Classifications

• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K31/00—Medicinal preparations containing organic active ingredients
  • A61K31/33—Heterocyclic compounds
  • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
  • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
  • A61K31/47—Quinolines; Isoquinolines
  • A61K31/48—Ergoline derivatives, e.g. lysergic acid, ergotamine
• • A—HUMAN NECESSITIES
  • A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
  • A23K—FODDER
  • A23K20/00—Accessory food factors for animal feeding-stuffs
  • A23K20/10—Organic substances
  • A23K20/111—Aromatic compounds
• • A—HUMAN NECESSITIES
  • A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
  • A23K—FODDER
  • A23K20/00—Accessory food factors for animal feeding-stuffs
  • A23K20/10—Organic substances
  • A23K20/116—Heterocyclic compounds
  • A23K20/137—Heterocyclic compounds containing two hetero atoms, of which at least one is nitrogen
• • A—HUMAN NECESSITIES
  • A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
  • A23K—FODDER
  • A23K50/00—Feeding-stuffs specially adapted for particular animals
  • A23K50/10—Feeding-stuffs specially adapted for particular animals for ruminants
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K9/00—Medicinal preparations characterised by special physical form
  • A61K9/0012—Galenical forms characterised by the site of application
  • A61K9/0019—Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P3/00—Drugs for disorders of the metabolism
  • A61P3/12—Drugs for disorders of the metabolism for electrolyte homeostasis
  • A61P3/14—Drugs for disorders of the metabolism for electrolyte homeostasis for calcium homeostasis

Definitions

• the present invention relates to a veterinary composition and to a method for the treatment of post-partum hypocalcemia by administering said composition during dry period.
• the veterinary compositions and method of treatment according to the invention do not affect the milk-producing ability and/or milk quality of the ruminant during subsequent lactations.
• lactation In dairy ruminants, lactation generally lasts for 5 to 20 months. In dairy cows it is most often 10 months. After this lactation period, milking is stopped, generally suddenly, and the dairy ruminant is supposed to produce no more milk until calving, when the subsequent lactation begins. This period between the cessation of milking and the subsequent lactation, the latter being generally at parturition (or calving with respect to cows), known as the “dry period”, is generally set at about 2 months (i.e. 56-70 days) in dairy cows.
• this dry period necessitates several dietary changes and transitions to adapt to the physiological needs of an animal that is no longer producing milk.
• These dietary changes cause numerous physiological disruptions and stresses in ruminants, such as disruptions of the balance of the digestive flora, decreases in stomach capacity and absorption with changes in the size of the rumen and the villi of the ruminal mucosa.
• this dry period leads to a metabolism in ruminants that is very different from that observed during lactation.
• the ruminant is in a state of metabolic maladjustment resulting in an energy deficit, whereas the need to produce milk is again at a maximum.
• Post-partum hypocalcemia also known as Milk fever
• Early clinical or preclinical symptoms can include excitability, nervousness, shifting of weight, and shuffling of hind feet.
• Post-partum hypocalcemia is a common cause of poor labor (dystocia), stillborn calves and apparent sudden death of dairy ruminants and more particularly dairy cows.
• Clinical hypocalcemia is the most recognized disease in dairy cattle by dairy farmers, with an incidence rate around 5%, which could sometimes reach 20%. Incidence increases with higher milk production and successive lactation.
• the concentration of calcium in blood is tightly regulated through control of absorption of dietary calcium and release or uptake of calcium from bone.
• PTH parathyroid hormone
• 1,25-dihydroxy vitamin D3 control these processes.
• PTH parathyroid hormone
• PTH acts on the kidney and results in the conversion of a vitamin D metabolite into 1,25-dihydroxy vitamin D3.
• 1,25- dihydroxy vitamin D3 can regulate the absorption of calcium from the small intestine through active transport.
• adequate magnesium and a slightly less alkaline blood pH are needed, thus illustrating the need to provide adequate amounts of magnesium in pre-fresh diets and balance these diets to provide a negative cation-to-anion difference (DCAD) in order to prevent hypocalcemia.
