Protective Effect of Zanthoxyliun leprieurii Fruits on Reproductive Organ Weight and Serum Metabolite Profile, Testicular Structure and Function Impairment in Male Cavy (Cavia porcellus) Exposed to Hyperthermia
- 1. Department of Agronomy and Agricultural Sciences, University of Dschang, Cameroon
Abstract
The present work was carried out in order to evaluate the effects of high temperature in male guinea pig (Cavia porcellus) reproductive characteristics and mitigation strategy using aqueous extract (AE), of Zanthoxylium leprieurii fruits. For this purpose, seventy-two (72), adult male guinea pigs aged about 4 months and weighing between 350-400 g were divided into 6 groups of 12 guinea pigs each, comparable in terms of body weight (bw). The six group were randomly subjected to the treatments as follow: T0 (neutral control coexposed to 20-25°C + 2 ml/kg bw of distilled water); T0- (negative control), T0+ (positive control), AE100, AE200 and AE400 were all exposed to temperature at 46 ± 1 °C and respectively received distilled water (2 ml/kg bw), vitamin C (200 mg/kg bw); 100, 200 and 400 mg/kg bw aqueous extract of Z. leprieurii). The exposure time was 6 hours per day for 60 days. At the end of the trial, samples were collected for analysis of reproductive characteristics. Results showed that serum levels of follicle stimulating hormone (FSH), luteinizing hormone (LH) and testosterone ; the weight of testes and vas deferens, the epididymal sperm mobility and density were significantly (p<0.05) greater in heat stressed guinea pigs treated with vitamin C and Z. leprieurii AE at 200 and 400 mg/kg bw compared to negative control (T0-). Serum Heat Shock Protein (HSP), concentrations were significantly (p<0.05) higher (82.27 ± 1.63 ng/ml), in heat-stressed guinea pigs treated at 400 mg/kg bw of AE compared to negative control (T0-) (43.01 ± 1.34 ng/ml). In conclusion, the oral administration of Z. leprieurii fruit aqueous extract reduced the negative impact of elevated temperatures in male guinea pig reproductive characteristics.
Keywords
Male guinea pig ,Reproduction ,Hyperthermia, Zanthoxylium leprieurii
Citation
Aime LF, Narcisse VB, Herve T, Dorice AK, Nadege DM, et al. (2020) Protective Effect of Zanthoxyliun leprieurii Fruits on Reproductive Organ Weight and Serum Metabolite Profile, Testicular Structure and Function Impairment in Male Cavy (Cavia porcellus) Exposed to Hyperthermia. Ann Reprod Med Treat 4(1): 1022.
INTRODUCTION
According to the Intergovernmental Conference report on Climate Change [1], the Earth’s temperature is increasing by around 0.2°C per decade. In the year 2100, it would have increased from 1.4 to 5.8°C. According to Hansen [2], and Emtnan et al. [3], the increase in temperature, greatly affect reproductive performance in mammals. Ambient temperatures above 20- 25°C in the temperate zone and 25-37°C in the tropical zone are sensitive to induce oxidative stress in animals [4,5]. Heat stress resulting from high temperature disrupts homeostasis. It negatively affects the semen quality and quantity, the testis structure and function [6]. These effects subsequently induce sub-fertility and infertility [7].
Thermal shocks both high temperatures and low temperatures are the causes of an overproduction of oxygen reactive species in which free radicals [8]. According to Kumar and Gandhi [9], high temperature creates an imbalance between the activated oxygen reactive species and the antioxidant defense system. This imbalance favors the accumulation of free radicals which cause lipid peroxidation and consequently the deterioration of reproductive performance [10]. Several studies have reported that an increase (acute or chronic) in testicular temperature adversely affects spermatogenesis, resulting in a decrease of the density of spermatozoa [11-13]. As a solution, the antioxidant capacities of animals can be enhanced by nutritional supplements such as vitamins A, E and C and some minerals including Selenium and Zinc [9]. On the other hand, study on some plants and plant
by-products, showed that they have molecules with antioxidant properties which can be used in animal production neutralize the negative effects of high temperatures. This is the case of green tea extracts [14], aqueous extracts of guava leaves [15], and essential oil of guava leaves [16]. The same properties are also founded in several spices such as Zanthoxylum leprieurii which is used to boost food flavor [17].
