TY - JOUR
T1 - Stabilization of atherosclerotic plaque by pitavastatin in Watanabe heritable hyperlipidemic rabbits
T2 - A serial tissue-characterizing intravascular ultrasound study
AU - Haruta, Hironori
AU - Hiro, Takafumi
AU - Mitsumata, Masako
AU - Takayama, Tadateru
AU - Sudo, Mitsumasa
AU - Li, Yuxin
AU - Takahashi, Rie
AU - Taniguchi, Yoshiki
AU - Shiomi, Masashi
AU - Hirayama, Atsushi
N1 - Publisher Copyright:
© 2015 Japanese College of Cardiology.
PY - 2016/2/1
Y1 - 2016/2/1
N2 - Background: To examine the effects of pitavastatin on atherosclerotic plaque in Watanabe heritable hyperlipidemic (WHHL) rabbits using serial in vivo tissue-characterizing intravascular ultrasound. Methods: A total of 11 WHHL rabbits of 10-12 weeks of age were divided into two groups, control and pitavastatin-administered groups. A total of 29 atherosclerotic plaque segments from control group and 43 plaque segments from the pitavastatin group were serially imaged by 40. MHz intravascular ultrasound in vivo with a tissue characterization software (iMAP™, Boston Scientific, Natick, MA, USA) at the baseline and the follow-up (16th week). Results: The level of low-density lipoprotein cholesterol was significantly decreased in pitavastatin group. During the follow-up period, plaque area was significantly increased in the control group, whereas it was not significantly changed in the pitavastatin group. The fibrotic, necrotic, and necrotic plus lipidic areas were significantly increased in the control group, while no significant change was revealed for tissue profile in pitavastatin group. The change in the percent areas of fibrotic and lipidic plus necrotic tissues were significantly different between the two groups especially in the superficial half portion of plaque. Conclusions: These data indicate that pitavastatin could attenuate atherosclerotic plaque formation and that it could stabilize the plaque in WHHL rabbits. Considering the fact that these were observed even with a high follow-up level of cholesterol, these data might come from the pleiotropic effects of pitavastatin.
AB - Background: To examine the effects of pitavastatin on atherosclerotic plaque in Watanabe heritable hyperlipidemic (WHHL) rabbits using serial in vivo tissue-characterizing intravascular ultrasound. Methods: A total of 11 WHHL rabbits of 10-12 weeks of age were divided into two groups, control and pitavastatin-administered groups. A total of 29 atherosclerotic plaque segments from control group and 43 plaque segments from the pitavastatin group were serially imaged by 40. MHz intravascular ultrasound in vivo with a tissue characterization software (iMAP™, Boston Scientific, Natick, MA, USA) at the baseline and the follow-up (16th week). Results: The level of low-density lipoprotein cholesterol was significantly decreased in pitavastatin group. During the follow-up period, plaque area was significantly increased in the control group, whereas it was not significantly changed in the pitavastatin group. The fibrotic, necrotic, and necrotic plus lipidic areas were significantly increased in the control group, while no significant change was revealed for tissue profile in pitavastatin group. The change in the percent areas of fibrotic and lipidic plus necrotic tissues were significantly different between the two groups especially in the superficial half portion of plaque. Conclusions: These data indicate that pitavastatin could attenuate atherosclerotic plaque formation and that it could stabilize the plaque in WHHL rabbits. Considering the fact that these were observed even with a high follow-up level of cholesterol, these data might come from the pleiotropic effects of pitavastatin.
KW - Intravascular ultrasound
KW - Low-density lipoprotein cholesterol
KW - Plaque
KW - Statin
KW - WHHL-MI rabbit
UR - http://www.scopus.com/inward/record.url?scp=84955405042&partnerID=8YFLogxK
U2 - 10.1016/j.jjcc.2015.04.015
DO - 10.1016/j.jjcc.2015.04.015
M3 - Article
C2 - 26194868
AN - SCOPUS:84955405042
SN - 0914-5087
VL - 67
SP - 205
EP - 211
JO - Journal of Cardiology
JF - Journal of Cardiology
IS - 2
ER -