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慢性睡眠剥夺损害生长中大鼠的骨形成并下调骨组织中的PI3K/AKT信号通路。

Chronic Sleep Deprivation Impaired Bone Formation in Growing Rats and Down-Regulated PI3K/AKT Signaling in Bone Tissues.

作者信息

Duan Xiaoye, Pan Qi, Guo Lixin

机构信息

Department of Endocrinology, Beijing Hospital, National Center of Gerontology, Institute of Geriatric Medicine, Chinese Academy of Medical Sciences, Beijing, People's Republic of China.

Graduate School of Peking Union Medical College, Chinese Academy of Medical Sciences, Beijing, People's Republic of China.

出版信息

Nat Sci Sleep. 2022 Apr 14;14:697-710. doi: 10.2147/NSS.S351850. eCollection 2022.

Abstract

BACKGROUND

This study aimed to assess the effects of chronic sleep deprivation (CSD) on bone metabolism in growing rats and the likely underlying mechanism.

METHODS

Twenty 5-week-old male Wistar rats and randomly divided into the CSD and normal control (NC) groups after one-week acclimatization. After a 6-week intervention of sleep deprivation, the distal femurs of both groups were harvested for micro-computed tomography scans and histological analysis. Meanwhile, the femur tissues were measured the mRNA and protein expression via RNA sequencing and immunohistochemical analysis. Serum bone turnover markers were evaluated at 0, 2, 4, and 6 weeks.

RESULTS

CSD impaired the bone growth, showing an imbalance of bone turnover status, dysphasia in the metaphysis growth plate, and deterioration of bone microarchitecture. Further, CSD suppressed bone formation, showing that the expression of osteogenesis-related proteins (col1α1 and osteocalcin) and mRNA () are down-regulated. Differentially expressed genes were detected, and functional enrichment analyses revealed that the PI3K/AKT pathway was significantly down-regulated in the CSD group.

CONCLUSION

These results suggest that CSD can significantly impaire bone health, and it may exert these effects in part by suppressing bone formation and osteoblast differentiation, and inactivating the PI3K/AKT signaling pathway.

摘要

背景

本研究旨在评估慢性睡眠剥夺(CSD)对生长中大鼠骨代谢的影响及其潜在机制。

方法

20只5周龄雄性Wistar大鼠,经1周适应性饲养后随机分为CSD组和正常对照组(NC)。经过6周的睡眠剥夺干预后,采集两组大鼠的股骨远端进行显微计算机断层扫描和组织学分析。同时,通过RNA测序和免疫组织化学分析测定股骨组织中mRNA和蛋白质表达。在第0、2、4和6周评估血清骨转换标志物。

结果

CSD损害骨生长,表现为骨转换状态失衡、干骺端生长板发育异常以及骨微结构恶化。此外,CSD抑制骨形成,表现为成骨相关蛋白(col1α1和骨钙素)和mRNA的表达下调。检测到差异表达基因,功能富集分析显示CSD组中PI3K/AKT通路显著下调。

结论

这些结果表明,CSD可显著损害骨骼健康,其可能部分通过抑制骨形成和成骨细胞分化以及使PI3K/AKT信号通路失活来发挥这些作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/052c/9015811/a42007a35a08/NSS-14-697-g0001.jpg

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