Dracaena arborea improves sperm characteristics and antioxidant enzymes in adult male rats with experimental varicocele

Pierre Watcho; Baudouin Yannick Petnga Tchatat; Patrick Brice Defo Deeh; Georges Romeo Bonsou Fozin; Modeste Wankeu-Nya

JBRA Assist. Reprod. 2021;25(3):329-336
ORIGINAL ARTICLE
doi: 10.5935/1518-0557.20200098

Dracaena arborea improves sperm characteristics and antioxidant enzymes in adult male rats with experimental varicocele

Pierre Watcho¹, Baudouin Yannick Petnga Tchatat¹, Patrick Brice Defo Deeh¹, Georges Romeo Bonsou Fozin¹, Modeste Wankeu-Nya²

¹Animal Physiology and Phytopharmacology Laboratory, University of Dschang, Box 67 Dschang, Cameroon
²Department of Animal Organisms Biology, University of Douala, P.O. BOX, 24157, Douala, Cameroon

Corresponding author:
Pierre Watcho Animal Physiology and Phytopharmacology Laboratory University of Dschang Dschang, Cameroon Email: pierre.watcho@univ-dschang.org pwatcho@yahoo.fr.

ABSTRACT
Objective: We evaluated the preventive effects of aqueous and ethanolic extracts of Dracaena arborea on sperm characteristics and oxidative stress markers in adult male rats with varicocele.
Methods: Thirty-six male Wistar rats were randomly distributed into 6 groups (6 animals/group) and treated for 30 days as follows: (1), normal rats receiving distilled water (10 ml/kg); (2), sham operated rats receiving distilled water (10 ml/kg); (3), varicocele rats receiving distilled water (10 ml/kg); (4), varicocele rats receiving vitamin E (150 mg/kg); (5-6), varicocele rats administered respectively with aqueous (500 mg/kg) and ethanolic (100 mg/kg) extracts of D. arborea. All rats (except normal and sham-operated groups) underwent varicocele induction. At the end of the treatment period, sexual organ weights, oxidative stress, sperm characteristics and some biochemical parameters were measured.
Results: A significant decrease (p<0.01) in sperm density (137.81±7.76 vs. 175.83±4.86), sperm motility (55.43±4.49 vs. 77.96± 3.15) and sperm normality (44.75±2.80 vs. 79.25±1.84) was noticed in varicocele-untreated rats compared with controls. Varicocele also induced oxidative stress by decreasing superoxide dismutase (SOD) and catalase activities, and increasing malondialdehyde (MDA) levels. These alterations were prevented by D. arborea. For instance, the aqueous extract of D. arborea (500 mg/kg) significantly increased (p<0.05-0.001) testes and epididymis weights, sperm viability and sperm motility, while the ethanolic extract (100 mg/kg) increased sperm normality compared with varicocele-untreated rats. D. arborea extracts also decreased MDA levels, but elevated catalase activity.
Conclusions: Dracaena arborea prevents the deleterious effects of varicocele and could be considered as an alternative treatment of this physiopathology.

