Evidences for the Involvement of Monoaminergic and GABAergic Systems in Antidepressant-like Activity of Tinospora cordifolia in Mice

Indian Journal of Pharmaceutical Sciences 761 November December 2008 Mental depression represents a major public health problem worldwide. The high prevalence of suicide in depressed patients (up to 15%) coupled with complications arising from stress and its effects on the cardiovascular system have suggested that it will be the second leading cause of death by the year 20201. The use of alternative medicines is increasing worldwide day by day. Hypericum perforatum, a well known plant has been proven to be effective antidepressant in clinical studies2. Thus, there is a constant need to identify newer natural antidepressants with greater efficacy, and to explore their potential over synthetic antidepressants. Tinospora cordifolia (Family: Menispermaceae), a well known plant of Indian medicinal system, was selected for evaluating antidepressant-like activity in laboratory animals, since this plant has been reported to possess antistress activity3,4. According to the Ayurvedic System of Medicine, T. cordifolia is an antigout, analgesic,


MATERIALS AND METHODS
Swiss mice of either sex, weighing around 20-25 g were purchased from Disease-free Small Animal House, Chaudhary Charan Singh Haryana Agricultural University, Hisar (Haryana, India).Male and female animals were housed separately in groups of 6 per cage (polycarbonate cage size: 29×22×14 cm) under laboratory conditions with alternating light and dark cycle of 12 h each.The animals had free access to food and water.The animals were kept fasted 2 h before and 2 h after drug administration.The animals were acclimatized for at least five days before behavioral experiments which were carried out between 09:00 and 17:00 h.The experimental protocol was approved by Institutional Animals Ethics Committee (IAEC) and animal care was taken as per the guidelines of Committee for the Purpose of Control and Supervision of Experiments on Animals (CPCSEA), Govt. of India (Registration No. 0436).

Collection of plant material:
The dried stems of T. cordifolia were purchased from the commercial market, New Delhi and were authenticated as Tinospora cordifolia (Wild.)Miers ex Hook.f. and Thoms from Raw Materials Herbarium and Museum section of National Institute of Science Communication and Information Resources, New Delhi (Ref.No. NISCAIR/RHMD/Consult/06/741/58).

Preparation of petroleum ether extract:
The dried stems were grounded to coarse powder.About 1kg of powdered drug was extracted with petroleum ether (60-80 o ) using Soxhlet apparatus at 70° till siphoning solution became colorless.The solvent was recovered by distillation and the extract was dried by using water bath at 50-60°.The dried petroleum ether extract was yellowish in color and the yield was 0.89%.The dried extract was stored in air tight container and kept in a refrigerator.

Preliminary phytochemical screening:
For preliminary phytochemical screening, petroleum ether extract was tested for the presence of alkaloids, glycosides, carbohydrates, sterols, phenolic compounds and tannins, ß avonoids, saponins, proteins and amino acids following the standard procedures 30 .The extract of T. cordifolia was emulsiÞ ed in 10% v/v Tween 80. Imipramine, sertraline, prazosin and baclofen were separately dissolved in normal saline (0.9% NaCl).Sulpiride was dissolved in normal saline followed by the addition of one drop of glacial acetic acid.p-CPA was dissolved in minimum quantity of 0.1N sodium hydroxide solution and pH was adjusted to 7.0 with 0.1N hydrochloric acid 31 .

Tail suspension test (TST):
TST, commonly employed behavioral model for screening antidepressant-like activity in mice, was Þ rst discovered by Steru et al. 32 .The test was conducted as previously followed 31 .Animals were moved from their housing colony to laboratory in their own cages and allowed to adapt to the laboratory conditions for 1-2 h.Each mouse was individually suspended to the edge of a table, 50 cm above the ß oor, by adhesive tape placed approximately 1 cm from the tip of the tail.Each animal under test was both acoustically and visually isolated from other animals during test.The total period of immobility was recorded manually for 6 min.Animal was considered to be immobile when it didn't show any body movement, hung passively and completely motionless.The test was conducted in a dim lighted room and each mouse was used only once in the test.The observer, recording the immobility of animals, was blind to the drug treatments given to the animals under study.

Forced swimming test (FST):
FST, the most frequently used behavioral model for screening antidepressant-like activity in rodents, was first proposed by Porsolt et al 33 .The procedure was same as previously followed 31 .Animals were moved from their housing colony to laboratory in their own cages and allowed to adapt to the laboratory conditions for 1-2 h.Mice were individually forced to swim in open glass chamber (25×15×25 cm 3 ) containing fresh water to a height of 15 cm and maintained at 26±1°.Water in the chamber was changed after subjecting each animal to FST because used-water has been shown to alter the behavior 34 .Each animal showed vigorous movement during initial 2 min period of the test.The duration of immobility was manually recorded during the next 4 min of the total 6 min testing period.Mice were considered to be immobile when they ceased struggling and remained ß oating motionless in water, making only those movements necessary to keep their head above water.The test was conducted in a dim lighted room and each mouse was used only once in the test 35 .The observer, recording the immobility of animals, was blind to the drug treatments given to the animals under study.

