摘要
切除3月龄SD大鼠双侧卵巢12周后,其骨形成的参数值明显增加(%L.Pm+58%,BFR/BV+105%,BFR/BS+74%,%0.Pm+188%),同时骨吸收的参数值增加(%Er.Pm+155%),荧光标记周长与吸收周长的比率-41%,由于骨吸收大于骨形成,骨质丢失(%Tb.Ar-59%,Tb.Th一14%),出现高转换型骨质疏松。分别用蛇床子素(osthole)6.7mg·kg ̄(-1)ig,每周6次,尼尔雌醇(nilestriol)1mg·kg ̄(-1)ig,每周1次,持续12周,均能明显抑制去卵巢诱导的骨高转换,防止骨质丢失。但蛇床子素抑制骨高转换的效应比尼尔雌醇低(蛇床子素治疗组比尼尔雌醇治疗组%Tb.Ar一55%)。
Thirty-one 3-month-old ♀ Sprague -Dawley rats were randomly divided into 5groups,basal control(group 1,killed at the begining),aging control(group 2),ovariectomized(OVX,group3),OVX with nilestriol treatment group(group 4)and OVX with osthole treatmentgroup(group 5).Group 2 and group 3 ig with water 5 ml· kg -1 and group 5 ig with osthole 6.7m8· kg-1, all once a day for 6 d;group4ig with nilestriol 1 mg· kg-1,once a week.After 12weeks,all rats were killed.The proximal tibiae of rats were processed to undecalcified sections at 20um thickness for histomorphometric analysis.OVX was shown to reduce markedly the trabecular bonemass(%Tb.Ar一59%)due to increase of bone turnover with the result that bone resorption exceededbone formation, as compared with aging controls.In contrast,treatment of OVX rats with Ostholeand nilestriol increased significantly the trabecular area(increased 68%and 274%compared with thatof OVX respectively).Our results indicate that osthole and nilestriol treatment provides protectionagainst osteoporosis in OVX rats.The protective mechanism of osthole and nilestriol involvessupressiOn of bone turnover,but the effects of osthole is lower than that of nilestriol(trabecular areadecreased 55%more in osthole group than that with nilestriol treatment).Our finding may providetheoretical evidence for the clinical use of osthole or nilestriol for treatment and prevention ofosteoporosis.
出处
《药学学报》
CAS
CSCD
北大核心
1996年第5期327-332,共6页
Acta Pharmaceutica Sinica
基金
国家自然科学基金
关键词
蛇床子
香豆素
蛇床子素
尼尔雌醇
骨质疏松
Common onidium fruit
Coumarins
Osthole
Nilestriol
Osteoporosis
Bonehistomorphometry