代谢组学揭示了羟基红花黄A对实验性创伤性脑损伤后神经发生和轴突再生的影响。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2023-12-01 DOI:10.1080/13880209.2023.2229379
En Hu, Teng Li, Zhilin Li, Hong Su, Qiuju Yan, Lei Wang, Haigang Li, Wei Zhang, Tao Tang, Yang Wang
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引用次数: 0

摘要

背景:羟基红花黄色素A(HSYA)是红花治疗创伤性脑损伤的主要生物活性成分。目的:探讨HSYA对脑外伤后神经发生和轴突再生的治疗作用及其可能机制。材料和方法:雄性Sprague-Dawley大鼠随机分为Sham组、控制皮层冲击组和HSYA组。首先,采用改良的神经严重程度评分(mNSS)、足部损伤试验、苏木精-伊红染色、尼氏染色以及Tau1和双皮质素(DCX)的免疫荧光来评估HSYA对第14天TBI的影响。接下来,通过病理学专业网络药理学和非靶向代谢组学筛选HSYA对TBI后神经发生和轴突再生的影响因素。然后,通过免疫荧光对核心效应物进行验证。结果:HSYA减轻了mNSS、足部故障率、炎症细胞浸润和Nissl身体损失。此外,HSYA在TBI后不仅增加了海马DCX,还增加了皮质Tau1和DCX。代谢组学表明,HSYA显著调节富含“精氨酸代谢”和“苯丙氨酸、酪氨酸和色氨酸代谢“的海马和皮层代谢产物,包括l-苯丙氨酸、鸟氨酸、l-(+)-瓜氨酸和精氨酸琥珀酸。网络药理学表明,神经营养因子(BDNF)和信号转导和转录激活因子3(STAT3)是HSYA TBI神经发生和轴突再生网络的核心节点。此外,HSYA治疗后,皮层和海马中的BDNF和生长相关蛋白43(GAP43)显著升高。讨论和结论:HSYA可能通过调节皮层和海马代谢、BDNF和STAT3/GAP43轴促进神经发生和轴突再生,从而促进TBI的恢复。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Metabolomics reveals the effects of hydroxysafflor yellow A on neurogenesis and axon regeneration after experimental traumatic brain injury.

Context: Hydroxysafflor yellow A (HSYA) is the main bioactive ingredient of safflower (Carthamus tinctorius L., [Asteraceae]) for traumatic brain injury (TBI) treatment.

Objective: To explore the therapeutic effects and underlying mechanisms of HSYA on post-TBI neurogenesis and axon regeneration.

Materials and methods: Male Sprague-Dawley rats were randomly assigned into Sham, controlled cortex impact (CCI), and HSYA groups. Firstly, the modified Neurologic Severity Score (mNSS), foot fault test, hematoxylin-eosin staining, Nissl's staining, and immunofluorescence of Tau1 and doublecortin (DCX) were used to evaluate the effects of HSYA on TBI at the 14th day. Next, the effectors of HSYA on post-TBI neurogenesis and axon regeneration were screened out by pathology-specialized network pharmacology and untargeted metabolomics. Then, the core effectors were validated by immunofluorescence.

Results: HSYA alleviated mNSS, foot fault rate, inflammatory cell infiltration, and Nissl's body loss. Moreover, HSYA increased not only hippocampal DCX but also cortical Tau1 and DCX following TBI. Metabolomics demonstrated that HSYA significantly regulated hippocampal and cortical metabolites enriched in 'arginine metabolism' and 'phenylalanine, tyrosine and tryptophan metabolism' including l-phenylalanine, ornithine, l-(+)-citrulline and argininosuccinic acid. Network pharmacology suggested that neurotrophic factor (BDNF) and signal transducer and activator of transcription 3 (STAT3) were the core nodes in the HSYA-TBI-neurogenesis and axon regeneration network. In addition, BDNF and growth-associated protein 43 (GAP43) were significantly elevated following HSYA treatment in the cortex and hippocampus.

Discussion and conclusions: HSYA may promote TBI recovery by facilitating neurogenesis and axon regeneration through regulating cortical and hippocampal metabolism, BDNF and STAT3/GAP43 axis.

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