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Influences of Saliva Substitutes on Salivary Enzymatic Activity

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°íÈ«¼·, À̽¿ì,
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°íÈ«¼· ( Kho Hong-Seop ) - ¼­¿ï´ëÇб³ Ä¡°ú´ëÇÐ ±¸°­³»°úÁø´ÜÇб³½Ç
À̽¿ì ( Lee Seung-U ) - ¼­¿ï´ëÇб³ Ä¡°ú´ëÇÐ ±¸°­³»°úÁø´ÜÇб³½Ç

Abstract

Ÿ¾×ÀÇ º¸È£ÀÛ¿ëÀº ÁַΠŸ¾× ´ç´Ü¹éÁúÀÇ »ý¹°ÇÐÀû, ¹°¸®Àû, ±¸Á¶Àû ¼ºÁú ¹× À¯µ¿ÇÐÀû ¼ºÁú°ú °ü·ÃÀÌ ÀÖ´Ù. ±×·¯¹Ç·Î ÀÌ»óÀûÀΠŸ¾× ´ëüÁ¦ÀÇ °³¹ßÀ» À§Çؼ­´Â ÀÎü Ÿ¾×ÀÇ »ý¹°ÇÐÀû ¼ºÁú »Ó¸¸ ¾Æ´Ï¶ó À¯µ¿ÇÐÀû Ư¼ºÀ» ÀÌÇØÇÏ¿©¾ß ÇÑ´Ù. º» ¿¬±¸ÀÇ ¸ñÀûÀº Ÿ¾× ´ëüÁ¦°¡ ÀÎü Ÿ¾×¿¡ Á¸ÀçÇÏ´Â È¿¼ÒÀÇ È°¼º¿¡ ¹ÌÄ¡´Â ¿µÇâÀ» ÆľÇÇÏ°í ´Ù¾çÇÑ Å¸¾× ´ëüÁ¦ÀÇ Á¡µµ¿Í ÀÎü Ÿ¾×ÀÇ Á¡µµ¸¦ ºñ±³Çϱâ À§Çؼ­ ½ÃÇàµÇ¾ú´Ù. Moi-Stir, Stoppers4, MouthKote, Saliva Orthana ¹× ¼­¿ï´ëÇб³Ä¡°úº´¿ø Ÿ¾× ´ëüÁ¦(SNU)¸¦ »ç¿ëÇÏ¿´À¸¸ç, lysozyme È°¼ºÀº turbidimetric ¹ýÀ¸·Î, peroxidase È°¼ºÀº NbsSCN ¹ýÀ¸·Î, ¥á-amylase È°¼ºÀº maltotriose¿Í °áÇÕµÈ 2-chloro-p-nitrophenol¸¦ »ç¿ëÇÏ¿© ½ÃÇàÇÏ¿´´Ù. Ÿ¾× ´ëüÁ¦ÀÇ pH¸¦ ÃøÁ¤ÇÏ¿´À¸¸ç cone-and-plate ÇüÅÂÀÇ Á¡µµ°è¸¦ ÀÌ¿ëÇÏ¿© ´Ù¾çÇÑ Àü´ÜÀ²¿¡¼­ Á¡µµ¸¦ ÃøÁ¤ÇÏ¿´´Ù. º» ¿¬±¸¿¡ »ç¿ëµÈ ´Ù¾çÇÑ Å¸¾× ´ëüÁ¦´Â Ÿ¾× È¿¼Ò È°¼º¿¡ °¢±â ´Ù¸¥ ¿µÇâÀ» ¹ÌÃÆ´Ù. Stoppers4´Â hen egg-white lysozyme, bovine lactoperoxidase (bLP) ¹× ¥á-amylase È°¼ºÀ» Áõ°¡½ÃÄ×°í, Saliva Orthana¿Í SNU´Â bLP È°¼ºÀº ÀúÇØÇÏ¿´À¸¸ç ¥á-amylase È°¼ºÀº Áõ°¡½ÃÄ×´Ù. MouthKote´Â ¥á-amylase È°¼ºÀ» ÀúÇØÇÏ¿´À¸¸ç, Moi-Stir´Â bLP¿Í ¥á-amylase È°¼ºÀ» ÀúÇØÇÏ¿´´Ù. Ÿ¾× ´ëüÁ¦ÀÇ pH´Â Ÿ¾× ´ëüÁ¦ÀÇ Á¾·ù¿¡ µû¶ó ¸Å¿ì ´Þ¶ú´Ù. Stoppers4, MouthKote ¹× Saliva Orthana´Â ³·Àº Àü´ÜÀ²¿¡¼­´Â ÀÎü Ÿ¾×º¸´Ù ³·Àº Á¡µµ¸¦ ³ôÀº Àü´ÜÀ²¿¡¼­´Â ÀÎü Ÿ¾×º¸´Ù ³ôÀº Á¡µµ¸¦ ³ªÅ¸³»¾ú´Ù. Moi-Stir¿Í SNU´Â ÀÎü Ÿ¾×º¸´Ù ¸Å¿ì ³ôÀº Á¡µµ¸¦ ³ªÅ¸³»¾ú´Ù. °á·ÐÀûÀ¸·Î º» ¿¬±¸°á°ú´Â °¢°¢ÀÇ Å¸¾× ´ëüÁ¦´Â °¢±â ´Ù¸¥ »ý¹°ÇÐÀû ±â´É°ú À¯µ¿ÇÐÀû Ư¼ºÀ» °¡Áö°í ÀÖÀ½À» ¾Ë ¼ö ÀÖ´Ù. Ÿ¾× ´ëüÁ¦ÀÇ »ç¿ëÀº »ç¿ëÇϴ Ÿ¾× ´ëüÁ¦ÀÇ Á¾·ù¿¡ µû¶ó Ÿ¾× È¿¼Ò È°¼º¿¡ °¢±â ´Ù¸¥ ¿µÇâÀ» ¹ÌÄ¡°í ±Ã±ØÀûÀ¸·Î´Â ±¸°­°Ç°­¿¡ ´Ù¸¥ ¿µÇâÀ» ¹ÌÄ¥ ¼ö ÀÖÀ» °ÍÀÌ´Ù.

