Isolation and Aphrodisiac Screening of the Fruits of Durio zibenthinus Linn.

MATERIALS AND METHODS

Collection and Identification of Plant
The plant fruits were collected in the month of August 2008 from the State Horticulture Farm, Burliar, The Niligiris, Tamil Nadu, India. The plant was authenticated by comparing it with authentic specimen at the Botanical survey of India, Coimbatore, Tamil Nadu, India.

Extraction of the Fruits of Durio zibenthinus Linn.
The fresh fruits of Durio zibenthinus Linn. which were made free from mud and other impurities and dried in shade. The dried fruit pulp was then powdered and subjected to successive hot extraction using non polar to polar solvents. The solvents used for successive extracts were petroleum ether, chloroform, ethyl acetate and aqueous alcohol.

To 380 g of dried fruit pulp powder, 1.5 L of petroleum ether was added and extracted at 60°C for 24 h in a Soxhlet apparatus. After 24 h the petroleum ether fraction was filtered through a Whattman filter paper and the marc was again successively extracted using chloroform, ethyl acetate and aqueous alcohol respectively by the same procedure. All the extracts were then concentrated and dried under reduced pressure with a controlled temperature (40-55°C) using the rotary evaporator (Kokate et al., 1997).

Isolation of Phytoconstituents of Durio zibenthinus Linn. Extracts
The petroleum ether extract was subjected to isolation of phytoconstituents by counter current method using various solvents like acetone, chloroform, methanol and hexane.

In vivo Screening Studies of the Petroleum Ether Extract and Isolated Compound (3-β-hydroxy-21-Normethyl-19-vinylidenylursane)
The sexually active male Swiss mice (25-35 g) were grouped separately and divided into 5 groups, each group consisting of 6 animals. Group I received solvent control (0.3% CMC), group II received petroleum ether extract 200 mg kg^-1 b.wt. in 0.3% CMC, group III received petroleum ether extract 400 mg kg^-1 b.wt. in 0.3% CMC, group IV received isolated compound (3-β-hydroxy-21-Normethyl-19-vinylidenylursane) 20 mg kg^-1 b.wt. in 0.3% CMC and group V received isolated compound (3 β-hydroxy-21-Normethyl-19-vinylidenylursane) 40 mg kg^-1 b.wt. in 0.3% CMC, daily, orally using oral catheter. Sexual behavior was observed in a dim light at day time in specially designed cages having glass on all sides and measuring 50x30x30 cm (Fig. 3). The male experimental mice were transferred to the cage and the female mice in oestrous phase were introduced with males.

Fig. 3:	Male mice showing mounting behavior

The first 15 min were considered as acclimatization period (Ageel et al., 1994). The activities of male mice in each group were recorded individually for 60 min after 30 min of the drug administration on 1st, 7th and 14th day treatments. The parameters viz. mounting (Subramoniam et al., 1997), intromission (Suresh-Kumar et al., 2000), sperm count and sperm motility were observed.

Sperm Count
One milliliter of diluting fluid (sodium bicarbonate 5 g and formalin neutral 1 mL in 100 mL of distilled water) was measured into a clean test tube. To this 0.1 mL of seminal fluid collected from epididymis using forced extraction was added, which yields a 1:10 dilution. Neubauer’s chamber (0.0025 mm², Tiefe depth profounder 0.100 mm, Superior Marienfield Germany) was filled with the diluted seminal fluid. The chamber was left on the bench for 2 min. This allows the immobilized sperms to settle down. Then the numbers of sperms in the four corner squares covering 4 mm² were counted under the high power objective (40x) (Mukherjee, 1997). Sperm count was calculated as per the formula:

Sperm Motility
Single Cauda of the epididymis was punctured with a 21 gauge hypodermic needle. Fluid content from the epididymal lumen was collected. A small drop of fluid was placed in pre-warmed microscopic slide, approximately at body temperature. The drop was covered with a cover slip by the WET MOUNTING TECHNIQUE. The cover slip was rimmed with vaseline to avoid drying. The slide was examined under the high power objective (40X) with reduced illumination. Several fields were scanned until a total of at least 200 sperms have been observed. The percentage of sperm showing actual progressive motion was calculated. Sperm motility was expressed in terms of the percentage of sperms which were active (Mukherjee, 1997).

RESULTS

Isolation of Phytoconstituents of Durio zibenthinus Linn. Extracts
The phytoconstituents present in the petroleum ether extract of Durio zibenthinus Linn. were isolated by counter current extraction and were partially characterized by ¹H NMR, ¹³C NMR and Mass are shown in the Fig. 4-6. Compound I (Fig. 4 and 5, the ¹H NMR spectrum displayed signals for two tertiary methyl groups at δ 0.68 (s, 3H) and 1.01 (s, 3H) and three secondary methyl groups at δ 0.93 (d, 3H), 0.81 (d, 3H) and 0.83 (d, 3H) and primary methyl group at δ 0.85 (m, 3H). The broad singlet at δ 5.35 was attributed to H-6 and the hydroxyl methane proton signal at δ 3.55 was attributed to H-3 proton based on biogenetic considerations. From Fig. 7 the molecular ion peak was found to be 415.00, the above data and knowledge of known sterols the compound I was found to be β-Sitosterol).

Compound II (Fig. 10), the ¹H NMR spectrum showed signals for six C-methyl singlet’s at δ 0.76, 0.78, 0.88, 0.94, 0.98 and 1.01, an allylic methyl group at δ 1.68, Fig. 11 showed signals for a vinylidene grouping exhibited by a pair of doublet signals at δ 4.56 and 4.68 each integrating for one proton and a hydroxy methine group at δ 3.19 (dd) which may be placed between a tetrasubstituted sp³ carbon atom and a methylene grouping. From a biogenetic point of view, the C-3 hydroxy group was assigned equatorial β-orientation, it is common feature in Triterpenoids.

