Role of P-glycoprotein in mediating rivastigmine effect on amyloid-β brain load and related pathology in Alzheimer's disease mouse model

BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE

卷:1862

Article

Mohamed, Loqman A.¹  Keller, Jeffrey N.²  Kaddoumi, Amal¹ 

[1] Univ Louisiana Monroe, Sch Pharm, Dept Basic Pharmaceut Sci, 1800 Bienville Dr, Monroe, LA 71201 USA

[2] Louisiana State Univ, Pennington Biomed Res Ctr, Baton Rouge, LA 70808 USA

关键词: Rivastigmine;    P-glycoprotein;    Alzheimer's disease;    Amyloid-beta;    Neuroprotection;    Astrogliosis;   

DOI  :  10.1016/j.bbadis.2016.01.013

来源: Elsevier

【 摘 要 】

Recently, we showed that rivastigmine decreased amyloid-beta (A beta) brain load in aged rats by enhancing its clearance across the blood-brain barrier (BBB) via upregulation of P-glycoprotein (P-gp) and low-density lipoprotein receptor-related protein 1 (LRP1). Here, we extend our previous work to clarify P-gp role in mediating rivastigmine effect on A beta brain levels and neuroprotection in a mouse model of Alzheimer's disease (AD) that expresses different levels of P-gp. APPSWE mice were bred with mdr1a/b knockout mice to produce littermates that were divided into three groups; APP(+)/mdr1(+/+), APP(+)/mdr1(+/-) and APP(+)/mdr1(-/-). Animals received rivastigmine treatment (0.3 mg/kg/day) or vehicle for 8 weeks using Alzet osmotic mini-pumps. ELISA analysis of brain homogenates for A beta showed rivastigmine treatment to significantly decrease A beta brain load in APP(+)/mdr1(-/-) by 25% and in APP(+)/mdr1+(/-) mice by 21% compared to their vehicle treated littermates, but not in APP(+)/mdr1(-/-) mice. In addition, rivastigmine reduced GFAP immunostaining of astrocytes by 50% and IL-1 beta brain level by 43% in APP(+)/mdr1(+/+) mice, however its effect was less pronounced in P-gp knockout mice. Moreover, rivastigmine demonstrated a P-gp expression dependent neuroprotective effect that was highest in APP(+)/mdr1(+/+) > APP(+)/mdr1(+/-)>APP(+)/mdr1(-/-) as determined by expression of synaptic markers PSD-95 and SNAP-25 using Western blot analysis. Collectively, our results suggest that P-gp plays important role in mediating rivastigmine non-cholinergic beneficial effects, including A beta brain load reduction, neuroprotective and anti-inflammatory effects in the AD mouse models. (C) 2016 Elsevier B.V. All rights reserved.

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