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Topic:Intramuscular Administration

Intramuscular administration in horses involves the injection of medications directly into the muscle tissue. This method is commonly used for delivering vaccines, antibiotics, and other therapeutic agents. The technique requires knowledge of equine anatomy to ensure the injection is placed in the correct location, such as the neck or hindquarters, to minimize discomfort and avoid complications. Proper intramuscular administration can facilitate the absorption of medications into the bloodstream, allowing for effective therapeutic interventions. This page compiles peer-reviewed research studies and scholarly articles that explore the techniques, benefits, and potential complications associated with intramuscular administration in equine practice.
The pharmacokinetics of meclofenamic acid in the horse.
Journal of veterinary pharmacology and therapeutics    June 1, 1981   Volume 4, Issue 2 147-156 doi: 10.1111/j.1365-2885.1981.tb00724.x
Snow DH, Baxter P, Whiting B.The pharmacokinetics of meclofenamic acid were studied in Thoroughbred horses and in ponies. After intravenous (i.v.) administration of either 2 mg/kg or 4 mg/kg sodium meclofenamate the elimination half-life was of the order of 0.9 h while the volume of distribution was found to be 0.128 litre/kg. Elimination was in accordance with a one-compartment model. Following oral administration of either meclofenamic acid (4 mg/kg) or sodium meclofenamate (4 mg/kg) a much longer terminal half-life than that calculated for Kel from i.v. data was found. This anomaly indicated that the 'flip-flop' phenom...
Pharmacokinetics and behavioral effects of methylphenidate in Thoroughbred horses.
American journal of veterinary research    May 1, 1981   Volume 42, Issue 5 722-726 
Shults T, Kownacki AA, Woods WE, Valentine R, Dougherty J, Tobin T.In horses given (rapid IV) methylphenidate (Ritalin, alpha-phenyl-2-piperidinacetic acid methyl ester; 0.70 mg/kg), plasma concentrations of the drug decreased rapidly at first, with an apparent alpha half-life of about 19 minutes, and then more slowly, with an apparent beta half-life of about 2.4 hours. These data were well fitted by a 2-compartment open model. In blood, about 40% of the methylphenidate present was in the plasma fraction, and of this, about 80% was plasma-protein bound. If given by subcutaneous or IM injection, plasma concentrations of methylphenidate peaked in about 1 hour a...
Aqueous procaine penicillin G in the horse: serum, synovial, peritoneal, and urine concentrations after single-dose intramuscular administration.
American journal of veterinary research    April 1, 1981   Volume 42, Issue 4 629-631 
Stover SM, Brown MP, Kelly RH, Farver TB, Knight HD.Six adult mares were given a single dose of aqueous suspension procaine penicillin G (300,000 IU/ml) IM at a dosage of 22,000 IU/kg of body weight (15.4 mg of penicillin G/kg). Serum, synovial fluid, peritoneal fluid, and urine penicillin concentrations were measured serially over a 48-hour period. The mean peak serum penicillin concentration was 1.42 microgram/ml at 3 hours. Penicillin was detected in synovial fluid and peritoneal fluid, which obtained mean peak penicillin concentrations of 0.62 microgram/ml and 0.58 microgram/ml, at 4 hours and 3 hours, respectively. These concentrations ste...
The disposition and metabolism of the synthetic prostaglandin fluprostenol (ICI 81,008) in the horse.
Xenobiotica; the fate of foreign compounds in biological systems    September 1, 1980   Volume 10, Issue 9 715-723 doi: 10.3109/00498258009108378
Chapman DI, Moss MS, Tomlinson PW, Harrison MP, Simmons PJ.1. Following single intramuscular doses of [14C]fluprostenol (0.5--2.4 micrograms/kg) to three female horses and to three gelded male horses, radioactivity was present in the plasma within 5 min; peak concn. (0.32--1.30 ng/ml fluprostenol equiv.) occurred 5 to 90 min after injection. Radioactivity was still present in the plasma of the females after three days. About 88% of fluprostenol is bound to plasma proteins. 2. Radioactivity was present in the parotid saliva of the gelded male horses within 10 min. Peak concn. (45--91 pg/ml fluprostenol equiv.) occurred from 5 min to 1 h after injection...
The immune response of horses to tetanus toxoid.
