Maruvada Subha, Hynynen Kullervo
Department of Radiology, Division of MRI, Brigham and Women's Hospital, Boston, MA 02139, USA.
Ultrasound Med Biol. 2004 Jan;30(1):67-74. doi: 10.1016/j.ultrasmedbio.2003.08.005.
This study is an investigation of the therapeutic ultrasound (US) effects on the blood vessels of optically transparent fish in vivo. Although many investigators have characterized cavitation in vivo using remote-sensing methods (i.e., measuring the acoustic emissions caused by oscillating bubbles) very few have made direct observations of cavitation-induced damage. Anesthetized glass catfish, which are optically transparent, was injected with the contrast agent, Optison, and then insonified at pressures that ranged from 0.5-10 MPa (peak negative pressures). Two focused transducers were used in these experiments to cover a frequency range of 0.7-3.3 MHz. Sonications were pulsed with pulse durations of 100, 10, 1, 0.1 and 0.01 ms and a pulse repetition frequency (PRF) of 1 Hz. The entire length of one sonication at a specific pressure level was 20 s. An inverted microscope combined with a digital camera and video monitor were used optically to monitor and record US interaction with the blood vessels in the tail of the anesthetized fish at 200x magnification. The effects of the burst sonication were analyzed visually at each pressure level. For the 1.091-MHz sonications, the first type of damage that occurred due to the US interaction was structural damage to the cartilage rods that comprise the tail of the fish, and was characterized by a disintegration of the lining of the rod. Damage to the rods occurred, starting at 3.5 MPa, 3.1 MPa, 4.1 MPa and 5.5 MPa for the 100-ms, 10-ms, 1-ms and 100-micros sonications, respectively. The formation of large gas bubbles was observed in the blood vessels of the fish at threshold values of 3.8 MPa, 3.8 MPa and 5.3 MPa, for the 100-ms, 10-ms and 1-ms sonications, respectively. Neither gas bubble formation nor hemorrhaging was observed during 100-micros sonications. Bubble formation was always accompanied by an increase of damage to the rods at the area surrounding the bubble. At 1.091 MHz, petechial hemorrhage thresholds were observed at 4.1 MPa, 4.1 MPa and 6.1 MPa, respectively, for the three pulse durations. The thresholds for damage were the lowest for the 0.747-MHz sonications: they were 2.6 MPa for damage to the rods, 3.7 MPa for gas bubble formation and 2.4 MPa for hemorrhaging.
本研究旨在调查治疗性超声(US)对体内光学透明鱼类血管的影响。尽管许多研究人员已使用遥感方法(即测量由振荡气泡引起的声发射)对体内空化进行了表征,但很少有人直接观察到空化诱导的损伤。将麻醉后的光学透明玻璃鲶鱼注射造影剂Optison,然后在0.5 - 10 MPa(峰值负压)的压力下进行超声辐照。在这些实验中使用了两个聚焦换能器,以覆盖0.7 - 3.3 MHz的频率范围。超声辐照采用脉冲形式,脉冲持续时间分别为100、10、1、0.1和0.01 ms,脉冲重复频率(PRF)为1 Hz。在特定压力水平下的一次超声辐照总时长为20 s。使用倒置显微镜结合数码相机和视频监视器进行光学监测,并以200倍放大率记录超声与麻醉鱼尾部血管的相互作用。在每个压力水平下直观分析脉冲超声辐照的效果。对于1.091 MHz的超声辐照,由于超声相互作用而发生的第一种损伤类型是对构成鱼尾的软骨棒的结构损伤,其特征是软骨棒内衬的崩解。对于100 - ms、10 - ms、1 - ms和100 - μs的超声辐照,软骨棒损伤分别在3.5 MPa、3.1 MPa、4.1 MPa和5.5 MPa开始出现。在100 - ms、10 - ms和1 - ms超声辐照的阈值分别为3.8 MPa、