Effect of Repeated GnRH Injection and Intra-vaginal Mechanical Stimulation on Reproductive Performance of Doe Rabbits
Various hormonal treatments were used for induction of ovulation to increase fertility of rabbits. Aim of the present study was to investigate the effect of repeated GnRH injections or Intra-Vaginal Mechanical Stimulation (IVMS) at mating for six consecutive litters, on fertility of naturally mated New Zealand White rabbit does. Does failed to kid after one service were mated in the next parity. Kindling Rate (KR), Number of Total (NTB) and Live Borns (NLB), Viability Rate (VR) and average Kit Weight (AKW) at birth as well as Gestation Period Length (GPL) were recorded after kidding for six consecutive parities. Also, concentrations of Follicle Stimulating Hormone (FSH) and Luteinzing Hormone (LH) were determined after mating of the 2nd litter. Results reveled that GnRH treatment showed highest (p<0.05) KR (71.4%), NTB (6.16/litter), NLB (5.53/litter) and VR (89.8%) and shortest (p<0.05) GPL (30.93 d). However, IVMS showed highest (p<0.05) AKW (66.59 g). Highest (p<0.05) VR was at the 1st and 2nd parity (87.5 and 84.5%), lowest at the 3rd parity (73.8%) and modest between 4th-6th parity. At 2, 3 and 4 h post-mating, FSH concentration was 12.04, 12.90 and 9.58 ng mL-1, while LH concentration was 16.0, 10.38 and 9.63 ng mL-1, respectively. The current study indicated that repeated injection with 0.2 mL GnRH analogue/doe (Receptal) at mating for 6 consecutive litters resulted in the best reproductive performance of rabbit does, leading to improving fertility of NZW does.
May 25, 2011; Accepted: July 02, 2011;
Published: September 05, 2011
In rabbits, ovulation is a neuroendocrine reflex that is physiologically induced
at the condition of natural breeding. The mechanisms whereby rabbit does become
spontaneous ovulators are still unclear, but are likely associated to factors
interfering with the control of the gonadal axis involving the hypothalamic
centers responsible for GnRH release (Theau-Clement et
al., 2008). The application of some of the exogenous hormonal substances
may cause fertility disorders in does. For example, equine Chorionic Gonadotropin
(eCG) is known to reduce fertility due to immunogenicity if used routinely (Rebollar
et al., 2006).
Ovulation has to be induced artificially in does by intramuscular injection
of either Gonadotropin-releasing Hormone (GnRH), or its synthetic analogues
(Moce et al., 2003; Rommers
et al., 2004; Quintela et al., 2004).
Highly potent, long-acting synthetic analogue of GnRH have been produced and
is available commercially (e.g., gonadoreline, buserelin, fertirelin acetate,
desloreline and fertagyl. These compounds proved a new tool for inducing endogenous
Follicle-Stimulating Hormone (FSH) and Luteinzing Hormone (LH) release and induce
ovulation in all mammalian species (Taponen et al.,
2003). In this concern, Bonanno et al. (2008)
induced ovulation in rabbits at Artificial Insemination (AI) by intramuscular
(i.m) injection of 0.8 μg of synthetic GnRH (buserelin).
In addition, ovulation can be induced by the sight of a sexually active male,
by mating with a vasectomized male, a female mounting another female (Laborda
et al., 2008). Also, mechanical stimulation of rabbit vagina could
be used as a tool of increasing fertility as a routine work in rabbit farms
in Egypt. Unfortunately, there is no information in the literature on the effect
of intravaginal mechanical stimulation on reproductive performance of rabbits.
Therefore, the objective of this study was to evaluate the reproductive performance of NZW rabbit does at 6 consecutive litters as affected by the repeated stimulation of ovulation by GnRH injection as a tool to mimic hypothalamic stimulation for multiple asynchronous ovulations, or intra-vaginal mechanical stimulation at mating.
