6
Minchenko et al. / International Journal of Radiation Medicine 2001, 3 (3-4): 106-117 3apel{JWR 1O.1v1., A6pClJ1106 B1O. HOBbIe aHTl1re- HbI TKaHeBOH COBMeCTI1MOCTHL1eJIOBeKa.Me,[lI1I.:(I1- Ha, MocKBa, 1986, 174 c. [Zaretskaya Yzl.ll1., Abramou VYzI. New Antigenes of Hu- man Tissue Compatibility. Meditsina Publishing House, ivloscow, 1986, 174 p.] H6axJ-teJ-tlcoAI AIIropHTMbI MeTO,[la rpyrrnoBo- ro )"-IeTa apryMeHToB npl1 HenpepbIBHbIX 116l1Hap- HbIX npH3HaKax. TIpenpl1HT AH YKpaI1HbI, Kl1eB, 1992. [IuakbnenkoA. G. Algori thms of Methods of Group Account of Arguments at Unceasing and BinalY Signs. Preprint, Academy of Sciences of Ukraine, Kiev, 1992]. H6axJ-teHlCO AI, 3au1.£eJ-tJCo fO.fl., JI.uMum- p06 B,l1,. TIpHH5!Tl1e peIlleI-IHH Ha OCHOBe caMOOp- raHl13aI.:(HH. COBeTCKoe pa,[lHO, MocKBa, 1976,21 C. [IuakbnenkoA. G., Zaycbenko YlI.P., Dimitrou YD. Decision Making on the Base of Self-organization. Soviet Radio Pub- lishing House, Moscow, 1976,21 p.] MuJ-t1.£eJ-lJCO JK.H. feHeTI1L1eCKHe CHCTeMbI KpO- BH L1eJIOBeKa npH pa,[lHaI.:(110HHOM 06JIYLleHHH. JJ:I1CC.... ~\OK.6HOJI. HayK, Kl1eB, HI1I1 reMaTOJIOrl1H H nepeJII1BaH!15! KpOBH M3 YKpaI1HbI, 1995,326 C. . [Mincbenko].N. Genetic Blood Systems at Exposure to Radiation. Dissertation of Doctor of Biological Sciences, Kiev, Research Institute for Haematology and Blood Trans- fusion, 1995, 326 p.]. MuJ-t1.£eJ-tlco JK.H., JIecpmep A.B., KaJluJ-tu1.£eJ-tJCo c.E. I1HTerpl1pOBaHHa5! cpe,[la.[(JI5! CTaTHCTI1L1eCKOH 06pa60TKH 3KcnepHMeHTaJIbHbIX ,[IaHHbIX MeTO,[la- MI1 nonyJI5!I.:(HOHHOH CTaTI1CTHKH MEDSTAT. B KH.: TIporpaMHble npo,[IyKTbI YKpal1Hbl. KaTaJIOr, 1994, BbII1. 2, C. 34-35. [Mincbenko}.N., LejrerA. v, KalinclJenkoS.B. Integrated En- vironment for Statistical Processing of Experimental Data with Methods of Population Statistics MEDSTAT.Catalogue «Software of Ukraine·>, 1994, Issue 2, pp. 34-35.] ne6J-tUl{JCUUJIA. CTaTI1CTHLleCKa5! OI.:(eHKa aCCOI.:(l1a- I.:(I1HHLA-aHTl1reHOB C 3a60JIeBaHH5!MH. BeCTH. AMH CCCP, 1988,7: 48-51. [Peunitsky L.A. Statistical evaluation of associations of I-ILA-anti- gens with diseases. Vest. AMN SSSR, 1988,7: 48-51] np02paMMbt npRMo2o CUJ-tme3aMooeneu (no npl1H- I.:(l1nycaMoopraHH3aI.:(I1H).I1HCTI1TyT KH6epHeTHKH, KHeB, BbII1. 1-3, 1975. [Programmes oj Direct Syntheses oJ Models (on the principle of self-organisation). Institute of Cybernetics, Kiev, Issues. 1-3, 1975] CmenaJ-t06a E.M. TIpOrH0311pOBaHI1e 3,[10pOBb5!l1eTeH paHHero B03paCTa. 113,[1aTeJIbCTBOTOMcKoro yHI1BepCH- TeTa, TOMCK, 1987, 156 C. [Stepanoua E.I. Health Forecasting in Children of Early Age. The Publishers of Tomsk University, Tomsk, 1987, 156 p.] Wa6anuJ-t BH., Cepo6aJI,ll,. MI1HWIeCKa5! HMlVryHO- reMaTOJIOfl15!. Mel1l1I.:(I1Ha,JIeHI1Hrpa,[l, 1988, 310 c. [SlJahaljn VN., SerouaL.D. Clinical Immunohaematology, Medit- sina Publishing House, Leningrad, 1988, 310 p,] BebeslJko VG., MinclJenkoj.N. Immunogenetic blood factors in ARS patients. In.: Proceedings of the European Federation ofImmunological Societies. 10th Meeting, 10- 12 September 1990, Edinburgh, 1990, pp. 3-11. Kissmeyer-Nielsen F, SvejegaardA., Hauge M. Gene- tics of the human HLA transplantation system. Nature, 1968, 219(159): 1116-1119. Mattiuz PL., Inde D, PiazzaA. et al. Histocompatibil- ityTesting. Copenhagen, 1970, pp. 193-205. MinclJenkoj. (,MEDSTAT·>. Catalogue of Exhibitors & Their Production in the Ukrainan Stand of the Innovation Forum, Kyiv, 1995, pp. 74-75. Simons M., Tait B (Eds.) Detection of immune-associ- ated genetic markers of human disease. Churchill living- stone, London, 1984. Svejgaard A., Hauge M., ]ersild C. The HLA System: Monographs in Human Genetics. Basel. 1975, vol. 7, pp.127-134. w 5" ~ w 7- J,. :JJ Q) Co - a' t... :JJ S S CD "TI Co -..I N 0 ..• ~~F;: 'Rr,,1 1i:is :oan to: C.'\S . ':-\! RiVt'f lie1. 01-l4.32lO··0012 117

