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KMID : 0365819730130010215
Journal of Pusan Medical College
1973 Volume.13 No. 1 p.215 ~ p.221
The Effect of Organic Phosphorus and Chlorinated Hydrocarbon Compounds on 3¥â-Hydroxysteroid Dehydrogenase Activity in Adreanls of Rat

Abstract
Recently, dipterex, DDVP and EPN have attracted wide interests as insecticides. The toxicities and mechanisms of action of these agents have not as yet been explained thoroughly.
So far as I kno , the work reported here is the first attempt specifically designed to study the effect of organic phosphorus n ad chlorinated hydrocarbon compounds on 3(3-hydroxysteroid dehydrogenase acti¡©vity in, adrenals of rat.
Rats were used as experimental animals throughout this study. Sixty rats were divided into 12 groups;
Group 1: control, Group 2: EPN injected. Gronp 3: dipterex injected, Group 4: DDVP injected, Group 5: DDT injected, Group 6: BHC injected, Group 7: EPN plus DDT injected, Group 8: EPN plus BHC injected, Group 9: dipterex plus DDT injected, Group 10: dipterex plus BHC injected, Group 11: DDVP plus DDT injected, Group 12: DDVP plus BHC injected.
The activity was determined at 37¡ÆC by monitoring formation of DPNH at 340 m¥ì in a Beckman DU spectrophotometer. Each cuvette contained 0.75 ml. of homogenate, 50 mM sodium phosphate buffer(pH 7.2), 40 mM nicotinamide, 5 mM disodium EDTA, 7 mM (3-mercaptoethanol,1 mM KCN, 0.3 mM DPN+ and the designated amounts of substrate in 0. 1 ml. of propylene glycol with a total volume of 3.0ml.. The results of this investigation were as follows:
1. 3j3-Hydroxysteroid dehydrogenase activities of adrenals of rat determined with 6-estradiol, allop¡©regnanolone, and 17x- hydroxypregnenolone as its substrate were 550, 224, and 2O5¥ì mole of product/ min. /g of wet tissue, respectively.
2. 3(3-Hydroxysteroid dehydrogenate activity was inhibited by EPN, dipterex, DDVP and DDT when determined with (3-estradiol as a substrate.
3. 3(3-Hydroxysteroid dehydrogenase activity was inhibited by EPN plus DDT, dipterex plus DDT, and DDVP plus BHC when determined with (3-estradiol as a substrate.
4. W-Hydroxystero d dehydrogenas^ activity was activated by dipterex plus BHC and DDVP plus BHC, but it was inhibited by dipterex plus DDT, when determined with allopregnanolone as a substrate.
5. 3/3-Hydroxysteroid dehydrogenase activity was inhibited by DDVP plus DDT and DDVP plus BHC, when determined with 17a-hydroxypregnenolone as a substrate.
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