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氧化应激介导血管迂曲。

Oxidative Stress Mediates Vascular Tortuosity.

作者信息

Fumoto Toshio, Kinoshita Shouhei, Sasaki Takao, Shimamura Norihito, Ohkuma Hiroki

机构信息

Department of Neurosurgery, Graduate School of Medicine, Hirosaki University, 5-Zaifuchou, Hirosaki, Aomori 036-8562, Japan.

出版信息

Antioxidants (Basel). 2021 Jun 7;10(6):926. doi: 10.3390/antiox10060926.

Abstract

Vascular tortuosity is associated with various disorders and is being increasingly detected through advances in imaging techniques. The underlying mechanisms for vascular tortuosity, however, remain unclear. Here, we tested the hypothesis that oxidative stress mediates the generation of tortuous vessels. We used the bilateral common carotid artery (CCA) ligation model to induce vascular tortuosity. Both young and adult rats showed basilar artery tortuous morphological changes one month after bilateral CCA ligation. These tortuous changes were permanent but more pronounced in the adult rats. Microarray and real-time PCR analysis revealed that these tortuous changes were accompanied by the induction of oxidative stress-related genes. Moreover, the indicated model in rabbits showed that tortuous morphological changes to the basilar artery were suppressed by antioxidant treatment. These results are highly suggestive of the significance of oxidative stress in the development of vascular tortuosity. Although further studies will be needed to elucidate the possible mechanisms by which oxidative stress enhances vascular tortuosity, our study also points toward possible prophylaxis and treatment for vascular tortuosity.

摘要

血管迂曲与多种疾病相关,并且随着成像技术的进步越来越多地被检测到。然而,血管迂曲的潜在机制仍不清楚。在此,我们检验了氧化应激介导迂曲血管生成的假说。我们使用双侧颈总动脉(CCA)结扎模型诱导血管迂曲。年轻和成年大鼠在双侧CCA结扎后1个月均出现基底动脉迂曲的形态学变化。这些迂曲变化是永久性的,但在成年大鼠中更明显。微阵列和实时PCR分析显示,这些迂曲变化伴随着氧化应激相关基因的诱导。此外,兔的所示模型表明,抗氧化剂治疗可抑制基底动脉的迂曲形态学变化。这些结果强烈提示氧化应激在血管迂曲发展中的重要性。尽管需要进一步研究来阐明氧化应激增强血管迂曲的可能机制,但我们的研究也指出了血管迂曲可能的预防和治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9dbc/8228074/076e778467e9/antioxidants-10-00926-g001.jpg

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