Keywords: Varicocele, Dracaena arborea, antioxidant, rat

INTRODUCTION
Infertility is defined as an incapacity for a couple to give birth after one year of regular and unprotected sexual intercourse (Drissi et al., 2015). In Cameroon, approximately 25% of couples experience reproductive difficulties (Nana et al., 2011); in about 50% of cases in general, male responsibility is diagnosed (Fainberg & Kashanian, 2019). Various causes of male infertility such as genetic predisposition, lifestyle, medications (Fainberg & Kashanian, 2019) and varicocele (Bolat et al., 2016) have been identified. Varicocele is characterized by abnormal tortuosity and dilation of the gonadal veins that drain the testis and is responsible for more than 15% of cases of male infertility (Jo et al., 2016). This prevalence increases significantly in men after puberty (Razi et al., 2011). Varicocele mainly affects the left testes (85%), and may be due to a higher probability of absence of left spermatic venous valves and to a low blood flow rate in the left renal vein compared with the inferior vena cava (Muratorio et al., 2013; Rehman et al., 2019). This pathology generates multiple consequences such as pain, hypoxia of the genital tissues, reflux of metabolites and hyperthermia, which then creates oxidative stress leading to testicular lesions, sperm injuries, hypoandrogenism and infertility (Muratorio et al., 2013; Bolat et al., 2016).
Several treatment options have been designed to attenuate pain, to stop the progression of the testicular lesions, to improve spermatogenesis and endocrine function of the testis; varicocelectomy, radiation, embolization, drugs (chorionic gonadotropic hormone) and sclerotherapy (Muratorio et al., 2013) are applied in patients suffering from varicocele. Indeed, these practices are associated with various side effects, including allergies to anaesthesia, hydrocele and infections, because the hormone therapy used is mostly from animal origin and often carries pathogenic germs. Moreover, a high recurrence rate and controversial effects on pregnancy (Zhu et al., 2019) very often follow surgery. Despite the beneficial effects of these treatment options, fewer studies have focused on the role of antioxidants as adjunct therapy along with surgery or hormonotherapy. The search for an effective alternative treatment from plants without side effects is on demand. Previous studies showed the efficacy of some plants in improving sperm parameters through antioxidant properties in experimental varicocele rats (Heidari et al., 2015).
Dracaena arborea is a plant used by traditional healers as an aphrodisiac to treat sexual dysfunctions. Previous studies carried out by our research group demonstrated that the aqueous (500 mg/kg) and ethanolic (100 mg/kg) extracts of D. arborea stimulate copulatory activity of normal and androgen-deprived (castrated) rats through dopaminergic and/or cholinergic pathway (Watcho et al., 2007), protect and regulate the increased rate of testicular germ cell death by apoptosis in streptozotocin-induced diabetic rats (Wankeu-Nya et al., 2013), and possess aphrodisiac property capable of alleviating erectile dysfunction caused by streptozotocin-induced diabetes in rats (Wankeu-Nya et al., 2014). D. arborea also delays the pro-ejaculatory effect of dopamine and oxytocin in the spine of male rats by preventing the contractions of the bulbospongiosus muscles through the blockade of dopaminergic and oxytocinergic receptors (Watcho et al., 2014). Moreover, we showed that D. arborea possesses androgenic properties, responsible for its alleviating effects on diabetes-induced reproductive complications in rats (Wankeu-Nya et al., 2019). A recent study also showed that the mixture of Mondia whitei, D. arborea, and Bridelia ferruginea possesses sexual stimulant effects in normal and prediabetic male Wistar rats (Watcho et al., 2019). Based on the above-mentioned findings, the present study was undertaken to evaluate the preventive effects of aqueous and ethanol extracts from the root barks of D. arborea on some fertility parameters of experimental varicocele rats.

MATERIALS AND METHODS
Plant collection, extract preparation and dose selection
Dracaena arborea roots were harvested in Bagnoun, Nde Division in the West Region of Cameroon. The plant was identified by Dr. Tatcham (Botany Department, Faculty of Science, University of Dschang, Cameroon) and authenticated at the National Herbarium under voucher number 25361/SFR/Cam.
The roots were cut into small pieces, shade-dried, later transformed into powder using an electric grinder and the powder obtained was used to prepare the extracts. The aqueous extract was obtained by macerating D. arborea powder (800g) in distilled water (5L) for 72h. After filtration, the filtrate was oven-dried at 45°C and 39.68g of a brownish residue was obtained (extraction yield: 4.96%) (Wankeu-Nya et al., 2013; 2014).
For the ethanolic extract, 1kg of D. arborea powder was macerated in 5L of ethanol (95%) for 72 hours. After filtration, the filtrate was evaporated under reduced pressure using a rotative evaporator and 30g of the brownish residue was obtained (an extraction yield of 3%) (Wankeu-Nya et al., 2013; 2014).
The doses of plant extracts and vitamin E were chosen from previous studies (Watcho et al., 2007; Wankeu-Nya et al., 2013; 2014; Khosravanian et al., 2015). The working solutions of aqueous and ethanolic extracts were prepared in distilled water and administered at 500 mg/kg and 100 mg/kg, respectively, according to our pilot studies (Watcho et al., 2007; Wankeu-Nya et al., 2013; 2014).

