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小鼠淋巴功能的无创定量成像

Noninvasive quantitative imaging of lymph function in mice.

作者信息

Kwon Sunkuk, Sevick-Muraca Eva M

机构信息

Division of Molecular Imaging, Department of Radiology, Baylor College of Medicine, Houston, TX 77030-3411, USA.

出版信息

Lymphat Res Biol. 2007;5(4):219-31. doi: 10.1089/lrb.2007.1013.

Abstract

BACKGROUND

Whereas functional lymph imaging in rodents is imperative for drug discovery of lymph therapeutics, noninvasive imaging of propulsive lymph function in rodents has not been reported previously. Herein, we present a noninvasive and rapid approach to measure lymphatic function in a rodent model using a near-infrared (NIR) dye to minimize background autofluorescence and maximize tissue penetration.

METHODS AND RESULTS

Mice were dynamically imaged following intradermal (i.d.) injection of 2 to 10 microL of 1.3 mM of indocyanine green (IC-Green) into the tail and the limb. Our results demonstrate the ability to image the IC-Green trafficking from the lymph plexus, through lymph vessels and lymphangions, to the ischial nodes in the tail, and to the axillary nodes in the limb. Our results show that lymph flow velocity from the propelled IC-Green "packet" in the lymph vessels in the tail ranged from 1.3 to 3.9 mm/s and the fluorescence intensity peaks repeated on an average of every 51.3 +/- 17.4 seconds in five animals. While pulsatile lymph flow was detected in the deep lymph vessels, lymph propulsion was not visualized in the superficial lymphatic network in the tail. In axillary lymphatic imaging, propulsive lymph flow was also detected. The intensity profile shows that the lymph flow velocity ranged from 0.28 to 1.35 mm/s at a frequency ranging from 0.72 to 11.1 pulses per minute in five animals.

CONCLUSIONS

Our study demonstrates the ability to noninvasively and quantitatively image propulsive lymph flow, which could provide a new method to investigate lymph function and its change in response to potential therapeutics.

摘要

背景

尽管啮齿动物的功能性淋巴成像对于淋巴治疗药物的发现至关重要,但此前尚未有关于啮齿动物推进性淋巴功能的无创成像报道。在此,我们提出一种无创且快速的方法,使用近红外(NIR)染料来测量啮齿动物模型中的淋巴功能,以最小化背景自发荧光并最大化组织穿透深度。

方法与结果

在小鼠的尾巴和肢体皮内(i.d.)注射2至10微升1.3 mM的吲哚菁绿(IC-绿)后进行动态成像。我们的结果表明能够对IC-绿从淋巴丛,通过淋巴管和淋巴节,流向尾巴的坐骨淋巴结以及肢体的腋窝淋巴结的过程进行成像。我们的结果显示,尾巴淋巴管中被推进的IC-绿“包块”的淋巴流速范围为1.3至3.9毫米/秒,五只动物中荧光强度峰值平均每51.3±17.4秒重复一次。虽然在深部淋巴管中检测到搏动性淋巴流,但在尾巴的浅表淋巴网络中未观察到淋巴推进。在腋窝淋巴成像中,也检测到了推进性淋巴流。强度分布图显示,五只动物的淋巴流速范围为0.28至1.35毫米/秒,频率范围为每分钟0.72至11.1次搏动。

结论

我们的研究证明了无创和定量成像推进性淋巴流的能力,这可为研究淋巴功能及其对潜在治疗的反应变化提供一种新方法。

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