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多柔比星化疗会影响骨骼肌细胞内和细胞间游离氨基酸池。

Doxorubicin chemotherapy affects the intracellular and interstitial free amino acid pools in skeletal muscle.

机构信息

Biomolecular Sciences, Laurentian University, Sudbury, Ontario, Canada.

Division of Medical Sciences, Northern Ontario School of Medicine, Sudbury & Thunder Bay, Ontario, Canada.

出版信息

PLoS One. 2018 Apr 4;13(4):e0195330. doi: 10.1371/journal.pone.0195330. eCollection 2018.

Abstract

Skeletal muscle (SM) health and integrity is dependent on the dynamic balance between protein synthesis and degradation, and central to this process is the availability of amino acids (AA) in the amino pool. While Doxorubicin (DOX) remains one of the most widely used chemotherapeutic agents for the treatment of solid and hematological malignancies, little is known of the effect of the drug on SM, particularly its effect on the availability of amino acids in the tissue. The purpose of this study was to examine the effect of DOX administration on vascular, interstitial and intracellular concentrations of AA in SM of the rat up to 8 days after the administration of a 1.5 or 4.5 mg/kg i.p. dose of DOX. In the plasma, total amino acids (TAA) were significantly increased compared to control where greater (P<0.05) concentrations were observed following the 1.5 mg/kg dose compared to the 4.5 mg/kg dose. Compared to control, the 1.5 mg/kg dose resulted in an increase (P<0.05) in interstitial TAA whereas the 4.5 mg/kg resulted in a sustained decrease (P<0.05). Intracellular TAA, essential amino acids (EAA) and branched-chain amino acids (BCAA) where significantly increased in each muscle group analyzed, following the 1.5 and 4.5 mg/kg doses compared to control. This study provides important insight into the amino acid response following DOX chemotherapy and presents a substantial foundation for future studies focused on reducing SM damage and recovery by targeting amino acid metabolism.

摘要

骨骼肌 (SM) 的健康和完整依赖于蛋白质合成和降解的动态平衡,而这一过程的核心是氨基酸 (AA) 在氨基酸池中的可用性。多柔比星 (DOX) 仍然是治疗实体瘤和血液系统恶性肿瘤最广泛使用的化疗药物之一,但人们对该药物对 SM 的影响知之甚少,特别是其对组织中氨基酸可用性的影响。本研究旨在检查 DOX 给药对大鼠 SM 血管、间质和细胞内 AA 浓度的影响,直至给药后 8 天,给予大鼠 1.5 或 4.5 mg/kg i.p. DOX 剂量。在血浆中,总氨基酸 (TAA) 与对照组相比显著增加,其中观察到 1.5 mg/kg 剂量比 4.5 mg/kg 剂量更高 (P<0.05)。与对照组相比,1.5 mg/kg 剂量导致间质 TAA 增加 (P<0.05),而 4.5 mg/kg 剂量导致持续减少 (P<0.05)。与对照组相比,1.5 和 4.5 mg/kg 剂量导致每个分析的肌肉群中的细胞内 TAA、必需氨基酸 (EAA) 和支链氨基酸 (BCAA) 均显著增加。本研究为 DOX 化疗后氨基酸反应提供了重要的见解,并为未来专注于通过靶向氨基酸代谢减少 SM 损伤和恢复的研究提供了重要基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efe9/5884546/31994ce65b0b/pone.0195330.g001.jpg

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