TABLE 3.
Experimental approaches for increasing ABCB1 expression.
| Experimental approach | References |
| β-catenin signalinga | Lim et al., 2008 |
| Colupulone analogsb | Bharate et al., 2015 |
| Exosomesc | Pan et al., 2020 |
| Ketone bodies | Versele et al., 2020 |
| NMDA receptor agonists | Bauer et al., 2008 |
| Nocodazoled | Ding et al., 2021 |
| Oleocanthal | Abuznait et al., 2013 |
| Pirenzepinee | Paganetti et al., 2014 |
| Prevention of ABCB1 ubiquitination | Hartz et al., 2018 |
| PXR agonistsf | Hartz et al., 2010; Wolf et al., 2012; Lemmen et al., 2013; Zoufal et al., 2020b |
| TGF-β1 | Baello et al., 2014 |
| Vitamin D receptor activation | Durk et al., 2012 |
aβ-catenin signaling was activated by inhibitors of glycogen synthase kinase-3β in primary rat brain endothelial cells and immortalized human brain endothelial cells (Lim et al., 2008).
bColupulone analogs are PXR activators (Bharate et al., 2015).
cABCB1-expressing human brain microvascular endothelial cell-derived exosomes were transplanted into a transgenic mouse model of AD by Pan et al. (2020).
dNocodazole is a microtubule inhibitor which prevented ABCB1 internalization and subsequent degradation by the ubiquitin–proteasome system in Tg2576 mice (Ding et al., 2021).
eAdministration of Pirenzepine, a selective M1 receptor antagonist, lowered cerebral Aβ in AβPPPS1, hAβPPSL, and AβPP/PS1 transgenic mice (Paganetti et al., 2014).
fPXR agonists include hyperforin, an active ingredient in St. John’s wort (Lemmen et al., 2013). Zoufal et al. (2020b) administered the rodent PXR activator 5-pregnen-3β-ol-20-one-16α-carbonitrile to APP/PS1-21 mice to activate cerebral ABCB1. ABCB1, ATP-binding cassette sub-family B member 1; NMDA, N-methyl-D-aspartate; PXR, pregnane X receptor; TGF-β1, tumor growth factor β1.