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大鼠骨骼中甲状旁腺激素(PTH)分解代谢与合成代谢治疗方案的分子特征:DNA微阵列分析

Molecular profile of catabolic versus anabolic treatment regimens of parathyroid hormone (PTH) in rat bone: an analysis by DNA microarray.

作者信息

Onyia Jude E, Helvering Leah M, Gelbert Lawrence, Wei Tao, Huang Shuguang, Chen Peining, Dow Ernst R, Maran Avudaiappan, Zhang Minzhi, Lotinun Sutada, Lin Xi, Halladay David L, Miles Rebecca R, Kulkarni Nalini H, Ambrose Emily M, Ma Yanfei L, Frolik Charles A, Sato Masahiko, Bryant Henry U, Turner Russell T

机构信息

Integrative Biology, Lilly Research Labs, Indianapolis, Indiana 46285, USA.

出版信息

J Cell Biochem. 2005 May 15;95(2):403-18. doi: 10.1002/jcb.20438.

Abstract

Teriparatide, human PTH (1-34), a new therapy for osteoporosis, elicits markedly different skeletal responses depending on the treatment regimen. In order to understand potential mechanisms for this dichotomy, the present investigation utilized microarrays to delineate the genes and pathways that are regulated by intermittent (subcutaneous injection of 80 microg/kg/day) and continuous (subcutaneous infusion of 40 microg/kg/day by osmotic mini pump) PTH (1-34) for 1 week in 6-month-old female rats. The effect of each PTH regimen was confirmed by histomorphometric analysis of the proximal tibial metaphysis, and mRNA from the distal femoral metaphysis was analyzed using an Affymetrix microarray. Both PTH paradigms co-regulated 22 genes including known bone formation genes (i.e., collagens, osteocalcin, decorin, and osteonectin) and also uniquely modulated additional genes. Intermittent PTH regulated 19 additional genes while continuous treatment regulated 173 additional genes. This investigation details for the first time the broad profiling of the gene and pathway changes that occur in vivo following treatment of intermittent versus continuous PTH (1-34). These results extend previous observations of gene expression changes and reveal the in vivo regulation of BMP3 and multiple neuronal genes by PTH treatment.

摘要

特立帕肽,即人甲状旁腺激素(1-34),一种治疗骨质疏松症的新疗法,根据治疗方案会引发明显不同的骨骼反应。为了了解这种二分法的潜在机制,本研究利用微阵列来描绘在6月龄雌性大鼠中,由间歇性(皮下注射80微克/千克/天)和连续性(通过渗透微型泵皮下输注40微克/千克/天)甲状旁腺激素(1-34)调节1周的基因和通路。通过对近端胫骨干骺端进行组织形态计量学分析来确认每种甲状旁腺激素治疗方案的效果,并使用Affymetrix微阵列分析来自远端股骨干骺端的mRNA。两种甲状旁腺激素治疗模式共同调节22个基因,包括已知的骨形成基因(即胶原蛋白、骨钙素、核心蛋白聚糖和骨连接蛋白),并且还独特地调节其他基因。间歇性甲状旁腺激素调节另外19个基因,而连续性治疗调节另外173个基因。本研究首次详细描述了间歇性与连续性甲状旁腺激素(1-34)治疗后体内发生的基因和通路变化的广泛概况。这些结果扩展了先前对基因表达变化的观察,并揭示了甲状旁腺激素治疗对骨形态发生蛋白3和多个神经元基因的体内调节作用。

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