RESUMO
OBJECTIVES: Our objective was to evaluate the pharmacokinetics of nelfinavir (NFV) (625 mg tablets) 1250 mg twice daily during pregnancy and postpartum. METHODS: The participants were HIV-1-infected pregnant women enrolled in P1026s and receiving NFV (625 mg tablets) 1250 mg twice daily as part of routine clinical care. Intensive steady-state 12-h NFV pharmacokinetic profiles were performed during pregnancy and postpartum. The target NFV area under the plasma concentration-time curve (AUC(0-12)) was >or=10th percentile NFV AUC(0-12) in non-pregnant historical controls (18.5 microg h/mL). RESULTS: Of 27 patients receiving NFV, pharmacokinetic data were available for four (second trimester), 27 (third trimester) and 22 (postpartum) patients. The NFV maximum concentration (C(max)), 12-h post-dose concentration (C(12)) and AUC(0-12) were significantly lower during the third trimester compared to postpartum (PAssuntos
Infecções por HIV/tratamento farmacológico
, Inibidores da Protease de HIV/farmacocinética
, HIV-1
, Nelfinavir/farmacocinética
, Complicações Infecciosas na Gravidez/tratamento farmacológico
, Adolescente
, Adulto
, Área Sob a Curva
, Contagem de Linfócito CD4
, Esquema de Medicação
, Feminino
, Infecções por HIV/metabolismo
, Inibidores da Protease de HIV/administração & dosagem
, Humanos
, Recém-Nascido
, Nelfinavir/administração & dosagem
, Gravidez
, Complicações Infecciosas na Gravidez/metabolismo
, Infecção Puerperal/tratamento farmacológico
, Infecção Puerperal/metabolismo
, RNA Viral
, Carga Viral
, Adulto Jovem
RESUMO
Luteinizing hormone and LH-RH-like immunoreactivity were measured in the jugular venous plasma of Clun Forest ewes at various stages of the oestrous cycle. Blood samples were collected through jugular venous cannulae every 2 h for at least 20 days from three ewes during the breeding season. The ewes were checked twice daily for oestrus using a vasectomized ram. Plasma LH peaks of apparent height 112-192 ng NIH-LH-S17 equivalents/ml were detected at oestrus with basal levels of 2-15 ng/ml during most of the remainder of the 17-day oestrous cycle. Peaks of LH-RH-like immunoreactivity occurred at various times of the cycle. The apparent maximal level of these peaks was 220 pg/ml compared with basal levels of less than 10 pg/ml. Further ewes (two for each group) were sampled at 4 min intervals for 12 h, (1) from onset of oestrus, (2) 36-48 h after onset of oestrus or (3) on day 10 of the oestrous cycle. In the ewes sampled at oestrus, peaks of LH-RH-like immunoreactivity were detected before, during and after the preovulatory LH peak. Those detected after the LH peak were unassociated with any further increases in the plasma LH level. In the ewes sampled 36-48 h after onset of oestrus and on day 10 of the cycle, several peaks of LH-RH-like immunoreactivity unassociated with any increases in the LH level were detected. These peaks, and those detected at oestrus, had durations of only one or two samples, and in some cases reached levels of several ng/ml compared with basal levels of less than 10 pg/ml. The significance of these results is discussed.
Assuntos
Estro , Hormônio Luteinizante/sangue , Ovinos/fisiologia , Animais , Feminino , Veias Jugulares , Hormônio Luteinizante/imunologia , GravidezRESUMO
The pineal indole 5-methoxytryptophol (ML) has been shown to have an antigonadal activity when administered to experimental animals, but data on its normal pattern of secretion have been lacking. Using a new gas chromatography-mass spectrometry assay, the concentration of ML at various phases of the human menstrual cycle has been studied. Daily samples were obtained throughout the month from five women with a normal cycle and two women taking an oral contraceptive. In women with a normal cycle levels of ML were found to be significantly lower in the last third of their cycle; this change was not seen in women taking an oral contraceptive who had low levels throughout the month. The changes in concentration of ML did not correlate with the changes in concentration of gonadotrophins.
