Saroj Neeshu, Shanker Shiv, Serrano-Hernández Eduardo, Manjarrez-Gutiérrez Gabriel, Mondragón José-Antonio, Moreno-Martínez Saidel, Jarillo-Luna Rosa A, López-Sánchez Pedro, Terrón José A
Departamento de Farmacología, Centro de Investigación y de Estudios Avanzados del IPN, Av. Instituto Politécnico Nacional 2508, La Laguna Ticomán, CP 07360, México.
Sección de Estudios de Posgrado e Investigación, Escuela Superior de Medicina del IPN, Plan de San Luis y Díaz Mirón s/n, Casco de Sto. Tomás, Mexico.
Psychoneuroendocrinology. 2025 Jan;171:107219. doi: 10.1016/j.psyneuen.2024.107219. Epub 2024 Oct 22.
It has been shown that chronic restraint stress (CRS) increases adrenal 5-HT levels and turnover through a mechanism that appears unrelated to tryptophan hydroxylase (TPH). In the present study we re-analyzed the effects of CRS (20 min/day) for 14 days relative to control (CTRL) conditions on TPH expression, distribution, and activity in rat adrenal glands. On day 15, adrenal glands were collected for TPH1 and TPH2 immunohistochemistry, Western blot, and RT-PCR; TPH activity was estimated by quantification of 5-hydroxytryptophan (5-HTP) and, indirectly, through measurement of 5-HT and 5-hydroxindolacetic acid (5-HIAA) levels and turnover (5-HIAA/5-HT ratio) by HPLC. TPH expression and activity in the dorsal raphe nucleus (DRN) were also determined for comparison. TPH1 and TPH2 immunostaining was observed in the adrenal medulla, and measurable levels of TPH1 and TPH2 protein and mRNA were detected in rat adrenal glands from CTRL animals. CRS exposure noticeably increased TPH2- but not THP1-immunostaining in the medulla and the outer adrenocortical areas of left (LAG) but not of right adrenal glands (RAG). In addition, CRS exposure increased TPH2 protein and mRNA levels in LAG; however, both measures decreased in DRN. Finally, CRS treatment produced an increase and a decrease of TPH activity and 5-HT turnover in LAG and DRN, respectively. Results indicate that TPH is indeed expressed in rat adrenal glands. Exposure to CRS upregulates TPH2 in LAG, while inducing downregulation of it in the DRN. Then, the increased levels of 5-HT in LAG from CRS-exposed animals likely results from TPH2-mediated synthesis.
研究表明,慢性束缚应激(CRS)通过一种似乎与色氨酸羟化酶(TPH)无关的机制增加肾上腺5-羟色胺(5-HT)水平和周转率。在本研究中,我们重新分析了相对于对照(CTRL)条件,持续14天、每天20分钟的CRS对大鼠肾上腺中TPH表达、分布和活性的影响。在第15天,收集肾上腺用于TPH1和TPH2免疫组织化学、蛋白质印迹法和逆转录聚合酶链反应(RT-PCR);通过对5-羟色氨酸(5-HTP)进行定量来估计TPH活性,并间接通过高效液相色谱法(HPLC)测量5-HT和5-羟吲哚乙酸(5-HIAA)水平及周转率(5-HIAA/5-HT比值)来估计TPH活性。还测定了中缝背核(DRN)中的TPH表达和活性以作比较。在肾上腺髓质中观察到了TPH1和TPH2免疫染色,并且在来自CTRL动物的大鼠肾上腺中检测到了可测量水平的TPH1和TPH2蛋白质及信使核糖核酸(mRNA)。CRS暴露显著增加了左侧肾上腺(LAG)而非右侧肾上腺(RAG)髓质和肾上腺皮质外层区域中TPH2的免疫染色,但未增加TPH1的免疫染色。此外,CRS暴露增加了LAG中TPH2蛋白质和mRNA水平;然而,这两种指标在DRN中均下降。最后,CRS处理分别导致LAG中TPH活性和5-HT周转率增加以及DRN中TPH活性和5-HT周转率降低。结果表明TPH确实在大鼠肾上腺中表达。暴露于CRS会使LAG中的TPH2上调,同时导致DRN中的TPH2下调。那么,来自CRS暴露动物的LAG中5-HT水平升高可能是由TPH2介导的合成所致。