Astronauts are classified as radiation workers due to the presence of
ionizing radiation in space. For the assessment of health risks, physi
cal dosimetry has been indispensable. However, the change of the locat
ion of dosimeters on the crew members, the variation in dose rate with
location inside the spacecraft and the unknown biological effects of
microgravity can introduce significant uncertainties in estimating exp
osure. To circumvent such uncertainty, a study on the cytogenetic effe
cts of space radiation in human lymphocytes was proposed and conducted
for Mir-18, a 115-day mission. This study used fluorescence in situ h
ybridization (FISH) with whole-chromosome painting probes to score chr
omosomal exchanges and the Giemsa staining method to determine the fre
quency of dicentrics. The growth kinetics of cells and sister chromati
d exchanges (SCEs) were examined to ensure that chromosomal aberration
s were scored in the first mitosis and were induced primarily by space
radiation. Our results showed that the frequency of chromosomal aberr
ations increased significantly in postflight samples compared to sampl
es drawn prior to flight, and that the frequency of SCEs was similar f
or both pre- and postflight samples. Based on a dose-response curve fo
r preflight samples exposed to gamma rays, the absorbed dose received
by crew members during the mission was estimated to be about 14.75 cSv
. Because the absorbed dose measured by physical dosimeters is 5.2 cGy
for the entire mission, the RBE is about 2.8. (C) 1997 by Radiation R
esearch Society.