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4623
Devarakonda Ramadevi et al, J. Global Trends Pharm Sci, 2017; 8(4): 4623 - 4628
approved by the institutional ethics The normal rectal temperature and its
committee and as per CPCSEA guidelines. hourly variation were recorded at the
Chemicals: Paracetamol and Typhoid beginning of the experiment using a digital
vaccine were purchased from Apollo tele thermometer[6]. Animals were fasted
medical store, Visakhapatnam. All other for 24 hours before giving the drugs, but
chemicals used for this study were of water freely permitted, pyrexia was
analytical grade. induced by the administration of TAB
Pyrexia Induced in Rats by Typhoid vaccine. The vaccine was given intra
Vaccine peritonially in a dilution of 1/15 in normal
The room temperature was saline to all animals[7]. After two hours of
maintained at 30ºC. Only animals with a the administration of TAB Vaccine, the
body temperature of at least 38ºC (Max) rectal- temperature of each rat was taken
were taken into the test. Typhoid- and found to be fairly stabilized.
Paratyphoid A & B vaccine (0.3 ml) was 1. The first group of rats were given
injected i.p. for rats of each group. the vehicle (0.1% Sodium CMC).
Standard paracetamol (I.V.) was injected
2. The second group was given
30 minutes before administration of paracetamol 100 mg/kg body
Typhoid-Paratyphoid A, B vaccine. The weight orally which was used as
rectal temperature of each animal was reference standard drug.
recorded initial and at the interval of 30 3. The third group was given plant
minute after treatment using treatment extract orally at a dose of 100
using tele thermometer up to 3 hours(4,5).
mg/kg body weight
In the LD50 value determination, we 4. The fourth group was given the
observed that the Leaf extract was safe to plant extract orally at a dose of 200
use in animals and showed no mortality up mg/kg body weight.
to 2000 mg/kg body weight. Therefore
5. The fifth group was administered
2000 mg/kg dose was considered as a safe
with plant extract 400 mg/kg body
dose. 1/5 th (400 mg/kg body wt.) , 1/10th
weight orally . The rectal
(200 mg/kg body w.t) and
temperature of rats were taken
1/20th(100mg/kg body w.t) of that was
using an electronic digital tele
selected for all in vivo experiments as
thermometer. The results were
maximal dose.
evaluated by one way ANOVA.
EXPERIMENTAL DESIGN
DISCUSSION
In the experiment, a total of 30 rats
Antipyretics are the agents which
were used. The rats were divided into 5
reduce the elevated body temperature.
groups comprising of 6 animals in each
Regulation of body temperature requires a
group as follows: Group : Control
delicate balance between production and
Group I : Rats received Paracetamol
loss of heat, and the hypothalamus
(10mg/kg.) only 1 day around 1 hr before
regulates the set point at which body
measurement of Body temperature by the
temperature is maintained. In fever this set
help of digital tele thermometer.
point elevates and a drug like paracetamol
Group II: Rats received Methanol Extract
does not influence body temperature when
of F.hispida (100mg/kg p.o.)
it is elevated by the factors such as
Group IV: Rats received Methanol
exercise or increase in ambient
Extract of F. hispida (200mg/kg p.o.) [8,9]
temperature . Experimental studies
Group V: Mice received Methanol Extract
reveals that extracts of Ficus hispida (at
of F.hispida (400mg/kg p.o)
dose 400 mg/kg) produced an antipyretic
Experimental Animals: Albino rats of action by decreasing the body temperature
either sex weighing between 170-220 gms in the model of fever in rats.
were arranged in five groups of six each.
4624
Devarakonda Ramadevi et al, J. Global Trends Pharm Sci, 2017; 8(4): 4623 - 4628
F.hispida extract(100mg/kg)
110
o hour
after vaccination
105
0.5 hr
1 hr
temp
100 1.5 hr
2 hr
95 2.5 hr
3 hr
90
r
hr
hr
hr
n
hr
hr
hr
u
tio
ho
3
5
5
na
0.
1.
2.
o
c ci
va
r
te
af
time
4625
Devarakonda Ramadevi et al, J. Global Trends Pharm Sci, 2017; 8(4): 4623 - 4628
F.hispida extract(200mg/kg)
110
0 hr
After vaccination
105
0.5 hr
1 hr
temp
100 1.5 hr
2 hr
95 2.5 hr
3 hr
90
ci hr
hr
hr
hr
n
hr
hr
hr
tio
0
3
5
5
na
0.
1.
2.
c
va
r
fte
A
time
F.hispida extract(400mg/kg)
110
0 hr
After vaccination
105
0.5 hr
1 hr
temp
100 1.5 hr
2 hr
95 2.5 hr
3 hr
90
hr n
io .5 h
r hr hr hr hr hr
0 t 1 5 2 5 3
in
a 0 1. 2.
cc
r va
fte
A
time
4626
Devarakonda Ramadevi et al, J. Global Trends Pharm Sci, 2017; 8(4): 4623 - 4628
CONTROL
110
0hr
after vaccine
Temperature(C)
105
0.5hr
1hr
100 1.5hr
2hr
95 2.5hr
3hr
90
r e r r r r r r
0h cin .5h 1h .5h 2h .5h 3h
c 0 1 2
r va
a fte
Time(hrs)
PARACETAMOL(150mg/kg)
110
0hr
after vaccine
Temperature(C)
105
0.5hr
1hr
100 1.5hr
2hr
95 2.5hr
3hr
90
r
r
r
r
ne
0h
1h
2h
3h
5h
5h
5h
ci
0.
1.
2.
c
r va
te
af
Time(hrs)
REFERENCES: 2. ZipcodeZoo. Archieved from the
1. The Ayurvedic Pharmacopoeia of original on august
India part I Vol. II Government of 30,2010.Retrieved april 17,2012
India, Ministry of health and 3. Encyclopedia of Medicinal Plants.
family welfare department of 4. The assay of anti-pyretic drugs in
Indian system of medicine and mice, using intracerebral injection
homoeopathy of pyretogenins C.H.Cashin and
4627
Devarakonda Ramadevi et al, J. Global Trends Pharm Sci, 2017; 8(4): 4623 - 4628
ChristeneE.Br.J.Pharmac.(1968),34
,148-158
5. Kumar,A.,Dora J. Singh A and
Tripathi, R. Review of King Bitter
(Kalmegh), International Journal
of Research in Pharmacy and
Chemistry,Vol II .2012
6. Chidambaram K, Albert J,
Karpagam K, Sivasubramanian N.
Antipyretic activity of Crataeva
magna bark on Tab- Vaccine
induced pyrexia. International
Journal of Pharmaceutical Science
& Research 2011; 2(4): 856-59.
7. British Pharmacopoeia (1963).
8. Goodman SL.Gilman A.The
Pharmacological Basis of
Therapeutics.IX Edition.
9. Bhargava S.Evaluation of
antipyretic of Sudarshan chuma:an
Ayurved formulation,International
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