MATERIALS AND METHODS
Animals and management: The experimental work was carried out in a private Rabbit Production Farm in Zian location, Dakahlyia governorate, Egypt, during the period from August 2009 to March 2010. Total of 63 virgin New Zealand White (NZW) rabbit does (7-8 months of age and 3.5-3.85 kg body weight) as well as 18 fertile NZW rabbit bucks (10-13 months of age and 4-4.25 kg body weight) were used in the present study. All animals were healthy and clinically free of external parasites.
All does and bucks were housed in a naturally ventilated building and kept individually in flat deck cages (50x60x40 cm) only for does equipped with automatic water dispensers and internal nest boxes. Animals received a commercial diet containing 10.5 MJ digestible energy per kg, 18.5% crude protein and 12.5% crude fiber according to their physiological condition. Water was provided ad libitum all over the experimental period. Average of ambient temperature during the experimental period ranged from 15.4°C in December to 30.0°C in August, while relative humidity ranged from 65% in November to 81% in August.
Does and bucks were kept under the same management system. Cages and nest boxes were cleaned and disinfected regularly before each kindling. Light in the rabbit farms was controlled to allow 14-16 h per day during the period of the study. Urine and feces dropped from the cages on the floor were cleaned every day in the morning.
Experimental design: The experimental rabbit does were divided into similar three treatment groups (21 in each) according to their live body weight. Does in the 1st group (control) were injected with 0.2 mL saline solution at mating (without treatment). Does in the 2nd group (GnRH) were intramuscularly injected at mating with 0.2 ml/doe of GnRH analogue (Receptal, Intervet International B.V. Boxmeer-Holland, each ml of Receptal contained 0.0042 mg Buserelin acetate equivalent to 0.004 mg Buserelin). In the 3rd group, vagina of each doe was stimulated mechanically immediately before mating by thermometer (IVMS). All treatments were applied at mating for six consecutive litters.
Reproductive management: On day of mating, receptive doe was transferred to the cage of buck and returned back to her own cage after mating. On day 27 of mating, the nest boxes were supplied with wooden straw to help the doe in preparing a worm comfortable nest for the kits of her litter. Does were mated 10-12 days after parturition of each litter. At the same time, does failed to kid from the previous mating in each treatment group were mated. After parturition, the size of the litter (total and live borns at birth) was recorded and rabbit kits were weaned up to the age of 35 days.
Blood samples and hormonal assay: Blood samples were taken from does
in each group at 2, 3 and 4 h after mating. Blood samples were collected by
puncture of the ear vein in heparinized clean test tubes and immediately centrifuged
(4000 g) for 15 min. Then, plasma was separated and stored at -20°C until
assay. Plasma concentrations of FSH and LH were determined in duplicate by radioimmunoassay
(RIA), using AFP- 472176 and AFP-3120489 antibodies for FSH and LH, respectively,
provided by the National Institute of Diabetes and Digestive and Kidney Diseases
(Harbor UCLA Medical Center, CA, USA). The dilutions antibody used were 1:45,000
and 1:1,500,000 for FSH and LH, respectively. Hormones were iodinated with 125I,
using the chloramine-T- method (Greenwood et al.,
1963). The assay sensitivity was 1.0 and 0.05 ng mL-1 for FSH
and LH, respectively. The intra-assay coefficients of variation, estimated from
plasma pool measured 8 times in the same assay, were <8% for both hormones.
Data recorded: Within 12 h after kindling of each litter, total number of kits (live and dead) was calculated, dead kits were removed and then size and weight of live kits were recorded. Kindling rate (number of kindled does per number of mated doesx100), viability rate (number of live per total number of kitsx100) and length of gestation period (day) were calculated.
Statistical analysis: Data obtained in this study were statistically
analyzed using computer program of SAS (2004). Factorial
ANOVA (GLM) was used to perform the effect of treatment, litter number and their
interaction different traits studied. Also, the effect of treatment, time post-mating
and their interaction only for the 2nd litter on concentration of
FSH and LH in blood plasma was performed. Multiple rang test (Duncan,
1955) was employed to test statistical differences among means at (p<0.05).
