The direct physiological actions of specific short-chain amino acid compounds, known as peptides, that result in a measurable reduction of anxiety, stress, and associated autonomic nervous system hyperactivity. These effects modulate the neuroendocrine stress axis, promoting a state of mental calm and emotional equilibrium. Clinical observation often correlates these actions with improved resilience against psychological stressors and enhanced parasympathetic tone.
Origin
The term originates from the Greek words “anxio” (anxiety) and “lytic” (to loosen or dissolve), combined with “peptide,” referring to the molecular structure. In a clinical context, the concept stems from the discovery of endogenous neuropeptides and their synthetic analogs that interact with central nervous system receptors to mediate fear and anxiety responses. This pharmacological domain is integral to neuroendocrinology and psychoneuroimmunology research.
Mechanism
Anxiolytic peptides typically exert their function by binding to specific receptor sites within the central nervous system, such as GABA-A receptors or opioid receptors, often influencing neurotransmitter release. They can modulate the hypothalamic-pituitary-adrenal (HPA) axis by reducing the release of corticotropin-releasing hormone (CRH) and subsequent cortisol production. This targeted neuromodulation decreases neuronal excitability, effectively dampening the physiological cascade that defines an anxious state and supporting HPA axis homeostasis.
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