Animals
We used adult male Wistar rats (2.5 months old; 190-210g body weight) in this current study. They were obtained from the animal house of the Faculty of Science, University of Dschang, Cameroon. The animals were maintained in a standard environment (22-25°C; approximately 12hrs of light and 12hrs of dark cycle), had food, and water ad libitum. The project was presented and validated by the Scientific Committee of the Department of Animal Biology, University of Dschang, which follows the internationally accepted standard ethical guidelines for laboratory animal use and care as described in the European Economic Community guidelines, EEC Directive 2010/63/EU, of the 22 September 2010 (European Union, 2010).

Varicocele induction
Varicocele was induced as described by Turner (2001). Briefly, the upper left abdominal quadrant was exposed using a midline laparotomy incision, and the left renal vein was carefully dissected at the middle of the insertion of the spermatic vein. A 20-gauge needle was placed over the renal vein and tied using a silk suture. Thereafter, the needle was slowly removed and the midline incision was sutured using a silk thread. The dilation of the spermatic vein at the time of slaughtering was the criterion, which confirmed the varicocele in rats. Rats in the sham group underwent a similar procedure without renal vein ligation.

Experimental protocol
Thirty-six animals (12 without varicocele and 24 with varicocele) were randomly distributed into 6 groups of 6 animals in each, and treated as follows: Group 1, normal rats receiving distilled water (10 ml/kg. bw); Group 2, sham operated rats receiving distilled water (10ml/kg. bw); Group 3, varicocele rats receiving distilled water (10 ml/kg. bw); Group 4, varicocele rats treated with vitamin E (150 mg/kg. bw); Groups 5 and 6, varicocele rats administered respectively with aqueous (500 mg/kg) and ethanolic (100 mg/kg) extracts of D. arborea. The rats were orally treated with vehicle and drugs for 30 days. At the end of the treatment period, we measured the testes and epididymis weights, sperm characteristics as well as oxidative stress-related biochemical parameters.

Tissue preparation and sample analysis
A day after the last treatment (day 31), all rats were sacrificed under diazepam (10 mg/kg) and ketamine (50 mg/kg) anaesthesia. Testes and epididymis were removed, cleared from adhering tissue, washed in saline solution and weighed. Relative sexual organ weights were calculated using the following formula: Relative sex organ weight = (absolute sexual organ weight/body weight) × 100. The left and right epididymis were used for sperm count, sperm motility and sperm morphology. The left and right testes were homogenised in Tris buffer (PH = 7.4) to make 15% (g/ml) homogenate and 100 µl of this homogenate were used for measurement of oxidative stress markers (MDA, SOD and catalase) and total protein levels.

Sperm density and motility
Immediately after sacrifice, the left and right epididymides cauda of each rat were minced and thoroughly mixed in 10 ml of warm (36°C) 0.9% NaCl. 20 µl of this mixture were transferred to a Malassez haemocytometer and examined under a light microscope (OLYMPUS, X400). Motile and non-motile spermatozoa were counted in 10 fields and the percentage of motile spermatozoa determined using the following formula:
Percentage of motile spermatozoa (%) = (number of motile spermatozoa/total number of counted spermatozoa) × 100 (Ngoula et al., 2007).
For sperm density, a twenty-fold dilution was made by mixing the sperm suspension with 0.9% NaCl solution and the mixture was shacked gently. 20 µl of this mixture were transferred to a Malassez haemocytometer, observed under a light microscope (OLYMPUS, X400), and spermatozoa were counted in 10 fields (Ngoula et al., 2007).

