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Topic:Drug

The topic of drugs and horses encompasses the study of various pharmacological agents used in equine medicine for therapeutic purposes. This includes the administration of medications for pain management, disease treatment, and performance enhancement. The pharmacokinetics and pharmacodynamics of drugs in horses are key areas of research, as they determine the absorption, distribution, metabolism, and excretion of these substances. Additionally, the topic covers the detection and regulation of substances in competitive equestrian sports to ensure fair play and animal welfare. This page compiles peer-reviewed research studies and scholarly articles that explore the effects, safety, and regulatory aspects of drug use in equine health and performance.
The search for the ultimate equine sedative: are we ‘Waiting for Godot’? Combined use of detomidine with opiates in the horse.
Equine veterinary journal    March 1, 1989   Volume 21, Issue 2 96-97 
Jöchle W, Vähä-Vahe T.No abstract available
Doping in race horses.
Journal of the South African Veterinary Association    March 1, 1989   Volume 60, Issue 1 4-6 
Debackere M.No abstract available
Bioavailability and pharmacokinetics of sulfamethazine in the pony.
Journal of veterinary pharmacology and therapeutics    March 1, 1989   Volume 12, Issue 1 99-102 doi: 10.1111/j.1365-2885.1989.tb00647.x
Wilson RC, Hammond LS, Clark CH, Ravis WR.No abstract available
Single-dose pharmacokinetics of detomidine in the horse and cow.
Journal of veterinary pharmacology and therapeutics    March 1, 1989   Volume 12, Issue 1 65-72 doi: 10.1111/j.1365-2885.1989.tb00643.x
Salonen JS, Vähä-Vahe T, Vainio O, Vakkuri O.The pharmacokinetics of detomidine, a novel analgesic sedative, was studied in the major target species after high (80 micrograms/kg) i.v. and i.m. doses. In addition, drug residues in some organs were determined. Concentrations were measured using a sensitive, detomidine-specific radio-immunoassay method. Rapid absorption following i.m. dosing occurred. Absorption half-lives were 0.15 h (horse) and 0.08 h (cattle). The mean peak concentration in the horse (51.3 ng/ml) was achieved in 0.5 h and in the cow (65.8 ng/ml) in 0.26 h. The areas under the concentration curve after i.m. dosing were 66...
[Anesthesia of horses in the standing position].
Archiv fur experimentelle Veterinarmedizin    March 1, 1989   Volume 43, Issue 2 199-213 
Bülow A, Bülow T, Mill J, Dietz O.Painful interventions can be performed on horse in standing position by means of sedative analgesia, also called standing-position anaesthesia. Combinations of anaesthetics are quite often used, in that context, for the purpose of producing analgetic effects stronger and more reliable than those that would be obtainable from one anaesthetic alone. The following combinations were comparatively tested for their analgetic and sedative effects and their effects upon the organism: Chloralhydrate with Ursonarkon (oxazolidone), Chloralhydrate with Rompun (xylazine), Chloralhydrate with morphine hydro...
ELISA detection of fentanyl in horse urine and plasma.
Journal of veterinary pharmacology and therapeutics    March 1, 1989   Volume 12, Issue 1 1-4 doi: 10.1111/j.1365-2885.1989.tb00633.x
Delbeke FT, Debackere M.The prototype of a commercial ELISA test kit designed for fentanyl determination in human urine has been evaluated for screening fentanyl in horse urine and plasma. The measurement of fentanyl after intravenous (2 mg) and intramuscular (0.25 mg) administration in undiluted plasma was not reproducible while accurate quantification of fentanyl in urine greatly depends on the composition of the horse urine. The ELISA assay, however, is simple and could be successfully used for quantitative measurements in diluted urine and for rapid qualitative screening for fentanyl in large numbers of urine sam...
Immunoassay detection of drugs in racing horses. IX. Detection of detomidine in equine blood and urine by radioimmunoassay.
Research communications in chemical pathology and pharmacology    February 1, 1989   Volume 63, Issue 2 263-279 
Wood T, Tai CL, Taylor DG, Woods WE, Wang CJ, Houtz PK, Tai HH, Weckman TJ, Yang JM, Sturma L.Detomidine is a potent non-narcotic sedative agent which is currently in the process of being approved for veterinary clinical use in the United States. Since no effective screening method in horses is available for detomidine, we have developed an 125I radioimmunoassay for detomidine in equine blood and urine as part of a panel of tests for illegal drugs in performance horses. Our 125I radioimmunoassay has an I-50 for detomidine of approximately 2 ng/ml. Our assay shows limited cross-reactivity with the pharmacodynamically similar xylazine, but does not cross-react with acepromazine, epinephr...