• DCAD negative cation-to-anion difference
• such specific diets might not suffice to avoid hypocalcemia.
• some dairy cows may experience subclinical hypocalcemia which do not show clinical symptoms but have a low blood concentration of calcium usually within 24 hours after calving.
• a way to know whether dairy cows are experiencing subclinical hypocalcemia is to analyze blood for the concentration of calcium within the first 1 to 2 days after calving. Dairy cows with blood calcium concentrations at or below 8.8 mg/dl (2.2 mmol/1) but not showing clinical signs are considered subclinically hypocalcemic. It is estimated that the economic cost of subclinical hypocalcemia in a dairy herd is four times the cost of clinical cases, resulting in a substantial impact on profitability of dairy operations. Post-partum hypocalcemia impacts fresh cow health, future milk production, and reproductive performance. Studies also have shown that immune function is compromised in dairy cows with low blood calcium concentrations.
• prolactin inhibitor-based compositions such as Galastop ®
• the present invention relates to veterinary composition
• veterinary composition comprising cabergoline for use to treat post-partum hypocalcemia of a dairy ruminant, wherein said composition is administered to the dairy ruminant during the dry period and preferably at the time of the implementation of the dry period, i.e. at the time of the dry-off
• compositions are administered in effective therapeutic amounts, during the dry period and preferably at dry-off of dairy ruminants, in order to treat hypocalcemia in the subsequent lactation period(s), especially at and after parturition.
• compositions are administered to ruminants once and/or several times, preferably once.
• compositions according to the invention does not affect the milk-producing ability and/or milk quality of the ruminant during the subsequent lactation.
• the present invention also relates to kits for treating post-partum hypocalcemia in ruminants.
• cabergoline for manufacture of a veterinary composition for treating post-partum hypocalcemia in ruminants, wherein said composition is administered to ruminants during the dry period and preferably at dry-off of ruminants.
• a method for treating post-partum hypocalcemia in ruminants wherein a veterinary composition comprising cabergoline is administered in a therapeutically effective amount during the dry period and preferably at dry-off of ruminants.
• dry period includes the period of time between last milking of the lactation period and the subsequent lactation of the subsequent lactation period, which starts generally at parturition.
• the dry period generally lasts about 2 months, more specifically from 45 to 70 days in dairy cows.
• last milking dry-off
• milking cessation can be used interchangeably. They correspond to the time of the implementation of the dry period.
• post-partum hypocalcemia and “milk fever” can be used interchangeably and refer more specifically to clinical or subclinical hypocalcemia at parturition and more specifically at calving for dairy cows, and as detailed above.
• Dairy cows with blood calcium concentrations at or below 8.8 mg/dl (2.2 mmol/1) but not showing clinical signs are considered subclinically hypocalcemic.
• Clinical signs of milk fever of dairy ruminants include, but are not limited to tremor in muscles of the head and limbs, recumbency, lethargy, cold feeling of extremity, or hypothermia.
• treatment As used herein, the terms “treatment”, “treating”, and “treat” are defined as acting upon post-partum hypocalcemia with cabergoline or composition comprising the same to reduce or to anneal the risk of developing post-partum hypocalcemia or to reduce or alleviate one or more, preferably all, symptoms of post-partum hypocalcemia.
• the symptoms include, but are not limited to, tremor in muscles of the head and limbs, recumbency, lethargy, cold feeling of extremity, or hypothermia. It thus includes preventive and/or curative treatment.
• Treatment includes: (a) reducing the risk of occurrence of post-partum hypocalcemia or milk fever in a dairy ruminant (b) impeding the initiation of reduction of blood calcium level, and/or (c) increasing blood calcium level or maintaining blood calcium level at a normal level, preferably to attain a blood calcium concentration higher than or equal to 2.1 mmol/1 in ruminants or preferably to 2.2 mmol/1.
• the treatment, or more specifically prevention, of post-partum hypocalcemia includes the treatment, or more specifically prevention, of tremor in muscles of the head and limbs, recumbency, lethargy, cold feeling of extremity, or hypothermia due to hypocalcemia in dairy ruminants.
