摘要
目的:研究下坡跑对生长期和去卵巢小鼠骨中Ⅰ型胶原蛋白表达和骨量的影响。方法:80只4周龄C57BL/6雌性小鼠适应性喂养1周后随机分为安静组(C组)、运动组(D组)、安静去卵巢组(C+OVX组)、运动去卵巢组(D+OVX组)和安静假手术组(C+SHAM组),每组16只。D组和D+OVX组进行8周下坡跑训练,剩余3组不训练。最后1次训练结束24 h后,处死C组和D组小鼠;C+OVX组和D+OVX组小鼠进行去卵巢手术,C+SHAM组进行假手术,术后安静状态下喂养6周,静养结束后,处死这3组小鼠。结果:(1)8周下坡跑训练结束后,小鼠骨中COL1α1 mRNA和Ⅰ型胶原蛋白表达上调有统计学意义,骨组织形态计量学指标和骨量增加有统计学意义;(2)去卵巢6周后,小鼠骨中COL1α1 mRNA和Ⅰ型胶原蛋白表达上调有统计学意义,骨组织形态计量学指标和骨量提高有统计学意义。结论:下坡跑可能通过上调骨中COL1α1 mRNA和Ⅰ型胶原蛋白表达来改善骨组织形态结构和骨量,且这种作用在去卵巢后仍然存在。
Objective: The purpose of this study was to research the effect of downhill running on expression of type I collagen and bone mass in growth and ovariectomized mice. Methods: 80 four-week-old C57BL/6 female mice were randomly divided into 5 groups as control group (C), downhill running group (D), ovariectomized control group (C+OVX), ovariectomized exercise group (D+OVX) and control sedentary group (C+SHAM). D Group and D+ OVX group were forced to downhill running for eight weeks while the residual groups received no training. C and D group mice were sacrificed after the 8 week training program; C+OVX and D+OVX group mice were subjected to ovariectomy 24 h after the last training and C+SHAM group mice reveived a sham parallel. Then C+OVX, D+OVX and C+SHAM group mice were killed 6 week later. Results: (1)After 8 weeks training, the expression of COLlcdmRNA and type I collagen in bone were significantly upregulated, the indexs of bone histomorphometry and bone mass were significantly increased; (2) After 6 weeks, the COL1α1 mRNA and type I collagen were remain significantly upregulated, the index of bone histomorphometry and bone mass were remain significantly increased. Conclusions: Downhill running can increase the trabecular structure of cancellous and bone mass by upregulating the expression of COL1α1 mRNA and type I collagen in bone and also this effect can extend at least six weeks in ovariectomized mice.
出处
《天津体育学院学报》
CAS
CSSCI
北大核心
2013年第5期427-430,共4页
Journal of Tianjin University of Sport
关键词
下坡跑
生长期
去卵巢
I型胶原蛋白
骨形成
downhill running
growth period
ovariectomized
type I collagen
bone formation