[Anesthesia of horses with xylazine and ketamine. 1. Anesthesia of foals].
Tierarztliche Praxis    January 1, 1989   Volume 17, Issue 4 388-393 
Schmidt-Oechtering GU.The anaesthesia with Xylazine and Ketamine in 24 foals is described. Special qualities of this form of anaesthesia and dosages for foals of different age are discussed. The combination of Xylazine and Ketamine is well suited for the anaesthesia of foals of all age and risk-groups. The induction takes place quickly and calmly, without signs of cardiorespiratory depression. The maintenance of anaesthesia is possible, without any problem, by repeated injection with Xylazine and Ketamine, as well as by inhalation anaesthesia with volatile anaesthetics. The recovery is short; the animals rise swift...
Narcotic analgesics, their detection and pain measurement in the horse: a review.
Equine veterinary journal    January 1, 1989   Volume 21, Issue 1 4-12 doi: 10.1111/j.2042-3306.1989.tb02081.x
Kamerling S, Wood T, DeQuick D, Weckman TJ, Tai C, Blake JW, Tobin T.Narcotic analgesics produce pharmacological effects by interacting with specific opiate receptors. At least five major types of opiate receptors have been recognised. These include mu (morphine) and kappa (ethylketazocine) receptor types. Narcotic analgesics which interact with mu receptors produce locomotor and autonomic stimulation at doses that produce little or no analgesia. Therefore, use of these drugs as analgesics in equine medicine has not been very satisfactory. Theoretical considerations suggested that the role of kappa agonists in equine analgesia be investigated. Using a pure kapp...
Pharmacokinetics and body fluid and endometrial concentrations of ormetoprim-sulfadimethoxine in mares. Brown MP, Gronwall RR, Houston AE.Six healthy adult mares were each given an oral loading dose of ormetoprim(OMP)-sulfadimethoxine (SDM) at a dosage of 9.2 mg of OMP/kg and 45.8 mg of SDM/kg, followed by four maintenance doses of 4.6 mg of OMP/kg and 22.9 mg of SDM/kg, at 24 h intervals. Ormetoprim and SDM concentrations were measured in serum, synovial fluid, peritoneal fluid, cerebrospinal fluid, urine and endometrium. The highest mean serum OMP concentration was 0.92 micrograms/mL 0.5 h after the first dose; the highest mean SDM concentration was 80.9 micrograms/mL 8 h after the first dose. The highest mean synovial fluid c...
The determination of non-steroidal anti-inflammatory drugs by GC-MS-MS in equine urine.
Journal of pharmaceutical and biomedical analysis    January 1, 1989   Volume 7, Issue 12 1617-1622 doi: 10.1016/0731-7085(89)80173-6
de Jong EG, Kiffers J, Maes RA.Results are given for a more sensitive screening procedure for non-steroidal anti-inflammatory drugs using GC-MS-MS. By monitoring a selected characteristic reaction for each drug very low detection limits are reached even in a difficult biological matrix such as equine urine. Detection down to 5 ng ml-1 for ibuprofen, ibufenac, alclofenac, fenoprofen, ketoprofen, naproxen and diclofenac is possible in contrast to the 0.5 microgram ml-1 limit for normal GC-MS detection. Examples are given of real positive cases for diclofenac and ibuprofen.
A preliminary comparison of lidocaine and xylazine as epidural analgesics in ponies.
Veterinary surgery : VS    January 1, 1989   Volume 18, Issue 1 85-86 doi: 10.1111/j.1532-950x.1989.tb01046.x
Fikes LW, Lin HC, Thurmon JC.Xylazine (0.35 mg/kg) or lidocaine (0.35 mg/kg) was injected into the epidural space of six ponies to compare their effectiveness as epidural analgesics. Each pony received both treatments at 1 week intervals with the order of treatments randomized. Xylazine produced analgesia of significantly longer duration (247 +/- 58 minutes) than that produced by an equal dose of lidocaine (135 +/- 22 minutes). Mild transient ataxia of no clinical significance developed in all ponies with both treatments. Spinal cords were removed from two ponies and examined histologically. No discernible pathologic chan...
