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2.
Jpn J Pharmacol ; 78(1): 55-61, 1998 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-9804062

RESUMO

The catastrophic epidemic of subacute myelo-optic neuropathy (SMON) affected Japan around 1970 with thousands of victims. The cause was attributed to high doses of locally acting oxyquinolines. It has been speculated that oxyquinoline derivatives of the clioquinol type can disturb the retention of vitamin B12 through chelation of Co2+. In the present paper, possible effects of clioquinol on the uptake and tissue distribution of [57Co]-cyanocobalamin have been studied in mice. In vivo experiments showed markedly decreased accumulation of radiolabelled vitamin B12 in the kidney and skin in animals that were pre-treated with clioquinol. The chloroform:water partition coefficients for [57Co]-cyanocobalamin in the presence or absence of clioquinol were also determined. No statistically significant alterations in the partition coefficient for [57Co]-cyanocobalamin in the presence of clioquinol was evident, indicating that clioquinol does not bind cobalt. In addition, transmethylation reactions in the CNS in mice treated with clioquinol were studied. Specific activities of methionine adenosyltransferase, and S-adenosylhomocysteine levels were not affected. In contrast, clioquinol treatment caused a significant increase in the levels of S-adenosylmethionine in the brain. The data of the present study show that clioquinol treatment can affect the accumulation of vitamin B12 in the kidney and the skin but not in the brain. These results do not support the hypothesis that clioquinol causes its damage to the nervous system by a direct chemical interaction with vitamin B12.


Assuntos
Vitamina B 12/farmacocinética , Animais , Anti-Infecciosos Locais/farmacologia , Autorradiografia , Encéfalo/efeitos dos fármacos , Encéfalo/metabolismo , Clorofórmio/química , Clioquinol/farmacologia , Radioisótopos de Cobalto , Rim/efeitos dos fármacos , Rim/metabolismo , Fígado/efeitos dos fármacos , Fígado/metabolismo , Masculino , Metionina Adenosiltransferase/efeitos dos fármacos , Metionina Adenosiltransferase/metabolismo , Metilação/efeitos dos fármacos , Camundongos , Camundongos Endogâmicos , S-Adenosil-Homocisteína/metabolismo , S-Adenosilmetionina/efeitos dos fármacos , S-Adenosilmetionina/metabolismo , Contagem de Cintilação , Solubilidade/efeitos dos fármacos , Distribuição Tecidual , Vitamina B 12/análise , Vitamina B 12/metabolismo , Água/química
3.
Eur Neuropsychopharmacol ; 8(2): 153-7, 1998 May.
Artigo em Inglês | MEDLINE | ID: mdl-9619694

RESUMO

Levels of cholecystokinin (CCK) peptides were measured in the CSF from 105 patients suffering from major depressive disorders admitted to a research psychiatric ward for diagnostic evaluation, by a radioimmunoassay method using two different antibodies. Relations between CCK levels and parameters of depression, anxiety, and suicidal behaviour were investigated. Significant inverse correlations were found between CCK levels and certain depression and anxiety parameters. Patients who had made one or more suicide attempts tended to have higher CSF CCK levels than those who had not. No correlations were found between CSF CCK and 5-HIAA or HVA, or with plasma cortisol.


Assuntos
Colecistocinina/líquido cefalorraquidiano , Transtorno Depressivo/líquido cefalorraquidiano , Transtorno Depressivo/psicologia , Suicídio/psicologia , Adulto , Idoso , Ansiedade/psicologia , Glicemia/metabolismo , Feminino , Ácido Homovanílico/líquido cefalorraquidiano , Humanos , Hidrocortisona/sangue , Ácido Hidroxi-Indolacético/líquido cefalorraquidiano , Masculino , Pessoa de Meia-Idade , Radioimunoensaio
4.
Neuropeptides ; 32(2): 103-8, 1998 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-9639247

