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.
Disposition of ampicillin sodium in horses, ponies and donkeys after intravenous administration.
Equine veterinary journal. Supplement    February 1, 1992   Issue 11 59-61 doi: 10.1111/j.2042-3306.1992.tb04775.x
Horspool LJ, Sarasola P, McKellar QA.No abstract available
Influence of feeding schedule on the absorption of orally administered flunixin in the horse.
Equine veterinary journal. Supplement    February 1, 1992   Issue 11 62-65 doi: 10.1111/j.2042-3306.1992.tb04776.x
Welsh JC, Lees P, Stodulski G, Cambridge H, Foster AP.The effects of access to hay and of restricted feeding on the pharmacokinetics of flunixin administered orally to six healthy ponies were compared in a cross-over study. No access to feed for a few hours before and after flunixin administration resulted in rapid absorption with a mean peak plasma concentration of 2.84 +/- 0.28 micrograms/ml attained in an average time of 0.76 +/- 0.18 h, followed by an exponential decline in plasma concentration. A lower peak plasma concentration was obtained when ponies had free access to hay before and after drug dosing. The mean maximum concentration (Cmax)...
The pharmacology and pharmacokinetics of high-dose methocarbamol in horses.
Equine veterinary journal. Supplement    February 1, 1992   Issue 11 41-44 doi: 10.1111/j.2042-3306.1992.tb04771.x
Muir WW, Sams RA, Ashcraft S.The haemodynamic, respiratory and behavioural effects and pharmacokinetics of methocarbamol were studied in eight healthy, adult horses after intravenous (i.v.) and oral administration of large dosages. Heart rate, cardiac output, mean pulmonary arterial blood pressure, systolic, diastolic and mean aortic blood pressure, respiratory rate and arterial blood gases did not change after either i.v. (30 mg/kg bodyweight [bwt]) or oral (50 and 100 mg/kg bwt) dosages of methocarbamol. Mild to moderate depression was observed in five of eight horses administered i.v. methocarbamol, and in all horses a...
The veterinary importance of the toxic syndrome induced by ionophores.
Veterinary and human toxicology    February 1, 1992   Volume 34, Issue 1 66-70 
Novilla MN.Monensin, lasalocid, salinomycin, narasin and maduramicin are carboxylic ionophores intended for use as anticoccidial drugs for poultry and as growth promotants for ruminants. Generally, ionophores have been found safe and effective in the target animals receiving recommended dosage levels. However, toxic syndromes can result from overdosage and misuse situations. More information and reports of adverse reactions are available for monensin than the other ionophores because of monensin's longstanding and widespread use in the poultry and livestock industries. Care must be exercised in the diagn...
A comparison of injectable anaesthetic regimens in Mammoth asses.
Equine veterinary journal. Supplement    February 1, 1992   Issue 11 37-40 doi: 10.1111/j.2042-3306.1992.tb04770.x
Matthews NS, Taylor TS, Hartsfield SM, Williams JD.Xylazine (1.1 mg/kg body weight [bwt])-ketamine (2.2 mg/kg bwt) (X/K) anaesthesia was evaluated, in nine Mammoth asses, for effectiveness and compared with two other injectable anaesthetic combinations: xylazine (1.1 mg/kg bwt)-butorphanol (0.044 mg/kg bwt)-ketamine (2.2 mg/kg bwt) (X/B/K); and xylazine (1.1 mg/kg bwt)-tiletamine-zolazepam (1.1 mg/kg bwt) (X/T). All drugs were given intravenously (i.v.). Heart rate, respiratory rate, systolic blood pressure, arterial blood pH, PCO2, PO2, recumbency time and number of attempts to stand were measured. Quality of induction and recovery, muscle re...
The effects of famotidine, ranitidine and magnesium hydroxide/aluminium hydroxide on gastric fluid pH in adult horses.
Equine veterinary journal. Supplement    February 1, 1992   Issue 11 52-55 doi: 10.1111/j.2042-3306.1992.tb04773.x
Murray MJ, Grodinsky C.Gastric fluid pH was measured in five adult horses following nasogastric administration of famotidine, 0.5, 1.0, and 2.0 mg/kg bodyweight (bwt); ranitidine, 4.4 and 6.6 mg/kg bwt and an antacid containing magnesium hydroxide (40 mg/ml) and aluminium hydroxide (45 mg/ml), 120 and 180 ml. Fluid was aspirated through a 16 French nasogastric feeding tube at 15 min intervals, and pH was measured using a pH meter. Basal gastric fluid pH was measured at 20 min intervals for 6 h in each horse and, with the exception of two measurements of 4.66 and 4.17, ranged from 1.42 to 2.41, with a mean pH of 1.88...
