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Environmental and Molecular Mutagenesis - Legacy Tobacco ...

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78 1989 EMS Abstracts<br />

Notes<br />

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

221<br />

SEL3CPIVE ANTIMUTAUENIC ACTZVITY GF TERKNALIA 1C~E9J~L! IN SALhiONEL14<br />

TyyUlhUk2= . I .S .GRLVER <strong>and</strong> Saroj bAl,p . School of Lite Sciences, Guru<br />

Nanak Lev University, Amritsar-143005, India .<br />

Tecmiralin chebula is a eommon medicinal plant whose fruit is used in<br />

"Ayurvedic" <strong>and</strong> "Unani' system of medicine as caaninative, exFectorant<br />

<strong>and</strong> gastric disorders . Antimutagenicity of its water <strong>and</strong> chloroform<br />

extracts of dried f wits was determined against two direct acting<br />

mutagens, sodium azide <strong>and</strong> 4-nitro-o-phecylenediamine (NPD) in strains<br />

TA1o0 <strong>and</strong> TA1535 <strong>and</strong> TA97a <strong>and</strong> TA98 respectively <strong>and</strong> S9 dependent<br />

mutagen 2-aminofluorene (2-AF) in TA97a <strong>and</strong> TA9S of ~ .S,ynhimurium . It was'<br />

obse rved that water ext ract s reduced NrL i nduced hi a revertant s i n both<br />

TA97a <strong>and</strong> TA98 significantly but did not have any perceptible effect<br />

against sodium az ;de induced his+ revertant in TA100 <strong>and</strong> TA1535 of<br />

.Z,tvl)hlm yrium, The pre-incubation studies where the extract was incubated<br />

at 370C for 30 minutes with the said mutegen prior to plating enhanced<br />

the inhibitory effect . Autoclaving the water extract reduced its effect<br />

but the reduction was not significant . The water extracts inhibited signi .<br />

ficantly 2-AF reduced his+ revertants too in all the strains tested but<br />

its effect inTA98 was striking as it reduced the revertants to spontaneous<br />

level . No inhibitory effect was observed in any of the strains <strong>and</strong> against<br />

all the test mutagens with chloroform extract . It appears that inhibitory<br />

factor (antimutagen) is water soluble, heat stable <strong>and</strong> desnutagen .<br />

COMYARISON OF TF1E ANTIMITTAUENIC EFFECT ( .F WACER Ey.TRAGTS OF TWU<br />

DIFFEFtEhT VARIETIES OF INLIAN CGUSEbF :NIQf . I .S .GRGVER 6, AjpLMD liaur,<br />

School of Life Sciences,Guru Nanak l :ev University, Amrit :.;ar, 1NDIA .<br />

Indian gooseberry (Llnbiica Officinalis) is a very comnon medicinal<br />

plant <strong>and</strong> its fruit is thv richest source of Vitamin C . Nntimutagenicity<br />

ot the wate r extracts ot its two difterent varletiess was<br />

tested against two direct acting.mutagens, sodium azido <strong>and</strong> 4-nltrcL<br />

o-phenylenediaminr in TA1535 <strong>and</strong> 'l'A98 respectively using thn Ames<br />

test . water extract of var .-I reduced the his+ revertants in TA98<br />

upto 5r/. but its effect was not significant in TA1535 . Pre-incubation<br />

of the extract with the mutagen at 370C for 30 min did~not have a<br />

significant eff--ct in TA98 but reduction'of his+ revertants in TA1535<br />

was . enhanced by pre-incubating the extract with sodium azide . Auto-oclaving<br />

of ext ract reduced its inhibitory effect in TA98 but promoted<br />

its effect in TA1535 . Water ext ract of var .-II showed a maximum of<br />

52% inhibition in the sodium ezide inLluced frequency of his+<br />

revertants in TA1535 but its effect was corvparatively less in TA98 .<br />

P re-incubation of the extracts with the mutagen increased the<br />

inhibitory effect in both the strains . 1Heating of the extracts did<br />

rnt have -a significant effect on its inhibitory activity . Thus it<br />

may be concluded from the results that both th ese varieties may have<br />

different nutagenic facto rs .<br />

222<br />

A GENETIC ASSAY FOR TNE DETECTION OF INEUPLOIDY AN? CLASTOGENICITY USING A<br />

NONOCBRONOSONAL HYBRID CELL LINE . R . 6ud1 , R .S . Athwal . <strong>and</strong> S .S . S<strong>and</strong>hu2 . 1Nsw<br />

Jersey Medical School, Newark, NJ 07103 USA ; 2U .S . <strong>Environmental</strong> Protection Agency,<br />

RTP, NC 27711 USA .<br />

We have developed an assay for induced chromosomal anomalies based on the<br />

quantitation of loss of a chromosome or chromosomal segment by growth of cells in<br />

selection media . For this purpose, a mouse/human hybrid cell line containing human<br />

chromosome 5 as the only human component has been produced . This chromosome S<br />

carries two dominant selectable markers, Ecogpt, <strong>and</strong> a gene for sensitivity to<br />

diptheria toxin (DTs) . Cultivation of these cells in DNEN containing mycophenolic<br />

acid <strong>and</strong> xanthine (NX medium) selects for Ecogpt <strong>and</strong> thus for the retention of<br />

chromosome 5 . The growth of these cells in the medium containing 6•thioguanine <strong>and</strong><br />

diptheria toxin (DT) gives the frequency of chromosome loss . Similarly, growth of<br />

hybrid cells in MX medium containing DT (10'10l1) selects for the cells that have lost<br />

the segment of chromosome 5 carrying DTs gene while retaining Ecogpt . This provides<br />

a method to quantitate induced chromosome breaks . Preliminary results using model<br />

compounds show a dose-related response for induced aneuploidy <strong>and</strong> chromosome breaks .<br />

The same cell line can also be used to quantitate induced point mutations by growth<br />

in the medium containing ouabain (10-3M) . A unified genetic assay for multiple<br />

endpoints will enable the evaluation of test chemicals at doses relevant to human<br />

exposure . (This is an abstract of a proposed presentation <strong>and</strong> does not necessarily<br />

reflect U .S . EPA policy .)<br />

50869 3590<br />

223

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