While there are no magic elixirs that can replace the need for sound management and husbandry, producers can use various hormonal treatments to help maintain reproductive efficiency. These hormonal treatments can be used to induce puberty and synchronize estrus in gilts, minimize the wean-to-estrus interval in sows, and treat the anestrous condition in gilts and sows. To effectively use these hormonal treatment strategies, a clear understanding of the interrelationships among reproductive hormones is necessary.
This publication gives a brief overview of the reproductive anatomy of the female and addresses how the hormones involved in female reproduction change and influence one another during an estrous cycle. Also, several hormonal treatments that can be used to manipulate the estrous cycle of swine are discussed.
The hypothalamus, which is located at the base of the brain, produces and secretes gonadotropin-releasing hormone (GnRH). This hormone stimulates the release of follicle- stimulating hormone (FSH) and luteinizing hormone (LH) from the anterior pituitary gland. GnRH production and release from the hypothalamus are controlled by hormonal feedback from the ovaries.
The pituitary gland, located beneath the hypothalamus, is divided into an anterior and posterior portion. The anterior pituitary synthesizes and secretes FSH and LH. FSH stimulates follicle growth of the ovaries and estrogen release from the ovaries. LH is responsible for the release of eggs from the follicles (ovulation) and the development, maintenance, and function of the corpus luteum, or yellow body. Because the pig is a multiparous species (gives birth to multiple offspring), there will be several corpora lutea present on each ovary.
The posterior portion of the pituitary gland is responsible for the release of oxytocin, which is involved in farrowing (parturition) and milk ejection.
The ovaries are a part of the female reproductive tract that is located in the abdominal and pelvic cavities. The ovaries produce the eggs and the two classes of female sex hormones, estrogens (the most important being estradiol) and progestins (the most important being progesterone). Each egg develops within a fluid-filled follicle located on the ovary. These follicles produce estradiol. At the time of ovulation, the wall of each mature follicle ruptures, and an egg with the surrounding fluid is released into the tubular part of the reproductive tract. The cells remaining in each ruptured follicle grow and fill the empty space left by the ovulated egg and fluid, forming a corpus luteum. Each corpus luteum produces progesterone.
Estradiol is involved in mating behavior, secondary sex characteristics, maintenance of the female duct system, and mammary growth. Progesterone is responsible for the maintenance of pregnancy and is also involved in mammary growth.
The oviduct is the portion of the reproductive tract that receives the eggs after ovulation. It has a funnel-shaped portion located close to the ovary called the infundibulum, which aids in the entry of the eggs into the oviduct. The oviduct is the site where fertilization of the eggs occurs. Fertilized eggs remain in the oviduct approximately 2 days before they enter the uterus.
The uterus in swine consists of a short uterine body and two long uterine horns. Before implantation, the uterus secretes proteins, carbohydrates, and lipids that provide nourishment for the preimplantation embryo. Following implantation, nourishment for the developing embryo is provided by the blood supply of the dam to the embryonic membranes (placenta) that are attached to the uterine wall. The nutrients are then transported to the embryo by the umbilical vein.
The uterus is the major source of prostaglandin F-2 alpha (PGF) in the pig. This hormone is involved in regulating the life span of the corpora lutea in cycling and pregnant gilts and sows. At the time of farrowing, PGF (and oxytocin) stimulates uterine contractions, which are involved in expulsion of the newborn pigs.
The cervix is located between the uterus and vagina and consists of muscular and dense connective tissue. Typically, the cervical opening into the body of the uterus is small and plugged with cervical mucus. At farrowing the walls of the cervix relax, allowing the pigs to pass from the uterine horns into the vagina. The cervix also serves as the site of semen deposition. During mating the cervix constricts around the boar's penis, and this pressure is the stimulus that causes the boar to ejaculate.
The tubular portion of the tract leading posterior from the cervix to the urethral opening is the vagina. The visible, external portion of the tract is referred to as the vulva. When the female approaches or is in standing heat (the period when she is receptive to the boar), the vulva will often become red and swollen.
