Evaluation of Anti-Diabetic Activity of Leaves and Fruits of Ficus religiosa Linn

 

RB Goswami1*, Neelima Goswami2, P Khare1, S Choudhary3 and AK Pathak3

1Sagar Institute of Research, Technology and Science – Pharmacy Bhopal

2Sagar Institute of Research and Technology-Pharmacy Bhopal

3Department of Pharmacy, Barkatullah University, Bhopal-462 026 (M.P.)

 

 

ABSTRACT:

The ethanolic extract of the leaves and fruits of Ficus religiosa Linn. was evaluated for its antidiabetic activity in normal rats and alloxan induced diabetic rats. Fruit extracts were found to have no effect on normal rats while they were effective in lowering the elevated blood glucose level in experimental diabetic rats. Fruit extract in a dose of 250 mg/kg body weight was found to be more effective than 100 mg/kg body weight.

 

KEYWORDS: Ficus religiosa, Antidiabetic, Alloxan diabetic model.

 

INTRODUCTION:

Ficus religiosa Linn. (Syn: Peepal, Ashvatha) is a large perennial tree belonging to the family Moraceae. It is found throughout the plains of India up to 170 m altitude in the Himalayas and planted especially near temples1. Anti-diabetic activity has been attributed to the genus Ficus, as Ficus bengalensis2,3 . Ficus racemosa4 are reported to decrease the blood glucose level.   Ficus religiosa stem bark is reported to be antidiabetic due to b-sitosterol-D-glucoside4 and its root bark also reduces blood sugar level5. Flavonoids6 are present in Ficus religiosa which are also present in several other plants having antidiabetic activity like Bridelia ferruginea7 Ficus bengalensis3, Vaccinum myrtillus8 and Pterocarpus marsupium9  Based on the above information the present study was carried out to evaluate the antidiabetic activity of the fruits of this plant in experimental animal models using rats.

 

MATERIALS AND METHODS:

Plants material:

Matured leaves and fruits were collected from the plant of Barkatullah University campus, Bhopal in the month of March-April. The plant parts were identified and authenticated by Pharmacognosy section of Department of Pharmacy, Barkatullah University, Bhopal, voucher Specimen No. (BUPH-4014). Leaves and fruits were dried in shade for 15-20 days. Dried plant material was pulverized to coarse powder form and subjected to further studies.

 

Animals Used:

Healthy and 2-3 months old albino Wister rats of either sex (weighing 140-160gm) were procured from DRDE, Gwalior and maintained at 24-28°C throughout the experiment. All the animals were fed on standard diet and water ad-libitum and maintained in large spacious polypropylene cages and well-ventilated animal house with 12-hour dark and light cycle. The institutional ethical committee, Department of Pharmacy, Barkatullah University, Bhopal approved the use of animals in the present study.

 

EXPERIMENTAL METHOD:

Preparation of Extract and Standard Drug:

The coarsely powdered air-dried materials were extracted with cold maceration process separately, using 95% ethanol as solvent. The filtrate was concentrated to yield a semisolid mass (Yield: leaves – 11.24% w/w and fruits 21.56% w/w on dry basis).


TABLE 1: Effect of Ethanolic Extracts of Leaves and Fruits of Ficus religiosa in Alloxan Induced Diabetic Rat

Group

Treatment

Dose/kg body wt.

Blood Glucose Level (Mg/dl) After Days

% Blood Glucose

Change

Before Treatment

0

7

14

21

I.

Vehicle control (Normal)

80.22±2.10

80.22±2.10

81.96±2.14

84.81±1.58

83.12±1.48

---

II.

Leaf Ext. alone, 250mg (Normal)

79.80±3.61

79.80±3.61

80.22±1.47

83.14±1.32

80.24±1.12

---

III.

Fruit Ext. alone, 250mg (Normal)

80.47±4.54

80.47±4.54

81.63±1.66

83.25±1.61

82.15±1.41

 

---

IV.

Diabetic control (Diabetic)

81.75±2.14

248.33±0.91

285.77±3.09

267.92±1.65

259.92±1.65

---

V.

Leaf Ext. 100mg(Diabetic)

84.31±1.54

249.44±4.87

241.87±6.58

236.88±0.96*

230.1±0.96*

7.75%

VI.

