| PATENT ASSIGNEE'S COUNTRY | USA |
| UPDATE | 12.00 |
| PATENT NUMBER | This data is not available for free |
| PATENT GRANT DATE | 26.12.00 |
| PATENT TITLE |
Small molecules that increase the conversion of food to body weight gain |
| PATENT ABSTRACT |
The present invention relates to peptide-like compounds, eg aminocarboxylic acid amide derivatives, and to methods of using same in the field of general health care, for example, to improve resistance to stress, improve production of desired characteristics or useful products in animals, to increase weight gain, and to decrease feed efficiency. The invention has applications in the field of animal husbandry. It also relates to administering beta-alethine to improve feed efficiency in an animal, comprising administering to animal an amount of .beta.-alethine sufficient to reduce the amount of food required to increase a unit of weight in the animal. |
| PATENT INVENTORS | This data is not available for free |
| PATENT ASSIGNEE | This data is not available for free |
| PATENT FILE DATE | 24.02.99 |
| PATENT REFERENCES CITED | Knight, G.D. et al. Seemingly Diverse Activities of B-Alethine. Cancer Research. Nov. 1, 1994, pp. 5636-5642, vol. 54, see especially Abstract, Figure 1 and pp. 5636-5637 |
| PATENT PARENT CASE TEXT | This data is not available for free |
| PATENT CLAIMS |
What is claimed is: 1. A method of lowering feed efficiency in an animal, comprising administering to the animal an amount of .beta.-alethine sufficient to reduce the amount of food required to increase a unit of weight in the animal. 2. A method of increasing weight gain in an animal, comprising administering to the animal an amount of .beta.-alethine sufficient to increase weight gain in the animal. 3. A method of increasing the conversion of food to body weight in an animal, comprising administering an amount of .beta.-alethine sufficient to increase conversion of food to body weight. 4. The method of claim 3, wherein the animal is a livestock animal. 5. The method of claim 3, wherein the animal is a human. 6. A method of treating or preventing weight loss associated with a disease in an animal, comprising administering an amount of .beta.-alethine sufficient to treat or prevent weight loss. 7. A method of treating or preventing cachexia in an animal, comprising administering .beta.-alethine in an amount sufficient to treat or prevent cachexia. 8. The method of claim 6, wherein the disease is anorexia nervosa, bulimia, AIDS, cancer, or Crohn's disease. 9. A method of decreasing mortality among a population of livestock animals, comprising administering to the animals an amount of .beta.-alethine sufficient to decrease mortality in the population of animals. 10. A method of increasing the ability of an animal to withstand environmental stressors selected from the group consisting of food deprivation, temperature changes, and exposure to pathogens, comprising administering to the animal an amount of .beta.-alethine sufficient to increase the ability of the animal to withstand the environmental stressors. 11. The method of claim 10, wherein the environmental stressor is food deprivation. 12. The method of claim 10, wherein the environmental stressor is a temperature change. 13. The method of claim 10, wherein the environmental stressor is exposure to pathogens. 14. The method as in one of claims 6 or 10, wherein the animal is a bird. 15. The method of claim 14, wherein the bird is a chicken. 16. The method of claim 14, wherein the .beta.-alethine is administered in ovo. 17. The method of claim 1-7, or 10, wherein the .beta.-alethine is administered subcutaneously. 18. The method as in either claim 6 or claim 7, wherein the animal is a mammal. 19. The method as in either claim 6 or claim 7, wherein the mammal is a human. 20. A method of preventing disease in an animal raised in crowded living conditions comprising administering to the animal an amount of .beta.-alethine sufficient to prevent said disease. |
| PATENT DESCRIPTION |
FIELD OF THE INVENTION The present invention relates to peptide-like compounds, eg aminocarboxylic acid amide derivatives, and to methods of using same in the field of general health care, for example, to improve resistance to stress, improve production of desired characteristics or useful products in animals, to increase weight gain, and to decrease feed efficiency. The invention has applications in the field of animal husbandry. BACKGROUND OF THE INVENTION In the area of animal husbandry, antimicrobials, including antibacterials, are used routinely for prophylaxis, chemotherapy and growth promotion. Animals receiving antibiotics in their feed, gain four to five percent more body weight than animals that do not receive antibiotics. They are important for sustainable livestock production ad for the control of animal infections that could be passed on to humans. However, microbiological and clinical evidence is mounting that resistant bacteria or resistance determinants might be passed from animals to humans, resulting in human infections that are more difficult to treat. With a marked increase