Suppr超能文献

大鼠椎管和脊髓在性成熟后仍继续生长:解剖学研究和分子假说。

Spinal Canal and Spinal Cord in Rat Continue to Grow Even after Sexual Maturation: Anatomical Study and Molecular Proposition.

机构信息

Department of Orthopaedic Surgery, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, Kita-15 Nishi-7, Kita-ku, Sapporo 060-8638, Japan.

出版信息

Int J Mol Sci. 2022 Dec 16;23(24):16076. doi: 10.3390/ijms232416076.

Abstract

Although rodents have been widely used for experimental models of spinal cord diseases, the details of the growth curves of their spinal canal and spinal cord, as well as the molecular mechanism of the growth of adult rat spinal cords remain unavailable. They are particularly important when conducting the experiments of cervical spondylotic myelopathy (CSM), since the disease condition depends on the size of the spinal canal and the spinal cord. Thus, the purposes of the present study were to obtain accurate growth curves for the spinal canal and spinal cord in rats; to define the appropriate age in weeks for their use as a CSM model; and to propose a molecular mechanism of the growth of the adult spinal cord in rats. CT myelography was performed on Lewis rats from 4 weeks to 40 weeks of age. The vertical growth of the spinal canal at C5 reached a plateau after 20 and 12 weeks, and at T8 after 20 and 16 weeks, in males and females, respectively. The vertical growth of the C5 and T8 spinal cord reached a plateau after 24 weeks in both sexes. The vertical space available for the cord (SAC) of C5 and T8 did not significantly change after 8 weeks in either sex. Western blot analyses showed that VEGFA, FGF2, and BDNF were highly expressed in the cervical spinal cords of 4-week-old rats, and that the expression of these growth factors declined as rats grew. These findings indicate that the spinal canal and the spinal cord in rats continue to grow even after sexual maturation and that rats need to be at least 8 weeks of age for use in experimental models of CSM. The present study, in conjunction with recent evidence, proposes the hypothetical model that the growth of rat spinal cord after the postnatal period is mediated at least in part by differentiation of neural progenitor cells and that their differentiation potency is maintained by VEGFA, FGF2, and BDNF.

摘要

虽然啮齿动物已被广泛用于脊髓疾病的实验模型,但它们的椎管和脊髓的生长曲线的细节以及成年大鼠脊髓生长的分子机制仍然未知。当进行颈椎病(CSM)实验时,这些信息尤为重要,因为疾病状况取决于椎管和脊髓的大小。因此,本研究的目的是获得大鼠椎管和脊髓的准确生长曲线;确定作为 CSM 模型使用的合适周龄;并提出大鼠成年脊髓生长的分子机制。对 4 至 40 周龄的 Lewis 大鼠进行 CT 脊髓造影。雄性和雌性大鼠的 C5 椎管垂直生长在 20 周和 12 周后达到平台期,T8 椎管在 20 周和 16 周后达到平台期。C5 和 T8 脊髓的垂直生长在雌雄大鼠中均在 24 周后达到平台期。C5 和 T8 的脊髓可用垂直空间(SAC)在两性中在 8 周后没有显著变化。Western blot 分析显示,4 周龄大鼠颈段脊髓中 VEGFA、FGF2 和 BDNF 表达水平较高,随着大鼠生长,这些生长因子的表达水平下降。这些发现表明,大鼠的椎管和脊髓在性成熟后仍在继续生长,并且需要至少 8 周龄才能用于 CSM 的实验模型。本研究结合最近的证据,提出了假设模型,即大鼠脊髓在出生后的生长至少部分是由神经祖细胞的分化介导的,其分化潜能由 VEGFA、FGF2 和 BDNF 维持。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验