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Topic:Phenobarbital

Phenobarbital is a barbiturate commonly used in veterinary medicine for its anticonvulsant properties, particularly in the management of seizure disorders in horses. It acts by depressing the central nervous system, thereby reducing the frequency and severity of seizures. The pharmacokinetics of phenobarbital in horses, including its absorption, distribution, metabolism, and excretion, are subjects of ongoing research to optimize therapeutic regimens. Dosing must be carefully managed to balance efficacy with potential side effects, such as sedation and hepatotoxicity. This page compiles peer-reviewed research studies and scholarly articles that explore the pharmacological properties, therapeutic applications, and safety considerations of phenobarbital in equine medicine.
Induction of cytochrome P450 enzymes in primary equine hepatocyte culture.
Toxicology in vitro : an international journal published in association with BIBRA    August 1, 2013   Volume 27, Issue 7 2023-2030 doi: 10.1016/j.tiv.2013.07.009
Stefanski A, Mevissen M, Möller AM, Kuehni-Boghenbor K, Schmitz A.In this study, we established cell culture conditions for primary equine hepatocytes allowing cytochrome P450 enzyme (CYP) induction experiments. Hepatocytes were isolated after a modified method of Bakala et al. (2003) and cultivated on collagen I coated plates. Three different media were compared for their influence on morphology, viability and CYP activity of the hepatocytes. CYP activity was evaluated with the fluorescent substrate 7-benzyloxy-4-trifluoromethylcoumarin. Induction experiments were carried out with rifampicin, dexamethasone or phenobarbital. Concentration-response curves for...
Exposure to phenobarbital in a foal after nursing a mare treated with phenobarbital.
Journal of veterinary internal medicine    February 22, 2008   Volume 22, Issue 1 227-230 doi: 10.1111/j.1939-1676.2007.0036.x
Wong DM, Papich MG, Davis JL.No abstract available
Perinatal asphyxia syndrome in the foal: review and a case report.
Irish veterinary journal    December 1, 2004   Volume 57, Issue 12 707-714 doi: 10.1186/2046-0481-57-12-707
Galvin N, Collins D.: This report presented a brief overview of the literature on the perinatal asphyxia syndrome (PAS) in foals as a prelude to a description of the investigation and treatment of acute onset seizures in a 24-hour-old Thoroughbred colt foal.PAS can cause a wide variety of clinical abnormalities, of which seizures due to encephalopathy are the most significant. The structural and biochemical components of CNS neurones are disrupted by the shift from oxidative to anaerobic metabolism, with a resultant deficit in cellular energy. The cells succumb to the combined effects of acidosis, neurotoxic acti...
Pharmacokinetics of phenobarbital after repeated oral administration in normal horses.
Journal of veterinary pharmacology and therapeutics    September 1, 1992   Volume 15, Issue 3 301-304 doi: 10.1111/j.1365-2885.1992.tb01020.x
Reimer JM, Sweeney RW.No abstract available
A pharmacokinetic study of phenobarbital in mature horses after oral dosing.
Journal of veterinary pharmacology and therapeutics    December 1, 1987   Volume 10, Issue 4 283-289 doi: 10.1111/j.1365-2885.1987.tb00103.x
Ravis WR, Duran SH, Pedersoli WM, Schumacher J.The pharmacokinetics of phenobarbital were determined in six mature horses after a single oral dose. Horses were administered a 5.5 mg/kg of body weight oral dose of phenobarbital tablets. Based on the combined evaluation of i.v. and oral results, phenobarbital displayed two-compartment pharmacokinetics in the horse with a terminal half-life of 19.0 +/- 4.4 (mean +/- SD) h. This half-life is considerably shorter than those reported for dogs and humans. The steady-state volume of distribution (Vdss/F) and the total body clearance (Clt/F) of phenobarbital were 0.753 +/- 0.115 l/kg and 27.9 +/- 9...
Effects of phenobarbital treatment on 3-methylindole toxicosis in ponies.
American journal of veterinary research    April 1, 1986   Volume 47, Issue 4 901-905 
Turk MA, Thomas DE.To study the role of cytochrome P-450-dependent mixed function oxidase reactions in equine 3-methylindole (3MI) toxicosis, ponies were given 20 mg of phenobarbital/kg of body weight at 72, 60, 48, 36, and 24 hours before 100 mg of oral 3MI/kg to induce cytochrome P-450 or no treatment (controls). Maximal 3MI plasma concentration was decreased and clearance was faster in phenobarbital-treated ponies. Plasma 3MI was still detectable 12 and 36 hours after dosing in phenobarbital-treated and control ponies, respectively. Phenobarbital treatment induced a distribution phase with transition from a 1...
[Pharmacological studies on doping drugs for race horses. IV. Chlorpromazine and phenobarbital (author’s transl)].
Nihon juigaku zasshi. The Japanese journal of veterinary science    April 1, 1975   Volume 37, Issue 2 133-139 doi: 10.1292/jvms1939.37.133
Fujii S, Inada S, Yoshida S, Kusanagi C, Mima K.No abstract available