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¹é¼­¿¡¼­ ½ÇÇèÀû Ä¡¾ÆÀ̵¿½Ã Ä¡Á¶°ñ Èí¼ö¿¡ ¹ÌÄ¡´Â BisphosphonateÀÇ ¿µÇâ-»ýÈ­ÇÐÀû ¹× Á¶Á÷ÇÐÀû °üÂû-

Effects of Bisphosphonate on Alveolar Bone Resorption during Experimental Tooth Movement in Rats -Biochemical £¦ Histological Observations-

Korean Journal of Orthodontics 1999³â 29±Ç 1È£ p.95 ~ 106
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Abstract

¹é¼­¿¡¼­ ½ÇÇèÀû Ä¡¾Æ À̵¿½Ã bisphosphonate°¡ ÆÄ°ñ¼¼Æ÷ÀÇ Çü¼º¿¡ ¹ÌÄ¡´Â ¿µÇâ°ú °ñ Èí
¼ö ¾ïÁ¦±âÀüÀ» ±Ô¸íÇÏ°í µ¶¼ºÀ¯¹«¸¦ ¾Ë¾Æº¸°íÀÚ ÇÏ¿´´Ù. üÁß 260-350gÀÇ ¿õ¼º ¹é¼­ 87¸¶¸®
¸¦ Á¤»ó±º(ÀåÄ¡ºñÀåÂø +0.9£¥ NaCl), ´ëÁ¶±º(ÀåÄ¡ÀåÂø +0.9£¥ NaCl) ¹× ÀåÄ¡ÀåÂøÈÄ
bisphosphonate Åõ¿©±º(À¸·Î ºÐ·ùÇÏ¿´´Ù. »ó¾Ç ÁÂÃø Á¦ 1´ë±¸Ä¡¸¦ ±Ù½ÉÀ¸·Î Ä¡¾ÆÀ̵¿ÀÌ ÀÏ
¾î³ªµµ·Ï 50-70gÀÇ ±³Á¤·ÂÀ» °¡ÇÏ°í, ±³Á¤ÀåÄ¡ ÀåÂøÈÄ 1ÀÏ, 3ÀÏ ¹× 7ÀÏ°¿¡ Çü¼º acid
phosphatase¿Í lactate dehydrogenase(LDH)ÀÇ È°¼ºµµ¸¦ ÃøÁ¤ÇÏ°í, ¶ÇÇÑ Á¦ 1´ë±¸Ä¡¸¦ Æ÷ÇÔ
ÇÑ »ó¾Ç°ñ ÀϺο¡¼­ ÆÄ°ñ¼¼Æ÷¼ö ¹× °ñÈí¼ö Á¤µµ¸¦ Á¶Á÷ÇÐÀûÀ¸·Î °üÂûÇÏ¿© ´ÙÀ½°ú °°Àº ¼ºÀû
À» ¾ò¾ú´Ù.
1, Acid phosphatase È°¼ºµµ´Â ÀåÄ¡ÈÄ 1ÀÏ°¿Í 3ÀÏ°¿¡ ´ëÁ¶±º°ú bisphophonate Åõ¿©±º¿¡¼­
¸ðµÎ Á¤»ó±º¿¡ ºñÇØ 2-3¹è ³ô¾ÒÀ¸³ª, 7ÀÏ°¿¡´Â Á¤»ó±º°ú À¯ÀÇÇÑ Â÷À̸¦ º¸ÀÌÁö ¾Ê¾Ò´Ù.
2. LDHÈ°¼ºµµ´Â bisphosphonate 4§·°ú 20§·/§¸Åõ¿©±º¿¡¼­ Àü ½ÇÇè±â°£¿¡ °ÉÃÄ Áõ°¡µÈ ¾ç
»óÀ» º¸¿´À¸³ª 0.8§·°ú 100§·/§¸Åõ¿©±º¿¡¼­´Â À¯ÀÇÇÑ Â÷À̸¦ ³ªÅ¸³»Áö ¾Ê¾Ò´Ù.
3. °ñÈí¼ö´Â ÀåÄ¡ÈÄ 1ÀÏ°¿¡ ´ëÁ¶±º°ú bisphosphonate Åõ¿©±º¿¡¼­ ¸ðµÎ °üÂûµÇÁö ¾Ê¾ÒÀ¸³ª,
3ÀÏ ÀÌÈÄ¿¡ ³ªÅ¸³ª 7ÀÏ°±îÁö °è¼ÓµÇ¾ú´Ù, Bisphosphonate 4, 20 ¹× 100§·/§¸±º¿¡¼­ÀÇ °ñÈí
¼öÁ¤µµ´Â 3ÀÏ°¿¡´Â ´ëÁ¶±º¿¡ ºñÇØ ¹Ì¾àÇÏ¿´À¸³ª 7ÀÏ°¿¡´Â ´ëÁ¶±º°ú À¯»çÇÏ°Ô ³ªÅ¸³µ´Ù.
4. ÆÄ°ñ¼¼Æ÷°¡ 1ÀÏ°¿¡ ´ëÁ¶±ºÀ̳ª bisphosphonate Åõ¿©±º ¸ðµÎ¿¡¼­ °ÅÀÇ °üÂûÇÒ ¼ö ¾ø¾ú´Ù.
3ÀÏ°¿¡ ´ëÁ¶±º¿¡¼­´Â ÆÄ°ñ¼¼Æ÷°¡ ´Ù·® ÃâÇöÇÏ¿´À¸³ª bisphosphonate Åõ¿©±º¿¡¼­´Â ¾à¹°ÀÇ
¿ë·®ÀÌ Áõ°¡ÇÔ¿¡ µû¶ó °¨¼ÒÇÏ¿© ³ªÅ¸³µ´Ù.
ÀÌ»óÀÇ °á°ú·Î ½ÇÇèÀû Ä¡¾ÆÀ̵¿½Ã ÆÄ°í¼¼Æ÷ÀÇ Çü¼º¾ïÁ¦°¡ bisphosphonate ¿¡ ÀÇÇÑ °ñÈí¼ö
¾ïÁ¦±âÀüÀÌ ¾Æ´ÔÀ» ¾Ë ¼ö ÀÖ¾ú°í, bisphosphonate´Â Åõ¿©·®ÀÌ Áõ°¡¿¡ µû¸¥ ¶Ñ·ÇÇÑ ¼¼Æ÷µ¶¼º
Àº °üÂûµÇÁö ¾Ê¾ÒÀ¸¸ç, °ñÈí¼ö ¾ïÁ¦È¿°ú¸¦ Áö¼Ó½ÃÅ°±â À§Çؼ­ ¾à¹°ÀÌ ¹Ýº¹ÀûÀ¸·Î Åõ¿©µÇ¾î
¾ß ÇÒ ÇÊ¿ä°¡ ÀÖÀ½ÀÌ ½Ã»çµÇ¾ú´Ù.
#ÃÊ·Ï#
This study was performed to examine the effect of bisphosphonate, an inhibitor of
bone resorption, on the formation of osteoclast and bone resorption during experimental
tooth movement. Whether bisphosphonate has a cytotoxicity in high dose was also
examined. Eighty-seven male Sprague-Dawley rats. Weighing 260-350g, were classified
