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DOI 10.1210/jc.2010-2961

Медицинская библиотека · The Journal of clinical endocrinology and metabolism · 2011

Insulin suppresses the expression of amyloid precursor protein, presenilins, and glycogen synthase kinase-3beta in peripheral blood mononuclear cells.

Dandona Paresh, Mohamed Islam, Ghanim Husam, Sia Chang Ling, Dhindsa Sandeep, Dandona Sonny, Makdissi Antoine, Chaudhuri Ajay

СтатьяПоддержка NIH: внешняя программаПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

OBJECTIVE

Our objective was to determine whether peripheral blood mononuclear cells express amyloid precursor protein (APP) and other mediators involved in the pathogenesis of Alzheimer's disease and whether their expression is suppressed by insulin.

RESEARCH DESIGN AND

METHODS

Ten obese type 2 diabetic patients were infused with insulin (2 U/h with 100 ml 5% dextrose/h) for 4 h. Patients were also infused with 5% dextrose/h or normal physiological saline for 4 h, respectively, on two other days as controls. Blood samples were obtained at 0, 2, 4, and 6 h.

RESULTS

Insulin infusion significantly suppressed the expression of APP, presenilin-1, presenilin-2, and glycogen synthase kinase-3β in peripheral blood mononuclear cells. Dextrose and saline infusions did not alter these indices. Insulin infusion also caused significant parallel reductions in nuclear factor-κB binding activity and plasma concentrations of serum amyloid A and intercellular adhesion molecule-1.

CONCLUSIONS

A low dose infusion of insulin suppresses APP, presenilin-1, presenilin-2, and glycogen synthase kinase-3β, key proteins involved in the pathogenesis of Alzheimer's disease, in parallel with exerting its other antiinflammatory effects.

Для цитирования: Dandona Paresh, Mohamed Islam, Ghanim Husam, Sia Chang Ling, Dhindsa Sandeep, Dandona Sonny, Makdissi Antoine, Chaudhuri Ajay. Insulin suppresses the expression of amyloid precursor protein, presenilins, and glycogen synthase kinase-3beta in peripheral blood mononuclear cells.. The Journal of clinical endocrinology and metabolism. 2011. DOI: 10.1210/jc.2010-2961.

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