v,cricket.biol.sc.edu/papers/chernobyl/stepanova misharina...Stepanova, Misharina / International Journal of Radiation Medicine 2001, 3 (3-4): 118-122 One of the most effective methods,

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Page 1: v,cricket.biol.sc.edu/papers/chernobyl/stepanova misharina...Stepanova, Misharina / International Journal of Radiation Medicine 2001, 3 (3-4): 118-122 One of the most effective methods,

Minchenko et al. / International Journal of Radiation Medicine 2001, 3 (3-4): 106-117

3apel{JWR 1O.1v1.,A6pClJ1106B1O. HOBbIe aHTl1re­HbI TKaHeBOH COBMeCTI1MOCTHL1eJIOBeKa.Me,[lI1I.:(I1­Ha, MocKBa, 1986, 174 c.[Zaretskaya Yzl.ll1., Abramou VYzI. New Antigenes of Hu­man Tissue Compatibility. Meditsina Publishing House,ivloscow, 1986, 174 p.]

H6axJ-teJ-tlcoAI AIIropHTMbI MeTO,[la rpyrrnoBo­ro )"-IeTa apryMeHToB npl1 HenpepbIBHbIX 116l1Hap­HbIX npH3HaKax. TIpenpl1HT AH YKpaI1HbI, Kl1eB,1992.[IuakbnenkoA. G. Algori thms of Methods of Group Accountof Arguments at Unceasing and BinalY Signs. Preprint,Academy of Sciences of Ukraine, Kiev, 1992].

