TY - JOUR

T1 - Small molecule β-amyloid inhibitors that stabilize protofibrillar structures in vitro improve cognition and pathology in a mouse model of Alzheimer's disease

AU - Hawkes, Cheryl A.

AU - Deng, Le Hua

AU - Shaw, James E.

AU - Nitz, Mark

AU - McLaurin, Joanne

PY - 2010/1/1

Y1 - 2010/1/1

N2 - β-Amyloid (Aβ) peptides are thought to play a major role in the pathogenesis of Alzheimer's disease. Compounds that disrupt the kinetic pathways of Aβ aggregation may be useful in elucidating the role of oligomeric, protofibrillar and fibrillar Aβ in the etiology of the disease. We have previously reported that scyllo-inositol inhibits Aβ42 fibril formation but the mechanism(s) by which this occurs has not been investigated in detail. Using a series of scyllo-inositol derivatives in which one or two hydroxyl groups were replaced with hydrogen, chlorine or methoxy substituents, we examined the role of hydrogen bonding and hydrophobicity in the structure-function relationship of scyllo-inositol-Aβ binding. We report here that all scyllo-inositol derivatives demonstrated reduced effectiveness in preventing Aβ42 fibrillization compared with scyllo-inositol, suggesting that scyllo-inositol interacts with Aβ42 via key hydrogen bonds that are formed by all hydroxyl groups. Increasing the hydrophobicity of scyllo-inositol by the addition of two methoxy groups (1,4-di-O-methyl-scyllo-inositol) produced a derivative that stabilized Aβ42 protofibrils in vitro. Prophylactic administration of 1,4-di-O-methyl-scyllo-inositol to TgCRND8 mice attenuated spatial memory impairments and significantly decreased cerebral amyloid pathology. These results suggest that Aβ aggregation can be targeted at multiple points along the kinetic pathway for the improvement of Alzheimer's disease-like pathology.

AB - β-Amyloid (Aβ) peptides are thought to play a major role in the pathogenesis of Alzheimer's disease. Compounds that disrupt the kinetic pathways of Aβ aggregation may be useful in elucidating the role of oligomeric, protofibrillar and fibrillar Aβ in the etiology of the disease. We have previously reported that scyllo-inositol inhibits Aβ42 fibril formation but the mechanism(s) by which this occurs has not been investigated in detail. Using a series of scyllo-inositol derivatives in which one or two hydroxyl groups were replaced with hydrogen, chlorine or methoxy substituents, we examined the role of hydrogen bonding and hydrophobicity in the structure-function relationship of scyllo-inositol-Aβ binding. We report here that all scyllo-inositol derivatives demonstrated reduced effectiveness in preventing Aβ42 fibrillization compared with scyllo-inositol, suggesting that scyllo-inositol interacts with Aβ42 via key hydrogen bonds that are formed by all hydroxyl groups. Increasing the hydrophobicity of scyllo-inositol by the addition of two methoxy groups (1,4-di-O-methyl-scyllo-inositol) produced a derivative that stabilized Aβ42 protofibrils in vitro. Prophylactic administration of 1,4-di-O-methyl-scyllo-inositol to TgCRND8 mice attenuated spatial memory impairments and significantly decreased cerebral amyloid pathology. These results suggest that Aβ aggregation can be targeted at multiple points along the kinetic pathway for the improvement of Alzheimer's disease-like pathology.

KW - Hydrogen bonding

KW - Hydrophobicity

KW - Morris water maze

KW - Scyllo-inositol

KW - TgCRND8 mice

U2 - 10.1111/j.1460-9568.2009.07052.x

DO - 10.1111/j.1460-9568.2009.07052.x

M3 - Journal article

C2 - 20074226

AN - SCOPUS:74549169940

VL - 31

SP - 203

EP - 213

JO - European Journal of Neuroscience

JF - European Journal of Neuroscience

SN - 0953-816X

IS - 2

ER -