Cited by 41Coenzyme Q10 studies and effectsCardiac Fibrosis and RemodelingAntioxidant Activity and Oxidative Stress

Effect of pretreatment with coenzyme Q10 on isoproterenol-induced cardiotoxicity and cardiac hypertrophy in rats

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Ghule, Arvindkumar E., Kulkarni, Chetan P., Bodhankar, Subhash L., Pandit, Vijaya A.·2009·Current Therapeutic Research

Abstract

BACKGROUND: Coenzyme Q10 (CoQ10) is a lipid-soluble, vitamin-like substance found in the hydrophobic interior of the phospholipid bilayer of most cellular membranes. It appears to be involved in the coordinated regulation between oxidative stress and antioxidant capacity of heart tissue when the heart is subjected to oxidative stress in various pathogenic conditions. OBJECTIVE: The objective of the present study was to investigate the effect of pretreatment with CoQ10 (100 mg/kg) on isoproterenol (ISO)-induced cardiotoxicity and cardiac hypertrophy in rats. METHODS: Albino male Wistar rats (250-300 g) were evenly divided by lottery method into 1 of the following 3 groups: the ISO group (olive oil 2 mL/kg orally for 18 days and ISO 1 mg/kg IP from days 9-18); the CoQ10 + ISO group (CoQ10 100 mg/kg orally for 18 days and ISO 1 mg/kg IP from days 9-18); and the control group (olive oil 2 mL/kg orally for 18 days and water IP from days 9-18). Twenty-four hours after the last dose of water or ISO, the rats were anesthetized and an ECG was recorded. Blood was withdrawn by retro-orbital puncture for estimation of serum creatine kinase-MB (CK-MB) isoenzyme levels, lactate dehydrogenase (LDH) levels, and aspartate aminotransferase activities. The animals were euthanized using an overdose of ether. The hearts of 6 animals from each group were used for estimation of superoxide dismutase (SOD) activity, reduced glutathione (GSH) concentration, lipid peroxidation (LPO), malondialdehyde (MDA), and total protein concentration. Histopathology of the 2 remaining hearts in each group was carried out by a blinded technician. RESULTS: A total of 24 rats (8 in each group) were used in this study; all rats survived to study end. Compared with the control group, the ISO-treated rats had a significant change in heart to body weight ratio (P < 0.001); significant changes in the endogenous antioxidants (ie, significantly higher myocardial MDA concentration [P < 0.001]; significantly lower myocardial GSH concentration [P < 0.001] and SOD activity [P < 0.01]); and significantly higher serum activities of marker enzymes (eg, CK-MB [P < 0.001] and LDH [P < 0.001]). Compared with the ISO group, the CoQ10 + ISO group had a significant change in heart to body weight ratio (P < 0.001); significant changes in the endogenous antioxidants (ie, significantly lower MDA concentration [P < 0.05]; significantly higher myocardial GSH concentration [P < 0.001] and SOD activity [P < 0.05]); and significantly lower serum activities of marker enzymes (eg, CK-MB [P < 0.05] and LDH [P < 0.01]). CONCLUSION: Pretreatment with CoQ10 (100 mg/kg) for 18 days was associated with moderate protection against ISO-induced cardiotoxicity and cardiac hypertrophy, and with lower myocardial injury by preserving endogenous antioxidants and reducing LPO in rat heart.

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Crossref · 10.1016/j.curtheres.2009.12.004

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  • CoQ10 could reduce CK activity in isoprenaline-induced cardiac hypertrophy and cardiotoxicity in rats.

    “This was also in agreement with previous work that reported that CoQ10 could reduce CK activity in isoprenaline-induced cardiac hypertrophy and cardiotoxicity in rats”

    From Can coenzyme Q10 alleviate the toxic effect of fenofibrate on skeletal muscle? (2023) · cites this paper as Ghule et al. 2009

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Authors
Ghule, A. E., Kulkarni, C. P., Bodhankar, S. L., & Pandit, V. A.
Affiliations
Bharati Vidyapeeth (Deemed to be University) (IN)
Corresponding author
Bodhankar, Subhash L.
Venue
Current Therapeutic Research
Publisher
Elsevier BV
Published
2009-12
Volume
70
Issue
6
Pages
460-471
ISSN
0011-393X (ISSN-L)
OpenAlex
W2160073318
Cited by
41
References
34
Citations by year
2026: 2 · 2025: 4 · 2024: 1 · 2023: 3 · 2022: 6 · 2021: 4 · 2020: 1 · 2018: 4 · 2017: 1 · 2016: 2 · 2015: 2 · 2014: 2 · 2013: 5 · 2012: 3
FWCI
0.54
Type
journal article
Language
en
Open access
Locations
  • Current Therapeutic Research (publishedVersion)
  • Europe PMC (PubMed Central) (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Coenzyme Q10 studies and effects
  • Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Cardiac Fibrosis and Remodeling
  • Health Sciences › Medicine › Biochemistry › Antioxidant Activity and Oxidative Stress
Keywords
coenzyme Q10, isoproterenol, cardiotoxicity, cardiac hypertrophy, oxidative stress, antioxidant defense, lipid peroxidation, malondialdehyde, superoxide dismutase, glutathione, creatine kinase-MB, lactate dehydrogenase, aspartate aminotransferase, myocardial injury, cardioprotection, heart-to-body weight ratio

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