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Cytogenetical Studies on Biological Effects of Low Dose (Rate) Radiation

https://repo.qst.go.jp/records/60656
https://repo.qst.go.jp/records/60656
f5788011-86be-4bda-bc2a-58bb996aa051
Item type 会議発表用資料 / Presentation(1)
公開日 2004-11-12
タイトル
タイトル Cytogenetical Studies on Biological Effects of Low Dose (Rate) Radiation
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 Hayata, Isamu

× Hayata, Isamu

WEKO 601511

Hayata, Isamu

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Yoshida, Mitsuaki

× Yoshida, Mitsuaki

WEKO 601512

Yoshida, Mitsuaki

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Kanda, Reiko

× Kanda, Reiko

WEKO 601513

Kanda, Reiko

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Bing, Wang

× Bing, Wang

WEKO 601514

Bing, Wang

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Minamihisamatsu, Masako

× Minamihisamatsu, Masako

WEKO 601515

Minamihisamatsu, Masako

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Akiyma, Miho

× Akiyma, Miho

WEKO 601516

Akiyma, Miho

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Vares, Guillaume

× Vares, Guillaume

WEKO 601517

Vares, Guillaume

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早田 勇

× 早田 勇

WEKO 601518

en 早田 勇

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吉田 光明

× 吉田 光明

WEKO 601519

en 吉田 光明

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神田 玲子

× 神田 玲子

WEKO 601520

en 神田 玲子

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王 冰

× 王 冰

WEKO 601521

en 王 冰

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南久松 眞子

× 南久松 眞子

WEKO 601522

en 南久松 眞子

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穐山 美穂

× 穐山 美穂

WEKO 601523

en 穐山 美穂

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Guillaume Vares

× Guillaume Vares

WEKO 601524

en Guillaume Vares

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抄録
内容記述タイプ Abstract
内容記述 In this presentation I will first introduce the advantage of using human lymphocytes for the study of biological effects of low dose (rate) radiation, and the results of cytogenetical studies in high background radiation area (HBRA) we performed in the previous nuclear cross-over study. Then I will talk about our plan for the new nuclear cross-over study where we will investigate the biological effects of low dose of dose rate radiation in mouse.
When human peripheral lymphocytes are exposed to radiation or chemicals in vivo, their resultant chromosome aberrations are different. The former induces chromosome type aberrations involving both chromatids of chromosomes and the latter induces chromatid type aberrations involving only one of the two chromatids. At the metaphase stage in the first cell division cycle after exposure to those clastogens, these two kinds of aberrations show morphologically different features. But they become indistinguishable in the succeeding cell divisions, because the chromatid type rearrangement is copied on both chromatids to become chromosome type. If a cell has a dicentric (chromosome type aberration) accompanied by a fragment to be lost during cell division, the cell is considered in the first cell division cycle. Since most chemical mutagens induce chromatid type aberrations a dicentric accompanied by a fragment is an excellent marker of radiation exposures.
Dicentrics and translocations are induced in the human peripheral lymphocytes in about equal frequency by radiation(1). The former is unstable to be eliminated through cell division, while the latter is stable to be accumulated in the human body. A radiation induced translocation is not distinguished from a chemically induced translocation, and therefore translocations are the indicator of total effect of all kinds of clastogenic factors. Induction yield of a dicentric per cSv with X or gamma rays is reported to be 0.3 per 1000 cells in the human lymphocytes (2). If the average dose of exposure per year in human body is assumed to be 0.24 cSv (3), 4.68 dicentrics and 4.68 translocations per 1000 cells would be induced by radiation in the body in 65 years.
In the high background radiation area (HBRA) in the Guang-dong province of China where the level of natural radiation is three to five times higher than that in the control area (CA) (4), increase of the frequencies of dicentrics was found in the peripheral lymphocytes of the residents. But the increase of translocations in HBRA was within the range of individual variation in CA (5-7). The frequency of translocations was much higher than the expected value induced by the accumulated dose of radiation both in HBRA and CA. Smoking contributed to the induction of the chromosome aberrations more than the elevated natural radiation in those areas (8).
The targets of our research in the new nuclear cross-over study are as follows
A)The minimum radiation dose that can be detected by chromosome analysis in mouse.
B)Development of the methods to detect chromosome aberrations to be induced by radiation in comparison to those by all kinds of clastogens in mouse.
C)Adaptive response in the irradiated mouse fetus to be examined by chromosome analysis.
In mouse, turnover or cell division cycle of lymphocytes is shorter than that in human. Lymphocyte culture is not easy, and induction rates of dicentrics and translocations by radiation have not yet been extensively studied in mouse. The shape of mouse chromosomes is all acrocentrics, while the majority of human chromosomes are meta-or submetacentrics. It was reported that the morphology of chromosome influences the yield of dicentrics (1). Therefore, the ratio of dicentrics in comparison to translocations to be induced by radiation in mouse would not be the same as that of human. The life span of mouse is about 3 years, while that of human is about 80 years. Therefore, the background frequency of chromosome aberrations in the adult due to natural radiation would be much smaller in mouse than in human.
Thus mouse chromosome aberrations could be more sensitive biological indicator of man-made radiation exposures than human chromosome aberrations. We investigate chromosomes of the mice which are irradiated chronically at low dose or dose rate with or without a chemical mutagen in the new nuclear cross-over study.
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 International Workshop on Biological Responses to Low Dose Radiation
発表年月日
日付 2004-08-26
日付タイプ Issued
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