Evaluating the Efficacy and Moderators of Algorithm-Guided Antidepressant Treatments of Major Depressive Disorder

Author(s):  
Huifeng Zhang ◽  
Zhiguo Wu ◽  
Lan Cao ◽  
Yousong Su ◽  
Fan Wang ◽  
...  
2014 ◽  
Vol 18 (5) ◽  
pp. 567-577 ◽  
Author(s):  
Yoshihiko Matsumoto ◽  
Chiara Fabbri ◽  
Silvia Pellegrini ◽  
Stefano Porcelli ◽  
Pierluigi Politi ◽  
...  

2021 ◽  
Vol 22 (17) ◽  
pp. 9225
Author(s):  
Rosa Estrada-Reyes ◽  
Daniel B. Quero-Chávez ◽  
Citlali Trueta ◽  
Armida Miranda ◽  
Marcela Valdés-Tovar ◽  
...  

Major depressive disorder is a disabling disease with the number of affected individuals increasing each year. Current antidepressant treatments take between three to six weeks to be effective with forty percent of patients being resistant to treatment, making it necessary to search for new antidepressant treatments. Ketamine, a phencyclidine hydrochloride derivative, given intravenously, induces a rapid antidepressant effect in humans. In mice, it causes increased neurogenesis and antidepressant-like effects. However, it also produces psychomimetic effects in humans and in rodents increases the locomotor activity. In contrast, melatonin, a hormone secreted by the pineal gland and synthesized in extrapineal sites, increases new neuron formation and causes antidepressant-like effects in adult rodents with no collateral effects. Here, we assessed the effects of a non-effective dose of ketamine in combination with melatonin (KET/MEL), both on neurogenesis as well as on the antidepressant-like effect in mice. Our results showed that KET/MEL combination increased neurogenesis and produced antidepressant-like effects without altering locomotor activity after both single and triple administration protocols. Our data strongly suggest that KET/MEL combination could be used to simultaneously promote neurogenesis, reverting neuronal atrophy and inducing antidepressant-like effects.


Biomedicines ◽  
2021 ◽  
Vol 9 (11) ◽  
pp. 1659
Author(s):  
Miguel A. Ortega ◽  
Miguel Angel Alvarez-Mon ◽  
Cielo García-Montero ◽  
Oscar Fraile-Martinez ◽  
Guillermo Lahera ◽  
...  

Major Depressive Disorder (MDD) represents a major global health concern, a body-mind malady of rising prevalence worldwide nowadays. The complex network of mechanisms involved in MDD pathophysiology is subjected to epigenetic changes modulated by microRNAs (miRNAs). Serum free or vesicles loaded miRNAs have starred numerous publications, denoting a key role in cell-cell communication, systematically and in brain structure and neuronal morphogenesis, activity and plasticity. Upregulated or downregulated expression of these signaling molecules may imply the impairment of genes implicated in pathways of MDD etiopathogenesis (neuroinflammation, brain-derived neurotrophic factor (BDNF), neurotransmitters, hypothalamic-pituitary-adrenal (HPA) axis, oxidative stress, circadian rhythms...). In addition, these miRNAs could serve as potential biomarkers with diagnostic, prognostic and predictive value, allowing to classify severity of the disease or to make decisions in clinical management. They have been considered as promising therapy targets as well and may interfere with available antidepressant treatments. As epigenetic malleable regulators, we also conclude emphasizing lifestyle interventions with physical activity, mindfulness and diet, opening the door to new clinical management considerations.


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