (PgE2) near hypothalamic area and thereby trigger the hypothalamus to elevate the body temperature. When body temperature becomes high, the temperature regulatory system, which is governed by a nervous feedback mechanism, dilates the blood vessels and increases sweating to reduce the temperature. When the body temperature becomes low, hypothalamus protects the internal temperature by vasoconstriction. High fever often increases faster disease progression by increasing tissue catabolism, laxmideepak.pharma@gmail.com Available Online at: www.ijrpp.com Print ISSN: 2278 - 2648 Online ISSN: 2278 - 2656 (Research article) ANTIPYRETIC ACTIVITY OF WHOLE PLANT OF LEPIDAGATHIS BREWER’S YEAST INDUCED HYPER Rajendar Rao.V, 3 Mikkilineni Sindhu Devi, 4 Chandrashekar.B. Sri Balaji College Of Pharmacy, Choppadandi, Karimnagar, A.P, India. ________________________________________________________________ The objective of the present work was to study the antipyretic activity of whole plant of Lepidagathis cristata belongs to family Acantahaceae. The Petroleum ether extract was taken for the study and evaluated for antipyretic yeast induced pyrexia in Wister strain albino rats. The Petroleum ether extracts at a dose of 100mg/kg & 200mg/kg were evaluated for antipyretic activity. The extract of Lepidagathis cristata significant (P < 0.01) dose dependent antipyretic effect in yeast induced elevation of body temperature in experimental Lepidagathis cristata plant have significant antipyretic activity when compared , Antipyretic activity, Brewer’s yeast. ______________________________________________________________________ Pyrexia or fever is caused as a secondary impact of infection, malignancy or other diseased states. It is the function to create an environment where infectious agents or damaged tissues cannot survive. Normally, the infected or damaged tissue initiates the enhanced formation of pro-inflammatory (cytokines, such as interleukin 1, , , and ), which increase the synthesis of prostaglandin E2 (PgE2) near hypothalamic area and thereby trigger the hypothalamus to elevate the body temperature. When body temperature becomes high, the temperature regulatory system, which is governed by a edback mechanism, dilates the blood vessels and increases sweating to reduce the temperature. When the body temperature becomes low, hypothalamus protects the internal temperature by vasoconstriction. High fever often increases faster y increasing tissue catabolism, dehydration, and existing complaints, COX expression to reduce the elevated body temperature by inhibiting PgE2 biosynthesis. These synthetic agents irreversibly inhibit COX-2 with a high selectivity and are toxic to the hepatic cells, glomeruli, cortex of brain, and heart muscles. Natural COX lower selectivity with fewer side effects [1,2]. A natural antipyretic agent with reduced or no toxicity is therefore, essential. Hence, the present study was designed to determine the antipyretic effect of petroleum ether extract of Lepidagathis cristata Lepidagathis cristata Willd. (family: Acantahaceae) Crested Lepidagathis is a perennial herb, with almost no stem. Branches, 20 cm long, arise out of a globose head on the ground, and spread out. Flowers also arise stalk less from this globose head. Flowers are pale pink, 2-lipped. The upper lip is notched, and the lower lip is divided into 3 lobes. Chattisgarh, they use this herb in treatment of International Journal of Research in Pharmacology and Pharmacotherapeutics 14 (Research article) LEPIDAGATHIS ED HYPER PYREXIA Chandrashekar.B. ________________________________________________________________ Lepidagathis cristata Willd, belongs to family Acantahaceae. The Petroleum ether extract was taken for the study and evaluated for antipyretic yeast induced pyrexia in Wister strain albino rats. The Petroleum ether extracts at a dose of Lepidagathis cristata plant showed a c effect in yeast induced elevation of body temperature in experimental plant have significant antipyretic activity when compared ______________________________________________________________________ dehydration, and existing complaints, COX-2 expression to reduce the elevated body temperature by inhibiting PgE2 biosynthesis. These synthetic agents 2 with a high selectivity and hepatic cells, glomeruli, cortex of brain, and heart muscles. Natural COX-2 inhibitors have lower selectivity with fewer side effects [1,2]. A natural antipyretic agent with reduced or no toxicity is therefore, essential. Hence, the present study was gned to determine the antipyretic effect of Lepidagathis cristata. Willd. (family: Acantahaceae) Crested Lepidagathis is a perennial herb, with almost no stem. Branches, 20 cm long, arise out of a globose ad on the ground, and spread out. Flowers also arise stalk less from this globose head. Flowers are pale lipped. The upper lip is notched, and the lower lip is divided into 3 lobes. Medicinal uses: In Chattisgarh, they use this herb in treatment of fever International Journal of Research in Pharmacology and Pharmacotherapeutics