Interactions between chloramphenicol, acepromazine, phenylbutazone, rifampin and thiamylal in the horse.
Equine veterinary journal    January 1, 1989   Volume 21, Issue 1 34-38 doi: 10.1111/j.2042-3306.1989.tb02086.x
Burrows GE, MacAllister CG, Tripp P, Black J.The potential for interactions between chloramphenicol, phenylbutazone, acepromazine and thiamylal and chloramphenicol, rifampin, and phenylbutazone were evaluated in two groups of experiments. In the first, five horses were given thiamylal intravenously (iv) (6.6 mg/kg) after pretreatment with acepromazine, and the time of recumbency was determined. Administration of chloramphenicol iv (25 mg/kg) 1 h prior to anaesthesia significantly lengthened the recumbency time from 21.8 +/- 4.8 mins to 36.0 +/- 8.3 mins. There was an apparent but not statistically significant decrease in recumbency time ...
Immunoassay detection of drugs in racing horses. XI. ELISA and RIA detection of fentanyl, alfentanil, sufentanil and carfentanil in equine blood and urine.
Research communications in chemical pathology and pharmacology    January 1, 1989   Volume 63, Issue 1 129-152 
Tobin T, Kwiatkowski S, Watt DS, Tai HH, Tai CL, Woods WE, Goodman JP, Taylor DG, Weckman TJ, Yang JM.We have developed and evaluated a one step enzyme-linked immunosorbent assay (ELISA) test for sufentanil and a 125I radioimmunoassay test for alfentanil as part of a panel of pre- and post-race tests for narcotic analgesics in racing horses. Our sufentanil ELISA test detects sufentanil with an I-50 of about 0.5 ng/ml. The test is rapid and economical in that it can be read with an inexpensive spectrophotometer, or even by eye. The test readily detects the presence of sufentanil or its metabolites in equine blood and urine from 1 to 24 hours respectively after administration of therapeutic or s...
In vitro susceptibility of Pseudomonas mallei to antimicrobial agents.
Comparative immunology, microbiology and infectious diseases    January 1, 1989   Volume 12, Issue 1-2 5-8 doi: 10.1016/0147-9571(89)90003-9
Al-Izzi SA, Al-Bassam LS.Pseudomonas mallei was isolated from pus samples obtained from 34 mallein-positive horses. The isolates were subjected to in vitro sensitivity test using 16 different antimicrobial discs. All isolates (34) were sensitive to sulfamethizole, gentamycin, tetracycline, sulfathiazole, kanamycin, tobramycin, streptomycin and a combination of trimethoprim and sulfamethoxazole while none of them were sensitive to cephalothin, colistin, ampicillin, penicillin and nitrofurantoin. Rifapicin, chloramphenicol and carbenicillin were effective against 32, 26 and 18 isolates respectively. The minimum inhibito...
Screening, confirmation and quantification of boldenone sulfate in equine urine after administration of boldenone undecylenate (Equipoise).
Journal of chromatography    December 9, 1988   Volume 433 9-21 doi: 10.1016/s0378-4347(00)80580-0
Weidolf LO, Chichila TM, Henion JD.Methods for screening by thin-layer chromatography, quantification by high-performance liquid chromatography with ultraviolet detection and confirmation by gas chromatography-mass spectrometry of boldenone sulfate in equine urine after administration of boldenone undecylenate (Equipoise) are presented. Sample work-up was done with C18 liquid-solid extraction followed by solvolytic cleavage of the sulfate ester. Confirmatory evidence of boldenone sulfate in equine urine was obtained from 2 h to 42 days following a therapeutic intramuscular dose of Equipoise. The use of 19-nortestosterone sulfat...
Misuse of antibiotics in horses.
The Veterinary record    December 3, 1988   Volume 123, Issue 23 608 
Robinson LR.No abstract available
Drug-sensitivity of Klebsiella pneumoniae derived from horses.
Nihon juigaku zasshi. The Japanese journal of veterinary science    December 1, 1988   Volume 50, Issue 6 1268-1270 doi: 10.1292/jvms1939.50.1268
Eguchi M, Kuniyasu C, Ohmae K, Kashiwazaki M.No abstract available
Clinical pharmacokinetics of metronidazole in horses.