• the present invention relates to a veterinary composition
• a veterinary composition comprising cabergoline for use to treat, or more specifically to prevent from, milk fever, wherein said composition is administered to ruminants during the dry period and preferably at dry-off
• the present invention also relates to a veterinary composition
• a veterinary composition comprising cabergoline administered in a single administration and/or in repeated administrations, preferably in a single administration, during the dry period and preferably at dry-off, for use to treating milk fever in dairy ruminants.
• Administration of said compositions to dairy ruminants according to the invention allows more specifically to maintain a blood calcium concentration higher than or equal to 2.1 mmol/1 in ruminants or preferably to 2.2 mmol/1. More particularly, said administration does not require any specific diet and more specifically any diet regimen aiming at maintaining a satisfactory blood calcium concentration in ruminants (such as diets with adequate amounts of magnesium and balance these diets to provide a DCAD).
• compositions used according to the invention allow to maintain such blood concentration during the dry period and more specifically at parturition and after parturition, i.e. at the subsequent lactation.
• the present invention also relates to a method of preventing and/or reducing post partum hypocalcemia in dairy ruminants, as well as to a method of preventing dairy ruminants from milk fever, comprising an administration according to an effective therapeutic regimen of the veterinary compositions comprising cabergoline to ruminants during the dry period and preferably at dry-off
• said veterinary compositions are administered to dairy cows.
• the veterinary compositions for use according to the invention are administered after the last milking.
• the veterinary compositions are preferably administered within the first 5, the first 4 or the first 2 hours after the last milking, preferably within the first 30 minutes (such as 15-20 minutes) after the last milking.
• compositions and the methods according to the present invention are attractive to farmers as their use can maintain a satisfactory blood calcium concentration, without worrying about a specific blood calcium concentration increasing-regimen, resulting in a simplified herd management, and savings in terms of disease treatment costs when lactation is resumed.
• the administration of the compositions according to the present invention thus enables better management of dietary programs during the dry period.
• Cabergoline whose chemical name is /V-[3-(dimethylamino)propyl]-V- [(ethylamino)carbonyl]-6-(2-propenyl)-8g-ergoline-8-carboxamide, is an anti-prolactin agonist compound specific for D2 dopamine receptors. It is in particular described in the patent US 4,526,892. Its chemical structural formula is the following:
• Cabergoline is the active ingredient in human drugs marketed under the names Dostinex ® and Cabaser ® . Also, it is the basic active ingredient in veterinary compositions marketed under the name Galastop ® for bitches prone to lactations of false pregnancy, and under the name Velactis ® for use in dairy cows for the reduction of udder involution duration during the dry period in the dairy cow and is administered as a single intramuscular injection. Neither of these cabergoline-based compositions, is administered to ruminants in order to treat milk fever in dairy ruminants.
• the effective amounts or therapeutic doses are likely to vary according to the ruminants to be treated.
• the dosages, also called therapeutic regimens, can easily be determined by systematic tests on the basis of the example below and are within the ability of persons skilled in the art.
• the effective therapeutic doses according to the present invention are between 1 and 50 pg/kg, or between 5 to 11 pg/kg, and more preferably about 6 to 9 pg/kg.
• the amount of cabergoline which is administered is from 0.25 to 7 mg, preferably from 0.3 to 6 mg, and more specifically 1-6 mg, per dairy ruminant.
• the amount of cabergoline which is administered is from 2 to 7 mg, preferably from 3 to 6 mg, and more specifically 5-6 mg, per dairy cow.
• the term “ruminants” refers to herbivorous mammals such as, for example, bovines, ovines, caprines, camelids or bovids.
• the dairy ruminants of the invention are preferably gestating ruminants.
• the compositions according to the invention are administered to milk-producing gestating ruminant mammals, preferably such as dairy cows, sheep and goats, and more preferably dairy cows.
• the veterinary compositions of the present invention can be administered in association with standard treatments for treating and/or preventing intra mammary inflammations and intra mammary infections (such as mastitis) of ruminants.
