Bangladesh J Pharmacol. 2013; 8: 102-106


| Research | Article |

Potential anti-diabetic activity of Bombax ceiba

Chetan J. Bhavsar1 and Gokul S. Talele2

1R.C. Patel Institute of Pharmaceutical Education and Research, Shirpur, Dhule, India; 2NGSPM’s College of Pharmacy, Brahma Valley Educational campus, Trimbak road, Anjaneri, Nashik, India.

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Bombax ceiba bark extract was evaluated for its hypoglycemic and hypolipidemic potential through normal and streptozotocin-induced diabetic rats administered with graded oral doses (200, 400, 600 mg/kg/day) for 21 days. The results showed that a dose of 600 mg/kg of B. ceiba extract is the most effective to cause significant (p<0.001) hypoglycemic and/or hypolipidemic effects on streptozotocin-induced diabetic rats. This dose also significantly (p<0.001) lowered the total cholesterol and triglyceride level in severely diabetic rats. Phytochemical and GC-MS studies confirmed the presence of the triterpenoid compounds in the extract, which may account for its significant hypoglycemic activity. The present study thus provides a scientific rationale


Kantesavar botanical name Bombax ceiba L barkfamily Malvaceae is commonly known as silk cotton tree, found in dry, moist and mixed deciduous forest, throughout in India. The tender bark is used as famine food, demulcent, emetic and tonic, and its aqueous extract mixed with curd to check blood-dysentery. Externally it is used as styptic and also for fomenting wounds (The wealth of India, 2005). The bark reported to contain Shamiminol: a new aromatic glycoside from the stem bark of B. ceiba (Faizi et al., 2011). The bark is also reported to have anti-oxidant activity (Gandhare et al., 2012). Cardioprotective effect of B. ceiba flowers has been reported by (Patel et al., 2011). Pharmacognostical, phytochemical and biological evaluations of the stem bark of B. ceiba were carried out (Ansari et al., 2007).

The tribal’s of toranmal use and prescribe the extract in the form of powder for the treatment of diabetes, however there is no scientific proof regarding its use as an anti-diabetic agent in modern literature. Thus the present study was undertaken to find out the anti-diabetic activity of the extract in streptozotocin-induced hyperglycemic rat using glibenclamide as reference standard.

Materials and Methods

The bark was collected from Toranmal, Maharashtra, India in December 2007 and authenticated from Botany department of Dr. P.R. Ghogre Science College Dhule, Maharashtra. A voucher specimen (HRPIPER-02) has been conserved for future reference. The bark was washed, cleaned, shade-dried, pulverized and passed through a 40-mesh sieve, and kept in a well-closed container for further extraction.


Diagnostic kits for estimation of triglyceride and cholesterol were purchased from Pointe Scientific Inc., Michigan, USA, for measurement of glucose from RFCL Limited, Haridwar, India

Preparation of bark extract

The bark powder (1 kg) was successively extracted with petroleum ether (60°-80°), ethyl acetate and ethanol with hot continuous percola-tion. All the extracts were screened for preliminary phytochemical test, out of the three extracts screened; only ethyl acetate extract showed Libermann-Burchards test positive for the presence of triterpenoids. Accurately weighed 3 g of ethyl acetate extract was dissol-ved in ethyl acetate and shaken well, this solution then treated with 5%hydrochloric acid for several times, resulted in formation of two layers, which then separated by separating funnel. Aqueous layer was discarded and ethyl acetate layer was treated with 5% potassium hydroxide and shaken for 3 days. Formed two layers were then separated by separating funnel. Ethyl acetate layer was collected, evaporated, dried and used for further study.


Animal experimentation part was performed by strictly adhering to Indian regulations and approved by the Institutional Research Committee (Approval letter no. RCPIPER/2008-9/12). Wister rats weighing 250-300 g were used for the study. Animals were maintained under controlled environmental conditions: 12 hours light-dark cycles with ad libitum access to standard rodent chow and water. Food was removed 4 hours before experiments were conducted.

Acute toxicity study

Healthy adult Wistar rats (male) were subjected to acute toxicity studies as per guideline (AOT No. 425) suggested by Organization for Economic Co-operation and Development (OECD) (2001). The rats were observed by housing them individually in the polypropylene metabolic cages continuously for 2 hours for behavioral, neurological and autonomic profiles; and for any lethality during next 48 hours.

