Cerebral ischemia/reperfusion

脑缺血 / 再灌注
  • 文章类型: Journal Article
    无论在缺血性卒中的发病机制方面取得的进展,它仍然是成人残疾和死亡的主要原因。迄今为止,缺血性中风最有效的治疗方法是及时再通闭塞的动脉。然而,短的时间窗和再灌注损伤极大地限制了其应用和功效。线粒体功能障碍和ATP耗竭已被认为是缺血性中风后神经病理生理学的标志。线粒体移植是缺血性卒中的一种新的潜在治疗干预措施,在过去的几年中引起了广泛的关注。本文总结并讨论了线粒体移植在体外和体内缺血性中风模型中的作用。此外,综述和讨论了促进线粒体移植的药理干预措施。我们还讨论了线粒体移植在缺血性中风的临床应用中的潜在挑战。
    Regardless of the progress made in the pathogenesis of ischemic stroke, it remains a leading cause of adult disability and death. To date, the most effective treatment for ischemic stroke is the timely recanalization of the occluded artery. However, the short time window and reperfusion injury have greatly limited its application and efficacy. Mitochondrial dysfunction and ATP depletion have become regarded as being hallmarks of neuropathophysiology following ischemic stroke. Mitochondrial transplantation is a novel potential therapeutic intervention for ischemic stroke that has sparked widespread concern during the past few years. This review summarizes and discusses the effects of mitochondrial transplantation in in vitro and in vivo ischemic stroke models. In addition, pharmacological interventions promoting mitochondrial transplantation are reviewed and discussed. We also discuss the potential challenges to the clinical application of mitochondrial transplantation in the treatment of ischemic stroke.
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  • 文章类型: Journal Article
    虾青素是由各种微生物和海洋动物产生的脂溶性类胡萝卜素,包括细菌,酵母,真菌,微藻,虾和龙虾。虾青素有抗氧化剂,抗炎和抗凋亡特性。这些特征表明虾青素具有健康益处并防止各种疾病。由于它能够穿越血脑屏障,虾青素因其对神经系统疾病的保护作用而受到关注,包括老年痴呆症,帕金森病,肌萎缩侧索硬化,脑缺血/再灌注,蛛网膜下腔出血,创伤性脑损伤,脊髓损伤,认知障碍和神经性疼痛。以往对虾青素神经效应的研究大多基于动物模型和细胞实验。因此,虾青素对人类的生物学效应及其潜在机制仍未完全了解。本文综述了虾青素的神经保护作用,探讨其作用机制,并提请注意其作为治疗剂的潜在临床意义。
    Astaxanthin is a lipid‑soluble carotenoid produced by various microorganisms and marine animals, including bacteria, yeast, fungi, microalgae, shrimps and lobsters. Astaxanthin has antioxidant, anti‑inflammatory and anti‑apoptotic properties. These characteristics suggest that astaxanthin has health benefits and protects against various diseases. Owing to its ability to cross the blood‑brain barrier, astaxanthin has received attention for its protective effects against neurological disorders, including Alzheimer\'s disease, Parkinson\'s disease, amyotrophic lateral sclerosis, cerebral ischemia/reperfusion, subarachnoid hemorrhage, traumatic brain injury, spinal cord injury, cognitive impairment and neuropathic pain. Previous studies on the neurological effects of astaxanthin are mostly based on animal models and cellular experiments. Thus, the biological effects of astaxanthin on humans and its underlying mechanisms are still not fully understood. The present review summarizes the neuroprotective effects of astaxanthin, explores its mechanisms of action and draws attention to its potential clinical implications as a therapeutic agent.
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