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____________________
* Corresponding author:
1
Sruthi.B
St.Peter’s institute of Pharmaceutical Sciences,
Hanamkonda, A.P, India
Email: burugula.shruthi@gmail.com
Available Online at: www.ijrpp.com
DIURETIC ACTIVITY OF
CARICA L. FRUITS
*1
Sruthi.B, 2
Sunny.G, 3
Hajra Naz
1,2,3
St.Peter’s institute of Pharmaceutical sciences
4
P.R.R.M. College of Pharmacy, Kadapa, Andhra Pradesh, India
________________________________________________________________________
ABSTRACT
Ethanol extracts of Ficus carica L. fruits were tested for diuretic activity in rats. The parameters studied on
individual rat were total urine volume, urine concentration of Na+, K
of Ficus carica, L. (100 and 200mg/kg of body weight) showed
excretion. Furosemide was used as the reference diuretic. Based on the above results, we can conclude that
carica L. treatment produced a marked diuresis when rats were acutely treated. In our study, no lethality was
observed at least for the dose (2000mg/kg body weight), and duration used. The best results of urine output
observed with the ethanolic extract of
support the traditional uses of Ficus carica L.
Keywords: Ficus carica L., diuretic activity,
_____________________________________________________________
INTRODUCTION
Diuretics not only alter the excretion of Na
may modify renal handling of other cations (
H+
, Ca2+
, and Mg2+
), anions (e.g.,Cl–
, HCO3
–
and uric acid. In addition, diuretics may alter renal
hemodynamics indirectly. Diuretics remain the
cornerstone for the treatment of edema or volume
overload, particularly that owing to congestive heart
failure, ascites, chronic renal failure, and nephr
syndrome. Naturally occurring diuretics include
caffeine in coffee, tea, and cola, which inhibit Na +
reabsorption. Hence search for a new diuretic agent
retains therapeutic efficacy and yet devoid of
potassium loss is justified [1,2].
Ficus carica L. (family-Moraceae) is a tree of small
dimension that produces copious milky latex and
fruits, which are actually a synconium, i.e. a fleshy
hollow receptacle with a small opening at the apex
partly closed by small scales. The latex of the unripe
fruit and other parts of the tree cause severe
irritation to the skin, if not removed promptly. The
institute of Pharmaceutical Sciences,
Available Online at: www.ijrpp.com Print ISSN: 2278 - 2648
Online ISSN: 2278 - 2656
(Research article)
DIURETIC ACTIVITY OF ETHANOLIC EXTRACTS OF FICUS
Naz, 4
S.Sakthivel
institute of Pharmaceutical sciences, Hanamkonda, A.P, India
P.R.R.M. College of Pharmacy, Kadapa, Andhra Pradesh, India- 516 003.
________________________________________________________________________
fruits were tested for diuretic activity in rats. The parameters studied on
individual rat were total urine volume, urine concentration of Na+, K- and Cl-. In the present study ethanol extracts
(100 and 200mg/kg of body weight) showed an increase in urine volume, cation and anion
Furosemide was used as the reference diuretic. Based on the above results, we can conclude that
treatment produced a marked diuresis when rats were acutely treated. In our study, no lethality was
observed at least for the dose (2000mg/kg body weight), and duration used. The best results of urine output
observed with the ethanolic extract of Ficus carica L. fruits obtained through this evaluation. These findings
Ficus carica L. as diuretic agents.
diuretic activity, Lipschitz test.
________________________________________________________________________
Diuretics not only alter the excretion of Na+
but also
may modify renal handling of other cations (e.g., K+
,
–
, and H2
PO4
–
),
and uric acid. In addition, diuretics may alter renal
hemodynamics indirectly. Diuretics remain the
cornerstone for the treatment of edema or volume
overload, particularly that owing to congestive heart
failure, ascites, chronic renal failure, and nephrotic
Naturally occurring diuretics include
caffeine in coffee, tea, and cola, which inhibit Na +
reabsorption. Hence search for a new diuretic agent
retains therapeutic efficacy and yet devoid of
Moraceae) is a tree of small
dimension that produces copious milky latex and
fruits, which are actually a synconium, i.e. a fleshy
hollow receptacle with a small opening at the apex
partly closed by small scales. The latex of the unripe
other parts of the tree cause severe
irritation to the skin, if not removed promptly. The
latex is widely applied on warts, skin ulcers,
soresand abnormal growth. It also lowers the levels
of total cholesterol, triglycerides and total
cholesterol/HDL cholesterol ratio. In addition,
carica L. has been used to treat many other medical
conditions such as cough, flu, asthma, cancer,
abscesses, constipation, diabetes, gingivitis and used
as a diuretic [3]. The aim of this present study was
the diuretic activity of ethanolic extracts of
carica fruits.
