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impact of latex and plant extract of and the recovery of latex toxicity ...

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Procedure:<br />

To <strong>the</strong> tubes labeled 'test' <strong>and</strong> 'blank' 0.5 ml <strong>of</strong> para-nitrophenyl phosphate <strong>and</strong> 0.5<br />

ml <strong>of</strong> glycine buffer was added. The tubes were placed in a water bath at 37'~<br />

for 5<br />

minutes. The reaction was initiated by <strong>the</strong> addition <strong>of</strong> 0.1 ml <strong>of</strong> sample to <strong>the</strong> test<br />

<strong>and</strong> 0. I ml <strong>of</strong> distilled water to <strong>the</strong> blank. Exactly after 30 minutes <strong>of</strong> incubation at<br />

37'~.~he reaction was arrested by addition <strong>of</strong> 10 ml <strong>of</strong> NaOH. The tubes were mixed<br />

well <strong>and</strong> <strong>the</strong> colour developed was read at 410 nm, in a spectrophotometer, against<br />

<strong>the</strong> blank. 0.1 ml <strong>of</strong> concentrated Hydrochloric acid was added, mixed <strong>and</strong> <strong>the</strong> optical<br />

density was read at 410 nm against <strong>the</strong> blank. The difference in <strong>the</strong> two absorbance<br />

was taken as <strong>the</strong> measure <strong>of</strong> enzyme activity. Suitable st<strong>and</strong>ards were mn along with<br />

<strong>the</strong> assay. The alkaline Phosphatase activity was calculated from <strong>the</strong> calibration<br />

curve obtained using para-nitrophenol st<strong>and</strong>ard. The enzyme activity is expressed as<br />

p moles <strong>of</strong> para nitrophenol formed per hour per mg protein.<br />

Toxicity Impact on Acetylcholinesterase<br />

The important toxic property <strong>of</strong> pesticides is inhibiting <strong>the</strong>ir target enzyme acetyl<br />

cholinesterase (AChE), <strong>and</strong> as well studied (O'Brein, lP67;Corbelt,1974),most <strong>of</strong><br />

<strong>the</strong> chemical pesticides are similar with <strong>the</strong> ester part <strong>of</strong> <strong>the</strong> acetylcholine <strong>and</strong> <strong>the</strong>y<br />

react with esterase part <strong>of</strong> AChE after entering into <strong>the</strong> exposed fish The conversion<br />

<strong>of</strong> acetic acid <strong>and</strong> choline catalysed by AChE is considered to be <strong>the</strong> reaction in<br />

synaptic transmission(Bachelard,l976).Decrease in AChE activity <strong>and</strong> increased<br />

accumulation <strong>of</strong> AChE was observed in fresh water mussel treated with<br />

demacron(Vijendrababu <strong>and</strong> Vasudev,l984),with Fenotrothion in Senex senex<br />

(Bagyalarmi <strong>and</strong> Ramamur~,l980) <strong>and</strong> many organophosphates in fishes were<br />

reported(March et a1 .,1956;Murphy el aL,1968).A drop in AChE in vertebrates<br />

caused various neurobiological changes that reduce <strong>the</strong> animal survival ability.<br />

Fishes were exposed to three sublethal concentrations <strong>of</strong> <strong>latex</strong>, <strong>latex</strong> with<br />

supplements <strong>and</strong> <strong>plant</strong> <strong>extract</strong>. The tissues <strong>of</strong> gill, liver <strong>and</strong> brain excised <strong>and</strong> are<br />

used for <strong>the</strong> following experiment.

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