Division of Cardiovascular Medicine, University of Iowa Carver College of Medicine, Iowa City, Iowa, United States of America.
PLoS One. 2013 Jun 6;8(6):e65201. doi: 10.1371/journal.pone.0065201. Print 2013.
There are no rigorously confirmed effective medical therapies for calcific aortic stenosis. Hypercholesterolemic Ldlr (-/-) Apob (100/100) mice develop calcific aortic stenosis and valvular cardiomyopathy in old age. Osteoprotegerin (OPG) modulates calcification in bone and blood vessels, but its effect on valve calcification and valve function is not known.
To determine the impact of pharmacologic treatment with OPG upon aortic valve calcification and valve function in aortic stenosis-prone hypercholesterolemic Ldlr (-/-) Apob (100/100) mice.
Young Ldlr (-/-) Apob (100/100) mice (age 2 months) were fed a Western diet and received exogenous OPG or vehicle (N = 12 each) 3 times per week, until age 8 months. After echocardiographic evaluation of valve function, the aortic valve was evaluated histologically. Older Ldlr (-/-) Apob (100/100) mice were fed a Western diet beginning at age 2 months. OPG or vehicle (N = 12 each) was administered from 6 to 12 months of age, followed by echocardiographic evaluation of valve function, followed by histologic evaluation.
In Young Ldlr (-/-) Apob (100/100) mice, OPG significantly attenuated osteogenic transformation in the aortic valve, but did not affect lipid accumulation. In Older Ldlr (-/-) Apob (100/100) mice, OPG attenuated accumulation of the osteoblast-specific matrix protein osteocalcin by ∼80%, and attenuated aortic valve calcification by ∼ 70%. OPG also attenuated impairment of aortic valve function.
OPG attenuates pro-calcific processes in the aortic valve, and protects against impairment of aortic valve function in hypercholesterolemic aortic stenosis-prone Ldlr (-/-) Apob (100/100) mice.
目前尚无经严格证实的有效医学疗法可用于治疗钙化性主动脉瓣狭窄。载脂蛋白 B 基因敲除合并 LDL 受体基因敲除(Ldlr -/- )的 Apob(100/100 )小鼠在老年时会发展为钙化性主动脉瓣狭窄和瓣叶心肌病变。骨保护素(Osteoprotegerin,OPG)可调节骨骼和血管中的钙化,但它对瓣膜钙化和瓣膜功能的影响尚不清楚。
旨在确定 OPG 药物治疗对易患主动脉瓣狭窄的高胆固醇血症 LDLR(-/-)Apob(100/100 )小鼠主动脉瓣钙化和瓣膜功能的影响。
年轻的 LDLR(-/-)Apob(100/100 )小鼠(2 月龄)给予西方饮食,并每周接受 3 次外源性 OPG 或载体(每组 12 只)治疗,直至 8 月龄。在进行瓣膜功能的超声心动图评估后,对主动脉瓣进行组织学评估。老年 LDLR(-/-)Apob(100/100 )小鼠从 2 月龄开始给予西方饮食。OPG 或载体(每组 12 只)从 6 至 12 月龄开始给药,随后进行瓣膜功能的超声心动图评估,随后进行组织学评估。
在年轻的 LDLR(-/-)Apob(100/100 )小鼠中,OPG 显著抑制了主动脉瓣的成骨转化,但不影响脂质蓄积。在老年 LDLR(-/-)Apob(100/100 )小鼠中,OPG 使成骨细胞特异性基质蛋白骨钙素的蓄积减少了约 80%,并使主动脉瓣钙化减少了约 70%。OPG 还减轻了主动脉瓣功能的损害。
OPG 可抑制主动脉瓣的促钙化过程,并可防止高胆固醇血症易患主动脉瓣狭窄的 LDLR(-/-)Apob(100/100 )小鼠主动脉瓣功能受损。