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单次低剂量辐射对幼年大鼠脑室下区细胞的影响。

Effects of single low dose irradiation on subventricular zone cells in juvenile rat brain.

作者信息

Amano Toshiyuki, Inamura Takanori, Wu Chun-Ming, Kura Shinobu, Nakamizo Akira, Inoha Satoshi, Miyazono Masayuki, Ikezaki Kiyonobu

机构信息

Department of Neurosurgery, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka, 812-8582, Japan.

出版信息

Neurol Res. 2002 Dec;24(8):809-16. doi: 10.1179/016164102101200771.

Abstract

Although the juvenile human brain is relatively radioresistant, irradiation can result in brain growth retardation, progressive mental disturbance, and neurologic abnormalities. As neural stem cells or progenitor cells may be a target of radiation injury and may play an important role in the brain's functional recovery, we examined the effects of whole brain irradiation on these cells in juvenile rat. Six-week-old Wistar rats, where the brain is still growing, were irradiated with single doses of 1, 2, or 3 Gy X-ray. We measured their body and brain weights at 30 or 60 days after irradiation. The chronological changes of the subventricular zone (SVZ) were examined at 6 h, 2, 7, 14, 30, or 60 days after irradiation by immunohistochemistry, specifically looking at the neural stem cells or progenitor cells using anti-nestin antibodies specific for these cells. The rate of brain weight gain of irradiated rats significantly decreased in comparison to controls, although that of body weight gain was similar among them. Multiple apoptotic cells appeared in the SVZ at 6 h after irradiation with simultaneous reduction in nestin-positive cells (69% of the control). The cell levels recovered within a week, with the nestin-positive cells reaching maximal numbers (182%) on Day 14. Nestin-positive cells returned to baseline levels within 30 days (96%) and remained unchanged for the subsequent 60 days. The X-ray dosage did not affect these findings. Our findings revealed that single low dose X-ray administration reversibly affected the levels of neural stem and progenitor cells in the SVZ region. These results suggest that continuous multiple administrations of X-rays in clinical treatment may affect irreversible changes on neural stem or progenitor cells, causing brain growth retardation, or dysfunction.

摘要

尽管幼年人类大脑对辐射相对具有抗性,但辐射仍可导致脑发育迟缓、进行性精神障碍和神经异常。由于神经干细胞或祖细胞可能是辐射损伤的靶点,并且可能在大脑功能恢复中发挥重要作用,我们研究了全脑照射对幼年大鼠这些细胞的影响。六周龄的Wistar大鼠,其大脑仍在生长,接受了1、2或3 Gy的单次X射线照射。我们在照射后30天或60天测量了它们的体重和脑重。通过免疫组织化学在照射后6小时、2天、7天、14天、30天或60天检查脑室下区(SVZ)的时间变化,具体使用针对这些细胞的抗巢蛋白抗体观察神经干细胞或祖细胞。与对照组相比,照射大鼠的脑重增加率显著降低,尽管它们的体重增加率相似。照射后6小时,SVZ中出现多个凋亡细胞,同时巢蛋白阳性细胞减少(为对照组的69%)。细胞水平在一周内恢复,巢蛋白阳性细胞在第14天达到最大数量(为对照组的182%)。巢蛋白阳性细胞在30天内恢复到基线水平(为对照组的96%),并在随后的60天内保持不变。X射线剂量不影响这些结果。我们的研究结果表明,单次低剂量X射线给药可逆地影响了SVZ区域神经干细胞和祖细胞的水平。这些结果表明,临床治疗中连续多次给予X射线可能会对神经干细胞或祖细胞产生不可逆的变化,导致脑发育迟缓或功能障碍。

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