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1.
Transl Psychiatry ; 5: e674, 2015 Nov 03.
Artigo em Inglês | MEDLINE | ID: mdl-26529427

RESUMO

Chronic ventromedial prefrontal cortex (vmPFC) deep brain stimulation (DBS) improves depressive-like behaviour in rats via serotonergic and neurotrophic-related mechanisms. We hypothesise that, in addition to these substrates, DBS-induced increases in hippocampal neurogenesis may also be involved. Our results show that stress-induced behavioural deficits in the sucrose preference test, forced swim test, novelty-suppressed feeding test (NSFT) and elevated plus maze were countered by chronic vmPFC DBS. In addition, stressed rats receiving stimulation had significant increases in hippocampal neurogenesis, PFC and hippocampal brain-derived neurotrophic factor levels. To block neurogenesis, stressed animals given DBS were injected with temozolomide. Such treatment reversed the anxiolytic-like effect of stimulation in the NSFT without significantly affecting performance in other behavioural tests. Taken together, our findings suggest that neuroplastic changes, including neurogenesis, may be involved in specific anxiolytic effects of DBS without affecting its general antidepressant-like response.


Assuntos
Comportamento Animal/fisiologia , Estimulação Encefálica Profunda , Plasticidade Neuronal/fisiologia , Estresse Psicológico/fisiopatologia , Estresse Psicológico/terapia , Animais , Modelos Animais de Doenças , Masculino , Neurogênese/fisiologia , Ratos , Ratos Endogâmicos F344
2.
Eur J Clin Chem Clin Biochem ; 35(6): 475-81, 1997 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-9228332

RESUMO

This study describes the value of using the fraction of free prostate-specific antigen as a further marker in the early detection of prostate cancer. This newly introduced marker is compared to the usual battery of age-dependent total prostate-specific antigen, prostate-specific antigen density (microg/l x g tissue) and prostate-specific antigen velocity (microg/l x year). Determination of total prostate-specific antigen and free prostate-specific antigen was performed on fresh serum samples obtained from 3470 symptomatic patients aged 45-80 attending the Urology Clinics, or their General Practitioners. Among them, 310 patients had total prostate-specific antigen above the age-dependent cut-off, and/or free/total prostate-specific antigen under 11%, with different prostate-specific antigen densities and velocities. Only 147 patients complied to undergo biopsy: in 72 of those patients, benign prostatic disease was histologically confirmed, while in 75 patients primary prostate cancer was histologically confirmed. Total and free prostate-specific antigen levels were determined using the third generation DPCs prostate-specific antigen assay performed on the Immulite automated immunoassay instrument. Total prostate-specific antigen age reference values were adopted from Oesterling et al. (J Am Med Ass 1993; 270:860-4); the prostate-specific antigen density was considered suspicious of prostate cancer if it was greater than 0.15 microg/l prostate-specific antigen per gram tissue (Seaman et al. Urol Clin N Am 1993; 20:653); prostate-specific antigen velocity greater than 0.75 microg/l x year (Carter et al., J Am Med Ass 1992; 267:215) was considered suspicious for prostate cancer. Of the 147 patients, 75 had prostate cancer and 72 had benign prostatic hypertrophy. The difference between prostate cancer and benign prostatic hypertrophy was significantly reflected only by free/total prostate-specific antigen and prostate-specific antigen velocity. These parameters also provided the best sensitivity and specificity. Only these parameters proved to be significant when using a backwards logistic regression model (prostate-specific antigen velocity, p = 0.007 odds ratio 2.782; free/total prostate-specific antigen %, p = 0.016 odds ratio 2.678). Combinations of various parameters became significant when including free/total prostate-specific antigen, increasing prostate cancer detection to 88%. We conclude that free/total prostate-specific antigen is the most significant among prostate-specific antigen quantities (total age-dependent prostate-specific antigen, prostate-specific antigen density and prostate-specific antigen velocity). Adding this parameter to other prostate-specific antigen parameters improves the discrimination between prostate cancer and benign prostatic hypertrophy for the population at risk.


Assuntos
Antígeno Prostático Específico/sangue , Idoso , Idoso de 80 Anos ou mais , Envelhecimento/sangue , Envelhecimento/imunologia , Algoritmos , Humanos , Masculino , Pessoa de Meia-Idade , Razão de Chances , Valor Preditivo dos Testes , Hiperplasia Prostática/sangue , Hiperplasia Prostática/diagnóstico , Hiperplasia Prostática/imunologia , Neoplasias da Próstata/sangue , Neoplasias da Próstata/diagnóstico , Neoplasias da Próstata/imunologia , Valores de Referência , Sensibilidade e Especificidade
3.
World J Urol ; 14(1): 59-61, 1996.
Artigo em Inglês | MEDLINE | ID: mdl-8646243

RESUMO

Two cases of spermatic cord leiomyosarcoma are described. Preoperative ultrasound disclosed a paratesticular tumor. Inguinal orchiectomy was performed; there was no adjuvant treatment. Currently there is no evidence of disease after 12 and 24 months of follow-up. The literature on this rare condition is reviewed.


Assuntos
Leiomiossarcoma/patologia , Cordão Espermático/patologia , Idoso , Seguimentos , Humanos , Leiomiossarcoma/cirurgia , Masculino , Orquiectomia , Cordão Espermático/diagnóstico por imagem , Cordão Espermático/cirurgia , Ultrassonografia
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