Drug disposition in the neonatal animal, with particular reference to the foal.
Abstract: Differences between neonatal and adult animals in their response to drugs can usually be attributed to altered disposition (ie, distribution, metabolism and excretion) processes during the neonatal period. These alterations affect the plasma concentrations as well as the concentrations of drug attained at the receptor site. Some characteristics of the neonatal period include greater absorption from the gastrointestinal tract, lower extent of plasma protein binding, increased apparent volume of distribution of drugs that distribute in extracellular fluid or total body water, increased permeability of the 'blood-brain' barrier and slower elimination of many drugs. The hepatic microsomal oxidative reactions and glucuronide conjugation are deficient metabolic pathways for a varying period of time, usually up to six weeks after birth or even longer in some species. Decreased metabolism can affect the duration of action of lipid-soluble drugs. Functional immaturity of the kidneys decreases the renal excretion of polar drugs and drug metabolites. Overall renal function appears to reach maturity within two weeks after birth in ruminant species and pigs, while maturation may take at least four weeks in other species of domestic animals. Considerable physiological and biochemical development takes place during the first five days after birth with maturation continuing more slowly over the succeeding five weeks. The time it takes for any process to reach functional maturity depends on the process in question and varies with the species of animal. The absorption, disposition and pharmacological response to drugs during the first 24 h after birth may be unique to that time and, because of lack of information, are impossible to predict.(ABSTRACT TRUNCATED AT 250 WORDS)
Publication Date: 1984-07-01 PubMed ID: 6479135DOI: 10.1111/j.2042-3306.1984.tb01945.xGoogle Scholar: Lookup
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- Comparative Study
- Journal Article
Summary
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The research article investigates how newborn animals, specifically foals, handle drugs differently than their adult counterparts due to changes in drug distribution, metabolism, and excretion during their early life stages. These alterations can influence drug concentrations in plasma and at receptor sites.
Drug Disposition in Neonates
- Newborn animals, or neonates, react differently to drugs compared to adults due to modifications in the processes of drug distribution, metabolism, and excretion. These changes can affect the drug concentrations in the blood plasma and at the locations where the drug behaves (receptor sites).
Characteristics of the Neonatal Period
- The neonatal period, the time just after birth, exhibits several distinguishing characteristics that influence drug disposition. These include enhanced absorption of drugs from the gastrointestinal tract, diminished binding of drugs with proteins in the blood plasma, and an increased volume of distribution of drugs in the extracellular fluid or total body water.
- The ‘blood-brain’ barrier, a filtering mechanism of the body that keeps the circulating blood away from the brain extracellular fluid, is more permeable in newborns which allows more of the drug to penetrate.
- Many drugs are eliminated more slowly in newborns due to the immaturity of drug metabolism and excretion pathways.
Metabolic and Renal Function Development
- Newborn animals have deficient hepatic microsomal oxidative reactions and glucuronide conjugation (types of drug metabolism) for some time after birth. This could affect the duration of action of certain lipid-soluble drugs.
- Also, due to the kidneys’ functional immaturity, the renal excretion of polar drugs and drug metabolites is decreased.
- In terms of overall renal function, maturity usually is reached within two weeks after birth in ruminants and pigs, whereas, in other domestic animals, it might take at least four weeks.
Continuing Maturation After Birth
- Significant physiological and biochemical development occurs in the first five days after birth with maturation continuing more slowly over the next five weeks.
- The time taken for any process to reach functional maturity depends on the process itself and varies with the species of animal.
- The absorption, disposition and response to drugs in the first 24 hours after birth may be unique to that period.
Cite This Article
APA
Baggot JD, Short CR.
(1984).
Drug disposition in the neonatal animal, with particular reference to the foal.
Equine Vet J, 16(4), 364-367.
https://doi.org/10.1111/j.2042-3306.1984.tb01945.x Publication
Researcher Affiliations
MeSH Terms
- Absorption
- Animals
- Animals, Newborn / growth & development
- Animals, Newborn / metabolism
- Anti-Infective Agents / metabolism
- Blood-Brain Barrier / drug effects
- Cattle / metabolism
- Female
- Half-Life
- Horses / growth & development
- Horses / metabolism
- Kidney / metabolism
- Kinetics
- Liver / metabolism
- Pharmaceutical Preparations / metabolism
- Swine / metabolism
- Tissue Distribution
Citations
This article has been cited 6 times.- Gold JR, Grubb T, Court MH, Villarino NF. Pharmacokinetics of acetaminophen after a single Oral administration of 20 or 40 mg/kg to 7-9 Day-old foals. Front Vet Sci 2023;10:1198940.
- Ekstrand C, Nostell K, Gehring R, Bondesson U, Bröjer J. The disposition of trimethoprim and sulfadiazine in neonatal foals after intravenous administration. Vet Med Sci 2022 May;8(3):1065-1071.
- Brown MP, Gronwall RR, Houston AE. Pharmacokinetics and body fluid and endometrial concentrations of ormetoprim-sulfadimethoxine in mares. Can J Vet Res 1989 Jan;53(1):12-6.
- Baggot JD. Clinical pharmacokinetics in veterinary medicine. Clin Pharmacokinet 1992 Apr;22(4):254-73.
- Riond JL, Müller P, Wanner M. The influence of age on the pharmacokinetics of aditoprim in pigs after intravenous and oral administration. Vet Res Commun 1992;16(5):355-64.
- Paegelow JL, Schoonover MJ, Young JM, Maxwell LK, Taylor JD, Gilliam LL, Holbrook TC. Pharmacokinetics of amikacin after intravenous, intra-articular, and combined intravenous and intra-articular administration in healthy neonatal foals. J Vet Intern Med 2024 May-Jun;38(3):1825-1834.
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