Cited by 332Mitochondrial Function and PathologyNeurological Disorders and TreatmentsAlzheimer's disease research and treatments

Mitochondria-targeted peptide antioxidants: Novel neuroprotective agents

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Szeto, Hazel H.·2006·The AAPS Journal

Abstract

Increasing evidence suggests that mitochondrial dysfunction and oxidative stress play a crucial role in the majority of neurodegenerative diseases. Mitochondria are a major source of intracellular reactive oxygen species (ROS) and are particularly vulnerable to oxidative stress. Oxidative damage to mitochondria has been shown to impair mitochondrial function and lead to cell death via apoptosis and necrosis. Because dysfunctional mitochondria will produce more ROS, a feed-forward loop is set up whereby ROS-mediated oxidative damage to mitochondria favors more ROS generation, resulting in a vicious cycle. It is now appreciated that reduction of mitochondrial oxidative stress may prevent or slow down the progression of these neurodegenerative disorders. However, if mitochondria are the major source of intracellular ROS and mitochondria are most vulnerable to oxidative damage, then it would be ideal to deliver the antioxidant therapy to mitochondria. This review will summarize the development of a novel class of mitochondria-targeted antioxidants that can protect mitochondria against oxidative stress and prevent neuronal cell death in animal models of stroke, Parkinson's disease, and amyotrophic lateral sclerosis.

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  • SS-31 is a small water-soluble tetrapeptide that accumulates within the mitochondrion and binds to cardiolipin in the inner mitochondrial membrane where it scavenges ROS and prevents lipid peroxidation.

    “Szeto–Schiller-31 (SS-31) (Bendavia/elamipretide; Stealth Peptides) is a small water-soluble tetrapeptide that accumulates within the mitochondrion and binds to cardiolipin in the inner mitochondrial membrane where it scavenges ROS and prevents lipid peroxidation (921) (FIGURE 14).”

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References 83 · Cited by 332

Research works printed but not linked: 3

  1. Beal MF . Oxidatively modifi ed proteins in aging and disease. Free Radic Biol Med . 2002 ; 32 : 797 -803 .
  2. Giasson BI , Ischiropoulos H , Lee VM , Trojanowski JQ . The relationship between oxidative/nitrative stress and pathological inclusions in Alzheimer ' s and Parkinson ' s diseases. Free Radic Biol Med . 2002 ; 32 : 1264 -1275 .
  3. Erdelyi K , Bakondi E , Gergely P , Szabo C , Virag L . Pathophysiologic role of oxidative stress-induced poly(ADP-ribose) polymerase-1 activation: focus on cell death and transcriptional regulation. Cell Mol Life Sci . 2005 ; 62 : 751 -759 .

Authors
Szeto, H. H.
Affiliations
Cornell University (US)
Corresponding author
Szeto, Hazel H.
Venue
The AAPS Journal
Published
2006-09
Volume
8
Issue
3
Pages
E521-E531
ISSN
1550-7416 (ISSN-L)
OpenAlex
W2089982008
Cited by
332
References
83
Citations by year
2026: 8 · 2025: 10 · 2024: 11 · 2023: 11 · 2022: 14 · 2021: 22 · 2020: 20 · 2019: 17 · 2018: 16 · 2017: 9 · 2016: 11 · 2015: 15 · 2014: 24 · 2013: 13 · 2012: 28
FWCI
1.33
Type
journal article
Language
en
Open access
Locations
  • The AAPS Journal (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • National Institute on Drug Abuse (DA08924, P01 DA 08924, P01DA008924)
  • National Institute of Neurological Disorders and Stroke (R21NS048295, R21-NS-48295)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
  • Life Sciences › Neuroscience › Neurology › Neurological Disorders and Treatments
  • Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
Keywords
mitochondria-targeted antioxidants, mitochondrial dysfunction, oxidative stress, reactive oxygen species, neurodegenerative diseases, neuroprotection, neuronal cell death, stroke, Parkinson's disease, amyotrophic lateral sclerosis
MeSH terms
Antioxidants, Humans, Mitochondria, Parkinson Disease, Apoptosis, Reactive Oxygen Species, Oxidative Stress, Neuroprotective Agents, Neurodegenerative Diseases

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