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Antidepressive and anxiolytic effects of ayahuasca: a systematic literature review of animal and human studies – Revista Brasileira de Psiquiatria

Sorgente: Antidepressive and anxiolytic effects of ayahuasca: a systematic literature review of animal and human studies

Rev. Bras. Psiquiatr. vol.38 no.1 São Paulo Jan./Mar. 2016

http://dx.doi.org/10.1590/1516-4446-2015-1701

Review Articles

Antidepressive and anxiolytic effects of ayahuasca: a systematic literature review of animal and human studies

Rafael G. dos Santos1  , Flávia L. Osório1  2  , José Alexandre S. Crippa1  2  , Jaime E. C. Hallak1  2 

1Departamento de Neurociências e Ciências do Comportamento, Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo (USP), Ribeirão Preto, SP, Brazil

2Instituto Nacional de Ciência e Tecnologia – Medicina Translacional, Ribeirão Preto, SP, Brazil

ABSTRACT

Objective:

To conduct a systematic literature review of animal and human studies reporting anxiolytic or antidepressive effects of ayahuasca or some of its isolated alkaloids (dimethyltryptamine, harmine, tetrahydroharmine, and harmaline).

Methods:

Papers published until 3 April 2015 were retrieved from the PubMed, LILACS and SciELO databases following a comprehensive search strategy and using a predetermined set of criteria for article selection.

Results:

Five hundred and fourteen studies were identified, of which 21 met the established criteria. Studies in animals have shown anxiolytic and antidepressive effects of ayahuasca, harmine, and harmaline, and experimental studies in humans and mental health assessments of experienced ayahuasca consumers also suggest that ayahuasca is associated with reductions in anxiety and depressive symptoms. A pilot study reported rapid antidepressive effects of a single ayahuasca dose in six patients with recurrent depression.

Conclusion:

Considering the need for new drugs that produce fewer adverse effects and are more effective in reducing anxiety and depression symptomatology, the described effects of ayahuasca and its alkaloids should be further investigated.

Key words: Psychedelic agents; dimethyltryptamine; harmine; monoamine oxidase inhibitors; therapeutic use

Introduction

Ayahuasca is a Quechua name used to describe a pan-Amazonian botanical hallucinogenic beverage produced by boiling the stems of the liana Banisteriospsis caapi with the leaves of the shrub Psychotria viridis.1,2B. caapi is rich in β-carbolines such as harmine, tetrahydroharmine (THH), and harmaline, while P. viridis contains considerable amounts of the hallucinogenic tryptamine N,N-dimethyltryptamine (DMT), a 5-HT1A/2A/2C agonist.1 2 3 45 Pure DMT is not psychoactive after oral administration,6 but liver and gastrointestinal monoamine oxidase A (MAO-A) inhibition by the β-carbolines in ayahuasca – especially by harmine – allows DMT to reach the systemic circulation and the brain, where it activates 5-HT1A/2A/2C receptors in frontal and paralimbic areas.5,7,8

Ayahuasca has been traditionally used by indigenous and mestizo populations of Amazonian countries such as Brazil, Colombia, Peru, and Ecuador for magical-religious and therapeutic purposes.1,2 However, in the last 25 years, ritual and therapeutic use of ayahuasca has spread from small cities in the Amazonian jungle to the urban centers of South America, United Sates, Europe, Asia, and Africa.9

Anecdotal evidence, studies conducted among ayahuasca consumers, and preliminary studies in patients suggest that ayahuasca has broad therapeutic potential, especially for the treatment of substance dependence and anxiety and mood disorders.10 11 12 13 14 15 16 1718 Moreover, pharmacological studies of acute ayahuasca administration to healthy volunteers and mental health assessments of long-term ayahuasca consumers suggest that this compound is relatively safe.4,5,7,1015,19 2021

Thus, this study aimed to conduct a systematic literature review of animal and human studies that investigated anxiolytic and antidepressive effects of ayahuasca or of some of its isolated alkaloids (dimethyltryptamine, harmine, THH, and harmaline).

Methods

Data for this systematic review were collected in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines (PRISMA; http://www.prisma-statement.org/usage.htm).

Data acquisition

We attempted to identify all animal and human studies available for review as of 3 April 2015 in which the anxiolytic or antidepressive effects of ayahuasca or of some of its isolated alkaloids (dimethyltryptamine, harmine, THH, and harmaline) were analyzed.

Search strategy

The electronic PubMed (1 January 1966 to 3 April 2015), LILACS (1 January 1982 to 3 April 2015), and SciELO (1 January 1998 to 3 April 2015) databases were searched. The following keywords were used: ayahuasca OR dimethyltryptamine OR harmine OR tetrahydroharmine OR harmaline AND anxiety OR anxiogenic OR anxiolytic OR depression OR depressive OR antidepressive OR antidepressant. References were retrieved by searching the aforementioned electronic databases and handsearching of reference lists of the identified literature. All studies published up to 3 April 2015, without language restriction, were included.

Eligibility criteria

The inclusion and exclusion criteria listed below were established prior to the literature search.

Article type. Journal articles, abstracts, letters, conference abstracts, books, and book chapters were included. Case reports, comments, and editorials were excluded.

Study design. The review included (i) animal models of anxiety or depression; (ii) experimental studies of ayahuasca administration to healthy volunteers that assessed anxiety or depressive-like symptoms with validated scales; (iii) observational studies of ayahuasca consumers that assessed anxiety or depressive symptoms with validated scales; and (iv) clinical trials involving patients with a diagnosis of anxiety or depressive disorder based on DSM criteria.

Participants/sample. Rodents (rat or mouse), healthy human volunteer (including ayahuasca consumers), and patients with a diagnosis of anxiety or depressive disorder based on DSM criteria.

