Effect of mouse strain as a background for Alzheimer’s disease models on the clearance of amyloid-β

Abstract

Novel animal models of Alzheimer’s disease (AD) are relentlessly being developed and existing ones are being fine-tuned; however, these models face multiple challenges associated with the complexity of the disease where most of these models do not reproduce the full phenotypical disease spectrum. Moreover, different AD models express different phenotypes that could affect their validity to recapitulate disease pathogenesis and/or response to a drug. One of the most important and understudied differences between AD models is differences in the phenotypic characteristics of the background species. Here, we used the brain clearance index (BCI) method to investigate the effect of strain differences on the clearance of amyloid β (Aβ) from the brains of four mouse strains. These mouse strains, namely C57BL/6, FVB/N, BALB/c and SJL/J, are widely used as a background for the development of AD mouse models. Findings showed that while Aβ clearance across the blood-brain barrier (BBB) was comparable between the 4 strains, levels of LRP1, an Aβ clearance protein, was significantly lower in SJL/J mice compared to other mouse strains. Furthermore, these mouse strains showed a significantly different response to rifampicin treatment with regard to Aβ clearance and effect on brain level of its clearance-related proteins. Our results provide for the first time an evidence for strain differences that could affect ability of AD mouse models to recapitulate response to a drug, and opens a new research avenue that requires further investigation to successfully develop mouse models that could simulate clinically important phenotypic characteristics of AD.

Introduction

Alzheimer’s disease (AD) is the most common cause of progressively irreversible dementia among elderly that is characterized by complex neuropathological lesions. Extensive research has identified amyloid-β (Aβ) and tau-related neuropathologies in the brains of AD patients as the main underlying causes of neurodegeneration, cognitive decline and memory loss [1, 2]. Aβ peptides are 39–43 amino acid peptides derived from proteolytic hydrolysis of amyloid-β protein precursor (AβPP) in neurons and other cells [3, 4]. The level of Aβ in the brain is controlled by its production and clearance; chronic imbalance between these two processes may result in accumulation of Aβ in the brain [5]. In very rare cases of AD (familial AD), Aβ accumulation is related to its overproduction [4]. However, mounting evidence suggests that Aβ accumulation in the brain of late-onset “sporadic” AD patients and in some cases of familial AD is related to its impaired clearance from brain [6]. Brain clearance of Aβ takes place by three major pathways, transport across blood-brain barrier (BBB), degradation in the brain tissue, and bulk flow of cerebrospinal fluid (CSF), however, clearance across the BBB is considered to be the most efficient route for removing Aβ from the brain [7].

Mouse is a widely used animal model to study AD pathology and to develop therapeutic approaches to fight AD. Over the last decades, several transgenic mouse models were developed to express different pathological alterations of AD including amyloid pathology, cerebral amyloid angiopathy, tau pathologies, synaptic loss, dystrophic neurites, reactive gliosis, as well as impairments in synaptic plasticity and learning and memory [8]. Such mouse models exhibit above characteristics to varying extents, and many available studies independently showed a significant difference in AD pathology between different mouse models [9–11]. Although several AD models are made congenic on inbred strains, usually C57BL/6J, to stabilize the genetic background, most of transgenic mouse models used to model AD are from different strains [12]. Therefore, strain variability could make the expression of pathological AD phenotype, or the relevance of potential pathogenic mechanisms, difficult to ascertain. Moreover, strain variability could explain differences in drug responses observed between different studies.

Aβ is considered an efficient target for the development of therapeutic agents that enhance its clearance and thus slow AD progression and related pathologies [5]. Many clinically used drugs and herbal medicines have been investigated for their role in decreasing Aβ accumulation [13]. For example, rifampicin, a widely used antibiotic, was able to attenuate the rate of cognitive decline in mild to moderate AD patients after 3-month course of 300 mg/day dose [14]. Moreover, we previously reported rifampicin potential to enhance Aβ clearance across the BBB by increasing the expression and activity of Aβ transport proteins namely low density lipoprotein receptor related protein-1 (LRP1) and P-glycoprotein (P-gp) [15].

In this study we investigated differences in Aβ clearance between wild-type mouse strains that have been used as background inbred for the development of transgenic AD mouse models. Moreover, we assessed the clearance of Aβ from the brain of these mouse strains after treatment with rifampicin.

