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Biochem Pharmacol ; 65(10): 1755-60, 2003 May 15.
Artigo em Inglês | MEDLINE | ID: mdl-12754112

RESUMO

Helicobacter pylori infection can be associated with chronic gastric inflammation and hypochlorhydria with increased levels of the proinflammatory cytokines. The current study investigated the effects of TNF-alpha on programmed death of gastric parietal cells. TNF-alpha induced apoptosis of parietal cells in isolated perfused rat stomachs at 10ng/mL. In isolated and highly enriched rat parietal cells, 10ng/mL TNF-alpha induced a 2.6-fold increase in the apoptotic rate. The 55kDa protein of TNFR-1 but not the 75kDa of TNFR-2 was detected by Western blot analysis. TNF-alpha-induced apoptosis of isolated parietal cells was inhibited by pretreatment with different NF-kappaB-inhibitors, nitric oxide synthase inhibitors and with antisense-oligodeoxynucleotides against the p65 subunit of NF-kappaB. Investigation of downstream signaling pathways of apoptosis revealed that TNF-alpha induced the expression of iNOS, but failed to stimulate the activity of caspase 3. The TNF-alpha effect on gastric parietal cells may contribute to the atrophy and hypochlorhydria of the gastric mucosa observed during chronic H. pylori infection.


Assuntos
Apoptose , Células Parietais Gástricas/efeitos dos fármacos , Fator de Necrose Tumoral alfa/farmacologia , Animais , Caspase 3 , Caspases/metabolismo , NF-kappa B/metabolismo , Óxido Nítrico Sintase/metabolismo , Óxido Nítrico Sintase Tipo II , Células Parietais Gástricas/citologia , Células Parietais Gástricas/enzimologia , Células Parietais Gástricas/metabolismo , Ratos , Receptores do Fator de Necrose Tumoral/metabolismo
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