Cardiovascular effects of dopexamine HCl in conscious and halothane-anaesthetised horses.
Equine veterinary journal. Supplement    February 1, 1992   Issue 11 24-29 
Muir WW.The cardiovascular effects of serial increasing infusions of dopexamine HCl were investigated in six conscious (1, 2, 4, 6, 10 micrograms/kg bodyweight [bwt]/min) and eight (0.5, 1, 5, 10, 20 micrograms/kg bwt/min) halothane-anaesthetised horses. Dopexamine produced dose-dependent increases in heart rate, +dP/dtmax' -dP/dtmax and cardiac output, and a decrease in systemic vascular resistance in conscious and halothane-anaesthetised horses. Mean arterial blood pressure did not change in conscious horses but increased to a maximum value at 10 micrograms/kg bwt/min in halothane-anaesthetised hors...
Sympatho-adrenal activity and the clinical sedative effect of detomidine in horses.
Equine veterinary journal. Supplement    February 1, 1992   Issue 11 66-68 doi: 10.1111/j.2042-3306.1992.tb04777.x
Raekallio M, Leino A, Vainio O, Scheinin M.Thirty-nine horses were given detomidine 10 micrograms/kg bodyweight (bwt) intravenously (iv) and six horses were given a corresponding volume of saline solution before minor procedures. Venous blood samples were collected for catecholamine and cortisol determination immediately before the detomidine or saline injection and 20 mins after it. The behaviour of the horse at the time of detomidine injection and the extent of sedation were evaluated. Plasma adrenaline, noradrenaline and the catecholamine metabolites, 3,4-dihydroxyphenylglycol (DHPG) and 3,4-dihydroxyphenylacetic acid (DOPAC), and c...
Endothelium-dependent relaxation to alpha-methyl-5-hydroxytryptamine in isolated horse coronary arteries.
Japanese journal of pharmacology    January 1, 1992   Volume 58 Suppl 2 322P 
Obi T, Kabeyama A, Nishio A.No abstract available
Cardiovascular effects and fatalities associated with intravenous administration of doxycycline to horses and ponies.
Equine veterinary journal    January 1, 1992   Volume 24, Issue 1 41-45 doi: 10.1111/j.2042-3306.1992.tb02777.x
Riond JL, Riviere JE, Duckett WM, Atkins CE, Jernigan AD, Rikihisa Y, Spurlock SL.Intravenous use of doxycycline in horses is associated with deleterious side effects on the cardiovascular system which may result in fatalities. At dosages and infusion rates used in these studies, supraventricular tachycardia, systemic arterial hypertension, clinical signs of discomfort, collapse and death were observed. Results of the present study suggest that the intravenous use of doxycycline should be avoided in horses.
Equine piroplasmosis: a review.
The British veterinary journal    January 1, 1992   Volume 148, Issue 1 6-14 doi: 10.1016/0007-1935(92)90061-5
de Waal DT.This review focuses on equine piroplasmosis with specific reference to its distribution, diagnosis and clinical and pathological signs. The more common used drugs are discussed both with reference to treatment and chemosterilization. Areas requiring further research are also briefly mentioned.
Inhibition of equine complement activity by polysulfated glycosaminoglycans.
American journal of veterinary research    January 1, 1992   Volume 53, Issue 1 87-90 
Rashmir-Raven AM, Coyne CP, Fenwick BW, Gaughan EM, Andrews GA, DeBowes RM.The ability of polysulfated glycosaminoglycans (PSGAG) to inhibit the complement cascade was evaluated. The role of complement in inflammation and infection has been well documented. Inhibition of the complement cascade by PSGAG could explain why intra-articularly administered PSGAG diminish diarthrodial joint inflammation and potentiate septic arthritis in horses. Hemolytic complement testing was performed to evaluate the effect of PSGAG on the equine classical and alternate pathways of complement, using rabbit erythrocytes as the target cells. Concentration of PSGAG between 0.2 mg/ml and 0.6...
The pharmacokinetics of a slow-release theophylline preparation in horses after intravenous and oral administration.
