Analyze Diet

Topic:Pharmacology

Pharmacology in horses involves the study and application of drugs and medications to diagnose, treat, and prevent diseases and conditions in equine species. This field encompasses the understanding of pharmacokinetics and pharmacodynamics specific to horses, including how drugs are absorbed, distributed, metabolized, and excreted by the equine body. Commonly studied pharmacological agents in horses include non-steroidal anti-inflammatory drugs (NSAIDs), antibiotics, sedatives, and anthelmintics. Research in equine pharmacology focuses on determining appropriate dosages, understanding drug interactions, and minimizing adverse effects. This page compiles peer-reviewed research studies and scholarly articles that investigate the efficacy, safety, and regulatory aspects of pharmacological interventions in equine veterinary practice.
Electron capture detection of an apomorphine heptafluorobutyrate derivative at low picogram levels.
Research communications in chemical pathology and pharmacology    November 1, 1976   Volume 15, Issue 3 447-455 
Miller JR, Blake JW, Tobin T.An electron capturing derivative of apomorphine was prepared by incubating the drug with heptafluorobutyric anhydride (HFBA), triethylamine and heat. Mass spectral analysis suggests that HFBA reacts with both phenolic hydroxyl groups on apomorphine to give a derivative detectable at low picogram levels. This method is sufficiently sensitive for pharmacokinetic studies in the horse and is likely applicable to other dopaminergic analogues of apomorphine.
Summary of the effect of prostalene, a new synthetic prostaglandin, on the breeding efficiency of mares.
Veterinary medicine, small animal clinician : VM, SAC    November 1, 1976   Volume 71, Issue 11 1616-1623 
Averkin G, Schiltz R.No abstract available
Broad-spectrum penicillins.
Modern veterinary practice    November 1, 1976   Volume 57, Issue 11 936-940 
Clark CH.No abstract available
Effects of repeated daily injections of prostaglandin F2alpha on ovaries in mares.
Prostaglandins    November 1, 1976   Volume 12, Issue 5 881-894 doi: 10.1016/0090-6980(76)90061-7
Douglas RH, Ginther OJ.In experiment 1, seven groups of pony mares (2 or 3/group) were given either no injections (controls), or 5 (5X) or 10 (10X) daily subcutaneous (SC) injections of 1.25 mg PGF2alpha beginning on days 1, 7 or 13 post-ovulation. Compared to controls (24.5 days), the interovulatory interval was longer (P less than ..05) for day 7, 10X (33.5 days) and day 13, 10X mares (49.0 days) but was not different for the remaining groups. In experiment 2, nine groups of pony mares (4/group) were given either no injections (controls) or 1 (1X) or 10 (10X) daily SC injections of 1.25 mg PGF2alpha beginning on d...
[Banmith paste for planful strongyles control in the horse].
DTW. Deutsche tierarztliche Wochenschrift    October 5, 1976   Volume 83, Issue 10 431-432 
Ende H, Stoye M.No abstract available
Effects of Saffan administered intravenously in the horse.
The Veterinary record    October 2, 1976   Volume 99, Issue 14 270-272 doi: 10.1136/vr.99.14.270
Eales FA.Saffan was injected intravenously on 41 occasions in 11 horses and ponies to investigate its possible use in clinical equine anaesthesia. The optimum dose for induction was 1-90 mg per kg. This dose was divided into two halves, the first half given in five seconds and the second half, containing suxamethonium chloride 0.1 mg per kg, in the next 10 seconds. Induction was associated with excitement for up to 30 secs after the assumption of recumbency. At this dose rate anaesthesia lasted five to eight minutes. Muscle relaxation was poor. Recovery was associated with marked tactile and audible hy...
Drug interactions in the horse: effect of furosemide on plasma and urinary levels of phenylbutazone.
Research communications in chemical pathology and pharmacology    October 1, 1976   Volume 15, Issue 2 257-265 
Roberts BL, Blake JW, Tobin T.Horses pretreated with 6.6 mg/kg of phenylbutazone were injected with 1 mg/kg of furosemide intravenously. Furosemide had no clinically significant effect on either plasma levels or plasma half-life of phenylbutazone. Furosemide reduced urinary levels of phenylbutazone 18-fold to concentrations which may result in inconsistent drug detection in routine screening tests. The results show that it is not possible to monitor compliance with phenylbutazone medication rules by means of urinalysis alone if the use of furosemide is permitted. Furosemide treatment, however, does not interfere with monit...
The use of Dopram as a respiratory stimulant following Immobilon in the pony.
