| Literature DB >> 28993937 |
Nailya Chaizhunusova1, Madina Madiyeva2, Kimio Tanaka3, Masaharu Hoshi4, Noriyuki Kawano4, Yoshihiro Noso5, Nobuo Takeichi5,6, Tolebay Rakhypbekov1, Nailya Urazalina1, Galina Dovgal1, Tamara Rymbaeva2, Sholpan Tokanova1, Meruert Beisengazina1, Kulypash Kembayeva1, Ken Inoue7.
Abstract
More than 400 nuclear explosion tests were conducted at the Semipalatinsk Nuclear Test Site (SNTS) and significant radioactive substances were released. The long-term consequences of the activities at the SNTS and the appearance of any hereditary effects remain insufficiently studied about 25 years after the test site was closed. The population living in villages near the SNTS are considered to have been heavily exposed to external and internal radiation. This study aims to perform an assessment and comprehensive cytogenetic analysis of the inhabitants living near the SNTS, and their first-(F1) and second-(F2) generation children. Residents of the East Kazakhstan region living in the area covered by the former SNTS were included in the study. To evaluate the hereditary effects of nuclear testing, comprehensive chromosome analyses were performed in lymphocytes using conventional Giemsa and fluorescent in situ hybridization methods in 115 F1 and F2 descendants in the villages of Dolon and Sarzhal, which were heavily contaminated. The parents of the subjects had permanently lived in the villages. A higher number of stable-type chromosome aberrations such as translocations was found in these residents than in 80 residents of the control area, Kokpecty, which indicates the possibility that radiation had biological effects on the exposed subjects.Entities:
Keywords: Chromosome aberrations; FISH method; Hereditary effects; Semipalatinsk Nuclear Test Site
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Year: 2017 PMID: 28993937 DOI: 10.1007/s00411-017-0717-2
Source DB: PubMed Journal: Radiat Environ Biophys ISSN: 0301-634X Impact factor: 1.925