Interventions. All designs evaluating the effect of ayahuasca or its alkaloids on anxiety and depressive measures were included.

Comparisons. The main comparators considered were placebo and established pharmacotherapy regimens for anxiety and mood disorders (e.g., imipramine).

Outcomes. Studies investigating the effect of ayahuasca or its alkaloids on anxiety or depressive-like behavioral or biochemical parameters (animal studies) or symptoms (human studies) were included.

Data extraction

All studies were screened by two independent reviewers, with discrepancies resolved by a third reviewer. Names of authors, year of publication, study design (experimental, observational, clinical trial), characteristics of the participants (species, sample size), response criteria (anxiolytic or antidepressive effect), type of intervention (drug, dose), and type of outcome measure (anxiety or depression model or scale) were recorded for all included articles. The sample was divided into (i) animal and (ii) human studies for the sake of clarity and to facilitate interpretation of results.

Results

Study selection

A flow diagram illustrating the different phases of the systematic review is presented in Figure 1.

Figure 1 Flow diagram illustrating the different phases of the systematic review. 

The literature search yielded 514 separate references. Owing to overlap of coverage between the databases, four of the references were found to be duplicates. A total of 510 citations were reviewed for abstract screening (first pass). Following this pass, 21 potentially relevant references were identified. Full-text reports of these citations were obtained for a more detailed evaluation. Following detailed examination of the reports, all 21 citations were included.

Studies were classified according to the species (animal, human), compound (ayahuasca, DMT, harmine, THH, harmaline), and behavior/symptom (anxiolytic, antidepressive) assessed. The included publications comprised 10 animal studies (two on the anxiolytic effect of harmaline, nine on the antidepressive effect of harmine, and one on the antidepressive effect of ayahuasca) and 11 human studies (three experimental studies, seven observational studies, and one clinical trial).

Animal studies

Anxiolytic effects of harmaline

A study in mice examined the effects of harmaline on state anxiety employing the elevated plus maze test.22 Lower doses of harmaline (5-10 mg/kg) increased anxiety, while higher doses (20 mg/kg) produced anxiolytic effects. Another study in mice investigated the anxiolytic activity of harmaline using the marble burying test, an animal model of obsessive-compulsive disorder (OCD), and reported that animals treated with 5-7.5 mg/kg harmaline buried a significantly greater number of marbles, which suggests an anxiolytic effect.23

Antidepressive effects of harmine

A study in mice using the forced swim test (FST) as an animal model of depression reported that harmine (5-15 mg/kg via intraperitoneal [i.p.] injection) dose-dependently reduced immobility time in this test, which indicates antidepressive effects.24 These effects were reversed after treatment with a γ-aminobutyric acid (GABAA) receptor antagonist, suggesting involvement of this receptor in the antidepressive effects of harmine.

Since 2009, our group has published several studies describing the antidepressive properties of harmine.2530 In the first of these studies, the effects of harmine (5-15 mg/kg) were assessed in rats using the FST.25 Moreover, hippocampal levels of brain-derived neurotrophic factor (BDNF), an endogenous protein that plays critical roles in neuroplasticity and depression, were assessed in harmine-treated rats. Harmine (10-15 mg/kg) reduced immobility time and increased both climbing and swimming time in rats, which suggests antidepressant effects. Furthermore, harmine (15 mg/kg) increased BDNF levels in the rat hippocampus. A subsequent study assessed the effects of chronic treatment with harmine (5-15 mg/kg/day for 14 days) using the FST in rats.26 All doses of harmine reduced immobility and increased swimming time. Moreover, harmine at 5-10 mg/kg increased climbing time, whereas the higher doses (10-15 mg/kg) increased BDNF levels in the rat hippocampus.

The antidepressive effects of harmine (15 mg/kg/day for 7 days) were assessed in rats using another animal model of depression, the chronic mild stress (CMS) model.27 In this study, sweet food consumption, adrenal gland weight, adrenocorticotropic hormone (ACTH), and hippocampal BDNF levels were also assessed. The CMS model induced lower consumption of sweet foods, which is postulated to reflect anhedonia, a core symptom of depressive episodes in humans. Moreover, CMS induced adrenal gland hypertrophy and increased ACTH and BDNF levels. Harmine treatment reversed anhedonia and the increase in adrenal gland weight, and normalized ACTH and BDNF levels. A recent study also used the CMS model and showed that harmine (15 mg/kg/day for 7 days) reversed increased sucrose intake and prefrontal cortex citrate synthase activity in stressed rats.30

Considering the involvement of reactive oxygen species (ROS), energy metabolism, and mitochondrial function in the pathophysiology of depression, our group investigated the effects of acute and chronic administration of harmine on several parameters of oxidative stress,30 mitochondrial function, and cellular energy metabolism,29,30 For instance, the effects of harmine on lipid and protein oxidation levels (markers of oxidative stress) and on activity of the antioxidant enzymes superoxide dismutase (SOD) and catalase (CAT) in the rat brain were evaluated.29 Acute (5-15 mg/kg) and chronic (5-15 mg/kg/day for 14 days) harmine treatments reduced lipid and protein oxidation in the rat prefrontal cortex and hippocampus, while SOD and CAT activity were increased in the same brain regions.

