Cited by 40Alzheimer's disease research and treatmentsDementia and Cognitive Impairment ResearchCholinesterase and Neurodegenerative Diseases

SkQ1 Suppresses the p38 MAPK Signaling Pathway Involved in Alzheimer’s Disease-Like Pathology in OXYS Rats

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Muraleva, Natalia A., Stefanova, Natalia A., Kolosova, Nataliya G.·2020·Antioxidants

Abstract

Alzheimer’s disease (AD) is the most common type of dementia and is currently incurable, and mitogen-activated protein kinase (MAPK) p38 is implicated in the pathogenesis of AD. p38 MAPK inhibition is considered a promising strategy against AD, but there are no safe inhibitors capable of penetrating the blood–brain barrier. Earlier, we have shown that mitochondria-targeted antioxidant plastoquinonyl-decyltriphenylphosphonium (SkQ1) at nanomolar concentrations can prevent, slow down, or partially alleviate AD-like pathology in accelerated-senescence OXYS rats. Here we confirmed that dietary supplementation with SkQ1 during active progression of AD-like pathology in OXYS rats (aged 12–18 months) suppresses AD-like pathology progression, and for the first time, we showed that its effects are associated with suppression of p38 MAPK signaling pathway (MAPKsp) activity. Transcriptome analysis, western blotting, and immunofluorescent staining revealed that SkQ1 suppresses p38 MAPKsp activity in the hippocampus at the level of expression of genes involved in the p38 MAPKsp and reduces the phosphorylation of intermediate kinases (p38 MAPK and MK2) and a downstream protein (αB-crystallin). Thus, the anti-AD effects of SkQ1 are associated with improvement in the functioning of relevant signaling pathways and intracellular processes, thus making it a promising therapeutic agent for human AD.

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  • AD-related cognitive decline, behavioural test scores and senescence-associated myocardial disease may improve in murine models upon long-term or limited intake of SkQ1.

    “Finally, AD-related cognitive decline, behavioural test scores and senescence-associated myocardial disease may improve in murine models upon long-term (lifelong) or limited (between 12 and 18 months of age) intake of SkQ1 [77,78,99,100,101].”

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Authors
Muraleva, N. A., Stefanova, N. A., & Kolosova, N. G.
Affiliations
  • Institute of Cytology and Genetics (RU)
  • Novosibirsk Institute of Organic Chemistry (RU)
Corresponding author
Muraleva, Natalia A.
Venue
Antioxidants
Publisher
MDPI AG
Published
2020-07-28
Volume
9
Issue
8
Pages
676
ISSN
2076-3921 (ISSN-L)
OpenAlex
W3045571752
Cited by
40
References
32
Citations by year
2026: 7 · 2025: 7 · 2024: 6 · 2023: 9 · 2022: 5 · 2021: 4 · 2020: 2
FWCI
3.01
Type
journal article
Language
en
Open access
Locations
  • Antioxidants (publishedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
Funders
  • Ministry of Science and Higher Education of the Russian Federation (14.W03.31.0034)
  • Russian Foundation for Basic Research (18-015-00336)
Topics
  • Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
  • Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
  • Health Sciences › Medicine › Pharmacology › Cholinesterase and Neurodegenerative Diseases
Keywords
SkQ1, p38 MAPK signaling, Alzheimer's disease, OXYS rats, mitochondria-targeted antioxidants, alphaB-crystallin, hippocampus, dietary supplementation, blood-brain barrier, neuroprotection

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