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The protection of APP17-mer peptide against neuronal apoptosis induced by aβ25-35 / 中国药理学通报
Chinese Pharmacological Bulletin ; (12): 31-35, 2002.
Artículo en Chino | WPRIM | ID: wpr-857418
ABSTRACT

AIM:

To examine the effects of the APP17-mer peptide against 2Aβ25-35-induced apoptosis and gain some insight into the neuroprotective mechanism of the APP17-mer peptide.

METHODS:

Protective effects of APP17-mer peptide against Aβ25-35- induced apoptosis in SH-SY5Y cell was proved by cell morphology, LM-PCR DNA ladder assay and FCM assay. The antiapoptotic mechanism of APP17-mer peptide was investigated using the MTT assay to measure mitochondrial energy redox state, using the fluorescent probe DCF-DA, Rhodamine 123 to measure relative levels of cellular peroxides and mitochondrial membrane potential and using Western blot for AIF and NF-kB to detect the expression of AIF and NF-KB.

RESULTS:

Damage of cell morphology was ameliorated by pretreating with APP17-mer peptide. The apoptotic rate of the SH-SY5Y cells exposed to Aβ25-35 in the presence of APP17-mer peptide decreased from 63.75% to 28.25%. Exposure of SH-SY5Y to Aβ25-35 for 48 h resulted in an increase in DCF-DA fluorescence, a decrease in Rhodamine 123 fluorescence and MTT reduction, the results were weakened by pre-incubating with APP17-me.r peptide for 30 minutes. Treatment of cells with APP17-mer peptide resulted in a significant attenuation in the expression of AIF and a strong increase in the expression of NF-KB.

CONCLUSION:

APP17-mer is protective against cell apoptosis induced by Aβ25-35 by provoking and sustaining upregulation of a key antiapoptotic transcription factor NF-KB, by suppressing oxyradical production and by preserving mitochondrial function and inhibiting the release of apoptotic protein from mitochondria.

Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Idioma: Chino Revista: Chinese Pharmacological Bulletin Año: 2002 Tipo del documento: Artículo

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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Idioma: Chino Revista: Chinese Pharmacological Bulletin Año: 2002 Tipo del documento: Artículo