Marthi Katalin, Hansen Søren B, Jakobsen Steen, Bender Dirk, Smith Stefan Bo, Smith Donald F
PET Center, Aarhus University Hospital, Nørrebrogade 44, Aarhus C 8000, Denmark.
Appl Radiat Isot. 2003 Aug-Sep;59(2-3):175-9. doi: 10.1016/s0969-8043(03)00156-8.
Central adrenoceptors cannot currently be studied by PET neuroimaging due to a lack of appropriate radioligands. The fast-acting antidepressant drug mirtazapine, radiolabelled for PET, may be of value for assessing central adrenoceptors, provided that the radiation dosimetry of the radioligand is acceptable. To obtain that information, serial whole-body images were made for up to 70 min following intravenous injection of 326 and 185 MBq [N-methyl-11C]mirtazapine (specific activities E.O.S. of 119 and 39G Bq/micromol, respectively) in a healthy volunteer. Ten source organs plus remaining body were considered in estimating absorbed radiation doses calculated using MIRD 3.1. The highest absorbed organ doses were found to the lungs (3.4 x 10(-2) mGy/MBq), adrenals (1.2 x 10(-2) mGy/MBq), spleen (1.2 x 10(-2) mGy/MBq), and gallbladder wall (1.1 x 10(-2) mGy/MBq). The effective dose was estimated to be 6.8 x 10(-3) mSv/MBq, which is similar to that produced by several radioligands used routinely for neuroimaging.
由于缺乏合适的放射性配体,目前正电子发射断层扫描(PET)神经成像无法对中枢肾上腺素能受体进行研究。用于PET的放射性标记速效抗抑郁药米氮平,若放射性配体的辐射剂量测定结果可接受,则可能对评估中枢肾上腺素能受体有价值。为获取该信息,在一名健康志愿者静脉注射326和185 MBq [N-甲基-¹¹C]米氮平(比活度分别为119和39 GBq/μmol)后,连续进行长达70分钟的全身成像。在使用MIRD 3.1估算吸收辐射剂量时,考虑了十个源器官及剩余身体部分。发现肺部(3.4×10⁻² mGy/MBq)、肾上腺(1.2×10⁻² mGy/MBq)、脾脏(1.2×10⁻² mGy/MBq)和胆囊壁(1.1×10⁻² mGy/MBq)的吸收器官剂量最高。有效剂量估计为6.8×10⁻³ mSv/MBq,这与几种常用于神经成像的放射性配体产生的剂量相似。