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The Synergistic Effects of 5-HT2A and TRP Agonism/Antagonism in Reducing Inflammation for Enhanced Mental and Physical Health.

Robert B. Kargbo

ACS Medicinal Chemistry Letters August 10, 2023 DOI: 10.1021/acsmedchemlett.3c00276 (opens in new tab)

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AI-extracted from the abstract
Characteristics Patent highlight Peer reviewed
Interventions 5-HT2A serotonin receptor agonist TRP receptor agonist TRP receptor antagonist
Topics Serotonin
Key points Describes patent-disclosed compositions combining at least one 5-HT2A serotonin receptor agonist with a TRP receptor agonist, and possibly a TRP receptor antagonist, intended to reduce inflammation and improve or maintain mental and physical health across conditions including depression, pain, anxiety, and PTSD. The authors contend that SSRIs have limited effectiveness and slow onset, and that alternative interventions are needed for diagnosed depression and for enhancing creativity, mindfulness, sexual desire, and well-being in people without a depression diagnosis.

Abstract

Depression is a widespread issue in the United States and the leading cause of disability globally, impacting people of all ages. Although selective serotonin reuptake inhibitors (SSRIs) are commonly used for treatment, they have limited effectiveness and may take weeks to show results. There is a pressing need for fast and effective solutions for various types of depression, including chronic, clinical, situational, and undiagnosed cases. Alternative interventions are necessary not only for diagnosed depression but also for enhancing creativity, mindfulness, sexual desire, and overall well-being in individuals without a medical diagnosis of depression. This Patent Highlight discloses compositions designed to reduce inflammation and improve or maintain mental and physical health. These compositions target issues like depression, pain, mood disorders, anxiety, PTSD, digestive problems, relaxation, focus, creativity, and aim to decrease reliance on pharmaceutical and illicit drugs. The compositions involve combinations of at least one 5-HT2A serotonin receptor agonist and one TRP receptor agonist, possibly including a TRP receptor antagonist.

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