The effects of harmine on energy metabolism in the rat brain were assessed by evaluation of mitochondrial respiratory chain (complexes I, II, II-III, and IV) and creatine kinase activity.29 Acute (5-15 mg/kg) treatment with harmine increased creatine kinase activity in the prefrontal cortex (all doses) and striatum (5 mg/kg), while the higher dose (15 mg/kg) decreased creatine kinase in the striatum. Regarding the mitochondrial respiratory chain, harmine increased the activity of complex I in the prefrontal cortex (15 mg/kg) and striatum (10 mg/kg). Chronic treatment with harmine (5-15 mg/kg/day for 14 days) increased creatine kinase in the prefrontal cortex (5 mg/kg) and striatum (5-10 mg/kg), and increased the activity of complex I in the prefrontal cortex (5 mg/kg) and of complex IV in the striatum (10 mg/kg). Acute and chronic treatment with harmine did not alter complex II or II-III activity. These findings suggest that the mechanism of action of the antidepressive effects of harmine may involve, at least in part, activity of creatine kinase and of the mitochondrial respiratory chain, depending on dose and brain area.

As noted previously, a study in rats using the CMS model reported that harmine (15 mg/kg/day for 7 days) reversed the increased activity of citrate synthase, an enzyme involved in mitochondrial function, in the rat prefrontal cortex.30

Taken together, these findings support the hypothesis that the antidepressive effects of harmine could be mediated by regulation of cell energy homeostasis, mitochondrial functions, and oxidative stress.

Table 1 shows preclinical evidence of the antidepressive-like effects of harmine in laboratory animals.

Table 1 Antidepressive-like effects of harmine in animal models 

Reference Model Animal Results Dose
Farzin & Mansouri24 FST Mouse Reduced immobility 5-15 mg/kg (acute)
Fortunato25 FST Rat Reduced immobility, increased climbing and swimming, increased BDNF levels in the hippocampus 10-15 mg/kg (acute)
Fortunato26 FST Rat Reduced immobility, increased climbing and swimming, increased BDNF levels in the hippocampus 5-15 mg/kg/day (14 days)
Fortunato27 CMS Rat Reversed anhedonia, reduced adrenal gland weight, normalized ACTH and BDNF levels 15 mg/kg/day (7 days)
Réus28 Acute and chronic treatment Rat Reduced lipid/protein oxidation and increased superoxide dismutase/catalase activity in prefrontal cortex and hippocampus 5-15 mg/kg (acute)5-15 mg/kg/day (14 days)
Réus29 Acute and chronic treatment Rat Increased creatine kinase and complex I/IV activity in the prefrontal cortex and striatum 5-15 mg/kg (acute)5-15 mg/kg/day (14 days)
Abelaira30 CMS Rat Reversed sucrose intake and prefrontal cortex citrate synthase activity 15 mg/kg/day (7 days)

ACTH = adrenocorticotropic hormone; BDNF = brain-derived neurotrophic factor; CMS = chronic mild stress; FST = forced swim test.

Antidepressive effects of ayahuasca

A study in rats showed that orally administered ayahuasca (5 mg/kg) decreased immobility time in the FST. Lower (2.5 mg/kg) and higher doses (10 mg/kg) did not produce significant effects, and the number of dives was not altered by ayahuasca administration.31

Human studies

Relaxation and increased positive mood after DMT administration

In an open-label trial involving the intramuscular administration of 0.7 mg/kg DMT to 15 healthy volunteers, 93% of the participants self-reported feelings of relaxation.32 A double-blind, placebo-controlled, randomized study involving the administration of four doses of intravenous DMT (0.04-0.4 mg/kg) to 15 healthy volunteers reported that non-hallucinogenic doses of DMT (0.05 mg/kg) produced relaxation in some participants.33 A study that assessed the effects of oral and smoked DMT (25 mg) in six healthy volunteers reported that while oral DMT did not produce any psychoactive effects, smoked DMT was fully psychoactive and increased positive mood.6

Mental health assessments of ayahuasca consumers

In a study among first-time ayahuasca consumers, 28 volunteers were evaluated 1-4 days before and 1-2 weeks after their first participation in an ayahuasca ritual in the Santo Daime or União do Vegetal religions.34 Ayahuasca consumption was associated with reduced psychiatric symptoms and increased serenity and tranquility. In a follow-up study performed after 6 months with 23 of the initial 28 volunteers, ayahuasca use was associated with reduced psychiatric symptoms, improved mental health, confidence, and optimism.35

One study assessed psychiatric symptoms and neurocognitive functions in 15 experienced (at least 10 years of continuous use) members of the União do Vegetal religion, and reported an absence of mental health or cognitive problems.10 Instead, ayahuasca consumers showed reduced psychopathology, which included a reduction in anxiety and depression symptoms. A reduction in anxiety and depression symptoms was also observed in other studies. In a study which evaluated psychiatric symptoms in 40 adolescent (age 15-19 years) members of the União do Vegetal who had consumed ayahuasca at least 24 times in the last 2 years, the ayahuasca-using group had a reduced incidence of anxiety symptoms when compared to a non-ayahuasca-using control group.36 Moreover, a study with 32 long-term (lifetime 269±314.7 ceremonies; range, 20-1300) North American Santo Daime members reported that ayahuasca use was associated with reduced anxiety and depression symptoms.12 In a study performed among 127 long-term (at least 15 years of continuous use) Santo Daime and Barquinha members, which included a 1-year follow-up, ayahuasca use was not associated with any psychiatric symptoms, and religion participants showed better neuropsychological performance and reduced psychopathology, including anxiety- and depression-related symptoms.15

The effects of ayahuasca on psychometric measures of anxiety, panic-like, and hopelessness were assessed in experienced (at least 10 years of continuous use) Santo Daime members during one of their rituals (Oração, “prayer”). Questionnaires were administered 1 hour after ayahuasca ingestion in a double-blind, placebo-controlled design. Participants showed reduced panic and hopelessness symptoms after ayahuasca intake, and ayahuasca did not modify state or trait anxiety.11

Clinical trials

Our group performed the first clinical trial involving the administration of ayahuasca to patients with recurrent depression.18 A single dose of ayahuasca was administered to six volunteers with a current depressive episode in an open-label trial conducted in an inpatient psychiatric unit. Ayahuasca administration significantly reduced depressive symptoms from baseline 1, 7, and 21 days after drug intake, according to the Hamilton Rating Scale for Depression (HAM-D), the Montgomery-Åsberg Depression Rating Scale (MADRS), and the Anxious-Depression subscale of the Brief Psychiatric Rating Scale (BPRS). These results suggest fast-acting anxiolytic and antidepressant effects of ayahuasca in patients with a depressive disorder.