H6axJ-teHlCO AI, 3au1.£eJ-tJCofO.fl., JI.uMum­p06 B,l1,. TIpHH5!Tl1e peIlleI-IHH Ha OCHOBe caMOOp­raHl13aI.:(HH. COBeTCKoe pa,[lHO, MocKBa, 1976,21 C.[IuakbnenkoA. G., Zaycbenko YlI.P., Dimitrou YD. DecisionMaking on the Base of Self-organization. Soviet Radio Pub­lishing House, Moscow, 1976,21 p.]

MuJ-t1.£eJ-lJCOJK.H. feHeTI1L1eCKHe CHCTeMbI KpO­BH L1eJIOBeKa npH pa,[lHaI.:(110HHOM 06JIYLleHHH.JJ:I1CC.... ~\OK.6HOJI. HayK, Kl1eB, HI1I1 reMaTOJIOrl1HH nepeJII1BaH!15! KpOBH M3 YKpaI1HbI, 1995,326 C.

. [Mincbenko].N. Genetic Blood Systems at Exposure toRadiation. Dissertation of Doctor of Biological Sciences,Kiev, Research Institute for Haematology and Blood Trans­fusion, 1995, 326 p.].

MuJ-t1.£eJ-tlcoJK.H., JIecpmep A.B., KaJluJ-tu1.£eJ-tJCoc.E. I1HTerpl1pOBaHHa5! cpe,[la.[(JI5! CTaTHCTI1L1eCKOH06pa60TKH 3KcnepHMeHTaJIbHbIX ,[IaHHbIX MeTO,[la­MI1 nonyJI5!I.:(HOHHOH CTaTI1CTHKH MEDSTAT. B KH.:

TIporpaMHble npo,[IyKTbI YKpal1Hbl. KaTaJIOr, 1994,BbII1.2, C. 34-35.[Mincbenko}.N., LejrerA. v, KalinclJenkoS.B. Integrated En­vironment for Statistical Processing of Experimental Datawith Methods of Population Statistics MEDSTAT.Catalogue«Software of Ukraine·>, 1994, Issue 2, pp. 34-35.]

ne6J-tUl{JCUUJIA. CTaTI1CTHLleCKa5! OI.:(eHKa aCCOI.:(l1a­I.:(I1HHLA-aHTl1reHOB C 3a60JIeBaHH5!MH. BeCTH. AMHCCCP, 1988,7: 48-51.[Peunitsky L.A. Statistical evaluation of associations of I-ILA-anti­gens with diseases. Vest. AMN SSSR, 1988,7: 48-51]

np02paMMbt npRMo2o CUJ-tme3aMooeneu (no npl1H­I.:(l1nycaMoopraHH3aI.:(I1H).I1HCTI1TyT KH6epHeTHKH, KHeB,BbII1.1-3, 1975.[Programmes oj Direct Syntheses oJ Models (on the principle ofself-organisation). Institute of Cybernetics, Kiev, Issues. 1-3, 1975]

CmenaJ-t06a E.M. TIpOrH0311pOBaHI1e 3,[10pOBb5!l1eTeHpaHHero B03paCTa. 113,[1aTeJIbCTBOTOMcKoro yHI1BepCH­TeTa, TOMCK, 1987, 156 C.[Stepanoua E.I. Health Forecasting in Children of Early Age. ThePublishers of Tomsk University, Tomsk, 1987, 156 p.]

Wa6anuJ-t BH., Cepo6aJI,ll,. MI1HWIeCKa5! HMlVryHO­reMaTOJIOfl15!. Mel1l1I.:(I1Ha,JIeHI1Hrpa,[l, 1988, 310 c.[SlJahaljn VN., SerouaL.D. Clinical Immunohaematology, Medit­sina Publishing House, Leningrad, 1988, 310 p,]

BebeslJko VG., MinclJenkoj.N. Immunogenetic bloodfactors in ARS patients. In.: Proceedings of the EuropeanFederation ofImmunological Societies. 10th Meeting, 10­12 September 1990, Edinburgh, 1990, pp. 3-11.