Materials and Methods

Animals

C57BL/6, FVB/N, BALB/c and SJL/J wild-type male mice were purchased from Harlan Laboratories (Houston, TX). The mice were 7–8 weeks old with an average body weight of 20 g. Mice were kept under standard environmental conditions (22°C, 35% relative humidity, 12 h dark/light cycle) with free access to tap water and standard rodent food. After shipping, mice were allowed to adapt to the new environment for one week before initiating the experiments. All animal experiments were approved by the Institutional Animal Care and Use Committee of the University of Louisiana at Monroe and all surgical and treatment procedures were consistent with the IACUC policies and procedures.

Animals’ treatment with rifampicin

Animals of each strain were divided into two treatment groups; control and rifampicin groups. Each group contained at least four animals. Drug administration was started at 8–9 weeks of age and continued for 3 weeks in all experiments. Mice of control groups received intraperitoneal normal saline once daily. Mice of rifampicin groups received intraperitoneal rifampicin at dose of 20 mg/kg once daily. Treatments were given intraperitoneal to avoid variability associated with oral administration when given with food where the administered dose will be influenced by the amount of food ingested by each mouse, as well as rifampicin stability.

Brain clearance of ¹²⁵I-Aβ₄₀

At the end of treatment period, mice were prepared for brain clearance index study (BCI%) to assess the clearance of ¹²⁵I-Aβ₄₀ 24 h after the last dose of rifampicin [15]. Aβ₄₀ and Aβ₄₂ share similar clearance pathway [16, 17], however Aβ₄₀ was used in the BCI% experiments because unlike Aβ₄₂ it has lower tendency to aggregate and for practicality reasons as it has much faster clearance rate than Aβ₄₂ [18, 19]. In-vivo ¹²⁵IAβ₄₀ clearance was investigated using the BCI method as described previously [7]. In brief, a stainless steel guide cannula was implanted stereotaxically into the right caudate nucleus of mouse brain that was anesthetized with intraperitoneal xylazine and ketamine (20 and 125 mg/kg, respectively; HenrySchein, NY). After 12 h recovery period, animals were re-anesthetized and tracer fluid (0.5 ml) containing ¹²⁵I-Aβ₄₀ (30 nM, PerkinElmer, MA) and ¹⁴C-inulin (0.02 mCi, American Radiolabeled Chemicals, MO) prepared in extracellular fluid buffer (ECF) was administered. Thirty minutes’ post ¹²⁵I-Aβ₄₀ injection, brain tissues were rapidly collected for ¹²⁵I-Aβ₄₀ analysis. Calculations of ¹²⁵I-Aβ₄₀ clearance were performed as described previously [7]. Using the trichloroacetic acid (TCA) precipitation assay, intact (precipitate) and degraded (supernatant) ¹²⁵I-Aβ₄₀ were determined in brain tissue using a Wallac 1470 Wizard Gamma Counter (PerkinElmer, MA). ¹⁴C-Inulin in precipitate and supernatant were also determined using a Wallac 1414 WinSpectral Counter (PerkinElmer, MA). The brain clearance index of ¹²⁵I-Aβ₄₀ from the brain, (BCI_Total(%)), i.e. clearance across the BBB and brain degradation was calculated according to Equation 1. Clearance of ¹²⁵I-Aβ₄₀ across the BBB (BCI_BBB(%)) and brain degradation (BCI_Degradation(%)) were defined by Equations 2 and 3, respectively.

$${\mathit{BCI}}_{\mathit{Total}}(\%)=100-\left[\frac{\left(\frac{\text{Amount}\text{of}\text{intact}{}^{125}\mathrm{I}-\mathrm{A}{\beta }_{40}\text{in}\text{the}\text{brain}}{\text{Amount}\text{of}{}^{14}\mathrm{C}-\text{inulin}\text{in}\text{the}\text{brain}}\right)}{\left(\frac{\text{Amount}\text{of}\text{intact}{}^{125}\mathrm{I}-\mathrm{A}{\beta }_{40}\text{injected}\text{into}\text{the}\text{brain}}{\text{Amount}\text{of}{}^{14}\mathrm{C}-\text{inulin}\text{injected}}\right)}\times 100\right]$$ (Eq. 1)

$${\mathit{BCI}}_{\mathit{BBB}}(\%)=100-\left[\frac{\left(\frac{\text{Amount}\text{of}\text{total}{}^{125}\mathrm{I}-\mathrm{A}{\beta }_{40}\text{in}\text{the}\text{brain}(\text{intact}\text{and}\text{degraded})}{\text{Amount}\text{of}{}^{14}\mathrm{C}-\text{inulin}\text{in}\text{the}\text{brain}}\right)}{\left(\frac{\text{Amount}\text{of}\text{intact}{}^{125}\mathrm{I}-\mathrm{A}{\beta }_{40}\text{injected}\text{into}\text{the}\text{brain}}{\text{Amount}\text{of}{}^{14}\mathrm{C}-\text{inulin}\text{injected}}\right)}\times 100\right]$$ (Eq. 2)

$${\mathit{BCI}}_{\mathit{Degradation}}(\mathit{\%})={\mathit{BCI}}_{\mathit{Total}}(\mathit{\%})-{\mathit{BCI}}_{\mathit{BBB}}(\mathit{\%})$$ (Eq. 3)

