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Radiation exposure at early stage of life

https://repo.qst.go.jp/records/70318
https://repo.qst.go.jp/records/70318
bf1d7fc2-8eae-41cb-9e7f-09e79cb51e34
Item type 会議発表用資料 / Presentation(1)
公開日 2010-11-12
タイトル
タイトル Radiation exposure at early stage of life
言語
言語 eng
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_c94f
資源タイプ conference object
アクセス権
アクセス権 metadata only access
アクセス権URI http://purl.org/coar/access_right/c_14cb
著者 Shimada, Yoshiya

× Shimada, Yoshiya

WEKO 690457

Shimada, Yoshiya

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Nishimura, Mayumi

× Nishimura, Mayumi

WEKO 690458

Nishimura, Mayumi

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Imaoka, Tatsuhiko

× Imaoka, Tatsuhiko

WEKO 690459

Imaoka, Tatsuhiko

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Kakinuma, Shizuko

× Kakinuma, Shizuko

WEKO 690460

Kakinuma, Shizuko

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Takabatake, Takashi

× Takabatake, Takashi

WEKO 690461

Takabatake, Takashi

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Shang, Yi

× Shang, Yi

WEKO 690462

Shang, Yi

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Amasaki, Yoshiko

× Amasaki, Yoshiko

WEKO 690463

Amasaki, Yoshiko

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Hirano, Shinobu

× Hirano, Shinobu

WEKO 690464

Hirano, Shinobu

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Yamada, Yutaka

× Yamada, Yutaka

WEKO 690465

Yamada, Yutaka

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Takeda, Shino

× Takeda, Shino

WEKO 690466

Takeda, Shino

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島田 義也

× 島田 義也

WEKO 690467

en 島田 義也

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西村 まゆみ

× 西村 まゆみ

WEKO 690468

en 西村 まゆみ

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今岡 達彦

× 今岡 達彦

WEKO 690469

en 今岡 達彦

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柿沼 志津子

× 柿沼 志津子

WEKO 690470

en 柿沼 志津子

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高畠 貴志

× 高畠 貴志

WEKO 690471

en 高畠 貴志

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尚 奕

× 尚 奕

WEKO 690472

en 尚 奕

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甘崎 佳子

× 甘崎 佳子

WEKO 690473

en 甘崎 佳子

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坂入 しのぶ

× 坂入 しのぶ

WEKO 690474

en 坂入 しのぶ

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山田 裕

× 山田 裕

WEKO 690475

en 山田 裕

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武田 志乃

× 武田 志乃

WEKO 690476

en 武田 志乃

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抄録
内容記述タイプ Abstract
内容記述 Given both the established vulnerability of children to ionizing radiation and a progressive increase in the use of medical radiation, understanding the relationship between children's health outcome and radiation exposure is critical for our children's wellbeing. These conditions have forced the radiation-regulatory bodies to draft global initiatives on radiation protection for children. In order to obtain the parameters of radiation protection for children, we have studied the effect of gamma-rays, X-rays, neutrons and heavy ions on cancer induction and lifespan shortening of fetuses and children. Final goals of this research group are to propose age-weighting factors and relative biological effectiveness (RBE) of neutrons and heavy ions for fetuses and children for radiation protection.
(1) Lifespan shortening
Female and male B6C3F1 mice, which have been used in a wide variety of toxicological studies, were exposed to gamma rays (137Cs), carbon ions (energy, 290 MeV/u; LET, 13 keV/um) and neutrons (energy, 2 MeV) at various ages during fetal to mature adulthood periods. The ages examined were pre-implantation, major organogenesis, late fetal, neonatal, prepubertal, post-pubertal and mature adult stages. Male mice at the neonatal stage were more sensitive than those at the adult stage. Surprisingly, irradiation at the late fetal stage had little influence on lifespan shortening for both genders. Irradiation with carbon ions at the adult stage shortened the lifespan to a similar extent as that with gamma-rays, suggesting a small RBE of carbon ions. Carbon ions were more potent, however, in reducing lifespan than gamma rays when fetal and neonatal mice were exposed.
(2) Cancer induction
Radiation risks are dependent upon both tissue types and the age at exposure. Breast is one of the most susceptible organs to radiation-associated cancer risk. The data suggest that gamma irradiation at prepubertal stage at 1 Gy resulted in the highest incidence of mammary carcinomas than other stages. On the other hand, the dose-effect relationship of lung tumors did not change much depending on the age at irradiation.
The age effect on tumor development of kidney, brain (medulloblastoma), intestine, and lymphoid organ (thymus) was examined using mutant and genetically engineered animals of human cancer models. Peri-natal and infant stages were the most sensitive to the development of tumors of kidney and brain in Eker rats and Ptch1+/- mice, respectively. Brain tumors developed in a dose-dependent fashion with considerable effects even at a low dose of 100 mGy. We found intra-chromosomal deletions at Ptch1 locus in radiation-induced tumors, which was not observed in spontaneous tumors. This molecular change enabled us to identify the radiation-induced tumors even at a low dose as low as 50 mGy. Irradiation at the infant stage induced more intestinal tumors in ApcMin/+ mice than that at the adult stage, and the second hit event was, again, intra-chromosomal deletions. The incidence of T-cell lymphomas was the highest in Mlh1-/- mice exposed at infant stage, but the late fetal mice were unexpectedly resistant. In the lymphomas from Mlh1-/- mice, the frequent frame shift mutations at mononucleotide repeat sequences in Ikaros were observed.
(3) Uranium
Health effects for children in depleted uranium-polluted areas and uranium mining areas are of recent concerns. Uranium and its compounds have the potential to cause nephrotoxicity. We found that elimination of uranium was delayed in neonates than adults, and that rapidly growing S3 segments during infant period re-accumulated the uranium, thereby resulting in persistent apoptotic figures observed.
\n In conclusion, peri- and post-natal ages are the most susceptible for radiation carcinogenesis.
会議概要(会議名, 開催地, 会期, 主催者等)
内容記述タイプ Other
内容記述 NIRS-Workshop as an IAEA Collaborating Centre
発表年月日
日付 2010-11-12
日付タイプ Issued
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