Purpose: To define the fractionation effect, including the magnitude and ki
netics of dose compensation, on days 3 and 8 after a single priming dose of
8 Gy.
Materials and methods: Graded radiation doses were given to the snouts of C
3H/Neu mice in 1 to 5 fractions within a time period of less than or equal
to 36 h, or in four fractions with intervals from 5 min to 4 h. Each protoc
ol was terminated by a top-up dose of 2.5 Gy to a 3 x 3 mm(2) test area in
order to precipitate the subclinical damage induced by the snout treatment
and to generate the full dose response.
Results: No significant increase in isoeffective dose by increasing Fractio
n numbers or by increasing interfraction intervals could be detected at eac
h time point after the priming treatment. This indicates that the effect of
dose fractionation was entirely lost.
Conclusions: The loss of fractionation effect may be interpreted as a subst
antial impairment of the processes underlying recovery from sublethal damag
e as a consequence of a repopulation-inducing priming dose given 3 days or
8 days in advance.