Kissmeyer-Nielsen F, SvejegaardA., Hauge M. Gene­tics of the human HLA transplantation system. Nature,1968, 219(159): 1116-1119.

Mattiuz PL., Inde D, PiazzaA. et al. Histocompatibil­ityTesting. Copenhagen, 1970, pp. 193-205.

MinclJenkoj. (,MEDSTAT·>. Catalogue of Exhibitors &Their Production in the Ukrainan Stand of the Innovation

Forum, Kyiv, 1995, pp. 74-75.Simons M., Tait B (Eds.) Detection of immune-associ­

ated genetic markers of human disease. Churchill living­stone, London, 1984.

Svejgaard A., Hauge M., ]ersild C. The HLA System:Monographs in Human Genetics. Basel. 1975, vol. 7,pp.127-134.

w 5"~w7-

J,. :JJQ)Co- a't... •

:JJ SS CD"TI Co-..I

N

00..•

~~F;:'Rr,,1 1i:is :oan to: C.'\S

. ':-\! RiVt'f lie1.

01-l4.32lO··0012

117

Page 2: v,cricket.biol.sc.edu/papers/chernobyl/stepanova misharina...Stepanova, Misharina / International Journal of Radiation Medicine 2001, 3 (3-4): 118-122 One of the most effective methods,

Stepanova, Misharina / International Journal of Radiation Medicine 2001, 3 (3-4): 118-122

CYTOGENETICAL EFFECTS IN PERIPHERAL BLOOD LYMPHOCYTESAMONG CHILDREN IN REMOTE TERMS AFTER PRENATAL

IRRADIATION

UVlTorEHETVI\.IECKVlE 3CbCbEKTbiB J1V1MCbOUVjTAXnEPVlCbEPVI\.IECKO~KPOBVI AETE~ B OTAA11EHHbl~ nEPVlOA

nOCJ1E nPEHATAJ1bHOrO 05J1YLlEHVlS1

E.!. Stepanova,].A. MisharinaResearch Centre for Radiation Medicine, Academy of Medical Sciences of Ukraine.

\'VHO Collaborating Centre53 Melnikov Street, Kiev, 04050, Ukraine088511318

I111I111111111111111111111111111111111111111111111

~

E.H. CTeIIaHo~.a,)K.A. MnmapnHaHaY'lHbIH l\eHTp pa,l\l1al\110HIIOH Me,11I1l\I1HblAMH YKpal1l-lbl,

COTPY,l\HI1'lJIOIl\I1Hl\eHTp B0304050, YKpa}IHa, KHeB, YJI.MeJlbHI1KOBa,53

Abstract

Though the chromosome structural anomalies incidence elevation is marked in remote terms after the Cherno­

byl accident among children exposed to acute irradiation in prenatal period. Stable damage is prcvalent with

identified breaks preferred localisation in 1,2, 3, 5, 7, 11, 13, 17 chromosomes. Both stable and unstable induced

chromosome aberrations with 1,4,5,9, 17,22 chromosomes elevated damaging are observed in children ex­

posed to chronic radiation impact.

Keywords: children, prenatal irradiation, radiation Jeffect, aberration chromosomes.

INTRODUCTION

After the Chernobyl accident a cytogenetic exami­

nation of reprcsentatives of different categories

of the irradiated contingents, including children

population exposed to ionising radiation in the

different periods of ontogenesis, was carried outby native and foreign scientists (Stepanova E.!.,

1996). Using the data obtained, possibility of cy­

togenetic parameter usage as the most correct bio­logical indicator of human irradiation was con­

firmed, as well as necessity of further data storage

concerning frequencies, types and features ofhu­

man genome damage in the remote period of the

Chernobyl catastrophe was indicated (Pilins­kaya M. et a!., 1998).

