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      Adaptive response in human blood lymphocytes exposed to non-ionizing radiofrequency fields: resistance to ionizing radiation-induced damage

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          Abstract

          The aim of this preliminary investigation was to assess whether human peripheral blood lymphocytes which have been pre-exposed to non-ionizing radiofrequency fields exhibit an adaptive response (AR) by resisting the induction of genetic damage from subsequent exposure to ionizing radiation. Peripheral blood lymphocytes from four healthy donors were stimulated with phytohemagglutinin for 24 h and then exposed for 20 h to 1950 MHz radiofrequency fields (RF, adaptive dose, AD) at an average specific absorption rate of 0.3 W/kg. At 48 h, the cells were subjected to a challenge dose (CD) of 1.0 or 1.5 Gy X-irradiation (XR, challenge dose, CD). After a 72 h total culture period, cells were collected to examine the incidence of micronuclei (MN). There was a significant decrease in the number of MN in lymphocytes exposed to RF + XR (AD + CD) as compared with those subjected to XR alone (CD). These observations thus suggested a RF-induced AR and induction of resistance to subsequent damage from XR. There was variability between the donors in RF-induced AR. The data reported in our earlier investigations also indicated a similar induction of AR in human blood lymphocytes that had been pre-exposed to RF (AD) and subsequently treated with a chemical mutagen, mitomycin C (CD). Since XR and mitomycin-C induce different kinds of lesions in cellular DNA, further studies are required to understand the mechanism(s) involved in the RF-induced adaptive response.

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          Most cited references43

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          SAS for Mixed Models

          The indispensable, up-to-date guide to mixed models using SAS®. Discover the latest capabilities available for a variety of applications featuring the MIXED, GLIMMIX, and NLMIXED procedures in this valuable edition of the comprehensive mixed models guide for data analysis, completely revised and updated for SAS®9. The theory underlying the models, the forms of the models for various applications, and a wealth of examples from different fields of study are integrated in the discussions of these models: random effect only and random coefficients models split-plot, multilocation, and repeated measures models hierarchical models with nested random effects analysis of covariance models spatial correlation models generalized linear mixed models nonlinear mixed models Professionals and students with a background in two-way ANOVA and regression and a basic knowledge of linear models and matrix algebra will benefit from the topics covered. Includes a free CD-ROM with example SAS code!
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            The in vitro micronucleus technique.

            M Fenech (2000)
            The study of DNA damage at the chromosome level is an essential part of genetic toxicology because chromosomal mutation is an important event in carcinogenesis. The micronucleus assays have emerged as one of the preferred methods for assessing chromosome damage because they enable both chromosome loss and chromosome breakage to be measured reliably. Because micronuclei can only be expressed in cells that complete nuclear division a special method was developed that identifies such cells by their binucleate appearance when blocked from performing cytokinesis by cytochalasin-B (Cyt-B), a microfilament-assembly inhibitor. The cytokinesis-block micronucleus (CBMN) assay allows better precision because the data obtained are not confounded by altered cell division kinetics caused by cytotoxicity of agents tested or sub-optimal cell culture conditions. The method is now applied to various cell types for population monitoring of genetic damage, screening of chemicals for genotoxic potential and for specific purposes such as the prediction of the radiosensitivity of tumours and the inter-individual variation in radiosensitivity. In its current basic form the CBMN assay can provide, using simple morphological criteria, the following measures of genotoxicity and cytotoxicity: chromosome breakage, chromosome loss, chromosome rearrangement (nucleoplasmic bridges), cell division inhibition, necrosis and apoptosis. The cytosine-arabinoside modification of the CBMN assay allows for measurement of excision repairable lesions. The use of molecular probes enables chromosome loss to be distinguished from chromosome breakage and importantly non-disjunction in non-micronucleated binucleated cells can be efficiently measured. The in vitro CBMN technique, therefore, provides multiple and complementary measures of genotoxicity and cytotoxicity which can be achieved with relative ease within one system. The basic principles and methods (including detailed scoring criteria for all the genotoxicity and cytotoxicity end-points) of the CBMN assay are described and areas for future development identified.
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              Adaptive response of human lymphocytes to low concentrations of radioactive thymidine.

              When human lymphocytes were cultured with [3H]thymidine, which acts as a source of low-level chronic radiation, and then exposed to 150 rad of x-rays at 5, 7, 9, or 11 hours before fixation, the yield of chromatid aberrations was less than the sum of the yields of aberrations induced by [3H]thymidine and x-rays separately. Often fewer aberrations were found after exposure to radiation from both sources than were found after exposure to x-rays alone. At the same fixation times, nonradioactive thymidine did not affect the yield of x-ray-induced aberrations. The same phenomenon occurred at earlier fixation times, after exposure to 30 or 40 rad of x-rays and [3H]thymidine. This response is analogous to the adaptive response to alkylating agents whereby prior treatment with small doses for a long period reduces the damage occurring from large doses of similar agents given for a short time.
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                Author and article information

                Journal
                J Radiat Res
                J. Radiat. Res
                jrr
                jrr
                Journal of Radiation Research
                Oxford University Press
                0449-3060
                1349-9157
                March 2014
                26 August 2013
                26 August 2013
                : 55
                : 2
                : 210-217
                Affiliations
                [1 ]CNR – Institute for Electromagnetic Sensing of the Environment, via Diocleziano 328, 80124, Napoli, Italy
                [2 ]National Institute of Nuclear Physics, Section of Napoli, via Cintia, 80126, Napoli, Italy
                [3 ]Department of Physics, University of Naples Federico II, CMSA via Cintia, 80126, Napoli, Italy
                [4 ]Centre of Radioprotection and Health Physics, University of Naples Federico II, via Cintia, 80126, Napoli, Italy
                [5 ]Department of Radiology, University of Texas Health Science Centre, 7703 Floyd Curl Drive – MC 7800, San Antonio, TX 78229-3900, USA
                Author notes
                [* ]Corresponding author: CNR-Institute for Electromagnetic Sensing of Environment, via Diocleziano, 328, 80124 Naples, Italy. Tel: +39-081-762-0659; Fax: +39-081-570-5734. Email: scarfi.mr@ 123456irea.cnr.it
                Article
                rrt106
                10.1093/jrr/rrt106
                3951069
                23979077
                cf69e642-7289-4103-aa05-b7907e45427d
                © The Author 2013. Published by Oxford University Press on behalf of The Japan Radiation Research Society and Japanese Society for Therapeutic Radiology and Oncology.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/3.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 21 May 2013
                : 25 July 2013
                : 27 July 2013
                Page count
                Pages: 8
                Categories
                Biology

                Oncology & Radiotherapy
                radiofrequency,adaptive response,micronucleus,x-rays,human lymphocytes
                Oncology & Radiotherapy
                radiofrequency, adaptive response, micronucleus, x-rays, human lymphocytes

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