Veterinary research communications    January 1, 1992   Volume 16, Issue 2 131-138 doi: 10.1007/BF01839010
Errecalde JO, Landoni MF.The pharmacokinetics of a slow-release theophylline formulation was investigated following intravenous and oral administration at 10 mg/kg in horses. A tricompartmental model was selected to describe the intravenous plasma profile. The elimination half-life (t1/2 beta) was 16.91 +/- 0.93 h, the apparent volume of distribution (Vd) was 1.35 +/- 0.18 L/kg and the body clearance (ClB) was 0.061 +/- 0.009 L kg-1 h. After oral administration the half-life of absorption was 1.24 +/- 0.30 h, and the calculated bioavailability was above 100%. The t1/2 beta after oral administration was 18.51 +/- 1.75 ...
Ketamine, Telazol, xylazine and detomidine. A comparative anesthetic drug combinations study in ponies.
Acta veterinaria Scandinavica    January 1, 1992   Volume 33, Issue 2 109-115 doi: 10.1186/BF03547317
Lin HC, Branson KR, Thurmon JC, Benson GJ, Tranquilli WJ, Olson WA, Vähä-Vahe AT.This study was designed to assess the effects of 5 anesthetic drug combinations in ponies: (1) ketamine 2.75 mg/kg, xylazine 1.0 mg/kg (KX), (2) Telazol 1.65 mg/kg, xylazine 1.0 mg/kg (TX), (3) Telazol 2 mg/kg, detomidine 20 micrograms/kg (TD-20), (4) Telazol 2 mg/kg, detomidine 40 micrograms/kg (TD-40), (5) Telazol 3 mg/kg, detomidine 60 micrograms/kg (TD-60). All drugs were given iv with xylazine or detomidine preceding ketamine or Telazol by 5 min. Heart rate was decreased significantly from 5 min to arousal after TD-20 but only at 60 and 90 min after TD-40 and TD-60 respectively. Respirato...
Identification of detomidine carboxylic acid as the major urinary metabolite of detomidine in the horse.
European journal of drug metabolism and pharmacokinetics    January 1, 1992   Volume 17, Issue 1 13-20 doi: 10.1007/BF03189982
Salonen JS, Vuorilehto L, Gilbert M, Maylin GA.Horse urine was investigated for metabolites by chromatography and mass spectrometry following the oral administration of the large animal analgesic sedative detomidine to two stallions and intravenous administration of [3H]-detomidine to a mare. Detomidine carboxylic acid and hydroxydetomidine glucuronic acid conjugate were identified in the urine after the oral doses. In addition, traces of free hydroxydetomidine were observed. About half of the radioactivity of [3H]-detomidine was excreted in the urine in 12 h after the i.v. dose (80 micrograms/kg). Most of the excretion occurred between 5 ...
Muscarinic receptor subtypes in equine tracheal smooth muscle.
Veterinary research communications    January 1, 1992   Volume 16, Issue 4 301-310 doi: 10.1007/BF01839329
Yu M, Robinson NE, Wang Z, Derksen FJ.Selective muscarinic receptor antagonists were used to identify muscarinic receptor subtypes in equine trachealis strips. The M1 receptor antagonist pirenzepine (10(-7) mol/L to 3 x 10(-5) mol/L) and the M3 receptor antagonist 4-diphenylacetoxy-N-methylpiperidine (4-DAMP, 10(-9) mol/L to 3 x 10(-7) mol/L3) dose dependently inhibited the contractile responses to electrical field stimulation (EFS) and exogenous acetylcholine (ACh). Schild plots yielded a pA2 value for pirenzepine vs ACh of 6.75 +/- 0.09, which is consistent with the affinity for M2 or M3 receptors, and a pA2 value for 4-DAMP vs ...
Bee venom melittin is a potent toxin for reducing the threshold for calcium-induced calcium release in human and equine skeletal muscle.
Life sciences    January 1, 1992   Volume 51, Issue 22 1731-1738 doi: 10.1016/0024-3205(92)90302-6
Fletcher JE, Tripolitis L, Beech J.The modulation of Ca2+ release by synthetic bee venom melittin was examined in equine and human terminal cisternae-containing fractions. Melittin (0.1 microM) decreased the threshold of Ca(2+)-induced Ca2+ release by 20% in equine muscle and by 36% in human muscle. If terminal cisternae fractions were first preloaded with Ca2+ to greater than about 75% of the threshold of Ca(2+)-induced Ca2+ release and then melittin added, an immediate and sustained release of Ca2+ occurred in preparations from both species. Addition of melittin after a Ca2+ preload of < 50% of the threshold of Ca(2+)-induced...