Sperm viability and morphology
To determine sperm viability, 10 µl of sperm suspension were thoroughly mixed with 10 µl of eosin (1℅) and 30 µl of nigrosin (5%) on a slide. The eosin-nigrosin staining procedure was done in respect to the guidelines of the World Health Organization (WHO) on the examination and processing of semen published in 2010 (WHO, 2010). The mixture of stained sperm was smeared on the slide and examined under a light microscope (OLYMPUS, 40X). Ten (10) fields on the slide were selected in order to appreciate sperms that were stained pink or red (considered dead), and the unstained sperms (considered viable). The percentage of sperm vitality was expressed using the formula below:

Where %SPZv: percentage of viable spermatozoa; SPZn: number of viable spermatozoa; SPZt: total number of counted spermatozoa.
The sperm morphology was determined using eosin/nigrosin staining. Ten microliters of eosin (1%) and thirty microliters of nigrosin (5%) were added to 10 µl of sperm suspension. The prepared smear was used after incubation for 5 min in an oven (45°C). Ten (10) fields on the slide were selected in order to appreciate various abnormalities of spermatozoa (head and tail abnormalities, cytoplasmic droplets, tailless spermatozoa). For each field, the percentage of normal spermatozoa was calculated and the mean percentage of all slides was determined using the following formula (Ngoula et al., 2007):

Where %SPZn: percentage of normal spermatozoa; SPZn: number of normal spermatozoa; SPZt: total number of counted spermatozoa.

Oxidative stress parameters
The testis was crushed in a mortar containing tampon tris, then cold centrifuged for 10 minutes at 3,000xg and 10% supernatant was collected from the homogenate. The supernatant was used for protein, MDA, SOD and catalase analysis. The proteins were measured using a commercial kit (Roche diagnostics cobas c-1111) and protocols were performed according to the manufacturer’s instructions. The MDA content was measured using thiobarbituric acid reaction (Soni et al., 2018). The tissue SOD and catalase activities were evaluated as described by Théophile et al. (2006).

Statistical analysis
The results are presented as mean ± S.E.M. One-way analysis of variance (ANOVA) followed by Tukey-HSD post-hoc test were used to determine statistical differences. All analysis were performed using the Statistica software (version 8.0, StatSoft, Inc., Tulsa, USA).

RESULTS
Effectivity of varicocele after surgery
Figure 1 shows the normal aspect of the internal spermatic vein (1A) and a dilated testicular vein (1B). Out of 32 rats that underwent varicocele induction, 24 showed a clear dilation of the left internal spermatic vein, whereas 04 cases of death and 04 cases of failure of induction were noticed, giving a success percentage of induction of 75%.

Figure 1. Aspect of the internal spermatic vein (A) before and (B) after partial ligation of the left renal vein.

Effect of different treatments on the relative weight of testes and epididymis
As shown in figure 2 A-B, no statistical changes in both testicular and epididymal weights in the normal and sham operated groups were found. However, the epididymal weight (left and right) of varicocele rats receiving distilled water was significantly lowered (p<0.05) compared to controls. The aqueous extract of D. arborea significantly increased (p<0.05) the testicular (left testis) and epididymal (left and right epididymides) weights, compared to varicocele rats administered with distilled water (Figure 2 A-B).

Figure 2. Effects of different treatments on the relative weights of testes (A) and epididymis (B). Values are mean±SEM. *:p<0.05 compared to distilled water; α:p<0.05 compared to normal; N: normal; S.O: sham operated; DW: distilled water; Vit E: vitamin E; A.E: aqueous extract; E.E: ethanolic extract.

Effect of different treatments on sperm parameters
In varicocele rats treated with distilled water, sperm density (in both epididymides), sperm viability (in the left epididymis), sperm motility (in the right epididymis) and sperm normality (in both epididymides) were significantly reduced, compared with normal rats. Vitamin E significantly increased (p<0.05-0.001) sperm density (in both epididymis) and sperm normality (in the right epididymis), compared with varicocele rats treated with distilled water. D. arborea extracts improved sperm parameters after treatment. Thus, the aqueous and ethanolic extracts of D. arborea significantly increased sperm viability and sperm normality compared to distilled water group (Table 1).

