在n-甲基- n-亚硝基脲诱导的小鼠乳腺癌模型中,芦丁对阿霉素诱导的认知功能障碍有保护作用,同时保留了阿霉素的抗癌潜力。

G. Ramalingayya, K. Gourishetti, P. Nayak, C. Rao, A. Kishore, S. Alnaseer, S. Hussain, K. Nandakumar
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引用次数: 10

摘要

化疗脑是一种重要的化疗后并发症,目前尚无批准的治疗方法。我们之前已经发现,芦丁抑制阿霉素(Dox-)诱导的健康大鼠认知能力下降。然而,重要的是要确定它在患有乳腺癌的大鼠中起作用,而不影响Dox的抗肿瘤潜力。用n -甲基-n -亚硝基脲(i.p)腹腔灌胃诱导雌性大鼠乳腺癌。发生乳腺癌的大鼠在用对照物或芦丁预处理后再用阿霉素治疗。Dox暴露后(50天),分别使用新的对象识别任务和Morris水迷宫评估情景记忆和空间记忆。通过测量肿瘤的重量、体积和组织学分析来评估肿瘤的进展。采集血样估计血液学参数。测定脑匀浆的氧化状态和TNF-α水平。Dox治疗显著减小了肿瘤的大小和体积。芦丁预处理未显著改变Dox的抑瘤潜能,提示其不影响Dox的抗癌活性。此外,芦丁还能改善dox诱导的认知能力下降、骨髓抑制和脑氧化应激。目前的研究表明,芦丁对dox诱导的认知能力下降和骨髓抑制有保护作用,但不影响其抗肿瘤潜能。
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Rutin Protects against Doxorubicin-Induced Cognitive Dysfunction While Retaining the Anticancer Potential of Dox in a Murine Model of N-Methyl-N-Nitrosourea - Induced Mammary Carcinoma.
Chemobrain is a significant post-chemotherapy complication for which no approved treatments are available. We had previously identified that rutin inhibits doxorubicin (Dox-) -induced cognitive decline in healthy rats. However, it was important to also establish that it does so in rats with mammary carcinoma without compromising Dox's antitumor potential. Mammary carcinoma was induced in female rats by intraperitonial administration of N-methyl-N-nitrosourea (i.p.). Rats that developed mammary carcinoma were treated with Dox after pretreatment with vehicle or rutin. After Dox exposure (50 days), episodic and spatial memory was assessed using the novel object recognition task and the Morris water maze, respectively. Tumor progression was evaluated by measurement of tumor weight and volume and histological analysis. Blood samples were collected to estimate hematological parameters. Oxidative status and TNF-α levels were estimated in brain homogenates. Dox treatment significantly reduced tumor size and volume. Pretreatment with rutin did not significantly alter Dox's tumor suppression potential, suggesting that it does not influence Dox's anticancer activity. In addition, rutin ameliorated Dox-induced cognitive decline, myelosuppression, and brain oxidative stress. The present study indicates that rutin protects against Dox-induced cognitive decline and myelosuppression without affecting its antitumor potential.
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