Amyloid-β oligomers in the nucleus accumbens decrease motivation via insertion of calcium-permeable AMPA receptors
It is essential to identify the neuronal mechanisms of Alzheimer's Disease (AD)-associated neuropsychiatric symptoms, e.g., apathy, before improving the life quality of AD patients. Here, we focused on the nucleus accumbens (NAc), a critical brain region processing motivation, also known to dis...
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| Veröffentlicht in: | Molecular psychiatry Jg. 27; H. 4; S. 2146 - 2157 |
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| Format: | Journal Article |
| Sprache: | Englisch |
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01.04.2022
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| Abstract | It is essential to identify the neuronal mechanisms of Alzheimer's Disease (AD)-associated neuropsychiatric symptoms, e.g., apathy, before improving the life quality of AD patients. Here, we focused on the nucleus accumbens (NAc), a critical brain region processing motivation, also known to display AD-associated pathological changes in human cases. We found that the synaptic calcium permeable (CP)-AMPA receptors (AMPARs), which are normally absent in the NAc, can be revealed by acute exposure to Aβ oligomers (AβOs), and play a critical role in the emergence of synaptic loss and motivation deficits. Blockade of NAc CP-AMPARs can effectively prevent AβO-induced downsizing and pruning of spines and silencing of excitatory synaptic transmission. We conclude that AβO-triggered synaptic insertion of CP-AMPARs is a key mechanism mediating synaptic degeneration in AD, and preserving synaptic integrity may prevent or delay the onset of AD-associated psychiatric symptoms. |
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| AbstractList | It is essential to identify the neuronal mechanisms of Alzheimer’s Disease (AD)-associated neuropsychiatric symptoms, e.g., apathy, before improving the life quality of AD patients. Here, we focused on the nucleus accumbens (NAc), a critical brain region processing motivation, also known to display AD-associated pathological changes in human cases. We found that the synaptic calcium permeable (CP)-AMPA receptors (AMPARs), which are normally absent in the NAc, can be revealed by acute exposure to Aβ oligomers (AβOs), and play a critical role in the emergence of synaptic loss and motivation deficits. Blockade of NAc CP-AMPARs can effectively prevent AβO-induced downsizing and pruning of spines and silencing of excitatory synaptic transmission. We conclude that AβO-triggered synaptic insertion of CP-AMPARs is a key mechanism mediating synaptic degeneration in AD, and preserving synaptic integrity may prevent or delay the onset of AD-associated psychiatric symptoms. It is essential to identify the neuronal mechanisms of Alzheimer's Disease (AD)-associated neuropsychiatric symptoms, e.g., apathy, before improving the life quality of AD patients. Here, we focused on the nucleus accumbens (NAc), a critical brain region processing motivation, also known to display AD-associated pathological changes in human cases. We found that the synaptic calcium permeable (CP)-AMPA receptors (AMPARs), which are normally absent in the NAc, can be revealed by acute exposure to Aβ oligomers (AβOs), and play a critical role in the emergence of synaptic loss and motivation deficits. Blockade of NAc CP-AMPARs can effectively prevent AβO-induced downsizing and pruning of spines and silencing of excitatory synaptic transmission. We conclude that AβO-triggered synaptic insertion of CP-AMPARs is a key mechanism mediating synaptic degeneration in AD, and preserving synaptic integrity may prevent or delay the onset of AD-associated psychiatric symptoms.It is essential to identify the neuronal mechanisms of Alzheimer's Disease (AD)-associated neuropsychiatric symptoms, e.g., apathy, before improving the life quality of AD patients. Here, we focused on the nucleus accumbens (NAc), a critical brain region processing motivation, also known to display AD-associated pathological