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in the presenoe of specific inhibitors of cytochrome P-450 . In these eorditions, vanadyl<br />

genotwcicity renaiz>aa unaffected, while the presenoe of inhibitors determined an increase<br />

in mitotic yene conversion an3 point reverse mutation irr3uaed by vanadate . Therefore,<br />

tcrmooxygenase system cytochrome P-450 depertflent is probably involved in the vanaditm tretabolism<br />

reducirg vanadate, but not oxidating vanadyl ..<br />

183<br />

DIFFEREhTIAL MUTAGENIC RESPOOiSE CF A SYtVCi-ic .~l'IC pYR::THRCID, DELTAMETHR4tv,<br />

IN SUB-MAN:MALIAN AND MAMNALIAN TEST SYSTfVIS . G . G<strong>and</strong>hi, J .b . Chowt9'tury,<br />

P .K .Sareen <strong>and</strong> I .S .Grover, Scliool of Life Scit•aces,GNDU,Amritsar,India .<br />

Deltamethrin is one of the most commonly used pesticides in North<br />

India . Mence,•-tts genoto•ricity was studied for germ-cell mutagenesis in<br />

Dromvhil~ <strong>and</strong> for clastogenicity in the mouse bone-marrow !• :0 test . LM<br />

(solvent) exhibited mutation rates comparable to the norn :al control v luas<br />

while EMS elicited a positive response in all the test assays . il.iA<br />

were exposed to media containing varying concentrations of the insecticide<br />

(0 .2, 0 .4, 0 .6, 0 .8 <strong>and</strong> 1 .0 ppn) for the induction of dominant<br />

lethals . A steady but non-significant increase in lethality fr(m 32 .58:4<br />

at 0 .20 ppm to 5O .05X at 1 .00 ppm was ob served . Also none of the concentrations<br />

i nduced significa nt SLRLs (2 .45%) even at the highest eoncent ration<br />

tested (0 .80 pgo) . Cytogenetic damage in mice was screened for three<br />

ip administered doses (32 .50, 162 .50 <strong>and</strong> 300 .00 tng/kg b .w), selected from<br />

estimated LD50 (325 mg/),-.g b .w) . significant genetic damage (1 .26 <strong>and</strong><br />

'1 .35% micronucleated PCES) was observed at the two higher doses . The PCE/<br />

tCZ<br />

ratio demonstrated a significant ir.crease in the percentage of pCES,<br />

at lower doses sig nifying a stimulatcry eff ect of deltamethrin . Though,<br />

deltameth rin showed no germ-cell mutagenesis in ro• :nnhd .11, yet it acted<br />

as a strong clastogerl/sPindle ir4fibitor in the mouse . Its differential<br />

response has rather made it desirable to investigate its ; genotoxicity in<br />

oth er systems too .<br />

184<br />

RFGULA'TION OF NUM,AN DNA GLYCOSYLASFS 'rdAT INT'fTA'TF gAgfy FXCISION RFPAIR OF OXii)ATTVE<br />

PYHf,lIjL2F MODIFICA'TTONS . Tapan Cang-il y <strong>and</strong> aahum J . Duker, Temple University<br />

School of Nndicine, Philadelphia, PA (OSA)<br />

DNA oxid,rrive damap,ea are among the most frequPOt~ tyoes encountered in the<br />

lifetime of a cell . TheaPe can result from ionizing or gamma radiation <strong>and</strong> froaa<br />

activated oxygen species Renerated from metabolic procesees . Fxciaion of oxidized<br />

bases from DNA of hurnan cella ia initiated by DNA qlycosylaees . The oxidized<br />

t7yminrc moiety 5-hydroxyrethyluracil is removed frorn DNA by 5-hydroxyerethyluracil-<br />

DNA e,lycosylase . A redoxyendonuclease, active against a wide variety of substrates,<br />

has ;lycosylic activity aF,ai .ist many modified DNA pyrimidiiea . We studied<br />

re.gul .ation of these enzymes in proliferating human cella . Both glycosylases were<br />

assayed by measurement of direct telease of modified free bases from their DNA<br />

substrates . Serum-atimulated JI-38 Sunan cells were the sources of enzyme<br />

a .tiviries assayed in crude extracts as a function of cell division . 5hydroxyaret.hyluracil-DNA<br />

qlycosylase activity did not vary significantly during the<br />

cell cycle . ny contrast, the glycosylic activity of the redoxyendonucleaee<br />

increased four-fold as a function of cell growth . Maximum stimulation was obtained<br />

during peak DNA synthesis . Tnis enzyme activity increased once again aa thn cella<br />

entered a second growth cycle . This ia similar to the stimulation observed for<br />

uracil-UNA glycosylase in a aynchronous cell population . Theae results indicate<br />

that the glycosylasea that initiate base excision repair of oxidised DNA are not<br />

coor3inately induced during the cell cycle .<br />

185<br />

LATE EFFECTS OF FEMALE SEX HORMONES<br />

han Fengeing, )laog Hsnyfug, <strong>and</strong> Yu Yannao, Dept . of Blological Effect of<br />

Radislion, Laboratory of tnduslrial Nygiens, Ministry of Public Health . I<br />

Xinkang Street, Desheng.enr,l, Beijing, (China)<br />

Inj . Hydroxyprugesterone Co . (containing hydroxyprogesterons capruste (P)<br />

250 •g <strong>and</strong> estradiol valerate (E) S sfgi .l of vehit•ls, .EP) was Isjecled<br />

intrseuscularly into fe .ale Vister rats <strong>and</strong> different strains of rtee of both<br />

sexes with doses of 5 to 100 ti .es that used Is huans ones or twice a month for<br />

10 to 24 ti .es . In so .e experl .ents EP was co .bined with •hole-body 3 Gy ga. .a<br />

radiation once or twice . The purpose of this work was to detsr .ine whether F•P<br />

would possess carcleogenleity or not <strong>and</strong> whether synergistic cercinogeeicily<br />

would exist when EP had been ad .lnistered In coebination of ga . .a radletion .<br />

Results show that EP has ubvious carcloogenicity/tu .our lncidence was siegnifi-<br />

http://legacy.library.ucsf.edu/tid/clb93d00/pdf<br />

1989 EMS Abstracts 65<br />

Notes

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