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Neurodegenerative Disorders: From Molecules to Potential Cures

A special issue of Molecules (ISSN 1420-3049). This special issue belongs to the section "Bioorganic Chemistry".

Deadline for manuscript submissions: closed (30 April 2022) | Viewed by 2562

Special Issue Editors


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Guest Editor
Department of Chinese Pharmaceutical Sciences and Chinese Medicine Resources, China Medical University, Taichung 40438, Taiwan
Interests: neurodegenerative disorders; Alzheimer’s disease; Parkinson’s disease; behavioral pharmacology; neuropharmacology; antioxidants; neuroinflammation; pharmacognosy; medicinal herbs
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Guest Editor
Department of Pharmacology, China Medical University Taichung, Taichung, Taiwan
Interests: neurodegenerative disorders; pharmacology and toxicology; signal transduction; neuroinflammation; animal behavior

Special Issue Information

Dear Colleagues,

Neurodegenerative disorders (NDs) are characterized by the progressive and irreversible loss of selected neuronal populations in the peripheral or central nervous system (CNS). Neuronal loss in the CNS leads to an impairment of motor, behavioral and/or cognitive function. NDs mainly include Alzheimer’s disease (AD), Parkinson’s disease (PD), Huntington’s disease (HD), amyotrophic lateral sclerosis (ALS), cerebral ischemia reperfusion injury (IR), etc. Already, many of the pathological mechanisms underlying these above NDs have been mentioned, such as genetic mutation, microRNA (miRNA) network alteration, glutamate excitotoxicity, oxidative stress, neuroinflammation, mitochondria dysfunction, endoplasmic reticulum stress, proteostasis failure, autophagy dysfunction, cerebral microvascular damages, etc. Most of the previous studies suggest that these NDs are caused by multiple pathological mechanisms or processes, although each ND has its own different clinical characteristics, neuropathological targets, and loss of selected neuronal populations. Recent reports indicated that medicinal herbs and/or natural products possess substantial pharmacological activities, including antioxidant, anti-inflammatory, antiapoptotic, autophagy-inducible and ubiquitin-proteasome system-modulating activities. Accordingly, these multitargeted medicinal herbs and/or natural products are most likely to have potential advantages against these NDs. Thus, based on these above backgrounds, this Special Issue is dedicated to presenting the molecular pathological mechanisms of NDs, and the molecular mechanisms of medicinal herbs and/or natural products in the treatment of these NDs. Additionally, review articles summarizing the molecular pathological mechanisms of NDs and the anti-NDs and/or neuroprotective mechanisms of medicinal herbs and/or natural products are also a focus of this Special Issue.

Dr. Chi-Rei Wu
Prof. Dr. Dah-Yuu Lu
Guest Editors

Manuscript Submission Information

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Keywords

  • Neurodegenerative disorders
  • Alzheimer’s disease
  • Parkinson’s disease
  • Cerebral ischemia reperfusion injury
  • Molecular pathological mechanism
  • Medicinal herbs
  • Natural products.

Published Papers (1 paper)

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Research

16 pages, 3451 KiB  
Article
Deficiency in Androgen Receptor Aggravates Traumatic Brain Injury-Induced Pathophysiology and Motor Deficits in Mice
by Yu-Hsin Chen, Yen-Chou Chen, Ling-Ling Hwang, Liang-Yo Yang and Dah-Yuu Lu
Molecules 2021, 26(20), 6250; https://0-doi-org.brum.beds.ac.uk/10.3390/molecules26206250 - 15 Oct 2021
Cited by 3 | Viewed by 1890
Abstract
Androgens have been shown to have a beneficial effect on brain injury and lower reactive astrocyte expression after TBI. Androgen receptors (ARs) are known to mediate the neuroprotective effects of androgens. However, whether ARs play a crucial role in TBI remains unknown. In [...] Read more.
Androgens have been shown to have a beneficial effect on brain injury and lower reactive astrocyte expression after TBI. Androgen receptors (ARs) are known to mediate the neuroprotective effects of androgens. However, whether ARs play a crucial role in TBI remains unknown. In this study, we investigated the role of ARs in TBI pathophysiology, using AR knockout (ARKO) mice. We used the controlled cortical impact model to produce primary and mechanical brain injuries and assessed motor function and brain-lesion volume. In addition, the AR knockout effects on necrosis and autophagy were evaluated after TBI. AR knockout significantly increased TBI-induced expression of the necrosis marker alpha-II-spectrin breakdown product 150 and astrogliosis marker glial fibrillary acidic protein. In addition, the TBI-induced astrogliosis increase in ARKO mice lasted for three weeks after a TBI. The autophagy marker Beclin-1 was also enhanced in ARKO mice compared with wild-type mice after TBI. Our results also indicated that ARKO mice showed a more unsatisfactory performance than wild-type mice in a motor function test following TBI. Further, they were observed to have more severe lesions than wild-type mice after injury. These findings strongly suggest that ARs play a role in TBI. Full article
(This article belongs to the Special Issue Neurodegenerative Disorders: From Molecules to Potential Cures)
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