The Onderstepoort journal of veterinary research    December 1, 1979   Volume 46, Issue 4 211-216 
Jansen BC, Knoetze PC.An intramuscular injection of 8-16 Lf tetanus toxoid in water-in-oil emulsion protected adult horses against tetanus for at least 128 weeks. A booster dose of 8 Lf toxoid in aqueous solution protected them for a further period of at least 3 1/2 years. Colostral immunity protected foals for at least 10 weeks. An intramuscular injection of 8 Lf toxoid in water-in-oil emulsion given to foals from immune dams when they were 10-18 weeks old did not elicit any antibody response. They did respond, however, to a booster injection of 8 Lf toxoid in aqueous solution given 12 weeks after the first dose. ...
Studies related to the metabolism of anabolic steroids in the horse: testosterone.
Xenobiotica; the fate of foreign compounds in biological systems    May 1, 1979   Volume 9, Issue 5 269-279 doi: 10.3109/00498257909038730
Houghton E, Dumasia MC.1. After intramuscular administration of [4-14C]testosterone to two cross-bred gelded horses, 45% of the radioactivity was excreted in urine in 96 h. Small amounts of urinary activity could still be detected at 200 h. 2. Neutral metabolites obtained after both enzyme and acid hydrolysis of urine samples have been investigated by g.l.c.-mass spectrometry. 3. 5 alpha-Androstane-3 beta, 17 alpha-diol was found only in the enzyme-hydrolysable extract and testosterone only in the acid-hydrolysable extract. 5 alpha-Androstane-3 beta, 17 beta-diol and 3 beta-hydroxy-5 alpha-androstan-17-one were foun...
Adrenal gland function in the horse: effects of cosyntropin (synthetic) and corticotropin (natural) stimulation.
American journal of veterinary research    May 1, 1979   Volume 40, Issue 5 724-726 
Eiler H, Goble D, Oliver J.The plasma concentration of hydrocortisone was determined in mares given either cosyntropin (100 IU, given IV) or corticotropin (200 IU, given IM). Plasma hydrocortisone concentrations of the mares treated with cosyntropin increased by 46%, 57% and 80% at 30, 60, and 120 minutes, respectively, when compared with base-line values; these values returned to base line at 240 minutes. In mares treated with corticotropin, mean plasma hydrocortisone concentrations increased by 42%, 143%, 101% and 155% at 30, 60, 120, and 240 minutes, respectively, when compared with base-line values. Differences in t...
Critical test evaluation of butamisole against gastrointestinal parasites of horses and ponies.
American journal of veterinary research    January 1, 1979   Volume 40, Issue 1 139-141 
Grieve RB, Moore BG, Bradley RE.A critical test was performed to evaluate the anthelmintic properties of an injectable butamisole formulation and to compare the efficiency with that of a commercially available piperazine-thiabendazole anthelmintic. The test was done in 10 horses and 15 ponies with naturally acquired parasitic infections. Butamisole was administered at the dose level of 2.5 or 3.75 mg/kg of body weight by either subcutaneous or deep intramuscular injection. Given at the dose level of 2.5 mg/kg, butamisole was highly effective (99%) against Strongylus vulgaris and moderately effective (49%) against Parascaris ...
Evaluation of xylazine, guaifenesin, and ketamine hydrochloride for restraint in horses.
American journal of veterinary research    August 1, 1978   Volume 39, Issue 8 1274-1278 
Muir WW, Skarda RT, Sheehan W.A combination of intramuscular xylazine plus intravenous guaifenesin and ketamine hydrochloride was evaluated as a method for chemical restraint and casting of the adult horse. This drug combination provided safe and rapid induction of the horse and uneventful recovery from lateral recumbency. Cardiopulmonary function remained within base-line values for the adult horse, although cardiac output, arterial blood pressure, and arterial partial pressure of oxygen were decreased from base-line values. Xylazine, guaifenesin, and ketamine hydrochloride provided safe induction to general anesthesia wi...
Absorption of sodium benzylpenicillin from the equine uterus after local Lugol’s lodine treatment, compared with absorption after intramuscular injection.
Equine veterinary journal    July 1, 1978   Volume 10, Issue 3 174-175 doi: 10.1111/j.2042-3306.1978.tb02251.x
Allen WE, Clarke AR.Plasma concentrations of sodium benzylpenicillin following intrauterine infusion were increased by reducing the volume of solution and expelling air from the vagina after infusion. Instillation of 10 per cent Lugol's iodine solution into the uterus before penicillin infusion further increased the absorption rate, although peak plasma levels of penicillin were less than half those which resulted from intramuscular injection of the same dose.
The mini-pig as a model for penetration of penicillins.
