Aim of study: Ancient literature alluded to the use of a number of plants/preparations as sex enhancer. One of such botanicals is Phoenix dactylifera in which the pollen grain has been acclaimed to be used as an aphrodisiac. However, the validity has not been scientifically tested. Dopamine is known to facilitate male sexual function. Therefore, the present study was undertaken to evaluate the effect of aqueous extract of Phoenix dactylifera pollen on the sexual behavior of male rats and to measure of serum Estradiol and Testostrone. Also, dopamine transmission in the nucleus accumbence (NAc) was studied in male rats using in vivo microdialysis. Methods and Materials: sixty male rats were randomized into 6 groups (A-F). Group A received 0.2 ml of Normal Saline mixed with Dimethyl Sulphate (DMSO), while groups B-F were injected same volume containing 35 mg/kg, 70 mg/kg, 105 mg/kg, 140 mg/kg and 350 mg/kg of DPP extract, respectively. Sexual behavioral parameters including mounting, intromission and ejaculation frequencies and latencies were recorded in male rats one hour after injection of extract by mating with a receptive female (1:1). The male serum testosterone and estradiol concentrations were also determined. Results: All doses stimulated male sexual behavior. Extract significantly increased mount, ejaculation, intromission frequencies and ejaculation latency in comparison to controlled ones (p < 0.001). Mount and intromission latencies significantly reduced (p < 0.001). Maximum effect was observed in dose 140 mg/kg. This extract was found to enhance Testestrone, Estradiol and the orientation of males toward female ones by increasing mounting and ano-genital investigatory behavior. Conclusions: Data from this study identified that the aqueous extract of Phoenix dactylifera pollen grain enhanced sexual behaviour in male rats. The improved sexual appetitive behaviour in male rats may be attributed, to the alkaloids, saponins, and or flavonoids since these phytochemicals has engorgement, androgen enhancing. Also, our findings support the traditional use of this plant as acclaimed aphrodisiac and for the treatment of pre-ejaculation and impotency.
Male sexual behavior comprises a complex pattern of genital and somatomotor responses, elicited, directed, and maintained by external and internal signals. It includes copulation as well as precopulatory behaviors that allow the male to detect and locate a mate, assess her potential mating appropriateness, and stimulate a receptive response [1,2]. For a normal sexual intercourse in males, the sexual organs and factors relating to erection of the copulatory organ must function as normally [
Male reproductive capacity was found to be deficient in no less than 50% of infertile couples [
Traditional medicines are gaining importance and nowadays are being studied to find the scientific basis of their therapeutic actions [8,9]. Plant-derived chemicals are used to relieve sexual dysfunction and they have sex enhancing potentials. These phytochemicals increase libido, sexual potency and sexual pleasure [5,6]. The use of herbal medicine has become increasingly popular worldwide especially in the Asian and African countries [
The various parts of Phoenix dactylifera widely are used in traditional medicine for the treatment of various disorders which include memory disturbances, fever, inflammation, paralysis, loss of consciousness and nervous disorders [11,12]. Suspension of Phoenix dactylifera date palm pollen (DPP) is an herbal mixture that is widely used as a folk remedy for curing male infertility in traditional medicine. Date palm fruit suspensions improve the sperm count, motility, morphology, and DNA quality with a concomitant increase in the weights of testis and epididymis [
Samples of the plant were collected from botanical garden at Bushehr city (South of Iran), Iran.
Phoenix dactylifera pollen grain is a small and oval shape gametocyte with a fine bark. After removing the bark, pollen grain washed with distilled water and then dried. Dried pollen grain was pulverized with a small electric blender (blender model/Pars khazar, Iran). 100 gram of powder was extracted in 0.5 liter of warm distilled water (30˚C) with constant shaking (magnetic shaker model). The solution was passed through a filter paper and lyophilized. After vaporizing of water, the resultant yield was reconstituted in normal saline to give the required doses of 35, 70, 105, 144 and 350 mg/kg used in our study. Solutions were stored in refrigerator (2˚C - 8˚C). The doses were mixed with Dimethyl Sulphate (DMSO) and IP injection was done 1 hour before experimentations with volume of 0.2 ml/rat.