• mastitis examples include local disinfectants for udders, antibiotics such as penicillins of group M, cephalosporine, gentamycin or even enzymes such as lysozymes or muramidase, and also teat-sealants
• post-partum hypocalcemia also known as Milk fever
• Milk fever is caused by a temporary blood calcium deficiency which usually occurs around the time of parturition, more specifically at calving with respect to dairy cows. Milk fever generally occurs within the next 12-24 hours following parturition.
• post-partum hypocalcemia is treated within the next 12-24 hours following parturition.
• the treatment of post partum hypocalcemia of the invention includes reducing or annealing the risk of developing post-partum hypocalcemia, especially within the next 12-24 hours following parturition.
• preventing and/or reducing post-partum hypocalcemia in a dairy ruminant refers to a treatment where the ruminant presents or attains a satisfactory blood calcium concentration which is generally higher than or equal to 2.1 mmol/1, preferably 2.2 mmol/L.
• compositions used according to the present invention can be administered according to many ways of administration that are well known in the field and adapted to the treatment of each of these animals. They are preferably administered orally or parenterally. It is even more preferred to administer them through intramuscular or subcutaneous injection or by intramammary administration. According to a particular embodiment, they are intramammary or preferably intramuscularly administered.
• They can thus be in the form of an oral, intramammary or injectable liquid solution or suspension, or in solid or semi-solid form.
• compositions used can further comprise ingredients conventionally used in pharmacy for the preparation of liquid formulations for intramammary administration.
• injectable preparations are prepared by mixing effective therapeutic amounts of cabergoline as described above with a solvent, a pH regulator, a buffer agent, a suspending agent, a solubilizing agent, a stabilizer, a tonicity agent and/or a preservative, and by transforming the mixture into a subcutaneous or intramuscular injection according to a conventional method.
• DMSO dimethyl sulfoxide
• oily solvents such as medium-chain triglycerides, or a mixture of capric acid, caprylic acid and triglycerides such as that marketed under the name Mygliol ® 812.
• the injectable preparations can be lyophilized according to a conventional method.
• suspending agents include methyl cellulose, polysorbate 80, hydroxy ethylcellulose, xanthan gum, sodium carboxymethylcellulose and polyethoxylated sorbitan monolaurate.
• solubilizing agents include polyoxyethylene hardened castor oil, polysorbate 80, nicotinamide, polyethoxylated sorbitan monolaurate, macrogol and castor oil fatty acid ethyl ester.
• stabilizers include sodium sulfite, sodium metalsulfite and ether, while preservatives include methyl p-hydroxybenzoate, ethyl p-hydroxybenzoate, sorbic acid, benzyl alcohol, phenol, cresol and chlorocresol.
• An example of a tonicity agent is mannitol.
• the present invention further relates to a kit for veterinary use for treating, more specifically reducing or annealing, post-partum hypocalcemia, in dairy ruminants, where the kit includes a veterinary composition comprising cabergoline, as defined above, for use to treat post-partum hypocalcemia in dairy ruminants.
• the kits according to the present invention can include at least one compartment for an optionally sterile packaging including an effective therapeutic amount of cabergoline as described above, for administration to ruminants.
• the kit includes the means enabling the administration of the compositions by the chosen route, such as intramammary or intramuscularly route, as well as instructions relating to the mode of administration of the veterinary compositions according to the invention.
• the cabergoline composition is a solution comprising cabergoline with dimethyl sulfoxide and medium-chain triglycerides, as excipients. It corresponds to the product called VelactisTM (cabergoline 1.12mg/mL).
• the total number of cows included in the study was 255 (126 in the Tested group and 129 in Placebo group). Both groups were comparable in their baseline criteria at inclusion. Milk fever was assessed and recorded at calving in both groups by veterinarians.
• a veterinary composition comprising cabergoline reduces the risk of developing milk fever in a very satisfactory and simple way. It is also important to note that such treatment does not affect the milk-producing ability and/or milk quality (e.g. SCC) of the ruminant during subsequent lactations.
• SCC milk quality

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• 2021
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