changes in human cases. We found that the synaptic calcium permeable (CP)-AMPA receptors (AMPARs), which are normally absent in the NAc, can be revealed by acute exposure to Aβ oligomers (AβOs), and play a critical role in the emergence of synaptic loss and motivation deficits. Blockade of NAc CP-AMPARs can effectively prevent AβO-induced downsizing and pruning of spines and silencing of excitatory synaptic transmission. We conclude that AβO-triggered synaptic insertion of CP-AMPARs is a key mechanism mediating synaptic degeneration in AD, and preserving synaptic integrity may prevent or delay the onset of AD-associated psychiatric symptoms. |
| Author | Ma, Yao-Ying Wen, Di Mustaklem, Richie Mustaklem, Basil Ma, Tao Zhang, Yihong Zhou, Miou Guo, Changyong |
| Author_xml | – sequence: 1 givenname: Changyong orcidid: 0000-0001-6541-240X surname: Guo fullname: Guo, Changyong organization: Department of Pharmacology and Toxicology, Indiana University School of Medicine, Indianapolis, IN, 46202, USA – sequence: 2 givenname: Di orcidid: 0000-0001-6918-0394 surname: Wen fullname: Wen, Di organization: Department of Pharmacology and Toxicology, Indiana University School of Medicine, Indianapolis, IN, 46202, USA – sequence: 3 givenname: Yihong surname: Zhang fullname: Zhang, Yihong organization: Department of Pharmacology and Toxicology, Indiana University School of Medicine, Indianapolis, IN, 46202, USA – sequence: 4 givenname: Richie surname: Mustaklem fullname: Mustaklem, Richie organization: Department of Pharmacology and Toxicology, Indiana University School of Medicine, Indianapolis, IN, 46202, USA – sequence: 5 givenname: Basil surname: Mustaklem fullname: Mustaklem, Basil organization: Department of Pharmacology and Toxicology, Indiana University School of Medicine, Indianapolis, IN, 46202, USA – sequence: 6 givenname: Miou orcidid: 0000-0001-8188-7392 surname: Zhou fullname: Zhou, Miou organization: Graduate College of Biomedical Sciences, Western University of Health Sciences, Pomona, CA, 91766, USA – sequence: 7 givenname: Tao orcidid: 0000-0002-0763-7261 surname: Ma fullname: Ma, Tao organization: Department of Neurobiology and Anatomy, Wake Forest University School of Medicine, Winston-Salem, NC, 27101, USA – sequence: 8 givenname: Yao-Ying orcidid: 0000-0003-3735-8412 surname: Ma fullname: Ma, Yao-Ying email: ym9@iu.edu, ym9@iu.edu organization: Stark Neurosciences Research Institute, Indiana University School of Medicine, Indianapolis, IN, 46202, USA. ym9@iu.edu |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/35105968$$D View this record in MEDLINE/PubMed |
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| CitedBy_id | crossref_primary_10_1002_advs_202204717 crossref_primary_10_1002_alz_14499 crossref_primary_10_1042_BST20231385 crossref_primary_10_1016_j_bcp_2024_116622 crossref_primary_10_1016_j_ejphar_2022_175188 crossref_primary_10_3390_ijms23052618 crossref_primary_10_4103_NRR_NRR_D_24_01052 crossref_primary_10_1162_netn_a_00423 crossref_primary_10_1007_s11596_025_00003_9 crossref_primary_10_3390_ijms25010111 crossref_primary_10_1093_jnen_nlae093 crossref_primary_10_3389_fnagi_2024_1487875 |
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| DOI | 10.1038/s41380-022-01459-0 |
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| SubjectTerms | alpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid Alzheimer Disease - pathology Alzheimer's disease Amyloid beta-Peptides - metabolism Calcium - metabolism Calcium permeability Emotional behavior Humans Mental disorders Motivation Neurodegeneration Neurodegenerative diseases Nucleus accumbens Nucleus Accumbens - metabolism Oligomers Quality of life Receptors, AMPA - metabolism Receptors, Calcium-Sensing Synapses - metabolism Synaptic transmission α-Amino-3-hydroxy-5-methyl-4-isoxazole propionic acid α-Amino-3-hydroxy-5-methyl-4-isoxazole propionic acid receptors β-Amyloid |
| Title | Amyloid-β oligomers in the nucleus accumbens decrease motivation via insertion of calcium-permeable AMPA receptors |
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