Brain microvessels isolation

Brain microvessels were isolated as described previously [15]. Briefly, collected brains were homogenized in ice-cold DPBS with Dounce homogenizer. One volume Ficoll (30%) was added to the brain homogenate to a final concentration of 15%; the mixture was mixed and then centrifuged (5000 rpm for 10 min, 4°C). The resulting pellets were suspended in ice-cold DPBS containing 1% bovine serum albumin (BSA) and passed over a glass beads column. Microvessels adhering to the glass beads were collected by gentle agitation in 1% BSA in DPBS. Isolated microvessels were used for Western blotting studies.

Western blot analysis

Protein extracts were prepared from brain microvessels or brain tissue using RIPA buffer containing complete mammalian protease inhibitor mixture followed by centrifugation at 14,000 rpm for 1 h at 4°C. The supernatant was collected as the protein extract and stored at −80°C to the time of the experiment. Protein samples, 25 μg, were resolved on 7.5% SDS-polyacrylamide gels and transferred onto a nitrocellulose membrane. Membranes were blocked with 2% BSA and incubated overnight with monoclonal antibodies for P-gp (C-219; Covance Research Products, MA), LRP1 (Calbiochem, NJ), insulin-degrading enzyme (IDE), neprilysin (NEP), GAPDH or actin (Santa Cruz Biotechnology, TX). For antigen detection, the membranes were washed and incubated with HRP-labeled secondary IgG anti-mouse antibody for P-gp and GAPDH, anti-rabbit antibody for LRP1 and NEP (Santa Cruz Biotechnology) and anti-goat antibody for actin and IDE (Santa Cruz Biotechnology). The bands were visualized using Pierce chemiluminescence detection kit (Thermo Scientific; Rockford, IL). Quantitative analysis of the immunoreactive bands was performed using Li-Core luminescent image analyzer (LI-COR Biotechnology Inc., Lincoln, NE) and band intensity was measured by densitometric analysis. Three independent Western blotting experiments were carried out for each treatment group.

Measurement of rifampicin concentrations in plasma and brain homogenate samples

Rifampicin levels in plasma and brain homogenate were quantified using LC/MS/MS system. Mice plasma and brain homogenate were mixed with methanol to precipitate proteins in a ratio of 1:2 (v/v). The samples were vortexed for 30 seconds and centrifuged at 14,000 rpm for 10 min at 4°C. The clear supernatant was directly injected into the LC/MS/MS system. Chromatographic separation of rifampicin was performed on Kinetex XB-C18 reversed phase column (100 × 4.6 mm i.d., 2.6 μm; Phenomenex, CA) with an ODS guard column (4 mm × 3 mm; Phenomenex) using Agilent 1100 series LC system (Agilent Technologies, CA) and 3200 QTRAP LC/MS/MS system (Applied Biosystems/MDS Sciex, Foster City, CA) at flow rate of 0.5 ml/min. The injection volume was 10 μl. The mobile phase used was methanol/ammonium acetate 10 mM, pH 6.8 (70:30, v/v). The analyte was detected using electrospray ionization interface operated in positive mode. Instrument control and data acquisition were carried out by the Analyst 1.4.1 software (Applied Biosystems). The analyte was detected and quantified by MS/MS in multiple-reaction monitoring (MRM) method. The peak signals of transition from the parent ion to its major fragment m/z 823.3→791 was measured.

Statistical analysis

Unless otherwise indicated, the data were expressed as mean ± SEM (n=4). The experimental results were statistically analyzed for significant difference using two-tailed Student’s t-test for 2 groups, and one-way analysis of variance (ANOVA) for more than two group analysis. Values of p<0.05 were considered statistically significant.

