Mitochondria-targeted peptide antioxidants: Novel neuroprotective agents
Open accessAbstract
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).”
From Sources of Vascular Nitric Oxide and Reactive Oxygen Species and Their Regulation (2019) · cites this paper as [921]
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References 83 · Cited by 332
Research works printed but not linked: 3
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- 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 .
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- Authors
- Szeto, H. H.
- Affiliations
- Cornell University (US)
- Corresponding author
- Szeto, Hazel H.
- ORCID
- Szeto, Hazel H.
- Venue
- The AAPS Journal
- Published
- 2006-09
- Volume
- 8
- Issue
- 3
- Pages
- E521-E531
- ISSN
- 1550-7416 (ISSN-L)
- PMC
- PMC2761060
- 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
- bronze
- doi.org
- Licence
- www.springer.com/tdm (tdm)
- 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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