Leaf Ext.

250mg (Diabetic)

89.6±6.14

248.71±5.55

239.55±2.20

232.15±1.06*

228.15±1.06*

8.26%

VII.

Fruit Ext. 100mg (Diabetic)

82.7±5.17

247.14±3.62

230.59±5.09

219.64±3.02**

198.51±0.21**

19.67%

VIII.

Fruit Ext. 250mg (Diabetic)

90.1±5.17

250.50±4.33

237.16±1.65

211.58±0.79**

190.21±0.21**

24.06%

IX.

Glibenclamide.600 µg (Diabetic)

89.5±1.3 7

234.73±1.59

201.48±2.64

156.31±2.15**

101.51±0.19**

56.75%

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
* Significant, ** Highly Significant

Values are given as mean ± S.D. for 6 rats in each group, Values not sharing common superscripts differ significantly at P <0.001

 

 


Both the extracts indicated the presence of carbohydrates, proteins and amino acids, sterols and saponins while fruit extract also showed the presence of phenolic compounds on qualitative chemical analysis10. The extract was suspended in 0.3% w/v carboxy methyl cellulose (CMC) solution11. Suspension of each extract was given orally in a dose of 100mg/kg body wt. and 250mg/kg body wt. to selected groups of animals once daily through out the experiment. Glibenclamide at a dose of 600 mg/kg (in 0.3%CMC) was used as standard drug and given orally, once daily throughout the experiment.

 

Induction of Diabetes:

Experimental diabetes in rats was induced by injecting alloxan monohydrate intraperitoneally at a single dose of 150 mg/kg body wt. (5% w/v solution in sterile water) to overnight fasted animals12. After 72 hrs of alloxan administration13, blood was collected from sino-ocular puncture in a centrifuge tube containing anticoagulant (10% sodium citrate solution) and the plasma was separated by centrifugation at 3000 rpm for 10 min. and immediately blood sugar level was analyzed in autoanalyzer (GOD-POD method)14. Rats with blood glucose levels of 200-300 mg/dl were considered as diabetic and were employed in the study.

 

Experimental design:

The rats were divided into 9 groups of 6 rats each. All animals were allowed free access to food and water. The rats of group I, group II and group III were normal while the rats of group IV to group IX were diabetic surviving. The treatment was carried out for 21 days12.

 

Group I:  Normal rats treated with vehicle alone.

Group II: Normal rats treated with leaf extract, 250 mg/kg

Group III: Normal rats treated with fruit extract, 250 mg/kg

Group IV: Diabetic rats treated with vehicle alone.

Group V: Diabetic rats treated with leaf extract, 100 mg/kg

Group VI:  Diabetic rats treated with leaf extract, 250 mg/kg

Group VII: Diabetic rats treated with fruit extract, 100 mg/kg

Group VIII: Diabetic rats treated with fruit extract, 250 mg/kg

Group IX: Diabetic rats treated with Glibenclamide, 600 µg/kg

At 0, 7, 14, and 21 day, the animals were deprived of food overnight and blood was collected next morning for analysis. Percent change of blood glucose was calculated as function of time by applying the formula:

                                                 Gx - Go

% Blood Glucose Change   =   ――――― x 100

                                                     Go

Where, Gx = Initial values

Go = Values at minutes time interval.

 

Statistical Analysis:

Values are represented as means ± S.D. for 6 animals in each group. Data are analyzed using one-way analysis of variance (ANOVA). Individual groups are compared critically (Table-I).

 

RESULTS AND DISCUSSION:

In the present study of antidiabetic activity in rats, alloxan was used as toxicant, which has been known to induce diabetes mellitus in experimental animals, due to massive reduction of the β-cells of islets of langerhans and induce hyperglycemia. Induction of diabetes in rats in present study was confirmed as a significant rise in blood glucose level. Ficus religiosa fruit extract was found to reverse this effect to some extent, when given orally, daily for 21 days. The effect of extract is compared with a clinically used sulphonyl urea derivative, Glibenclamide as standard drug which is known to lower blood glucose level by stimulating, β-cells to release insulin. It is used in present study to compare the efficacy of the drug in normal and alloxanized diabetic rats.