The study adheres to the principles of laboratory care established by Ethic Committee of Tehran University of Medical Sciences. A total of 120 animals made up of equal number of male and female rats were used for this study in a complete randomized design. Healthy sexually experienced male rats after sex screening test (wistar albino), 4 months old, weighting between 280 - 320 grams and females, 3 months old weighting between 220 - 250 grams were selected from our department (physiology department of Tehran university of medial sciences). Male and female rats were housed separately 4 to a glass cage placed in a well-ventilated animal room. Room temperature was 22˚C ± 2˚C with humidity of 60%. Animals were housed in a reversed light-dark cycle (light on: 7 p.m to 7 a.m). Animals were acclimated for about 4 weeks before the experimentation. They were allowed free access to food pellets and water ad libitum. Before experiments, sex screening test was done. In this test, male rats must exhibit consistent parameters of sexual behavior, including intromission within 30 sec of the presentation of female, ejaculation within 15 min of the first intromission. Experiments were done in dark period in a dim red florescent lamp.
Sixty female rats were used as mating stimulus. The females were bilaterally ovariectomized via lumbar incisions under ketamine (100 µl/0.1 kg of rat) and xylazin (10 µl/0.1 kg of rat) anesthesia at least two weeks before the experiments began. The females were rendered sexually receptive by single subcutaneous injections of estradiol benzoate (10 µg) 52 h and progesterone (1 mg) 4 h, prior to pairing. Estrous females displayed a high degree of lordosis responding and proceptivity.
Sixty male rats were randomly grouped into 6 (A-F) consisting of 10 animals each. Animals in group A, which served as the control, received 0.2 ml of saline mixed with DMSO (IP injection). Animals in groups B, C, D, E and F were treated with doses of 35, 70, 105, 140 and 350 mg/kg of the extract, respectively, with volume of 0.2 ml/rat. All administrations were done daily at the time of during 8:00 a.m and 9:00 a.m. The experimental rats allowed free access to rat pellets and water.
A Plexiglas observation cage (0.3 m × 0.5 m × 0.3 m) with a mesh plate in the middle was put on a metal box that has an oblique mirror within. One hour after the treatment, the male rat was placed in this cage. After 10 minutes, a sexually receptive female rat was introduced on the other side of the cage (Anticipatory phase) and after 10 minutes, the mesh plate was removed for 30 minutes (Consummatory phase). Sexual behaviors of a male with female were observed from the cage side for proceptive and precopulatory behaviors. Sexual behavior parameters were monitored for 30 min observatory period by camera (Panasonic model with O-Lux) and direct observations.
If male rat couldn’t have an intromission within the first 15 minutes, that rat was removed and replaced with a new one According to the standard and basic procedures, the following male sexual parameters were recorded or calculated for the observatory period. 1—Mount Latency (ML), time from introduction of the female until the first mount. 2—Intromission Latency (IL), time from introduction of the female until the first intromission. 3—Ejaculation Latency (EL), time from the first intromission until ejaculation. 4—Mount Frequency (MF), the number of mounts in a series. 5—Intromission Frequency (IF), the number of intromissions in a series. 6—Ejaculation frequency (EF), the number of times there was expulsion of semen by males after vaginal penetration-characterized by rhythmic contraction of the posterior abdomen. 7— Post-Ejaculatory Interval (PEI), the time from the occurrence of ejaculation until the initiation of a new series, as indicated by the next intromission. Other computed male sexual behavioural parameters include: % index of libido = (number mated/number paired) × 100; % mounted = (number mounted/number paired) × 100; % intromitted = (number of rats that intromitted/number paired) × 100; % ejaculated = (number of rats that ejaculated/number paired) × 100; copulatory efficiency = (number of intromissions/ number of mounts) × 100; intercopulatory efficiency = average time between intromissions [13-16].
The testosterone. Estradiol and Dopamine enzyme immunoassay test kits were used according to their manufacture’s instruction (ABO Switzerland Co.), while estradiol benzoate and progesterone were products of Sigma Chemical (Germany).
After finding the effective dose (140 mg/kg), we measured the Dopamine concentration of nucleus accumbence in male rats using in vivo microdialysis in aperiod of 70 minutes.
After recording of the sexual behavior parameters and at the end of experiments, all male rats were deeply anaesthetized With Ketamine and Xylazine. Blood samples were collected from the aorta, centrifuged and the serum separated, Samples stored at −20˚C for the measurement of testosterone and estradiol.
All treated rats were observed any signs of toxicity (Salivation, lachrymation, ptosis, squinted eyes, writhing, convulsions, tremors) stress (erection of fur), diarrhea and changes in behaviour (such as spontaneous movements in the cage, climbing, cleaning of face, nongenital self grooming). In addition, food and water intake were noted.