Discussion

In this systematic review, we identified 21 studies on the anxiolytic and antidepressive effects of ayahuasca and its alkaloids that met our inclusion criteria. Despite the small number of studies and the high degree of heterogeneity among them, the reported results consistently show that these compounds have anxiolytic and antidepressive properties. These findings will be discussed in detail below.

Research performed among ayahuasca consumers over the last 20 years shows that users of this substance do not exhibit symptoms of psychiatric disorders or neurocognitive problems, but instead show normal or better cognitive function, increased well-being and spirituality, and reduced psychopathology, including anxiety and depression symptoms.1012,14,15,3436 Moreover, DMT administration to healthy volunteers suggest that this tryptamine may have anxiolytic properties.6,32,33

Studies in rodents have reported that the β-carbolines harmine and harmaline, as well as ayahuasca, produce anxiolytic or antidepressive effects. As harmaline acts as a MAO-A inhibitor,3,5 the anxiolytic effects of this compound22,23 could be theoretically explained by an enhancement of serotonin concentrations in the brain after MAO-A inhibition.37 Nevertheless, the mechanisms of action responsible for the anxiolytic and antidepressive properties of harmine and harmaline are not completely understood, and other non-serotonergic mechanisms could also be involved.

Specifically, the antidepressive effects of harmine are apparently independent of its effects as a MAO-A inhibitor,3,5 and seem to be mediated by regulation of cell energy homeostasis, mitochondrial functions and oxidative stress,2830 and modulation of BDNF, an endogenous protein involved in neuroplasticity and depressive symptoms.2527 Harmine and harmaline also bind to 5-HT2A receptors.3840 Since hallucinogens increase cortical glutamate levels following activation of 5-HT2A receptors, increasing the expression of BDNF in prefrontal areas,41 4243 the agonist action of harmine and harmaline in this serotonergic receptor could also lead to increased BDNF levels.2527

A study suggested that the GABAA receptor could be involved in the antidepressive effects of harmine.24 Nevertheless, some studies suggest that harmine, harmaline, and THH display little affinity for benzodiazepine receptors.38,39

Regarding DMT, there is evidence that 5-HT1A/2A/2C receptor agonists modulate emotional processing, reduce anxiety and depressive symptoms, and increase positive mood. Interestingly, cortical expression of 5-HT1A/2A/2C receptor is altered in post-mortem samples of depressed patients.43 Therapeutic drugs that are 5-HT1A receptor agonists produce anxiolytic and antidepressive effects in animals and humans,37,43,44 and 5-HT2A/2C receptor agonists produce anxiolytic and antidepressive effects in animals.45 4647 Moreover, there is increasing evidence that anxiety and depressive symptoms are associated with inflammatory processes, and 5-HT1A/2A/2C receptor agonists have anti-inflammatory properties.43,48 4950

Other 5-HT1A/2A/2C receptor agonists, such as psilocybin and lysergic acid diethylamide (LSD), also produce reductions in anxiety and depressive symptoms and increases in positive mood. In the mid-1950s and 1960s, several studies investigated the potential therapeutic use of psilocybin and LSD in the treatment of disorders such as neurosis and OCDs, and as an adjunctive therapy in the terminally ill.42,51 52 53 54 5556 However, a definite conclusion regarding the potential beneficial effects of these compounds cannot be drawn from previous investigations, since many of these studies had important methodological limitations, such as lack of a control group or randomization, absence of double-blind/placebo-controlled designs, and limited follow-up data.42,5156

Recent studies reported that psilocybin produces anxiolytic effects in mice in the marble burying test, an animal model of OCD,57 and that LSD produced antidepressive-like effects and normalized learning behavior and hippocampal serotonin 5-HT2 signaling in a rat model of depression (olfactory bulbectomy).58

As previously reported, smoked DMT increased positive mood in healthy voluntters,6 and both psilocybin59 60 61 6263 and LSD64 also increased positive mood in experimental studies in humans. Case reports56,65 66 6768 and clinical trials69 suggest that psilocybin and LSD may be beneficial for patients with OCD. Moreover, psilocybin- and LSD-assisted psychotherapy has been shown to reduce anxiety and depressive-like symptoms in patients with anxiety and depression associated with life-threatening diseases such as advanced-stage cancer.70 7172

The antidepressive properties of ayahuasca could also be related to alterations of cortical connectivity in the default mode network (DMN), a group of brain areas involved in introspection, meditative states, daydreaming, imagination, and mind-wandering. Depressive states are associated with increased rumination, a self-referential process that may become difficult to disengage and is associated with increased activity of the DMN, and acute ayahuasca administration (2.2 mL/kg of body weight) significantly reduced DMN activation.73 A recent study evaluated cortical thickness in 22 regular users of ayahuasca (average 5.3 years of continuous use; range: 2-13 years) using magnetic resonance imaging (MRI) and reported significant cortical thinning in the posterior cingulate cortex (PCC), a key node of the DMN.74

Regarding other serotonergic hallucinogens, a recent functional MRI (fMRI) study involving intravenous administration of psilocybin (2 mg) to 15 healthy volunteers reported significant decreased cerebral blood flow in several brain areas including the PCC and the medial prefrontal cortex (mPFC), another important component of the DMN.75 A subsequent study reported increased functional connectivity of the DMN and the task-positive network (TPN), involved in goal-directed attentional tasks.76 Since the DMN and TPN have opposite functions, the authors suggested that the subjective effects of hallucinogens, as well as psychotic and meditative states, could be caused by disruption of DMN-TPN functional connectivity. This disruption would obfuscate the separateness of internally and externally focused states, profoundly altering cognition, perceptions, emotions, and consciousness. However, no significant change was observed in DMN-TPN connectivity after acute ayahuasca administration. Thus, further studies are needed to better explore the subjective and therapeutic effects of serotonergic hallucinogens.

