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经前期烦躁障碍女性单核白细胞中 β- Arrestin1 水平降低可能与睾酮和催乳素紊乱有关。

Testosterone and Prolactin Perturbations Possibly Associated with Reduced Levels of β-Arrestin1 in Mononuclear Leukocytes of Women with Premenstrual Dysphoric Disorder.

机构信息

Meharry Medical College, 1005 Dr. D. B. Todd Jr. Blvd, Nashville, TN 37208, USA.

出版信息

Int J Mol Sci. 2023 Oct 22;24(20):15449. doi: 10.3390/ijms242015449.

DOI:10.3390/ijms242015449
PMID:37895130
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10607656/
Abstract

Previously, we reported that a reduction in β-Arrestin1 protein levels in peripheral blood mononuclear leukocytes (PBMC) significantly correlated with the severity of depression symptoms in women with premenstrual dysphoric disorder (PMDD). This study aimed to determine whether the reduced premenstrual β-Arrestin1 protein levels were associated with changes in the regulator for late luteal phase progesterone secretion. The study participants ( = 25) were non-pregnant women between 18 and 42 years of age not taking any antidepressants or receiving therapy and experiencing the luteal phase of menstruation. ELISA determined the β-Arrestin1 protein in PBMC; testosterone and prolactin levels from the plasma were determined by radioimmunoassay. Reduced levels of β-Arrestin1 protein in women with Hamilton Rating Scale for Depression (HAM-D) scores above 19 were observed alongside significantly higher plasma testosterone and prolactin concentrations. Understanding the mechanism underlying the initiation of PMDD will allow for identification of a key perturbed metabolic enzyme that can serve as a target for drug development to ensure the alleviation of PMDD, which has been suggested earlier as a risk factor for developing major depressive disorders.

摘要

先前,我们曾报道外周血单个核细胞(PBMC)中β-arrestin1 蛋白水平的降低与经前期烦躁障碍(PMDD)女性抑郁症状的严重程度显著相关。本研究旨在确定黄体晚期孕激素分泌调节剂的变化是否与降低的经前期β-arrestin1 蛋白水平相关。研究参与者(n=25)为年龄在 18 至 42 岁之间、未服用任何抗抑郁药或接受治疗且正处于月经黄体期的非孕妇。ELISA 法测定 PBMC 中的β-arrestin1 蛋白;放射免疫法测定血浆中的睾酮和催乳素水平。汉密尔顿抑郁量表(HAM-D)评分大于 19 的女性β-arrestin1 蛋白水平降低,同时血浆睾酮和催乳素浓度显著升高。了解 PMDD 起始的机制将有助于确定关键的代谢酶扰动,这可以作为药物开发的靶点,以确保缓解 PMDD,先前已提出 PMDD 是发展为重度抑郁症的一个风险因素。

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本文引用的文献

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