用[99mTc]Tc-巯基乙酰三甘氨酸 SPECT 测量异氟醚麻醉深度和持续时间对小鼠肾功能的影响。

IF 3.1 3区 医学 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
Fabian Schmitz-Peiffer, Mathias Lukas, Ajay-Mohan Mohan, Jakob Albrecht, Jörg R Aschenbach, Winfried Brenner, Nicola Beindorff
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引用次数: 0

摘要

背景:在使用半静态动态单光子发射计算机断层扫描(SPECT)进行肾脏闪烁成像的 86 只重症联合免疫缺陷(SCID)小鼠中,研究了麻醉深度的影响以及不同麻醉床和不同处理程序的潜在影响。因此,在低麻醉(80-90 次/分)和深麻醉(40-45 次/分)时,异氟醚浓度根据呼吸频率进行调整。在低麻醉状态下,我们还测试了单鼠床与三鼠床酒店的影响;酒店小鼠分别在 1 号、2 号和 3 号位置注射示踪剂前约 30 分钟、20 分钟和 10 分钟连续麻醉。SPECT 开始后,静脉注射约 28 MBq 的[99mTc]Tc-MAG3。使用时间-活性曲线计算峰值时间(Tmax)、T50(50%清除率)和T25(75%清除率):结果:低度和深度麻醉对应的异氟醚浓度中值分别为 1.3% 和 1.5%,心率无显著差异(p = 0.74)。低度麻醉导致主动脉血液清除半衰期缩短(p = 0.091),相对肾脏示踪剂流入率增加(p = 0.018)。在低麻醉状态下,Tmax 有提前的趋势(p = 0.063),T50(p = 0.40)和 T25(p = 0.24)没有差异。差异随深度麻醉而增加。与单只小鼠扫描相比,位置 1 中的酒店小鼠显示出延迟的 Tmax、T50 和 T25(p 结论):肾脏闪烁扫描时应避免深度麻醉和长时间低麻醉,因为它们会导致血液清除半衰期延长、肾脏流入延迟和/或 Tmax 延迟。反之,则应首选呼吸频率高(80-90 rpm)、持续时间短(≤ 20 分钟)的低麻醉,以获得具有代表性且差异较小的数据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of isoflurane anaesthesia depth and duration on renal function measured with [99mTc]Tc-mercaptoacetyltriglycine SPECT in mice.

Background: The influence of anaesthetic depth and the potential influence of different anaesthetic beds and thus different handling procedures were investigated in 86 severe combined immunodeficient (SCID) mice using semi-stationary dynamic single photon emission computed tomography (SPECT) for kidney scintigraphy. Therefore, isoflurane concentrations were adjusted using respiratory rate for low (80-90 breath/min) and deep anaesthesia (40-45 breath/min). At low anaesthesia, we additionally tested the influence of single bed versus 3-mouse bed hotel; the hotel mice were anaesthetized consecutively at ~ 30, 20, and 10 min before tracer injections for positions 1, 2, and 3, respectively. Intravenous [99mTc]Tc-MAG3 injection of ~ 28 MBq was performed after SPECT start. Time-activity curves were used to calculate time-to-peak (Tmax), T50 (50% clearance) and T25 (75% clearance).

Results: Low and deep anaesthesia corresponded to median isoflurane concentrations of 1.3% and 1.5%, respectively, with no significant differences in heart rate (p = 0.74). Low anaesthesia resulted in shorter aortic blood clearance half-life (p = 0.091) and increased relative renal tracer influx rate (p = 0.018). A tendency toward earlier Tmax occurred under low anaesthesia (p = 0.063) with no differences in T50 (p = 0.40) and T25 (p = 0.24). Variance increased with deep anaesthesia. Compared to single mouse scans, hotel mice in position 1 showed a delayed Tmax, T50, and T25 (p < 0.05 each). Furthermore, hotel mice in position 1 showed delayed Tmax versus position 3, and delayed T50 and T25 versus position 2 and 3 (p < 0.05 each). No difference occurred between single bed and positions 2 (p = 1.0) and 3 (p = 1.0).

Conclusions: Deep anaesthesia and prolonged low anaesthesia should be avoided during renal scintigraphy because they result in prolonged blood clearance half-life, delayed renal influx and/or later Tmax. Vice versa, low anaesthesia with high respiratory rates of 80-90 rpm and short duration (≤ 20 min) should be preferred to obtain representative data with low variance.

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来源期刊
EJNMMI Research
EJNMMI Research RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING&nb-
CiteScore
5.90
自引率
3.10%
发文量
72
审稿时长
13 weeks
期刊介绍: EJNMMI Research publishes new basic, translational and clinical research in the field of nuclear medicine and molecular imaging. Regular features include original research articles, rapid communication of preliminary data on innovative research, interesting case reports, editorials, and letters to the editor. Educational articles on basic sciences, fundamental aspects and controversy related to pre-clinical and clinical research or ethical aspects of research are also welcome. Timely reviews provide updates on current applications, issues in imaging research and translational aspects of nuclear medicine and molecular imaging technologies. The main emphasis is placed on the development of targeted imaging with radiopharmaceuticals within the broader context of molecular probes to enhance understanding and characterisation of the complex biological processes underlying disease and to develop, test and guide new treatment modalities, including radionuclide therapy.
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