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血红蛋白作为一种假过氧化物酶及氧化应激相关疾病的药物靶点。

Hemoglobin as a pseudoperoxidase and drug target for oxidative stress-related diseases.

作者信息

Won Woojin, Lee Elijah Hwejin, Gotina Lizaveta, Chun Heejung, Lee Jae-Hun, Bhalla Mridula, Park Uiyeol, Kim Daeun, Kim Tai Young, Choi Ji Won, Kim Yoowon, Park Sun Jun, Lim Jiwoon, Park Jong-Hyun, Kim Hyeon Jeong, Heo Jun Young, Chung Woosuk, Oh Myung Jin, An Hyun Joo, Lee Junghee, Oh Soo-Jin, Ryu Hoon, Pae Ae Nim, Park Ki Duk, Lee C Justin

机构信息

Center for Cognition and Sociality, Institute for Basic Science (IBS), Daejeon, Republic of Korea.

Center for Brain Disorders, Brain Science Institute, Korea Institute of Science and Technology (KIST), Seoul, Republic of Korea.

出版信息

Signal Transduct Target Ther. 2025 Aug 22;10(1):270. doi: 10.1038/s41392-025-02366-w.

Abstract

Hemoglobin (Hb) is well known for transporting oxygen in the blood, but its role in the brain remains poorly understood. Here, we identified Hb in the cytosol, mitochondria, and nuclei of hippocampal and substantia nigra astrocytes and dopaminergic neurons. As a pseudoperoxidase, Hb decomposes hydrogen peroxide (HO) and mitigates HO-induced oxidative damage. However, in Alzheimer's disease, Parkinson's disease, and aging, excessive HO diminishes astrocytic Hb, perpetuating a vicious cycle of oxidative stress and neurodegeneration. To counter the harmful effects of aberrant HO production in diseases, we developed KDS12025, a BBB-permeable small molecule that enhances Hb pseudoperoxidase activity 100-fold, even at a low level of Hb. KDS12025 and its analogs achieve this enhancement through its electron-donating amine group, possibly stabilizing the complex between Hb, HO, and KDS12025. KDS12025 reduces astrocytic HO, alleviates astrogliosis, normalizes Hb, and reverts to a virtuous cycle of redox balance, preventing neurodegeneration without altering the oxygen-transport function of Hb. Gene silencing of Hb abrogates the impact of KDS12025 in both culture and animal models, confirming the necessity of Hb for the effects of KDS12025. KDS12025 extends survival and improves motor function even in severe amyotrophic lateral sclerosis and aging. Furthermore, the enrichment of astrocytic Hb in the nucleolus highlights a novel antioxidative mechanism potentially protecting against nuclear oxidative damage. Our findings suggest that Hb is a new therapeutic target for neurodegenerative diseases, with KDS12025 emerging as a first-in-class approach that enhances Hb pseudoperoxidase activity to reduce HO. Increasing Hb pseudoperoxidase activity with KDS12025 mitigates oxidative stress and alleviates neurodegeneration in AD, PD, and ALS patients and increases the degree of aging, with broad applicability for numerous oxidative-stress-driven diseases.

摘要

血红蛋白(Hb)因在血液中运输氧气而广为人知,但其在大脑中的作用仍知之甚少。在此,我们在海马体和黑质星形胶质细胞及多巴胺能神经元的胞质溶胶、线粒体和细胞核中鉴定出了Hb。作为一种假过氧化物酶,Hb分解过氧化氢(HO)并减轻HO诱导的氧化损伤。然而,在阿尔茨海默病、帕金森病和衰老过程中,过量的HO会减少星形胶质细胞中的Hb,使氧化应激和神经退行性变的恶性循环持续存在。为了对抗疾病中异常产生的HO的有害影响,我们开发了KDS12025,一种可透过血脑屏障的小分子,即使在Hb水平较低时也能将Hb假过氧化物酶活性提高100倍。KDS12025及其类似物通过其供电子胺基团实现这种增强,可能稳定了Hb、HO和KDS12025之间的复合物。KDS12025降低星形胶质细胞中的HO,减轻星形胶质细胞增生,使Hb正常化,并恢复到氧化还原平衡的良性循环,在不改变Hb氧运输功能的情况下预防神经退行性变。在细胞培养和动物模型中,对Hb进行基因沉默消除了KDS12025的作用,证实了Hb对KDS12025发挥作用的必要性。即使在严重的肌萎缩侧索硬化症和衰老模型中,KDS12025也能延长生存期并改善运动功能。此外,核仁中星形胶质细胞Hb的富集突出了一种潜在的新型抗氧化机制,可保护细胞核免受氧化损伤。我们的研究结果表明,Hb是神经退行性疾病的一个新的治疗靶点,KDS12025作为一种一流的方法出现,可增强Hb假过氧化物酶活性以减少HO。用KDS12025提高Hb假过氧化物酶活性可减轻氧化应激,缓解阿尔茨海默病、帕金森病和肌萎缩侧索硬化症患者的神经退行性变,并延缓衰老程度,对众多由氧化应激驱动的疾病具有广泛的适用性。

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