Cited by 54Mitochondrial Function and PathologyCoenzyme Q10 studies and effectsAutophagy in Disease and Therapy

Insulin Attenuates Diabetes-Related Mitochondrial Alterations: A Comparative Study

Moreira, P., Rolo, A., Sena, C., Seica, R., Oliveira, C., Santos, M.·2006·Medicinal Chemistry

Abstract

This study evaluated and compared the effect of insulin treatment on the status of brain, heart and kidney mitochondria isolated from 12-week streptozotocin (STZ)-induced diabetic rats versus STZ-diabetic animals treated with insulin during a period of 4 weeks. Mitochondria isolated from 12-week citrate (vehicle)-treated rats were used as control. Several mitochondrial parameters were evaluated: respiratory indexes (state 3 and 4 of respiration, respiratory control and ADP/O ratios), transmembrane potential, depolarization and repolarization levels, ATP, glutathione and coenzyme Q contents, production of hydrogen peroxide, superoxide dismutase, glutathione peroxidase and glutathione reductase activities and the ability of mitochondria to accumulate calcium. We observed that diabetes promoted a significant decrease in kidney and brain mitochondrial coenzyme Q9 content while this parameter was increased in heart mitochondria. Furthermore, diabetes induced a significant increase in hydrogen peroxide production in kidney mitochondria this effect being accompanied by a significant increase in glutathione peroxidase and reductase activities. Furthermore, brain mitochondria isolated from diabetic animals presented a lower ATP content and ability to accumulate calcium. In contrast, heart and kidney mitochondria presented a slight higher capacity to accumulate calcium. Insulin treatment normalized the levels of coenzyme Q9 and glutathione peroxidase and reductase activities and increased ATP content and the ability to accumulate calcium. Altogether these results suggest that insulin treatment attenuates diabetes-induced mitochondrial alterations protecting against the increase in oxidative stress and improving oxidative phosphorylation efficiency. In this line, insulin therapy, besides its well-known importance in the maintenance of glycemic control, may help to protect against mitochondrial dysfunction associated to several age-related disorders such as diabetes.

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Crossref · 10.2174/157340606776930754

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References 2 · Cited by 54

Authors
Moreira, P., Rolo, A., Sena, C., Seica, R., Oliveira, C., & Santos, M.
Affiliations
  • Centro de Neurociências e Biologia Celular (PT)
  • University of Coimbra (PT)
Corresponding author
Santos, M.
Venue
Medicinal Chemistry
Published
2006-05-01
Volume
2
Issue
3
Pages
299-308
ISSN
1573-4064 (ISSN-L)
OpenAlex
W2143258411
Cited by
54
References
2
Citations by year
2026: 1 · 2025: 1 · 2024: 2 · 2023: 1 · 2022: 6 · 2021: 2 · 2020: 2 · 2019: 1 · 2018: 1 · 2017: 6 · 2016: 1 · 2015: 1 · 2014: 4 · 2013: 6 · 2012: 3
FWCI
1.49
Type
journal article
Language
en
Open access
closed
Locations
  • Medicinal Chemistry (publishedVersion)
  • PubMed (publishedVersion)
Funders
Fundação para a Ciência e a Tecnologia
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Coenzyme Q10 studies and effects
  • Health Sciences › Medicine › Epidemiology › Autophagy in Disease and Therapy
Keywords
insulin therapy, diabetes mellitus, mitochondrial dysfunction, streptozotocin-induced diabetes, coenzyme Q9, oxidative stress, hydrogen peroxide, glutathione peroxidase, glutathione reductase, mitochondrial calcium accumulation, ATP levels, mitochondrial respiration, membrane potential, brain mitochondria, heart mitochondria, kidney mitochondria
MeSH terms
Animals, Body Weight, Brain, Calcium, Diabetes Mellitus, Experimental, Insulin, Male, Mitochondria, Organ Size, Phosphorylation, Streptozocin, Rats, Wistar, Oxidative Stress, Rats

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