Vildagliptine protects SH-SY5Y human neuron-like cells from Aβ 1–42 induced toxicity, in vitro
The amyloid β (A β ) toxic fibrils is thought to play a central role in the onset and progression of Alzheimer’s disease (AD) because of it is a main formation of senile plaques. Diabetic patients are more vulnerable to caught Alzheimer’s disease. Vildagliptine, a novel anti diabetic agent, has been...
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Veröffentlicht in: | Cytotechnology (Dordrecht) 2019-04, Vol.71 (2), p.635-646 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | The amyloid β (A
β
) toxic fibrils is thought to play a central role in the onset and progression of Alzheimer’s disease (AD) because of it is a main formation of senile plaques. Diabetic patients are more vulnerable to caught Alzheimer’s disease. Vildagliptine, a novel anti diabetic agent, has been reported to exert protective effects on AD rat models in restricted study. We aimed to investigate any protective effects of vildagliptine against A
β
fibrils on SH-SY5Y cell line. Vildagliptine decreased PSEN1 and PSEN2 mRNA levels which enroll A
β
production. In addition, vildagliptin was downregulated caspase-3 and caspase-9 expression levels which were evoked by A
β
. Also we confirmed cellular viability with real time cell analyzer and MTT assay. Our data exposed that vildagliptine has lowering effect on GSK3
β
and Tau phosphorylation. However we did not get protective effect of vildagliptine against A
β
toxicity on mitochondrial membrane potential. These results indicate that vildagliptine exerts a protective effect against A
β
by decreasing apoptosis related proteins, lowering GSK3
β
and Tau phosphorylation levels in addition to expression of PSEN1 and PSEN2 mRNA downregulation effect. |
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ISSN: | 0920-9069 1573-0778 |
DOI: | 10.1007/s10616-019-00312-7 |