 

Table-I depicts the blood glucose level of different groups of rats on day 0, 7, 14, and 21. Blood glucose level was significantly (p<0.001) increased in diabetic control Group IV as compared to vehicle control Group I. Administration of Ficus religiosa fruit extract (100 and 250 mg/kg body wt. to Group VII and Group VIII respectively) and Glibenclamide Group IX significantly (p<0.001) decreased the blood glucose level as compared to diabetic control Group IV and both the doses of fruit extracts were comparable to standard drug, Glibenclamide (insignificant difference). Maximum effect was observed at 250 mg/kg of fruit extract on day 21, while leaves are not more effective compare than fruits on blood glucose level. The groups treated with extract alone, at a dose of 250 mg/kg of leaf and fruit extract Group II and Group III found to be insignificant when compared with vehicle control Group I. It may be concluded that fruits and leaves are not showing any reduction in normal blood glucose level in normal animals.

 

ACKNOWLEDGEMENT:

We are thankful to Dr. A. K. Pathak, Dean and Head of Department of Pharmacy, Barkatullah Vishwavidyalaya, Bhopal for authentication of plant, providing valuable advices for completing research and allowing us to carry out the present work in his Laboratory.

 

REFERENCES:

1.     Anonymous, “The wealth of India, A dictionary of Indian Raw Materials and Industrial products”, Council of Scientific and Industrial research, New Delhi Vol.-IV, 1956, 38.

2.     Rastogi, R.P. and Mehrotra, B. N; ”Compendium of Indian Medicinal Plants”. Vol. V., CDRI, Lucknow and CSIR, New Delhi, 1998; 188 and 371.

3.     Cherian, S Et.al ‘Antidiabetic effect of a glycoside of pelargonidin isolation from the bark of Ficus bengalensis Linn’, Indian J. Biochem. Biophys. (29), 1992, 380-82.

4.     Prajapati, N.D., Purohit, S.S., Sharma, A.K. and Kumar, T. “A Handbook of Medicinal Plants: A Complete Source Book”, Aggrobios. (India), 2003; 238-239

5.     Asolkar, L.V., Kakkar, K.K and Chakre, O.J. “Second Supplement to Glossary of Indian Medicinal Plants with Active Principles”, CSIR, New Delhi, 1992, 314

6.     Chevallier, A. “Encyclopedia of Medicinal Plants”, Dorling Indesley, Great Britain, 1996, 212

7.     Craker, L.E., and Simon, J.E. “Herbs, Spices and Medicinal Plants: Recent Advance in Botany, Horticulture and Pharmacology”; CBS Publishers and Distributors, New Delhi, Vol. III, 2002, 53

8.     Dandia, P.S. and Vohora, S.B.; “Research and Development of Indigenous Drugs”, Institute of History of Medicine and Medical Research. 1st Ed., New Delhi, 1989, 336

9.     Manickam, M., Et al.; ‘Antihyperglycemic Activity of Phenolics from Pterocarpus marsupium, Journal of Natural Product. 60: 1997; 609-610.

10.   Anonymous, “Quality Control Methods for Medicinal Plant Material”, World Health Organization, Geneva, 1998, 190.

11.   Dhanabal, S.P. Etal., ‘Antihyperglycemic Activity of Polygala Arvensis in Alloxan Diabetic Rats’; Indian Drugs. 41 (11): 2004, 690.

12.   Mukherjee, P. K ”Quality Control of Herbal Drug”, 1st  Edn., Business Horizons, Pharmaceutical Publishers, New Delhi, 2002, 13

13.   Prince, P.S, Et al. ‘Hypoglycemic Activity of Syzygium  cumini   Seed:  Effect  on  Liquid  Peroxidation  in   Alloxan  Diabetic Rats’. Journal of Ethanopharmacology. 61(1):1998; 1-7.

14.   Tietz, N.W. “Fundamental of Clinical Chemistry”, 2nd Ed., W.B. Saunders Co, Toronto; 1992; 242

 

 

Received on 21.11.2009

Accepted on 25.12.2009   

© A&V Publication all right reserved

Research Journal of Pharmacognosy  and Phytochemistry. 2(1): Jan.-Feb. 2010, 61-63