Home > Research > Publications & Outputs > Acylated Ghrelin as a Multi-Targeted Therapy fo...

Links

Text available via DOI:

View graph of relations

Acylated Ghrelin as a Multi-Targeted Therapy for Alzheimer's and Parkinson's Disease.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

Published

Standard

Acylated Ghrelin as a Multi-Targeted Therapy for Alzheimer's and Parkinson's Disease. / Reich, Niklas; Hölscher, Christian.
In: Frontiers in Neuroscience, Vol. 14, 614828, 14.12.2020.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

Harvard

APA

Vancouver

Reich N, Hölscher C. Acylated Ghrelin as a Multi-Targeted Therapy for Alzheimer's and Parkinson's Disease. Frontiers in Neuroscience. 2020 Dec 14;14:614828. doi: 10.3389/fnins.2020.614828

Author

Bibtex

@article{cd9c3e42ac0c49f9a2a6b98ba2f44d28,
title = "Acylated Ghrelin as a Multi-Targeted Therapy for Alzheimer's and Parkinson's Disease.",
abstract = "Much thought has been given to the impact of Amyloid Beta, Tau and Alpha-Synuclein in the development of Alzheimer's disease (AD) and Parkinson's disease (PD), yet the clinical failures of the recent decades indicate that there are further pathological mechanisms at work. Indeed, besides amyloids, AD and PD are characterized by the culminative interplay of oxidative stress, mitochondrial dysfunction and hyperfission, defective autophagy and mitophagy, systemic inflammation, BBB and vascular damage, demyelination, cerebral insulin resistance, the loss of dopamine production in PD, impaired neurogenesis and, of course, widespread axonal, synaptic and neuronal degeneration that leads to cognitive and motor impediments. Interestingly, the acylated form of the hormone ghrelin has shown the potential to ameliorate the latter pathologic changes, although some studies indicate a few complications that need to be considered in the long-term administration of the hormone. As such, this review will illustrate the wide-ranging neuroprotective properties of acylated ghrelin and critically evaluate the hormone's therapeutic benefits for the treatment of AD and PD.",
keywords = "growth hormone secretagogue receptor 1 alpha, mitochondrial dysfunction, inflammation, autophagy, insulin resistance, dopamine, neurodegeneration, ghrelin",
author = "Niklas Reich and Christian H{\"o}lscher",
year = "2020",
month = dec,
day = "14",
doi = "10.3389/fnins.2020.614828",
language = "English",
volume = "14",
journal = "Frontiers in Neuroscience",
issn = "1662-453X",
publisher = "Frontiers Media S.A.",

}

RIS

TY - JOUR

T1 - Acylated Ghrelin as a Multi-Targeted Therapy for Alzheimer's and Parkinson's Disease.

AU - Reich, Niklas

AU - Hölscher, Christian

PY - 2020/12/14

Y1 - 2020/12/14

N2 - Much thought has been given to the impact of Amyloid Beta, Tau and Alpha-Synuclein in the development of Alzheimer's disease (AD) and Parkinson's disease (PD), yet the clinical failures of the recent decades indicate that there are further pathological mechanisms at work. Indeed, besides amyloids, AD and PD are characterized by the culminative interplay of oxidative stress, mitochondrial dysfunction and hyperfission, defective autophagy and mitophagy, systemic inflammation, BBB and vascular damage, demyelination, cerebral insulin resistance, the loss of dopamine production in PD, impaired neurogenesis and, of course, widespread axonal, synaptic and neuronal degeneration that leads to cognitive and motor impediments. Interestingly, the acylated form of the hormone ghrelin has shown the potential to ameliorate the latter pathologic changes, although some studies indicate a few complications that need to be considered in the long-term administration of the hormone. As such, this review will illustrate the wide-ranging neuroprotective properties of acylated ghrelin and critically evaluate the hormone's therapeutic benefits for the treatment of AD and PD.

AB - Much thought has been given to the impact of Amyloid Beta, Tau and Alpha-Synuclein in the development of Alzheimer's disease (AD) and Parkinson's disease (PD), yet the clinical failures of the recent decades indicate that there are further pathological mechanisms at work. Indeed, besides amyloids, AD and PD are characterized by the culminative interplay of oxidative stress, mitochondrial dysfunction and hyperfission, defective autophagy and mitophagy, systemic inflammation, BBB and vascular damage, demyelination, cerebral insulin resistance, the loss of dopamine production in PD, impaired neurogenesis and, of course, widespread axonal, synaptic and neuronal degeneration that leads to cognitive and motor impediments. Interestingly, the acylated form of the hormone ghrelin has shown the potential to ameliorate the latter pathologic changes, although some studies indicate a few complications that need to be considered in the long-term administration of the hormone. As such, this review will illustrate the wide-ranging neuroprotective properties of acylated ghrelin and critically evaluate the hormone's therapeutic benefits for the treatment of AD and PD.

KW - growth hormone secretagogue receptor 1 alpha

KW - mitochondrial dysfunction

KW - inflammation

KW - autophagy

KW - insulin resistance

KW - dopamine

KW - neurodegeneration

KW - ghrelin

U2 - 10.3389/fnins.2020.614828

DO - 10.3389/fnins.2020.614828

M3 - Journal article

VL - 14

JO - Frontiers in Neuroscience

JF - Frontiers in Neuroscience

SN - 1662-453X

M1 - 614828

ER -