Table 1. Effects of different treatments on sperm parameters

Effect of different treatments on sperm abnormalities
In the left epididymis of varicocele rats treated with distilled water, head abnormality, tail abnormality and cytoplasmic droplets were significantly increased (p<0.001), compared with normal rats. In the contralateral epididymis, there were no significant changes in sperm abnormalities between untreated varicocele and normal rats. The effects of vitamin E on sperm abnormalities were more pronounced in the left epididymis, where a decrease in head (23.99%) and tail abnormalities (37.99 %) was recorded compared with untreated varicocele rats. The aqueous and ethanolic extracts of D. arborea significantly reduced head abnormality (p<0.001) in the left epididymis compared to the rats in the distilled water group. The ethanolic extract significantly reduced (p<0.01) the cytoplasmic droplets in the left epididymis compared to those in the distilled water group. The aqueous extract was more efficient in preventing sperm abnormalities (Table 2).

Table 2. Effects of different treatments on sperm abnormalities

Effect of different treatments on biochemical parameters
In all varicocele rats, testicular protein levels were lowered in the left testis. Vitamin E significantly (p ?0.05) increased the testicular protein content (in the right testis) after treatment (Figure 3).

Figure 3. Effects of different treatments on testicular protein levels. Values are mean ± SEM. *: p<0.05 compared to distilled water; N: normal; S.O: sham operated; DW: distilled water; Vit E: vitamin E; A.E: aqueous extract; E.E: ethanolic extract.

The induction of varicocele was associated with oxidative stress, characterized by the significant decrease (in the left testis) (p<0.01) of catalase and SOD activities, and elevated lipid peroxidation. In the left testis, the aqueous and ethanolic extracts of D. arborea significantly increased (p<0.05) catalase activity, but decreased MDA levels, compared with untreated varicocele animals ().

Figure 4. Effects of different treatments on testicular MDA (A) SOD (B) and catalase (C) activities. Values are mean ± SEM. *: p<0.05 compared to distilled water; ^aa: p<0.01: compared to normal; ^bb: p<0.01 compared to sham operated; N: normal; S.O: sham operated; DW: distilled water; Vit E: vitamin E; A.E: aqueous extract; E.E: ethanolic extract.

