» Articles » PMID: 35890196

Nutraceutical Interventions for Post-Traumatic Stress Disorder in Animal Models: A Focus on the Hypothalamic-Pituitary-Adrenal Axis

Overview
Publisher MDPI
Specialty Chemistry
Date 2022 Jul 27
PMID 35890196
Authors
Affiliations
Soon will be listed here.
Abstract

Post-traumatic stress disorder (PTSD) occurs after exposure to traumatic events and is characterized by overwhelming fear and anxiety. Disturbances in the hypothalamic-pituitary-adrenal (HPA) axis are involved in the pathogenesis of mood disorders, including anxiety, PTSD, and major depressive disorders. Studies have demonstrated the relationship between the HPA axis response and stress vulnerability, indicating that the HPA axis regulates the immune system, fear memory, and neurotransmission. The selective serotonin reuptake inhibitors (SSRIs), sertraline and paroxetine, are the only drugs that have been approved by the United States Food and Drug Administration for the treatment of PTSD. However, SSRIs require long treatment times and are associated with lower response and remission rates; therefore, additional pharmacological interventions are required. Complementary and alternative medicine therapies ameliorate HPA axis disturbances through regulation of gut dysbiosis, insomnia, chronic stress, and depression. We have described the cellular and molecular mechanisms through which the HPA axis is involved in PTSD pathogenesis and have evaluated the potential of herbal medicines for PTSD treatment. Herbal medicines could comprise a good therapeutic strategy for HPA axis regulation and can simultaneously improve PTSD-related symptoms. Finally, herbal medicines may lead to novel biologically driven approaches for the treatment and prevention of PTSD.

Citing Articles

Bidirectional mechanism of comorbidity of depression and insomnia based on synaptic plasticity.

Meng F, Wang L Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2024; 48(10):1518-1528.

PMID: 38432881 PMC: 10929903. DOI: 10.11817/j.issn.1672-7347.2023.230082.


Diosgenin normalization of disrupted behavioral and central neurochemical activity after single prolonged stress.

Malik H, Usman M, Arif M, Ahmed Z, Ali G, Rauf K Front Pharmacol. 2023; 14:1232088.

PMID: 37663254 PMC: 10468593. DOI: 10.3389/fphar.2023.1232088.

References
1.
Logue M, van Rooij S, Dennis E, Davis S, Hayes J, Stevens J . Smaller Hippocampal Volume in Posttraumatic Stress Disorder: A Multisite ENIGMA-PGC Study: Subcortical Volumetry Results From Posttraumatic Stress Disorder Consortia. Biol Psychiatry. 2017; 83(3):244-253. PMC: 5951719. DOI: 10.1016/j.biopsych.2017.09.006. View

2.
Guillen-Burgos H, Gutierrez-Ruiz K . Genetic Advances in Post-traumatic Stress Disorder. Rev Colomb Psiquiatr (Engl Ed). 2018; 47(2):108-118. DOI: 10.1016/j.rcp.2016.12.001. View

3.
May B, Lu C, Lu Y, Zhang A, Xue C . Chinese herbs for memory disorders: a review and systematic analysis of classical herbal literature. J Acupunct Meridian Stud. 2013; 6(1):2-11. DOI: 10.1016/j.jams.2012.11.009. View

4.
An L, Zhang Y, Liu X, Yu N, Chen H, Zhao N . Total flavonoids extracted from xiaobuxin-tang on the hyperactivity of hypothalamic-pituitary-adrenal axis in chronically stressed rats. Evid Based Complement Alternat Med. 2009; 2011:367619. PMC: 3136372. DOI: 10.1093/ecam/nep218. View

5.
Raymundi A, Silva T, Sohn J, Bertoglio L, Stern C . Effects of ∆-tetrahydrocannabinol on aversive memories and anxiety: a review from human studies. BMC Psychiatry. 2020; 20(1):420. PMC: 7448997. DOI: 10.1186/s12888-020-02813-8. View