MATERIALS AND METHODS
Plant material
The fruits of Ficus carica L. was collected from
Tirumala hills, Tirupati, Andhra Pradesh. India. It
was identified and authenticated by Prof.
Chetty, K., Taxonomist, S.V. University, Tirupati,
Andhra Pradesh, India. A voucher specimen has
been kept in our laboratory for future reference.
International Journal of
Research in Pharmacology and
Pharmacotherapeutics
23
(Research article)
FICUS
________________________________________________________________________
fruits were tested for diuretic activity in rats. The parameters studied on
. In the present study ethanol extracts
an increase in urine volume, cation and anion
Furosemide was used as the reference diuretic. Based on the above results, we can conclude that Ficus
treatment produced a marked diuresis when rats were acutely treated. In our study, no lethality was
observed at least for the dose (2000mg/kg body weight), and duration used. The best results of urine output
fruits obtained through this evaluation. These findings
___________
latex is widely applied on warts, skin ulcers,
soresand abnormal growth. It also lowers the levels
of total cholesterol, triglycerides and total
lesterol ratio. In addition, Ficus
has been used to treat many other medical
conditions such as cough, flu, asthma, cancer,
abscesses, constipation, diabetes, gingivitis and used
as a diuretic [3]. The aim of this present study was
ctivity of ethanolic extracts of Ficus
MATERIALS AND METHODS
was collected from
Tirumala hills, Tirupati, Andhra Pradesh. India. It
was identified and authenticated by Prof. Madhava
, Taxonomist, S.V. University, Tirupati,
Andhra Pradesh, India. A voucher specimen has
been kept in our laboratory for future reference.
International Journal of
Research in Pharmacology and
Pharmacotherapeutics
24
Sruthi.B et al / Int. Jour. of Res. in Pharmacology and Pharmacotherapeutics Vol-1[1] 2012 [23-26]
www.ijrpp.com
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 Ethanol (90%) 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 10.5%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 the Purpose of 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 Ethanol extracts of Ficus carica
L. fruit 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
2000 mg/kg doses. Hence, 1/10th
(200mg/kg) and
1/5th
(400mg/kg) of this dose was selected for
further study [4].
Diuretic activity
Group I received 2% v/v aqueous tween 80 solutions
(5ml/kg, p.o.). Group II received Furosemide
(100mg/kg, i.p), Group III and Group IV received 200
and 400mg/kg of EEFC suspended in 2% v/v aqueous
tween 80 solutions, p.o. respectively. Four groups of
six rats in each and were fasted and deprived of
water for eighteen hours prior to the experiment.
The first group of animals serving as control,
received 2% v/v aqueous tween 80 solutions (5ml/kg,
p.o.); the second group received furosemide (100
mg/kg, i.p.) in 2% v/v aqueous tween 80 solutions;
the third, fourth groups received the EEFC at the
doses of 200 mg/kg and 400 mg/kg respectively, in
2% v/v aqueous tween 80 solutions. The animals
were fasted overnight (18 h) prior to the test but
with free access to tap water only and then drugs
were administered to respective groups.
Immediately, after administration, the animals were
placed in metabolic cages, specially designed to
separate urine and feaces, kept at room temperature
of 25± 0.5°C throughout the experiment. The urine
was collected in measuring cylinders up to 5 h after
dosing. During this period, no food or water was
made available to animals. The parameters taken for
individual rat were volume of urine output, total
concentration of Na+
, K+
, and Clˉ in the urine. Na+
, K+
concentrations were measured by Flame photometry
[5], and Clˉ concentration was estimated by titration
[6] with silver nitrate solution (N/50) using three
drops of 5% Potassium chromate solution as an
indicator. Appearance of brick red precipitate was
taken as the end point [7,8].
The volume of the urine excreted in 5 h
study by each group was expressed as percent of the
liquid administered giving rise to a measure of
“Urinary Excretion” (U.E) - Independent of group
weight.
Total urinary
output
Urinary ______________________
excretion (U.E) = Total liquid
Administered
Diuretic U.E in test group
Index = ____________________
U.E in control group
Mean urine volume
of test
Lipschitz ______________________
Value = Mean urine volume
of Standard
Statistical analysis
The data were expressed as Mean ± S.E.M and
statistically analyzed using one-way ANOVA
followed by Tukey-Kramer’s multiple comparison
test, p<0.05 was considered as significant.