As it is generally known the mutagenous effect in­

duced by ionising radiation in human somatic and

sex cells can cause some pathologic states with the

genetic component (including oncopathology and

haemoblastoses), therefore the frequency of chro­

mosome abnormalities in peripheral blood lym­phocytes is considered as one of criteria of in­

creased risk for the irradiated contingent.

Concerning this studies of small doses of ionisingradiation effect on a genome of somatic cells is now

represen ted as one of the most actual problems. An

assessment of the structural damages in chromo­somes, which are markers of radiation effect is of

the great importance.

118

BBE.II:EHHE

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(Stepanova El, 1996). TIOJIY'-IeHHblepe3YJIbTaThI IIO,[\TBepiK­,l\aIOT B03MOiKHOCTb HCnOJIb30BaHH5I lI,HTOrCHeTH'-IeCKHX

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nOBpeiK,l\eHH5I reHOMa 'Ie.rrOBeKa B OT,l\aJIeHHblr1 rrepHO,l\

LJepH06billbCK0r1 KanC'rpocpbI (Pilinskaya M. et a!., 1998).

KaK H3BeCTHO, MYTareHHblrI .3cpcpeKT, HI-I,[(ylI,HpoBaHIlbltt

HOHH3Hp)'IOIlJ,HMH31IY'-IcHHeMBCOMaTH'IeCKHXH nOJIOBbLX

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RC"tIRN i~;s :Jan to: C.~~

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?O. Gox 30;2, C,lumb"" 011432W.00121

Page 3: v,cricket.biol.sc.edu/papers/chernobyl/stepanova misharina...Stepanova, Misharina / International Journal of Radiation Medicine 2001, 3 (3-4): 118-122 One of the most effective methods,

Stepanova, Misharina / International Journal of Radiation Medicine 2001, 3 (3-4): 118-122

One of the most effective methods, permitting torealise a bio-indication of radiation effect, as well

as to identify the chromosomal nature of geneticaldisorders is the method of differentiated G-colour­

ing, which allows not only to reveal structural dam­ages, but also to establish a localisation of sites witha heightened chromosomal fragility (Ohtaki K.,

1992).

SUBJECTS AND METHODS

In remote period after the Chernobyl catastrophe42 children exposed to ionising radiation duringintrauterine development and 15 children of con­trol group were examined.

The first group consisted of 22 children, born bypreg­nant at moment of the accident who were evacuated

from Pripyat (they can be referred to the variant ofacute single according to the type of irradiation).

The second group included 20 children exposed toionising radiation as during intrauterine develop­ment, as further years of life (living in N arodichsk)'district of Zhitomir region);

The third group (control) consisted of 15 children(date of birth - 1986) living in «clear» regions ac­cording to the radiation conditions.

The equivalent radiation doses to foetal red bonemarrow during acute irradiation ranged from 10 to376 mSv, and during chronic irradiation of children,including the antenatal period - from 4.7 to 52 mSv

A cytogenetic examination conducted after thecomplex clinical examination and medicogenetic

consultation of nuclear proband family, both basicand control groups. Thus, diseases related to disor­ders of DNA repair and chromosome instabilitywere eliminated. For 3 months before examinationchildren did not suffer from diseases of virus infec­

tion, they were not under exposure to prophylac­tic inoculation, i.e. the majority of factors whichcould influence the results of cytogenetic analysiswere eliminated.

The complex clinical and cytogenetic examinationsof children of 10-12 years old were conducted.

For preparations of metaphase chromosomes to beobtained the heparinised blood was cultivated dueto standard semimicromethod in the nutrient me­

dium HAM'S F-l °«<Seromed», Germany), contain­

ing L-glutamine, with an addition of embryoniccalves serum «<Seromed», Germany) and phytohe­magglutinin (PHA-M, <·Difco>" USA) for48-50 hours(the last 2 hours - with a colchicine, <.Merk», Ger­

many). This allowed to analyse cells which weremainly presented in the first postradiation mitosis.

