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In vivo MRI volumetric measurement of prostate regression and growth in mice

机译:小鼠体内前列腺退缩和生长的体内MRI体积测量

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Background Mouse models for treatment of late-stage prostate cancer are valuable tools, but assessing the extent of growth of the prostate and particularly its regression due to therapeutic intervention or castration is difficult due to the location, small size and interdigitated anatomy of the prostate gland in situ. Temporal monitoring of mouse prostate regression requires multiple animals and examination of histological sections. Methods Initially, T2-weighted magnetic resonance imaging (MRI) was performed on normal year-old C57/BL6 mice. Individual mice were repeatedly imaged using inhalation anesthesia to establish the reproducibility of the method and to follow hormone manipulation of the prostate volume. Subsequently, MRI fat signal was suppressed using a chemical shift-selective (CHESS) pulse to avoid signal contamination and enhance discrimination of the prostate. Results High field (7T) MRI provides high resolution (117 × 117 μm in plane), highly reproducible images of the normal mouse prostate. Despite long imaging times, animals can be imaged repeatedly to establish reliability of volume measurements. Prostate volume declines following castration and subsequently returns to normal with androgen administration in the same animal. CHESS imaging allowed discrimination of both the margins of the prostate and the dorsal-lateral lobes of the prostate (DLP) from the ventral lobes (VP). Castration results in a 40% reduction in the volume of the DLP and a 75% reduction in the volume of the VP. Conclusion MRI assessment of the volume of the mouse prostate is precise and reproducible. MRI improves volumetric determination of the extent of regression and monitoring of the same mouse over time during the course of treatment is possible. Since assessing groups of animals at each time point is avoided, this improves the accuracy of the measurement of any manipulation effect and reduces the number of animals required.
机译:背景技术用于治疗晚期前列腺癌的小鼠模型是有价值的工具,但是由于前列腺的位置,体积小和相互交叉的解剖结构,很难评估前列腺的生长程度,尤其是由于治疗干预或去势而导致的退化程度原地。小鼠前列腺消退的时间监测需要多只动物并检查组织学切片。方法最初,对正常一岁的C57 / BL6小鼠进行T2加权磁共振成像(MRI)。使用吸入麻醉对每只小鼠重复成像,以建立该方法的可重复性并跟踪激素对前列腺体积的控制。随后,使用化学位移选择性(CHESS)脉冲抑制了MRI脂肪信号,以避免信号污染并增强对前列腺的辨别力。结果高场(7T)MRI可提供正常小鼠前列腺的高分辨率(平面上为117×117μm),高度可重复的图像。尽管成像时间长,但可以对动物重复成像以建立体积测量的可靠性。 cast割后前列腺体积下降,随后在同一只动物中服用雄激素后恢复正常。 CHESS成像可从腹侧凸角(VP)分辨出前列腺的边缘和前列腺的背侧凸角(DLP)。去势导致DLP的体积减少40%,VP的体积减少75%。结论MRI对小鼠前列腺体积的评估是准确且可重复的。 MRI可以改善对消退程度的体积确定,并且可以在治疗过程中随时间监视同一只小鼠。由于避免了在每个时间点评估动物群,因此提高了任何操纵效果的测量准确性,并减少了所需动物的数量。

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