Animal and human studies suggest that ayahuasca and its alkaloids can produce anxiolytic and antidepressive effects, which are probably mediated by agonist action on 5-HT1A/2A/2C receptors. These receptors are involved in emotional processing, regulation of BDNF brain levels, anti-inflammatory actions, and altered DMN functional connectivity. However, the mechanisms of action involved in these therapeutic effects are not completely understood, and, at least in the case of harmine, may include non-serotonergic mechanisms that regulate cell energy homeostasis, mitochondrial functions, and oxidative stress.

Considering that the average time necessary for the onset of therapeutic action of commercially available antidepressants is 2 weeks,77 the fast antidepressant action of ayahuasca reported in our preliminary clinical trial is promising. Recently, our group increased the number of depressive patients receiving ayahuasca treatment and used single photon emission computed tomography (SPECT) to assess regional cerebral blood flow after drug administration. Our results suggest similar positive effects as described in our pilot study.78

In summary, the results of this systematic review suggest that ayahuasca and its alkaloids have anxiolytic and antidepressive properties. These results are supported by studies using rodent models of anxiety and depressive disorders, experimental studies in healthy volunteers, observational studies in ayahuasca consumers, and preliminary data from depressed patients.

Investigation of these compounds could provide new pharmacological treatments with fast-acting beneficial effects for patients with anxiety and depressive disorders. Further studies are needed to replicate these findings.

Limitations of the present review include the small number of studies, especially clinical trials, and the heterogeneity among reviewed reports. Furthermore, most evidence showing anxiolytic and antidepressive effects of ayahuasca or its alkaloids comes from rodent studies. Thus, it is premature to extrapolate these results to humans until more research is conducted.

With the exception of a single pilot study, the human studies included in this review were mostly experimental and observational in nature. The experimental studies described had small sample sizes and were not designed to assess anxiolytic or antidepressive effect. An important limitation of observational studies with long-term ayahuasca consumers is that it is generally very hard to differentiate whether the improvements described are a consequence of the ingestion of ayahuasca or of joining a religious group, which can improve quality of life and well-being.79 Experimental and observational studies provide weak evidence of causality, and until more clinical trials are developed, the available evidence in humans must be considered preliminary.

Despite these limitations, the results showing anxiolytic and antidepressive effects of ayahuasca and its alkaloids are relatively constant, and have been reported in rodents, healthy volunteers, and depressed patients.

Acknowledgements

This work was funded by Funda��o de Amparo � Pesquisa do Estado de S�o Paulo (FAPESP; process 15/02848-2) and Coordena��o de Aperfei�oamento de Pessoal de N�vel Superior (CAPES).

References

1. Schultes RE, Ceballos LF, Castillo A. El desarrollo histórico de la identificación de las malpigiáceas empleadas como alucinógenos. Am Indig. 1986;46:9-47. [ Links ]

2. Schultes RE, Hofmann A. Plants of the gods: their sacred, healing, and hallucinogenic powers. Rochester: Healing Arts; 1992. [ Links ]

3. McKenna DJ, Towers GH, Abbott F. Monoamine oxidase inhibitors in South American hallucinogenic plants: tryptamine and beta-carboline constituents of ayahuasca. J Ethnopharmacol. 1984;10:195-223. [ Links ]

4. Riba J, Rodríguez-Fornells A, Urbano G, Morte A, Antonijoan R, Montero M, et al. Subjective effects and tolerability of the South American psychoactive beverage Ayahuasca in healthy volunteers. Psychopharmacology (Berl). 2001;154:85-95. [ Links ]

5. Riba J, Valle M, Urbano G, Yritia M, Morte A, Barbanoj MJ. Human pharmacology of ayahuasca: subjective and cardiovascular effects, monoamine metabolite excretion, and pharmacokinetics. J Pharmacol Exp Ther. 2003;306:73-83. [ Links ]

6. Riba J, McIlhenny EH, Bouso JC, Barker SA. Metabolism and urinary disposition of N,N-dimethyltryptamine after oral and smoked administration: a comparative study. Drug Test Anal. 2015;7:401-6. [ Links ]

7. Riba J, Romero S, Grasa E, Mena E, Carrió I, Barbanoj MJ. Increased frontal and paralimbic activation following ayahuasca, the pan-Amazonian inebriant. Psychopharmacology (Berl). 2006;186:93-8. [ Links ]

8. de Araujo DB, Ribeiro S, Cecchi GA, Carvalho FM, Sanchez TA, Pinto JP, et al. Seeing with the eyes shut: neural basis of enhanced imagery following Ayahuasca ingestion. Hum Brain Mapp. 2012;33:2550-60. [ Links ]

9. Labate BC, Rose IS, dos Santos RG. Ayahuasca religions: a comprehensive bibliography and critical essays. Santa Cruz: Multidisciplinary Association for Psychedelic Studies; 2009. [ Links ]

10. Grob CS, McKenna DJ, Callaway JC, Brito GS, Neves ES, Oberlaender G, et al. Human psychopharmacology of hoasca, a plant hallucinogen used in ritual context in Brazil. J Nerv Ment Dis. 1996;184:86-94. [ Links ]