in the prevalence and distribution of antimicrobial-resistant infections in hospitals and the community the question has been raised as to how this escalation of resistance could have been influenced by the use of antimicrobials in livestock production. Antimicrobials are used extensively in livestock, fish and plant production. Most are administered to livestock animals in subtherapeutic doses as growth promoters which boost the utilization of the genetic potential for growth of pigs and poultry, improve feed conversion and reduce waste production output from intensive livestock production. They are also used prophylactically to prevent diseases, for example, after commingling of animals from different farms, or among animals raised in crowded conditions with thousands of animals living under confinement on a single premises. Antimicrobial use leads to the selection of resistant forms of bacteria in the ecosystem of use. Low level, long-term exposure to antimicrobials may have a greater selective potential than short-term, full-dose therapeutic use because full doses are more likely to kill all of the targeted bacteria in the host, making it less likely that resistant bacteria will emerge. Adverse consequences of selecting resistant bacteria include an increase in the prevalence of resistant bacteria in animals, causing diseases that won't respond to known antimicrobials; the transfer of resistant pathogens to humans via direct contact with animals, or through the consumption of contaminated food or water; the transfer of resistance genes to human bacteria; an increase in the incidence of human infection caused by resistant pathogens; and potential therapeutic failures in animals and humans. Antibiotic resistance that arises in animal husbandry affects such zoonotic pathogens as Salmonella serovars and Campylobacter, both of which are associated with diarrheal diseases, and human and animal commensals such as Escherichia coli and enterococci. Because the human and animal microbial ecosystems are inextricably intertwined, microbial antibiotic resistance readily crosses boundaries so that antibiotics given to animals and closely related antibiotic compounds used in human therapy have been exerting selective pressure on their target bacteria for decades. Specifically, the introduction of fluorquinolones for use in poultry caused a dramatic rise in the prevalence of fluoroquinolone-resistant Campylobacter jejuni isolated in live poultry, poultry meat and from infected humans. The use of avoparcin as a growth-promoting feed additive for pigs and poultry has contributed to the reservoir of transferable resistance genes to glycopeptides, including vancomycin, in the commensal enterococci of animals. Multiresistant Escherichia coli have been selected by use of broad spectrum antimicrobials in both livestock and humans. The problems caused by the prolific use of a wide variety of antimicrobials in animal husbandry is a driving force for the development of antibiotic resistance in certain pathogenic bacterial species. The problems of resistance reach beyond the country of origin because meat products are traded worldwide. The present invention is therefore directed to a nontoxic, non-antimicrobial agent that can replace or supplement the use of antibiotics in the animal husbandry of livestock animals to increase health and general well-being, productivity, feed efficiency and weight gain. The present invention is also directed to such an agent that increases the vitality of livestock animals as is indicated by their ability to withstand environmental stressors such as wide variations in temperature, food deprivation which can occur under crowded condition, and exposure to pathogenic bacteria and viruses. DETAILED DESCRIPTION OF THE INVENTION In order that the present invention may be fully understood the following detailed description is set forth. The invention describes a variety of small molecules that improve health and general well-being, increase body weight, lower feed efficiency, and help animals overcome environmental stress such as exposure to infection, temperature change, and/or food deprivation. This invention relates to the use of many kinds of small molecules, including .beta.-alethine, a naturally occurring disulfide, to (1) improve general health and well being; (2) increase the ability of an animal to resist environmental stressors, including temperature change, food deprivation, and exposure to pathogenic bacteria and viruses; (3) increase the production of desired characteristics or useful products from animals, (4)increase weight gain, or (5)decrease feed efficiency in animals. The present invention also relates to the use of small molecules, including .beta.-alethine, to decrease mortality during shipping or transport of livestock. Other compounds, structurally similar to .beta.-alethine, including both disulfides and thiols, are also within the present invention. Taurox.TM. compounds (described in U.S. Ser. No. 08/733,174), and small molecules having immunoregulatory isomers such as mevalonate and mevalonolactone (described in U.S. Pat. Nos. 5,849,777 and 5,783,594, and U.S. Ser. No. 09/033,098 which are incorporated in their entirety by reference) can also be used for the various embodiments of the present invention. The disulfide .beta.