Zanthoxylum leprieurii is one of the spice plants commonly used in Central and West Africa for traditional medicine. Root and bark decoctions are said to have excellent diuretic and purgative activities [18]. They are also used as analgesics and against heart palpitations [19]. The Z. leprieurii is rich in various bioactive molecules (phenols, flavonoids, tannins, terpenoids and saponins). These molecules possess diverse biological properties including antioxidant activity [20], which can be used in animal production to limit the oxygen reactive species attacks. This study was designed to test the protector effects of Z. leprieurii fruit aqueous extract on genital organs weight and histopathological changes, sperm characteristics, serum level of reproductive hormones and HSPs in heat- stress male guinea pigs.
MATERIALS AND METHODS
Collection and preparation of Z. leprieurii fruit aqueous extract
The seeds of Zanthoxylium were bought from Dschang (Menoua division in Cameroon), local market. They were dried sheltered from the sun, and then ground at the mill. The obtained powder was used for extractions, using 6 liters of distilled water for 1 kilogram of powder. The filtrate was dried in the oven at 45°C to obtain a paste used to prepare the Z. leprieurii aqueous extract at different concentrations.
Experimental animals and design
Seventy-two male cavies (Cavia porcellus) weighing 330.56 ± 23.62g, with average age of 3-4 months were used. The cavies were reared in the Teaching and Research Farm of the University of Dschang (Cameroon). They were identified using numbered earrings and housed in identical cages of dimensions 100 cm ×80 cm × 60 cm (length, width and height) under 12 hours’ light/day and had free access to feed and water.
Animals were divided into six groups of twelve animals each, randomly assigned in terms of body weight. They were subjected to the following treatments: T0 (neutral control): 20-25 °C + 2 ml/ kg bw of distilled water and T0- (negative control), T0+ (positive control), AE100, AE200 and AE400. Animals from T0- to AE400 were all exposed to 46 ± 1°C and respectively received distilled water (2 ml/kg bw), vitamin C (200 mg/kg bw); 100, 200 and 400 (mg/kg bw AE from Z. leprieurii). The exposure time was 6 hours per day for 60 days.
Data collection
Twenty-four hours after the last exposure to heat and administration of doses of vitamin C and Z. leprieurii fruit aqueous extract, each animal was anesthetized using ether vapor and blood samples were collected by cardiac puncture for determination of hormone levels and HSP-40. Thereafter, animal were sacrified, testes, epididymides, vas deferens and sexual accessory glands were excised and weighed. The cauda epididymides were weighed and immersed in 5 ml 0.9% NaCl solution (37 °C), for sperm characteristics. Briefly, a drop of the latter solution was placed on a slide, observed at 40X magnification under the microscope and sperm mobility examined as reported by Boiti et al. [21]. Sperm count was done using the Thomas haemocytometer. Briefly, defined aliquots of the sperm was dissolved and immobilized in 10 % Formol/NaCl solution. After gentle stirring of the sample, spermatozoa were counted microscopically using hemacytometer chamber in a total of 10 square out of two chamberfields.
Evaluation of reproductive hormones and Heat Shock Protein (HSP)
Serum levels of testosterone, FSH and LH were measured using ELISA kit from Omega Diagnostics (Scotland, United Kingdom). HSP levels in serum samples were determined using guinea pig Heat Shock Protein 40 (HSP-40) ELISA kit (ABclonal Biotechnology Co., Lto China), as per instructions from the manufacturer.
Histology
The right testis was fixed by immersion in 10% NaCl solution for 1 week and then washed, dehydrated in ascending grade alcohol bath, clarified in xylene immersion, and embedded in paraffin. Sections of 5μm were stained with hematoxylin–eosin for histological observations under a light microscope (400×).
