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.
Stability of cephalosporins in horse serum.
Antimicrobial agents and chemotherapy    January 1, 1977   Volume 11, Issue 1 174-175 doi: 10.1128/AAC.11.1.174
Foglesong MA.The antibiotic activity of cephalothin, cephaloridine, cephalexin, cephaloglycin, cefazolin, and cefamandole was determined after storage for up to 30 days in horse serum at -10 and 4 degrees C. Cephalothin, cefamandole, cefazolin, and cephalexin were stable for at least 30 days at -10 degrees C, whereas cephaloridine lost 29% of its initial activity and cephaloglycin lost more than 50%. Cefamandole, cefazolin, and cephalexin could only be stored for 3 days at 4 degrees C without significant loss in activity, whereas cephalothin, cephaloridine, and cephaloglycin could be stored for only 1 day....
Liver fluke infection in horses and ponies.
Equine veterinary journal    January 1, 1977   Volume 9, Issue 1 29-31 doi: 10.1111/j.2042-3306.1977.tb03969.x
Owen JM.Thirty eight cases of Fasciola hepatica infection in horses with associated clinical signs are reported. A method of examining large amounts of faeces for fluke is described. A safe method of treatment for infected horses is given which involves oral medication with oxyclozanide at a dose rate of 15 ml/50 kg body weight.
Metabolism of biogenic amines in the pulmonary circulation.
Bibliotheca anatomica    January 1, 1977   Issue 16 Pt 2 387-389 
Gillis CN.No abstract available
Rapid heterolysis of indophenyl acetate by a constituent of a preparation of horse serum cholinesterase.
Enzyme    January 1, 1977   Volume 22, Issue 2 130-136 doi: 10.1159/000458777
Hubbard CD, Shoupe TS.A transient phase for the hydrolysis of indophenyl acetate by the commercial preparation of horse serum cholinesterase was observed on a stopped-flow spectrophotometer. It was found that the transient process is a reaction of the ester with a major component of the preparation and is not caused by the serum cholinesterase enzyme. This noncholinesterase component was isolated and the dependence of its concentration and that of the ester upon the transient liberation of the indophenolate ion were determined. Studies with the isolated component and subsequent analyses have led to the tentative id...
The effect of parenteral acepromazine and xylazine on intraocular pressure in the horse.
Veterinary medicine, small animal clinician : VM, SAC    December 11, 1976   Volume 71, Issue 12 1727-1730 
McClure JR, Gelatt KN, Gum GG, Manning JP.No abstract available
Evaluation of an enteric-coated microencapsulated formulation of trichlorfon in horses.
Veterinary medicine, small animal clinician : VM, SAC    December 1, 1976   Volume 71, Issue 12 1737-1742 
Greve JH, Paul JW.No abstract available
Penicillins in veterinary practice.
Modern veterinary practice    December 1, 1976   Volume 57, Issue 12 1019-1023 
Clark CH.No abstract available
[Effectiveness of fenbendazole (Panacur-Hoechst) and cambendazole (MSD) against roundworms in horses’ alimentary tract].
Medycyna weterynaryjna    December 1, 1976   Volume 32, Issue 12 734-737 
Furmaga S, Gundlach L, Patyra J.No abstract available
[Gastric juice–an effective drug].
Veterinariia    November 1, 1976   Issue 11 28-29 
Malysheva NI, Dieva VT, Divina EG, Chuklov NF, Mengel' IV.No abstract available
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...