The preparations were obtained after hypotonictreatment (0.075 M solution KCl at temperature37 'C) and thrice-repeated fixing with ethanol and

O,lJ,HHMH3 HaH60JIee .3cpcpeKTHBHbIXMeTO,lJ,OB,KOTOpbIHrr03BOJI5IeToCYIl~eCTBJI5ITb6HOHH,lJ,HKaIJ;HlOpa,lJ,HaIJ;HOH­Horo B03,lJ,eHCTBillI,a TaIOKeH,lJ,eHTHcpHIJ;HpOBaTbXpOMO­COMHYJOrrpHpo,lJ,y reHeTH'-IeCKHX HapyrneHHH, 5IBJI5IeTC5IMeTO,lJ,,lJ,HcpcpepeHIJ;HpOBaHHoH G-oKpacKH, KOTOpbIHrr03BOJI5IeTHe TOJIbKOBbI5IBHTbCTPYKTYpHble rrOBpeJK,lJ,e­HillI, HO H YCTaHoBHTb JIOKaJIH3aL\HlOcaHToB rroBbIIlleH­HOH JIOMKOCTHXpOMOCOM (Ohtaki K., 1992).

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119

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Stepanova, Misharina / International Journal of Radiation Medicine 2001, 3 (3-4): 118-122

glacial acetic acid in ratio 3:1.For obtaining differen­tially G-coloured chromosomes the preparationswere dipped into Trypsin (2 S mg: 100 ml of distilledwater) for 4 seconds. To colouring Gimza's methodwas applied.

Cytogenetic analysis was carried out using a visualkaryotyping of individual chromosomes. Not lessthan 200 metaphases responding to necessary re­quirements were analysed in each examined pa­

tient. All the aberrations of chromosome (translo­cation, deletion, inversion, acentric fragments, di­centrics and ring chromosomes) and chromatid

(single fragments, exchanges) types (with the ex­ception of gaps) were taken into account.

RESULTS AND DISCUSSION

The results of cytogenetic examination of childrenof control group testify to that the mutation rate inthe somatic cells was at the population level. So, amean frequency of aberrant cells and chromosome

aberrations in group, showed through structuralabnormalities of both chromosome and chroma­

tid types, being identical was 2.71±0.61 %.The aber­rations of chromosome type were representedmainly by pair fragmcnts (0.57±0.23%) and anoma­lous monocentrics (mainly by terminal deletionswithout acentric fragments) (0.43±0.15%). Thenumber of aberrations with chromatid type was1.57±0.38%, which were represented only by singlefragments.

In children examined at the age of 10-11, whose redbone matTOW was inadiated during intrauterine de­velopment in doses from 10 to 376 mSv, the amountof the aberrant cells (8.66± 1.23%) and the mean fre­quency of chromosome aberrations (9.07±1.34%)exceeded parameters of the control (P<O.oS). Thus,the individual frequency of aberrant chromosomesranged from 2 up to 18.5 per 100 cells. In 17 childrenthe level of abenant cells exceeded 3%.The majorityof chromosome damages were represented by theabetTations of chromosome type (7.2±1.l7%), whilethe stable structural abnormalities (translocation, in­version, deletions) were registered in 21 children andconsisted of S.64±0.94%, that significantly exceededthe control parameters (P<O.OS). The unstable chro­mosome damages were registered with the frequen­cy of 1.43±0.3 S%and were mainly represented by pairfragments, dicentric and ring chromosomes, that canbe a consequence of abenation preservation of thistype aswell as in the founder cells, and in the fraction

of long-living peripheral lymphocytes.

The number of aberrations of chromatid type (sin­gle fragments and exchanges) was 2±0.2S% and itdid not differ from data on the children in control

group (P>O.OS).