RESUMO

The neurotoxin DSP-4 has, in this laboratory, previously been shown to upregulate cholecystokinin (CCK) binding in the frontal cortex and the hippocampus in rats. The present study investigated the effect of DSP-4 on CCK peptide levels and CCK receptor binding in some rat brain areas. Sprague-Dawley rats were given single injections of DSP-4 (10 and 50 mg/kg) and examined after 1 week. Wistar rats were given an injection of DSP-4 (50 mg/kg) and evaluated 1 week and 4 months after treatment. No significant changes in CCK levels or in CCK binding were found. It has been found that stress produced by handling of the rats immediately before decapitation can result in an increase in cortical CCK receptor binding. This finding led to the speculation that the upregulation of CCK binding after DSP-4 treatment which was reported earlier, reflects a stress-potentiating effect of DSP-4.


Assuntos
Adrenérgicos/farmacologia , Benzilaminas/farmacologia , Química Encefálica/efeitos dos fármacos , Colecistocinina/metabolismo , Receptores da Colecistocinina/metabolismo , Agonistas alfa-Adrenérgicos/análise , Agonistas alfa-Adrenérgicos/farmacocinética , Animais , Peso Corporal/efeitos dos fármacos , Masculino , Neuropeptídeos/metabolismo , Norepinefrina/análise , Norepinefrina/farmacocinética , Radioimunoensaio , Ratos , Ratos Sprague-Dawley , Ratos Wistar , Receptor de Colecistocinina A , Receptor de Colecistocinina B
5.
Exp Neurol ; 145(2 Pt 1): 580-5, 1997 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-9217094

RESUMO

In the present study, levels of S-adenosylmethionine (SAM) and S-adenosylhomocysteine (SAH) in whole blood as well as L-methionine S-adenosyltransferase (MAT) activity in erythrocytes were assayed in a series of 20 patients with Parkinson's disease and 12 healthy control subjects. A significant difference was found with regard to SAM levels between patients and controls, with the detected levels being 383.1 +/- 41.5 nM for the parkinsonian patients and 680.6 +/- 30.9 nM for the controls. With regard to SAH, we found no difference between the groups. The catalytic activity of MAT was increased by 30% in patients compared to controls, with the Vmax for methionine being 17.9 +/- 3.7 and 13.9 +/- 2.2 pmol/mg/h, respectively.


Assuntos
Eritrócitos/enzimologia , Metionina Adenosiltransferase/metabolismo , Doença de Parkinson/metabolismo , S-Adenosil-Homocisteína/metabolismo , S-Adenosilmetionina/metabolismo , Antiparkinsonianos/administração & dosagem , Cromatografia Líquida de Alta Pressão , Eritrócitos/química , Feminino , Humanos , Levodopa/administração & dosagem , Masculino , Pessoa de Meia-Idade , Doença de Parkinson/tratamento farmacológico
6.
Naunyn Schmiedebergs Arch Pharmacol ; 355(1): 57-63, 1997 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-9007843

RESUMO

Cholecystokinin (CCK) is a neuropeptide recently implicated in affective disorders. This study aimed at measuring the levels of different molecular forms of CCK and the binding characteristics of CCKB receptors in the rat brain after three weeks of treatment with four different antidepressants, imipramine, amitriptyline, desipramine, and citalopram (all at the dose of 10 mg/kg once per day i.p.). Chronic treatment with imipramine and desipramine had a significant immobility-reducing effect in the Porsolt's swim test. The effect of amitriptyline, albeit in the same direction, was not significant, and citalopram had no effect in this test. In the elevated plus-maze test of anxiety, all drugs tended to increase the number of open arm entries and the ratio open/total arm entries, but only the effects of imipramine were statistically significant. None of the treatments affected the total levels of CCK or the levels of CCK-8-sulphated, CCK-8-nonsulphated, CCK-5, or CCK-4 in the frontal cortex. There was no effect of the treatments on CCKB receptor binding in the frontal cortex, hippocampus, or striatum. Imipramine and amitriptyline, however, increased the affinity of CCKB receptor binding in the hypothalamus. Thus, no consistent effect of chronic antidepressant treatment on the CCK-ergic neurotransmission in the rats was found.


