Torner Luz, Plotsky Paul M, Neumann Inga D, de Jong Trynke R
Centro de Investigación Biomédica de Michoacán, Instituto Mexicano del Seguro Social, Morelia, Mexico; Max Planck Institute of Psychiatry, Munich, Germany.
Department of Psychiatry and Behavioral Sciences, Emory University School of Medicine, Atlanta, GA, USA.
Psychoneuroendocrinology. 2017 Mar;77:165-174. doi: 10.1016/j.psyneuen.2016.12.006. Epub 2016 Dec 16.
The oxytocin (OXT) system is functionally linked to the HPA axis in a reciprocal and complex manner. Certain stressors are known to cause the simultaneous release of OXT and adrenocorticotrophic hormone (ACTH) followed by corticosterone (CORT). Furthermore, brain OXT attenuates ACTH and CORT responses. Although there are some indications of CORT influencing OXT neurotransmission, specific effects of CORT on neurohypophyseal or intra-hypothalamic release of OXT have not been studied in detail. In the present set of experiments, adult male rats were adrenalectomized (ADX) or sham-operated and fitted with a jugular vein catheter and/or microdialysis probe targeting the hypothalamic paraventricular nucleus (PVN). Blood samples and dialysates were collected before and after forced swimming (FS) and analyzed for CORT, ACTH and AVP concentrations (in plasma) and OXT concentrations (in plasma and dialysates). Experimental treatments included acute infusion of CORT (70 or 175μg/kg i.v.) 5min prior to FS, or subcutaneous placement of 40% CORT pellets resulting in stable CORT levels in the normal basal range. Although ADX did not alter basal OXT concentrations either in plasma or in microdialysates from the PVN, it did cause an exaggerated peripheral secretion of OXT and a blunted intra-PVN release of OXT in response to FS. CORT pellets did not influence either of these ADX-induced effects, while acute infusion of 175μg/kg CORT rescued the stress-induced rise in OXT release within the PVN and modestly increased peripheral OXT secretion. In conclusion, these results indicate that CORT regulates both peripheral and intracerebral OXT release, but in an independent manner. Whereas the peripheral secretion of OXT occurs simultaneously to HPA axis activation in response to FS and is modestly influenced by CORT, HPA axis activation and circulating CORT strongly contribute to the stress-induced stimulation of OXT release within the PVN.
催产素(OXT)系统与下丘脑-垂体-肾上腺(HPA)轴以一种相互且复杂的方式存在功能联系。已知某些应激源会导致OXT和促肾上腺皮质激素(ACTH)同时释放,随后是皮质酮(CORT)。此外,脑内OXT会减弱ACTH和CORT反应。尽管有一些迹象表明CORT会影响OXT神经传递,但CORT对神经垂体或下丘脑内OXT释放的具体影响尚未得到详细研究。在本系列实验中,成年雄性大鼠接受肾上腺切除术(ADX)或假手术,并安装颈静脉导管和/或针对下丘脑室旁核(PVN)的微透析探针。在强迫游泳(FS)前后采集血样和透析液,分析其中CORT、ACTH和精氨酸加压素(AVP)的浓度(血浆中)以及OXT的浓度(血浆和透析液中)。实验处理包括在FS前5分钟静脉内急性注射CORT(70或175μg/kg),或皮下植入40% CORT丸剂以使CORT水平稳定在正常基础范围内。尽管ADX并未改变血浆或PVN微透析液中的基础OXT浓度,但它确实导致FS后OXT外周分泌增加以及PVN内OXT释放减弱。CORT丸剂并未影响ADX诱导的这些效应中的任何一个,而急性注射175μg/kg CORT可挽救应激诱导的PVN内OXT释放增加,并适度增加外周OXT分泌。总之,这些结果表明CORT以独立的方式调节外周和脑内OXT释放。在FS时,OXT外周分泌与HPA轴激活同时发生,并受到CORT的适度影响,而HPA轴激活和循环CORT对应激诱导的PVN内OXT释放刺激有强烈作用。