Institute of Pathophysiology, Faculty of Medicine, Comenius University, Sasinkova 4, 81108 Bratislava, Slovakia.
Department of Cell Systems and Anatomy, UT Health San Antonio, Long School of Medicine, San Antonio, TX 78229, USA.
Int J Mol Sci. 2022 Dec 19;23(24):16187. doi: 10.3390/ijms232416187.
Anxiety disorders are the most common mental diseases. Anxiety and the associated physical symptoms may disturb social and occupational life and increase the risk of somatic diseases. The pathophysiology of anxiety development is complex and involves alterations in stress hormone production, neurosignaling pathways or free radical production. The various manifestations of anxiety, its complex pathophysiological background and the side effects of available treatments underlie the quest for constantly seeking therapies for these conditions. Melatonin, an indolamine produced in the pineal gland and released into the blood on a nightly basis, has been demonstrated to exert anxiolytic action in animal experiments and different clinical conditions. This hormone influences a number of physiological actions either via specific melatonin receptors or by receptor-independent pleiotropic effects. The underlying pathomechanism of melatonin's benefit in anxiety may reside in its sympatholytic action, interaction with the renin-angiotensin and glucocorticoid systems, modulation of interneuronal signaling and its extraordinary antioxidant and radical scavenging nature. Of importance, the concentration of this indolamine is significantly higher in cerebrospinal fluid than in the blood. Thus, ensuring sufficient melatonin production by reducing light pollution, which suppresses melatonin levels, may represent an endogenous neuroprotective and anxiolytic treatment. Since melatonin is freely available, economically undemanding and has limited side effects, it may be considered an additional or alternative treatment for various conditions associated with anxiety.
焦虑障碍是最常见的精神疾病。焦虑及相关躯体症状可能会干扰社交和职业生活,并增加患躯体疾病的风险。焦虑发展的病理生理学是复杂的,涉及应激激素产生、神经信号通路或自由基产生的改变。焦虑的各种表现、其复杂的病理生理背景以及现有治疗方法的副作用,都促使人们不断寻求这些疾病的治疗方法。褪黑素是一种在松果腺中产生并在夜间释放到血液中的吲哚胺,已被证明在动物实验和不同的临床情况下具有抗焦虑作用。这种激素通过特定的褪黑素受体或受体非依赖性多效性作用影响许多生理作用。褪黑素在焦虑中有益的潜在病理机制可能在于其拟交感神经作用、与肾素-血管紧张素和糖皮质激素系统的相互作用、中间神经元信号的调节及其非凡的抗氧化和自由基清除特性。重要的是,这种吲哚胺在脑脊液中的浓度明显高于血液。因此,通过减少抑制褪黑素水平的光污染来确保足够的褪黑素产生,可能代表一种内源性神经保护和抗焦虑治疗。由于褪黑素是自由可用的,经济上要求不高,副作用有限,因此它可以被认为是与焦虑相关的各种疾病的附加或替代治疗方法。