RESULTS AND DISCUSSION
The diuretic activity of the EEFC was significant
when compared to control (Table 1). Furosemide
(100mg/kg) treated animals very significantly (p <
0.01) increased the urinary output and electrolyte
excretion of Na+
, K+
and Clˉ as compared to control.
The graded doses of the EEFC in 2% v/v aqueous
tween 80 solutions showed a very significant
increase in diuresis, natriuresis, kaliuresis and total
chloride excretion, which was comparable to the
action of Furosemide. The diuretic index of the two
different doses, i.e., 200 mg/kg and 400 mg/kg body
weight was found to be 2.0433 and 2.7154
25
Sruthi.B et al / Int. Jour. of Res. in Pharmacology and Pharmacotherapeutics Vol-1[1] 2012 [23-26]
www.ijrpp.com
respectively (Table 2) where the diuretic activity of
EEFC at a dose of 400 mg/kg body weight was found
to be extremely significant (p < 0.01).
Based on the above results, we can conclude that
Ficus carica L. treatment produced a marked diuresis
when rats were acutely treated. In our study, no
lethality was observed at least for the dose
(2000mg/kg body weight), and duration used. The
best results of urine output observed with the
ethanolic extract obtained through this evaluation.
However, advanced toxicological studies remain to
be performed in other animals before its
recommendation to the clinical studies.
Table 1: Effect of Ethanol extract of Ficus carica (L.) on urine volume and electrolyte
concentration in Rats.
Groups
Treatment &
Dose
Mean urine
volume (ml)
Electrolyte excretion
Na+
mMoles/L
K+
mMoles/L
Na+
/ K+
ratio
Clˉ
mMoles/L
I
2% v/v tween 80
solution 5ml/kg, p.o
3.69 ±0.06 72.60±0.26 48.65±0.15 1.4922 103.65±0.16
II
Furosemide 100mg/kg,
i.p
11.25±0.05**
120.30
±0.35**
82.20
±2.96**
1.4635 138 ±0.31**
III
EEFC
200 mg/kg, p.o
7.54 ±0.04*
102.25
±0.35*
71.22
±1.50*
1.4357
105.12
±0.17*
IV
EEFC
400 mg/kg, p.o
10.02 ±0.05**
114.90
±0.14**
74.36
±1.14**
1.5452 128 ±0.22**
Values are expressed as mean ± SEM (n = 6); *p < 0.05 and **p < 0.01 compared with control (One way ANOVA
followed by Tukey-Kramer’s multiple comparison test).
Table 2: Diuretic effect of Ethanol extract of Ficus carica (L.) in comparison to control &
standard.
Groups
Treatment &
Dose
Diuretic Index Lipschitz value
I
2% v/v aqueous tween 80 solution,
5ml/kg, p.o
-- --
II
Furosemide
100mg/kg, i.p
3.0487 --
III
EEFC
200 mg/kg, p.o
2.0433 0.6702
IV
EEFC
400 mg/kg, p.o
2.7154 0.8907
26
Sruthi.B et al / Int. Jour. of Res. in Pharmacology and Pharmacotherapeutics Vol-1[1] 2012 [23-26]
www.ijrpp.com
REFERENCES
1. Brunton LL, Lazo JS, Parker KL. Goodman &
Gilman's The Pharmacological Basis of
Therapeutics, 11th edition. McGraw-Hill
(New York), 2006.
2. Rang HP, Dale MM, Ritter JM. In: Text book
of Pharmacology. 2nd ed. Churchill
Livingstone, pp 428-38; 1994.
3. Madhava Chetty K. Yucca gloriosa Linn.
Chittoor medicinal plants, Himalaya Book
Publications, Tirupati, 2005, pp 60.
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. Beckette AH, Stenlake JB. Practical
Pharmaceutical Chemistry, Part I, 1st
edition, CBS Publishers (New Delhi), 197;
1997.
6. Jeffery GH, Bassett J, Mendham J, Denny.
Vogel’s Textbook of Quantitative Chemical
Analysis, 5th
edition. Addison Westley
Longman (England) pp 801; 1989.
7. Lipschitz WL, Haddian Z, Kerpscar A.
Bioassay of Diuretics, .Pharmacol.Exp.Ther.,
79: 97- 110; 1943.
