The Radioprotective Effect of Procaine and Procaine-Derived Product Gerovital H3 in Lymphocytes from Young and Aged Individuals

Author:

Ungurianu Anca1ORCID,Margina Denisa1ORCID,Borsa Claudia2ORCID,Ionescu Cristina2,von Scheven Gudrun3,Oziol Lucie4,Faure Philippe5ORCID,Artur Yves5,Bürkle Alexander3,Gradinaru Daniela1ORCID,Moreno-Villanueva Maria36ORCID

Affiliation:

1. Department of Biochemistry, Faculty of Pharmacy, Carol Davila University of Medicine and Pharmacy, RO-020956 Bucharest, Romania

2. Department of Biology of Aging, Ana Aslan National Institute of Gerontology and Geriatrics, RO-011241 Bucharest, Romania

3. Department of Biology, Molecular Toxicology Group, University of Konstanz, D-78457 Konstanz, Germany

4. Faculty of Pharmacy, CNRS UMR 8079, University of Paris-Sud, F-92296 Châtenay-Malabry, France

5. Centre for Taste and Feeding Behavior, UMR CNRS 6265-INRA 1324-University of Burgundy-AgroSup, F-21000 Dijon, France

6. Department of Sport Science, Human Performance Research Centre, University of Konstanz, D-78457 Konstanz, Germany

Abstract

Ionizing radiation induces genomic instability in living organisms, and several studies reported an ageing-dependent radiosensitivity. Chemical compounds, such as scavengers, radioprotectors, and modifiers, contribute to reducing the radiation-associated toxicity. These compounds are often antioxidants, and therefore, in order to be effective, they must be present before or during exposure to radiation. However, not all antioxidants provide radioprotection. In this study, we investigated the effects of procaine and of a procaine-based product Gerovital H3 (GH3) on the formation of endogenous and X-ray-induced DNA strand breaks in peripheral blood mononuclear cells (PBMCs) isolated from young and elderly individuals. Interestingly, GH3 showed the strongest radioprotective effects in PBMCs from young subjects, while procaine reduced the endogenous amount of DNA strand breaks more pronounced in aged individuals. Both procaine and GH3 inhibited lipid peroxidation, but procaine was more effective in inhibiting mitochondria free radicals’ generation, while GH3 showed a higher antioxidant action on macrophage-induced low-density lipoprotein oxidation. Our findings provide new insights into the mechanisms underlying the distinct effects of procaine and GH3 on DNA damage.

Funder

EU-FP7 Project

Publisher

Hindawi Limited

Subject

Cell Biology,Aging,General Medicine,Biochemistry

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