After recording the sexual behavioral parameters, Data was expressed as mean ±SD and analyzed. Statistical analysis was done by Kruskal Wallis test (ANOVA). The comparison of means between control and each experimental group was done by the Wilcoxon-test. P < 0.05 was regarded as significant. SPSS software version 11 and Excel 2007 were used for analyzing.
The effects of various doses of DPP on sexual behavior are summarized in Tables 1 and 2. Intrapritonaly (IP) injection of various concentration of DPP modified all parameters. Maximum effect was observed in rats treated with dose 140 mg/kg of DDP. The aqueous extract of DPP produced a significant increase in MF, IF, EJF, EJL, PEI and decrease in ML, IL (p < 0.05). Treated male rats displayed vigorous ano-genital sniffing and mounting on females and restricted them to one side of cage (
The extract produced a significant increase in the penile erection index as compared to control value. There were homosexual mountings in the treated animals after experimentations. Our studies on the orientation of male towards the female rats showed that males treated with the extract displayed more frequent and vigorous anogenital sniffing and mounting on females, as compared to controlled cases. The orientation towards environment (climbing on cage wall, raring and exploration) was found to be inconsistently reduced whereas towards self (genital grooming) was increased. The rats treated with the extract tended to show confinement to a particular area of the cage (around female) showing restriction in movement.
There was an increase in the blood level of Estradiol and Testosterone (Figures 1 and 2). As shown in Figures, the effective dose for estradiol and testosterone was 140 mg/kg.
Releasing of Dopamine increased significantly in the nucleus accumbence when a receptive female was introduced behind a screen (P < 0.001). During copulation, Dopamine increased markedly in control and extracted rats. Improving of sexual behavior and Dopamine release was higher in treated rats with extract in comparison with control (P < 0.001).
There were no defects and clinical signs of toxicity, stress or changes in behaviour and appearance evident.
Values are presented as mean ± SD. All latencies and interval are expressed in seconds. Significant from control: *p < 0.05, §p < 0.01, ¥p < 0.001; N/group = 10 rats; $= Max. Effect.
Values are presented as mean ± SD. Significant from control. *p < 0.05, §p < 0.01, ¥p < 0.001; N/group = 10.
Diarrhea was observed in animal treated with 350 mg/kg. The food and water intake of all treated rats was similar to those of controls.
Many plants with medicinal properties are effective as aphrodisiac through mechanisms such as vasodilation, generation of nitric oxide, elevation of androgens and gonadotropins [
Administration of the Aqueous extract at all dose levels modified rat copulatory behavior as well as orientation activities, the main determinant for measuring male sexual behavior [
by the aqueous extract might be responsible for the enhanced sexual behaviour in the animals [
Extract prolonged the ejaculatory latency in male rats, indicating an increase of ejaculatory threshold [
Increased MF and IF in treated rats, indicating the sexual motivation and efficiency of erection and penile orientation. Increasing of the libido might be the result of increasing several hormones that are secreted from pituitary. The main components of DPP are stroids, flavonoids, saponins, and lipid. These agents can increase sexual behavior. They stimulate endogenous testosterone levels probably by raising the level of luteinizing hormones (LH) [24-26]. Following adequate erection and activity of muscles, intromission is possible and increasing of IF by the extract show the activation of penile erection mechanism. Alkaloids of DPP have estrogenic properties [27,28] that induce vasodilation of blood vessels of penis which results in erection [
Steroidogenesis produces steroid hormones that they increase dehydroepiandrosterone. The last agent enhances sexual behavior and prolongs EF and reduces EL, PEI and intercopulatory intervals. All of these mechanisms are central. Peripheral acting of alkaloids can relax smooth muscles of corpus [
Finally, our study showed that DPP possess facilitatory effects that increase sexual arousal, the state of sexual excitement or desire during sexual interaction. Dose 140 mg/kg had greater activity in stimulating of erection, genital grooming and orientation activities of male rats. In addition of improving the sperm quality [
This study was supported by Vice Chancellor for Research of Tehran University of Medical Sciences, Tehran, Iran (No. 90). Authors wish to thank Mr. Ghasemi and Mr. Sohanaki (instructors of medical physiology) and also Mr. Fanaee and Mr. Bakhshesh (Ph.D. students of medical physiology) for their technical assistances.