The hormonal changes associated with puberty are poorly understood. Research shows that many of the hormonal events associated with estrus can occur before the age when gilts normally exhibit estrus. For example, the hypothalamus can secrete GnRH, the anterior pituitary can secrete FSH and LH, and ovulation can be stimulated to occur well before gilts are old enough to begin exhibiting estrus. Puberty is attained only when these individual events begin to occur at regular
intervals and when the gonadotropins (FSH and LH) are produced at high enough levels to initiate follicle growth, oocyte (egg) maturation, and ovulation.
Figure 1. Changes in reproductive hormones throughout the estrous cycle. (LH = luteinizing hormone; FSH = follicle-stimulating hormone; PGF = prostaglandin F-2 alpha; GnRH = gonadotropin-releasing hormone.)
Figure 2. Interactions among the female reproductive hormones.
Around days 12 to 14 of the estrous cycle, progesterone concentrations begin to decline. If the female is not pregnant at this time, PGF is released from the uterus and causes the rapid regression or destruction of the corpora lutea (a process called luteolysis). With the destruction of the corpora lutea, progesterone levels rapidly decline, and their inhibitory control on the growth of follicles is removed. Following luteolysis, a slight increase in FSH secretion and an increase in the number of LH pulses occur that stimulate follicular growth. This part of the estrous cycle is called the follicular phase. As the follicles develop, they produce estradiol, which increases steadily during the latter stages of the estrous cycle. Once estradiol concentrations reach a high enough level, the preovulatory surge of FSH and LH occurs, and ovulation follows. Estradiol is also responsible for the characteristic responses of a gilt or sow in estrus or standing heat (swollen and red vulva, immobile stance, and erect ears).
To effectively stimulate puberty in gilts, it is critical to know the pubertal status in a group of gilts and the typical age of the onset of puberty under the conditions of the specific farm. Puberty usually occurs in gilts at 6 to 7 months of age, but it can vary considerably based on the genetics and management of the gilts. Gilts should not be treated with hormones to induce puberty unless they are within 1 month of the natural onset of estrus. If gilts are too young, estrus might be induced,
but they will often return to an anestrous state. If gilts are within 30 days of the natural onset of puberty, most will respond to treatment with gonadotropins by expressing estrus and continuing to cycle.
Puberty in gilts can be induced by treatment with a single 5-ml injection of P.G.600® (Intervet Inc.). This compound is a combination of pregnant mare serum gonadotropin (PMSG; 400 IU) and human chorionic gonadotropin (hCG; 200 IU). PMSG mimics the reproductive hormone FSH and results in follicular growth, increased levels of estradiol, and estrus. The hCG component of P.G.600 mimics the hormone LH that leads to ovulation. Numerous studies have shown that a high percentage (50 percent to 70 percent) of prepubertal gilts injected with P.G.600 will exhibit estrus within 7 days following treatment (Figure 3).
Figure 3. Inducing puberty in gilts with P.G.600. Prepubertal (noncycling) gilts are given P.G.600 at 5 to 6 months of age (within 1 month of the natural onset of puberty).
The lack of response to treatment with P.G.600 is most often associated with treating gilts that have already reached puberty. Cycling gilts will not respond to P.G.600 during the luteal phase of the estrous cycle because of the negative feedback of progesterone. The benefits of P.G.600 treatment if gilts are injected during the follicular phase of the estrous cycle are questionable because estradiol concentrations have already begun to increase, leading to higher levels of FSH and LH.
Because producers typically do not breed gilts at the time of puberty, an effective means of synchronizing the second estrus period would be beneficial. While P.G.600 can be used to effectively induce puberty in a group of gilts, all of the gilts may not return to heat at the same time in subsequent periods due to variations in length of estrous cycles.
A strategy that one could theoretically use to resynchronize the second estrus in P.G.600-treated gilts is to give a luteolytic dose of lutalyse (PGF; 2-ml) approximately 18 days after inducing puberty with a single 5-ml injection of P.G.600 (Figure 4). The corpora lutea in pigs will not undergo luteolysis in response to a luteolytic dose of lutalyse during the first 12 days of the estrous cycle. However, beyond day 12 of the estrous cycle, lutalyse will cause the corpora lutea to regress, leading to a decrease in the concentration of progesterone, followed by follicular growth, estrus, and ovulation. Therefore, one can speculate that giving a single injection of lutalyse to a group of gilts 18 days after P.G.600 treatment should result in a more synchronous second estrus.