Results

¹²⁵IAβ₄₀ Brain clearance index and expression of Aβ clearance proteins in C57BL/6, BALB/c, FVB/N and SJL/J mice

Aβ clearance from the brains of selected four mouse strains have been measured using the BCI% method. BCI% method is a modified method from the brain efflux index (BEI%) technique that we have developed previously to calculate total Aβ clearance, i.e. clearance across the BBB and clearance by parenchymal degradation of Aβ [7]. Total clearance of ¹²⁵I-Aβ₄₀ from the brains of the 4 mouse strains was comparable with BCI_Total(%) of 57.2% ± 2.7%, 60.6% ± 1.9%, 59.7% ± 2.1% and 61.3 ± 1.7% (Fig. 1A) in C57BL/6, BALB/c, FVB/N and SJL/J, respectively. Similarly, BCI_BBB(%) and BCI_Degradation(%) were comparable among the strains with ~35% of Aβ was estimated to be cleared across the BBB and ~23% by brain degradation (Fig. 1B & C). On the other hand, western blot analyses of different Aβ clearance proteins in the mice brains showed similar levels of P-gp, NEP and IDE among all mouse strains, but significantly lower levels of LRP1 at the BBB of SJL/J mice. Densitometric analyses of western blot bands showed ~20% reduction in LRP1 levels in SJL/J mice compared to the other investigated strains (p = 0.026, Fig. 1C)

Figure 1. ¹²⁵I-Aβ₄₀ clearance from the brain of C57BL/6, BALB/c, FVB/N and SJL/J wild-type mice.

Total ¹²⁵I-Aβ₄₀ brain clearance (BCI_Total(%)) (A), BBB ¹²⁵I-Aβ₄₀ clearance (BCI_BBB(%)) (B) and clearance of ¹²⁵I-Aβ₄₀ by brain degradation (BCI_Degradation(%)) (C) from the brain of C57BL/6, BALB/c, FVB/N and SJL/J wild-type mice. (D) Representative western blot and densitometry analysis of P-gp, LRP1 and protein loading control (GAPDH) in the brain tissue of C57BL/6, BALB/c, FVB/N and SJL/J wild-type mice. (E) Representative western blot quantitative fold change for IDE, NEP and protein loading control (GAPDH) in the brain tissue of C57BL/6, BALB/c, FVB/N and SJL/J wild-type mice. The data are expressed as mean ± SEM of n = 4 mice; * p<0.05 and ns is not significant.

Effect of rifampicin treatment on Aβ clearance from the brains of C57BL/6, BALB/c, FVB/N and SJL/J mice

Next, the effect of rifampicin treatment on Aβ clearance was evaluated after three weeks’ treatment course of intraperitoneal rifampicin (20 mg/kg once daily). Aβ clearance experiments were performed 24 h after the last injection of rifampicin or vehicle. After 24 h from the last injection of rifampicin, plasma and brain homogenate concentrations of rifampicin were negligible (lower than the method limit of detection of 1 ng/ml) as determined by LC/MS/MS. This observation is important to exclude any inhibitory effect of rifampicin on Aβ transport proteins and thus Aβ clearance [15]. Thirty minutes post ¹²⁵I-Aβ₄₀ microinjection, the BCI_Total% values in C57BL/6, BALB/c and FVB/N and SJL/J mice were 82.4% ± 2.4%, 87.7% ± 1.1%, 77.9% ± 1.8% and 50.5 ± 2.5% respectively (Fig. 2A). These results indicate rifampicin increased Aβ-BCI_Total(%) by 18–27% in C57BL/6, BALB/c and FVB/N mice, while decreased by ~11% in SJL/J mice (Fig. 2A). The increase in total Aβ clearance in C57BL/6, BALB/c and FVB/N is specifically owed to the enhanced removal of Aβ across the BBB where rifampicin caused a significant increase in the BBB clearance of Aβ by 24%, 43%, and 33% from the brains of C57BL/6, BALB/c and FVB/N mice, respectively (Fig. 2B); while BBB clearance of Aβ did not change in SJL/J mice after rifampicin treatment (33.4 ± 2.9% and 31.3 ± 2.2% in rifampicin and control mice, respectively, Fig. 2B). Contrary to BBB Aβ clearance, brain degradation of Aβ measured as BCI_Degradation(%) was significantly decreased in BALB/c (18%), FVB/N (14%), and SJL/J (8%) after rifampicin treatment for three weeks (Fig. 2C, p<0.05). In C57BL/6 mice, however, rifampicin treatment did alter Aβ-BCI_Degradation(%) (22.8 ± 1.9% and 22.3 ± 0.8% in rifampicin and vehicle groups, respectively, Fig. 2C).