Measurement of MAO-A and MAO-B:
On 14 th day, mice were sacrificed after 6 min exposure to FST, and the brain samples were collected immediately on a ice plate.The collected brain samples were washed with cold 0.25M Sucrose, 0.1M Tris, 0.02M EDTA buffer (pH 7.4) and weighed.The whole procedure of brain isolation was completed within five minutes [36][37] .Mouse brain mitochondrial fractions were prepared following the procedure of Schurr and Livne 36 .The MAO activity was assessed spectrophotometrically [37][38][39] .Brieß y, the buffer washed brain sample was homogenized in 9 volumes of cold 0.25 M sucrose, 0.1 M Tris, 0.02 M EDTA buffer (pH 7.4) buffer and centrifuged twice at 800 g for 10 min at 4° in cooling centrifuge (Remi instruments, Mumbai).The pellet was discarded.The supernatant was then centrifuged at 12000 g for 20 min at 4° in cooling centrifuge.The precipitates were washed twice with about 100 ml of sucrose-Tris-EDTA buffer and suspended in 9 volumes of cold sodium phosphate buffer (10 mM, pH 7.4, containing 320 mM sucrose) and mingled well at 4° for 20 min.The mixture was then centrifuged at 15000 g for 30 min at 0° and the pellets were re-suspended in cold sodium phosphate buffer.The protein concentration was estimated by Lowry method using bovine serum albumin as the standard 40 .The assay mixture contained 100 µl of 4 mM 5-hydroxytryatpamine and 100 µl of 0.1 M benzylamine as the specific substrate for MAO-A and MAO-B, respectively, 150 µl solution of mitochondrial fraction and 2.75 ml sodium phosphate buffer (100 mM, pH 7.4).
For estimating MAO-B activity, 2.75 ml sodium phosphate buffer (100 mM, pH 7.4) and 100 µl of 0.1 M benzylamine were mixed in a quartz cuvette which was then placed in double beam spectrophotometer (Systronics 2203, Bangalore, India).This was followed by the addition of 150 µl solution of mitochondrial fraction to initiate the enzymatic reaction and the change in absorbance was recorded at wavelength of 249.5 nm for 5 min against the blank containing sodium phosphate buffer and benzylamine.
For estimating MAO-A activity, 2.75 ml sodium phosphate buffer (100 mM, pH 7.4) and 100 µl of 4 mM 5-hydroxytryptamine were mixed in a quartz cuvette which was then placed in double beam spectrophotometer (Systronics 2203, Bangalore, India).This was followed by the addition of 150 µl solution of mitochondrial fraction to initiate the enzymatic reaction and the change in absorbance was recorded at wavelength of 280 nm for 5 min against the blank containing sodium phosphate buffer and 5-hydroxytryptamine.

Measurement of locomotor activity:
To rule out the effects of the extract on immobility period, horizontal locomotor activities of control and test animals were recorded for a period of 10 min using Medicraft Photoactometer-Model No. 600-4D (INCO, Ambala, India).
Animals were divided into 25 groups and each group comprised of a minimum of 6 mice.The experimental protocol was divided into the following parts:

Antidepressant-like activity using tail suspension test:
In group 1 (control group), 10% v/v Tween 80 was administered orally for 14 consecutive days and on 14 th day, 60 min after the administration; immobility period was recorded in TST.In groups 2 and 3, imipramine (15 mg/kg) and sertraline (20 mg/kg) respectively were orally administered for 14 successive days and on 14 th day, 60 min after the administration; immobility period was recorded in TST.In groups 4, 5 and 6, petroleum ether extract (50, 100 and 200 mg/kg, p.o. respectively) of T. cordifolia was administered for 14 successive days and on 14 th day, 60 min after the administration, immobility period was recorded in TST.
Antidepressant-like activity using forced swim test: Group 7 to 12 were similar as mentioned under TST (Group 1 to 6) except that the immobility period was recorded using FST.Thus, group 7 was similar to group 1; group 8 was similar to group 2 and so on.