Assuntos
Antidepressivos/farmacologia , Encéfalo/efeitos dos fármacos , Colecistocinina/análise , Receptores da Colecistocinina/efeitos dos fármacos , Animais , Encéfalo/metabolismo , Colecistocinina/metabolismo , Lobo Frontal/química , Masculino , Aprendizagem em Labirinto/efeitos dos fármacos , Ratos , Ratos Wistar , Receptor de Colecistocinina B , Receptores da Colecistocinina/metabolismo
7.
Naunyn Schmiedebergs Arch Pharmacol ; 354(1): 59-66, 1996 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-8832589

RESUMO

Cholecystokinin (CCK) has been implicated in stress and anxiety disorders. We have studied the levels of different molecular forms of CCK and CCK receptor characteristics in rats kept for 1 h in individual cages and exposed to decapitation of conspecifics, and a control group which was decapitated immediately. Total CCK concentration was found to be increased in the hippocampus of stressed animals in the first experiment: this finding was not confirmed in further studies. No effect of stress was found on total CCK levels in the frontal cortex, hypothalamus, striatum, and septum. CCK-8-sulphated, CCK-8-nonsulphated, CCK-5, and CCK-4 were separated by HPLC and measured with two antibodies with different selectivity: no effect of stress was found on the levels of any of these molecular forms of CCK. Injection procedure and diazepam (5 mg/kg) administration had no effect on total CCK levels. Exposition of rats to the decapitation procedure increased [3H]-CCK-8 binding in the frontal and cerebral (whole-frontal) cortex. This effect could not be blocked by diazepam pretreatment. Injection procedure itself increased CCK receptor binding in the cerebral cortex, but the effect of this type of stress was smaller in magnitude. The upregulation of CCK receptors in stressed animals was due to the increased binding of radioligand on CCKB receptor subtype.


Assuntos
Colecistocinina/metabolismo , Receptores da Colecistocinina/metabolismo , Animais , Encéfalo/metabolismo , Masculino , Ligação Proteica , Ratos , Ratos Sprague-Dawley , Receptores da Colecistocinina/antagonistas & inibidores
8.
J Neural Transm (Vienna) ; 103(7): 851-60, 1996.
Artigo em Inglês | MEDLINE | ID: mdl-8872869

RESUMO

Cholecystokinin (CCK) is a peptide that can be found in the cerebral cortex in high concentrations and is involved in learning and memory as well as neurodegenerative processes. Cortical brain samples from 9 patients with Alzheimer's disease and 9 matched control cases were studied with respect to the concentrations of various molecular forms of CCK and the CCK receptor binding characteristics. No differences were found between patients and controls in any of these measures. Significant correlations were found between the concentrations of CCK-8 sulphated and the three nonsulphated CCK peptides measured. In addition, the concentrations of CCK-4 and CCK-5 showed a highly significant and positive correlation.


Assuntos
Doença de Alzheimer/metabolismo , Colecistocinina/metabolismo , Giro do Cíngulo/metabolismo , Receptores da Colecistocinina/metabolismo , Idade de Início , Idoso , Idoso de 80 Anos ou mais , Análise de Variância , Estudos de Casos e Controles , Feminino , Humanos , Modelos Lineares , Masculino , Pessoa de Meia-Idade , Fragmentos de Peptídeos/metabolismo , Sincalida/metabolismo , Tetragastrina/metabolismo
9.
Eur Neuropsychopharmacol ; 4(4): 469-77, 1994 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-7894257

