Aging, oxidative stress and degenerative diseases: mechanisms, complications and emerging therapeutic strategies

MR Chaudhary, S Chaudhary, Y Sharma, TA Singh… - Biogerontology, 2023 - Springer
Aging accompanied by several age-related complications, is a multifaceted inevitable
biological progression involving various genetic, environmental, and lifestyle factors. The …

Intrinsic factors behind long‐COVID: II. SARS‐CoV‐2, extracellular vesicles, and neurological disorders

YA El‐Maradny, A Rubio‐Casillas… - Journal of Cellular …, 2023 - Wiley Online Library
With the decline in the number of new Severe Acute Respiratory Syndrome Coronavirus 2
(SARS‐CoV‐2) infections, the World Health Organization announced the end of the SARS …

Mitochondrial Dyshomeostasis as an Early Hallmark and a Therapeutic Target in Amyotrophic Lateral Sclerosis

NV Belosludtseva, LA Matveeva… - International Journal of …, 2023 - mdpi.com
Amyotrophic lateral sclerosis (ALS) is a fatal multisystem disease characterized by
progressive death of motor neurons, loss of muscle mass, and impaired energy metabolism …

Translocator protein in the rise and fall of central nervous system neurons

G Cheung, YC Lin, V Papadopoulos - Frontiers in Cellular …, 2023 - frontiersin.org
Translocator protein (TSPO), a 18 kDa protein found in the outer mitochondrial membrane,
has historically been associated with the transport of cholesterol in highly steroidogenic …

Why are aging and stress associated with dementia, cancer, and other diverse medical conditions? Role of pineal melatonin interactions with the HPA axis in …

G Anderson - Melatonin Research, 2023 - melaonin-research.com
Pineal melatonin and the cortisol awakening response (CAR) are integral aspects of the
circadian rhythm. Pineal melatonin release during sleep is proposed to optimize …

Skeletal muscle dysfunction in amyotrophic lateral sclerosis: a mitochondrial perspective and therapeutic approaches

GB Kubat, P Picone - Neurological Sciences, 2024 - Springer
Amyotrophic lateral sclerosis (ALS) is a progressive and fatal neuromuscular disease that
results in the loss of motor neurons and severe skeletal muscle atrophy. The etiology of ALS …

[HTML][HTML] Mitophagy in neurodegenerative disease pathogenesis

K Yang, Y Yan, A Yu, R Zhang, Y Zhang… - Neural Regeneration …, 2024 - journals.lww.com
Mitochondria are critical cellular energy resources and are central to the life of the neuron.
Mitophagy selectively clears damaged or dysfunctional mitochondria through autophagic …

Current potential pathogenic mechanisms of copper-zinc superoxide dismutase 1 (SOD1) in amyotrophic lateral sclerosis

XX Wang, WZ Chen, C Li, RS Xu - Reviews in the Neurosciences, 2024 - degruyter.com
Amyotrophic lateral sclerosis (ALS) is a rare neurodegenerative disease which damages
upper and lower motor neurons (UMN and LMN) innervating the muscles of the trunk …

AAV-mediated upregulation of VDAC1 rescues the mitochondrial respiration and sirtuins expression in a SOD1 mouse model of inherited ALS

A Magrì, CLR Lipari, A Caccamo, G Battiato… - Cell Death …, 2024 - nature.com
Mitochondrial dysfunction represents one of the most common molecular hallmarks of both
sporadic and familial forms of amyotrophic lateral sclerosis (ALS), a neurodegenerative …

Keep in touch: a perspective on the mitochondrial social network and its implication in health and disease

S Barabino, S Lombardi, M Zilocchi - Cell Death Discovery, 2023 - nature.com
Mitochondria have been the focus of extensive research for decades since their dysfunction
is linked to more than 150 distinct human disorders. Despite considerable efforts …