11. Santos RG, Landeira-Fernandez J, Strassman RJ, Motta V, Cruz AP. Effects of ayahuasca on psychometric measures of anxiety, panic-like and hopelessness in Santo Daime members. J Ethnopharmacol. 2007;112:507-13. [ Links ]

12. Halpern JH, Sherwood AR, Passie T, Blackwell KC, Ruttenber AJ. Evidence of health and safety in American members of a religion who use a hallucinogenic sacrament. Med Sci Monit. 2008;14:SR15-22. [ Links ]

13. Fábregas JM, González D, Fondevila S, Cutchet M, Fernández X, Barbosa PC, et al. Assessment of addiction severity among ritual users of ayahuasca. Drug Alcohol Depend. 2010;111:257-61. [ Links ]

14. Barbosa PC, Mizumoto S, Bogenschutz MP, Strassman RJ. Health status of ayahuasca users. Drug Test Anal. 2012;4:601-9. [ Links ]

15. Bouso JC, González D, Fondevila S, Cutchet M, Fernández X, Ribeiro Barbosa PC, et al. Personality, psychopathology, life attitudes and neuropsychological performance among ritual users of Ayahuasca: a longitudinal study. PLoS One. 2012;7:e42421. [ Links ]

16. Thomas G, Lucas P, Capler NR, Tupper KW, Martin G. Ayahuasca-assisted therapy for addiction: results from a preliminary observational study in Canada. Curr Drug Abuse Rev. 2013;6:30-42. [ Links ]

17. Palhano-Fontes F, Alchieri JC, Oliveira JPM, Soares BL, Hallak JEC, Galvão-Coelho N, et al. The therapeutic potentials of ayahuasca in the treatment of depression. In: Labate BC, Cavnar C, editors. The therapeutic use of ayahuasca. Berlin: Springer-Verlag; 2014. p 23-39. [ Links ]

18. Osório Fde L, Sanches RF, Macedo LR, dos Santos RG, Maia-de-Oliveira JP, Wichert-Ana L, et al. Antidepressant effects of a single dose of ayahuasca in patients with recurrent depression: a preliminary report. Rev Bras Psiquiatr. 2015;37:13-20. [ Links ]

19. dos Santos RG, Valle M, Bouso JC, Nomdedéu JF, Rodríguez-Espinosa J, McIlhenny EH, et al. Autonomic, neuroendocrine and immunological effects of ayahuasca: a comparative study with d-amphetamine. J Clin Psychopharmacol. 2011;31:717-26. [ Links ]

20. dos Santos RG, Grasa E, Valle M, Ballester MR, Bouso JC, Nomdedéu JF, et al. Pharmacology of ayahuasca administered in two repeated doses. Psychopharmacology (Berl). 2012;219:1039-53. [ Links ]

21. dos Santos RG. Safety and side effects of ayahuasca in humans — an overview focusing on developmental toxicology. J Psychoactive Drugs. 2013;45:68-78. [ Links ]

22. Hilber P, Chapillon P. Effects of harmaline on anxiety-related behavior in mice. Physiol Behav. 2005;86:164-7. [ Links ]

23. Wu C, Jiang XL, Shen HW, Yu AM. Effects of CYP2D6 status on harmaline metabolism, pharmacokinetics and pharmacodynamics, and a pharmacogenetics-based pharmacokinetic model. Biochem Pharmacol. 2009;78:617-24. [ Links ]

24. Farzin D, Mansouri N. Antidepressant-like effect of harmane and other beta-carbolines in the mouse forced swim test. Eur Neuropsychopharmacol. 2006;16:324-8. [ Links ]

25. Fortunato JJ, Réus GZ, Kirsch TR, Stringari RB, Stertz L, Kapczinski F, et al. Acute harmine administration induces antidepressive-like effects and increases BDNF levels in the rat hippocampus. Prog Neuropsychopharmacol Biol Psychiatry. 2009;33:1425-30. [ Links ]

26. Fortunato JJ, Réus GZ, Kirsch TR, Stringari RB, Fries GR, Kapczinski F, et al. Effects of beta-carboline harmine on behavioral and physiological parameters observed in the chronic mild stress model: further evidence of antidepressant properties. Brain Res Bull. 2010;81:491-6. [ Links ]

27. Fortunato JJ, Réus GZ, Kirsch TR, Stringari RB, Fries GR, Kapczinski F, et al. Chronic administration of harmine elicits antidepressant-like effects and increases BDNF levels in the rat hippocampus. J Neural Transm. 2010;117:1131-7. [ Links ]

28. Réus GZ, Stringari RB, de Souza B, Petronilho F, Dal-Pizzol F, Hallak JE, et al. Harmine and imipramine promote antioxidant activities in prefrontal cortex and hippocampus. Oxid Med Cell Longev. 2010;3:325-31. [ Links ]

29. Réus GZ, Stringari RB, Gonçalves CL, Scaini G, Carvalho-Silva M, Jeremias GC, et al. Administration of harmine and imipramine alters creatine kinase and mitochondrial respiratory chain activities in the rat brain. Depress Res Treat. 2012;2012:987397. [ Links ]

30. Abelaira HM, Réus GZ, Scaini G, Streck EL, Crippa JA, Quevedo J. β-Carboline harmine reverses the effects induced by stress on behaviour and citrate synthase activity in the rat prefrontal cortex. Acta Neuropsychiatr. 2013;25:328-33. [ Links ]

31. Lima LM, Ferreira MS, Ávila AA, Perazzo FF, Schneedorf JM, Hinsberger A, et al. Ayahuasca central nervous system effects: behavioral study. Ärztezeitschrift Naturheilverfahren. 2006;47:476-80. [ Links ]

