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Diffusion Efficiency and Bioavailability of Resveratrol Administered to Rat Brain by Different Routes: Therapeutic Implications

机译:白藜芦醇通过不同途径给药于大鼠脑的扩散效率和生物利用度:治疗意义

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摘要

Resveratrol possesses anti-tumor activities against central nervous system (CNS) tumors in vitro but has not yet been used clinically due to its low bioavailability, particularly in the CNS. This study thus aimed to elucidate brain bioavailability of trans-resveratrol by monitoring brain concentrations and dwell times following administration of resveratrol through intragastric, intraperitoneal, external carotid artery/ECA and intrathecal routes. In parallel, we evaluated the biological responses of rat RG2 glioblastoma cells as well as RG2-formed rat intracranial glioblastomas treated with resveratrol via intrathecal administration. The results revealed that resveratrol was detected in rat brains except when administered systemically. Intrathecal administration of reseveratrol led to abundant apoptotic foci and increased staining of the autophagy proteins, LC-3 and Beclin-1 and shrinkage of the intracranial tumors. In conclusion, the BBB penetrability of resveratrol is remarkably increased by intracthecal administration. Regular short-term resveratrol treatments suppress growth and enhance autophagic and apoptotic activities of rat RG2 glioblastoma cells in vitro and in vivo. Therefore, intrathecal administration of resveratrol could be an optimal intervention approach in the adjuvant management of brain malignancies.Electronic supplementary materialThe online version of this article (doi:10.1007/s13311-014-0334-6) contains supplementary material, which is available to authorized users.
机译:白藜芦醇在体外具有抗中枢神经系统(CNS)肿瘤的抗肿瘤活性,但由于其生物利用度低而尚未在临床上使用,特别是在CNS中。因此,本研究旨在通过监测通过胃内,腹膜内,颈外动脉/ ECA和鞘内途径给药白藜芦醇后的脑浓度和停留时间,阐明反式白藜芦醇的脑生物利用度。同时,我们通过鞘内给药评估了大鼠RG2胶质母细胞瘤细胞以及用白藜芦醇治疗的RG2形成的大鼠颅内胶质母细胞瘤的生物学反应。结果表明,除全身给药外,在大鼠脑中均检测到白藜芦醇。鞘内注射白藜芦醇可导致大量凋亡灶,自噬蛋白LC-3和Beclin-1的染色增加,颅内肿瘤缩小。总之,通过皮内给药可明显提高白藜芦醇的BBB渗透性。常规的短期白藜芦醇治疗可在体外和体内抑制大鼠RG2胶质母细胞瘤细胞的生长并增强其自噬和凋亡活性。因此,鞘内注射白藜芦醇可能是脑恶性肿瘤辅助治疗的最佳干预方法。电子补充材料本文的在线版本(doi:10.1007 / s13311-014-0334-6)包含补充材料,可通过授权获得用户。

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