Silverstone P H, Hanstock C C, Rotzinger S
Department of Psychiatry, University of Alberta, Hanstock.
J Psychiatry Neurosci. 1999 May;24(3):222-6.
To study the effect of lithium administration on brain choline/creatine (Cho/Cr) ratios in healthy volunteers.
Double-blind, placebo-controlled, prospective study.
The Nuclear Magnetic Resonance Research Unit at the University of Alberta.
Sixteen healthy volunteers, recruited through advertisements. Subjects were excluded if they had a physical illness, or a personal or family history of psychiatric illness. The study period was from Feb. 6, 1996, to Mar. 21, 1996.
Subjects received a baseline proton magnetic resonance spectroscopy (1H MRS) scan, and then were instructed to take either lithium (1,200 mg) or placebo at night for 7 days. On Day 8, the subjects returned for a second 1H MRS scan. Study participants were seen by a physician at the beginning and at the end of the experiment, and had access to the physician throughout the study period.
Ratios of Cho/Cr measured in the temporal lobes by 1H MRS.
There were no significant differences in the Cho/Cr ratios between the 2 groups on the test day (placebo 0.748 [standard deviation 0.29] versus lithium 0.811 [SD 0.25]; F = 0.147, p = 0.72), and there was no significant change from baseline in either group (0.003 above baseline for placebo; 0.056 above baseline for lithium; F = 1.21, p = 0.32).
Lithium administration to healthy volunteers does not alter the Cho/Cr ratio in temporal lobe as measured by 1H MRS. The result concurs with reports that differences in Cho/Cr ratios observed in patients with bipolar disorder are likely specific to the illness, and are not the result of lithium therapy. Hence, alterations in choline function are not involved in the clinical effectiveness of lithium.
研究锂剂给药对健康志愿者脑内胆碱/肌酸(Cho/Cr)比值的影响。
双盲、安慰剂对照的前瞻性研究。
阿尔伯塔大学核磁共振研究室。
通过广告招募的16名健康志愿者。若受试者有躯体疾病、个人或家族精神病史,则被排除。研究期间为1996年2月6日至1996年3月21日。
受试者接受一次基线质子磁共振波谱(1H MRS)扫描,然后被指导在夜间服用锂剂(1200毫克)或安慰剂,持续7天。在第8天,受试者返回进行第二次1H MRS扫描。研究参与者在实验开始和结束时由医生诊查,且在整个研究期间可随时联系医生。
通过1H MRS测量颞叶的Cho/Cr比值。
在测试日,两组之间的Cho/Cr比值无显著差异(安慰剂组为0.748[标准差0.29],锂剂组为0.811[标准差0.25];F=0.147,p=0.72),且两组与基线相比均无显著变化(安慰剂组比基线高0.003;锂剂组比基线高0.056;F=1.21,p=0.32)。
对健康志愿者给予锂剂不会改变通过1H MRS测量的颞叶Cho/Cr比值。该结果与以下报道一致,即双相情感障碍患者中观察到的Cho/Cr比值差异可能是该疾病所特有的,而非锂剂治疗的结果。因此,胆碱功能的改变与锂剂的临床疗效无关。