Scandinavian journal of infectious diseases. Supplementum    January 1, 1978   Issue 14 135-142 
Bergan T, Versland I.To be active, antimicrobials must reach the bacteria in the infectious foci in adequate concentrations. Direct measurements of levels in the various foci are difficult to perform, but a number of animal models with artificial extravascular foci have been developed. In many ways, the physiology of pigs resemble that of humans. Consequently, it was thought that pigs might also parallel humans in the handling of penicillins. General pharmacokinetics of ampicillin and flucloxacillin and the penetration of the substances to subcutaneously implanted teflon tistisue chambers were investigated. Ampici...
An evaluation of chemical restraining agents in the horse.
The Veterinary record    July 9, 1977   Volume 101, Issue 2 30-33 doi: 10.1136/vr.101.2.30
MacKenzie G, Snow DH.An evaluation of acepromazine (0.5 mg/kg intramuscularly), azaperone (0.7 and 0.9 mg/kg intramuscularly) and xylazine (2.0 mg/kg intramuscularly) as chemical restraining agents was carried out in seven horses. (Xylazine and azaperone were used at the recommended dose rates; acepromazine at five times the recommended dose rates). Of the three drugs administered only azaperone produced sufficient sedation in all the horses to allow a percutaneous needle muscle biopsy to be taken from six muscles. With acepromazine and xylazine this procedure could be successfully carried out in five and four hor...
Therapeutic use of gentamicin in horses: concentrations in serum, urine, and synovial fluid and evaluation of renal function.
American journal of veterinary research    July 1, 1977   Volume 38, Issue 7 1085-1087 
Beech J, Kohn C, Leitch M, Weinstein AJ, Gallagher M.Serum, synovial fluid, and urine concentrations of gentamicin were measured in normal mature horses which had been given a single dose of the drug. Mean peak serum concentration (16.8 microgram/ml) occurred in horses 30 minutes after they were given a single intramuscular dose of 4.4 mg of gentamicin/kg of body weight. In horses given a smaller dose of gentamicin (1.7 mg/kg), mean peak serum concentrations of gentamicin (10.2 microgram/ml) appeared at 1 hour. Synovial fluid concentration was maximum at 2 hours for both doses; in horses given the larger dose, mean peak concentration was 6.4 mic...
The urinary excretion of synthetic corticosteroids by the horse.
The Veterinary record    May 21, 1977   Volume 100, Issue 21 447-450 doi: 10.1136/vr.100.21.447
Chapman DI, Whiteside J.A radioimmunoassay method has been developed that enables the administration of therapeutic doses of synthetic corticosteroids to be detected in horse urine. Fourteen proprietary preparations of these steroids have been given by intramuscular injection to ponies and thoroughbreds. The administration of some preperations could still be detected six days after a single intramuscular injection of a therapeutic dose. The route of injection of dexamethasone-21-sodium phosphate, whether intramuscular, intravenous or intra-articular, did not appear to alter the length of time over which the steroid o...
Biochemical and physiological effects of catecholamine administration in the horse.
Research in veterinary science    May 1, 1977   Volume 22, Issue 3 357-360 
Anderson MG, Aitken MM.Adrenaline was given intramuscularly to resting horses. It increased heart rate, sweating, blood levels of lactic dehydrogenase, aldolase, creatine kinase, glucose, lactate, free fatty acids and glycerol. Responses to isoprenaline, to noradenaline and to adrenaline after pretreatment with propranolol indicated that beta receptors were involved in stimulation of tachycardia, sweating, lipolysis and muscle glycogenolysis, and alpha receptors in stimulation of liver glycogenolysis and leakage of intracellular enzymes. The time course and relative magnitude of the effects on different enzymes was ...
Effect of imidocarb dipropionate and hemicastration on spermatogenesis in pony stallions.
American journal of veterinary research    January 1, 1977   Volume 38, Issue 1 139-141 
Frerichs WM.The effect of imidocarb dipropionate [3, 3' bis-(2-imidazolin-2-yl) carbanilide dipropionate] on spermatogenesis in 3 pony stallions was studied. The drug alone had no deleterious effect on spermatogenesis when given intramuscularly 4 times at a dosage level of 4 mg/kg at 72-hour intervals. Hemicastration, with or without subsequent drug treatment, caused almost complete cessation of spermatogenesis 30 days after the operation.
[Comparative studies on blood serum concentrations of Terramycin (oxytetracycline) following intravenous and intramuscular administration in horses].
DTW. Deutsche tierarztliche Wochenschrift    November 5, 1976   Volume 83, Issue 11 489-492 
Eidt E, Anhalt G, Froehner H.No abstract available
Excretion and metabolism of nikethamide in the horse.