8. Ratnasooriya WD, Pieris KPP, Samaratunga
U, Jayakody JRAC, Diuretic activity of
Spilanthes acmella flowers in rats. Journal
of Ethnopharmacology, 91: 317-320; 2004.

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Diuretic activity of ethanolic extracts of ficus carica l fruits ijrpp

  • 1. ____________________ * Corresponding author: 1 Sruthi.B St.Peter’s institute of Pharmaceutical Sciences, Hanamkonda, A.P, India Email: burugula.shruthi@gmail.com Available Online at: www.ijrpp.com DIURETIC ACTIVITY OF CARICA L. FRUITS *1 Sruthi.B, 2 Sunny.G, 3 Hajra Naz 1,2,3 St.Peter’s institute of Pharmaceutical sciences 4 P.R.R.M. College of Pharmacy, Kadapa, Andhra Pradesh, India ________________________________________________________________________ ABSTRACT Ethanol extracts of Ficus carica L. fruits were tested for diuretic activity in rats. The parameters studied on individual rat were total urine volume, urine concentration of Na+, K of Ficus carica, L. (100 and 200mg/kg of body weight) showed excretion. Furosemide was used as the reference diuretic. Based on the above results, we can conclude that carica L. treatment produced a marked diuresis when rats were acutely treated. In our study, no lethality was observed at least for the dose (2000mg/kg body weight), and duration used. The best results of urine output observed with the ethanolic extract of support the traditional uses of Ficus carica L. Keywords: Ficus carica L., diuretic activity, _____________________________________________________________ INTRODUCTION Diuretics not only alter the excretion of Na may modify renal handling of other cations ( H+ , Ca2+ , and Mg2+ ), anions (e.g.,Cl– , HCO3 – and uric acid. In addition, diuretics may alter renal hemodynamics indirectly. Diuretics remain the cornerstone for the treatment of edema or volume overload, particularly that owing to congestive heart failure, ascites, chronic renal failure, and nephr syndrome. Naturally occurring diuretics include caffeine in coffee, tea, and cola, which inhibit Na + reabsorption. Hence search for a new diuretic agent retains therapeutic efficacy and yet devoid of potassium loss is justified [1,2]. Ficus carica L. (family-Moraceae) is a tree of small dimension that produces copious milky latex and fruits, which are actually a synconium, i.e. a fleshy hollow receptacle with a small opening at the apex partly closed by small scales. The latex of the unripe fruit and other parts of the tree cause severe irritation to the skin, if not removed promptly. The institute of Pharmaceutical Sciences, Available Online at: www.ijrpp.com Print ISSN: 2278 - 2648 Online ISSN: 2278 - 2656 (Research article) DIURETIC ACTIVITY OF ETHANOLIC EXTRACTS OF FICUS Naz, 4 S.Sakthivel institute of Pharmaceutical sciences, Hanamkonda, A.P, India P.R.R.M. College of Pharmacy, Kadapa, Andhra Pradesh, India- 516 003. ________________________________________________________________________ fruits were tested for diuretic activity in rats. The parameters studied on individual rat were total urine volume, urine concentration of Na+, K- and Cl-. In the present study ethanol extracts (100 and 200mg/kg of body weight) showed an increase in urine volume, cation and anion Furosemide was used as the reference diuretic. Based on the above results, we can conclude that treatment produced a marked diuresis when rats were acutely treated. In our study, no lethality was observed at least for the dose (2000mg/kg body weight), and duration used. The best results of urine output observed with the ethanolic extract of Ficus carica L. fruits obtained through this evaluation. These findings Ficus carica L. as diuretic agents. diuretic activity, Lipschitz test. ________________________________________________________________________ Diuretics not only alter the excretion of Na+ but also may modify renal handling of other cations (e.g., K+ , – , and H2 PO4 – ), and uric acid. In addition, diuretics may alter renal hemodynamics indirectly. Diuretics remain the cornerstone for the treatment of edema or volume overload, particularly that owing to congestive heart failure, ascites, chronic renal failure, and nephrotic Naturally occurring diuretics include caffeine in coffee, tea, and cola, which inhibit Na + reabsorption. Hence search for a new diuretic agent retains therapeutic efficacy and yet devoid of Moraceae) is a tree of small dimension that produces copious milky latex and