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High-fat diet-associated cognitive decline: Is zinc finger protein 1 (ZPR1) the molecular connection?

Zinc finger protein 1 (ZPR1) is required for cellular replication and viability. Recently, ZPR1 variant rs964184 has been repeatedly linked to high plasma triglyceride levels, metabolic syndrome, type 2 diabetes mellitus (T2DM), and nonalcoholic fatty liver disease (NAFLD), suggesting its involvemen...

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Detalles Bibliográficos
Autores principales: Chittilla, Mythri, Akimbekov, Nuraly S., Razzaque, Mohammed S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8562238/
https://www.ncbi.nlm.nih.gov/pubmed/34746842
http://dx.doi.org/10.1016/j.crphys.2021.09.004
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author Chittilla, Mythri
Akimbekov, Nuraly S.
Razzaque, Mohammed S.
author_facet Chittilla, Mythri
Akimbekov, Nuraly S.
Razzaque, Mohammed S.
author_sort Chittilla, Mythri
collection PubMed
description Zinc finger protein 1 (ZPR1) is required for cellular replication and viability. Recently, ZPR1 variant rs964184 has been repeatedly linked to high plasma triglyceride levels, metabolic syndrome, type 2 diabetes mellitus (T2DM), and nonalcoholic fatty liver disease (NAFLD), suggesting its involvement in lipid metabolism. This article attempts to explain how ZPR1 contributes to the mechanism of high-fat diet-associated cognitive decline through three premises: i) high-fat diet results in cognitive decline, ii) ZPR1 deficiency also results in cognitive decline, and iii) high-fat diet results in ZPR1 deficiency. Therefore, ZPR1 has the potential to be the connection between high-fat diet and cognitive decline. The two modalities of cognitive decline caused by low concentrations of ZPR1 are reduced brain-derived growth factor (BDNF) synthesis and neuron death, both occurring in the hippocampus. Downregulation of ZPR1 may lead to decreased synthesis of BDNF due to reduced concentrations of peroxisome proliferator-activated receptor-gamma (PPAR-γ), tropomyosin receptor kinase B (Trk B), and cAMP response element-binding protein (CREB), resulting in reduced ability to form and retain long-term memory as well as reduced neuroplasticity. Likewise, low concentrations of ZPR1 facilitate neuron death by producing lower amount of spinal motor neuron (SMN) protein, causing genomic instability, activating mixed-lineage protein kinase 3 (MLK3), mitogen-activated protein kinase 7 (MKK7), and c-Jun N-terminal kinase 3 (JNK3) signal cascade, and ultimately resulting in the activation of Caspase 3.
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spelling pubmed-85622382021-11-04 High-fat diet-associated cognitive decline: Is zinc finger protein 1 (ZPR1) the molecular connection? Chittilla, Mythri Akimbekov, Nuraly S. Razzaque, Mohammed S. Curr Res Physiol Hypotheses & Intersections Zinc finger protein 1 (ZPR1) is required for cellular replication and viability. Recently, ZPR1 variant rs964184 has been repeatedly linked to high plasma triglyceride levels, metabolic syndrome, type 2 diabetes mellitus (T2DM), and nonalcoholic fatty liver disease (NAFLD), suggesting its involvement in lipid metabolism. This article attempts to explain how ZPR1 contributes to the mechanism of high-fat diet-associated cognitive decline through three premises: i) high-fat diet results in cognitive decline, ii) ZPR1 deficiency also results in cognitive decline, and iii) high-fat diet results in ZPR1 deficiency. Therefore, ZPR1 has the potential to be the connection between high-fat diet and cognitive decline. The two modalities of cognitive decline caused by low concentrations of ZPR1 are reduced brain-derived growth factor (BDNF) synthesis and neuron death, both occurring in the hippocampus. Downregulation of ZPR1 may lead to decreased synthesis of BDNF due to reduced concentrations of peroxisome proliferator-activated receptor-gamma (PPAR-γ), tropomyosin receptor kinase B (Trk B), and cAMP response element-binding protein (CREB), resulting in reduced ability to form and retain long-term memory as well as reduced neuroplasticity. Likewise, low concentrations of ZPR1 facilitate neuron death by producing lower amount of spinal motor neuron (SMN) protein, causing genomic instability, activating mixed-lineage protein kinase 3 (MLK3), mitogen-activated protein kinase 7 (MKK7), and c-Jun N-terminal kinase 3 (JNK3) signal cascade, and ultimately resulting in the activation of Caspase 3. Elsevier 2021-10-02 /pmc/articles/PMC8562238/ /pubmed/34746842 http://dx.doi.org/10.1016/j.crphys.2021.09.004 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Hypotheses & Intersections
Chittilla, Mythri
Akimbekov, Nuraly S.
Razzaque, Mohammed S.
High-fat diet-associated cognitive decline: Is zinc finger protein 1 (ZPR1) the molecular connection?
title High-fat diet-associated cognitive decline: Is zinc finger protein 1 (ZPR1) the molecular connection?
title_full High-fat diet-associated cognitive decline: Is zinc finger protein 1 (ZPR1) the molecular connection?
title_fullStr High-fat diet-associated cognitive decline: Is zinc finger protein 1 (ZPR1) the molecular connection?
title_full_unstemmed High-fat diet-associated cognitive decline: Is zinc finger protein 1 (ZPR1) the molecular connection?
title_short High-fat diet-associated cognitive decline: Is zinc finger protein 1 (ZPR1) the molecular connection?
title_sort high-fat diet-associated cognitive decline: is zinc finger protein 1 (zpr1) the molecular connection?
topic Hypotheses & Intersections
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8562238/
https://www.ncbi.nlm.nih.gov/pubmed/34746842
http://dx.doi.org/10.1016/j.crphys.2021.09.004
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