  • 2. 15 B.Deepak Kumar et al / Int. Jour. of Res. in Pharmacology and Pharmacotherapeutics Vol-1 [1] 2012 [14-17] www.ijrpp.com particularly in treatment of Malarial fever. The decoction of leaves is used internally for this purpose. Its utility in treatment of fever has given it the name Bukhar Jadi in reference literatures; the use of this herb in treatment of itchy affections of skin has been mentioned. The traditional healers of Chhattisgarh Plains are aware of this use. In many parts of Chhattisgarh, the cattle owners use the decoction of this herb to wash the cattle in rainy season in order to keep it free from flies [3]. Therefore, the main objectives of present study were to investigate the anti-pyretic activity of the Petroleum Ether Extract of Lepidagathis cristata is being reported here. MATERIALS AND METHODS Plant material The whole plant of Lepidagathis cristata was collected from Tirumala hills, Tirupati, Andhra Pradesh. India. It was identified and authenticated by Prof. Madhava Chetty, K., Taxonomist, S.V. University, Tirupati, Andhra Pradesh, India. A voucher specimen has been kept in our laboratory for future reference. Preparation of plant extract The collected whole plant was dried at room temperature, pulverized by a mechanical grinder, sieved through 40mesh. About 100g of powdered materials were extracted with petroleum ether (60°- 80°C) using soxhlet apparatus. The extraction was carried out until the extractive becomes colourless. The extract is then concentrated and dried under reduced pressure. The solvent free semisolid mass thus obtained is dissolved in tween 80 and used for the experiment. The percentage yield of prepared extracts was around 8.4%w/w. Animals Used Albino rats (180–200 g) of either sex were maintained in a 12 h light/dark cycle at a constant temperature 25 ◦C with free access to feed (Sai durga feeds and foods, Bangalore) and water. All animals were fasted prior to all assays and were allocated to different experimental groups each of six rats. Moreover, the animals were kept in specially constructed cages to prevent coprophagia during the experiment. All experiments were carried out according to the guidelines for care and use of experimental animals and approved by Committee for Control and Supervision of Experiments on Animals (CPCSEA). Ethical committee clearance was obtained from IAEC (Institutional Animal Ethics Committee) of CPCSEA. Acute toxicity study The acute toxicity of Petroleum Ether extracts of Lepidagathis cristata whole plant was determined as per the OECD guideline no. 423 (Acute Toxic Class Method) It was observed that the test extract was not lethal to the rats even at 2000mg/kg 2000mg/kg doses. Hence, 1/20th (100mg/kg) and 1/10th (200mg/kg) of this dose was selected for further study [4]. Experimental Design Group I: 2% v/v aqueous Tween 80 solutions (5 ml/kg body wt., p.o) [Control group] Group II: Paracetamol (150 mg/kg body wt., p.o) [Standard group] Group III: 100 mg/kg PELC suspended in 2% v/v aqueous Tween 80 solutions, p.o. Group IV: 200 mg/kg PELC suspended in 2% v/v aqueous Tween 80 solutions, p.o. Induction of Brewer’s Yeast-Induced Pyrexia The rats were divided into four groups of six each. The normal body temperature of each rat was measured rectally at predetermined intervals and recorded (Vogel, 2002). The rats were trained to remain quiet in a restraint cage. A thermometer probe was inserted 3-4 cm deep into the rectum and fastened to the tail by adhesive tape. Temperature was measured on a digital thermometer. After measuring the basal rectal temperature, the animals were injected subcutaneously with 10 ml/kg body wt. of 15% w/v suspension of brewer’s yeast, suspended in 0.5% w/v methylcellulose solution [5]. The rats were then returned to their housing cages. Nineteen hours after the yeast injection, the animals were again restrained in individual cages for rectal temperature recording. Drug Administration Nineteen hours after yeast injection, the PELC was administered orally at doses of 100 and 200mg/kg body wt. to two groups of animals, respectively. A similar volume (5 ml/kg body wt.) of 2% aqueous Tween 80 solutions was administered orally to the control group. The fourth group of animals received the standard drug, Paracetamol (150 mg/kg body wt.), orally. The rats were restrained for rectal temperature recording at the nineteenth hour, immediately before PELC or 2% aqueous Tween 80 solution or paracetamol administration, and again at one-hour intervals up to the four hours after yeast injection [6].
