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Tauroursodeoxycholic Acid Inhibited Apoptosis and Oxidative Stress in H2O2-Induced BMSC Death via Modulating the Nrf-2 Signaling Pathway: the Therapeutic Implications in a Rat Model of Spinal Cord Injury

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机构: [1]School of Pharmaceutical Sciences, Guangzhou University of Chinese Medicine, Guangzhou 510006, Guangdong, China [2]Lingnan Medical Research Center of Guangzhou University of Chinese Medicine, Guangzhou 510405, China [3]Guangzhou University of Chinese Medicine, Guangzhou 510405, China [4]Department of Spine Surgery, the First Afliated Hospital of Sun Yat-Sen University, Guangdong Provincial Key Laboratory of Orthopedics and Traumatology, Guangzhou 510080, Guangdong, China [5]State Key Laboratory of Dampness Syndrome of Chinese Medicine, Department of Orthopedic Surgery,, The Second Afliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou 510120, China [6]The First Afliated Hospital of Chinese Medicine, Guangzhou University of Chinese Medicine, Guangzhou 510405, China
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关键词: Bone marrow mesenchymal stem cells  TUDCA  Spinal cord injury  Apoptosis  Oxidative stress

摘要:
Spinal cord injury (SCI) is a prevalent and significant injury to the central nervous system, resulting in severe consequences. This injury is characterized by motor, sensory, and excretory dysfunctions below the affected spinal segment. Transplantation of bone marrow mesenchymal stem cells (BMSCs) has emerged as a potential treatment for SCI. However, the low survival as well as the differentiation rates of BMSCs within the spinal cord microenvironment significantly limit their therapeutic efficiency. Tauroursodeoxycholic acid (TUDCA), an active ingredient found in bear bile, has demonstrated its neuroprotective, antioxidant, and antiapoptotic effects on SCI. Thus, the present study was aimed to study the possible benefits of combining TUDCA with BMSC transplantation using an animal model of SCI. The results showed that TUDCA significantly enhanced BMSC viability and reduced apoptosis (assessed by Annexin V-FITC, TUNEL, Bax, Bcl-2, and Caspase-3) as well as oxidative stress (assessed by ROS, GSH, SOD, and MDA) both in vitro and in vivo. Additionally, TUDCA accelerated tissue regeneration (assessed by HE, Nissl, MAP2, MBP, TUJ1, and GFAP) and improved functional recovery (assessed by BBB score) following BMSC transplantation in SCI. These effects were mediated via the Nrf-2 signaling pathway, as evidenced by the upregulation of Nrf-2, NQO-1, and HO-1 expression levels. Overall, these results indicate that TUDCA could serve as a valuable adjunct to BMSC transplantation therapy for SCI, potentially enhancing its therapeutic efficacy.© 2023. The Author(s).

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大类 | 2 区 医学
小类 | 2 区 神经科学
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大类 | 2 区 医学
小类 | 2 区 神经科学
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第一作者机构: [1]School of Pharmaceutical Sciences, Guangzhou University of Chinese Medicine, Guangzhou 510006, Guangdong, China [2]Lingnan Medical Research Center of Guangzhou University of Chinese Medicine, Guangzhou 510405, China [3]Guangzhou University of Chinese Medicine, Guangzhou 510405, China
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通讯机构: [2]Lingnan Medical Research Center of Guangzhou University of Chinese Medicine, Guangzhou 510405, China [3]Guangzhou University of Chinese Medicine, Guangzhou 510405, China [5]State Key Laboratory of Dampness Syndrome of Chinese Medicine, Department of Orthopedic Surgery,, The Second Afliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou 510120, China
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