Equine veterinary journal    October 1, 1976   Volume 8, Issue 4 173-175 doi: 10.1111/j.2042-3306.1976.tb03334.x
Hillidge CJ.The effects of the analeptic agent, Dopram (doxapram hydrochloride) were investigated in 2 ponies during Immobilon - induced neuroleptanalgesia. Although Dopram was demonstrated to exert a degree of respiratory stimulation, this was concluded to provide no overall advantage. The etorphine-induced hypoxic hypoxia was only partially reversed, and there was additional cardiovascular stimulation, in contrast to the previously reported tendency for arterial blood pressure to return towards conscious control values during the course of action of Immobilon.
Stimulation of food intake in horses by diazepam and promazine.
Pharmacology, biochemistry, and behavior    October 1, 1976   Volume 5, Issue 4 495-497 doi: 10.1016/0091-3057(76)90116-7
Brown RF, Houpt KA, Schryver HF.In two adult horses doses of 0.02-0.03 mg/kg diazepam, intravenously, increased 1 hr intake 54-75% above control levels. Intake was stimulated when the diet was a high grain, calorically dense one and also when the diet was a high fiber, calorically dilute one. Two young rapidly growing weanling horses showed an even more pronounced stimulation of intake. Following diazepam 1 hr intake was increased 105-240% above control lelvels. Promazine at a dose of 0.5 mg/kg also stimulated intake in adult horses, but not as markedly as did diazepam. A transquilizer and a neuroleptic appear to have a stim...
Pharmacology of procaine in the horse: procaine esterase properties of equine plasma and synovial fluid.
American journal of veterinary research    October 1, 1976   Volume 37, Issue 10 1165-1170 
Tobin T, Blake JW, Sturma L, Arnett S.Procaine added to whole equine blood or diluted plasma was hydrolyzed with half times of approximately 9 and 12 minutes, respectively, at 37 C. This hydrolytic activity was sensitive to heating and physostigmine, but did not affect procainamide. At pharmacologic concentrations of procaine, the rate of the hydrolytic reaction depended directly on the concentrations of plasma or procaine in the system and was less in whole blood than in plasma. These properties are consistent with hydrolysis being due to plasma esterases operating at less than saturating procaine concentrations. These esterases ...
Pine oil toxicity in the horse: drug detection, residues and pathological changes.
Research communications in chemical pathology and pharmacology    October 1, 1976   Volume 15, Issue 2 291-301 
Tobin T, Swerczek TW, Blake JW.This report concerns the detection and acute toxicity of pine oil (a commercially available disinfectant) after intravenous administration in horses. alpha Terpineol was identified as a major constituent of pine oil. alpha Terpineol was recovered from equine tissues by extraction into heptane and detected by gas chromatography, using either flame ionization detection or pentafluoropropionic anhydride derivatization and electron capture detection. After intravenous injection of 0.1 ml/kg, death due to massive pulmonary edema occurred within minutes. In this animal blood and tissue levels of alp...
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...
The gas-liquid chromatograph and the electron capture detection in equine drug testing.
British journal of sports medicine    October 1, 1976   Volume 10, Issue 3 129-132 doi: 10.1136/bjsm.10.3.129
Blake JW, Tobin T.Three gas-liquid chromatographic (G.L.C.) procedures discussed have been designed around the four "esses" of detection tests--speed, sensitivity, simplicity, and specificity. These techniques are admirably applicable to the very low plasma drug levels encountered in blood testing under pre-race conditions. The methods are equally applicable to post-race testing procedures, where both blood and urine samples are tested. Drugs can only rarely be detected by the electron capture detector (E.C.D.) without a prior derivatization step, which conveys to the drug(s) high electron affinity. Because of ...
Research and identification of tranquillizers – use of retention index.
British journal of sports medicine    October 1, 1976   Volume 10, Issue 3 143-146 doi: 10.1136/bjsm.10.3.143
Courtot D.At the request of the Service des Haras, our laboratory works on the toxicological problems of the sport-horse. These studies have resulted in the setting up of an anti-doping control for equestrian competitions of various types, not only flat racing. During events, horses, must be calm and docile to the riders' order. Frequently, the latter use tranquillizers to try and win events. The analytical method for the research and identification of these compounds is described. The technique involves successively: 1. alkalinisation of the sample - saliva, blood or urine after enzymatic hydrolysis. 2...
Acute hemodynamic effects of furosemide administered intravenously in the horse.