Only the significant interactions were included in the discussion.
RESULTS AND DISCUSSION
Reproductive and litter size of doe rabbits
Effect of treatment: Results presented in Table 1
reveal that stimulation of ovulation by GnRH showed significantly (p<0.05)
the higher kindling rate (71.4%), litter size per doe as a total (6.16/litter)
and live kits (5.53/litter), viability rate (89.8%), kit weight (64.11 g) and
litter weight (345.5 g as compared to 48.4%, 5.67 and 3.91/litter, 70.0%, 60.83
g and 1.76/litter in the controls, respectively). The differences between GnRH
and IVMS groups in all traits weight were insignificant, but all values were
higher for GnRH than IVMS treatment. In general, reproductive index was the
highest (3.95) for GnRH-treated does, moderate in IVMS (3.46) and the lowest
in the control (1.89).
Localization of GnRH within the hypothalamus has been well documented in rabbits
(Arimura et al., 1973) and many investigators
reported improvement in kindling of rabbit does as affected by exogenous GnRH.
||Least square means and standard errors of means (SEM) of productive
and reproductive traits of doe rabbits as affected by stimulation treatment
and does parity
|a, b and c: Means denoted within the same raw for
group or parity having different superscripts are significantly different
at p≤0.05. IVMS: Intravaginal mechanical stimulation, RI: Reproductive
index. GPL: Gestation period length
In nearly similarity with the present results, Zapletal
et al. (1990) reported that the total annual fertility rate was higher
(73.02%, p<0.05) in rabbit group treated with lecirelin (GnRH) but with higher
litter size as a total and live borns (9.82 and 9.70, respectively) than those
obtained in the present study. It has been shown that GnRH mediates the hypothalamic
control of pituitary gonadotropin secretion and biosynthesis (Dekel
et al., 1988) to induce ovulation. However, the obtained improvement
in kindling rate and litter size of rabbit does treated with GnRH as compared
to the controls in this study was also due to the effects of GnRH on the ovary
include stimulation of oocyte maturation (Dekel et al.,
1988; Yang et al., 1995).
In addition, GnRH may interfere with the stimulatory effects of exogenous gonadotropin
on follicular development, corpus luteum establishment and oocyte maturation
(Zanagnolo et al., 1996). Some studies have shown
that GnRH and its analogues also exert a direct effect on gonadal function,
influencing rabbit oocyte maturation both in vivo and in vitro
(Yang et al., 1995; Yoshimura
et al., 1992). It has been suggested that GnRH induces oocyte maturation
via activation of specific GnRH receptors on granulosa cells (Koves
et al., 1989). Exposure to GnRH stimulates prostaglandin synthesis
in preovulatory follicles (Wong and Richards, 1992).
Increasing concentration of prostaglandin plays an important role in oocyte
maturation (Calder et al., 2001). According to
these studies, GnRH treatment increased number of kits per litter and decreased
kit weight at birth (Table 1), which is in good agreement
with the finding of Zapletal and Pavlik (2008), who
reported that the conception rates ranged from 10.0 to 89.5% for different GnRH
On the other hand, buserelin or triptorelin added to seminal doses (Viudes-de-Castro
et al., 2007) have been shown to be valid methods for inducing ovulation
in rabbit does submitted to artificial insemination. However, the hormonal doses
needed were high and the kindling rates obtained were similar or lower than
those for the control group. In agreement with the results of GnRH injection
intramuscularly, Ondruska et al. (2008) found
that supplementation of insemination dose at AI with GnRH-Lecirelinum (7.5 μg)
increased kindling rate (72.09%) as compared to 62.74% in the control group
(administered i.m. with 2.5 μg same synthetic GnRH immediately after AI).