-alethine, and .beta.-aletheine (the corresponding thiol) have a variety of diverse effects including use as a nontoxic anti-cancer agent, the ability to delay senescence in vivo and in vitro, and to facilitate the adaptation and differentiation of cultured cells. Knight et al., U.S. Pat. No. 5,643,966, and U.S. application Ser. Nos. 08/346,177, 08/468,043, and 08/468,041, which are incorporated herein by reference for all purposes. Beta-alethine has also been reported to be an adjuvant that stimulates antigen-specific immunoglobulin synthesis. (081733,174 incorporated herein by reference). In a first embodiment, it was discovered that small molecules that, including .beta.-alethine, and the ability of animals to withstand environmental stressors. To test the effects of .beta.-alethine on the ability of animals to withstand environmental stress, experimental chicks received a single injection of .beta.-alethine on the day of hatch, which was day one of an 18 day experiment. On day 8, a Newcastle disease live virus vaccine was administered. On Day 11, the chicks were stressed by simultaneous food withdrawal, temperature extremes, and aerosol exposure to E. coli 19B. Temperature stress continued through day 14. On day 18, all pens of chicks, were evaluated for weight gain and feed efficiency, adjusting for dead chicks, mortality was observed throughout the study. Beta-alethine decreased mortality as early as day seven, and mortality continued to be lower in .beta.-alethine-treated chicks through day 16 of the experiment in two pens and throughout the entire study in the other pen. .beta.-alethine enhanced the ability of chicks to survive environmental stressors that are commonly encountered in poultry houses where chickens are commercially raised in large numbers and are therefore routinely exposed to pathogenic viruses and bacteria. It is also possible that .beta.-alethine's ability to act as an adjuvant to stimulate an antigen-specific immune response to pathogens may have contributed to the decrease in mortality of chicks exposed to E. coli antigen. In a most preferred embodiment, approximately 50 ng/kg .beta.-alethine is administered to an animal to decrease mortality from environmental stressors and/or to enhance the ability of the animal to tolerate food deprivation or temperature extremes, and/or to enhance the likelihood that the animal will survive exposure to pathogenic viruses or bacteria. In another preferred embodiment, .beta.-alethine is administered at a dose of from about 200 pg to about 20 mg per kilogram. It is emphasized that the small molecules in the embodiment of the present invention can be administered at any time during the life of the animal, and periodic administrations throughout the life of the animal are anticipated to achieve the optimum benefit from the drug. In one preferred embodiment, the compounds of Formula I are injected in ovo. In another embodiment, the drugs are injected shortly after hatch administered by one of a variety of routes known in the art of veterinary medicine and animal husbandry and periodically thereafter. One embodiment of the present invention is directed to multiple administrations of Formula I compounds or other small molecules during the life of the animal. A particularly important time to administer drug is shortly before livestock animals such as cattle, pigs, sheep, fish, shrimp, shellfish and goats, are transported from one location to another in order to increase vitality of the animals and their ability to survive the stress of crowded conditions, exposure to pathogens, deprivation of food and water, and temperature changes. The use of the drugs disclosed herein to enhance the ability of an animal to withstand environmental stress includes human travel, shipment of cows, turkeys and other food or pet animals or desirable or valuable animals of all types, between sites used to rear or house them, weaning of animals including pigs, and farming of land animals and of tank and "open water" raising of fish and shellfish. It has also been discovered small molecules, including .beta.-alethine, increase the ability of an animal to combat external stress including stress imposed by chemical agents, all types of radiation, natural toxin, and all manner of infectious agents. In addition to protecting whole animals from internal and external stress, specific organs such as brains, skin, heart, liver and other vital tissues are protected from loss of mass and the adverse effects of stress or bacterial or viral disease. Animals (including but not limited to humans, livestock animals, chickens, birds, mammals, reptiles, shrimp, fish and shellfish) are frequently exposed to normal stress of growth and development and specific stress such as viral exposure and/or bacterial exposure. It has further been discovered that the compounds disclosed herein increase body weight and lower feed efficiency (i.e., the amount of feed required for weight gain) thus multiple uses in animal husbandry, and food production are discovered. Reduction of disability, stress induced illness, weight loss is advantageous at various times including but not limited to the treatment and/or prevention of loss of weight and life when animals are shipped and stressed including human travel, shipment of cows, turkeys and other food or pet animals between sites used to rear or house them, weaning of animals including pigs, and farming of land animals and of tank and "open water" raising offish and shellfish. The present invention is not limited to .beta.