Many of the protective functions of saliva can be attributed to the biological, physical, structural, and rheological characteristics of salivary glycoproteins. Therefore, the development of ideal saliva substitutes requires understanding of the rheological as well as biological properties of human saliva. In the present study, we investigated the changes of salivary enzymatic activities by saliva substitutes and compared viscosity of saliva substitutes with human saliva. Five kinds of saliva substitutes such as Moi-Stir, Stoppers4, MouthKote, Saliva Orthana, and SNU were used. Lysozyme activity was determined by the turbidimetric method. Peroxidase activity was determined with an NbsSCN assay. ¥á -Amylase activity was determined using a chromogenic substrate, 2-chloro-p-nitrophenol linked with maltotriose. The pH values of saliva substitutes were measured and their viscosity values were measured with a cone-and-plate digital viscometer at six different shear rates. Various types of saliva substitutes affected the activities of salivary enzymes in different ways. Stoppers4 enhanced the enzymatic activities of hen egg-white lysozyme, bovine lactoperoxidase (bLP), and ¥á-amylase. Saliva Orthana and SNU inhibited bLP activity and enhanced ¥á-amylase activity. MouthKote inhibited ¥á-amylase activity. Moi-Stir inhibited the enzymatic activities of bLP and ¥á-amylase. The pH values were very different according to the types of saliva substitutes. Stoppers4, MouthKote, and Saliva Orthana showed lower values of viscosity at low shear rates and higher values of viscosity at high shear rates compared with unstimulated and stimulated whole saliva. Moi-Stir and SNU displayed much higher values of viscosity than those of natural whole saliva. Collectively, our results indicate that each saliva substitute has its own biological and rheological characteristics. Each saliva substitute affects the enzymatic activity of salivary enzyme and finally oral health in different ways.

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Saliva substitute;Lysozyme;Peroxidase;Amylase;Saliva

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