RESUMO
Deep sea water (DSW) commonly refers to a body of seawater that is pumped up from a depth of over 200 m. It is usually associated with the following characteristics: low temperature, high purity, and being rich with nutrients, namely, beneficial elements, which include magnesium, calcium, potassium, chromium, selenium, zinc, and vanadium. Less photosynthesis of plant planktons, consumption of nutrients, and organic decomposition have caused lots of nutrients to remain there. Due to this, DSW has potential to become a good source for health. Research has proven that DSW can help overcome health problems especially related to lifestyle-associated diseases such as cardiovascular disease, diabetes, obesity, cancer, and skin problems. This paper reviews the potential health benefits of DSW by referring to the findings from previous researches.
Assuntos
Fluoxetina/efeitos adversos , Inibidores Seletivos de Recaptação de Serotonina/efeitos adversos , Distribuição de Qui-Quadrado , Ensaios Clínicos como Assunto/estatística & dados numéricos , Relação Dose-Resposta a Droga , Esquema de Medicação , Serviços de Informação sobre Medicamentos/estatística & dados numéricos , Humanos , Masculino , Pessoa de Meia-Idade , Vigilância de Produtos Comercializados/estatística & dados numéricos , Obras Médicas de Referência , Disfunções Sexuais Psicogênicas/induzido quimicamente , Disfunções Sexuais Psicogênicas/epidemiologiaRESUMO
OBJECTIVE: To determine the pattern of postneonatal childhood meningitis in Malaysia. METHODS: Retrospective cross-sectional study involving five pediatric departments in Malaysia. RESULTS: There were 435 cases of clinical meningitis admitted to the five centers. More than 90% of the patients were <5 years old, and one-half were <6 months of age. The estimated overall incidence of childhood meningitis in the first 5 years of life was 76.7 per 100000 per year. However, of the 435 cases only 71 (16.3%) fulfilled laboratory diagnostic criteria and in only 58 of these was an organism isolated. Nearly one-half (48%) of all bacteriologically proved cases were caused by Haemophilus influenzae type b (Hib). The mortality rate was 12.5% and 21 patients (30%) suffered neurologic sequelae. CONCLUSIONS: More than one-half of all cases of culture-positive childhood bacterial meningitis were caused by Hib, although successful isolation of a pathogen occurred in only a small proportion of cases. For this reason the true incidence of Hib meningitis in Malaysia remains unknown. These findings are consistent with previous studies in Malaysia.
Assuntos
Meningite por Haemophilus/epidemiologia , Criança , Pré-Escolar , Estudos Transversais , Haemophilus influenzae tipo b , Humanos , Incidência , Lactente , Malásia/epidemiologia , Estudos RetrospectivosRESUMO
Patulin is a mycotoxin produced by several species of fungi and is commonly found in fruits. It is regulated in several countries at a tolerance level of 50 micrograms/Kg. We investigated its ability to inhibit cell growth in hepatoma tissue culture and its ability to inhibit protein synthesis. It was found to be cytostatic at concentration of 1 microgram/mL (6.4 microM). It inhibits protein synthesis by two mechanisms: inhibition of amino acid uptake into the cell and their incorporation into proteins. The former mechanism appears to be more significant than the latter. This is consistent with previous work showing the ability of patulin to perturb plasma membrane function.
Assuntos
Neoplasias Hepáticas Experimentais/metabolismo , Proteínas de Neoplasias/antagonistas & inibidores , Patulina/farmacologia , Inibidores da Síntese de Proteínas/farmacologia , Animais , Divisão Celular/efeitos dos fármacos , Permeabilidade da Membrana Celular , Leucina/metabolismo , Neoplasias Hepáticas Experimentais/tratamento farmacológico , Proteínas de Neoplasias/biossíntese , Ratos , Células Tumorais CultivadasRESUMO
For a mixture of three normal distributions, which represent genotypes AA, Aa and aa, a method of estimation of the seven unknown parameters is proposed which works well whenever the phenotype (aa) is sufficiently well separated from the phenotype (AA, Aa). It is based on p-values of Kolmogorov's test of goodness of fit to normality. Initial parameter values for this iterative algorithm can be found by visual check and/or by using the EM algorithm. In an example of a data set of size 59 from a study of the metabolic rate of desipramine, the usefulness of this method is demonstrated. Extensions to more complex situations are feasible and are indicated at the end.