RESUMO

The distribution of the activity of the enzyme methionine adenosyltransferase (ATP:L-methionine S-adenosyltransferase, EC 2.5.1.6, MAT) was investigated in human postmortem brains of individuals without a known history of neuropsychiatric disorders. The brain regions were the frontal, temporal, parietal and occipital cortices, nucleus caudatus, putamen, globus pallidus, thalamus and white matter. The activities in the nucleus caudatus and putamen were approximately 25% higher than the activities in the seven other brain regions, however, not on a statistically significant level. The apparent values of MAT Km and Vmax in the parietal cortex were 11.41 +/- 3.51 microM methionine and 25.72 +/- 3.90 nmol/mg protein/h, respectively. In the frontal cortex, a significant positive correlation between age and the activity of MAT was found (r = 0.997, P < 0.01). Concerning MAT stability in the rat brain, there was a steady decrease in the activity with postmortem time in the brains kept for 0-72 h at room temperature (23 degrees C), which reached the level of significance at 24 h. The activity did not change significantly when the brains were kept for 120 h at 4 degrees C, or by freezing and thawing the tissue before analysis. In a parallel study in rats of different ages (2-22 months), a homogeneous distribution of SAM and SAH was observed in the cortex, striatum, midbrain, hypothalamus, brainstem and cerebellum. The lowest levels of SAM and the highest levels of SAH observed in the striatum gave the lowest SAM/SAH ratio. The SAH content of rat cerebral cortex was highest in the oldest group.(ABSTRACT TRUNCATED AT 250 WORDS)


Assuntos
Envelhecimento/metabolismo , Química Encefálica/fisiologia , Metionina Adenosiltransferase/metabolismo , S-Adenosil-Homocisteína/metabolismo , S-Adenosilmetionina/metabolismo , Idoso , Idoso de 80 Anos ou mais , Animais , Encéfalo/enzimologia , Cromatografia Líquida de Alta Pressão , Feminino , Humanos , Cinética , Masculino , Pessoa de Meia-Idade , Ratos , Ratos Sprague-Dawley , Espectrofotometria Ultravioleta
10.
Child Abuse Negl ; 14(2): 165-70, 1990.
Artigo em Inglês | MEDLINE | ID: mdl-2340427

RESUMO

This study analyzes factors related to the decision to divorce in intrafamilial sexual abuse cases. Data was collected on 128 cases of incest in St. Louis, Missouri, through the Washington University Child Guidance Center. Examination of multiple variables revealed there are differences between child sexual abuse cases that elect to stay together vs. those that divorce subsequent to the discovery of abuse. Families that broke up were more likely to have young child victims and have additional problems with domestic violence. The child was more likely to have revealed the abuse to the mother and have been believed by her in divorcing cases.


Assuntos
Abuso Sexual na Infância/psicologia , Divórcio/psicologia , Família , Adolescente , Criança , Abuso Sexual na Infância/epidemiologia , Pré-Escolar , Estudos Transversais , Divórcio/estatística & dados numéricos , Feminino , Seguimentos , Humanos , Incidência , Masculino , Missouri/epidemiologia
11.
Exp Clin Endocrinol ; 93(2-3): 307-12, 1989 May.
Artigo em Inglês | MEDLINE | ID: mdl-2550272

RESUMO

Insulin release in response to glucose was measured after culture of islets from ob/obmice in a medium deficient in Ca2+. When present at a concentration of 6 mmol/l, glucose inhibited, insulin release. After activation of the alpha2-adrenergic receptors by 1 mumol/l clonidine also 20 mmol/l glucose became inhibitory. The inhibitory action of glucose on insulin release disappeared in the presence of 1 mmol/l dibutyryl cyclic AMP. Raising the glucose concentration from 3 to 20 mmol/l resulted in increased cytoplasmic Ca2+ after an initial depression. Whereas clonidine removed the Ca2+ increase, this phase was partly restored after simultaneous addition of dibutyryl cyclic AMP. It is concluded that cyclic AMP plays a major role in controlling the balance between the stimulatory and inhibitory components in the glucose action on insulin release.


Assuntos
Bucladesina/farmacologia , Glucose/farmacologia , Insulina/metabolismo , Animais , Cálcio/análise , Cálcio/metabolismo , Clonidina/farmacologia , Citoplasma/análise , Citoplasma/metabolismo , Relação Dose-Resposta a Droga , Camundongos , Camundongos Obesos
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