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1.
J Clin Pharm Ther ; 43(3): 422-429, 2018 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-29265480

RESUMO

WHAT IS KNOWN AND OBJECTIVE: This study developed a population pharmacokinetic (PK) model of levetiracetam (LEV) for treating neonatal seizures (NS) and determined the influence of clinically relevant covariates to explain the interindividual variability and residual error. METHODS: Twenty newborns admitted to the Neonatal Intensive Care Unit at the Hospital Central "Dr. Ignacio Morones Prieto" were included. LEV doses were administered by intermittent infusion. Blood samples were drawn 3 times post-infusion. Levetiracetam was quantified by a chromatographic technique. NONMEM software was used to determine the population PK model of LEV in neonates and the influence of clinical covariates on drug disposition. RESULTS AND DISCUSSION: The LEV PK in neonates is described by a one-compartment open model with first-order elimination. The influence of creatinine clearance (CRCL) and body weight (BW) on clearance (CL[L/h] = 0.47*CRCL), as well as the volume of the distribution (Vd[L] = 0.65*BW) of LEV, were confirmed, considering interindividual variabilities of 36% and 22%, respectively, and a residual error of 13%. WHAT IS NEW AND CONCLUSION: Based on the PK of LEV in neonates and the influence of the final PK model, a priori dosing guidelines are proposed considering CRCL, BW and LEV plasma concentrations between 6 and 20 mg/L for NS treatment.


Assuntos
Anticonvulsivantes/farmacocinética , Modelos Biológicos , Piracetam/análogos & derivados , Convulsões/tratamento farmacológico , Anticonvulsivantes/administração & dosagem , Creatinina/análise , Relação Dose-Resposta a Droga , Feminino , Humanos , Recém-Nascido , Levetiracetam , Masculino , Piracetam/administração & dosagem , Piracetam/farmacocinética , Estudos Prospectivos , Distribuição Tecidual
2.
Neurologia (Engl Ed) ; 38(9): 671-680, 2023.
Artigo em Inglês | MEDLINE | ID: mdl-37858892

RESUMO

INTRODUCTION: Rafts are protein-lipid structural nanodomains involved in efficient signal transduction and the modulation of physiological processes of the cell plasma membrane. Raft disruption in the nervous system has been associated with a wide range of disorders. DEVELOPMENT: We review the concept of rafts, the nervous system processes in which they are involved, and their role in diseases such as Parkinson's disease, Alzheimer disease, and Huntington disease. CONCLUSIONS: Based on the available evidence, preservation and/or reconstitution of rafts is a promising treatment strategy for a wide range of neurological disorders.


Assuntos
Doença de Alzheimer , Cavéolas , Humanos , Cavéolas/química , Cavéolas/metabolismo , Microdomínios da Membrana/química , Microdomínios da Membrana/metabolismo , Colesterol/análise , Colesterol/química , Colesterol/metabolismo , Membrana Celular/metabolismo
3.
Neurologia (Engl Ed) ; 2021 Mar 13.
Artigo em Inglês, Espanhol | MEDLINE | ID: mdl-33726969

RESUMO

INTRODUCTION: Rafts are function-structural cell membrane nano-domains. They contribute to explain the efficiency of signal transduction at the low physiological membrane concentrations of the signaling partners by their clustering inside specialized signaling domains. DEVELOPMENT: In this article, we review the current model of the membrane rafts and their physio-pathological relevance in the nervous system, including their role in Parkinson, Alzheimer, and Huntington diseases. CONCLUSIONS: Rafts disruption/dysfunction has been shown to relate diverse neurological diseases. Therefore, it has been suggested that preservation of membrane rafts may represent a strategy to prevent or delay neuronal dysfunctions in several diseases.

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