Assuntos
Transtorno Depressivo/metabolismo , Desipramina/metabolismo , Genótipo , Adolescente , Adulto , Algoritmos , Transtorno Depressivo/tratamento farmacológico , Desipramina/sangue , Desipramina/uso terapêutico , Feminino , Humanos , Hidroxilação , Masculino , Pessoa de Meia-Idade , Modelos Genéticos , Fenótipo , Estatísticas não ParamétricasAssuntos
Lítio/farmacocinética , Idoso , Benzotiadiazinas , Contraindicações , Diuréticos , Interações Medicamentosas , Monitoramento de Medicamentos , Feminino , Humanos , Absorção Intestinal , Falência Renal Crônica/metabolismo , Lítio/uso terapêutico , Taxa de Depuração Metabólica , Gravidez , Inibidores de Simportadores de Cloreto de Sódio/farmacologia , Teofilina/farmacologiaRESUMO
There is wide interindividual variation in steady-state plasma concentration of desipramine and other tricyclic antidepressants primarily due to differences in rates of hydroxylation. Several studies have shown that the rate of hydroxylation of desipramine is correlated with the rate of hydroxylation of the genetic probe drug, debrisoquine, which is controlled by monogenic inheritance. However, no population studies of the polymorphic metabolism of antidepressants have been reported. In this study, 59 patients with endogenous depression received a fixed dose of desipramine and the steady-state plasma concentration of desipramine and 2-hydroxydesipramine were determined by high-pressure chromatography. A new statistical approach based on optimizing the fit to a specific stochastic model was utilized to separate the mixture of the three genotypes: homozygous extensive (AA), heterozygous extensive (Aa) and poor (aa) metabolizers. The proportions of the genotypes are 0.43, 0.45 and 0.12, respectively. The gene frequency of the low-activity allele is 0.34 and that of the high-activity allele is 0.66. The means (SD) of the desipramine/2-hydroxydesipramine metabolic ratios of the three genotypes are 1.71 (0.44), 3.32 (1.68) and 23.32 (10.03). These data suggest that the heterozygous genotype has half the metabolic activity of the homozygous extensive metabolizer and that the poor metabolizer genotype has negligible metabolic activity.
Assuntos
Antidepressivos Tricíclicos/metabolismo , Desipramina/análogos & derivados , Desipramina/metabolismo , Adolescente , Adulto , Antidepressivos Tricíclicos/sangue , Cromatografia Líquida de Alta Pressão , Transtorno Depressivo/metabolismo , Desipramina/sangue , Metabolismo Energético , Feminino , Genótipo , Humanos , Masculino , Matemática , Pessoa de Meia-Idade , Farmacogenética , Estatística como AssuntoRESUMO
An increase of the dose of trimipramine (TM) results in a markedly disproportionate increase of the steady-state plasma concentration of the major active metabolite desmethyltrimipramine (DMT). Ten patients receiving 75 mg/day of TM had a mean steady-state plasma concentration of 53.8 ng/ml TM and 26.3 ng/ml DMT. Ten others receiving 150 ng/ml TM had a mean concentration of 122.5 ng/ml TM and 133.8 ng/ml DMT. This is most likely due to the saturation within therapeutic dosage range of the subspecies of cytochrome P-450 responsible for hydroxylation of DMT. Available data on metabolism of tricyclic antidepressants shows that the hydroxylation of desmethylimipramine (desipramine) but not that of desmethylamitriptyline (nortriptyline) reaches saturation within therapeutic dosage range. Clinicians should take into consideration the possibility of dose-dependent kinetics when adjusting the dose of tricyclic antidepressants. This finding highlights the value of monitoring of blood levels of antidepressants.
Assuntos
Transtorno Depressivo/metabolismo , Dibenzazepinas/farmacocinética , Trimipramina/farmacocinética , Adulto , Transtorno Depressivo/tratamento farmacológico , Desipramina/administração & dosagem , Desipramina/sangue , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Trimipramina/administração & dosagem , Trimipramina/uso terapêuticoRESUMO
A 41-year-old man developed sleep apnea following abrupt cessation of amitriptyline. Cessation of antidepressants may result in excessive release of acetylcholine, which increases REM sleep. This in turn increases disordered breathing time and decreases nocturnal oxygenation. Sleep apnea did not recur when amitriptyline was reinstated and later gradually discontinued.
Assuntos
Amitriptilina/efeitos adversos , Síndromes da Apneia do Sono/etiologia , Síndrome de Abstinência a Substâncias/complicações , Adulto , Humanos , MasculinoRESUMO
Cocaine kinetics were studied in four subjects after intravenous and intranasal administration. For intravenous administration cocaine hydrochloride (32 mg) dissolved in physiological saline was injected in 1 ml volume over a 1 min period. Intranasal cocaine was administered as 100 mg powder consisting of an appropriate dose of cocaine hydrochloride (64 and 96 mg) mixed with lactose powder. Subjects were instructed to inhale the mixture through a 5 cm straw within 1 min. Cocaine kinetics, after intravenous injection, conform to a one-compartment open model with first-order elimination. After intranasal administration, cocaine kinetics conform to a one-compartment model with first-order absorption and first-order elimination. The mean half-life of cocaine for intravenous injection in four subjects was 41.4 +/- 8.2 min (mean +/- S.E.M.) and the range was 19 to 64 min. There were statistically significant differences in the mean area under the concentration-time curve (AUC) following intravenous and intranasal administration. The AUC was dose-dependent and the fraction of the dose absorbed after 64 mg intranasal cocaine was significantly lower than after 96 mg dose (p less than 0.05).
Assuntos
Cocaína/metabolismo , Administração Intranasal , Análise de Variância , Cocaína/administração & dosagem , Humanos , Individualidade , Injeções Intravenosas , Cinética , Modelos BiológicosRESUMO
Plasma thioridazine levels were estimated in seven retarded patients during the course of gradual phenobarbital withdrawal. In each patient, plasma levels of thioridazine plus metabolites increased with decreasing phenobarbital dose. Possible mechanisms of the interaction are discussed.