-alethine; molecules that are structurally or functionally similar to .beta.-alethine can also be used to accomplish the objectives of the present invention. The use of disulfides, thiols, Taurox compounds such as Taurox-SB and other amino-peptide like compounds disclosed in U.S. 48 can also be used for the embodiment described herein. Small molecules having isomers such as mevalonate and mevalonolactone (described in U.S. Pat. Nos. 5,849,777 and 5,783,594, and U.S. Ser. No. 09/033,098 which are incorporated in their entirety by reference). It was discovered that .beta.-alethine has a positive effect on weight gain and on lowering feed efficiency in animals by significantly increasing conversion of feed to weight; thus multiple uses in animal husbandry and food production are discovered. The results of one experiment using highly stressed male Peterson x Hubbard broiler chicks, show that the feed efficiency ratio of the .beta.-alethine-treated group was 7.9% lower relative to the negative controls. In a second study using a normal flock of Avian x Ross broiler chicks, an average decrease in feed efficiency ratios of about 4%. Therefore, another embodiment of the present invention is the use of .beta.-alethine or functionally or structurally similar compound, or other small molecules disclosed herein to decrease feed efficiency values. The deliverable weight ratio is similar to feed efficiency, but it includes an adjustment for the food consumed (and wasted) by chicks that do not survive. Experimental results show that .beta.-alethine caused a 10.8% improvement in final deliverable weight ratio (lower values) relative to controls. Therefore, another embodiment of the present invention is the use of .beta.-alethine or structurally similar or functionally similar molecule, to increase deliverable weight ratios in livestock animals or other animals including birds, fish, shellfish, bovine, porcine, and goats. The compounds can also be administered to animals to increase milk production, or to enhance production of other valuable or desirable characteristics such as improving fur, hooves, feathers, and so on. The compounds, especially beta-alethine and Taurox-SB (carbobenzoxy-beta-alanyl taurine) are useful in any animal raised as a pet or for food or to produce a desired product, including milk, wool, caviar, feathers, nails, fur, hooves . . . Increase products even if not increase efficiency. In another embodiment, small molecules, including .beta.-alethine, are administered to humans or other animals suffering from disease-associated weight loss in order to increase weight gain and/or to improve the utilization of food by increasing the conversion of food to body weight. Such illnesses include anorexia nervosa, AIDS, cachexia, Crohn's disease, or other illnesses or situations where the patient/animal ingests less food, or absorbs the nutrients from the food less efficiently than is desired. These compounds can also be used to treat underweight animals including humans, who do not have a disease, in order to increase body weight an/or the conversion of food to body weight. The compounds can be administered for this purpose at doses ranging from the picogram range to the miligram range, as needed, up to the maximum tolerated dose. Acceptable doses can be determined using routine practices. In one embodiment, .beta.-alethine is administered at relatively low doses once every 14 days or on a daily basis over extended periods of time to raise or maintain body weight, for example in relatively normal population including elderly, young or the sick. Alternatively, for example in a crisis situation, .beta.-alethine is administered at higher doses as needed and the amount administered is manipulated based on the response of the recipient. The compounds of Formula I for use in the various embodiments of the present invention, can be administered as needed by observing standard indicia of the progress of the disease using methods known to persons of ordinary skill in the art. The drugs are preferably administered on a daily or alternate-day regimen as described more fully below, until the desired results are achieved. Other regimens, such as weekly or biweekly regimens may suffice, particularly when a positive response is readily apparent. Decreases in dosages of the drugs, the frequency of administration, or both, can be made as normalization progresses. The methods of the present invention are not