DISCUSSION
Varicocele is a pathology characterized by the dilation of the pampiniform plexus veins, which negatively affects testicular function (spermatogenesis and steroidogenesis), leading to infertility (Bolat et al., 2016). The present study clearly demonstrated that the aqueous and ethanolic extracts of D. arborea improved fertility potential and prevented oxidative stress. This improvement (mainly in the left testis) was characterized by the significant increase in sperm viability, sperm motility and sperm normality as well as reduced sperm abnormalities and increased antioxidant enzymes.
Varicocele appears as the result of anatomical differences between the right and left spermatic veins. Indeed, the left internal spermatic vein enters the left renal vein at a right angle, while the right internal spermatic vein enters directly into the inferior vena cava at an acute angle. This increases the hydrostatic pressure in the venous pampiniform plexus, causing its dilation (Muratorio et al., 2013). In this study, after surgical blockade of the left renal vein, varicocele was evidenced by the visually apparent dilation of the left spermatic vein. Out of 32 rats submitted to varicocele induction, 24 showed a clear dilation of the left internal spermatic vein, and there were 04 cases of death and 04 cases of failure, giving a success percentage of 75%. Comparatively, this percentage is lower than, the 98.3% obtained by Zhou et al. (2015). This difference could rely on the surgical approach used in the two studies since Zhou et al. (2015) used the microsurgical approach. Testicular and epididymal weights are important markers of varicocele. Similar to previous studies (Saalu et al., 2009), testicular and epididymal weights were lowered in varicocele rats, compared to normal animals. Data from the literature indicate that varicocele is associated with an excessive production of reactive oxygen species (ROS), which induces apoptosis in the testes and causes degeneration of the germinal epithelium of seminiferous tubuli, leading to low testicular weight (Heidari et al., 2015; Soni et al., 2018). Since the epididymal activity depends on testicular function, this drop in testicular weight may partly justify the decrease seen in the epididymal weight. These decreases in testicular and epididymal weights seen in the untreated varicocele rats are similar to the findings of Saalu et al. (2009). Vitamin E prevented the decline in testicular and epididymal weights; this could probably be due to its powerful antioxidant potential. In rats treated with D. arborea extracts, the testicular and epididymal weights were significantly increased (p<0.05). These results indicate that D. arborea could protect and/or stimulate testicular functions (steroidogenesis and spermatogenesis) as suggested by Wankeu-Nya et al. (2013) who showed that in streptozotocin-diabetic rats, D. arborea extracts protect and regulate the testicular germ cells (Wankeu-Nya et al., 2013). Similarly, Heidari et al. (2015) reported that Pilea microphila significantly increased the testicular and epididymal weights of varicocele rats.
Varicocele is generally associated with abnormal sperm parameters (Yu et al., 2011; Muratorio et al., 2013). In the current study, sperm density was significantly reduced in the untreated varicocele rats. This result corroborates that of Soni et al. (2018) and could be justified by the adverse effects of the thermal stress, which negatively affects spermatogenesis and steroidogenesis, leading to low sperm density. Varicocele rats also exhibited low sperm motility and viability as well as elevated morphological abnormalities (Will et al., 2011; Razi et al., 2011). Under varicocele condition, spermatozoa, which are released in the germinal epithelium, carry more residual cytoplasm and are then considered as defective spermatozoa (Razi et al., 2011). Vitamin E and plant extracts prevented these abnormalities. The increase in spermatic density seen after treatment with D. arborea corroborates the findings of Heidari et al. (2015), who showed that varicocele rats treated with Pilea microphila exhibited a significant increase in sperm density. According to Muratorio et al. (2013), varicocele can slightly affect the contralateral normal testicle. D. arborea also improved sperm motility, viability and normality, and decreased sperm abnormalities, probably due to its antioxidant properties, which has already been previously reported (Nwaehujor et al., 2013). Similarly, Soni et al. (2018) and Zhu et al. (2019) showed respectively that motiliperm, a mixture of extracts of three medicinal herbs, has a protective effect in varicocele-induced oxidative injury in rat testis, and Morinda officinalis polysaccharides attenuate varicocele-induced spermatogenic impairment.
Several studies have reported that varicocele increases ROS production and negatively affects sperm quality (Sakamoto et al., 2008; Muratorio et al., 2013; Soni et al., 2018). In the present study, varicocele was associated with a significant increase in MDA concentration, but with low SOD and catalase activities. Under varicocele condition, there is an increase in testicular temperature, which causes ROS overproduction and lipid peroxidation of the spermatozoa membrane, leading to the death of germ cells (Sakamoto et al., 2008). SOD, an antioxidant enzyme, transforms the superoxide anion into hydrogen peroxide and oxygen, thus preventing it from exerting its noxious effects (Soni et al., 2018). The imbalance marked by increased MDA and decreased SOD and catalase activities due to varicocele was reversed by D. arborea extracts, with the highest effects observed in rats administered with the aqueous extract (500 mg/kg). In parallel, Heidari et al. (2015) reported that Pilea microphila decreased oxidative stress in the testis, by significantly increasing SOD activity after treatment. Additionally, a clinical study demonstrated that Jingling, a substance derived from a Chinese plant, increases catalase activity and prevents oxidative stress in men with varicocele (Yan et al., 2004). These protective properties of D. arborea extracts could be attributed to the presence of some bioactive compounds, such as sterols, phenols, flavonoids and saponins previously found in this plant (Watcho et al., 2007), which are powerful antioxidant compounds.

CONCLUSION
Our findings have demonstrated that D. arborea improved the testicular and epididymal weights as well as sperm characteristics and antioxidant enzymes in varicocele rats; hence suggesting D. arborea as a reliable therapeutic plant for patients suffering from varicocele and infertility.

Congress where the study was presented
The 24^th annual conference of the Cameroon Bioscience Society on the theme: “Bioscience research for Cameroon’s emergence” held in the University of Buea, Cameroon, on November-December 2017.

Disclosure statement
No potential conflict of interest was reported by the authors.

ACKNOWLEDGEMENTS
The authors would like to thank the University of Dschang for the research facilities.

CONCLUSION
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