Statistical analysis
Data were analyzed using SPSS IBM statistics software 20.0. Differences between groups were assessed using one-way analysis of variance (ANOVA), and specific differences between pairs of means assessed by Duncan’s test at 5% significance.
RESULTS
Effects of Z. leprieurii on reproductive organ weights in male guinea pig exposed to high temperature
Table 1 summarizes the effects of the Z. leprieurii fruit aqueous extract on the weight of genitals organs in male guinea pig subjected to heat stress. The relative weights of the testes, accessory glands and vas deferens decreased significantly (p<0.05), in heat stressed animals compared to the neutral control. In addition, the relative weight of the epididymis decreased nonsignificantly (p?0.05) in heat stressed animals compared to the neutral control. The administration of Z. leprieurii fruit aqueous extract at doses of 200 and 400 mg/kg bw induced a significant increase (p<0.05) of the weight of the testes, accessory glands and vas deferens compared to thermal stress exposed animals (T0-).
Effect of Z. leprieurii on reproductive hormones in male guinea pig exposed to high temperature
It appears that the concentrations of FSH, LH and testosterone decreased significantly (p <0.05), in guinea pigs subjected to heat stress compared to neutral controls. The administration of Z. leprieurii fruit aqueous extract whatever the dose and vit C led to a significant increase (p<0.05), in FSH compared to the negative controls (T0-). For LH, the increase was significant (p<0.05), only with vit C and Z. leprieurii fruit aqueous extract at 100 and 200 mg/kg bw. With respect to negative controls (T0-), the Z. leprieurii fruit aqueous extract at 200 and 400 mg/kg bw significantly increased the serum content in testosterone.
Table 1: Effects of Z. leprieurii fruit aqueous extract on the relative weight of genitals organ in heat stressed male guinea pig.
Relative weight of genital organs (g/100 g bw) | Controls | Doses of Z. leprieurii AE (mg/kg bw) | P Values | ||||
T0 (n=12) | T0- (n=12) | T0+ (n=12) | 100 (n=12) | 200 (n=12) | 400 (n=12) | 0 | |
Testis | 0.43±0.01b | 0.31±0.01e | 0.39±0.01c | 0.36±0.02d | 0.41±0.01bc | 0.51±0.02a | 0.56 |
Epididymis | 0.09±0.03 | 0.07±0.01 | 0.08±0.01 | 0.07±0.02 0 | 0.08±0.02 | 0.09±0.01 | 0 |
Accessory glands | 0.34±0.02c | 0.22±0.03d | 0.45±0.03b | 0.24±0.01d | 0.54±0.01a | 0.34±0.01c | 0 |
Vas deferens | 0.04±0.01b | 0.03±0.01c | 0.05±0.01a | 0.03±0.01c | 0.05±0.01a | 0.05±0.01a | 0 |
n= number of guinea pigs. (a, b, c, d, e): on the same line, the values affected by the same letter do not differ significantly (p?0.05). bw: body weight. p = probability. T0 = Neutral control (20-25 ° C + 2 ml / kg bw of distilled water). T0- = Negative control (46 ± 1 ° C + 2 ml / kg bw of distilled water). T0 + = Positive control (46 ± 1 ° C + 200 mg / kg bw of VC). AE100, AE200, AE400 = aqueous extract (mg / kg bw) + Temperatures (46 ± 1 ° C). VC: vitamin C
Table 2: Effects of Z. leprieurii fruit aqueous extract on serum reproductive hormones in heat stressed male guinea pig.