Anti-inflammatory drugs inhibit degradation of equine synovial fluid induced by free radicals.
Australian veterinary journal    December 1, 1991   Volume 68, Issue 12 403-405 doi: 10.1111/j.1751-0813.1991.tb03112.x
Auer DE, Ng JC, Reilly JS, Seawright AA.No abstract available
Furosemide-induced changes in plasma and blood volume of horses.
Journal of veterinary pharmacology and therapeutics    December 1, 1991   Volume 14, Issue 4 411-417 doi: 10.1111/j.1365-2885.1991.tb00855.x
Hinchcliff KW, McKeever KH, Muir WW.The effect of furosemide administration (1 mg/kg body weight, i.v.) on plasma and blood volumes in 6 intact and 4 splenectomized horses was measured using Evans blue dye dilution, hematocrit, and hemoglobin and plasma total solids concentrations. Body weight decreased by 33.6 +/- 3.3 and 33.7 +/- 0.8 g/kg 4 h after furosemide administration to intact and splenectomized mares, respectively. Plasma volume, estimated by Evans blue dye dilution, was reduced by 8.3 +/- 3.3% (mean +/- SE) 4 h after furosemide administration. The reduction in plasma volume was first detectable 5-10 min after furosemi...
Testosterone disposition after intramuscular injection in castrated thoroughbred race horses.
Journal of veterinary pharmacology and therapeutics    December 1, 1991   Volume 14, Issue 4 430-434 doi: 10.1111/j.1365-2885.1991.tb00859.x
Martinez R, Urquieta B, Altieri E, Garzón L, Cid E.No abstract available
The pharmacology of local anesthetics.
The Veterinary clinics of North America. Equine practice    December 1, 1991   Volume 7, Issue 3 489-500 doi: 10.1016/s0749-0739(17)30482-0
Day TK, Skarda RT.Understanding of the pharmacology of local anesthesia is important for selection of a local anesthetic for use in equine standing surgery. In general, the action potential is inhibited by local anesthetics by preventing the influx of sodium ions across the axonal membrane. The physicochemical properties of each local anesthetic determine the onset of action, potency, and duration of action. Procaine, chlorprocaine, lidocaine, and mepivacaine are the local anesthetics still used clinically in horses; lidocaine is the most widely used. The future of equine local anesthesia may see the introducti...
Standing rectal and tail surgery.
The Veterinary clinics of North America. Equine practice    December 1, 1991   Volume 7, Issue 3 649-667 doi: 10.1016/s0749-0739(17)30492-3
DeBowes RM.A variety of rectal, perirectal, and coccygeal surgeries can be performed in the standing equine patient if appropriate chemical and physical restraints are available and adequate regional anesthesia can be achieved. Some rectal tears and most rectal prolapses, mass lesions, perirectal abscesses, rectal biopsies, and selected injuries of the tail can be managed without prohibitive difficulty. Severe injuries that compromise the small colon cranial to the peritoneal reflection may require flank laparotomy, midline celiotomy, or humane euthanasia to manage the disease process effectively and app...
Mucosal histamine inhibits Na absorption and stimulates Cl secretion across equine tracheal epithelium.
The American journal of physiology    December 1, 1991   Volume 261, Issue 6 Pt 1 L456-L461 doi: 10.1152/ajplung.1991.261.6.L456
Tessier GJ, Traynor TR, Kannan MS, O'Grady SM.When the equine tracheal epithelium is mounted in Ussing chambers and bathed in plasma-like Ringer solution, the tissue generates a lumen-negative transepithelial potential (PD) of 22 mV and a short-circuit current (Isc) of 70-200 microA/cm2. Mucosal addition of 10 microM histamine produces a transient increase in the Isc followed by a return to baseline or below. Mucosal addition of 2 microM diphenhydramine inhibits the Isc response to mucosal histamine, whereas 100 microM mucosal cimetidine produces no effect. The average initial increases in Isc over time for mucosal vs. serosal histamine a...
Chemical restraint for surgery in the standing horse.
The Veterinary clinics of North America. Equine practice    December 1, 1991   Volume 7, Issue 3 521-533 doi: 10.1016/s0749-0739(17)30484-4
LeBlanc PH.Chemical restraint can be a useful pharmacologic tool to assist the veterinarian performing surgery in the standing horse. The agents discussed impose minimal adverse side effects and are considered relatively safe when administered in the doses described. Acetylpromazine, the most widely used tranquilizer, produces mild sedation but no analgesia. The use of tranquilizers for surgical procedures requires the combined use of either a local anesthetic technique or a sedative-hypnotic or opiate to provide analgesia. Sedative-hypnotics such as xylazine and detomidine or opiates such as morphine an...
