BiotechMed Center, BME Lab, Multimedia Systems Department, Faculty of Electronics, Telecommunications, and Informatics, Gdansk University of Technology, Gdansk 80-233, Poland.
Professor at the Faculty of Law and Forensic Sciences, Tecnológico de Antioquia University Institution, Medellín 050034, Colombia.
Soc Cogn Affect Neurosci. 2024 Oct 23;19(1). doi: 10.1093/scan/nsae069.
The hypothalamus-pituitary-adrenal axis (HPA axis) and the sympathetic-adrenal-medullary system (SAM system), two neuroendocrine systems associated with the stress response, have often been implicated to modulate decision-making in various domains. This systematic review summarizes the scientific evidence on the effects of pharmacological HPA axis and SAM system modulation on decision-making. We found 6375 references, of which 17 studies fulfilled our inclusion criteria. We quantified the risk of bias in our results with respect to missing outcome data, measurements, and selection of the reported results. The included studies administered hydrocortisone, fludrocortisone (HPA axis stimulants), yohimbine, reboxetine (SAM system stimulants), and/or propranolol (SAM system inhibitor). Integrating the evidence, we found that SAM system stimulation had no impact on risk aversion, loss aversion or intertemporal choice, while SAM system inhibition showed a tentative reduction in sensitivity to losses. HPA axis stimulation had no effect on loss aversion or reward anticipation but likely a time-dependent effect on decision under risk. Lastly, combined stimulation of both systems exhibited inconsistent results that could be explained by dose differences (loss aversion) and sex differences (risk aversion). Future research should address time-, dose-, and sex-dependencies of pharmacological effects on decision-making.
下丘脑-垂体-肾上腺轴(HPA 轴)和交感神经-肾上腺髓质系统(SAM 系统)是与应激反应相关的两个神经内分泌系统,它们经常被认为可以调节各种领域的决策。本系统综述总结了关于药物调节 HPA 轴和 SAM 系统对决策影响的科学证据。我们共检索到 6375 篇参考文献,其中 17 项研究符合我们的纳入标准。我们根据缺失结局数据、测量方法和报告结果的选择,对我们的结果进行了偏倚风险量化。纳入的研究给予了氢化可的松、氟氢可的松(HPA 轴兴奋剂)、育亨宾、瑞波西汀(SAM 系统兴奋剂)和/或普萘洛尔(SAM 系统抑制剂)。综合证据,我们发现 SAM 系统刺激对风险厌恶、损失厌恶或跨期选择没有影响,而 SAM 系统抑制对损失敏感性显示出暂时降低。HPA 轴刺激对损失厌恶或奖励预期没有影响,但可能对风险下的决策有时间依赖性影响。最后,两个系统的联合刺激表现出不一致的结果,可以用剂量差异(损失厌恶)和性别差异(风险厌恶)来解释。未来的研究应该关注药物对决策的时间、剂量和性别依赖性的影响。