fruits, which are actually a synconium, i.e. a fleshy hollow receptacle with a small opening at the apex partly closed by small scales. The latex of the unripe other parts of the tree cause severe irritation to the skin, if not removed promptly. The latex is widely applied on warts, skin ulcers, soresand abnormal growth. It also lowers the levels of total cholesterol, triglycerides and total cholesterol/HDL cholesterol ratio. In addition, carica L. has been used to treat many other medical conditions such as cough, flu, asthma, cancer, abscesses, constipation, diabetes, gingivitis and used as a diuretic [3]. The aim of this present study was the diuretic activity of ethanolic extracts of carica fruits. MATERIALS AND METHODS Plant material The fruits of Ficus carica L. was collected from Tirumala hills, Tirupati, Andhra Pradesh. India. It was identified and authenticated by Prof. Chetty, K., Taxonomist, S.V. University, Tirupati, Andhra Pradesh, India. A voucher specimen has been kept in our laboratory for future reference. International Journal of Research in Pharmacology and Pharmacotherapeutics 23 (Research article) FICUS ________________________________________________________________________ fruits were tested for diuretic activity in rats. The parameters studied on . In the present study ethanol extracts an increase in urine volume, cation and anion Furosemide was used as the reference diuretic. Based on the above results, we can conclude that Ficus treatment produced a marked diuresis when rats were acutely treated. In our study, no lethality was observed at least for the dose (2000mg/kg body weight), and duration used. The best results of urine output fruits obtained through this evaluation. These findings ___________ latex is widely applied on warts, skin ulcers, soresand abnormal growth. It also lowers the levels of total cholesterol, triglycerides and total lesterol ratio. In addition, Ficus has been used to treat many other medical conditions such as cough, flu, asthma, cancer, abscesses, constipation, diabetes, gingivitis and used as a diuretic [3]. The aim of this present study was ctivity of ethanolic extracts of Ficus MATERIALS AND METHODS was collected from Tirumala hills, Tirupati, Andhra Pradesh. India. It was identified and authenticated by Prof. Madhava , Taxonomist, S.V. University, Tirupati, Andhra Pradesh, India. A voucher specimen has been kept in our laboratory for future reference. International Journal of Research in Pharmacology and Pharmacotherapeutics
  • 2. 24 Sruthi.B et al / Int. Jour. of Res. in Pharmacology and Pharmacotherapeutics Vol-1[1] 2012 [23-26] www.ijrpp.com 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 Ethanol (90%) 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 10.5%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 the Purpose of 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 Ethanol extracts of Ficus carica L. fruit 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 2000 mg/kg doses. Hence, 1/10th (200mg/kg) and 1/5th (400mg/kg) of this dose was selected for further study [4]. Diuretic activity Group I received 2% v/v aqueous tween 80 solutions (5ml/kg, p.o.). Group II received Furosemide (100mg/kg, i.p), Group III and Group IV received 200 and 400mg/kg of EEFC suspended in 2% v/v aqueous tween 80 solutions, p.o. respectively. Four groups of six rats in each and were fasted and deprived of water for eighteen hours prior to the experiment. The first group of animals serving as control, received 2% v/v aqueous tween 80 solutions (5ml/kg, p.o.); the second group received furosemide (100 mg/kg, i.p.) in 2% v/v aqueous tween 80 solutions; the third, fourth groups received the EEFC at the doses of 200 mg/kg and 400 mg/kg respectively, in 2% v/v aqueous tween 80 solutions. The animals were fasted overnight (18 h) prior to the test but with free access to tap water only and then drugs were administered to respective groups. Immediately, after administration, the animals were placed in metabolic cages, specially designed to separate urine and feaces, kept at room temperature of 25± 0.5°C throughout the experiment. The urine was collected in measuring cylinders up to 5 h after dosing. During this period, no food or water was made available to animals. The parameters taken for individual rat were volume of urine output, total concentration of Na+ , K+ , and Clˉ in the urine. Na+ , K+ concentrations were measured