Literature DB >> 28231026

Late Administration of a Palladium Lipoic Acid Complex (POLY-MVA) Modifies Cardiac Mitochondria but Not Functional or Structural Manifestations of Radiation-Induced Heart Disease in a Rat Model.

Vijayalakshmi Sridharan1, John W Seawright1, Francis J Antonawich2,3, Merrill Garnett2, Maohua Cao1, Preeti Singh1, Marjan Boerma1.   

Abstract

Exposure of the heart to ionizing radiation can cause adverse myocardial remodeling. In small animal models, local heart irradiation causes persistent alterations in cardiac mitochondrial function and swelling. POLY-MVA is a dietary supplement that contains a palladium lipoic acid complex that targets mitochondrial complex I and has been demonstrated to have greater redox potential than lipoic acid alone. POLY-MVA improves mitochondrial function and anti-oxidant enzyme activity in the aged rat heart. In this study, we tested whether POLY-MVA can mitigate cardiac effects of ionizing radiation. Adult male rats were exposed to local heart X rays with a daily dose of 9 Gy for 5 consecutive days. Eighteen weeks after irradiation, POLY-MVA was administered orally at 1 ml/kg bodyweight per day during weekdays, for 6 weeks. Alterations in cardiac function as measured with echocardiography coincided with enhanced mitochondrial swelling, a reduction in mitochondrial expression of complex II, manifestations of adverse remodeling such as a reduction in myocardial microvessel density and an increase in collagen deposition and mast cell numbers. POLY-MVA enhanced left ventricular expression of superoxide dismutase 2, but only in sham-irradiated animals. In irradiated animals, POLY-MVA caused a reduction in markers of inflammatory infiltration, CD2 and CD68. Moreover, POLY-MVA mitigated the effects of radiation on mitochondria. Nonetheless, POLY-MVA did not mitigate adverse cardiac remodeling, suggesting that this tissue remodeling may not be alleviated by altering cardiac mitochondria alone. However, we cannot exclude the possibility that an earlier onset of POLY-MVA administration may have more profound effects on radiation-induced cardiac remodeling.

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Year:  2017        PMID: 28231026      PMCID: PMC5483333          DOI: 10.1667/RR14643.1

Source DB:  PubMed          Journal:  Radiat Res        ISSN: 0033-7587            Impact factor:   2.841


  18 in total

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4.  Irradiation induced modest changes in murine cardiac function despite progressive structural damage to the myocardium and microvasculature.

Authors:  Ingar Seemann; Karen Gabriels; Nils L Visser; Saske Hoving; Johannes A te Poele; Jeffrey F Pol; Marion J Gijbels; Ben J Janssen; Fijs W van Leeuwen; Mat J Daemen; Sylvia Heeneman; Fiona A Stewart
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Authors:  G D Cilliers; I S Harper; A Lochner
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9.  A novel technique for image-guided local heart irradiation in the rat.

Authors:  Sunil Sharma; Eduardo G Moros; Marjan Boerma; Vijayalakshmi Sridharan; Eun Young Han; Richard Clarkson; Martin Hauer-Jensen; Peter M Corry
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Authors:  Detcho A Stoyanovsky; Jianfei Jiang; Michael P Murphy; Michael Epperly; Xiaolan Zhang; Song Li; Joel Greenberger; Valerian Kagan; Hülya Bayır
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7.  Acquired Immunity Is Not Essential for Radiation-Induced Heart Dysfunction but Exerts a Complex Impact on Injury.

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8.  Radiation‑induced dysfunction of energy metabolism in the heart results in the fibrosis of cardiac tissues.

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9.  Pyrrolidine Dithiocarbamate Might Mitigate Radiation-Induced Heart Damage at an Early Stage in Rats.

Authors:  Yajing Wu; Lina Liu; Shengliang Lv; Yi Wang; Shuai Wang; Sheng Wang; Jiandong Zhang; Jun Wang
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10.  Differences in Expression of Mitochondrial Complexes Due to Genetic Variants May Alter Sensitivity to Radiation-Induced Cardiac Dysfunction.

Authors:  Rachel A Schlaak; Anne Frei; Gopika SenthilKumar; Shirng-Wern Tsaih; Clive Wells; Jyotsna Mishra; Michael J Flister; Amadou K S Camara; Carmen Bergom
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