32. Gillin JC, Kaplan J, Stillman R, Wyatt RJ. The psychedelic model of schizophrenia: the case of N,N-dimethyltryptamine. Am J Psychiatry. 1976;133:203-8. [ Links ]

33. Strassman RJ, Qualls CR, Uhlenhuth EH, Kellner R. Dose-response study of N,N-dimethyltryptamine in humans. II. Subjective effects and preliminary results of a new rating scale. Arch Gen Psychiatry. 1994;51:98-108. [ Links ]

34. Barbosa PC, Giglio JS, Dalgalarrondo P. Altered states of consciousness and short-term psychological after-effects induced by the first time ritual use of ayahuasca in an urban context in Brazil. J Psychoactive Drugs. 2005;37:193-201. [ Links ]

35. Barbosa PC, Cazorla IM, Giglio JS, Strassman R. A six-month prospective evaluation of personality traits, psychiatric symptoms and quality of life in ayahuasca-naïve subjects. J Psychoactive Drugs. 2009;41:205-12. [ Links ]

36. Da Silveira DX, Grob CS, de Rios MD, Lopez E, Alonso LK, Tacla C, et al. Ayahuasca in adolescence: a preliminary psychiatric assessment. J Psychoactive Drugs. 2005;37:129-33. [ Links ]

37. Nutt DJ. Overview of diagnosis and drug treatments of anxiety disorders. CNS Spectr. 2005;10:49-56. [ Links ]

38. Grella B, Dukat M, Young R, Teitler M, Herrick-Davis K, Gauthier CB, et al. Investigation of hallucinogenic and related beta-carbolines. Drug Alcohol Depend. 1998;50:99-107. [ Links ]

39. Glennon RA, Dukat M, Grella B, Hong S, Costantino L, Teitler M, et al. Binding of β-carbolines and related agents at serotonin (5-HT2 and 5-HT1A), dopamine (D2) and benzodiazepine receptors. Drug Alcohol Depend. 2000;60:121-32. [ Links ]

40. Grella B, Teitler M, Smith C, Herrick-Davis K, Glennon RA. Binding of β-carbolines at 5-HT2 serotonin receptors. Bioorg Med Chem Lett. 2003;13:4421-5. [ Links ]

41. Nichols DE. Hallucinogens. Pharmacol Ther. 2004;101:131-81. [ Links ]

42. Vollenweider FX, Kometer M. The neurobiology of psychedelic drugs: implications for the treatment of mood disorders. Nat Rev Neurosci. 2010;11:642-51. [ Links ]

43. Baumeister D, Barnes G, Giaroli G, Tracy D. Classical hallucinogens as antidepressants? A review of pharmacodynamics and putative clinical roles. Ther Adv Psychopharmacol. 2014;4:156-69. [ Links ]

44. Katzman MA. Current considerations in the treatment of generalized anxiety disorder. CNS Drugs. 2009;23:103-20. [ Links ]

45. Masuda Y, Sugiyama T. The effect of globopentaosylceramide on a depression model, mouse forced swimming. Tohoku J Exp Med. 2000;191:47-54. [ Links ]

46. Nic Dhonnchadha BA, Bourin M, Hascoët M. Anxiolytic-like effects of 5-HT2 ligands on three mouse models of anxiety. Behav Brain Res. 2003;140:203-14. [ Links ]

47. Nic Dhonnchadha BA, Hascoët M, Jolliet P, Bourin M. Evidence for a 5-HT2A receptor mode of action in the anxiolytic-like properties of DOI in mice. Behav Brain Res. 2003;147:175-84. [ Links ]

48. Nau F Jr, Yu B, Martin D, Nichols CD. Serotonin 5-HT2A receptor activation blocks TNF-α mediated inflammation in vivo. PLoS One. 2013;8:e75426. [ Links ]

49. dos Santos RG. Immunological effects of ayahuasca in humans. J Psychoactive Drugs. 2014;46:383-8. [ Links ]

50. Szabo A, Kovacs A, Frecska E, Rajnavolgyi E. Psychedelic N,N-dimethyltryptamine and 5-methoxy-N,N-dimethyltryptamine modulate innate and adaptive inflammatory responses through the sigma-1 receptor of human monocyte-derived dendritic cells. PLoS One. 2014;9:e106533. [ Links ]

51. Kurland AA, Pahnke WN, Unger S, Savage C. Psychedelic LSD research. In: Evans WO, Kline NS, editors. Psychotropic drugs in the year 2000. Use by Normal Humans. Springfield: Charles C. Thomas Publisher; 1971. p. 86-108. [ Links ]

52. McGlothlin WH, Arnold DO. LSD revisited. A ten-year follow-up of medical LSD use. Arch Gen Psychiatry. 1971;24:35-49. [ Links ]

53. Grispoon L, Bakalar JB. Psychedelic drugs reconsidered. New York: Basic Books; 1981. [ Links ]

54. Riedlinger TJ, Riedlinger JE. Psychedelic and entactogenic drugs in the treatment of depression. J Psychoactive Drugs. 1994;26:41-55. [ Links ]

55. Abraham HD, Aldridge AM, Gogia P. The psychopharmacology of hallucinogens. Neuropsychopharmacology. 1996;14:285-98. [ Links ]

56. Delgado PL, Moreno FA. Hallucinogens, serotonin and obsessive-compulsive disorder. J Psychoactive Drugs. 1998;30:359-66. [ Links ]

57. Matsushima Y, Shirota O, Kikura-Hanajiri R, Goda Y, Eguchi F. Effects of Psilocybe argentipes on marble-burying behavior in mice. Biosci Biotechnol Biochem. 2009;73:1866-8. [ Links ]