  • 3. 16 B.Deepak Kumar et al / Int. Jour. of Res. in Pharmacology and Pharmacotherapeutics Vol-1 [1] 2012 [14-17] www.ijrpp.com Evaluation of parameters Anti pyretic activity was evaluated by comparing initial rectal temperature (°C) before yeast injection, with rectal temperature (°C) after 18 hours of yeast injection at different time intervals [7,8]. Statistical Analysis All the values are expressed as mean ± S.E.M for 4 groups of six animals each. The data were analyzed for significance using the unpaired two-tailed Student’s t- test. RESULTS AND DISCUSSION The effect of PELC on yeast-induced pyrexia was studied, and it was found that PELC at doses of 100 mg/kg and 200 mg/kg caused significant lowering of body temperature up to fourth hour following its administration. This effect was maximum at a dose of 200 mg/kg, in a dose-dependent manner, and caused significant lowering of body temperature up to fourth hour after its administration. The subcutaneous injection of yeast suspension markedly elevated the rectal temperature at the nineteenth hour after administration. The results showed that the petroleum ether extracts of Lepidagathis cristata L. possesses a significant antipyretic effect in the yeast-provoked elevation of body temperature in rats, and its effect is comparable to that of Paracetamol (standard drug). The antipyretic effect started as early as the first hour after administration, and the effect was maintained for four hours after its administration. The standard drug paracetamol at the dose of 150 mg/kg significantly reduced the yeast-provoked elevation of body temperature [9]. The results obtained for both the standard drug-treated and PELC treated rats were compared with the control (2% aqueous Tween 80 solutions) group, and a significant reduction in the yeast-elevated rectal temperature was observed in the plant extract (Table 1). Table:- 1 Antipyretic effect of Petroleum ether extracts of Lepidagathis cristata. Treatment/Dose Initial rectal Temp. in °C before yeast injection Rectal temp. in °C after 18 hours of yeast injection (Mean±Sem) 0 hr 1 hr 2 hr 3 hr 4 hr Group I (2% aqueous Tween 80 solution, 5ml/kg, p.o) 37.05±0.02 39.16 ± 0.05 39.20 ± 0.04 39.42 ± 0.05 39.69 ± 0.04 39.95 ± 0.06 Group II (Paracetamol, 150mg/kg, p.o) 37.14±0.01 39.09 ± 0.03 38.44 ± 0.01a 38.16 ± 0.01 a 37.68 ± 0.05 a 37.21 ± 0.03 a Group III (PELC, 100mg/kg, p.o) 37.09±0.03 39.98 ± 0.01 39.50 ± 0.01b 39.34 ± 0.02 b 38.13 ± 0.05 b 37.51 ± 0.08 a Group IV (PELC, 200mg/kg, p.o) 37.10±0.07 40.12 ± 0.07 39.25 ± 0.01a 38.20 ± 0.03 a 37.65 ± 0.01 a 37.18 ± 0.05 a Each value represents mean ± SEM (n=6); a p<0.001,b p<0.01, as compared to control.
  • 4. 17 B.Deepak Kumar et al / Int. Jour. of Res. in Pharmacology and Pharmacotherapeutics Vol-1 [1] 2012 [14-17] www.ijrpp.com REFERENCES 1. Spacer CB, Breder CD. The neurologic basis of fever. N Engl J Med., 330, 1994, 1880-1886. 2. Cheng L, Ming-liang H, Lars B et al. Is COX-2 a perpetrator or a protector? Selective COX-2 inhibitors remain controversial. Acta Pharmacologica Sinica, 26, 2005, 926-933. 3. Madhava Chetty K. Lepidagathis cristata Willd. Chittoor medicinal plants, Himalaya Book Publications, Tirupati, 2005, pp 544. 4. OECD, 2002. Acute oral toxicity. Acute oral toxic class method guideline 423 adopted 23.03.1996. In: Eleventh Addendum to the, OECD, guidelines for the testing of chemicals organisation for economical co-operation and development, Paris, June, 2000. 5. Vogel HG. Drug Discovery and Evaluation Pharmacological Assays, 2nd edition, Springer, New York, 2002,716. 6. Turner RA. Screening method in Pharmacology, Academic Press, New York & London, 1965, 268. 7. Ghosh MN. Fundamentals of experimental pharmacology, 2nd edition, Scientific book Agency, Calcutta, 2005,156-157. 8. Kulkarni SK. Hand Book of Experimental Pharmacology, 3rd revised edition, Vallabh Prakashan, New Delhi, 2006, 178-180. 9. Rajnarayana K, Reddy MS. Chaluvadi MR. Bioflavonoids classification, pharmacological, biochemical effects and therapeutical potential. Indian J. of Pharmaceutical Sciences, 2006, 68(3), 380-384.