Environmental and Molecular Mutagenesis - Legacy Tobacco ...
Environmental and Molecular Mutagenesis - Legacy Tobacco ...
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