首页> 外文期刊>Addiction biology >Intranasal delivery of mesenchymal stem cell‐derived exosomes reduces oxidative stress and markedly inhibits ethanol consumption and post‐deprivation relapse drinking.
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Intranasal delivery of mesenchymal stem cell‐derived exosomes reduces oxidative stress and markedly inhibits ethanol consumption and post‐deprivation relapse drinking.

机译:间充质干细胞衍生的外索体的鼻内递送减少了氧化应激并显着抑制乙醇消费和剥夺后复发饮酒。

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Abstract Chronic ethanol consumption leads to brain oxidative stress and neuroinflammation, conditions known to potentiate and perpetuate each other. Several studies have shown that neuroinflammation results in increases in chronic ethanol consumption. Recent reports showed that the intra‐cerebroventricular administration of mesenchymal stem cells to rats consuming alcohol chronically markedly inhibited oxidative‐stress, abolished neuroinflammation and greatly reduced chronic alcohol intake and post deprivation relapse‐like alcohol intake. However, the intra‐cerebroventricular administration of living cells is not suitable as a treatment of a chronic condition. The present study aimed at inhibiting ethanol intake by the non‐invasive intranasal administration of human mesenchymal stem cell products: exosomes, microvesicles (40 to 150?nm) with marked antioxidant activity extruded from mesenchymal stem cells. The exosome membrane can fuse with the plasma membrane of cells in different tissues, thus delivering their content intracellularly. The study showed that the weekly intranasal administration of mesenchymal stem cell‐derived exosomes to rats consuming alcohol chronically (1) inhibited their ethanol intake by 84 percent and blunted the relapse‐like ‘binge’ drinking that follows an alcohol deprivation period and ethanol re‐access. (2) Intranasally administered exosomes were found in the brain within 24?hours; (3) fully reversed both alcohol‐induced hippocampal oxidative‐stress, evidenced by a lower ratio of oxidized to reduced glutathione, and neuroinflammation, shown by a reduced astrocyte activation and microglial density; and (4) increased glutamate transporter GLT1 expression in nucleus accumbens, counteracting the inhibition of glutamate transporter activity, reportedly depressed under oxidative‐stress conditions. Possible translational implications are envisaged.
机译:摘要慢性乙醇消耗导致脑氧化应激和神经炎症,众所周知的条件,并彼此延伸。几项研究表明,神经炎性炎症导致慢性乙醇消耗量的增加。最近的报道显示,脑内充质干细胞的脑内闭合性施用对饮酒的大鼠慢性抑制氧化胁迫,废除神经炎性和大大降低的慢性酒精摄入量和后剥夺复发样酒精摄入量。然而,脑内脑室内的活细胞施用不适合作为对慢性病症的治疗。本研究旨在通过非侵入性鼻内施用人间充质干细胞产物的乙醇摄入:外泌体,微缺血(40至150〜Nm),具有从间充质干细胞挤出的标记抗氧化活性。外渗膜可以与不同组织中细胞的血浆膜一起熔化,从而递送它们的内容物细胞内。该研究表明,每周鼻内鼻内施用间充质干细胞衍生的外索体对饮用醇慢性(1)抑制其乙醇摄入量84%,并钝化了遵循酒精剥夺期和乙醇的复发样的“狂欢”饮酒使用权。 (2)在24小时内的大脑中发现鼻内给药外泌体; (3)完全逆转醇诱导的海马氧化 - 应激,通过氧化降低的谷胱甘肽和神经炎性的较低比例证明,通过减少的星形胶质细胞活化和微胶质密度表示; (4)增加谷氨酸转运蛋白GLT1在核心腺中的表达,抵消抑制谷氨酸转运蛋白活性,据报道在氧化胁迫条件下抑制。设想可能的翻译含义。

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