Laboratório de Neurociência do Comportamento, Departamento de Psicologia, Pontifícia Universidade Católica do Rio de Janeiro, Rio de Janeiro, Brazil; Laboratório de Eletrofisiologia, Neuroplasticidade e Comportamento (LENC), Departamento de Psicologia, Pontifícia Universidade Católica do Rio de Janeiro, Rio de Janeiro, Brazil.
Laboratório de Neurociência do Comportamento, Departamento de Psicologia, Pontifícia Universidade Católica do Rio de Janeiro, Rio de Janeiro, Brazil.
Psychoneuroendocrinology. 2021 Oct;132:105354. doi: 10.1016/j.psyneuen.2021.105354. Epub 2021 Jul 9.
Anxiety is characterized as the emotional response in anticipation of a future threat. This hypervigilant state comprehends a cascade of neuroendocrine and physiological processes, involving the renin-angiotensin system (RAS) and hypothalamic-pituitary-adrenal axis (HPA). Excessive and chronic anxiety may ultimately lead to the development of anxiety disorders. This systematic review aimed to investigate experimental studies using animal models that explored the relationship between RAS and the HPA axis in anxiety disorders. A systematic search was conducted in MEDLINE/PubMed, Embase and Web of Science, and was performed according to PRISMA guidelines. The inclusion criteria was mainly the mention of RAS, HPA axis, and an anxiety disorder in the same study. Quality of studies was evaluated according to the table of risk of bias from SYRCLE. From 12 eligible studies, 7 were included. Research in rats and mice shows that the overactivation of the RAS and HPA axis triggers several neuroendocrine reactions, mainly mediated by AT1 receptors, which promote anxiety-like behaviors and positive feedback for its hyperactivation. On the contrary, the administration of antihypertensive drugs, such as angiotensin AT1 receptor blocker, propitiated the regulation of the RAS and HPA axis, maintaining homeostasis even amid aversive situations. Assessment of risk of bias revealed a pronounced unclear to high risk in several categories, which thus jeopardize the comparability and reproducibility of the results. Nonetheless, the preclinical evidence indicates that the hyperactivation of both RAS and HPA axis during stress exerts deleterious consequences, inducing anxiogenic responses. Moreover, the compiled results show that the modulation of both systems by the administration of AT1 receptor blockers produce anxiolytic effects in animal models and may constitute a new venue for the treatment of anxiety-like disorders.
焦虑被定义为对未来威胁的预期产生的情绪反应。这种高度警惕状态包含了一系列神经内分泌和生理过程,涉及肾素-血管紧张素系统(RAS)和下丘脑-垂体-肾上腺轴(HPA)。过度和慢性焦虑最终可能导致焦虑障碍的发展。本系统综述旨在调查使用动物模型的实验研究,以探讨 RAS 和 HPA 轴与焦虑障碍之间的关系。根据 PRISMA 指南,在 MEDLINE/PubMed、Embase 和 Web of Science 中进行了系统搜索。纳入标准主要是在同一项研究中提到 RAS、HPA 轴和焦虑障碍。根据 SYRCLE 的偏倚风险表评估研究质量。从 12 项合格研究中,有 7 项被纳入。大鼠和小鼠的研究表明,RAS 和 HPA 轴的过度激活引发了几种神经内分泌反应,主要由 AT1 受体介导,促进了类似焦虑的行为和对其过度激活的正反馈。相反,血管紧张素 AT1 受体阻滞剂等抗高血压药物的给药促进了 RAS 和 HPA 轴的调节,即使在厌恶的情况下也维持了体内平衡。偏倚风险评估显示,在几个类别中存在明显的不明确到高风险,这因此危及结果的可比性和可重复性。尽管如此,临床前证据表明,应激期间 RAS 和 HPA 轴的过度激活会产生有害后果,引起焦虑反应。此外,编译的结果表明,通过给予 AT1 受体阻滞剂对这两个系统进行调节,在动物模型中产生抗焦虑作用,并且可能为治疗类似焦虑障碍提供新的途径。