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Effect of Atorvastatin, a HMG-CoA Reductase Inhibitor, in Experimental Colitis in Mice

´ëÇѺ´¸®ÇÐȸÁö 2004³â 38±Ç 6È£ p.401 ~ 407
¹ÚÈ¿Áø, ¿À±ÇÀÍ, ½ÅÇü½Ä, Seo Jae-Nam, ¹Ú¿µÀÇ, ±èÅ¿î, ÃÖÀº¿µ,
¼Ò¼Ó »ó¼¼Á¤º¸
¹ÚÈ¿Áø ( Park Hyo-Jin ) 
¼­¿ï´ëÇб³ ÀÇ°ú´ëÇÐ º´¸®Çб³½Ç

¿À±ÇÀÍ ( Oh Kwon-Ik ) 
ÇѸ²´ëÇб³ ÀÇ°ú´ëÇÐ º´¸®Çб³½Ç
½ÅÇü½Ä ( Shin Hyung-Sik ) 
ÇѸ²´ëÇб³ ÀÇ°ú´ëÇÐ º´¸®Çб³½Ç
 ( Seo Jae-Nam ) 
ÇѸ²´ëÇб³ ÀÇ°ú´ëÇÐ º´¸®Çб³½Ç
¹Ú¿µÀÇ ( Park Young-Euy ) 
ÇѸ²´ëÇб³ ÀÇ°ú´ëÇÐ º´¸®Çб³½Ç
±èÅ¿î ( Kim Tae-Woon ) 
ÇѸ²´ëÇб³ ÀÇ°ú´ëÇÐ º´¸®Çб³½Ç
ÃÖÀº¿µ ( Choi Eun-Young ) 
¼­¿ï´ëÇб³ ÀÇ°ú´ëÇРƯ¼ö»ý¸íÀÚ¿ø¼¾ÅÍ

Abstract


Background: The statins, 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitors, are approved for cholesterol reduction, and may also be beneficial in the treatment of inflammatory disease. In this study, atorvastatin was tested in experimental colitis, a disease model of inflammatory bowel disease.

Methods: To induce colitis, dextran sodium sulfate (DSS) or trinitrobenzene sulfonic acid (TNBS) were administrated to C57BL/6 or BALB/c mice. Mice were monitored daily for loss of body weight and survival for indicated days. Colon length and histology were examined after sacrifice.

Results: The administration of DSS induced marked colonic inflammation and shortening, and resulted in a loss of body weight. DSS-induced colitis was not affected by atorvastatin treatment, but in contrast, the administration of atorvastatin relieved TNBS-induced colitis with a resultant rapid recovery of weight loss and a reduction in colonic length shortening. Histologically, inflammatory cell infiltration in the colonic wall, mucosal ulceration and crypt disruption were also suppressed in atorvastatin treated mice.

Conclusions: These results suggest that atorvastatin preserves intestinal integrity in colitis, probably via the modulation of Th cell-mediated immune response, in a manner independent of innate immunity.

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Atorvastatin;inflammatiory bowel disease;Experimental colitis;Th cell mediated immunity;Immunity; Natural

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