In children exposed to ionising radiation as in periodof prenatal development as at further stages of onto­genesis (chronic type of irradiation) and with the

120

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Stepanova, Misharina / International Journal of Radiation Medicine 2001, 3 (3-4): 118-122

equivalent exposure dose to red bone marrow for all

the pedods from 4.7 up to S2mSv, the mean frequen­cy of the aberrant cells and chromosome aberrations

in groups was 7.1S±2.39% and 7.63±2.92% respectively

and exceeded parameters of the control (P<O.OS).

The individual frequency of aberrant metaphasesranged from 1.5% up to 21 %. Thus the level of aber­

rant cells exceeded 3% in 14 children. The majority

of the registered damages was represented byaber­rations of chromosome type and was 77%.

The mean group level of unstable markers of irra­

diation (dicentric and ring chromosomes) (1.75±0.25%) significantly exceeded the parameters of the

control (P<O.OS). The significant augmentation of

stable (4.23± 1.06%) chromosome damages (P<O.OS)was also marked. Translocations and inversions

were registered in 14 children of them. Their mean

group frequency was 0.73 per 100 cells and statisti­

cally significantly exceeded parameters of the con­trol. The level of deletions also significantly exceed­

ed parameters of the control (P<O.OS) and was

(3.38±0.87%). The terminal deletions were prevailedin a spectrum of deletion chromosomes.

The aberrations of chroma tide type were registered

with the frequency of 1.6S±0.2% and correspond­ed to control group (P>O.OS).

The determination of a damage degree in somebands during formation of stable and unstable aber­

rations allowed to establish the significant exceed­

ing of an amount of breakages in chromosomes ofexposed groups in comparison with the control.

The comparative analysis of point distribution inchromosome breakage has shown non-random al­

location of chromosome damages (proportional­ly to the chromosome length and DNA contents in

them). However, for the first group the preliminarylocalisation of the identified breakages is character­istic in 1,2,3, 5, 7, 11, 13, 17 chromosomes. Chro­

mosomes 6, 10, 15,21, X were less damaged.

The increased damage of 1,4, 5,9, 17,22 chromo­

somes was observed in the second group. in 6, 8,

10, 19,20 chromosomes the breakages were regis­tered less often. The localisation of the heightened

fragility fields, that is characteristic for both groups,

is shown in table. It is necessary to mark, that nodamages of Y chromosome were detected as in

main as in control groups.

The predominant localisation of break points wasmarked in euchromatin sites of chromosomes, where

it is registered about 90% of all damages is registered.

06lI)"-Iemrn) c 3KB11BaneillH0I1 ,0;0301106JlyqeI-IJ.rn KpaCI-IOfO

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121

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Stepan ova, Misharina / International Journal of Radiation Medicine 2001,3 (3-4): 118-122

For establishment of possible correlation between

the frequency, type of structural damages in chro­mosomes and equivalent exposure doses of red

bone marrow it was carried out correlation analy­sis. In children exposed to acute prenatal irradia­

tion in the dose range from 10 up to 376 mSv the

availability of authentic correlation connection

between the frequency of aberrant cells (r=0.34),chromosome aberrations (r=0.39), as well as stable

chromosome damages of the apparatus (r=0.33)and equivalent exposure doses of red bone marrow

were established. Such dependencies were not es­

tablished in chronic type of irradiation to red bone

marrow in the range from 4.7 to 52 mSv.

Thus, in children exposed to acute prenatal irradi­

ation, the increase in the frequency of structural

chromosome anbnormalities with a predomina­

tion of stable damages and primary localisation ofthe identified breakages in 1, 2, 3, 5, 7, 11, 13, 17chromosomes is marked in remote terms after the

Chernobyl accident. In children exposed to chron­

ic irradiation the augmentation both stable and un­

stable induced chromosome aberation and height­ened damage of 1,4,5,9,17,22 chromosomes areobserved.

REFERENCES

Ohtaki KG-banding analysis of radiation-in­duced chromosome damage in lymphocytes of Hi­roshima A-bomb survivors. Jpn J Human Genet,1992, 37: 245- 262.