Figure 2. Effect of rifampicin treatment on ¹²⁵I-Aβ₄₀ clearance from the brain of C57BL/6, BALB/c, FVB/N and SJL/J wild-type mice.

Total ¹²⁵I-Aβ₄₀ brain clearance (BCI_Total(%)) (A), BBB ¹²⁵I-Aβ₄₀ clearance (BCI_BBB(%)) (B) and clearance of ¹²⁵I-Aβ₄₀ by brain degradation (BCI_Degradation(%)) (C) from the brain of normal saline and rifampicin treated mice. Significant enhancement in total and BBB clearance of ¹²⁵I-Aβ₄₀ from the brain was observed in all mouse strains after treatment with rifampicin except in SJL/J mice, where a significant reduction in ¹²⁵I-Aβ₄₀ clearance was observed after treatment with rifampicin. On the other hand, ¹²⁵I-Aβ₄₀ degradation was decreased significantly after treatment with rifampicin in all mouse strains except C57BL/6 mice. Data represent mean±SEM for n=4 mice; * p<0.05, ** p<0.01 and ns is not significant.

Effect of rifampicin on expression of brain Aβ clearance proteins

To explain the enhanced clearance of Aβ across the BBB, P-gp and LRP1 protein expressions were examined in mice brains’ capillaries. Consistent with the increased clearance of Aβ across the BBB, a significant increase in the expression of P-gp and LRP1 was observed with all mice species. Figure 3 shows a significant increase by 26, 20, 22 and 20% in P-gp expression; and 12, 15, 18 and 22% in LRP1 expression in the brains’ capillaries of C57BL/6, BALB/c, FVB/N and SJL/J mice (p<0.05), respectively (Fig. 3).

Figure 3. Rifampicin enhances P-gp and LRP1 expression in the brain microvessels of C57BL/6, BALB/c, FVB/N and SJL/J wild-type mice.

Western blot analysis showed significantly higher expression level of P-gp and LRP1 in brain microvessels of rifampicin treated mice compared to normal saline treated mice. (A) Representative western blot lanes for P-gp, LRP1 and protein loading control (GAPDH). (B) Quantitative fold increase in P-gp and (C) LRP1 expression in the brain microvessels of C57BL/6, BALB/c, FVB/N and SJL/J wild-type mice after normal saline or rifampicin treatment. The data are expressed as mean ± SEM of n = 3 independent experiments from n=4 mice; * p<0.05 and ** p<0.01.

On the other hand, rifampicin treatment increased the expression of brain Aβ-degrading enzymes NEP and IDE only in SJL/J mice, while other mouse strains did not show any change in the levels of these Aβ degrading enzymes (Fig. 4). In the brain of SJL/J mice, NEP and IDE expression increased by 20 ± 2.1% and 22 ± 1.5%, respectively (p < 0.05), after rifampicin treatment for three weeks. However, this increase in the expression of Aβ degrading enzymes did not enhance brain Aβ clearance in this mouse strain.

Figure 4. Effect of rifampicin on IDE and NEP expression in the brain tissue of C57BL/6, BALB/c, FVB/N and SJL/J wild-type mice.

Western blot analysis showed significantly higher expression of IDE and NEP only in the brain tissue of SJL/J mice after treatment with rifampicin. (A) Representative western blot lanes for IDE, NEP and protein loading control (GAPDH). (B) Quantitative fold change in IDE and (C) NEP expressions in the brain tissue of C57BL/6, BALB/c, FVB/N and SJL/J wild-type mice after normal saline or rifampicin treatment. The data are expressed as mean ± SEM of n = 3 independent experiments of n=4 mice; * p<0.05 and ns is not significant.

Discussion

Over the last two decades, several animal models have been developed to dissect the pathogenic mechanisms of AD [8, 11]. Most of the transgenic mice have been created in an attempt to generate models of human AD by overexpressing one or more mutations linked to familial AD. These mice successfully recapitulate many key aspects of AD [8]. Different background strains are being used to create transgenic mouse models. For example, PDAPP mice have been mostly studied on a highly mixed C57BL6/DBA/Swiss-Webster background. By contrast, Tg2576 mice are typically studied on a hybrid C57BL6/SJL background. Therefore, strain variability could make the expression of pathological Alzheimer’s phenotype, or the relevance of potential pathogenic mechanisms, difficult to ascertain [12]. Accordingly, in the current study we examined the effect of strain differences on one of AD pathological alterations, Aβ clearance across the BBB, and how this difference may affect a drug response in wild type mice.

