Àá½Ã¸¸ ±â´Ù·Á ÁÖ¼¼¿ä. ·ÎµùÁßÀÔ´Ï´Ù.

»êÈ­¼º ¼Õ»óÀ» ¹ÞÀº PC12 ¼¼Æ÷¿¡¼­ Diallyl Disulfide¿¡ ÀÇÇÑ Cytochrome c ¸Å°³¼º ¾ÆÆËÅä½Ã½º Â÷´Ü È¿°ú Diallyl Disulfide Inhibits Cytochrome c-Mediated Apoptosis in H2O2 Induced Death of Neuronal-differentiated PC12 Cells

´ëÇѽŰæ°úÇÐȸÁö 2004³â 22±Ç 4È£ p.375 ~ 381
°í¼ºÈ£, ±ÇÇõ¼º, ¹ÚÀ±ÁÖ, ±èÁرÔ, ±è±â¼®, ¼ÛÄ¡¿ø, ±èÁÖȯ, ±èÁÖÇÑ, ±è¸íÈ£, ±è°æ¼÷, À¯ÇöÁ¤, Á¤ÇرÇ, ±è½ÂÇö,
¼Ò¼Ó »ó¼¼Á¤º¸
°í¼ºÈ£ ( Koh Seong-Ho ) 
½ÄÇ°ÀǾàÇ°¾ÈÀüû ±¹¸³µ¶¼º¿¬±¸¿ø ÀϹݵ¶¼ººÎ ½Å°æµ¶¼º°ú

±ÇÇõ¼º ( Kwon Hyug-Sung ) 
½ÄÇ°ÀǾàÇ°¾ÈÀüû ±¹¸³µ¶¼º¿¬±¸¿ø ÀϹݵ¶¼ººÎ ½Å°æµ¶¼º°ú
¹ÚÀ±ÁÖ ( Park Youn-Joo ) 
½ÄÇ°ÀǾàÇ°¾ÈÀüû ±¹¸³µ¶¼º¿¬±¸¿ø ÀϹݵ¶¼ººÎ ½Å°æµ¶¼º°ú
±èÁرԠ( Kim Jun-Gyou ) 
½ÄÇ°ÀǾàÇ°¾ÈÀüû ±¹¸³µ¶¼º¿¬±¸¿ø ÀϹݵ¶¼ººÎ ½Å°æµ¶¼º°ú
±è±â¼® ( Kim Ki-Sok ) 
½ÄÇ°ÀǾàÇ°¾ÈÀüû ±¹¸³µ¶¼º¿¬±¸¿ø ÀϹݵ¶¼ººÎ ½Å°æµ¶¼º°ú
¼ÛÄ¡¿ø ( Song Chi-Won ) 
½ÄÇ°ÀǾàÇ°¾ÈÀüû ±¹¸³µ¶¼º¿¬±¸¿ø ÀϹݵ¶¼ººÎ ½Å°æµ¶¼º°ú
±èÁÖȯ ( Kim Ju-Hwan ) 
½ÄÇ°ÀǾàÇ°¾ÈÀüû ±¹¸³µ¶¼º¿¬±¸¿ø ÀϹݵ¶¼ººÎ ½Å°æµ¶¼º°ú
±èÁÖÇÑ ( Kim Ju-Han ) 
ÇѾç´ëÇб³ ÀÇ°ú´ëÇÐ ½Å°æ°úÇб³½Ç
±è¸íÈ£ ( Kim Myung-Ho ) 
ÇѾç´ëÇб³ ÀÇ°ú´ëÇÐ ½Å°æ°úÇб³½Ç
±è°æ¼÷ ( Kim Kyeong-Sook ) 
Á¤½Å°Ç°­¿¬±¸¼Ò
À¯ÇöÁ¤ ( Yu Hyun-Jeung ) 
ºÐ´çÁ¦»ýº´¿ø ½Å°æ°ú
Á¤ÇرǠ( Jung Hai-Kwan ) 
½ÄÇ°ÀǾàÇ°¾ÈÀüû ±¹¸³µ¶¼º¿¬±¸¿ø ÀϹݵ¶¼ººÎ ½Å°æµ¶¼º°ú
±è½ÂÇö ( Kim Seung-Hyun ) 
ÇѾç´ëÇб³ ÀÇ°ú´ëÇÐ ½Å°æ°úÇб³½Ç

Abstract


Background: The effects of diallyl disulfide (DADS), a garlic derived compound, on the viability and cell signaling-like the downstream signaling through cytochrome c, caspase-3, poly (ADP-ribose) polymerase (PARP) during an oxidative-stress induced injury were studied using H2O2 treated neuronal-differentiated PC12 cells by a nerve growth factor.

Methods: To evaluate the toxicity of the DADS itself, the viability of the differentiated PC12 cells treated with several concentrations of DADS was evaluated with 3,(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assays. To evaluate the protective effect of the low concentration of DADS from oxidative stress, the viability of the cells (DADS pretreated vs. not pretreated) was evaluated following the exposure to 100 µM H2O2. Additionally, the expression of caspase-3, PARP, and cytochrome c was examined using western blot analyses.

Results: The viability was not affected at low concentrations of DADS, up to 20 µM, but, over this concentration, it was decreased. Compared with the cells treated with only 100 µM H2O2, the pretreatment with low concentrations of DADS before exposure to 100 µM H2O2 increased the viability and induced the inhibition of caspase-3 activation, PARP cleavage, and cytochrome c release.

Conclusions: These results show that low concentrations of DADS shows neuroprotective effects by affecting the downstream signaling through cytochrome c, caspase-3, and PARP pathway and may be a new potential therapeutic strategy for neurodegenerative diseases associated with oxidative injury.

Å°¿öµå

Diallyl disulfide; Antioxidant; Apoptosis; Caspase-3; PARP

¿ø¹® ¹× ¸µÅ©¾Æ¿ô Á¤º¸

 

µîÀçÀú³Î Á¤º¸

KCI
KoreaMed
KAMS