SARS-CoV-2 infects alveolar epithelial cells by endocytosis through the angiotensin-converting enzyme II (ACE2) receptor, which initiates virus replication and its effects on the respiratory system.1 However, ACE2 receptors are also found on glial cells, the olfactory bulb, the hippocampus, the brainstem, and spinal neurons.2 Thus, the virus could enter the nervous system through the cribriform plate towards the olfactory bulb, altering the permeability of the blood-brain barrier to easily reach all parts of the nervous system.2Once the virus enters the interior of the cell through the ACE2 receptors, it interacts with the sigma-1 receptor, which is located in the endoplasmic reticulum, conditioning its structure to create the ideal conditions for replication.3It is suggested that sigma-1 receptor agonists could serve as a prophylactic treatment, since these drugs, by occupying this receptor, prevent modification of intracellular machinery to the needs of SARS-CoV-2, stopping the inflammatory process induced by the cytokine storm. For this reason, the use of fluvoxamine, donepezil, arketamine, among others, has been proposed.4Preliminary evidence has been found about the effects of antidepressants in relation to severe impairment and death5 in Covid-19. Lenze et al.6 found that a group treated with fluvoxamine had a lower probability of clinical deterioration. There is a significant association between antidepressant use (whether selective serotonin reuptake inhibitors or not) and a reduced risk of intubation or death.7Ayahuasca, a compound used in South American folk healing rituals, is currently being studied for its therapeutic potential to treat mental illnesses.8 It contains β-carbolines (harmine, harmaline and tetrahydroharmine), which are monoamine oxidase inhibitors, and a substance analogous to serotonin called N,N-dimethyltryptamine (DMT), which is responsible for rapid antidepressant and anxiolytic effects.9 In relation to Covid-19, preliminary evidence has been published on the use of DMT to treat mental health problems in recovered patients.10Various studies have shown that DMT is an agonist of the sigma-1 receptor, which is related to synaptic plasticity in dendritic growth, and that it has anti-inflammatory action, which could attenuate the pathophysiological neuroinflammation mechanism of neuropsychiatric and neurodegenerative diseases.11 Although this evidence supported the therapeutic potential of ayahuasca components for mental illnesses prior to the pandemic, in this new scenario these findings could lead to more effective forms of treatment against SARS-CoV-2 beyond neuropsychiatric diseases.Finally, by interacting with the sigma-1 receptor, the alkaloids found in ayahuasca might inhibit the replication of SARS-CoV-2 once inside the cell, preventing Covid-19 infection and, ultimately, the development of serious complications. It is an opportune time to develop studies on the evolution of COVID-19 among populations that regularly consume ayahuasca due to its potential preventive effects against SARS-CoV-2 infection.
Authors: Eric J Lenze; Caline Mattar; Charles F Zorumski; Angela Stevens; Julie Schweiger; Ginger E Nicol; J Philip Miller; Lei Yang; Michael Yingling; Michael S Avidan; Angela M Reiersen Journal: JAMA Date: 2020-12-08 Impact factor: 56.272
Authors: Peter Richardson; Ivan Griffin; Catherine Tucker; Dan Smith; Olly Oechsle; Anne Phelan; Michael Rawling; Edward Savory; Justin Stebbing Journal: Lancet Date: 2020-02-04 Impact factor: 79.321
Authors: David E Gordon; Gwendolyn M Jang; Mehdi Bouhaddou; Jiewei Xu; Kirsten Obernier; Kris M White; Matthew J O'Meara; Veronica V Rezelj; Jeffrey Z Guo; Danielle L Swaney; Tia A Tummino; Ruth Hüttenhain; Robyn M Kaake; Alicia L Richards; Beril Tutuncuoglu; Helene Foussard; Jyoti Batra; Kelsey Haas; Maya Modak; Minkyu Kim; Paige Haas; Benjamin J Polacco; Hannes Braberg; Jacqueline M Fabius; Manon Eckhardt; Margaret Soucheray; Melanie J Bennett; Merve Cakir; Michael J McGregor; Qiongyu Li; Bjoern Meyer; Ferdinand Roesch; Thomas Vallet; Alice Mac Kain; Lisa Miorin; Elena Moreno; Zun Zar Chi Naing; Yuan Zhou; Shiming Peng; Ying Shi; Ziyang Zhang; Wenqi Shen; Ilsa T Kirby; James E Melnyk; John S Chorba; Kevin Lou; Shizhong A Dai; Inigo Barrio-Hernandez; Danish Memon; Claudia Hernandez-Armenta; Jiankun Lyu; Christopher J P Mathy; Tina Perica; Kala Bharath Pilla; Sai J Ganesan; Daniel J Saltzberg; Ramachandran Rakesh; Xi Liu; Sara B Rosenthal; Lorenzo Calviello; Srivats Venkataramanan; Jose Liboy-Lugo; Yizhu Lin; Xi-Ping Huang; YongFeng Liu; Stephanie A Wankowicz; Markus Bohn; Maliheh Safari; Fatima S Ugur; Cassandra Koh; Nastaran Sadat Savar; Quang Dinh Tran; Djoshkun Shengjuler; Sabrina J Fletcher; Michael C O'Neal; Yiming Cai; Jason C J Chang; David J Broadhurst; Saker Klippsten; Phillip P Sharp; Nicole A Wenzell; Duygu Kuzuoglu-Ozturk; Hao-Yuan Wang; Raphael Trenker; Janet M Young; Devin A Cavero; Joseph Hiatt; Theodore L Roth; Ujjwal Rathore; Advait Subramanian; Julia Noack; Mathieu Hubert; Robert M Stroud; Alan D Frankel; Oren S Rosenberg; Kliment A Verba; David A Agard; Melanie Ott; Michael Emerman; Natalia Jura; Mark von Zastrow; Eric Verdin; Alan Ashworth; Olivier Schwartz; Christophe d'Enfert; Shaeri Mukherjee; Matt Jacobson; Harmit S Malik; Danica G Fujimori; Trey Ideker; Charles S Craik; Stephen N Floor; James S Fraser; John D Gross; Andrej Sali; Bryan L Roth; Davide Ruggero; Jack Taunton; Tanja Kortemme; Pedro Beltrao; Marco Vignuzzi; Adolfo García-Sastre; Kevan M Shokat; Brian K Shoichet; Nevan J Krogan Journal: Nature Date: 2020-04-30 Impact factor: 69.504