Prevention of estrus in sow and ruminants
Embodiments of the present invention provide a pharmaceutical intervention in neonatal to infantile pigs, ruminants, and other livestock that inhibits the activation of the HPG axis, growth of the gonads and inhibits gonadal production of sex hormones, which will prevent the estrous cycle until the age at slaughter. The invention comprises treatment with estrogen or estrogen in combination with androgen in the newborn to infantile females using extended drug delivery methods, with a defined duration of between 1-4 months or infantile period of growth, for the purpose of the prevention of the estrous cycle in female production animals. The drug delivery component may consist of biocompatible polymers in the form of pellets, microspheres, or gels, or in solvents or solutions (hereafter, drug complex). The invention embodies neonatal to infantile period treatment with a drug complex consisting of a hormone-based compound configured to inhibit development and function of hypothalamic Kisspeptin neurons, pituitary release of luteinizing hormone/follicle stimulating hormone and postnatal development of the ovary through the use of sustained but temporary release of the compounds into the body of an animal once the drug-carrier has been injected or implanted therein.
1 . A method for preventing the estrous cycle in the female pig or ruminants, which prevents the pubertal development of ovary, ovarian follicles, and production of estrogen until slaughter, comprising administering to said sow or ruminants a combination of an estrogen and androgen within a few weeks or months after birth during the neonatal to infantile period.
2 . The method of claim 1 , female ruminants include doe, heifer, ewe, and other female livestock.
3 . The method of claim 1 , wherein the administration is by subcutaneous injection, intra-muscular injection, or by nasal inhalation.
4 . The method of claim 1 , further comprising an implant wherein the implant comprises said estrogen and androgen.
5 . The method of claim 1 , wherein the estrogen and androgen target hypothalamus-pituitary axis and ovary development, respectively.
6 . The method of claim 4 , wherein the implant comprises a material or enclosure that provides sustained release of the compounds over during the neonatal/infantile period.
7 . The method of claim 1 , wherein the injected estrogen and androgen are not present in the blood or tissues when the animals are slaughtered for meat production.
8 . The method of claim 5 , wherein the material or enclosure that provides sustained release comprises biodegradable polymers or biocompatible materials.
9 . The method of any one of claim 5 , wherein the material or enclosure that provides sustained release is a form of capsule, pellets, microspheres, gel, or solution.
10 . The method of claim 1 , wherein the estrogen comprises estrogenic compounds selected from the group consisting of estradiol benzoate, estradiol valerate, and estradiol cypionate, with a dose range of 0.1-2 mg/kg bodyweight.
11 . The method of claim 1 , wherein the androgen comprises testosterone, testosterone esters, androstenedione, trenbolone, trenbolone esters, 5α-dihydrotestosterone, 5α-dihydrotestosterone esters, synthetic androgens that has androgenic activity, or equivalents with the dose range of 1-20 mg/kg bodyweight.
12 . The method of claim 1 , wherein the injected amount of the estrogen/androgen combination is in a dose sufficient to inhibit kisspeptin neurons in the hypothalamus, LH/FSH production in the pituitary, follicle development and production of estrogen in the ovary.
13 . The method of claim 8 , wherein the material or enclosure comprises silicone.