Pilinskaya M., Day R., rflald N. The cytogeneticconsequences of in children of continuosresidence

in towns contaminated by the Chernobyl accident(1986-1991): a methodological and epidemiolo-

122

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11.3KBI1BaJIeHTHbIMI1,l.103aMI106JTy'IeHI15I KpacHoro KOCT­Horo M03ra rrpOBe,l.1eH KOppeJI5I~I10HHbIH aHaJII13. Y ,l.1e­

TeH, rrO,l.1BeprIIII1XC5IoCTp0MY BHYTPHYTP06HOMY 06JTy'Ie­1-II1IOB W1arra30He ,l.103OT 10 ,l.10 376 M3B, YCTaHOBJIeHO

lIaJII1qI1e ,lJ;OCTOBepHoH KOppeJI5I~I10HHOH CB5I3I1Me~qaCTOTOH a6eppaHTHblx KJIeTOK (r=0,34), a6eppa~I1H

XpOMOCOM (r=0,39), TaK)Ke cTa6I1JIbHbIX rrOBpe)K)J;erII1HXpOMocoMHoro arrrrapaYa (r=0,33) 11 .3KBI1BaJIeHTHbIMl1

,lJ;03aMl106JTy'IeHl15I KpaCHoro KOCTHOrO M03ra. TIpl1 xpo­Hl1qeCKOM Tl1rre 06JTy'IeHl15I KpacHoro KOCTHoro M03ra,lJ;03aMI1B,l.1l1arra30He OT 4,7 ,lJ;052 M3B TaKlIX 3aBl1Cl1MOC­

TeH He YCTaHOBJIeHo.

TaKIIM 06pa30M, B OT,lJ;aJIeHHbIeCpOKlI rrOCJIe aBapl1l1 Ha

'LfA3C y ,l.1eTeH,nO,lJ;BeprIIIlIXC5IOCTp0MY BHYTPHYTP06HO-

. MY06JTy'IeHl1IO, OTMeQaeTC5I rrOBblIIIeHl1e QaCTOTbI ClPYK­TypHbIX aI-IOMaJIl1HXpOMOCOM C rrpeBaJIl1pOBaHl1eM CTa­6l1JIbHbIXnOBpe)K)J;emIH 11rrpel1MYIIIeCTBeHHOH JIOKaJI113a­

~l1eH I1,l.1eI-ITHcj:>l1~I1pOBaI-IHbIXp;13pbIBOB B 1, 2, 3, 5, 7, 11,

13-H 1117 -H XpOMOCOMax Y ,lJ;eT~H,nO,lJ;BeprIIIlIXC5IXPOHl1­QeCKoMY pa,z:J;I1a~I10I-IHoMYB03,lJ;eHCTBmO, Ha6mo,lJ;aeTC5I

YBeJIl1QeI-II1eKaK CTa6l1JIbHbIX, YaK 11HeCTa6l1JIbHbIX l1HAY­~l1pOBaHHbIX XpOMOCOMHbIX a6eppa~l1H 11nOBblIIIeHHa5I

rrOBpe)K)J;aeMOCTb 1,4, 5,9, 17 -H 1122-H XpOMOCOM.

gical report. In: AI. Nyagu, GN. Souchkevitch (Eds.) Pro­ceedings of the 2nd International Conference «Long-termHealth Consequences of the Chernobyl Disaster'>,]une 1­6, 1998, Kiev. Chernobylinterinform, Kiev, 1998, 115 p.

StepanovaE.1. Health condition of children irradiated

in utero. In: Proceedings of the International Conference

One Decade After Chernobyl. Summing up the Conse­quence of the Accident, Vienna, April 8-10, 1996, IAEAVienna, 1996, pp. 253-260.

RETt'RN t1~is ioan to: CAS

2'- 'W Ole:i:~i,gy RiVE-i nd.

?8. :.'0': 3G~2; ColumbuS, 0114::J2.1.O-0012