Mechanisms of action studies in tail suspension test:
In group 13 (sulpiride control), vehicle (10% v/v Tween 80) was administered orally for 14 consecutive days and on 14 th day, after 45 min of vehicle treatment; sulpiride (50 mg/kg, i.p.) was injected.After 45 min of injection, the animals were subjected to tail suspension test.In group 14, petroleum ether extract (50 mg/kg, p.o.) of T. cordifolia was administered for 14 consecutive days and on 14 th day, after 45 min of extract treatment; sulpiride (50 mg/kg, i.p.) was injected and the animals were subjected to tail suspension test after 45 min of the injection.In group 15 (baclofen control), vehicle (10% v/v Tween 80) was administered orally for 14 consecutive days and on 14 th day, after 45 min of vehicle treatment; baclofen (10 mg/kg, i.p.) was injected.After 45 min of injection, the animals were subjected to tail suspension test.In group 16, petroleum ether extract (50 mg/kg, p.o.) of T. cordifolia was administered for 14 consecutive days and on 14 th day, after 45 min of extract treatment; baclofen (10 mg/kg, i.p.) was injected and the animals were subjected to tail suspension test after 45 min of the injection.In group 17 (prazosin control), vehicle (10% v/v Tween 80) was administered orally for 14 consecutive days and on 14 th day, after 45 min of vehicle treatment; prazosin (62.5 µg/kg, i.p.) was injected.After 45 min of injection, the animals were subjected to tail suspension test.In group 18, petroleum ether extract (50 mg/kg, p.o.) of T. cordifolia was administered for 14 consecutive days and on 14 th day, after 45 min of extract treatment; prazosin (62.5 µg/kg, i.p.) was injected and the animals were subjected to tail suspension test after 45 min of the injection.In group 19 (p-CPA control), vehicle (10% v/v Tween 80) was administered orally for 14 consecutive days.pCPA (100 mg/kg, i.p.) was injected from 11 th to 14 th day after 45 min of vehicle treatment.On 14 th day, the animals were subjected to tail suspension test after 45 min of pCPA injection.In group 20, petroleum ether extract (50 mg/kg, p.o.) of T. cordifolia was administered for 14 consecutive days.pCPA (100 mg/kg, i.p.) was injected from 11 th to 14 th day after 45 min of vehicle treatment.On 14 th day, the animals were subjected to tail suspension test after 45 min of pCPA injection.

Estimation of brain MAO:
In group 21, vehicle (10% v/v Tween 80) was administered orally for 14 successive days and on 14 th day, 60 min after the administration; the animals were subjected to forced swim test for 6 min, and immediately brain samples were collected.MAO-A and MAO-B levels were measured in the brain samples.In group 22, imipramine (15 mg/kg, p.o.) was administered orally for 14 successive days and on 14 th day, 60 min after the administration; the animals were subjected to forced swim test for 6 min, and immediately brain samples were collected.MAO-A and MAO-B levels were measured in the brain samples.In group 23, petroleum ether extract (50 mg/ kg, p.o.) was administered orally for 14 successive days and on 14 th day, 60 min after the administration; the animals were subjected to forced swim test for 6 min, and immediately brain samples were collected.MAO-A and MAO-B levels were measured in the brain samples.

Measurement of locomotor activity:
In group 24, vehicle (10% v/v Tween 80) was administered orally for 14 successive days and on 14 th day, 60 min after the administration; locomotor activity was measured.In group 25, petroleum ether extract (50 mg/kg, p.o.) of T. cordifolia were administered for 14 consecutive days and on 14 th day, 60 min after the administration; locomotor activity was measured.

Statistical analysis:
All the results were expressed as mean±standard error mean (SEM).The data of all the groups were analyzed using one-way ANOVA followed by Dunnett's t-test using the software Sigma-Stat 3.5.The data for locomotor activity scores was subjected to Student's unpaired t-test.In all the tests, the criterion for statistical signiÞ cance was P<0.05.

RESULTS
The results of phytochemical screening indicated the presence of alkaloids, glycosides, carbohydrates, sterols and ß avonoids in petroleum ether extract.

Effect of petroleum ether extract on immobility periods in TST and FST:
Petroleum ether extract (50, 100 and 200 mg/kg, p.o.) administered for 14 successive days to mice signiÞ cantly decreased the immobility periods in both TST and FST, indicating signiÞ cant antidepressant-like activity.Among three doses, the dose of 50 mg/kg of petroleum ether extract decreased the immobility period to the greatest extent, thus showed most potent antidepressant-like action.Imipramine (15 mg/kg, p.o.) and sertraline (20 mg/kg, p.o.) administered for 14 successive days to mice signiÞ cantly decreased the immobility periods in both TST and FST as compared to control, thus showed signiÞ cant antidepressant-like action (Tables 1 and 2).

