Effect of Atorvastatin, a HMG-CoA Reductase Inhibitor, in Experimental Colitis in Mice
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
KMID : 0357920040380060401
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.
Å°¿öµå
Atorvastatin;inflammatiory bowel disease;Experimental colitis;Th cell mediated immunity;Immunity; Natural
¿ø¹® ¹× ¸µÅ©¾Æ¿ô Á¤º¸
µîÀçÀú³Î Á¤º¸