To assess the effect of strain differences on Aβ clearance from the brain, we measured Aβ₄₀ brain clearance in four mouse strains, C57BL/6, BALB/c, FVB/N and SJL/J mice. These mouse strains were selected because most of transgenic mice that have been developed to model AD used one of these mouse strains as a background [12]. Our findings showed similar basal Aβ clearance between these mouse strains, with significant contribution of BBB to the total Aβ clearance among all strains, which is consistent with our previous findings [7]. However, although all strains showed similar ¹²⁵I-Aβ₄₀ clearance, analysis of proteins expression showed SJL/J mice to have lower level of LRP1, which suggests species differences in the expression, trafficking, or degradation of this protein at the BBB. Interestingly, available studies showed a positive direct correlation between LRP1 expression and vascular lipid disposition in atherosclerosis, this correlation is consistent with our findings of low LRP1 level in SJL/J mice which are known to be resistant for the development of atherosclerotic lesions [20, 21].

Given the difficulty of performing studies in AD patients to validate different therapeutic approaches, the development of animal models has been a high AD research priority. However, although several mouse models are now being used to test therapeutic approaches, it is yet to be confirmed whether the results from AD mouse models are reliable predictors of drug efficacy in humans. Therefore, understanding differences in drugs response between different mouse strains would be of great importance to create a reliable mouse model. In this study we evaluated the effect of strain differences on drug response using rifampicin as a model drug for its effect on ¹²⁵I-Aβ₄₀ clearance from the brain of the four mouse strains. The choice of rifampicin because it is clinically used drug and our previous studies showed potential for this drug to enhance Aβ clearance from the brain through upregulation of Aβ transport proteins expressed at the BBB [15]. Our findings showed a differential response to rifampicin on ¹²⁵I-Aβ₄₀ clearance. Following three weeks of rifampicin treatment, Aβ brain total clearance (BCI_Total) increased by ~20% in the mouse strains C57BL/6, BALB/c, and FVB/N, but significantly reduced in SJL/J mice (Fig. 2). This enhanced total brain clearance was correlated with increased clearance across the BBB in 3 of the strains except in SJL/J mice. The increase in Aβ brain clearance across the BBB in C57BL/6, BALB/c, and FVB/N strains could be explained, at least in part, by the upregulation of Aβ transport proteins LRP1 and P-gp. Recent findings from our laboratory demonstrated major contribution of LRP1 and P-gp to the clearance of Aβ across the BBB of C57BL/6 that when modulated with selective inhibitors, with or without treatment with rifampicin, significantly reduced the clearance of Aβ [7]. However, while rifampicin increased expression of these proteins at the BBB of SJL/J mice, this increase was not able to enhance BBB or total clearance of Aβ, suggesting involvement of alternative or additional protein(s)/pathway(s) that significantly contribute to Aβ brain clearance to compensate for lower levels of LRP1 in SJL/J mice, which could be suppressed by rifampicin treatment. Further investigations are required to confirm and identify these proteins.

Degradation pattern and magnitude were also different. Rifampicin treatment significantly reduced Aβ degradation in BALB/c, FVB/N and SJL/J strains with highest reduction in BALB/c strain, but not in C57BL/6. Yet, this reduced degradation in BALB/c and FVB/N mice did not alter the total clearance which could be explained, at least in part, by the significant increase in Aβ clearance across the BBB. This result further signifies the important role of the BBB in the clearance of Aβ compared to other clearance mechanisms including degradation.

Collectively, findings from this study suggest strain differences in Aβ clearance, which were further emphasized with rifampicin treatment. SJL/J strain showed lower levels of Aβ transport protein LRP1, and different response in Aβ clearance to rifampicin treatment. Indeed, further studies on the effect of strain type of the background animal that is being used in the development of AD mouse model are required to achieve the goal of producing mouse models that could recapitulate clinically important phenotypic characteristics of AD.

Abbreviations

AD

Alzheimer’s disease

Aβ

amyloid-β

APP

amyloid-β precursor protein

BBB

blood-brain barrier

IDE

insulin degrading enzyme

LC/MS/MS

liquid Chromatography/tandem mass spectrometry

LRP1

low density lipoprotein receptor-related protein-1

NEP

neprilysin

NFT

neurofibrillary tangles

P-gp

P-glycoprotein

RAGE

receptor for advanced glycation end products

RAP

receptor associated protein

TCA

trichloroacetic acid