Effect of combination of Petroleum ether extract with sulpiride, baclofen, prazosin and P-CPA on immobility period in TST:
Sulpiride (50 mg/kg, i.p.), baclofen (10 mg/kg, i.p.) prazosin (62.5 µg/kg, i.p.) and p-CPA (100 mg/kg, i.p.) alone significantly increased the immobility period as compared to control group.Pretreatment of animals with sulpiride or baclofen or prazosin or p-CPA significantly reversed the decrease in immobility time elicited by petroleum ether extract at the dose 50 mg/kg (Table 3).

Effect of petroleum ether extract on brain monoamine oxidase (MAO) activities:
Petroleum ether extract (50 mg/kg) administered for 14 consecutive days to mice, significantly reduced the brain MAO-A and MAO-B levels as compared to the respective vehicle treated groups.The efÞ cacy of petroleum ether extract, was found to be comparable to imipramine (Figs. 1 and 2).

Effect on locomotor activity:
Petroleum ether extract (50 mg/kg, p.o.) administered for 14 successive days did not show any signiÞ cant change in the locomotor function of mice (642.8 ± 84.5) as compared to the vehicle treated group (737.3 ± 50.1).

DISCUSSION
In the present study, petroleum ether extract (50, 100 and 200 mg/kg, p.o.) administered for 14 successive days to mice produced signiÞ cant antidepressant-like effect in TST as well as in FST.The efÞ cacy of the extract was found to be comparable to imipramine (15 mg/kg, p.o.) and sertraline (20 mg/kg, p.o.).FST and TST are two commonly used behavioral despair models of depression.These models are widely employed in rodents to predict antidepressant potential by decrease of immobility period produced by several different classes of antidepressant drugs [32][33] .Petroleum ether extract at the dose of 50 mg/kg, p.o. (most effective dose) did not show any signiÞ cant change in locomotor functions of mice as compared to control, so it did not produce any motor effects.It conÞ rmed the assumption that the antidepressant-like effect of the extract was speciÞ c and not the false positive.The precise mechanisms by which petroleum ether extract   of T. cordifolia produced antidepressant-like effect are not completely understood.However according to our results, the antidepressant-like effect of the extract was significantly reversed by pretreatment of animals with prazosin (a α 1 -adrenoceptor antagonist), sulpiride (a selective dopamine D 2receptor antagonist), p-CPA (a serotonin synthesis inhibitor) and baclofen (GABA B agonist), when tested in TST.This suggested that the petroleum ether extract might produce antidepressant-like effect by interaction with α 1 -adrenoceptors, dopamine D 2receptors, serotonergic and GABA B receptors, hence increasing the levels of norepinephrine, dopamine and serotonin; and decreasing the levels of GABA in brains of mice.Levels of monoamines like norepinephrine, serotonin and dopamine are decreased in depression, so antidepressant drugs enhance the levels of these monoamines.GABA B receptor antagonism may serve as a basis for the generation of novel antidepressants 41 .
Moreover, petroleum ether extract also reduced the mouse whole brain MAO-A and MAO-B activities as compared to control, so it indicated that this extract inhibited the metabolism of monoamines, particularly serotonin and noradrenaline.Monoamine oxidase (MAO) regulates the metabolic degradation of catecholamines, serotonin and other endogenous amines in CNS.Inhibition of this enzyme causes a reduction in metabolism and subsequent increase in the concentration of biogenic amines.MAO-A preferentially metabolize adrenaline, nor-adrenaline and serotonin.MAO-B metabolizes phenylethylamines.Dopamine is metabolized by both MAO-A and MAO-B 42 .
Thus, petroleum ether extract of T. cordifolia showed antidepressant-like activity probably by inhibiting MAO-A and MAO-B, thus increasing the levels of monoamines like noradrenaline, serotonin, and dopamine; and decreasing the levels of GABA.This was also supported by the earlier study where petroleum ether extract of T. cordifolia showed antistress activity 4 .According to results of phytochemical screening and literature, the antidepressant-like action of petroleum ether extract might be due to the presence of berberine (alkaloid), since the latter compound has been reported to have antidepressant-like activity 43 , however the role of other constituents present in petroleum ether extract towards antidepressant-like activity needs to be explored.Therefore, T. cordifolia extract may have potential therapeutic value for the management of depressive disorders.

Fig. 1 :Fig. 2 :
Fig. 1: Effect of petroleum ether extract of T. cordifolia on MAO-A activity n=6 in each group; Values are in mean±SEM.Data was analyzed by one-way ANOVA followed by Dunnett's t-test.F (2,15)= 12.235; P< 0.05, *P< 0.05 when compared with vehicle treated group.