Administration of amyloid-β oligomer to the buccal ganglia may reduce food intake and cholinergic synaptic responses within the feeding neural circuit in Aplysia kurodai
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Nagahama, Tatsumi
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Toho Univ, Fac Pharmaceut Sci, Dept Biophys, Funabashi 2748510, Japan
Teikyo Heisei Univ, Fac Hlth & Med Sci, Tokyo 1708445, JapanToho Univ, Fac Pharmaceut Sci, Dept Biophys, Funabashi 2748510, Japan
Nagahama, Tatsumi
[1
,2
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Nakajima, Hiroshi
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Toho Univ, Fac Pharmaceut Sci, Dept Biophys, Funabashi 2748510, JapanToho Univ, Fac Pharmaceut Sci, Dept Biophys, Funabashi 2748510, Japan
Nakajima, Hiroshi
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]
Wakuta, Mizuki
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Toho Univ, Fac Pharmaceut Sci, Dept Biophys, Funabashi 2748510, JapanToho Univ, Fac Pharmaceut Sci, Dept Biophys, Funabashi 2748510, Japan
Wakuta, Mizuki
[1
]
Kasahara, Yuse
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Toho Univ, Fac Pharmaceut Sci, Dept Biophys, Funabashi 2748510, JapanToho Univ, Fac Pharmaceut Sci, Dept Biophys, Funabashi 2748510, Japan
Kasahara, Yuse
[1
]
Narita, Kouki
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Toho Univ, Fac Pharmaceut Sci, Dept Biophys, Funabashi 2748510, JapanToho Univ, Fac Pharmaceut Sci, Dept Biophys, Funabashi 2748510, Japan
Narita, Kouki
[1
]
Nagahama, Setsuko
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Teikyo Heisei Univ, Fac Hlth & Med Sci, Tokyo 1708445, JapanToho Univ, Fac Pharmaceut Sci, Dept Biophys, Funabashi 2748510, Japan
Nagahama, Setsuko
[2
]
机构:
[1] Toho Univ, Fac Pharmaceut Sci, Dept Biophys, Funabashi 2748510, Japan
[2] Teikyo Heisei Univ, Fac Hlth & Med Sci, Tokyo 1708445, Japan
Anorexia is a behavioral change caused by functional brain disorders in patients with Alzheimer's disease (AD). Amyloid-beta (1-42) oligomers (o-A beta) are possible causative agents of AD that impair signaling via synaptic dysfunction. In this study, we used Aplysia kurodai to study functional disorders of the brain through o-A beta. Administration of o-A beta to the buccal ganglia (feeding brain for oral movements) by surgical treatment signifi-cantly reduced food intake for at least five days. Furthermore, we explored the effects of o-A beta on the synaptic function in the feeding neural circuit, focusing on a specific inhibitory synaptic response in jaw-closing motor neurons produced by cholinergic buccal multi-action neurons because we recently found that this cholinergic response decreases with aging, which is consistent with the cholinergic hypothesis for aging. Administration of o-A beta to the buccal ganglia significantly reduced the synaptic response within minutes, whereas administration of amyloid-beta (1-42) monomers did not. These results suggest that o-A beta may impair the cholinergic synapses, even in Aplysia, which is consistent with the cholinergic hypothesis for AD.