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非吸烟者与吸烟者外周器官中A型单胺氧化酶的比较。

Comparison of monoamine oxidase a in peripheral organs in nonsmokers and smokers.

作者信息

Fowler Joanna S, Logan Jean, Wang Gene-Jack, Volkow Nora D, Telang Frank, Zhu Wei, Franceschi Dinko, Shea Colleen, Garza Victor, Xu Youwen, Ding Yu-Shin, Alexoff David, Warner Donald, Netusil Noelwah, Carter Pauline, Jayne Millard, King Payton, Vaska Paul

机构信息

Chemistry Department, Brookhaven National Laboratory, Upton, NY 11973, USA.

出版信息

J Nucl Med. 2005 Sep;46(9):1414-20.

Abstract

UNLABELLED

Smokers have reduced levels of brain monoamine oxidase A (MAO A) leading to speculation that MAO A inhibition by tobacco smoke may underlie some of the neurophysiologic effects of smoking. Because smoking exposes peripheral organs as well as the brain to MAO A-inhibitory compounds, we determined whether smokers would also have reduced MAO A in peripheral organs.

METHODS

We measured MAO A in peripheral organs in a group of 9 smokers and compared it with a group of nonsmokers studied previously. MAO A was measured using PET and serial scans with the MAO A-specific radiotracers (11)C-clorgyline and deuterium-substituted (11)C-clorgyline ((11)C-clorgyline-D2) using the deuterium isotope effect to assess binding specificity. The time course of radiotracer in the arterial plasma was also measured and data from the tissue time-activity curves and the arterial input function were analyzed using a 3-compartment model to estimate k(3), which represents the rate-limiting step for the irreversible binding of labeled clorgyline to MAO A.

RESULTS

Tracer uptake at plateau was reduced with deuterium substitution for the heart, lungs, and kidneys, indicating specificity for MAO. There was no difference in organ uptake at plateau between nonsmokers and smokers though, for the smokers, the efflux of tracer from peak uptake to plateau was slower for the lungs. The area under the time-activity curve for the arterial plasma was also significantly reduced for smokers versus nonsmokers and the reduction occurred in the first few minutes after radiotracer injection. Smokers had an approximately 50% reduction in k(3) when compared with nonsmokers; however, k(3) did not differ for nonsmokers and smokers for the heart and the kidneys.

CONCLUSION

Because MAO A breaks down serotonin, norepinephrine, dopamine, and tyramine, and because the lung is a major metabolic organ in degrading some of these substances, reduced lung MAO A may contribute to some of the physiologic effects of smoking. This study also revealed that the concentration of the radiotracers in the arterial plasma is significantly lower for the smoker versus the nonsmoker and that this appears to be caused in part by retention of the radiotracer in lungs. If this is generally true for other substances that are administered intravenously, then this needs to be considered as a variable that may contribute to different short-term behavioral responses to intravenously administered drugs for nonsmokers versus smokers.

摘要

未标注

吸烟者脑内单胺氧化酶A(MAO A)水平降低,这引发了一种推测,即烟草烟雾对MAO A的抑制作用可能是吸烟某些神经生理效应的基础。由于吸烟会使外周器官以及大脑接触到MAO A抑制性化合物,我们研究了吸烟者外周器官中的MAO A水平是否也会降低。

方法

我们测量了一组9名吸烟者外周器官中的MAO A,并将其与之前研究的一组非吸烟者进行比较。使用PET和MAO A特异性放射性示踪剂(11)C - 氯吉兰和氘取代的(11)C - 氯吉兰((11)C - 氯吉兰 - D2)进行系列扫描来测量MAO A,利用氘同位素效应评估结合特异性。还测量了动脉血浆中放射性示踪剂的时间进程,并使用三室模型分析组织时间 - 活性曲线和动脉输入函数的数据,以估计k(3),k(3)代表标记氯吉兰与MAO A不可逆结合的限速步骤。

结果

用氘取代后,心脏、肺和肾脏在平台期的示踪剂摄取减少,表明对MAO具有特异性。非吸烟者和吸烟者在平台期的器官摄取没有差异,不过对于吸烟者,示踪剂从摄取峰值到平台期的流出在肺部较慢。吸烟者动脉血浆时间 - 活性曲线下的面积也显著低于非吸烟者,且这种降低发生在放射性示踪剂注射后的最初几分钟内。与非吸烟者相比,吸烟者的k(3)降低了约50%;然而,心脏和肾脏的k(3)在非吸烟者和吸烟者之间没有差异。

结论

由于MAO A分解血清素、去甲肾上腺素、多巴胺和酪胺,并且由于肺是降解其中一些物质的主要代谢器官,肺中MAO A的减少可能导致吸烟的一些生理效应。这项研究还表明,吸烟者动脉血浆中放射性示踪剂的浓度显著低于非吸烟者,这似乎部分是由于放射性示踪剂在肺中的滞留所致。如果这对于静脉注射的其他物质普遍成立,那么这需要被视为一个可能导致非吸烟者和吸烟者对静脉注射药物产生不同短期行为反应的变量。

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