limited to any particular amount of the above-identified drugs, as therapeutically effective amounts can be determined by routine testing. The compounds of the present invention are typically used in the form of a pharmaceutical composition comprising one or more compounds of Formula I, or salt or hydrolyzable derivative thereof, together with a pharmaceutically acceptable or feed acceptable diluent or carrier. The compositions of the present invention are also so formulated. The dcompounds may be administered topically, orally, rectally, intravaginally intravenously, intraperitoneally, subcutaneously, intramuscularly or intranasally, or by other means known in the art, as appropriate for the effect sought. The drugs can also be administered transdermally using, for example, transdermal patches or transmucosally via sprays or other application. The drugs can be present in dosage unit form, for example, as a tablet, capsule or suppository, or formulated so as to be suitable for topical application (e.g., as a gel, cream, lotion or ointment). The compounds and compositions of the present invention can also be administered in liposomes, microemulsions, sprays, or via any alternative delivery system. Alternatively, the drugs can be present as a solution or suspension (e.g., sterile) suitable for administration by injection, inhalation, intranasally or dropwise to the eye or other sites as appropriate. The drugs of the invention can be prepared as a slow release formulation appropriate for internal or external use. Using techniques known in the art, they can also be trapped in or bound to a polymer, a solid support, a liposome or a gel. Beta-alethine, Taurox.TM. compounds and other compounds of Formula I, can be administered together with additional active agents such hormones, vitamins, cytokines, enzyme regulators, regulatory macromolecules, regulatory thiols or other small molecules. The compounds and compositions of the present invention are suitable for therapeutic use in humans and for veterinary treatment of similar conditions affecting warm-blooded animals, such as dogs, cats, horses, birds and cattle and for reptiles, and fish. For such purposes, the compounds can be administered in analogous amount and manner to those described above for administration to humans. Therapeutic administration of the beta-alethine and the Taurox-SB compounds may be performed by methods known to those skilled in the art including orally, transmucosally, sublingually, parenterally, intravenous, intramuscular or subcutaneous routes, direct delivery into the tumor, direct delivery into an affected body cavity by infusion, and oral or rectal administration. A therapeutic dose, of the compounds of Formula I for use with the methods and compositions of the present invention, is an amount that is effective to modulate cytokine production by immunocytes, or increase cytotoxic T lymphocytes, or active T cells, or increase cellular immunity, or increase PMBC proliferation. The amount of the compounds to be used and the frequency of exposure for statistically significant effects can be readily determined by one skilled in the art and will vary with the type of disease being treated or the cell type in the case of ex vivo therapy, and the effect sought. The term "statistically significant" is well known to those skilled in the art. Cells can be grown or stored in the presence of the compounds using any of a variety of available techniques, including growth on plastic or glass or other support (e.g., beads or hollow fibers), growth in suspension (e.g., in liquid or semisolid medium), growth in a bioreactor, or storage in a frozen or dried state. Primary cultures or serial cultures, or otherwise, can be used. The amount of the compound of the invention to be used and the frequency of exposures or statistically significant effects can be readily determined by one skilled in the art and will vary with the cell type, the compound used and the effect sought. In determining optimum concentrations, appropriate in vitro assays are run in the femtogram/ml to hundreds of mg/ml range. Various aspects of the present invention are described in greater detail in the non-limiting Examples that follow. Certain of the synthetic procedures for making small molecules that can be used in the present invention are described by Knight et al, Cancer Research 54:5623 (1994) or in U.S. Pat. No. 4,218,404, U.S. Ser. No. 08/733,174, or represent modifications thereof. These references are incorporated by reference herein in their entirety. In addition, the disclosures of WO 92/00955 and PCT/US91/04725 are relevant here, including the portions therein that related to syntheses, therapeutic regimens and cell culture treatment protocols, those regimens and protocols being applicable to the drugs of the present invention. These references are also incorporated by reference herein in their entirety. |
| PATENT EXAMPLES | This data is not available for free |
| PATENT PHOTOCOPY | Available on request |
|
Want more information ? Interested in the hidden information ? Click here and do your request. |