British journal of sports medicine    October 1, 1976   Volume 10, Issue 3 116-123 doi: 10.1136/bjsm.10.3.116
Delbeke FT, Debackere M.It is well known that nikethamide (N,N-diethylnicotinamide, CoramineR) is metabolized very rapidly to nicotinamide. Hence, there is difficulty in proving that nikethamide has been used as a doping substance because nicotinamide is a normal physiological metabolite in the organism as well as a vitamin preparation. However, an intermediate metabolite (N-ethylnicotinamide) was found by us in the urine of horses treated with CoramineR. This was characterized by gas chromatography/mass spectrometry, and synthesized and identified as being N-ethylnicotinamide. The excretion and metabolism of niketha...
A review of the pharmacology, pharmacokinetics and behavioral effects of procaine in thoroughbred horses.
British journal of sports medicine    October 1, 1976   Volume 10, Issue 3 109-116 doi: 10.1136/bjsm.10.3.109
Tobin T, Blake JW.Since procaine has both local anaesthetic and central stimulant actions its presence in the blood or urine of racing horses is forbidden. After rapid intravenous injection of procaine HC1 (2.5 mg/Kg) in thoroughbred mares plasma levels of this drug fell rapidly (t 1/2 alpha = 5 min) and then more slowly (t 1/2 beta = 50.2 min). These kinetics were well fitted by a two compartment open model (Model I). This model gave an apparent Vdbeta for procaine in the horse of about 3,500 litres. Since procaine was about 45% bound to equine plasma protein this gives a true Vdbeta for procaine of about 6,50...
Fluprostenol in mares: clinical trials for the treatment of infertility.
The Veterinary record    June 26, 1976   Volume 98, Issue 26 523-525 doi: 10.1136/vr.98.26.523
Cooper MJ.Fluprostenol (ICI 81,008) is a 16-aryloxyprostaglandin, structurally related to PGF2alpha. It is a highly potent luteolytic agent, being effective in thoroughbred mares at a single intramuscular dose of 250 mug and having a wide margin of safety in this species. A total of 941 mares have been treated with fluprostenol in an international trial, for various forms of infertility associated with abnormal persistence of luteal function. These mares were selected for treatment on the basis of clinical examination and 760 (approximately 80 per cent) responded fluprostenol by showing oestrus within s...
The applied pharmacology of azaperone in ponies.
Research in veterinary science    May 1, 1976   Volume 20, Issue 3 316-323 
Serrano L, Lees P.The butyrophenone tranquilliser, azaperone, was administered intramuscularly to ponies in five series of experiments, using a dose level of 0-4 mg/kg once and 0-8 mg/kg four times. An excellent or good sedative effect was usually obtained with both dose levels, but the response was more consistent with the higher dose. The onset of sedation was apparent within 10 min of administration, the maximal effect usually occurring between 20 and 60 min while sedation was no longer apparent after 2 to 6 h. Body temperature was reduced in all animals for at least 2 h and respiratory rate was increased in...
Effects of azaperone on cardiovascular and respiratory functions in the horse.
British journal of pharmacology    March 1, 1976   Volume 56, Issue 3 263-269 doi: 10.1111/j.1476-5381.1976.tb07637.x
Lees P, Serrano L.1 The butyrophenone tranquilizer, azaperone, was administered intramuscularly, at dose levels of 0.4 and 0.8 mg/kg, to ponies and its effects on cardiovascular and respiratory functions assessed. 2 Arterial blood pH, CO2 tension (PaCO2) and O2 tension (PaO2) remained relatively constant throughout the course of action of azaperone. 3 Azaperone did not modify plasma protein concentration but venous blood packed cell volume and haemoglobin concentration were reduced by 5 to 10% for at least 4 hours. These changes were probably caused by uptake of erythrocytes into the splenic reservoir. 4 Small ...
Plasma concentrations, plasma protein binding and residues of sulfamonomethoxine in pigs, horses and cattle.
Tijdschrift voor diergeneeskunde    October 15, 1975   Volume 100, Issue 20 1099-1104 
Rauws AG, van Schothorst M, Frik JF.The protein binding, the plasma half-life and the residue depletion of sulfamonomethoxine (SMM) after intramuscular administration were investigated in pigs, horses and cattle. Protein binding was weakly concentration-dependent. The bound fraction in plasma in the therapeutic range amounted to approximately 45, 40 and 50% for pigs, horses and cattle respectively, and the plasma half-lives were approximately 5.1, 5.7 and 3.1 hours respectively. SMM levels were less than 1 mug/g in muscle tissue after 36, 20 and 12 hours in pigs, horses and cattle respectively. In the kidney SMM levels were not ...
