Ca(v)3 T-Type Voltage-Gated Ca(2+) Channels and the Amyloidogenic Environment: Pathophysiology and Implications on Pharmacotherapy and Pharmacovigilance.

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Papazoglou A, Arshaad MI, Henseler C, Daubner J, Broich K, Hescheler J, Ehninger D, Haenisch B, Weiergraber M

Ca(v)3 T-Type Voltage-Gated Ca(2+) Channels and the Amyloidogenic Environment: Pathophysiology and Implications on Pharmacotherapy and Pharmacovigilance.

Int J Mol Sci. 2022 Mar 22;23(7):3457. doi: 10.3390/ijms23073457.

PubMed ID
35408817 [ View in PubMed
]
Abstract

Voltage-gated Ca(2+) channels (VGCCs) were reported to play a crucial role in neurotransmitter release, dendritic resonance phenomena and integration, and the regulation of gene expression. In the septohippocampal system, high- and low-voltage-activated (HVA, LVA) Ca(2+) channels were shown to be involved in theta genesis, learning, and memory processes. In particular, HVA Ca(v)2.3 R-type and LVA Ca(v)3 T-type Ca(2+) channels are expressed in the medial septum-diagonal band of Broca (MS-DBB), hippocampal interneurons, and pyramidal cells, and ablation of both channels was proven to severely modulate theta activity. Importantly, Ca(v)3 Ca(2+) channels contribute to rebound burst firing in septal interneurons. Consequently, functional impairment of T-type Ca(2+) channels, e.g., in null mutant mouse models, caused tonic disinhibition of the septohippocampal pathway and subsequent enhancement of hippocampal theta activity. In addition, impairment of GABA A/B receptor transcription, trafficking, and membrane translocation was observed within the septohippocampal system. Given the recent findings that amyloid precursor protein (APP) forms complexes with GABA B receptors (GBRs), it is hypothesized that T-type Ca(2+) current reduction, decrease in GABA receptors, and APP destabilization generate complex functional interdependence that can constitute a sophisticated proamyloidogenic environment, which could be of potential relevance in the etiopathogenesis of Alzheimer's disease (AD). The age-related downregulation of T-type Ca(2+) channels in humans goes together with increased Abeta levels that could further inhibit T-type channels and aggravate the proamyloidogenic environment. The mechanistic model presented here sheds new light on recent reports about the potential risks of T-type Ca(2+) channel blockers (CCBs) in dementia, as observed upon antiepileptic drug application in the elderly.

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