Base de dados : HANSEN
Pesquisa : APOPTOSE/EF DROGAS [Descritor de assunto]
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Id:18936
Autor:Vescovo, Giorgio; Ravara, Barbara; Angelini, Annalisa; Sandri, Marco; Carraro, Ugo; Ceconi, Claudio; Dalla Libera, Luciano
Título:Effect of thalidomide on the skeletal muscle in experimental heart failure
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Fonte:s.l; s.n; 2002. 6 p. ilus, tab.
Resumo:BACKGROUND: Tumour Necrosis Factor alpha (TNFalpha) has been shown to contribute to heart failure (CHF) progression. AIMS: We have tried to antagonise the detrimental effects of TNFalpha on skeletal muscle apoptosis, by using thalidomide, a drug that inhibits its biosynthesis. METHODS: CHF was induced in 20 rats by injecting monocrotaline, which determines right ventricle (RV) failure. After 2 weeks, when CHF developed, 12 rats were treated with thalidomide 3.5.mg/kg per day for 2 weeks. Eight had saline and served as CHF controls. RESULTS: Thalidomide failed to decrease TNFalpha and its second messenger sphingosine (SPH), but was able to prevent the shift toward the fast myosin heavy chains. In the Tibialis Anterior muscle of the thalidomide group, the degree of atrophy, the number of apoptotic nuclei and the levels of caspases, were similar to those of the CHF controls. CONCLUSIONS: Thalidomide, at the doses used in this study, which are the same employed for the treatment of tubercolosis, leprosy, AIDS and cancer in humans, did not lower either TNFalpha or SPH and only marginally influenced the apoptosis-induced muscle atrophy. Since other TNFalpha blockers are under investigation for improving the clinical status of patients with CHF, the present data could be relevant in the design of randomised clinical trials in humans. (AU).
Descritores:APOPTOSE/ef drogas
INSUFICIÊNCIA CARDIACA CONGESTIVA/ind quim
INSUFICIÊNCIA CARDIACA CONGESTIVA/patol
MONOCROTALINA/tox
MUSCULO ESQUELETICO/ef drogas
MUSCULO ESQUELETICO/patol
ATROFIA MUSCULAR/ind quim
ATROFIA MUSCULAR/patol
CADEIAS PESADAS DE MIOSINA/metab
RATOS SPRAGUE-DAWLEY
ESFINGOSINA/antag
ESFINGOSINA/metab
TALIDOMIDA/farmacol
FATOR DE NECROSE TUMORAL/antag
FATOR DE NECROSE TUMORAL/metab
DISFUNCAO VENTRICULAR DIREITA/ind quim
DISFUNCAO VENTRICULAR DIREITA/patol
Limites:ANIMAL
RATOS
Meio Eletrônico: - .
Localização:BR191.1; 09104/s


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Id:18498
Autor:Hernandez, M. O; Neves Junior, I; Sales, J. S; Carvalho, D. S; Sarno, E. N; Sampaio, E. P
Título:Induction of apoptosis in monocytes by Mycobacterium leprae in vitro: a possible role for tumour necrosis factor-alpha
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Fonte:s.l; s.n; 2003. 9 p. graf.
Resumo:A diverse range of infectious organisms, including mycobacteria, have been reported to induce cell death in vivo and in vitro. Although morphological features of apoptosis have been identified in leprosy lesions, it has not yet been determined whether Mycobacterium leprae modulates programmed cell death. For that purpose, peripheral blood mononuclear cells obtained from leprosy patients were stimulated with different concentrations of this pathogen. Following analysis by flow cytometry on 7AAD/CD14+ cells, it was observed that M. leprae induced apoptosis of monocyte-derived macrophages in a dose-dependent manner in both leprosy patients and healthy individuals, but still with lower efficiency as compared to M. tuberculosis. Expression of tumour necrosis factor-alpha (TNF-alpha), Bax-alpha, Bak mRNA and TNF-alpha protein was also detected in these cultures; in addition, an enhancement in the rate of apoptotic cells (and of TNF-alpha release) was noted when interferon-gamma was added to the wells. On the other hand, incubation of the cells with pentoxifylline impaired mycobacterium-induced cell death, the secretion of TNF-alpha, and gene expression in vitro. In addition, diminished bacterial entry decreased both TNF-alpha levels and the death of CD14+ cells, albeit to a different extent. When investigating leprosy reactions, an enhanced rate of spontaneous apoptosis was detected as compared to the unreactive lepromatous patients. The results demonstrated that M. leprae can lead to apoptosis of macrophages through a mechanism that could be at least partially related to the expression of pro-apoptotic members of the Bcl-2 protein family and of TNF-alpha. Moreover, while phagocytosis may be necessary, it seems not to be crucial to the induction of cell death by the mycobacteria. (AU).
Descritores:APOPTOSE/ef drogas
APOPTOSE/imunol
CELULAS CULTIVADAS
REGULACAO DA EXPRESSÃO GÊNICA
INTERFERON TIPO II/farmacol
HANSENIASE/imunol
PROTEINAS DE MEMBRANA/genet
MONOCITOS/imunol
MONOCITOS/patol
MYCOBACTERIUM LEPRAE/imunol
PENTOXIFILINA/farmacol
FAGOCITOSE/imunol
PROTEINAS PROTO-ONCOGÊNICAS/genet
FATOR DE NECROSE TUMORAL/imunol
Limites:HUMANO
MASCULINO
FEMININO
ADULTO
MEIA-IDADE
IDOSO
SUPPORT, NON-U.S. GOV'T
Meio Eletrônico: - .
Localização:BR191.1; 09128/s


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Id:16319
Autor:Sampaio, E. P; Hernandez, M. O; Carvalho, D. S; Sarno, E. N
Título:Management of erythema nodosum leprosum by thalidomide: thalidomide analogues inhibit M. leprae-induced TNFalpha production in vitro
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Fonte:s.l; s.n; 2002. 7 p. ilus, graf.
Descritores:APOPTOSE
CITOCINAS
CITOCINAS
ERITEMA NODOSO
IMUNOSSUPRESSORES
IMUNOSSUPRESSORES
INTERLEUCINA-12
MONOCITOS
MYCOBACTERIUM LEPRAE
MYCOBACTERIUM LEPRAE
RNA MENSAGEIRO
RNA MENSAGEIRO
RNA MENSAGEIRO
TALIDOMIDA
TALIDOMIDA
TALIDOMIDA
FATOR DE NECROSE TUMORAL/AI/GE
Localização:BR191.1; 08709/s


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Id:14375
Autor:Gupta, Anu; Sharma, V. K; Vohra, Harpreet; Ganguly, N. K
Título:Spontaneous apoptosis in peripheral blood mononuclear cells of leprosy patients: role of cytokines
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Fonte:s.l; s.n; 1999. 7 p. tab, graf.
Descritores:ANTICORPOS
ESPECIFICIDADE DE ANTICORPOS
ANTIGENOS CD28
APOPTOSE
CITOCINAS
CITOCINAS
INTERLEUCINA-1
INTERLEUCINA-6
INTERLEUCINA-6
IONOMICINA
HANSENIASE
HANSENIASE
LEUCOCITOS MONONUCLEARES
LEUCOCITOS MONONUCLEARES
ZINCO
CELULAS CULTIVADAS
FATOR DE NECROSE TUMORAL/AI/PH
Localização:BR191.1; 07501/s



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