by Flame photometry [5], and Clˉ concentration was estimated by titration [6] with silver nitrate solution (N/50) using three drops of 5% Potassium chromate solution as an indicator. Appearance of brick red precipitate was taken as the end point [7,8]. The volume of the urine excreted in 5 h study by each group was expressed as percent of the liquid administered giving rise to a measure of “Urinary Excretion” (U.E) - Independent of group weight. Total urinary output Urinary ______________________ excretion (U.E) = Total liquid Administered Diuretic U.E in test group Index = ____________________ U.E in control group Mean urine volume of test Lipschitz ______________________ Value = Mean urine volume of Standard Statistical analysis The data were expressed as Mean ± S.E.M and statistically analyzed using one-way ANOVA followed by Tukey-Kramer’s multiple comparison test, p<0.05 was considered as significant. RESULTS AND DISCUSSION The diuretic activity of the EEFC was significant when compared to control (Table 1). Furosemide (100mg/kg) treated animals very significantly (p < 0.01) increased the urinary output and electrolyte excretion of Na+ , K+ and Clˉ as compared to control. The graded doses of the EEFC in 2% v/v aqueous tween 80 solutions showed a very significant increase in diuresis, natriuresis, kaliuresis and total chloride excretion, which was comparable to the action of Furosemide. The diuretic index of the two different doses, i.e., 200 mg/kg and 400 mg/kg body weight was found to be 2.0433 and 2.7154
  • 3. 25 Sruthi.B et al / Int. Jour. of Res. in Pharmacology and Pharmacotherapeutics Vol-1[1] 2012 [23-26] www.ijrpp.com respectively (Table 2) where the diuretic activity of EEFC at a dose of 400 mg/kg body weight was found to be extremely significant (p < 0.01). Based on the above results, we can conclude that Ficus carica L. treatment produced a marked diuresis when rats were acutely treated. In our study, no lethality was observed at least for the dose (2000mg/kg body weight), and duration used. The best results of urine output observed with the ethanolic extract obtained through this evaluation. However, advanced toxicological studies remain to be performed in other animals before its recommendation to the clinical studies. Table 1: Effect of Ethanol extract of Ficus carica (L.) on urine volume and electrolyte concentration in Rats. Groups Treatment & Dose Mean urine volume (ml) Electrolyte excretion Na+ mMoles/L K+ mMoles/L Na+ / K+ ratio Clˉ mMoles/L I 2% v/v tween 80 solution 5ml/kg, p.o 3.69 ±0.06 72.60±0.26 48.65±0.15 1.4922 103.65±0.16 II Furosemide 100mg/kg, i.p 11.25±0.05** 120.30 ±0.35** 82.20 ±2.96** 1.4635 138 ±0.31** III EEFC 200 mg/kg, p.o 7.54 ±0.04* 102.25 ±0.35* 71.22 ±1.50* 1.4357 105.12 ±0.17* IV EEFC 400 mg/kg, p.o 10.02 ±0.05** 114.90 ±0.14** 74.36 ±1.14** 1.5452 128 ±0.22** Values are expressed as mean ± SEM (n = 6); *p < 0.05 and **p < 0.01 compared with control (One way ANOVA followed by Tukey-Kramer’s multiple comparison test). Table 2: Diuretic effect of Ethanol extract of Ficus carica (L.) in comparison to control & standard. Groups Treatment & Dose Diuretic Index Lipschitz value I 2% v/v aqueous tween 80 solution, 5ml/kg, p.o -- -- II Furosemide 100mg/kg, i.p 3.0487 -- III EEFC 200 mg/kg, p.o 2.0433 0.6702 IV EEFC 400 mg/kg, p.o 2.7154 0.8907
  • 4. 26 Sruthi.B et al / Int. Jour. of Res. in Pharmacology and Pharmacotherapeutics Vol-1[1] 2012 [23-26] www.ijrpp.com REFERENCES 1. Brunton LL, Lazo JS, Parker KL. Goodman & Gilman's The Pharmacological Basis of Therapeutics, 11th edition. McGraw-Hill (New York), 2006. 2. Rang HP, Dale MM, Ritter JM. In: Text book of Pharmacology. 2nd ed. Churchill Livingstone, pp 428-38; 1994. 3. Madhava Chetty K. Yucca gloriosa Linn. Chittoor medicinal plants, Himalaya Book Publications, Tirupati, 2005, pp 60. 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. Beckette AH, Stenlake JB. Practical Pharmaceutical Chemistry, Part I, 1st edition, CBS Publishers (New Delhi), 197; 1997. 6. Jeffery GH, Bassett J, Mendham J, Denny. Vogel’s Textbook of Quantitative Chemical Analysis, 5th edition. Addison Westley Longman (England) pp 801; 1989. 7. Lipschitz WL, Haddian Z, Kerpscar A. Bioassay of Diuretics, .Pharmacol.Exp.Ther., 79: 97- 110; 1943. 8. Ratnasooriya WD, Pieris KPP, Samaratunga U, Jayakody JRAC, Diuretic activity of Spilanthes acmella flowers in rats. Journal of Ethnopharmacology, 91: 317-320; 2004.