Figure 4. Synchronizing the second estrus in gilts with P.G.600 and lutalyse (PGF). Prepubertal (noncycling) gilts are given P.G.600 to induce puberty and then given a luteolytic dose of PGF 18 days later.
It should be noted that research has not been conducted to document the effectiveness of this hormonal treatment strategy.
Once gilts have begun cycling, the combination of P.G.600 and PGF is not an effective treatment for synchronizing estrus. In circumstances where the cyclic status of gilts is not known, or if it is known that most gilts are cyclic, one can synchronize estrus by pen-mating for 3 weeks and giving a 2-ml injection of lutalyse 2 weeks later (Figure 5). Research has shown that lutalyse is effective for inducing luteolysis, abortion, and a prompt return to estrus (typically within 3 to 7 days) in pregnant gilts beyond the second week of gestation and that subsequent fertility is acceptable if gilts are aborted during the first trimester. Although this method of estrus synchronization can be used successfully, it can increase the age at first farrowing and nonproductive days because gilts are bred at an age that is approximately equal to the age at third estrus rather than second estrus. Furthermore, many producers are hesitant to abort gilts after they have become pregnant.
Figure 5. Synchronizing estrus in cycling gilts with pen-mating and lutalyse (PGF). Cycling gilts are pen-mated for 3 weeks and then given a luteolytic dose of PGF 2 weeks later.
Another approach for synchronizing estrus in gilts that have attained puberty is to feed a progestin for 14 to 18 days. The progestin inhibits maturation of follicles and estrus while permitting the corpora lutea to regress naturally. After the progestin is withdrawn, the follicles mature, and estrus occurs within approximately 3 to 7 days. Studies demonstrate that feeding the progestin altrenogest (Regumate) at a rate of 15 to 20 mg per day for 14 to 18 days is effective for synchronizing estrus in cyclic gilts (Figure 6) and that subsequent litter size is not adversely affected. Unfortunately, this compound does not have Food and Drug Administration (FDA) approval for use in swine.
Figure 6. Synchronizing estrus in cycling gilts with altrenogest (Regumate). Cycling gilts are fed Regumate for 18 days.
As the time of weaning has been reduced from 35 to 42 days of age to 18 to 24 days of age, a higher percentage of sows have become anestrus or have experienced a delayed return to estrus after weaning. This appears especially true for the more prolific, modern, high-lean-growth genotypes. Also, these conditions are more likely to occur during the summer and fall months and are most common in first-litter sows.
A strategy for improving the weaning-to-estrus interval and reducing the anestrus condition in weaned sows is to administer a 2-ml injection of lutalyse within 24 hours after farrowing and to inject a 5-ml dose of P.G.600 to sows at the time of weaning (Figure 7). Additional benefits of the lutalyse treatment after farrowing for the current litter include reduced mortality in newborn pigs and heavier pigs at weaning.
Figure 7. Inducing a prompt return to estrus in weaned sows. Sows are given an injection of lutalyse shortly after farrowing and an injection of P.G.600 at the time of weaning.
The mechanisms by which these compounds improve sow reproductive performance are not completely understood. It is thought that lutalyse has a "cleaning out" effect on the sow's reproductive system by aiding in the expulsion of the tissues associated with pregnancy (placenta). Lutalyse treatment may improve litter weight gains in the current litter by a more rapid removal of the corpora lutea of pregnancy. This would be accomplished by earlier luteolysis and a more rapid removal of the negative effect that progesterone has on milk production. The administration of P.G.600 at the time of weaning most likely reduces the incidence of anestrus by stimulating follicular growth, thus increasing the concentration of estradiol.
None of the strategies discussed in this publication should be expected to achieve a 100 percent success rate. Also, these treatments will not likely be effective if used in an attempt to cover poor management and husbandry. However, when used correctly, the outcome from these hormonal treatments should be satisfactory.
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