Hormones concentrations | Controls | Doses of Z. leprieurii AE (mg/kg bw) | |||||
---|---|---|---|---|---|---|---|
T0 (n=12) | T0- (n=12) | T0+ (n=12) | AE100 (n=12) | AE200 (n=12) | AE400 (n=12) | P values | |
FSH (mUI ml-1) | 8.68±0.06d | 5.67±0.05f | 6.43±0.16e | 9.79±0.05b | 9.61±0.10c | 10.59±0.06a | 0 |
LH (mUI ml-1) | 1.09±0.02bc | 0.98±0.02cd | 1.38±0.01a | 1.23±0.27ab | 1.33±0.04a | 0.85±0.07d | 0 |
Testostérone (ng ml-1) | 0.55±0.02b | 0.38±0.03c | 0.43±0.02c | 0.42±0.01c | 1.27±0.06a | 0.55±0.04b | 0 |
n = number of guinea pigs. (a, b, c, d, e, f): on the same line, the values affected by the same letter do not differ significantly (p?0.05). bw: body weight. p = probability. T0 = Neutral control (20-25 ° C + 2 ml / kg bw of distilled water). T0- = Negative control (46 ± 1 ° C + 2 ml / kg bw of distilled water). T0 + = Positive control (46 ± 1 ° C + 200 mg / kg bw of VC). AE100, AE200, AE400 = aqueous extract (mg / kg bw) + Temperatures (46 ± 1° C). VC: vitamin C.
Effect of Z. leprieurii on sperm characteristics in guinea pig exposed to high temperature
Table 3 presents the effects of Z. leprieurii fruit aqueous extract on the characteristics of epididymal spermatozoa in the male guinea pig subjected to heat stress. It shows that the mobility, concentration and membrane integrity of the sperm decreased significantly (p <0.05), in guinea pigs subjected only to thermal stress compared to neutral controls. With respect to negative control, the vitamin C and Z. leprieurii fruit aqueous extract whatever the dose considered led to a significant increase (p <0.05), of these sperm characteristics.
Histological structure of the testes
Figure 1 Histological structures of testes in guinea pigs exposed to thermal stress and treated with Z. leprieurii fruit aqueous extract (HE x 400). St: seminiferous tube; Lst: lumen of the seminiferous tube; Is: interstitial space; Spm: sperm; GE: Germinal epithelium.T0 = Neutral control (20-25 ° C + 2 ml / kg bw of distilled water); T0- = Negative control (46 ± 1 ° C + 2 ml / kg bw of distilled water); T0 + = Positive control (46 ± 1 ° C + 200 mg / kg bw VC); AE100, AE200, AE400 = aqueous extract (mg / kg bw) + Temperatures (46 ± 1 ° C); VC: vitamin C; bw: body weight.Histological structures of testes in guinea pigs exposed to thermal stress and treated with Z. leprieurii fruit aqueous extract (HE x 400). St: seminiferous tube; Lst: lumen of the seminiferous tube; Is: interstitial space; Spm: sperm; GE: Germinal epithelium.T0 = Neutral control (20-25 ° C + 2 ml / kg bw of distilled water); T0- = Negative control (46 ± 1 ° C + 2 ml / kg bw of distilled water); T0 + = Positive control (46 ± 1 ° C + 200 mg / kg bw VC); AE100, AE200, AE400 = aqueous extract (mg / kg bw) + Temperatures (46 ± 1 ° C); VC: vitamin C; bw: body weight.
Figure 1 illustrates the effects of Z. leprieurii fruit aqueous extract on testicular structures in male guinea pigs subjected to thermal stress. In neutral control animals (T0), the architecture of the seminiferous tubes was normal. From the membrane to the lumen of the tubes, germ cells are observed at different stages of development. The lumen of the tubes contains many mature sperms. This cellular arrangement was disturbed in the T0- (negative control), guinea pigs where the lumen of the seminiferous tubes and the interstitial spaces showed degradation of the various cells. In heat stressed cavies treated with Z. leprieurii fruit aqueous extract or vitamin C, the absence of anomaly noted in negative control was recorded. Briefly, the seminiferous tubes were more structured and there were mature germ cells in the lumen.
Effect of Z. leprieurii and Z. leprieurii fruit aqueous extract on Heat Shock Protein in male guinea pig exposed to heat stress
Figure 2 Effects of Z. leprieurii fruit aqueous extract on the serum concentration of HSPs in the male guinea pig subjected to heat stress. (a, b, c, d): on the same histogram, the bars affected by the same letter do not differ significantly (p?0.05). T0 = Neutral control (20-25 ° C + 2 ml / kg bw of distilled water). T0- = Negative control (46 ± 1 ° C + 2 ml / kg bw of distilled water). T0 + = Positive control (46 ± 1 ° C + 200 mg / kg bw VC). AE100, AE200, AE400 = aqueous extract (mg / kg bw) + Temperatures (46 ± 1 ° C). VC: vitamin C. bw: body weight.
