Lysophospholipids: A Potential Drug Candidates for Neurodegenerative Disorders

Neurodegenerative diseases (NDs) commonly present misfolded and aggregated proteins. Considerable research has been performed to unearth the molecular processes underpinning this pathological aggregation and develop therapeutic strategies targeting NDs. Fibrillary deposits of α-synuclein (α-Syn), a...

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Main Authors: Tatsuya Karaki, Hisao Haniu, Yoshikazu Matsuda, Tamotsu Tsukahara
Format: Article
Language:English
Published: MDPI AG 2022-12-01
Series:Biomedicines
Subjects:
Online Access:https://www.mdpi.com/2227-9059/10/12/3126
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author Tatsuya Karaki
Hisao Haniu
Yoshikazu Matsuda
Tamotsu Tsukahara
author_facet Tatsuya Karaki
Hisao Haniu
Yoshikazu Matsuda
Tamotsu Tsukahara
author_sort Tatsuya Karaki
collection DOAJ
description Neurodegenerative diseases (NDs) commonly present misfolded and aggregated proteins. Considerable research has been performed to unearth the molecular processes underpinning this pathological aggregation and develop therapeutic strategies targeting NDs. Fibrillary deposits of α-synuclein (α-Syn), a highly conserved and thermostable protein, are a critical feature in the development of NDs such as Alzheimer’s disease (AD), Lewy body disease (LBD), Parkinson’s disease (PD), and multiple system atrophy (MSA). Inhibition of α-Syn aggregation can thus serve as a potential approach for therapeutic intervention. Recently, the degradation of target proteins by small molecules has emerged as a new therapeutic modality, gaining the hotspot in pharmaceutical research. Additionally, interest is growing in the use of food-derived bioactive compounds as intervention agents against NDs via functional foods and dietary supplements. According to reports, dietary bioactive phospholipids may have cognition-enhancing and neuroprotective effects, owing to their abilities to influence cognition and mental health in vivo and in vitro. However, the mechanisms by which lipids may prevent the pathological aggregation of α-Syn warrant further clarification. Here, we review evidence for the potential mechanisms underlying this effect, with a particular focus on how porcine liver decomposition product (PLDP)-derived lysophospholipids (LPLs) may inhibit α-Syn aggregation.
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spelling doaj.art-328e4b078c504538b4bb25e89ff77aa02023-11-24T13:27:16ZengMDPI AGBiomedicines2227-90592022-12-011012312610.3390/biomedicines10123126Lysophospholipids: A Potential Drug Candidates for Neurodegenerative DisordersTatsuya Karaki0Hisao Haniu1Yoshikazu Matsuda2Tamotsu Tsukahara3Department of Pharmacology and Therapeutic Innovation, Nagasaki University Graduate School of Biomedical Sciences, 1-14 Bunkyo-machi, Nagasaki 852-8521, JapanInstitute for Biomedical Sciences, Interdisciplinary Cluster for Cutting Edge Research, Shinshu University, 3-1-1 Asahi, Nagano 390-8621, JapanClinical Pharmacology Educational Center, Nihon Pharmaceutical University, Ina-machi, Saitama 362-0806, JapanDepartment of Pharmacology and Therapeutic Innovation, Nagasaki University Graduate School of Biomedical Sciences, 1-14 Bunkyo-machi, Nagasaki 852-8521, JapanNeurodegenerative diseases (NDs) commonly present misfolded and aggregated proteins. Considerable research has been performed to unearth the molecular processes underpinning this pathological aggregation and develop therapeutic strategies targeting NDs. Fibrillary deposits of α-synuclein (α-Syn), a highly conserved and thermostable protein, are a critical feature in the development of NDs such as Alzheimer’s disease (AD), Lewy body disease (LBD), Parkinson’s disease (PD), and multiple system atrophy (MSA). Inhibition of α-Syn aggregation can thus serve as a potential approach for therapeutic intervention. Recently, the degradation of target proteins by small molecules has emerged as a new therapeutic modality, gaining the hotspot in pharmaceutical research. Additionally, interest is growing in the use of food-derived bioactive compounds as intervention agents against NDs via functional foods and dietary supplements. According to reports, dietary bioactive phospholipids may have cognition-enhancing and neuroprotective effects, owing to their abilities to influence cognition and mental health in vivo and in vitro. However, the mechanisms by which lipids may prevent the pathological aggregation of α-Syn warrant further clarification. Here, we review evidence for the potential mechanisms underlying this effect, with a particular focus on how porcine liver decomposition product (PLDP)-derived lysophospholipids (LPLs) may inhibit α-Syn aggregation.https://www.mdpi.com/2227-9059/10/12/3126lysophospholipidsneurodegenerative diseasesamyloidα-synuclein
spellingShingle Tatsuya Karaki
Hisao Haniu
Yoshikazu Matsuda
Tamotsu Tsukahara
Lysophospholipids: A Potential Drug Candidates for Neurodegenerative Disorders
Biomedicines
lysophospholipids
neurodegenerative diseases
amyloid
α-synuclein
title Lysophospholipids: A Potential Drug Candidates for Neurodegenerative Disorders
title_full Lysophospholipids: A Potential Drug Candidates for Neurodegenerative Disorders
title_fullStr Lysophospholipids: A Potential Drug Candidates for Neurodegenerative Disorders
title_full_unstemmed Lysophospholipids: A Potential Drug Candidates for Neurodegenerative Disorders
title_short Lysophospholipids: A Potential Drug Candidates for Neurodegenerative Disorders
title_sort lysophospholipids a potential drug candidates for neurodegenerative disorders
topic lysophospholipids
neurodegenerative diseases
amyloid
α-synuclein
url https://www.mdpi.com/2227-9059/10/12/3126
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AT yoshikazumatsuda lysophospholipidsapotentialdrugcandidatesforneurodegenerativedisorders
AT tamotsutsukahara lysophospholipidsapotentialdrugcandidatesforneurodegenerativedisorders