American journal of veterinary research    October 1, 1976   Volume 37, Issue 10 1177-1180 
Muir WW, Milne DW, Skarda RT.Intravenous administration of furosemide in the horse resulted in an immediate and significant decrease in right atrial pressure, pulmonary arterial pressure, pulmonary arterial wedge pressure, cardiac output, and stroke volume (P less than 0.05). There was a significant increase in total systemic vascular resistance and heart rate (P less than 0.05). There were no significant alterations in mean arterial pressure. Coincidental with these hemodynamic changes were increased urine production and associated increase in packed cell volume and total serum protein. All variables except cardiac outpu...
The rate of rise of intraventricular pressure as an index of myocardial contractility in conscious and anaesthetised ponies.
Research in veterinary science    September 1, 1976   Volume 21, Issue 2 176-183 
Hillidge CJ, Lees P.Measurements of the rate of rise of left ventricular blood pressure (dP/dt) have been made in conscious and anaesthetised ponies. Concurrent measurements of heart rate, mean arterial pressure and left ventricular pressure were also made in order to assess their relationship to values of dP/dt. Thiopentone-halothane and thiopentone-ether anaesthesia reduced the maximal rate of rise of intraventricular pressure (dP/dt max) from conscious control levels. After correcting for variations in the loading conditions of the ventricle, the depressant effect of halothane was still apparent, but the actio...
Pharmacology of procaine in the horse: a preliminary report.
American journal of veterinary research    September 1, 1976   Volume 37, Issue 9 1107-1110 
Tobin T, Blake JW, Tai CY, Arnett S.Rapid intravenous injection of 1 g of procaine hydrochloride in Thoroughbred mares produced variable signs of central nervous system excitation for as long as 4 minutes. Plasma concentrations of procaine were similarly variable and transient, decreasing with a half-life of approximately 25 minutes. In vitro, plasma from freshly collected equine blood hydrolyzed procaine with a half-life of approximately 7.5 minutes. This hydrolysis was apparently due to plasma esterases. Penicillin, when added free or complexed as procaine-penicillin, did not protect procaine against hydrolysis by these plasma...
Selected topics in laboratory animal medicine. Volume V. Anesthesiology.
Aeromedical reviews    August 1, 1976   Volume 5 1-110 
Cramlet SH, Jones EF.No abstract available
Active-site labelling of kallikreins by chloromethylketone derivatives.
General pharmacology    August 1, 1976   Volume 7, Issue 2-3 163-166 doi: 10.1016/0306-3623(76)90055-0
Sampaio CA, Prado ES.Ala-Phe-Lys-CH2-Cl is a chloromethylketone derivative which is able to promote the inhibition of several proteolytic enzymes. In this paper the inhibition of horse urinary and plasmatic kallikreins is described and this inhibition is compared to that produced in human plasma kallikrein. This compound was designed based upon the structure of bradykinin. This enzyme substrate system can provide a model for the study of the interactions between bradykinin and its receptor. The inhibition of the enzymes was achieved both for its esterase and kinin-releasing activities.
The preparation and testing of antihuman lymphoblast globulin for clinical use.
Transplantation    August 1, 1976   Volume 22, Issue 2 167-175 doi: 10.1097/00007890-197608000-00012
Phillips AW, Woodrooffe JG, Courtenay JS, Whitaker AM, Thomas D, Woiwod AJ.Antibodies to cultured human lymphoblasts were raised in horses using a schedule employing both subcutaneous and intravenous routes of injection. Plasma from groups of horses was pooled and the IgG prepared from each pool was tested extensively for safety and immunosuppressive efficacy in vitro and in vivo. On the basis of the results of skin grafting in monkeys, only globulins derived from the first main bleeds were blended to produce a bulk for clinical use. One early pool of globulin was discarded because when undiluted, it was lethal in monkeys by the intravenous route, and another pool wa...
The selection of antibiotics.
The Veterinary record    July 24, 1976   Volume 99, Issue 4 61-64 doi: 10.1136/vr.99.4.61
Sanford J.The usefulness of an antibiotic depends not only upon its antibacterial potency and spectrum but also on the prevalence of resistant organisms and the extent and severity of the adverse reactions to which it may give rise. Variations in formulation of the same compound are reflected in differences in bioavailability. These may be intentional, as in the development of long-acting preparations, but may also be unexpected following differences in drug purity, content and gastro-intestinal absorption. Individual and species differences in treated animals also result in variations in bioavailabilit...
Foaling induced by a synthetic prostaglandin analogue (fluprostenol).