58. Buchborn T, Schröder H, Höllt V, Grecksch G. Repeated lysergic acid diethylamide in an animal model of depression: normalisation of learning behaviour and hippocampal serotonin 5-HT2 signalling. J Psychopharmacol. 2014;28:545-52. [ Links ]

59. Griffiths RR, Richards WA, McCann U, Jesse R. Psilocybin can occasion mystical-type experiences having substantial and sustained personal meaning and spiritual significance. Psychopharmacology (Berl). 2006;187:268-83. [ Links ]

60. Griffiths RR, Johnson MW, Richards WA, Richards BD, McCann U, Jesse R. Psilocybin occasioned mystical-type experiences: immediate and persisting dose-related effects. Psychopharmacology (Berl). 2011;218:649-65. [ Links ]

61. Studerus E, Kometer M, Hasler F, Vollenweider FX. Acute, subacute and long-term subjective effects of psilocybin in healthy humans: a pooled analysis of experimental studies. J Psychopharmacol. 2011;25:1434-52. [ Links ]

62. Kometer M, Schmidt A, Bachmann R, Studerus E, Seifritz E, Vollenweider FX. Psilocybin biases facial recognition, goal-directed behavior, and mood state toward positive relative to negative emotions through different serotonergic subreceptors. Biol Psychiatry. 2012;72:898-906. [ Links ]

63. Kraehenmann R, Preller KH, Scheidegger M, Pokorny T, Bosch OG, Seifritz E, et al. Psilocybin-induced decrease in amygdala reactivity correlates with enhanced positive mood in healthy volunteers. 2015;78:572-81. [ Links ]

64. Schmid Y, Enzler F, Gasser P, Grouzmann E, Preller KH, Vollenweider FX, et al. Acute effects of lysergic acid diethylamide in healthy subjects. Biol Psychiatry. 2015;78:544-53. [ Links ]

65. Leonard HL, Rapoport JL. Relief of obsessive-compulsive symptoms by LSD and psilocin. Am J Psychiatry. 1987;144:1239-40. [ Links ]

66. Hanes KR. Serotonin, psilocybin, and body dysmorphic disorder: a case report. J Clin Psychopharmacol. 1996;16:188-9. [ Links ]

67. Perrine DM. Hallucinogens and obsessive-compulsive disorder. Am J Psychiatry. 1999;156:1123. [ Links ]

68. Wilcox JA. Psilocybin and obsessive compulsive disorder. J Psychoactive Drugs. 2014;46:393-5. [ Links ]

69. Moreno FA, Wiegand CB, Taitano EK, Delgado PL. Safety, tolerability, and efficacy of psilocybin in 9 patients with obsessive-compulsive disorder. J Clin Psychiatry. 2006;67:1735-40. [ Links ]

70. Grob CS, Danforth AL, Chopra GS, Hagerty M, McKay CR, Halberstadt AL, et al. Pilot study of psilocybin treatment for anxiety in patients with advanced-stage cancer. Arch Gen Psychiatry. 2011;68:71-8. [ Links ]

71. Gasser P, Holstein D, Michel Y, Doblin R, Yazar-Klosinski B, Passie T, et al. Safety and efficacy of lysergic acid diethylamide-assisted psychotherapy for anxiety associated with life-threatening diseases. J Nerv Ment Dis. 2014;202:513-20. [ Links ]

72. Gasser P, Kirchner K, Passie T. LSD-assisted psychotherapy for anxiety associated with a life-threatening disease: a qualitative study of acute and sustained subjective effects. J Psychopharmacol. 2015;29:57-68. [ Links ]

73. Palhano-Fontes F, Andrade KC, Tofoli LF, Santos AC, Crippa JA, Hallak JE, et al. The psychedelic state induced by ayahuasca modulates the activity and connectivity of the default mode network. PLoS One. 2015;10:e0118143. [ Links ]

74. Bouso JC, Palhano-Fontes F, Rodríguez-Fornells A, Ribeiro S, Sanches R, Crippa JA, et al. Long-term use of psychedelic drugs is associated with differences in brain structure and personality in humans. Eur Neuropsychopharmacol. 2015;25:483-92. [ Links ]

75. Carhart-Harris R, Erritzoe D, Williams T, Stone JM, Reed LJ, Colasanti A, et al. Neural correlates of the psychedelic state as determined by fMRI studies with psilocybin. Proc Natl Acad Sci USA. 2012;109:2138-43. [ Links ]

76. Carhart-Harris R, Leech R, Erritzoe D, Williams TM, Stone JM, Evans J, et al. Functional connectivity measures after psilocybin inform a novel hypothesis of early psychosis. Schizophr Bull. 2013;39:1343-51. [ Links ]

77. Pacher P, Kecskemeti V. Trends in the development of new antidepressants. Is there a light at the end of the tunnel? Currt Med Chem. 2004;11:925-43. [ Links ]

78. Sanches RF, Osório Fde L, dos Santos RG, Macedo LR, Maia-de-Oliveira JP, Wichert-Ana L, et al. Antidepressant effects of a single dose of ayahuasca in patients with recurrent depression: a SPECT study. J Clin Psychopharmacol. I Forthcoming 2015. [ Links ]

79. Panzini RG, da Rocha NS, Bandeira DR, Fleck MPA. Qualidade de vida e espiritualidade. Rev Psiquiatr Clin. 2007;34:105-15. [ Links ]

Received: March 2, 2015; Accepted: May 5, 2015

Correspondence: Rafael G. dos Santos, Departamento de Neurociências e Ciências do Comportamento, Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, Hospital das Clínicas, 3° andar, Av. Bandeirantes, 3900, CEP 14040-900, Ribeirão Preto, SP, Brazil.E-mail: banisteria@gmail.com

Disclosure The authors report no conflicts of interest.

Creative Commons License This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

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