Fig. 4:	1H NMR of cmpd I isolated compound I

Fig. 5:	1H NMR of isolated compound I

Fig. 6:	13C NMR of isolated compound I

Fig. 7:	Mass of isolated compound I

Fig. 8:	1H NMR of isolated compound II

Fig. 9:	1H NMR of isolated compound II

Fig. 10:	1H NMR of isolated compound II

Fig. 11:	1H NMR of isolated compound II

Fig. 12:	13C NMR of isolated compound II

Fig. 13:	13C NMR of isolated compound II

The presence of C-3 hydroxy group was supported by C¹³ NMR (Fig. 12 and 13) signal at δ 79.00. The signals at δ 109.32 and 150.97 are due to unsaturated carbon atoms between C₂₀ and C₃₀. From Fig. 8 and 9 the signals at δ 2.38 is due to H-13β and at δ 1.9 is due to H-19.

From Fig. 14 the molecular ion peak was found to be 440.85, the above data suggested the compound II was (3-β-hydroxy-21-Normethyl-19-vinylidenylursane).

In vivo Screening Studies of the Petroleum Ether Extract and Isolated Compound (3-β-hydroxy-21-Normethyl-19-vinylidenylursane)
The parameters viz., mounting (Fig. 3), intromission, sperm count and sperm motility were observed and results are shown in the Table 1-5.

Fig. 14:	Mass of the isolated compound II

Table 1:	Control
Route of administration: Oral, Values are Mean±SEM of 6 animals, Statistical significance: d = ns = p>0.05, c = p<0.05, b = p<0.01, a = p<0.001 as compared to the solvent control group, Bonferroni compare selected pairs of columns

Table 2:	Petroleum ether extract 200 mg kg-1 b.wt. in 0.3% CMC
Route of administration: Oral, Values are Mean±SEM of 6 animals, Statistical significance: d = ns = p>0.05, c = p<0.05, b = p<0.01, a = p<0.001 as compared to the solvent control group, Bonferroni compare selected pairs of columns

Table 3:	Petroleum ether extract 400 mg kg-1 b.wt. in 0.3% CMC
Route of administration: Oral, Values are Mean±SEM of 6 animals, Statistical significance: d = ns = p>0.05, c = p<0.05, b = p<0.01, a = p<0.001 as compared to the solvent control group, Bonferroni compare selected pairs of columns

Table 4:	Isolated compound (3-β-hydroxy-21-Normethyl-19-vinylidenylursane) 20 mg kg-1 b.wt. in 0.3% CMC
Route of administration: Oral, Values are Mean±SEM of 6 animals, Statistical significance: d = ns = p>0.05, c = p<0.05, b = p<0.01, a = p<0.001 as compared to the solvent control group, Bonferroni compare selected pairs of columns

Table 5:	Isolated compound (3-β-hydroxy-21-Normethyl-19-vinylidenylursane) 40 mg kg-1 b.wt. in 0.3% CMC
Route of administration: Oral, Values are Mean±SEM of 6 animals, Statistical significance: d = ns = p>0.05, c = p<0.05, b = p<0.01, a = p<0.001 as compared to the solvent control group, Bonferroni compare selected pairs of columns

DISCUSSION

On the first day of the treatment all the treated groups showed increased copulatory sexual behavior in all the experimental animals as revealed by the results. The prolonged treatment of all the treated groups was highly effective to increase the sexual libidity as compared to the solvent control. This indicates that the aphrodisiac activity has been shown by the tested petroleum ether extract and isolated compound (3-β-hydroxy-21-Normethyl-19-vinylidenylursane) at all the tested dose levels. The order of potency for the petroleum ether extract and isolated compound (3-β-hydroxy-21-Normethyl-19-vinylidenylursane) were:

Finally, two compounds were isolated. The petroleum ether extract and isolated compound (3-β-hydroxy-21-Normethyl-19-vinylidenylursane) were screened for aphrodisiac activity. The petroleum ether extract at 400 mg kg^-1 b.wt. doses showed better aphrodisiac activity than all other treated doses.

In support to the above work, phytochemical investigations have shown the presence of glycoside, saponins, flavanoids and sterols in Durian fruit. It is likely that these steroidal constituent increase the steroidogenesis and elevate androgen levels which results in observed effect (Chauhan and Dixit, 2008). So, the petroleum ether extract showed better activity due to presences of sterols.

Generally sexual behaviours are enhanced by elevated testosterone levels. Drug induced changes in neurotransmitter levels or their action in the cells could also change sexual behavior. In this connection it should be remembered that on ethnomedical practices this herb is also considered as a nervous stimulant (Chopra et al., 1956). Investigations are in progress to explore the possible mechanism of action.

CONCLUSION

There can be no doubt that most herbs rely for their effects on a variety constituents and the idea of synergy within and between them. So this plant may also contain other constituents which also possess fertility enhancing activity. Hence, future study on this plant should be in isolation of other constituents which may show fertility enhancing activity. Once a molecule has been isolated which possess activity then its derivatives could be synthesized and QSAR studies can be conducted which gives optimized result for activity (Wolf, 1997).

ACKNOWLEDGMENT

We are thankful to the management of J.S.S. College of Pharmacy, Ooty, Tamil Nadu, India for sponsoring this project and Sir C.R. Reddy College of Pharmaceutical Sciences, Eluru, Andhra Pradesh, India for providing other facilities.