The Veterinary record    July 10, 1976   Volume 99, Issue 2 26-28 doi: 10.1136/vr.99.2.26
Rossdale Pd, Jeffcott LB, Allen WR.No abstract available
Influence of azaperone/metomidate anaesthesia on blood biochemistry in the horse.
The British veterinary journal    July 1, 1976   Volume 132, Issue 4 405-415 doi: 10.1016/s0007-1935(17)34641-9
Serrano L, Lees P, Hillidge CJ.Ponies were anaesthetized by administration of the ataractic, azaperone (0 · 2–0 · 8 mg/kg), in combination with the hypnotic, metomidate (3 · 5 mg/kg). Changes in blood biochemistry were measured during and following the course of action of these drugs. In control experiments, azaperone (0 · 4 and 0 · 8 mg/kg) was administered alone to other ponies. There were no significant changes in blood glucose concentration in either circumstance. Blood lactate and pyruvate concentrations and lactate/pyruvate ratio were not altered significantly by azaperone. However, moderate increases in lactat...
[Neuroleptic agents in veterinary medicine].
Veterinariia    July 1, 1976   Issue 7 99-100 
Cherviakov DK, Shityĭ AG, Rakhmaev SS.No abstract available
The problem of testing horse kidneys for the presence of antibiotics at meat inspection: how to avoid a false positive reaction.
Nordisk veterinaermedicin    July 1, 1976   Volume 28, Issue 7-8 377-380 
Korkeala H, Stabel-Taucher R, Pekkanen TJ.When 33 horse kidneys were tested for the presence of inhibitory substances by the Bacillus subtilis BGA method at pH 8 and the Micrococcus luteus ATCC 9341 method, 24 were positive and 9 negative. The pH of the seeded M. luteus test medium changed from pH 6.6 before incubation to 8.7 after 24 hours incubation at 30 degrees C. When the same 33 kidneys were tested by the B. subtilis BGA method, medium pH 6, and 15 of them also by the M. luteus method using a medium buffered to pH 6, all were negative. The cadmium concentration of the 33 horse kidneys was found to be 70.17 +/- 81.28 mg/kg wet we...
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 influence of hepatic microsomal amidopyrine demethylase activity on halothane hepatotoxicity in the horse.
The Journal of pathology    June 1, 1976   Volume 119, Issue 2 105-112 doi: 10.1002/path.1711190205
Gopinath G, Ford EJ.The hepatotoxic effect of oral halothane in the horse is increased by pretreatment with phenobarbitone or DDT but not by chlorpromazine. Phenobarbitone and DDT increase the activity of hepatic amidopyrine N-demethylase but chlorpromazine does not. Carbon disulphide protects the liver of the horse against halothane.
Pharmacological studies on the isolated taenia coli from the horse [proceedings].
West African journal of pharmacology and drug research    June 1, 1976   Volume 3, Issue 1 73P-74P 
Akubue PI.No abstract available
Studies on the development and chemotherapy of larvae of Parascaris equorum (Nematoda: Ascaridoidea) in experimentally and naturally infected foals.
The Journal of parasitology    June 1, 1976   Volume 62, Issue 3 453-459 
Lyons ET, Drudge JH, Tolliver SC.Experimentally induced infections of Parascaris equorum in worm-free pony foals required 14 to 17 days for migration of the larvae through the liver and lungs, and 79 to 110 days to become gametogenically functional. Treatment of experimentally infected or naturally exposed foals during the parenteral phase of development, using levamisole at 8 mg/kg, a mixture of levamisole at 8 mg/kg plus piperazine at 88 mg base equivalent/kg, or dl-tetramisole at 10 mg/kg, was quite efficacious in (1) reducing the number of P. equorum larvae recovered from the small intestines of the foals at necropsy, or ...
Critical tests of anthelmintic activity of a paste formulation of thiabendazole in horses.
American journal of veterinary research    June 1, 1976   Volume 37, Issue 6 701-702 
Lyons ET, Drudge JH, Tolliver SC.Critical tests of the activity on large strongyles, ascarids, mature pinworms, and bots were carried out in 11 horses intraorally treated with a paste formulation of thiabendazole. The dose level of 44 mg/kg was administered to 3 horses, and the dose level of 88 mg/kg to 8 horses. Removals of Strongylus vulgaris and mature Oxyuris equi were 100% at the 2 dose levels, and efficacy against Strongylus edentatus varied from 95 to 99% and 89 to 100% for the 44- and the 88-mg/kg dose levels, respectively. Strongylus equinus was completely removed from the 1 infected horse treated at the dose level o...