Chloramphenicol plasma levels in horses, cattle and sheep after oral and intramuscular administration.
Zentralblatt fur Veterinarmedizin. Reihe A    October 1, 1975   Volume 22, Issue 8 704-712 doi: 10.1111/j.1439-0442.1975.tb01482.x
De Corte-Baeten K, Debackere M.No abstract available
Effects of prostaglandin F2alpha on the oestrous cycle and pregnancy in mares.
Journal of reproduction and fertility. Supplement    October 1, 1975   Issue 23 257-261 
Douglas RH, Ginther OJ.Several experiments indicated that prostaglandin F2alpha (PGF2alpha) has luteolytic and abortifacient properties in mares. A single subcutaneous injection of 1-25 mg PGF2alpha on Day 6 of dioestrus was as effective as 10 mg PGF2alpha in inducing luteolysis. Oestrus and ovulation appeared to be synchronized when a single injection of 1-25 mg PGF2alpha was given on Days 7, 10 or 13 after ovulation but not on Days 1 or 4 after ovulation or on Day 2 of oestrus. Intramuscular administration was as effective as subcutaneous administration and 1-25 mg PGF2alpha was the minimal effective systemic dose...
Synchronization of oestrus in mares with a prostaglandin analogue and HCG.
Journal of reproduction and fertility. Supplement    October 1, 1975   Issue 23 269-274 
Palmer E, Jousset B.Following an initial observation period of 13 days when plasma progesterone levels were determined, synchronization of oestrus and ovulation was investigated in thirty-three mares treated with a prostaglandin analogue ('Equimate') and HCG. Two courses of treatment were given 8 days apart and each consisted of a single intramuscular injection of Equimate (250 mug) followed 6 days later by an intramuscular injection of HCG (2500 i.u.). The first course was designed to remove all luteal tissue and to induce ovulation of any follicles that developed in response to the withdrawal of progesterone. T...
The use of Gn-RH for controlling the oestrous cycle of the mare (preliminary report).
Journal of reproduction and fertility. Supplement    October 1, 1975   Issue 23 275-277 
Heinze H, Klug E.Clinical tests with synthetic gonadotrophin-releasing hormone (Hoechst) were made during the breeding seasons of 1973 and 1974, using 128 mares injected with 1-0 to 4-0 mg of the substance intramuscularly. The mares were placed in one of five groups based on ovarian condition determined by clinical evidence. Some success was obtained in the induction of ovulation in mares with inactive and sub-normally active ovaries and in a small group having cystic ovaries. A large proportion of mares having a mature follicle responded within 48 hr, but others with atretic follicles failed to respond. The u...
The use of prostaglandin F2alpha in controlling the oestrous cycle of the mare and steroid changes in the peripheral blood.
Journal of reproduction and fertility. Supplement    October 1, 1975   Issue 23 263-267 
Spincemaille J, Coryn M, Vandekerckhove D, Vandeplassche M.Prostaglandin F2alpha (PGF2alpha), administered by untrauterine infusion and intramuscular injection, was used to induce oestrus and ovulation in non-cyclic mares. A satisfactory response rate (80% or more) was obtained and the dose (2-5--7-5 mg) and the time taken for ovulation to occur (up to 9 days) was the same irrespective of the route of administration. Only about one-half of the mares conceived to mating at the induced oestrus but the low conception rate could be attributed to the infertile condition of the mares. Plasma progesterone remained at basal levels after PGF2alpha and oestroge...
Evaluation of xylazine as a sedative and preanesthetic agent in horses.
American journal of veterinary research    October 1, 1975   Volume 36, Issue 10 1421-1429 
McCashin FB, Gabel AA.Xylazine administered intramuscularly (IM) to horses at the dose level of 2 mg/kg was an effective sedative and preanesthetic for thiamylal sodium narcosis or thiamylal sodium and halothane anesthesia. Evaluation of response of cardiovascular, respiratory, and hepatic function did not indicate serious untoward effects, although cardiac and respiratory rate decreased, calculated vigor of left ventricular contraction decreased, calculated peripheral vascular resistance increased, and transient innocuous cardiac arrhythmias occurred. Effects of the anesthetics used on respiratory function (blood ...
[Iron Dextran Administered to Horses (author’s transl)].
Tijdschrift voor diergeneeskunde    May 15, 1975   Volume 100, Issue 10 562-563 
Wagenaar G.A description is given of three cases in which horses died very shortly after being given an intramuscular injection of iron dextran. The use of iron dextran in the case of horses is inadvisable.