Hyperpolarization-activated cyclic nucleotide gated channels: a potential molecular link between epileptic seizures and A[beta] generation in Alzheimer's disease

• Published in: Molecular neurodegeneration Vol. 7; no. 1; p. 50
• Main Authors: Saito, Yuhki, Inoue, Tsuyoshi, Zhu, Gang, Kimura, Naoki, Okada, Motohiro, Nishimura, Masaki, Kimura, Nobuyuki, Murayama, Shigeo, Kaneko, Sunao, Shigemoto, Ryuichi, Imoto, Keiji, Suzuki, Toshiharu
• Format: Journal Article
• Language: English
• Published: London BioMed Central Ltd 03.10.2012; BioMed Central
• Subjects: Advertising executives; Aging; Alzheimer's disease; Amyloid precursor protein; Brain; Cyclic nucleotides; Cynomolgus; Epilepsy; Excitability; ion channels (cyclic nucleotide-gated); Macaca fascicularis; Neurodegenerative diseases; Neurons; Primates; Proteins; Risk factors; Rodents; Science; Seizures; Seizures (Medicine); Temporal lobe; Japan
• ISSN: 1750-1326; 1750-1326
• DOI: 10.1186/1750-1326-7-50

Background One of the best-characterized causative factors of Alzheimer's disease (AD) is the generation of amyloid-[beta] peptide (A[beta]). AD subjects are at high risk of epileptic seizures accompanied by aberrant neuronal excitability, which in itself enhances A[beta] generation. However, the molecular linkage between epileptic seizures and A[beta] generation in AD remains unclear. Results X11 and X11-like (X11L) gene knockout mice suffered from epileptic seizures, along with a malfunction of hyperpolarization-activated cyclic nucleotide gated (HCN) channels. Genetic ablation of HCN1 in mice and HCN1 channel blockage in cultured Neuro2a (N2a) cells enhanced A[beta] generation. Interestingly, HCN1 levels dramatically decreased in the temporal lobe of cynomolgus monkeys (Macaca fascicularis) during aging and were significantly diminished in the temporal lobe of sporadic AD patients. Conclusion Because HCN1 associates with amyloid-[beta] precursor protein (APP) and X11/X11L in the brain, genetic deficiency of X11/X11L may induce aberrant HCN1 distribution along with epilepsy. Moreover, the reduction in HCN1 levels in aged primates may contribute to augmented A[beta] generation. Taken together, HCN1 is proposed to play an important role in the molecular linkage between epileptic seizures and A[beta] generation, and in the aggravation of sporadic AD.