Journal of veterinary pharmacology and therapeutics    December 1, 1988   Volume 11, Issue 4 417-420 doi: 10.1111/j.1365-2885.1988.tb00205.x
Baggot JD, Wilson WD, Hietala S.No abstract available
Epidural injection of xylazine for perineal analgesia in horses.
Journal of the American Veterinary Medical Association    December 1, 1988   Volume 193, Issue 11 1405-1408 
LeBlanc PH, Caron JP, Patterson JS, Brown M, Matta MA.Local anesthetics given in the epidural space of a horse may cause hind limb weakness in addition to analgesia. Because alpha 2 agonists given by epidural injection cause sensory blockade without motor effects in human beings and other species, their use in veterinary anesthesia is appealing. This study was designed to examine the effectiveness of xylazine HCl, an alpha 2 agonist commonly used in horses. Xylazine, 0.9% NaCl, and lidocaine were given by epidural injection to horses subjected to perineal electrical stimulation. Administration of xylazine (0.17 mg/kg of body weight, diluted to a ...
Studies on the effect of short term, high dose praziquantel treatment against protoscoleces of ovine and equine Echinococcus granulosus within the cyst, and in vitro. Richards KS, Riley EM, Taylor DH, Morris DL.Protoscoleces of Echinococcus granulosus were subjected to high concentrations of praziquantel (10-1000 micrograms/ml medium or cyst fluid) for a short, 10 min duration in vitro or in situ within cysts. Drug efficacy was then monitored either by in vitro culture in drug-free medium and/or by passage into rodents. The in vitro test of effectiveness suggested that ovine-derived protoscoleces were more sensitive than those of equine origin, and that the in vitro method of treatment was more successful than that performed in situ. However, the subsequent passage of treated protoscoleces, whether i...
Non-isotopic immunoassay drug tests in racing horses: a review of their application to pre- and post-race testing, drug quantitation, and human drug testing.
Research communications in chemical pathology and pharmacology    December 1, 1988   Volume 62, Issue 3 371-395 
Tobin T, Watt DS, Kwiatkowski S, Tai HH, Blake JW, McDonald J, Prange CA, Wie S.We have introduced large scale non-isotopic immunoassay testing into pre- and post-race drug testing in racehorses. The technologies utilized are Particle Concentration Fluorescence Immuno Assay (PCFIA) and the one-step Enzyme Linked Immuno Sorbent Assay (ELISA). These technologies are rapid, inexpensive, and highly effective. On introduction into post-race testing in the Western United States, these ELISA tests exposed several previously undetected patterns of drug abuse. The drugs detected were buprenorphine, oxymorphone, mazindol, sufentanil and cocaine. This led to the suspension of a larg...
Prokinetic effects of cisapride, naloxone and parasympathetic stimulation at the equine ileo-caeco-colonic junction.
Journal of veterinary pharmacology and therapeutics    December 1, 1988   Volume 11, Issue 4 322-329 doi: 10.1111/j.1365-2885.1988.tb00191.x
Ruckebusch Y, Roger T.The electromyogram of the terminal ileum, the caecum and the proximal right ventral colon was recorded in fasted conscious ponies receiving intravenously equiactive doses of pilocarpine (0.05 mg/kg) and carbachol (0.01 mg/kg) as acetylcholine analogues; cisapride (0.1 mg/kg) and metoclopramide (2 mg/kg) facilitating acetylcholine release from myenteric neurones and naloxone (0.05 mg/kg) as an antagonist of the endogenous inhibitory opioid system. Both cisapride and naloxone induced typical migrating spike bursts in the colon associated with contractions of caecal body and caecal base. Both pil...
Pharmacokinetics, bioavailability, and in vitro antibacterial activity of rifampin in the horse.
American journal of veterinary research    December 1, 1988   Volume 49, Issue 12 2041-2046 
Wilson WD, Spensley MS, Baggot JD, Hietala SK.The pharmacokinetics and bioavailability of rifampin were determined after IV (10 mg/kg of body weight) and intragastric (20 mg/kg of body weight) administration to 6 healthy, adult horses. After IV administration, the disposition kinetics of rifampin were best described by a 2-compartment open model. A rapid distribution phase was followed by a slower elimination phase, with a half-life (t1/2[beta]) of 7.27 +/- 1.11 hours. The mean body clearance was 1.49 +/- 0.41 ml/min.kg, and the mean volume of distribution was 932 +/- 292 ml/kg, indicating that rifampin was widely distributed in the body....