Assuntos
Indóis/sangue , Menstruação , Adulto , Anticoncepcionais Orais , Feminino , Hormônio Foliculoestimulante/sangue , Humanos , Hormônio Luteinizante/sangueRESUMO
OBJECTIVE: To assess the sensitivity and specificity of a new polymerase chain reaction (PCR) assay with uninterrupted reverse transcription and complementary DNA amplification (RT-PCR) for the diagnosis of enteroviral (EV) meningitis in children. DESIGN: A prospective, cohort study. SETTINGS: Two medical centers: 1 university hospital and 1 children's hospital in San Diego County, California, during a 5-week period. PATIENTS: All pediatric patients younger than 16 years who underwent a lumbar puncture for evaluation of possible meningitis. MAIN OUTCOME MEASURES: The results of cerebrospinal fluid (CSF) RT-PCR were compared with viral cultures and clinical histories. RESULTS: During the 5-week period, 90 patients were entered into the study. Nonpolio EVs were cultured from 10% (9/90) of the patients from the following sites: CSF, 6.7% (6/90) of the patients; stool, 19% (4/21) of the patients; and throat swabs, 5.6% (1/18) of the patients. The EV genome was detected in the CSF by using RT-PCR in 7 of 9 EV culture-positive patients. The sensitivity and specificity of the CSF RT-PCR assay to detect EV meningitis were 77.8% and 100%, respectively. This compared with a sensitivity of 66.7% for detection of EV in CSF by viral culture alone. CONCLUSION: The new RT-PCR assay is a rapid and reliable method for the detection of EV infection in childhood.
Assuntos
Infecções por Enterovirus/líquido cefalorraquidiano , Enterovirus/genética , Genoma Viral , Meningite Viral/líquido cefalorraquidiano , Reação em Cadeia da Polimerase/métodos , Cultura de Vírus/métodos , Criança , Pré-Escolar , Infecções por Enterovirus/virologia , Humanos , Lactente , Recém-Nascido , Meningite Viral/virologia , Estudos Prospectivos , Reprodutibilidade dos Testes , Sensibilidade e Especificidade , Transcrição GênicaRESUMO
The presence of peptidases in the rabbit hypothalamus capable of inactivating luteinizing hormone-releasing hormone (LH-RH) was investigated with the use of a sensitive and specific radioimmunoassay for the releasing hormone. Enzymes acting on LH-RH were found in two fractions from rabbit hypothalami, a particulate fraction and a supernatant fraction, which very rapidly inactivated the decapeptide. Peptidase activity in the particulate fraction from male and female rabbits was approximately the same, but the supernatant fraction from female animals had significantly greater peptidase activity than that from male animals. These findings confirm the hypothesis that rabbit hypothalamus contains peptidases which inactivate LH-RH, and give some indication that the enzymes may be involved in the control by the central nervous system of reproductive function.
Assuntos
Hormônio Liberador de Gonadotropina/fisiologia , Hipotálamo/enzimologia , Peptídeo Hidrolases/fisiologia , Animais , Feminino , Hormônio Liberador de Gonadotropina/isolamento & purificação , Masculino , Peptídeo Hidrolases/isolamento & purificação , CoelhosRESUMO
Peptidases inactivating luteinizing hormone-releasing hormone (LH-RH) were found to be present in two subcellular fractions prepared from the following areas of the central nervous system of male and female rats: thalamus, hypothalamus, cortex and cerebellum. LH-RH immunoreactivity was also detected in these fractions after peptidase activity had been removed by heat denaturation. These findings support the concept that LH-RH may have a role in modulating neuronal activity within the central nervous system (CNS).
RESUMO
Peptidases inactivating growth hormone-release-inhibiting hormone (somatostatin) were found to be present in two fractions prepared from the thalamus, hypothalamus, cortex and cerebellum of male and female rats. Somatostatin was also detected in significant quantities in fractions from the thalamus, hypothalamus, and cortex, after peptidase activity had been removed by heat denaturation. These results support the suggestion that somatostatin may function as a neurotransmitter or modulator of neuronal activity in the central nervous system.