|
|
Çѱ¹È¯°æ»ýÅÂÇÐȸ / v.20, no.3, 2006³â, pp.345-351
|
$Cd^{2+}$ÀÌ ºÏ¹æ»ê°³±¸¸®ÀÇ ³ÀÚ¼º¼÷°ú ¹è¾Æ¹ß´Þ¿¡ ¹ÌÄ¡´Â ¿µÇâ
( Effect of $Cd^{2+}$ on the Oocyte Maturation and Developmental Stages of Brown Frog Embryo, Rana dybowskii in vitro ) |
°í¼±±Ù; È£³²´ëÇб³ »ý¸í°úÇаú;
|
|
|
 |
|
|
ÃÊ ·Ï |
º» ¿¬±¸´Â ºÏ¹æ»ê°³±¸¸®ÀÇ ³ÀÚ ¹× ¹è¾Æ¸¦ Ȱ¿ëÇÏ¿© ³ÀÚ¼º¼÷Çö»ó°ú ¹è¾Æ¹ß´Þ°úÁ¤¿¡ ¹ÌÄ¡´Â $Cd^{2+}$ÀÇ µ¶¼ºÈ¿°ú¸¦ Á¶»çÇÏ¿´´Ù. °á°ú $Cd^{2+}$ 0.1ppm¿¡¼ ³ÀÚÀÇ ¼º¼÷Çö»óÀ» ¾ïÁ¦ÇÏ¿´À¸¸ç $Cd^{2+}$ ÀÛ¿ëÀÇ °¡¿ª¼ºÀ» Á¶»çÇϱâ À§ÇØ 3½Ã°£ µ¿¾È ³ÀÚµéÀ» $Cd^{2+}$¿¡ ³ëÃâ½ÃŲ ÈÄ º¸Åë¹è¾ç¾×À¸·Î ¿Å°Ü 17½Ã°£ ¹è¾çÇÑ °á°ú 1ppm¿¡¼´Â °¡¿ª¼ºÀ» ³ªÅ¸³»¾úÀ¸³ª 2.5ppm¿¡¼´Â ºñ°¡¿ªÀû ÀÎ ¼Õ»óÀ» ÁÖ¾ú´Ù. ¹ß´Þ ÁßÀÎ 2¼¼Æ÷ ¹è¾Æ¸¦ $Cd^{2+}$ÀÇ ¿©·¯ ³óµµ¿¡ ³ëÃâ½ÃŲ °á°ú 0.1ppm¿¡¼ ¹ß´ÞÀÌ ¾ïÁ¦µÇ¾úÀ¸¸ç ³ëÃâ½Ã°£ÀÌ ±æ¾îÁø 32¼¼Æ÷ ½Ã±â¿¡´Â ¼¼Æ÷ºØ±«Çö»óÀ» À¯¹ßÇÏ¿´´Ù. ÇÑÆí, Æ÷¹è±â ¹è¾Æ¸¦ $Cd^{2+}$ÀÇ ¿©·¯ ³óµµ¿¡ ³ëÃâ½Ã ÄÑ 96½Ã°£ ¹è¾çÇÑ ÈÄ À¯»ýÀÇ Ä¡»çÀ² ¹× ±âÇüÀ²À» ´ë»óÀ¸·Î probit ºÐ¼®¹ýÀ¸·Î Á¶»çÇÑ °á°ú LC50Àº 0.1ppm, EC50Àº 0.08ppm, TI´Â 5.0À» ³ªÅ¸³»¾î $Cd^{2+}$Àº ³ôÀº Ä¡»çÀ²À» ³ªÅ¸³»´Â ¹°Áú·Î ³ªÅ¸³µ´Ù. ±âÇü ¾ç»óÀº ôÃß±âÇüÀÌ 0.05ppm¿¡¼ 14.3%,²¿¸®±âÇüÀÌ 0.1ppm¿¡¼ 75.0%,º¹ºÎ±âÇü ÀÌ 0.01ppm¿¡¼ 66.7%¸¦ ³ªÅ¸³»¾ú°í profoundÇü ±âÇüÀÌ 0.1ppm¿¡¼ 25.0%¸¦ °¢°¢ ³ªÅ¸³ÂÀ¸¸ç $Cd^{2+}$ 0.1ppm¿¡¼ ¸Ó¸®¿¡¼ ²¿¸®±îÁöÀÇ ¼ºÀåÀ» ¾ïÁ¦ÇÏ¿´´Ù. °á·ÐÀûÀ¸·Î º» ¿¬±¸ÀÇ °á°úµéÀº $Cd^{2+}$ÀÌ ³ÀÚ¼º¼÷, ³ÇÒ ¹× ¹è¾ÆÀÇ ¹ß´Þ°úÁ¤¿¡ ³ôÀº µ¶¼ºÀÇ È¿°ú¸¦ °¡ÁüÀ» ³ªÅ¸³½´Ù. |
|
This study investigates the toxic effects of $Cd^{2+}$on frog (Rana dybowskii) by the determination of oocyte maturation and development of embryo exposure to different concentrations of the toxicant. The results show that $Cd^{2+}$ concentration of 0.1ppm suppressed the maturation of the oocytes. To examine the reversibility of the inhibitory effects, the oocytes were exposed to the $Cd^{2+}$ only for 3 hours, and then transferred to plain medium and cultured further for 17 hours. The oocytes were recovered from the toxic effect of the $Cd^{2+}$ when they were exposed to 1ppm, but not to 2.5ppm of the $Cd^{2+}$. The development of 2 cell embryos to 32 cell was completely suppressed at 0.1ppm and the longer the embryos were exposed to the $Cd^{2+}$, the more damage appeared to the embryos and the cytolysis of the 32 cell was induced by $Cd^{2+}$ at 0.1ppm. On the other hand, the embryos of blastula stage were cultured 96 hours in presence of the $Cd^{2+}$ at various concentrations and were examined. The rates of mortality and malformed larvae were investigated by probit analysis. From the results of LC$_{50}$ of 0.1ppm and EC$_{50}$ of 0.08ppm, Tl of 5.0 was derived, which indicates $Cd^{2+}$ is to be considered a teratogenic compound. Such specific malformations occurred in 14.3% as spine deformations at the 0.05ppm, in 75.0% as tail deformations at the 0.1ppm, in 66.7% as abdominal deformations at the 0.01ppm and in 26.0% as profound deformations at the 0.1ppm of $Cd^{2+}$ concentration which living embryos were exposed to. $Cd^{2+}$ suppressed growth to head-tail length at 0.1ppm. In conclusion, The study results reveal that $Cd^{2+}$ must be considered highly toxic effect to oocyte maturation and embryonic development. |
|
Ű¿öµå |
µ¶¼º;»ê°³±¸¸®;TOXICITY;RANA DYBOWSKII; |
|
|
|
 |
|
Çѱ¹È¯°æ»ýÅÂÇÐȸÁö / v.20, no.3, 2006³â, pp.345-351
Çѱ¹È¯°æ»ýÅÂÇÐȸ
ISSN : 1229-3857
UCI : G100:I100-KOI(KISTI1.1003/JNL.JAKO200634742870461)
¾ð¾î : Çѱ¹¾î |
|
³í¹® Á¦°ø : KISTI Çѱ¹°úÇбâ¼úÁ¤º¸¿¬±¸¿ø |
|
|
|
|
|