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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 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.
Formation of steroids by the pregnant mare. V. Metabolism of 14C-isopentenylpyrophosphate and 3H-dehydroisoandrosterone injected into the fetus.
Endocrinology    April 1, 1975   Volume 96, Issue 4 1009-1017 doi: 10.1210/endo-96-4-1009
Bhavnani BR, Martin LJ, Baker RD.A mixture of 1-14C-isopentenylpyrophosphate and 3H-dehydroisoandrosterone was injected into a horse fetus intramuscularly during laparotomy, after which maternal urine was collected for 4 days. Steroid conjugates in the urine were extracted with Amberlite XAD-2 resin, hydrolysed and separated into phenolic and neutral fractions. From the phenolic fraction estrone, 17alpha-estradiol, equilin and equilenin were isolated. Only estrone and 17alpha-estradiol contained both 3H and 14C, while the ring B unsaturated estrogens contained only 14C. From the neutral fraction 14C-labeled 3beta-hydroxy-5alp...
A pharmacological study of chloramphenicol in horses.
Canadian journal of comparative medicine : Revue canadienne de medecine comparee    April 1, 1975   Volume 39, Issue 2 216-223 
Sisodia CS, Kramer LL, Gupta VS, Lerner DJ, Taksas L.Pharmacological disposition of chloramphenicol was studied in horses. Minimum levels of the antibiotic (greater than or equal to 5 mu g/ml) in blood or plasma recommended to combat infections could not be achieved by 4.4 and 8.8 mg/kg I.V. or 30 and 50 mg/kg I.M. or 30 mg/kg oral (as palmitate salt) doses of chloramphenicol. Increasing the dose to 19.8 and 26.4 mg/kg I.V. provided such levels for about two and three hours respectively. A combination of 20 mg/kg I.V. and 30 mg/kg I.M. administered simultaneously did not provide more prolonged levels than 26.4 mg/kg I.V. alone. Chloramphenicol s...
Route of prostaglandin F2alpha injection and luteolysis in mares (38519). Douglas RH, Ginther OJ.Nine groups of pony mares (3/group) were used in a 3 times 3 factorial experiment. The factors were dose of PGF-2 alpha (0, 0.25 of 1.25 mg and route of administration (im, iu or il). Mares were laparotomized and treated on day 7 postovulation. Jugular blood was collected for progesterone RIA at 0 (pretreatment) and 1,6,12,24,48, and 72 hr posttreatment. In mares given either 0.25 mg or 1.25 mg PGF-2alpha, progesterone concentrations were not significantly different among the three routes at any of the posttreatment times studied except at 6 hr posttreatment. In mares given 0.25 mg, progestero...
Serum oxytetracycline concentrations after intravenous and intramuscular administration in horses.
Journal of the American Veterinary Medical Association    January 15, 1973   Volume 162, Issue 2 119-120 
Teske RH, Rollins LD, Condon RJ, Carter GG.No abstract available
Serum penicillin and dihydrostreptomycin concentrations in horses after intramuscular administration of selected preparations containing these antibiotics.
Journal of the American Veterinary Medical Association    September 1, 1972   Volume 161, Issue 5 490-495 
Rollins LD, Teske RH, Condon RJ, Carter GG.No abstract available
Comparison of immunization methods for producing reference adenovirus antisera in horses.
Applied microbiology    September 1, 1972   Volume 24, Issue 3 398-404 doi: 10.1128/am.24.3.398-404.1972
Hierholzer JC, Gamble WC, Quist KD, Chappell WA.Horses were immunized by a variety of inoculation procedures designed to determine the most efficient method of producing antisera to adenovirus types 25 to 31. The procedures evaluated included immunization by (i) direct intravenous (iv) injection, (ii) iv infusion, (iii) intramuscular (im) injection of virus with and without Freund's incomplete adjuvant, (iv) combined iv and im injections, and (v) combined iv infusion and im injection. The im schedule (no. 3) was superior to the others in terms of immunizing antigen and time required, and hemagglutination-inhibition (HI) and serum-neutralizi...
Ampicillinemia following single intramuscular injection of sodium ampicillin in horses.
Veterinary medicine, small animal clinician : VM, SAC    April 1, 1971   Volume 66, Issue 4 374 
Evans LH, Stewart JV, Huebner RA.No abstract available
[Penetration of streptomycin into the aqueous humor and cerebrospinal fluid in the horse following intra-muscular administration].
Zentralblatt fur Veterinarmedizin. Reihe A    April 1, 1970   Volume 17, Issue 4 378-379 
Kottman J, Hanák J, Zakopal J.No abstract available
Blood concentration of chloramphenicol in horses after intramuscular or oral administration.
Nihon juigaku zasshi. The Japanese journal of veterinary science    February 1, 1968   Volume 30, Issue 1 25-28 doi: 10.1292/jvms1939.30.25
Oishi S.No abstract available
Propagation of Western Equine Encephalitis Virus in Mice Following Intramuscular and Intranasal Inoculation. FROESCHLE JE.No abstract available