Ryberg Henrik, Norlén Anna-Karin, Landin Andreas, Johansson Per, Salman Zeinab, Wallin Anders, Svensson Johan, Ohlsson Claes
Department of Clinical Chemistry, Sahlgrenska University Hospital, Gothenburg, Sweden.
Sahlgrenska Osteoporosis Centre, Center for Bone and Arthritis Research (CBAR), Department of Internal Medicine and Clinical Nutrition, Institute of Medicine, University of Gothenburg, Gothenburg, Sweden.
Endocr Connect. 2023 Dec 14;13(1). doi: 10.1530/EC-23-0250. Print 2024 Jan 1.
Sex steroids exert important biological functions within the CNS, but the underlying mechanisms are poorly understood. The contribution of circulating sex steroids to the levels in CNS tissue and cerebrospinal fluid (CSF) has been sparsely investigated in human and with inconclusive results. This could partly be due to lack of sensitive validated assays. To address this, we validated a gas chromatography-tandem mass spectrometry (GC-MS/MS) assay for quantification of sex steroid hormones/precursors in CSF.
GC-MS/MS quantification of dihydrotestosterone (DHT, CSF lower limit of quantification, 1.5 pg/mL), testosterone (4.9), estrone (E1, 0.88), estradiol (E2, 0.25), dehydroepiandrosterone (DHEA, 38.4), androstenedione (4D, 22.3), and progesterone (P, 4.2) in CSF, and corresponding serum samples from 47 men.
Analyses of CSF revealed that DHEA was the major sex steroid (73.5 ± 31.7 pg/mL) followed by 4D (61.4 ± 29.6 pg/mL) and testosterone (49.5 ± 18.9 pg/mL). The CSF levels of DHT, E2, and E1 were substantially lower, and P was in general not detectable in CSF. For all sex steroids except E2, strong associations between corresponding CSF and serum levels were observed. We propose that testosteronein CSF is derived from circulating testosterone, DHT in CSF is from local conversion from testosterone, while E2 in CSF is from local conversion from 4D in CNS.
We describe the first thoroughly validated highly sensitive mass spectrometric assay for a broad sex steroid hormone panel suitable for human CSF. This assay constitutes a new tool for investigation of the role of sex steroid hormones in the human CNS.
In this study, a fully validated highly sensitive mass spectrometric assay for sex steroids was applied to human CSF. The results were used to describe the relative contribution of peripheral circulating sex steroids together with locally transformation of sex steroids to the levels in CSF. The results are of importance to understand the biological processes of the human brain.
性类固醇在中枢神经系统(CNS)中发挥着重要的生物学功能,但其潜在机制尚不清楚。循环性类固醇对中枢神经系统组织和脑脊液(CSF)中水平的贡献在人类中研究较少,且结果尚无定论。这部分可能是由于缺乏经过验证的灵敏检测方法。为解决这一问题,我们验证了一种气相色谱-串联质谱(GC-MS/MS)法,用于定量脑脊液中的性类固醇激素/前体。
采用GC-MS/MS法对47名男性脑脊液及相应血清样本中的双氢睾酮(DHT,脑脊液定量下限为1.5 pg/mL)、睾酮(4.9)、雌酮(E1,0.88)、雌二醇(E2,0.25)、脱氢表雄酮(DHEA,38.4)、雄烯二酮(4D,22.3)和孕酮(P,4.2)进行定量。
脑脊液分析显示,脱氢表雄酮是主要的性类固醇(73.5±31.7 pg/mL),其次是雄烯二酮(61.4±29.6 pg/mL)和睾酮(49.5±18.9 pg/mL)。脑脊液中双氢睾酮、雌二醇和雌酮的水平显著较低,脑脊液中一般检测不到孕酮。除雌二醇外,所有性类固醇在相应的脑脊液和血清水平之间均观察到强相关性。我们认为,脑脊液中的睾酮来源于循环睾酮,脑脊液中的双氢睾酮来源于睾酮的局部转化,而脑脊液中的雌二醇来源于中枢神经系统中雄烯二酮的局部转化。
我们描述了首个经过全面验证的、适用于人类脑脊液的、针对广泛的性类固醇激素组的高灵敏度质谱检测方法。该检测方法构成了一种研究性类固醇激素在人类中枢神经系统中作用的新工具。
在本研究中,一种经过充分验证的、高灵敏度的性类固醇质谱检测方法被应用于人类脑脊液。结果用于描述外周循环性类固醇以及性类固醇的局部转化对脑脊液中水平的相对贡献。这些结果对于理解人类大脑的生物学过程具有重要意义。