Experimental design

Group I: Normal control (vehicle treated); Group II: Diabetic control (streptozotocin 45 mg/kg); Group III: Diabetic rats orally administered glibenclamide (10 mg/kg) in 0.5 mL of 5%alcohol; Group IV: Diabetic rats orally administered B. ceiba extract (200 mg/kg) in 0.5 mL of 0.1%methylcellulose suspension; Group V: Diabetic rats orally administered B. ceiba extract (400 mg/kg) in 0.5 mL of 0.1% methylcellulose suspension; Group VI: Diabetic rats orally administered B. ceiba extract (600 mg/kg) in 0.5 mL of 0.1%methylcellulose suspension.

In vivo hypoglycemic activity

A freshly prepared solution of streptozotocin (45 mg/kg) in 0.1M citrate buffer, pH 4.5 was injected intraperitoneally to overnight fasted rats. After 3 days, blood glucose level was analysed and those rats above blood glucose 250 mg/dL were considered as diabetic. Treatment began 3 days after streptozotocin injection with various concentrations of B. ceiba extract once a day for 3 weeks/21 days. Fasting blood glucose level in all the rats were determined on 21th day by glucose oxidase method (Trinder, 1969). Blood samples withdrawn from retro orbital sinus on 22nd day and serum was separated from blood by centrifugation at 4,000 rpm for 10 min to obtain biochemical parameters.

Biochemical parameters

Total cholesterol and trigly-cerides in blood were determined by cholesterol esterase method (Allain et al., 1974) and lipoprotein lipase method (Muller et al., 1977) respectively. High density lipoprotein was determined by Burstein method (Burstein et al., 1970). Low density lipoprotein was analyzed by Friedewald method (Friedewald et al., 1972).

Histopathological studies

On 22nd day of study, rats were sacrificed by cervical dislocation. Pancrea samples were isolated from the control and treated groups of animals, washed separately with normal saline, and fixed in 10% neutral buffered formalin solution for 48 h. The formalin-fixed Pancrea samples were stained with hematoxylin-eosin for photomicroscopic observations.

GC-MS analysis of ethyl acetate fraction

Ethyl acetate fraction of B. ceiba was analyzed by GC-MS, gas chromatograph- Make: Perkin Elmer, USA, and Model: auto system XL, silica based capillary column was used for separation of component. Mass spectrometer- make; Turbomass spectrometer, Perkin Elmer, Detector: Flame Ionization Detector, Temperature range was 50°C to 450°C, used for determination of molecular weight of separated component.

Statistical analysis

Results were expressed as mean ± S.D. Data were analyzed using one-way analysis of variance (ANOVA) followed by Dunnett’s test. A value of p<0.05 was considered to be statistically significant.


Body weight was significantly lowered (23% on day 21) in the diabetic group throughout the research signifying the appropriateness of the animal model. Animal treated with the extract improved body weight (0.98%) on 14 days and after 21-day supplementation, 14.12% increase was observed which was significant. (data not shown).

Before the treatment, fasting blood glucose of all animals was within the normal range. Blood glucose was elevated significantly after 48 hours of streptozotocin injection and was monitored for 7 days. Animals having 250 mg/dL blood glucose were selected for the study. Oral administration of ethyl acetate extract for 21 days resulted in significant reduction of fasting blood glucose at a dose of 600 mg/kg body weight when compared with diabetic control (Table I). At a dose of 200 mg/kg body weight no significant reduction in blood glucose level was observed.

In B. ceiba ethyl acetate extract treated rats, a significant decrease (p<0.001) in serum cholesterol was observed at dose of 600 mg/kg body weight after the treatment period, when compared to the diabetic untreated rats.

Table I
Effect of 21 daily dose of various concentration of Bombax ceiba bark ethyl acetate extract on fasting plasma glucose, cholesterol, triglycerides, HDL and LDL concentrations of STZ-treated rats


Blood glucose

Total cholesterol




Normal control

161 ± 21c

1.7 ± 01c

0.69 ± 0.19c

1.1 ± 0.44b

1.1 ± 0.44c

Diabetic control

433 ± 11

2.3 ± 07

2.2 ± 0.10

0.59 ± 0.07

1.5 ± 0.17

Glibenclamide 10 mg/kg

159 ± 14c

1.8 ± 0.11c

2.1 ± 0.18

0.60 ± 0.08

1.4 ± 0.14

Bombax ceiba 200 mg/kg

424 ± 44

2.1 ± 0.14b

2.1 ± 56

0.81 ± 0.22

1.1 ± 0.17

Bombax ceiba 400 mg/kg

327 ± 80a

1.8 ± 0.06c

1.6 ± 0.24c

0.92 ± 0.96a

1.3 ± 0.26b

Bombax ceiba 600 mg/kg

156 ± 8.6c

1.8 ± 0.12c

0.9 ± 1.33c

0.99 ± 0.1a

0.8 ± 0.33c

Data are expressed as mean ± S.D; (n = 6); ap<0.05 significant from diabetic control; bp<0.01 significant from diabetic control; cp<0.001 significant from diabetic control

Treatment with the ethyl acetate extract and glibenclamide caused a significant decline in total cholesterol by 24% and 19% correspondingly.

