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1.
J Epidemiol Community Health ; 62(6): 538-44, 2008 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-18477753

RESUMO

OBJECTIVES: Adults in South Africa demonstrate rates of mental illness at or above levels elsewhere in the developing world. Yet there is a research gap regarding the social context surrounding mental health in this region. The objective of this analysis was to characterize the prevalence and correlates of depressive symptoms and perceived stress among a heterogeneous South African population. METHODS: Low-income adults (n = 257) in Capetown, Port Elizabeth and Durban were interviewed regarding demographics, income, subjective social status, life events and decision-making. The Center for Epidemiologic Studies Depression Scale (CES-D) and Cohen's Perceived Stress Scale (PSS) were used. RESULTS: CES-D scores were 18.8 (SD 11.7), with 50.4% of men and 64.5% of women exceeding the cut-off at which professional care is recommended (p = 0.03). PSS scores were 18.6 (SD 6.7), with a mean of 17.5 among men and 19.6 among women (p = 0.02). In multivariate regressions, increased CES-D scores were associated with more household members (p<0.1), lower educational attainment (p = 0.07), less income stability (p<0.07), lower subjective social status (p<0.01) and independent decision-making (p = 0.04). Increased PSS scores were associated with female gender (p<0.05), multiracial race (p<0.02), more household members (p<0.1), lower subjective social status (p<0.02) and recent birth or catastrophe (p<0.01). CONCLUSIONS: Depressive symptoms and perceived stress are public health concerns in this sample, with more symptoms among those with fewer resources. The prevention of mental illness is critical, especially in vulnerable populations.


Assuntos
Depressão/epidemiologia , Países em Desenvolvimento , Pobreza , Estresse Psicológico/epidemiologia , Adulto , Tomada de Decisões , Depressão/etnologia , Depressão/etiologia , Escolaridade , Etnicidade , Feminino , Humanos , Acontecimentos que Mudam a Vida , Modelos Lineares , Masculino , Estado Civil , Prevalência , Características de Residência , Distribuição por Sexo , África do Sul/epidemiologia , Estresse Psicológico/etnologia , Estresse Psicológico/etiologia
2.
Am J Physiol Regul Integr Comp Physiol ; 281(5): R1699-709, 2001 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-11641143

RESUMO

The goal of these studies was to examine the potential utility of bladder instilled K+ channel gene therapy with hSlo cDNA (i.e., the maxi-K channel) to ameliorate bladder overactivity in a rat model of partial urinary outlet obstruction. Twenty-two female Sprague-Dawley rats were subjected to partial urethral (i.e., outlet) obstruction, with 17 sham-operated control rats run in parallel. After 6 wk of obstruction, suprapubic catheters were surgically placed in the dome of the bladder in all rats. Twelve obstructed rats received bladder instillation of 100 microg of hSlo/pcDNA in 1 ml PBS during catheterization, and another 10 obstructed rats received 1 ml PBS (7 rats) or 1 ml PBS containing pcDNA only (3 rats). Two days after surgery cystometry was performed on all animals to examine the characteristics of the micturition reflex in conscious and unrestrained rats. Obstruction was associated with a three- to fourfold increase in bladder weight and alterations in virtually every micturition parameter estimate. PBS-injected obstructed rats routinely displayed spontaneous bladder contractions between micturitions. In contrast, hSlo injection eliminated the obstruction-associated bladder hyperactivity, without detectably affecting any other cystometric parameter. Presumably, expression of hSlo in rat bladder functionally antagonizes the increased contractility normally observed in obstructed animals and thereby ameliorates bladder overactivity. These initial observations indicate a potential utility of gene therapy for urinary incontinence.


Assuntos
Terapia Genética , Hipertonia Muscular/terapia , Canais de Potássio Cálcio-Ativados , Canais de Potássio/genética , Transgenes/genética , Obstrução Uretral/terapia , Bexiga Urinária/metabolismo , Administração Intravesical , Animais , Sequência de Bases , DNA/genética , DNA/metabolismo , Modelos Animais de Doenças , Feminino , Humanos , Canais de Potássio Ativados por Cálcio de Condutância Alta , Masculino , Dados de Sequência Molecular , Contração Muscular/fisiologia , Hipertonia Muscular/fisiopatologia , Tamanho do Órgão , Canais de Potássio/metabolismo , Ratos , Ratos Sprague-Dawley , Bexiga Urinária/citologia
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