TY - JOUR
T1 - Investigation of nebivolol as a novel therapeutic agent for the treatment of Alzheimer's disease
AU - Wang, Jun
AU - Wright, Harold M.
AU - Vempati, Prashant
AU - Li, Henry
AU - Wangsa, Julie
AU - Dzhuan, Anastasiya
AU - Habbu, Karishma
AU - Knable, Lindsay A.
AU - Ho, Lap
AU - Pasinetti, Giulio M.
PY - 2013
Y1 - 2013
N2 - Nebivolol is a selective β1 adrenergic receptor antagonist with nitric oxide-mediated vasodilatory properties utilized in the treatment of hypertension. Previously, nebivolol was shown to modulate amyloid-β protein precursor processing in vitro. In this study, we investigated the in vivo effects of nebivolol on the modulation of amyloid neuropathology in the Tg2576 mouse model of Alzheimer's disease (AD). We found that nebivolol is brain bioavailable and can be readily detected in the brain following three weeks of treatment at a dose of 1 mg/kg/day. Moreover, this treatment regime resulted in a significant reduction of amyloid-β neuropathology in the brain, and this reduction was inversely correlated with plasma levels of amyloid-β. Chronic nebivolol treatment of Tg2576 mice with established amyloid neuropathology and cognitive impairments significantly reduced brain amyloid content but failed to improve cognitive function. Our study demonstrates that nebivolol is highly tolerable and safe and can significantly reduce amyloid neuropathology in the brain, which could be one of the most important parameters for primary prevention of AD. Our studies support the continued investigation of nebivolol for the treatment of AD at very early stages of the disease.
AB - Nebivolol is a selective β1 adrenergic receptor antagonist with nitric oxide-mediated vasodilatory properties utilized in the treatment of hypertension. Previously, nebivolol was shown to modulate amyloid-β protein precursor processing in vitro. In this study, we investigated the in vivo effects of nebivolol on the modulation of amyloid neuropathology in the Tg2576 mouse model of Alzheimer's disease (AD). We found that nebivolol is brain bioavailable and can be readily detected in the brain following three weeks of treatment at a dose of 1 mg/kg/day. Moreover, this treatment regime resulted in a significant reduction of amyloid-β neuropathology in the brain, and this reduction was inversely correlated with plasma levels of amyloid-β. Chronic nebivolol treatment of Tg2576 mice with established amyloid neuropathology and cognitive impairments significantly reduced brain amyloid content but failed to improve cognitive function. Our study demonstrates that nebivolol is highly tolerable and safe and can significantly reduce amyloid neuropathology in the brain, which could be one of the most important parameters for primary prevention of AD. Our studies support the continued investigation of nebivolol for the treatment of AD at very early stages of the disease.
KW - Adrenergic receptor blocker
KW - Alzheimer's disease
KW - brain bioavailability
KW - inflammatory response
KW - plaque
UR - http://www.scopus.com/inward/record.url?scp=84873686079&partnerID=8YFLogxK
U2 - 10.3233/JAD-2012-120904
DO - 10.3233/JAD-2012-120904
M3 - Article
C2 - 23128558
AN - SCOPUS:84873686079
SN - 1387-2877
VL - 33
SP - 1147
EP - 1156
JO - Journal of Alzheimer's Disease
JF - Journal of Alzheimer's Disease
IS - 4
ER -