Sacred Maya incense, copal (Protium copal - Burseraceae), has antianxiety effects in animal models.

ETHNOPHARMACOLOGICAL RELEVANCE The Maya have traditionally used copal, Protium copal, as incense during ceremonies since pre-Columbian times. Anecdotally, copal (when burned as incense), is thought to elicit mentally uplifting and calming effects. The main objective of this study was to determine whether the incense elicits anxiolytic-like behavior in animal models using rats. A second objective was to characterize active constituents and discern potential mechanism(s) of action, specifically the involvement of the GABAergic and endocannabinoid (eCB) systems. Despite the extensive Central American use of this resin, there are currently no known scientific behavioral or pharmacological studies done with the incense. MATERIALS AND METHODS Quantification of the triterpenes in the copal resin and cold trapped incense was achieved by HPLC MS. Behavioral effects in rats were assessed using the elevated plus maze (EPM), social interaction (SI) test, conditioned emotion response (CER) and Novel object recognition (NOR) paradigms. Rats were exposed to burning copal (200 mg) over 5 min in a smoking chamber apparatus and then immediately tested in each behavioral paradigm. Follow-up SI tests were done using two antagonists flumazenil (1 mg/kg) and AM251 (1 mg/kg) administered systemically. Inhibition of MAGL (monoacylglycerol lipase) was measured by microplate assay with recombinant human enzyme and probe substrate. RESULTS Phytochemical analysis revealed that copal resin and incense had high α- and β-amyrins and low lupeol triterpene content. Exposure to Protium copal incense significantly reduced anxiety-like behavior in the SI and CER tests. In contrast, no anxiolytic effects were observed in the EPM. The CER effect was time dependent. Both flumazenil and AM251 blocked the anxiolytic activity of copal revealing the involvement of GABAergic and endocannabinoid systems. Copal, as well as the identified triterpenes, potently inhibited monoacylglycerol lipase (MAGL) activity in vitro (IC50 ≤ 811 ng/mL). CONCLUSIONS This is the first study to show that copal incense from Protium copal elicits anxiolytic-like effects in fear and social interaction models as evidenced by a reduced learned fear behavior and an increase in active social interaction. It's high α and β-amyrin content suggests behavioral effects may be mediated, in part, by the known action of these terpenes at the benzodiazepine receptor. Furthermore, P. copal's observed activity through the eCB system via MAGL offers a new potential mechanism underlying the anxiolytic activity.

[1]  H. Schiöth,et al.  Acute ghrelin administration reverses depressive-like behavior induced by bilateral olfactory bulbectomy in mice , 2012, Peptides.

[2]  S. Murch,et al.  Spiritual and ceremonial plants in North America: an assessment of Moerman's ethnobotanical database comparing Residual, Binomial, Bayesian and Imprecise Dirichlet Model (IDM) analysis. , 2013, Journal of ethnopharmacology.

[3]  P. Bandeira,et al.  Analgesic and anti-inflammatory activities of the isomeric mixture of alpha- and beta-amyrin from Protium heptaphyllum (Aubl.) march. , 2008 .

[4]  J. Palazón,et al.  Valuable medicinal plants and resins: Commercial phytochemicals with bioactive properties , 2010 .

[5]  M. Chaves,et al.  Anti-inflammatory effect of α,β-amyrin, a triterpene from Protium heptaphyllum, on cerulein-induced acute pancreatitis in mice , 2011, Inflammation Research.

[6]  J. Arnason,et al.  Characterization of the Anxiolytic Activity of Nunavik Rhodiola rosea , 2013, Planta Medica.

[7]  Daniele Piomelli,et al.  Discovery of potent and reversible monoacylglycerol lipase inhibitors. , 2009, Chemistry & biology.

[8]  Michael Davis,et al.  The role of the amygdala in emotional learning. , 1994, International review of neurobiology.

[9]  S. File,et al.  Anxiolytic and anxiogenic drug effects on exploratory activity in an elevated plus-maze: A novel test of anxiety in the rat , 1986, Pharmacology Biochemistry and Behavior.

[10]  S. File,et al.  A review of 25 years of the social interaction test. , 2003, European journal of pharmacology.

[11]  P. Bandeira,et al.  A possible mechanism for anxiolytic and antidepressant effects of alpha- and beta-amyrin from Protium heptaphyllum (Aubl.) March , 2006, Pharmacology Biochemistry and Behavior.

[12]  R. Zhou,et al.  Natural amber, copal resin and colophony investigated by UV-VIS, infrared and Raman spectrum , 2013 .

[13]  G. F. Passos,et al.  Activation of cannabinoid receptors by the pentacyclic triterpene α,β-amyrin inhibits inflammatory and neuropathic persistent pain in mice , 2011, PAIN®.

[14]  R N Walsh,et al.  The Open-Field Test: a critical review. , 1976, Psychological bulletin.

[15]  A. Tucker,et al.  Chemistry and ethnobotany of commercial incense copals copal blanco, copal oro, and copal negro, of North America , 2003, Economic Botany.

[16]  B. Nuttin,et al.  Contextual conditioning in rats as an animal model for generalized anxiety disorder , 2011, Cognitive, affective & behavioral neuroscience.

[17]  F. Graeff,et al.  Ethopharmacological analysis of rat behavior on the elevated plus-maze , 1994, Pharmacology Biochemistry and Behavior.

[18]  Carole Mathe,et al.  Analysis of Mexican reference standards for Bursera spp. resins by Gas Chromatography–Mass Spectrometry and application to archaeological objects , 2014 .

[19]  L. Spear,et al.  Social interactions in adolescent and adult Sprague–Dawley rats: Impact of social deprivation and test context familiarity , 2008, Behavioural Brain Research.

[20]  J. Panksepp,et al.  Social deprivation and play in rats. , 1980, Behavioral and neural biology.

[21]  Michael Davis,et al.  Fear-potentiated startle: A neural and pharmacological analysis , 1993, Behavioural Brain Research.

[22]  R. Ribeiro‐dos‐Santos,et al.  Evaluation of anti-inflammatory-related activity of essential oils from the leaves and resin of species of Protium. , 1999, Journal of ethnopharmacology.

[23]  File Se Animal models of different anxiety states. , 1995 .

[24]  K. Mackie,et al.  Monoacylglycerol lipase inhibitors produce pro- or antidepressant responses via hippocampal CA1 GABAergic synapses , 2016, Molecular Psychiatry.

[25]  J. Gertsch,et al.  The antinociceptive triterpene β‐amyrin inhibits 2‐arachidonoylglycerol (2‐AG) hydrolysis without directly targeting cannabinoid receptors , 2012, British journal of pharmacology.

[26]  C. Cartwright,et al.  CHEMICAL CHARACTERIZATION OF ANCIENT MESOAMERICAN ‘COPAL’ RESINS: PRELIMINARY RESULTS* , 2006 .

[27]  S. D. de Boer,et al.  A robust animal model of state anxiety: fear-potentiated behaviour in the elevated plus-maze. , 2003, European journal of pharmacology.

[28]  Marta Coelho Antunes,et al.  The novel object recognition memory: neurobiology, test procedure, and its modifications , 2011, Cognitive Processing.