TY - JOUR
T1 - Behavioral deficits and cholinergic pathway abnormalities in male Sanfilippo B mice
AU - Kan, Shih hsin
AU - Le, Steven Q.
AU - Bui, Quang D.
AU - Benedict, Braeden
AU - Cushman, Jesse
AU - Sands, Mark S.
AU - Dickson, Patricia I.
N1 - Publisher Copyright:
© 2016 Elsevier B.V.
PY - 2016/10/1
Y1 - 2016/10/1
N2 - Sanfilippo B syndrome is a progressive neurological disorder caused by inability to catabolize heparan sulfate glycosaminoglycans. We studied neurobehavior in male Sanfilippo B mice and heterozygous littermate controls from 16 to 20 weeks of age. Affected mice showed reduced anxiety, with a decrease in the number of stretch-attend postures during the elevated plus maze (p = 0.001) and an increased tendency to linger in the center of an open field (p = 0.032). Water maze testing showed impaired spatial learning, with reduced preference for the target quadrant (p = 0.01). In radial arm maze testing, affected mice failed to achieve above-chance performance in a win-shift working memory task (t-test relative to 50% chance: p = 0.289), relative to controls (p = 0.037). We found a 12.4% reduction in mean acetylcholinesterase activity (p < 0.001) and no difference in choline acetyltransferase activity or acetylcholine in whole brain of affected male animals compared to controls. Cholinergic pathways are affected in adult-onset dementias, including Alzheimer disease. Our results suggest that male Sanfilippo B mice display neurobehavioral deficits at a relatively early age, and that as in adult dementias, they may display deficits in cholinergic pathways.
AB - Sanfilippo B syndrome is a progressive neurological disorder caused by inability to catabolize heparan sulfate glycosaminoglycans. We studied neurobehavior in male Sanfilippo B mice and heterozygous littermate controls from 16 to 20 weeks of age. Affected mice showed reduced anxiety, with a decrease in the number of stretch-attend postures during the elevated plus maze (p = 0.001) and an increased tendency to linger in the center of an open field (p = 0.032). Water maze testing showed impaired spatial learning, with reduced preference for the target quadrant (p = 0.01). In radial arm maze testing, affected mice failed to achieve above-chance performance in a win-shift working memory task (t-test relative to 50% chance: p = 0.289), relative to controls (p = 0.037). We found a 12.4% reduction in mean acetylcholinesterase activity (p < 0.001) and no difference in choline acetyltransferase activity or acetylcholine in whole brain of affected male animals compared to controls. Cholinergic pathways are affected in adult-onset dementias, including Alzheimer disease. Our results suggest that male Sanfilippo B mice display neurobehavioral deficits at a relatively early age, and that as in adult dementias, they may display deficits in cholinergic pathways.
KW - Acetylcholinesterase
KW - Glycosaminoglycan
KW - Inborn error of metabolism
KW - Lysosomal
KW - Mucopolysaccharidosis
KW - Neurodegeneration
UR - http://www.scopus.com/inward/record.url?scp=84976557400&partnerID=8YFLogxK
U2 - 10.1016/j.bbr.2016.06.023
DO - 10.1016/j.bbr.2016.06.023
M3 - Article
C2 - 27340089
AN - SCOPUS:84976557400
SN - 0166-4328
VL - 312
SP - 265
EP - 271
JO - Behavioural Brain Research
JF - Behavioural Brain Research
ER -