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通过体内核磁共振波谱监测黄酮乙酸(NSC 347512)对小鼠肿瘤生理学的调节作用。

Flavone acetic acid (NSC 347512)-induced modulation of murine tumor physiology monitored by in vivo nuclear magnetic resonance spectroscopy.

作者信息

Evelhoch J L, Bissery M C, Chabot G G, Simpson N E, McCoy C L, Heilbrun L K, Corbett T H

机构信息

Department of Internal Medicine, Wayne State University School of Medicine, Detroit, Michigan 48201-1998.

出版信息

Cancer Res. 1988 Sep 1;48(17):4749-55.

PMID:3409216
Abstract

Flavone acetic acid (FAA), a new drug with broad activity against transplanted solid tumors of mice, induces nonrepairable DNA single strand breaks that correlate with therapeutic efficacy. To test the hypothesis that the inability of the cells to repair single strand breaks is associated with a disruption of tumor energy metabolism, in vivo 31P nuclear magnetic resonance (NMR) spectra were acquired from s.c. implanted Glasgow osteogenic sarcomas in C57BL/6 x DBA/2 F1 mice both before and after treatment with FAA i.v. at 100, 150, or 200 mg/kg and from a control (no treatment) group (n = 4 in each group). While FAA produced a dose-dependent decrease in both the nucleoside triphosphates level and pH, only treatment with an efficacious dose of 200 mg/kg resulted in both a reduction in pH and a complete loss of nucleoside triphosphates from the NMR spectrum at 4 h with no recovery until 48 h and little recovery out to 72 h. The ATP concentration determined by high pressure liquid chromatography in a parallel set of experiments was 5.59 +/- 1.16 (SE) mumol/g (wet weight) in control tumors (n = 9) and 0.24 +/- 0.12 mumol/g (wet weight) at 4 h after 200 mg/kg FAA (n = 7). To examine the possibility that the loss of ATP and decreased pH are associated with a reduction in tumor blood flow, we used 2H NMR to monitor the washout of D2O injected directly into the tumor both before and 4 h after treatment with 200 mg/kg FAA. The pretreatment tumor blood flow of 12.4 +/- 1.7 ml/min/100 g was reduced to 1.9 +/- 0.5 ml/min/100 g at 4 h after treatment (n = 3). The FAA-induced reduction of both tumor blood flow and ATP may play an important role in its mechanism of action and should be considered in the combination of FAA with other drugs or therapeutic modalities. In addition, because 31P NMR can be used clinically, it should provide a nonambiguous early indicator of activity for clinical trials of FAA.

摘要

黄酮醋酸(FAA)是一种对小鼠移植性实体瘤具有广泛活性的新药,可诱导与治疗效果相关的不可修复的DNA单链断裂。为了验证细胞无法修复单链断裂与肿瘤能量代谢紊乱相关的假说,在C57BL/6×DBA/2 F1小鼠体内,对皮下植入的格拉斯哥骨肉瘤在静脉注射100、150或200 mg/kg FAA治疗前后以及对照组(未治疗)组(每组n = 4)采集体内31P核磁共振(NMR)光谱。虽然FAA使三磷酸核苷水平和pH值呈剂量依赖性降低,但仅用有效剂量200 mg/kg治疗在4小时时导致pH值降低且三磷酸核苷从NMR光谱中完全消失,直到48小时才恢复,到72小时几乎没有恢复。在一组平行实验中,通过高压液相色谱法测定对照组肿瘤(n = 9)中的ATP浓度为5.59±1.16(SE)μmol/g(湿重),在200 mg/kg FAA治疗后4小时为0.24±0.12 μmol/g(湿重)(n = 7)。为了研究ATP丧失和pH值降低与肿瘤血流减少相关的可能性,我们使用2H NMR监测在200 mg/kg FAA治疗前后直接注入肿瘤的D2O的洗脱情况。治疗前肿瘤血流为12.4±1.7 ml/min/100 g,治疗后4小时降至1.9±0.5 ml/min/100 g(n = 3)。FAA诱导的肿瘤血流和ATP减少可能在其作用机制中起重要作用,在FAA与其他药物或治疗方式联合使用时应予以考虑。此外,由于31P NMR可用于临床,它应为FAA的临床试验提供明确的早期活性指标。

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