into normal (no appliance + 0.9£¥ NaCl), control (appliance + 0.9£¥ NaCl) and four
bisphosphonate-treated( appliance + 0.8§·, 4§·, 20§·, or 100§·/§¸) groups. The maxillary
left first molar was moved mesially with the tippping movement using 50-70g of force.
Bisphosphonate(etidronate disodium)was injected intraperitoneally with a dose of 0.8§·, 4
§·, 20§·, or 100§·/§¸ simultaneously with the application of the orthodontic force. They
were killed at day 1.3 or 7after the application of the orthodontic force. The activities of
serum acid phosphatase and lactate dehydrogenase (LDH) were assayed, and osteoclasts
and the degree of bone resorption were examined histologically.
The results obtained were as follows:
1. Acid phosphatase activities were significantly higher in the appliance groups, both
control and bisphosphonate-treated( 4, 20 and 100§·/§¸) groups, at days 1and 3 than
these in normal. At day 1, bisphosphonate -treated(4, 20§·/§¸) groups showed even
higher acid phosphatase than control. However, at day 7, no significant difference was
noted between the control and bisphosphonate-treated groups.
2. LDH activities in the 4, 20§·/§¸ bisphosphonate-treated groups were increased during
the experimental periods examined, but there were no significant differences in the 0.8,
100§·/§¸ bisphosphonate-treated groups.
3. There was no bone resorption at day 1, but severe bone resorption was observed at
days 3and 7 in the control. Bone resorption was reduced by bisphosphonate-treatment at
day 3. Bone resorption observed at day 7 was similar between the control and
bisphosphonate-treated groups.
4. Few osteoclasts were observed at the alveolar bone in the control and
biosphosphnate-treated groups at day 1. At day 3. numerous osteoclasts were shown in
the control, the degree of which was reduced in bisphosphonate-treated groups.
These results suggest that the inhibition of the osteoclast formation was not the
mechanism of bone resorption by the bisphosphonate-treatment during experimenal tooth
movement. There was no distinct cytotoxicity with a high dose of bisphosphonate. And
the drug should be administrated repeatedly to maintain the inhibitory effect of bone
resorption.

Å°¿öµå

Ä¡¾ÆÀ̵¿; Bisphosphonate; Acid phosphatase; LDH; ÆÄ°ñ¼¼Æ÷; Tooth movement; Bisphosphonate; Acid phosphatease; LDH; Osteoclast;

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