Spontaneous rate of sister chromatid exchanges (SCEs) and BrdU dose-response relationships in mitotic chromosomes of goat (Capra hircus L.).

The spontaneous level of sister chromatid exchange (SCEs) in the goat, estimated by exposing peripheral blood lymphocytes to 0.1 pg/ml of 5-bromodeoxyuridine (BrdU), was 3.28 k 1.71 SCE/cell, 1.64 SCE/cell generation and 0.027 SCE/chromosome. The dose-response curve of SCE/cell, observed by exposing the cells to 0.1, 0.25, 0.5, 1.0, 2.5, and 5.0 pg/ml of BrdU, rose rapidly from 0.1 to 0.5 pg/ml, remained fairly stable from 0.5 to 1.0 pg/ml and rose less rapidly from 1.0 to 5.0 pg/ml of BrdU. The frequency distribution of sister chromatid exchanges/cell and that of chromosomes showing various number of exchanges followed the Poisson probability at all BrdU levels; only at 5.0 pg/ml of BrdU was the fit found on the border of the 5 % probability level. The usefulness of determining the spontaneous level of SCE/cell in domestic animals is discussed in relation to its possible application for a more precise evaluation of the genotoxic effects of environmental pollutants. Din0 Di Berurdino, Departmeni of Animal Science, Via Universira 133, 80055 Portici-Napoli, ital

Genotoxicity of radiofrequency electromagnetic fields: Protocol for a systematic review of in vitro studies.

Abstract Background Exposure to radiofrequency electromagnetic fields (RF-EMF, 100 kHz – 300 GHz) emitted by wireless communication technologies is pervasive and ubiquitous. Concern has been raised about possible adverse effects to human health. In 2011 the International Agency for Research on Cancer has classified RF-EMF as possibly carcinogenic to humans, highlighting that the evidence is weak and far from conclusive. Updated systematic reviews of the scientific literature on this topic are lacking, especially for mechanistic studies. Objectives To develop a protocol for a systematic review of experimental studies investigating genotoxic effects induced by RF-EMF in in vitro cellular models. Genotoxicity is one of the key-biological indicators of carcinogenicity, and the most common characteristics of established carcinogens. The predefined procedures for conducting the systematic review are outlined below. Methods We will follow the guidelines developed by the National Toxicology Program-Office of Health Assessment and Translation (NTP-OHAT), adapted to the evaluation of in vitro studies. Eligibility criteria We will include experimental in vitro studies addressing the relationship between controlled exposures to RF-EMF and genotoxicity in mammalian cells only. Eligibility for inclusion will be further restricted to peer reviewed articles reporting findings from primary studies. Information sources We will search the scientific literature databases NCBI PubMed, Web of Science, and EMF-Portal. No filter on publication date will be applied. Only studies published in English will be considered. The reference lists of the included papers and available reviews will be screened for unidentified relevant papers. References will be managed through Endnote X9 software. Data extraction and synthesis of results Data from included papers will be extracted according to predefined forms. Heterogeneity within the available evidence will determine the type of evidence synthesis that is appropriate. Findings will be summarized in tables, graphical displays and in a narrative synthesis of the available evidences. A meta-analysis will be carried out if subgroups of studies homogeneous in terms of exposure characteristics, endpoint, and cell types will be identified. Risk of bias The internal validity of included studies will be assessed using the NTP-OHAT Risk of Bias Rating Tool for animal studies, adapted to in vitro studies. This stage of the process will be managed through the Health Assessment Workspace Collaborative (HAWC). Evidence appraisal To rate confidence in the body of evidence, we will use the OHAT GRADE-based approach for animal studies. Framework and funding This protocol concerns one of the evidence streams considered in a larger systematic review of the scientific literature on the potential carcinogenicity of RF-EMF, performed by scientists from several Italian public research agencies. The project is supported by the Italian Workers' Compensation Authority (INAIL) in the framework of the CRA with the Istituto Superiore di Sanita "BRiC 2018/06 – Scientific evidence on the carcinogenicity of radiofrequency electromagnetic fields"

Spontaneous rate of sister chromatid exchanges (SCEs) in mitotic chromosomes of sheep (Ovis aries L.) and comparison with cattle (Bos taurus L.), goat (Capra hircus L.) and river buffalo (Bubalus bubalis L.).

The spontaneous level of sister chromatid exchanges (SCEs) in the sheep, estimated by exposing peripheral blood lymphocytes in 0.1 microgram/ml of 5'-bromodeoxyuridine (BrdU), was 4.08 +/- 2.47 SCE/cell, 2.04 SCE/cell cycle, 0.038 SCE/chromosome. The dose-response relationships, observed by exposing the cells to 0.1, 0.25, 0.5, 1.0, 2.5, and 5.0 micrograms/ml of BrdU, rose rapidly from 0.1 to 0.25 microgram/ml, and less rapidly at higher concentrations, thus reaching a saturation level. The analysis of variance, performed on the square root transformed data at 0.1 and 5 micrograms/ml of BrdU, indicated significant differences (P < 0.001) among the four donors tested. The distribution of the SCE/cell frequencies in the cell population of the four donors followed the Poisson 'mixture' probability function, thus confirming previous findings. The spontaneous rate of SCE/cell of sheep is compared with those previously reported for cattle, goat and river buffalo. The theoretical and practical implications of the spontaneous sister chromatid exchanges are discussed in relation to their possible use in animal production for (a) better genetic evaluation of the breeding animals under selection, (b) more precise monitoring of the genotoxic effects of environmental pollutants

DNA Electrophoretic Migration Patterns Change after Exposure of Jurkat Cells to a Single Intense Nanosecond Electric Pulse

Intense nanosecond pulsed electric fields (nsPEFs) interact with cellular membranes and intracellular structures. Investigating how cells respond to nanosecond pulses is essential for a) development of biomedical applications of nsPEFs, including cancer therapy, and b) better understanding of the mechanisms underlying such bioelectrical effects. In this work, we explored relatively mild exposure conditions to provide insight into weak, reversible effects, laying a foundation for a better understanding of the interaction mechanisms and kinetics underlying nsPEF bio-effects. In particular, we report changes in the nucleus of Jurkat cells (human lymphoblastoid T cells) exposed to single pulses of 60 ns duration and 1.0, 1.5 and 2.5 MV/m amplitudes, which do not affect cell growth and viability. A dose-dependent reduction in alkaline comet-assayed DNA migration is observed immediately after nsPEF exposure, accompanied by permeabilization of the plasma membrane (YO-PRO-1 uptake). Comet assay profiles return to normal within 60 minutes after pulse delivery at the highest pulse amplitude tested, indicating that our exposure protocol affects the nucleus, modifying DNA electrophoretic migration patterns