Comparison of high-performance liquid chromatography with a radiometric assay for determination of the effect of intra-articular administration of corticosteroid and saline solution on synovial fluid hyaluronate concentration in horses.
American journal of veterinary research    December 1, 1991   Volume 52, Issue 12 1940-1944 
Tulamo RM.Two recently developed direct methods, radioassay-125I-labeled hyaluronic acid binding protein (125I-HABP)- and high-performance liquid chromatography (HPLC), were used to assess and compare the concentration of hyaluronate (HA) in synovial fluid of horses. Also determined were changes in the HA concentration in an experimental treatment model involving physiologic saline solution (PSS)-irrigated or methylprednisolone acetate-injected tarsocrural joints of clinically normal horses. Serum HA concentration was determined simultaneously, using the 125I-HABP assay. Synovial fluid HA concentration ...
Cardiovascular effects of low dose calcium chloride infusions during halothane anaesthesia in dorsally recumbent ventilated ponies.
Zentralblatt fur Veterinarmedizin. Reihe A    December 1, 1991   Volume 38, Issue 10 728-736 doi: 10.1111/j.1439-0442.1991.tb01072.x
Gasthuys F, De Moor A, Parmentier D.The effects of calcium chloride administered at low infusion rates on the cardiovascular depression and the blood calcium balance were studied during a constant halothane anaesthesia in dorsally recumbent ventilated ponies. A pronounced cardiopulmonary depression characterized by decreases of all cardiac parameters and lowering of the mean arterial blood pressure was observed after the initial anaesthetic stabilization period of 30 minutes in the ponies. A significant decrease in the total calcium plasma concentration together with a constant ionized and complexed calcium fraction was present ...
Medetomidine in horses.
The Veterinary record    November 23, 1991   Volume 129, Issue 21 476 doi: 10.1136/vr.129.21.476
Jones P, Hoare C.No abstract available
Effect of an isoxsuprine-resin preparation on blood flow in the equine thoracic limb.
The Veterinary record    November 9, 1991   Volume 129, Issue 19 427-429 doi: 10.1136/vr.129.19.427
Deumer J, de Haan F, Tulp MT, van den Hoven R.The effects of an oral isoxsuprine-resin preparation on the blood flow in the thoracic limb of seven horses was determined by thermography. Treatment with the oral resin preparation resulted in increased skin temperatures compared with the non-medicated controls. The maximal temperature differences, 2.2 degrees C for the horses treated with 0.9 mg/kg and 1.8 degrees C for the horses treated with 1.2 mg/kg, occurred four hours after dosing. Plasma total isoxsuprine, determined in three horses, was detectable two hours after oral dosing and maximal eight hours after dosing, but free isoxsuprine ...
Comparison of the sedative effects of medetomidine and xylazine in horses.
The Veterinary record    November 9, 1991   Volume 129, Issue 19 421-423 doi: 10.1136/vr.129.19.421
Bryant CE, England GC, Clarke KW.The sedative effects in horses of the new alpha 2 agonist medetomidine were compared with those of xylazine. Four ponies and one horse were treated on separate occasions with two doses of medetomidine (5 micrograms/kg bodyweight and 10 micrograms/kg bodyweight) and with one dose of xylazine (1 mg/kg bodyweight) given by intravenous injection. Medetomidine at 10 micrograms/kg was similar to 1 mg/kg xylazine in its sedative effect but produced more severe and more prolonged ataxia, and one animal fell over during the study. Medetomidine at 5 micrograms/kg produced less sedation but a similar deg...
Pharmacologic treatment of priapism in two horses.
Journal of the American Veterinary Medical Association    November 1, 1991   Volume 199, Issue 9 1183-1184 
Wilson DV, Nickels FA, Williams MA.Benztropine mesylate was used successfully to treat priapism that developed during anesthesia in 2 horses. After IV injection, there was a rapid resolution of signs in both horses, and no side effects were observed. The choice of an effective method to treat priapism is challenging because precise causes in most patients have not been well-defined. Benztropine mesylate is a synthetic compound resulting from the combination of the active portions of atropine and diphenhydramine, and is believed effective because of its central acetyl-choline-antagonizing properties.