Actions of the novel gastrointestinal prokinetic agent cisapride on equine bowel motility.
Journal of veterinary pharmacology and therapeutics    December 1, 1988   Volume 11, Issue 4 314-321 doi: 10.1111/j.1365-2885.1988.tb00190.x
King JN, Gerring EL.The effect of cisapride was evaluated on the normal fasting bowel motility of four ponies with chronically implanted electromechanical transducers. Cisapride was infused over 60-min periods at 0.05 mg/kg (n = 4), 0.1 mg/kg (n = 5) and 0.25 mg/kg (n = 5). It produced marked and prolonged increases in electrical and mechanical activity at all sites examined. In the stomach there was increased total contraction activity with increased contraction amplitude and a slight reduction in rate. In the small intestine there was an increase in irregular (phase II) activity with an increase in number and a...
Misuse of antibiotics in horses.
The Veterinary record    November 19, 1988   Volume 123, Issue 21 556 doi: 10.1136/vr.123.21.556-a
de Ban NE.No abstract available
[Pathogenesis and drug therapy of acute laminitis in horses: a literature review].
Tijdschrift voor diergeneeskunde    November 15, 1988   Volume 113, Issue 22 1237-1246 
Boosman R, Németh F.Impairment of the microcirculation in the distal part of the foot is an important factor in the aetiology of equine laminitis. To prevent the development of chronic laminitis and the resulting complications, two new therapeutical principles were tested in the treatment of acute laminitis. Thrombosis which frequently occurs in the corium of the foot, could be controlled by administration of anticoagulants such as heparin. Alpha-receptor blocking agents such as phenoxybenzamine were used, to improve the peripheral blood flow. The use of these drugs and that of anti-inflammatory agents during the...
World Association for the Advancement of Veterinary Parasitology (W.A.A.V.P.) guidelines for evaluating the efficacy of equine anthelmintics.
Veterinary parasitology    November 1, 1988   Volume 30, Issue 1 57-72 doi: 10.1016/0304-4017(88)90142-2
Duncan JL, Arundel JH, Drudge JH, Malczewski A, Slocombe JO.These guidelines have been designed to assist in the planning, operation and interpretation of studies which would serve to assess the efficacy of drugs against internal parasites of horses. Although the term anthelmintic is used in the title and text, these guidelines include studies on drug efficacy against larvae of horse bot flies, Gasterophilus spp, which are non-helminth parasites commonly occurring in the stomach of horses. The advantages, disadvantages and application of critical and controlled tests are presented. Information is also provided on selection of animals, housing, feed, do...
Disposition and excretion of flunixin meglumine in horses.
American journal of veterinary research    November 1, 1988   Volume 49, Issue 11 1894-1898 
Soma LR, Behrend E, Rudy J, Sweeney RW.The disposition of flunixin meglumine administered IV at a dosage of 1.1 mg/kg was described by a 2-compartment model; the alpha and beta half-lives (t1/2) were 0.61 and 1.5 hours, respectively. When administered IV at a rate of 2.2 mg/kg, the disposition was best described by a 3-compartment model, and the alpha, beta, and lambda t1/2 were 0.16, 1.52, and 6.00 hours, respectively. The zero-time plasma concentrations after flunixin meglumine was administered at 1.1 and 2.2 mg/kg were 9.3 +/- 0.76 and 21.5 +/- 7.4 mg/L, respectively. The bioavailability after oral administration of 1.1 mg/kg wa...
Oxfendazole: activity of a two-dose treatment regimen on natural infections of internal parasites of equids, with emphasis on migrating large strongyles in controlled tests in 1986 and 1987.
American journal of veterinary research    November 1, 1988   Volume 49, Issue 11 1923-1927 
Lyons ET, Tolliver SC, Drudge JH, Swerczek TW.Oxfendazole paste formulation was administered intraorally at a dosage of 10 mg/kg of body weight, twice (48 hours between treatments) in 5 controlled tests (experiments A, B, C, D, and E) to 18 equids (14 horses and 4 ponies) that were 5 to 24 months old in 1986 and 1987. Activity was evaluated against naturally acquired infections of various internal parasites, with emphasis on migratory stages of Strongylus vulgaris and S edentatus. The number of treated and nontreated equids in each experiment (horses in experiments A to D and ponies in experiment E) was: A, 1 and 1; B, 3 and 3; C, 3 and 1...
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