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Environmental and Molecular Mutagenesis - Legacy Tobacco ...

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1989 EMS Abstracts<br />

ester of I41M, 1L1M acetate (MAMoAC) in combination with porcine liver esteraee Notes<br />

(Carboxylic-ester hydrolase ; EC 3 .1 .1 .1) to study the mutagenic activity of NAM .<br />

MAMoAC produces a dose-dependant increase in the mutation rate in Salmonella<br />

typhimurium His G46 at concentrations of 2 .5-30 micromoles/plate following<br />

preincubation at 30oC for 90 minutes . Addition of porcine liver esterase increased<br />

the mutation rate from 14 to 2200 <strong>and</strong> from 375 to 5800 revertants per plate at 2 .5<br />

<strong>and</strong> 5 .0 micromoles/plate, respectively . This increased mutagenicity was dependant on<br />

esterase concentration (optimum 63 micrograms protein/ml) . The preincubation time<br />

was also critical for expression of the mutagenicity of the MAMoAC/esterasa reaction .<br />

The dose-response curve was shifted to steeper slopes by increasing the preincubation<br />

time up to 90 minutes . Our results indicate that the MAMoAC/esterase system is a<br />

convenient model with which to study the mutagenicity of 14AM .<br />

119<br />

ANALYSIS OF MULTIPLE CONGENITAL ANOMALIES /ICPEMC/<br />

Andrew Czeizel<br />

par men o uman Genetics <strong>and</strong> Teratology, National Institute of<br />

Hygiene, Budapest, Hungary<br />

Three indicator conditions of offspring : sentinel anomalies, Down<br />

syndrome <strong>and</strong> unidentified multiple oongenital anomalies /UIICAs/ are<br />

being evaluated within the Hungarian population-based surveillance<br />

of germinal mutations . Ul[CAs are possible indioators of germinal<br />

dominant gene <strong>and</strong> ohromosomal mutations . The component oongenital<br />

abnormalities of UMCAs were classified into 45 groups . These<br />

component congenital abnormalities were reduced to pairs A pair is<br />

a set of two independent component congenital abnormalities in index<br />

patients with two or more congenital abnormalities . Baseline figures<br />

of all component congenital abnormality pairs in 3,722 UMCAs were<br />

determined in the study period 1973-1982 . The observed annual data<br />

after 1982 were compared with expected occurrences based on baseline<br />

figures . This pair-wise evaluation of component congenital<br />

abnormalities within U11[CAs seems to be an adequate surveillance<br />

method to detect any time cluster of congenital abnormalit' pairs<br />

due to environmental factors including germinal mutagens . The<br />

Hungarian data will be presented concerning tpe Chernobyl nuclear<br />

power accident .<br />

120<br />

SJMAN MEIUPIC CHRObDSCMAL IIANW(£ IN ItffERCIIB MhIIES AE To ImCPIQI .<br />

T .V . Darmdaran an9 K .M . Marinuthu, Department of Genetics, P .(; .Institute of<br />

Basic Me icaT-Sciences, University of Madras,Taramani, Medras 600 113,MIA .<br />

lwenty one infertile males were studied using mitotic, meiotic <strong>and</strong><br />

histological techniques . Syphilis (2), lynphogranulana venerum (2) <strong>and</strong><br />

nonspecific chronic epididymo orchitis (17) were the various infections<br />

observed . Meiotic studies fran normal healthy men (11) formed the control<br />

data . Changes in the meiotic percentage cell dietribution pattern (MPM) t .es<br />

correlated with meiotic chromeanal anamolies . There was no change in WD<br />

in 2 patients, wtro had shawefl micronuclei of the spermatids <strong>and</strong> increased<br />

frequency of mitotic chrormeane aberrations . Altered MI (msiotic met.aphase<br />

I) <strong>and</strong> M II (meiotic metaphase II) values were noted in 2 patients who have<br />

sho.ed separation difficulties of MI <strong>and</strong> M II . Slight increase in SPM<br />

(Sbermatogonial metaphase) values were noted in two patients . Highly<br />

increased SPM value vss noticed with loss of architecture of bivalents <strong>and</strong><br />

M II elements were saen in a patient . Thus, the results abtained so far<br />

irdicate that though the actual mrJde of action could not be fully undertood<br />

the fact that the meiotic studies fro :n normal healthy control mmles did not<br />

shar any of these ananaliess oonfizm the possible clastogenic <strong>and</strong> autagenic<br />

action of these microbes on meiotic system .<br />

121<br />

MATERNAL UPTAKE AND TRANSFER TO EGGS OF A PROMUTAGEN<br />

(CYCLOPHOSPHAMIDE) BY AN ESTUARINE FISH, CYPRINODON VAR/EQATUS. C.B .<br />

Daniels, D . McMillin <strong>and</strong> J .C . Means . Institute for <strong>Environmental</strong> Studies, Louisiana State<br />

University, Baton Rouge, LA 70803 .<br />

The cytogenetic <strong>and</strong> mutagenic properties of cyclophosphamide (CP) have been shown to<br />

be a function of its metabolism to 4-hydroxycyclophosphamide . We have Initiated research to<br />

determine the availability of cyclophosphamide to developing eggs <strong>and</strong> to characterize the<br />

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

43

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