determination of genotoxic effect of insecticide deltametrine wp 250

NEW KNOWLEDGE JOURNAL OF SCIENCE
ISSN 1314 -5703
DETERMINATION OF GENOTOXIC EFFECT OF INSECTICIDE
DELTAMETRINE WP 250
KEMAJL KURTESHI1, KASUM LETAJ1, ZEQIR SHAQIRI2, ARBNOR ALIDEMA3
1
Department of Bilogy, Faculty of Natyral Science
UNIVERSITY OF PRISHTINA, 10000 Prishtinë, Kosovë
2
Faculty of Education, UNIVERSITY OF PRISHTINA, 10000 Prishtinë, Kosovë
3
PHARMACEUTICAL COMPANY REXALL, 10000 Prishtinë, Kosovë
Corresponding author: Address: Eqrem Qabej nn, Prishtinë, 10000, Kosovë
E-mail: [email protected]
Abstract
Micronucleus (MN) assay is an ideal monitoring
system that uses aquatic organisms to assess the
genotoxicity of water in the field and in the
laboratory.
The aim of this study it was to determinated the
genotoxic effect of insecticide deltametrine
250 WP through micronucleus in erythrocytes of
golden fish (Carasius aureus), after in vitro
treatement in aquarium for 8 days in 4 aquaria and
1 aquaria used as controll. Frequency of
micronuclei at treated fish it was higher compared
with controll group.
Key
word:
insecticide,
micronucleus, erythrocyte, fish
deltametrine,
Introduction
Various industrial and agricultural activities
increase pollution, particularly in the aquatic
environment, which is contaminated by various
toxic chemicals from the discharge of waste
waters and agricultural drainage(Isani, 2009).
These are responsible for multiple effects at the
organisms, including humans, affecting organ
function, reproductive status, species survival,
population size and ultimately biodiversity.
Among these, carcinogenic and mutagenic
compounds are the most problematic as their
effect may exert a damage beyond that of
individual and may be active through following
generations. Epizootic neoplasm has been found
in a variety of ectothermic species, such as shell
fish, echinoderms, jawless fish and bony fish.
Various investigations using fish for screening
the clastogenic effects of xenobiotics indicate
that these fish represent good experimental
models for genotoxicity studies (Pantaleao et
al., 2006).
Material and methods
Fish Carasius aureus were placed in five different
aquaria, each one containing tap water(negative
control) and four different aquaria containing
different dilution of fungicid propinebtriadimenol: (0.02ml insecticide /l water, 0.03ml
insecticide /l water, 0.04ml insecticide /l water,
0.05ml insecticide /l water ).
The fish was cut in caudal region and smears of
peripheral blood were made on grease
free clean slides. For each fish prepare four
slides. Slides were coded,for each fish. The
smears are air-dried and fixed in
absolute ethanol for 25 minute. The next day,the
slides were stained in giemsa(diluted in distilled
water in ratio 3:1 ) for 30 minutes (Schmid1975).
Stained slides were rinsed thorouhly in distilled
water,air-draid, and mounted with coverslip.
From each individual 2000 erythrocyte, 500 per
slides were scored under an oil-immersion
objective.
Results and disscusion
The results of average number of micronuclei (per
aquarium) in peripheral erythrocyte in fish species
Carasius aureus treated for 8 days, are sumarised
at the table 1.
According to investigation (Tab.1)in fishes treated
in concentration 0.05 ml fungicid/ l water is
proved
high
frequency,
statistically
significant,compared with control group of fish.
ANNIVERSARY INTERNATIONAL SCIENTIFIC AND APPLIED CONFERENCE – UARD, BULGARIA
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NEW KNOWLEDGE JOURNAL OF SCIENCE
Also it was verified that frequency of micronuclei
in peripheral erythrocite of Carasius aureus,
increase proportionallity with increase of
concentration of insecticide. Frequency of
micronuclei at fish Carasius aureus in first
aquarium with concetration 0.05 fungicid/ l water
was about fivefould high compared with control
fish.
Frequency of MN in second(with concentration of
insecticide 0.04 ml/l water) was about fourfold
higher and threefold in third aquarium compared
with control fish.
ISSN 1314 -5703
According to these results (tab.1) it can be
conclude that C.aureus exposed in different
concetration of insecticide deltametrine WP 250 is
verified the high frequency of micronuclei in
insecticide deltametrine concentration ratio 0.05
ml insecticid: 1l water(36.33MN), 0.04ml
insecticid:1l water ( 31.25MN), 0.03 ml
insecticid:1l water and 0.02 ml insecticid:1l water
(27.15 MN), which are statistically significant
compared with controll group(7.65 MN).
Statistical analysis is done by ststistical software
SigmaStat version 3.4, 2004 year.
Tab.1. Average number of micronuclei( MN) in 2000 erythrocytes of peripheral blood of fish Carasius
aureus after 8 days treatment in different dilution of insecticide deltametrine WP 250 / and statistical
analysis beetwen treated aquarium and control aquarium
Aquarium-1: 0.05 fungicid/ l
liter water
Average number of MN per
aquarium
36.33
31.25
Aquarium -2: 0.04ml/l
27.15
Aquarium -3: 0.03ml/l
21.47
Aquarium -4: 0.02ml/l
Aquarium -5: cotroll group
Significancy
Aquarium1:control group
P=<0.001,s
Aquarium2:control group
P=<0.001,s
Aquarium3:control group
P=<0.001,s
Aquarium4:control group
P=<0.001,s
7.65
Legend: s-significant Ns- not significant
Conclusion
Based on this investigation we can conclude that
insecticide deltametrine WP 250 is genotoxic, as
it were damage the chromosome of fish, seeing
that chromosome are fragmented, and formed the
small nucleic body called micronuclei.
The averge number of micronuclei it was higher,
at treated fish, statistically significant compared
with control group( P<0.001).
The averge number of micronuclei it was higher,
at treated fish, statistically significant compared
with control group( P<0.001).
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