Figure 2 illustrates the variation in the serum concentration of HSP 40 in animals subjected to heat stress and treated with Z. leprieurii fruit aqueous extract. It appears that the serum concentration of HSP 40 significantly (p <0.05) decreased in the animals subjected to heat stress compared to the neutral controls. The oral administration of vit C and Z. leprieurii fruit aqueous extract at doses of 200 and 400 mg / kg bw resulted in a significant increase (p <0.05) in the serum level of HSP 40 compared to the negative control. However, these values remain significantly (p <0.05) lower than those recorded in the neutral controls.
Table 3: Effects of Z. leprieurii fruit aqueous extract on the characteristics of epididymal spermatozoa in the male guinea pig subjected to heat stress.
Caudal epididymal sperm characteristics | Controls | Doses of Z. leprieurii AE (mg/kg bw) | |||||
T0 (n=12) | T0- (n=12) | T0+ (n=12) | AE100 (n=12) | AE200 (n=12) | AE400 (n=12) | P valu es | |
Mobility (%) Number/ | 73.33±0.58c | 23.33±0.58f | 55.02±0.91e | 66.33±0.58d | 85.02±0.00a | a 79.25±0.96b | 0 |
cauda epididymis (x107) | 6.19±0.37b | 2.11±0.14d | 4.63±0.32c | 4.52±0.18c | 6.25±0.35ab | 6.67±0.38a | 0 |
Number/g of epididymal tail (x106) | 42.24±0.35b | 15.21±0.21f | 23.22±0.58e | 46.38±0.46a | 27.66±0.63d 3 | 34.95±0.23c | 0 |
Membrane integrity | 66.75±0.51b | 19.25±0.87e | 52.51±0.58d | 55.25±0.65c | 75.02±0.86a | 65.22±0.84b | 0 |
n = number of guinea pigs. (a, b, c, d, e, f): on the same line, the values affected by the same letter do not differ significantly (p?0.05). bw: body weight. p = probability. T0 = Neutral control (20-25 ° C + 2 ml / kg bw of distilled water). T0- = Negative control (46 ± 1 ° C + 2 ml / kg bw of distilled water). T0 + = Positive control (46 ± 1 ° C + 200 mg / kg bw of VC). AE100, AE200, AE400 = aqueous extract (mg / kg bw) + Temperatures (46 ± 1° C). VC: vitamin C.
leprieurii fruits aqueous extract heat stressed animals resulted in a significant increase in the weight of the genital organs and the serum concentrations of reproductive hormones. These results are similar to those obtained by Emtenan et al. [3], and Roy et al. [22], in rats, treated with the aqueous extract of Ferula hermosis at the dose of 0.025 ml /100 g bw, and the methanolic extract of Mallotus roxburghianus at the dose of 400 mg/kg, respectively. These observations can be explained by the action of antioxidant compounds such as phenols, flavonoids, tannins, terpenoids and saponins present in the Z. leprieurii fruit aqueous extract. According to Hodek et al. [27], molecules with antioxidant properties neutralize free radicals or inhibit the enzymes responsible for their production. This effect protects animal cells including testis cells against reactive oxygen species attacks and increases their size and their secretory function [28]. In the other hand, Androgens and more particularly testosterone have anabolic properties characterized by the increase in protein synthesis and consequently the increase in muscle mass. One of the roles of androgens is to increase the volume and weight of the testis and epididymis by stimulating protein synthesis [29]. The increase in testosterone concentration recorded following the administration of the aqueous extract in this study would induce the elevated weight of reproductive organs.
