Cited by 256Coenzyme Q10 studies and effectsParkinson's Disease Mechanisms and TreatmentsNeurological diseases and metabolism

Coenzyme Q10 attenuates the 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) induced loss of striatal dopamine and dopaminergic axons in aged mice

Beal, M.Flint, Matthews, Russell T, Tieleman, Alide, Shults, Clifford W·1998·Brain Research

Abstract

We investigated whether oral administration of coenzyme Q10 (CoQ10) could attenuate 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) neurotoxicity in one-year-old mice. Four groups of one-year-old, male C57BL/6 mice received a either standard diet or a diet supplemented with CoQ10 (200 mg/kg/day) for five weeks. After four weeks, one group that had received the standard diet and one group that had received the CoQ10 supplemented diet were treated with MPTP. The four groups continued on their assigned diets for an additional week prior to sacrifice. Striatal dopamine concentrations were reduced in both groups treated with MPTP, but they were significantly higher (37%) in the group treated with CoQ10 and MPTP than in the group treated with MPTP alone. The density of tyrosine hydroxylase immunoreactive (TH-IR) fibers in the caudal striatum was reduced in both MPTP-treated groups, but the density of TH-IR fibers was significantly (62%) greater in the group treated with CoQ10 and MPTP than in the group treated with MPTP alone. Our results indicate that CoQ10 can attenuate the MPTP-induced loss of striatal dopamine and dopaminergic axons in aged mice and suggest that CoQ10 may be useful in the treatment of Parkinson's disease.

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Crossref · 10.1016/s0006-8993(97)01192-x

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  • CoQ10 provided significant protection against MPTP-induced dopamine depletion and loss of TH-IR neurons in aged mice.

    “We demonstrated CoQ10 provided significant protection against MPTP induced dopamine depletion and loss of TH-IR neurons in aged mice146.”

    From Mitochondrial Approaches for Neuroprotection (2008) · cites this paper as [146]

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References 35 · Cited by 256

Authors
Beal, M. F., Matthews, R. T., Tieleman, A., & Shults, C. W.
Affiliations
  • Massachusetts General Hospital (US)
  • University of California San Diego (US)
Corresponding author
Shults, Clifford W
Venue
Brain Research
Publisher
Elsevier BV
Published
1998-02
Volume
783
Issue
1
Pages
109-114
ISSN
0006-8993 (ISSN-L)
OpenAlex
W2032515864
Cited by
256
References
35
Citations by year
2025: 5 · 2024: 5 · 2023: 7 · 2022: 9 · 2021: 6 · 2020: 8 · 2019: 5 · 2018: 7 · 2017: 7 · 2016: 6 · 2015: 2 · 2014: 6 · 2013: 12 · 2012: 18
FWCI
2.68
Type
journal article
Language
en
Open access
closed
Locations
  • Brain Research (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • U.S. Department of Veterans Affairs
  • National Institutes of Health (5r01ns032365-03, 5p01ns031579-05)
  • National Institute on Aging (P01 AG 12992, P01AG012992)
  • National Institute of Neurological Disorders and Stroke (NS31579, NS32365)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Coenzyme Q10 studies and effects
  • Health Sciences › Medicine › Neurology › Parkinson's Disease Mechanisms and Treatments
  • Life Sciences › Neuroscience › Neurology › Neurological diseases and metabolism
Keywords
coenzyme Q10, MPTP-induced neurotoxicity, Parkinson's disease, striatal dopamine, dopaminergic axons, tyrosine hydroxylase, aged mice, neuroprotection, dietary supplementation
MeSH terms
Administration, Oral, Aging, Animals, Axons, Coenzymes, Corpus Striatum, Dopamine, Male, Mice, Inbred C57BL, Substantia Nigra, Ubiquinone, 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine, Mice

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