抗焦虑和抗抑郁植物次生代谢物的神经药理学研究

R. García-Ríos, A. Mora-Pérez, A. R. Ramos-Molina, César Soria-Fregozo
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引用次数: 7

摘要

抑郁和焦虑目前分别是世界范围内造成残疾的第二大和第五大常见原因,这一现实加剧了对新治疗方法的探索。由于草药提取物和次生代谢物具有抗抑郁和抗焦虑的特性,因此在传统医学中有许多草药提取物和次生代谢物的研究。关于代谢物如生物碱、萜烯、类黄酮和甾醇等的作用机制的临床和临床前研究已经证明其作用与临床有效药物产生的作用相似。这些代谢物通过与γ -氨基丁酸亚型A受体(GABA -受体)相互作用和刺激血清素能、去甲肾上腺素能和多巴胺能神经递质系统,在各种焦虑实验模型中显示出抗焦虑和抗抑郁作用。这些药理作用可归因于与单胺具有结构相似性的植物代谢物,这使得它们能够与受体结合。本章的目的是总结已确定的具有抗焦虑和抗抑郁特性的次级代谢物的各种作用机制。萜烯、生物碱、类黄酮和甾醇可以在焦虑和抑郁的神经生物学中涉及的神经传递系统的不同水平上相互作用,这表明它们有治疗这些精神疾病的潜力。
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Neuropharmacology of Secondary Metabolites from Plants with Anxiolytic and Antidepressant Properties
Depression and anxiety currently rank as the second and fifth most common causes worldwide of years lived with disability-a reality that has intensified the search for new treatments. There are many studies of herbal extracts and secondary metabolites from plants used in traditional medicine due to their antidepressant and anxiolytic properties. Clinical and preclinical studies about some of the mechanisms of action of metabolites like alkaloids, terpenes, flavonoids, and sterols, among others, have documented effects similar to those produced by clinically effective drugs. These metabolites have shown anxiolytic and antidepressant effects in various experimental models of anxiety by interacting with γ -aminobutyric acid subtype A receptors (GABA A -receptors) and by stimulating the serotonergic, noradrenergic, and dopaminergic neurotransmitter systems. These pharmacological effects can be attributed to plant metabolites that share structural similarities with monoamines, which allow them to bind to receptors. The objective of this chapter is to summarize the various mechanisms of action that have been identified in secondary metabolites with anxiolytic and antidepressant properties. Terpenes, alkaloids, flavonoids, and sterols can interact at different levels of the neurotransmission systems involved in the neurobiology of anxiety and depression, suggesting their potential for treating these mental illnesses. on MAO-B in the three
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