Significant increased level of HDL was observed in diabetic group of rats on treatment with the ethyl acetate extract, as compared with diabetic control. The LDL level fell to 54.24% at dose of 600 mg/kg body weight of B. ceiba ethyl acetate extract in diabetic group of animal.

Histological changes were shown in Figure 1. In streptozotocin-diabetic rats the islet is considerably reduced and shrunken. There is damage of some β-cells with central hyalinization; a few cells showed pyknotic nuclei and the number of cells were decreased (Figure 1a). After 22 days of oral administration with the extract, when blood glucose came down to normal level, islets of Langerhans also showed improvement in the β-cells granulation which is comparable to standard (Figure 1f).

Compounds in the ethyl acetate fractions were separated by Gas chromatogram with different retention time of which compound 1 (RT 40.54) and Compound 2 (RT 41.60) were found to have mass fragmentations pattern same as that of triterpenoids.


Antihyperglycemic activity of medicinal plants or plant derived products needs extensive research as the number of diabetic patients is continuously on the rise and according to WHO projections; it will be the single largest noncommunicable disease worldwide by the year 2025 with the largest diabetic population in India (Wild et al., 2004). Hypoglycemic effect of various triterpenoids and steroids from natural resources had been investigated and documented by various researchers (Sugihara et al., 2000; Tan et al., 2008; Hai-Xue et al., 2011). The extractis widely used and prescribed by tribal of India as an alternative or complementary diabetes treatment (Verma et al., 2011). The extract reported to have triterpenoids but its anti-diabetic activity is not investigated till date. In light of these facts, the present study was undertaken to evaluate the anti-diabetic status of the extract.

In the preliminary phytochemical investigation of all extracts, ethyl acetate extract shows the presence of triterpenoids and hence selected for anti-diabetic activity.

Among the various doses of ethyl acetate fraction of the bark extract, a dose of 400 mg/kg body weight and 600 mg/kg body weight showed significant antihyperglycemic effect in the streptozotocin-treated group. The administration of extract in the streptozotocin-treated group prevented increase in cholesterol and triglyceride concentrations. In diabetes, hyperglycemia is accompanied with dyslipidemia i.e. characterized by increase in LDL and fall in HDL (Bierman, et al., 1966). This altered serum lipid profile was reversed towards normal after treatment with the extract. Streptozotocin is a highly cytotoxic agent inducing diabetes by damaging the pancreatic β-cells that causes reduction in insulin release (Elsner. et al., 2000). The insulinogenic effect of various medicinal plant extracts resulting in activation of β-cells has been reported (Kedar and Chakrabarti, 1982). The possible mechanism through which the exerts its anti-hyperglycemic effect might have been due to the increased release of insulin from β-cells and/or regenerated β-cells. In this circumstance, a number of other plants have been reported to have antihyperglycemic activity with a stimulatory effect on insulin release (Esmaeili and Yazdanparas, 2004). Since the extract produced highly significant antihyperglycemic effect even in diabetic rats in which most of the β-cells are damaged, it is likely that the extract might have extrapancreatic mechanism of action

GC-MS is valuable tool for the separation and identification of natural constituents in extract (Jacques et al., 2007). Hence the ethyl acetate fractions subjected to GC-MS analysis. The total ion chromatogram of ethyl acetate extract two triterpenoids detected and identified by comparing the mass spectra of separated fraction with the Wiley library of the GC/MS). A compound was only considered positively identified when the percent of similarity was superior to 90%.


B. ceiba was found to lower blood glucose in streptozotocin-induced diabetic rats, the extract also has hypocholesterolemic and hypotriglyceridemic effects.

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The authors are grateful to Dr. SJ Surana, Principal, R. C. Patel Institute of Pharmaceutical Education and Research, Shirpur for providing all the facilities to carry out this study. Authors are also thankful to SICART, Anand, Gujarat for GC-MS study.


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