However, viability rate was not affected significantly by GnRH treatment (Ondruska
et al., 2008). The present results are nearly similar for kindling
rate with improving viability rate inspite the marked differences in level and
location of GnRH treatment. In this respect, Quintela et
al. (2004) used GnRH-buserelin in considerable higher concentrations
for intravaginal use (10 up to 20 times) compared with intramuscular control
(0.8 μg per female). Differences in kindling rate among treated groups
were not statistically significant in their experiments. After intravaginally
application of 20-times higher concentration of buserelin they obtained significantly
higher prolificacy in experimental females compared with the control (11.7 young
and 9.4 kits per litter, respectively). In conclusion, buserelin was evaluated
to determine potential negative effects on the sperm characteristics and no
detrimental effects were found on sperm motility, viability or acrosomal integrity
during 24 h of sperm incubation at 16°C. According to the previous results
and those obtained in our study, GnRH treatment to induce ovulation in rabbits
is depending on type of analogue, does of GnRH and location of treatment.
The obtained results clearly demonstrated that the GnRH analogue (buserelin) i.m. injected was extremely efficient, significantly increasing kindling rate and viability rate of kits at birth for 6 successive litters in comparison with IVMS and control.
Effect of parity: Results in Table 1 show that only viability rate of kits and litter weight at birth significantly (p<0.05) affected by parity. However, kindling rate, litter size (total and live), kit weight and gestation period were not affected significantly by parity. Generally, most of the studied traits were the highest at the 2nd parity and the lowest at the 3rd one.
Inspite the insignificant differences in kindling rate at different parities,
rabbit does showed pronounced increase in kindling rate from 66.7 % at the 1st
parity to 71.4% at the 2nd one and decreased to 57.1% at the 3rd
parity, then insignificantly increased with progress of parity up to 68.3%,
at the 6th parity. The noted increase in kindling rate and litter
size at the 2nd compared with 1st parity may be due to
linkage between pseudo-pregnant does and parity. In this respect, Theau-Clement
et al. (2008) recorded increasing the percentage of pseudo-pregnant
does in primiparous (31.2%) than in secondiparous does (12.2%, p<0.001).
|| Interaction between treatment and parity for number of live
kits at birth
|| Interaction between treatment and parity for viability rate
Yet, the components of litter size have been studied by genetic (Argente
et al., 1997) and phenotypic (Santacreu et
al., 1992) points of view.
Analysis of variance revealed that the effect of interaction between treatment and parity was significant (p<0.05) only on number of live kits/litter and viability rate, reflecting nearly similar trend of change (p<0.05) in GnRH and IVMS groups as compared to control group (Fig. 1, 2).
At the 1st and 2nd parities, number of live kits (Fig. 1) was significantly (p<0.05) greatest (6.09 and 6.14/litter), followed by IVMS (4.90 and 5.00/litter), and the lowest in control group trend (4.19 and 4.33/litter). At the 3rd parity, live kits decreased in GnRH and IVMS groups to the lowest values (4.67 and 3.90/litter, respectively) versus slight increase to the highest values (4.52/litter) in control group, but the differences were not significant. At the 4th parity, live kits showed marked increase to 5.67/litter in GnRH and to 5.81/litter in IVMS groups, being significantly higher than 2.95/litter in control group. At the 5th and 6th parities, live kits were significantly (p<0.05) higher in both GnRH (5.19 and 5.43/litter) and IVMS (5.28 and 5.57/litter) groups than in control group (3.67 and 3.81 /litter).
Regarding viability rate of kits, results illustrated in Fig. 2 show that at the 1st parity, viability rate was 84.69, 86.69 and 89.39% in control, GnRH and IVMS groups, respectively and the differences were not significant. Then, it showed similar trend to that of number of live/litter at subsequent parities. Viability rate was significantly (p<0.05) the highest at the 2nd, 3rd and 4th parities in GnRH group (99.21, 75.55 and 93.43%, respectively) and at the 5th and 6th parities in IVMS group (89.32 and 90.43%, respectively). Yet, kits of the control group showed significantly (p<0.05) the lowest viability at all parities, except for the 3rd one.
Based on the previous results of parity effect, GnRH treatment or IVMS at mating for 6 successive litters had beneficial effects on fertility and viability of kits at birth.