The density and mobility of sperm are considered to be the interesting sperm characteristics in animals to evaluate it fecundity [30]. The results of this work have shown a decrease in sperm concentration, mobility and membrane integrity in male cavies exposed to heat stress. These results are similar to those reported by Mishra et al. [31], in bulls (jersey), subjected to high temperature levels (25-35°C; 35°C and more), Abshenas et al. [14] in mice whose scrotum was subjected to heat stress at 42°C. Heat stress affects both mobility and density of spermatozoa [2,32], and induces azoospermia or oligospermia in animals [11]. In this study, the decline in sperm characteristics would be the result of disintegration of the plasma membrane and DNA of the sperm as a consequence of ROS attacks. Indeed, the plasma membrane of sperm is rich in polyunsaturated fatty acids [33, 34]. These characteristics make them vulnerable to radical attacks.
In the present work, the administration of the Z. leprieurii fruit aqueous extract at 100, 200 or 400 mg/kg bw protects the membrane of the spermatozoa, but also an increase in sperm concentration and mobility in heat stressed animals. These results corroborate those of Abshenas et al. [14], in mice subjected to 42°C for 49 days and treated with methanolic extract of Camellia sinensis at doses of 500 and 750 mg/kg bw. These effects observed in the present study is linked to the Z. leprieurii bioactive molecules with antioxidant properties, which have reduced or prevented the attacks of sperm by free radicals.
Hyperthermia induces the synthesis of “heat shock proteins” (HSP), most of which are chaperone molecules which are normally overexpressed by cells in response to inducible signals which can lead to proteins denaturation [35]. However, at a certain degree of temperature (generally from 42°C), there is inhibition of the synthesis of HSPs with the main consequence of an exponential increase in cellular apoptosis [36]. Exposure of the animals to 46°C revealed a significant drop in the serum concentration of HSPs 40. The administration of the Z. leprieurii fruit aqueous extract at 200 and 400 mg/kg bw concomitantly with the exposure of animals to 46 ºC considerably reduced the influence of heat stress on the serum concentrations of HSPs 40. This effect would result of the antioxidant property of the Z. leprieurii fruit aqueous which have reduced the stress in hyperthermia situation and subsequently avoid the cell deterioration.
CONCLUSION
The results of this study revealed that heat stress caused impairment of reproductive characteristics in male cavies, illustrated by markedly impairment in the testes structure and sperm characteristics, decreased of reproductive hormone concentrations and serum concentration of Heat Shock protein 40. The administration of Z. leprieurii fruit aqueous extract efficiently improved cavy reproductive characteristics. Based on these effects, the Z. leprieurii fruit aqueous extract at 200 and 400 mg/kg bw can be used in male animals to improve its reproductive performances.
ETHICS STATEMENT
All experiments were carried out in compliance with the recommendations Guide of the National Academy of Sciences on the care and use of laboratory Animals (NAS, 2013), and approved by the department of animal science.
FUNDING
The authors received no funding from an external source.
REFERENCES
1. Intergovernmental Panel on Climate Change IPCC. Climate Change: Synthesis Report; Summary for Policymakers. 2015.
4. Vale WG. Effects of environment on buffalo reproduction. Ital J Animal Sci. 2007; 6: 130-142.
6. Stearns SC. The Evolution of life histories. Oxford University Press; 1992.
17.Abdou BA. Contribution to the study of a functional food based on spices from Cameroon: Physico-chemical and functional characterization. Thèse de Doctorat PhD, Université de Ngaoundéré. 2009; 117.
19.Jirovetz L, Buchhauer G, Ngassoum M. Investigation of the essential oil from the dried fruits of Xylopia aethiopica (West African peppertree) and Xylopia parViflora from Cameroon. Ernaehrung. 1997; 21: 324- 325.
28.Gayrard V. Production et transport des spermatozoïdes. In: Physiologie de la reproduction des mammifères. 2007; 97-110.
30.Mishra SR, Kundu AK, Mahapatra APK. Effect of ambient temperature on membrane integrity of spermatozoa in different breeds of bulls. The Bioscan. 2013; 8: 181-183.
32.Hwang K, Lamb DJ. Molecular mechanisms of male infertility. In: Parekattil, S.J., Agarwal,
33.(Eds.), Male Infertility. Springer, New York. 2012.