Department of Emergency Medicine, University of California San Diego, La Jolla, California, United States.
Department of Radiology, University of California San Diego, La Jolla, California, United States.
J Appl Physiol (1985). 2024 Apr 1;136(4):949-953. doi: 10.1152/japplphysiol.00859.2023. Epub 2024 Feb 29.
Decompression sickness (DCS) is caused by gaseous nitrogen dissolved in tissues forming bubbles during decompression. To date, no method exists to identify nitrogen within tissues, but with advances in positron-emission tomography (PET) technology, it may be possible to track gaseous radionuclides into tissues. We aimed to develop a method to track nitrogen movement in vivo and under hyperbaric pressure that could then be used to further our understanding of DCS using nitrogen-13 (N). A single anesthetized female Sprague-Dawley rat was exposed to 625 kPa, composed of air, isoflurane, and N for 10 min. The PET scanner recorded N during the hyperbaric exposure with energy windows of 250-750 keV. The PET showed an increase in N concentration in the lung, heart, and abdominal regions, which all reached a plateau after ∼4 min. This showed that it is possible to gain noninvasive in vivo measurements of nitrogen kinetics through the body while at hyperbaric pressures. Tissue samples showed radioactivity above background levels in the blood, brain, liver, femur, and thigh muscle when assessed using a γ counter. The method can be used to evaluate an array of challenges to our understanding of decompression physiology by quantifying nitrogen load through γ counts of N, and signal intensity of the PET. Further development of the method will improve the specificity of the measured outcomes, and enable it to be used with larger mammals, including humans. This article describes a method for the in vivo quantification and tracking of nitrogen through the mammalian body whilst exposed to hyperbaric pressure. The method has the potential to further our understanding of decompression sickness, and quantitatively evaluate the effectiveness of both the treatment and prevention of decompression sickness.
减压病(DCS)是由于组织中溶解的氮气在减压过程中形成气泡而引起的。迄今为止,尚无方法可识别组织中的氮气,但随着正电子发射断层扫描(PET)技术的进步,有可能追踪气态放射性核素进入组织。我们旨在开发一种方法来跟踪体内氮气的运动和高压下的氮气运动,然后可以使用氮-13(N)来进一步了解 DCS。一只麻醉的雌性 Sprague-Dawley 大鼠暴露于由空气、异氟烷和 N 组成的 625 kPa 高压下 10 分钟。PET 扫描仪在高压暴露期间记录 N 的能量窗口为 250-750 keV。PET 显示肺、心脏和腹部区域的 N 浓度增加,在大约 4 分钟后达到平台。这表明在高压下通过身体获得氮动力学的非侵入性体内测量是可能的。使用γ计数器评估时,组织样本在血液、大脑、肝脏、股骨和大腿肌肉中显示出高于背景水平的放射性。该方法可以通过对 N 的γ计数和 PET 的信号强度来定量评估氮负荷,从而评估对我们对减压生理学理解的一系列挑战。该方法的进一步发展将提高测量结果的特异性,并使其能够与包括人类在内的大型哺乳动物一起使用。本文描述了一种在体内定量和跟踪氮的方法,同时在高压下暴露于哺乳动物体内。该方法有可能进一步了解减压病,并定量评估减压病的治疗和预防效果。