Concentration of gonadotrophins: Results in Table 2
show that stimulation of ovulation by GnRH led to significant (p<0.05) increase
in concentration of FSH and LH in blood plasma to 16.71 and 16.57 ng mL-1
as compared to 5.79 and 9.23 ng mL-1 in the control, respectively.
However, IVMS significantly (p<0.05) increased only FSH concentration as
compared to the control (14.02 vs. 5.79 ng mL-1).
|| Effect of type of stimulation and sampling time after mating
on concentration of FSH and LH in blood plasma of rabbit does
|a, b and c: Means denoted within the same column
for each effect having different superscripts are significantly different
at p<0.05. IVMS: Intravaginal mechanical stimulation
As affected by mating time, FSH concentration significantly decreased 4 h post-mating,
however, LH concentration showed significant decrease 3 h post-mating. At 2,
3 and 4 h post-mating, FSH concentration was 14.04, 12.90 and 9.58 ng mL-1,
while LH concentration was 16.0, 10.38 and 9.63 ng mL-1, respectively.
The insignificant interaction between treatment and mating time on concentration of both FSH and LH was reflected in the highest concentration in GnRH treatment 2 h post-mating.
In this study the changes occurring in plasma LH and FSH concentrations 2,
3 and 4 h post- mating may explain ovulation rate and litter size. The reproductive
hormone profile of FSH and LH in rabbit does have been studied at mating by
Ubilla et al. (1992, 2000
a,b). The FSH may influence the follicular growth;
meanwhile LH may determine the number of breakage of pre-ovulatory follicles.
According our results, there was association between FSH and LH peaks. Similar
findings were reported by Muelas et al. (2008)
and Rodriguez et al. (1989).
Many authors observed that the highest LH and FSH concentrations reached 60-90
min after exogenous administration of GnRH, decreasing to basal concentrations
4-5 h later (Mills and Gerardot, 1984; Rodriguez
et al., 1989; Rebollar et al., 1997).
In agreement with our results concerning the FSH, Muelas
et al. (2008) did not find change in FSH concentration 48 h before
or after mating and 2 h after mating. Also, Ubilla et
al. (2000b) did not find any difference in FSH concentrations between
48 h before and 7 h after AI. However, the present trend of change in LH was
comparable with that observed on rabbits by Muelas et
al. (2008), who found significant differences among LH plasma concentrations
measured 48 h before or after the mating (5.1 and 5.4 ng mL-1, respectively)
vs. 2 h after the mating (29.0 ng mL-1). Similar trend was
observed by Ubilla et al. (2000a). In accordance
with the marked increase in LH concentration in GnRH-treated does, Rodriguez
et al. (1989) showed that LH level sharply increased after 15 min
of GnRH challenge, being 200-1000%, depending on sexual receptivity of does
and GnRH dose. However, Muelas et al. (2008) found that
the LH levels were 4-6 fold higher 2 h after the mating in does with high ovulation
rate, which may explain the highest litter size of GnRH-treated does as compared
to the control group. In addition, This may explain the higher ovarian stimulation
and pituitary responsiveness after GnRH biostimulation. The pronounced reduction
in litter size with advancing parity may be related to that the response of
circulating FSH to active immunization against GnRH. In several species, active
immunization against GnRH consistently decreased LH secretion to undetectable
levels (Garza et al., 1986; Ondruska
et al., 2008).
Based on the foregoing results, stimulation of ovulation in rabbit does by 0.2 mL GnRH (receptal)/doe at mating for 6 consecutive litters can be successfully used to improve fertility of rabbits and their litter weight. Also, intra-vaginal mechanical stimulation at mating could have some advantages on rabbit fertility by avoiding the intramuscular application of GnRH analogues and probably reducing the sanitary risk derived from incorrect use of needles. Further studies are necessary for determining an optimal level of GnRH analogue at different times of mating in relation with the physiological status of rabbit does at the moment of mating.
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