AI Article Synopsis

  • This study investigates how low doses of X-ray radiation can protect fetal mice from teratogenic effects caused by higher-energy irradiations like accelerated heavy ions.
  • It was found that a low dose of X-rays significantly reduced issues like fetal death and malformations when followed by high doses of X-ray or heavy ion exposure.
  • The variability in adaptive response effectiveness was related to the type of radiation and its linear energy transfer (LET) value, highlighting the complexity of radiation effects on fetal development.

Article Abstract

Background: Adaptive response (AR) of low linear energy transfer (LET) irradiations for protection against teratogenesis induced by high LET irradiations is not well documented. In this study, induction of AR by X-rays against teratogenesis induced by accelerated heavy ions was examined in fetal mice.

Methods: Irradiations of pregnant C57BL/6J mice were performed by delivering a priming low dose from X-rays at 0.05 or 0.30 Gy on gestation day 11 followed one day later by a challenge high dose from either X-rays or accelerated heavy ions. Monoenergetic beams of carbon, neon, silicon, and iron with the LET values of about 15, 30, 55, and 200 keV/μm, respectively, were examined. Significant suppression of teratogenic effects (fetal death, malformation of live fetuses, or low body weight) was used as the endpoint for judgment of a successful AR induction.

Results: Existence of AR induced by low-LET X-rays against teratogenic effect induced by high-LET accelerated heavy ions was demonstrated. The priming low dose of X-rays significantly reduced the occurrence of prenatal fetal death, malformation, and/or low body weight induced by the challenge high dose from either X-rays or accelerated heavy ions of carbon, neon or silicon but not iron particles.

Conclusions: Successful AR induction appears to be a radiation quality event, depending on the LET value and/or the particle species of the challenge irradiations. These findings would provide a new insight into the study on radiation-induced AR in utero.

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http://dx.doi.org/10.1002/bdrb.21027DOI Listing

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