| Literature DB >> 31997405 |
Sarah C Hopp1,2.
Abstract
Calcium (Ca2+ ) is a ubiquitous mediator of a multitude of cellular functions in the central nervous system (CNS). Intracellular Ca2+ is tightly regulated by cells, including entry via plasma membrane Ca2+ permeable channels. Of specific interest for this review are L-type voltage-dependent Ca2+ channels (L-VDCCs), due to their pleiotropic role in several CNS disorders. Currently, there are numerous approved drugs that target L-VDCCs, including dihydropyridines. These drugs are safe and effective for the treatment of humans with cardiovascular disease and may also confer neuroprotection. Here, we review the potential of L-VDCCs as a target for the treatment of CNS disorders with a focus on microglia L-VDCCs. Microglia, the resident immune cells of the brain, have attracted recent attention for their emerging inflammatory role in several CNS diseases. Intracellular Ca2+ regulates microglia transition from a resting quiescent state to an "activated" immune-effector state and is thus a valuable target for manipulation of microglia phenotype. We will review the literature on L-VDCC expression and function in the CNS and on microglia in vitro and in vivo and explore the therapeutic landscape of L-VDCC-targeting agents at present and future challenges in the context of Alzheimer's disease, Parkinson's disease, Huntington's disease, neuropsychiatric diseases, and other CNS disorders.Entities:
Keywords: Alzheimer's disease; CACNA1C; CACNA1D; Cav1.2; Cav1.3; Huntington's disease; L-type voltage-dependent calcium channels; Parkinson's disease; aging; bipolar disorder; calcium; depression; microglia; neuroinflammation; neuropsychiatric diseases; schizophrenia
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Year: 2020 PMID: 31997405 PMCID: PMC9394523 DOI: 10.1002/jnr.24585
Source DB: PubMed Journal: J Neurosci Res ISSN: 0360-4012 Impact factor: 4.433