[1]
Bogenschutz, M.P.; Johnson, M.W. Classic hallucinogens in the treatment of addictions. Prog. Neuropsychopharmacol. Biol. Psychiatry, 2016, 64, 250-258.
[2]
Nichols, D.E. Hallucinogens. Pharmacol. Ther., 2004, 101, 131-181.
[3]
Olive, M.F.; Triggle, D.J. Drugs the straight facts: Peyote and mescaline; Chelsea House: New York, 2007.
[4]
Lopez-Gimenez, J.F.; Gonzalez-Maeso, J. Hallucinogens and Serotonin 5-HT2A Receptor-Mediated Signaling Pathways. Curr. Top. Behav. Neurosci., 2018, 36, 45-73.
[5]
Dinis-Oliveira, R.J. Metabolism of psilocybin and psilocin: Clinical and forensic toxicological relevance. Drug Metab. Rev., 2017, 49, 84-91.
[6]
El-Seedi, H.R.; De Smet, P.A.; Beck, O.; Possnert, G.; Bruhn, J.G. Prehistoric peyote use: Alkaloid analysis and radiocarbon dating of archaeological specimens of Lophophora from Texas. J. Ethnopharmacol., 2005, 101, 238-242.
[7]
Halpern, J.H.; Sherwood, A.R.; Hudson, J.I.; Yurgelun-Todd, D.; Pope, H.G., Jr Psychological and cognitive effects of long-term peyote use among Native Americans. Biol. Psychiatry, 2005, 58, 624-631.
[8]
Bullis, R.K. Swallowing the scroll: Legal implications of the recent Supreme Court peyote cases. J. Psychoactive Drugs, 1990, 22, 325-332.
[9]
Csordas, T.J.; Storck, M.J.; Strauss, M. Diagnosis and distress in Navajo healing. J. Nerv. Ment. Dis., 2008, 196, 585-596.
[10]
Carstairs, S.D.; Cantrell, F.L. Peyote and mescaline exposures: a 12-year review of a statewide poison center database. Clin. Toxicol. (Phila.), 2010, 48, 350-353.
[11]
Heffter, A. Ueber Cacteenalkaloide. (II. Mittheilung). Ber. Dtsch. Chem. Ges., 1896, 29, 216-227.
[12]
Späth, E. Über die anhalonium-alkaloide I. Anhalin und mezcalin. Monatsh. Chem., 1919, 40, 129-154.
[13]
Kyzar, E.J.; Nichols, C.D.; Gainetdinov, R.R.; Nichols, D.E.; Kalueff, A.V. Psychedelic Drugs in Biomedicine. Trends Pharmacol. Sci., 2017, 38, 992-1005.
[14]
Dyck, E.; Farrell, P. Psychedelics and psychotherapy in Canada: Humphry Osmond and Aldous Huxley. Hist. Psychol., 2018, 21, 240-253.
[15]
de Rios, M.D.; Grob, C.S.; Baker, J.R. Hallucinogens and redemption. J. Psychoactive Drugs, 2002, 34, 239-248.
[16]
Winkelman, M. Psychedelics as medicines for substance abuse rehabilitation: Evaluating treatments with LSD, Peyote, Ibogaine and Ayahuasca. Curr. Drug Abuse Rev., 2014, 7, 101-116.
[17]
Denber, H.C. Mescaline and lysergic acid diethylamide: Therapeutic implications of the drug-induced state. Dis. Nerv. Syst., 1969, 30(Suppl.), 23-27.
[18]
Barbosa, J.; Faria, J.; Queiros, O.; Moreira, R.; Carvalho, F.
Dinis-Oliveira, R.J. Comparative metabolism of tramadol and tapentadol: A toxicological perspective. Drug Metab. Rev., 2016, 48, 577-592.
[19]
Dinis-Oliveira, R.J. Metabolic Profile of Flunitrazepam: Clinical and Forensic Toxicological Aspects. Drug Metab. Lett., 2017, 11, 14-20.
[20]
Dinis-Oliveira, R.J. Metabolic profile of oxazepam and related benzodiazepines: clinical and forensic aspects. Drug Metab. Rev., 2017, 49, 451-463.
[21]
Dinis-Oliveira, R.J. Metabolic Profiles of Propofol and Fospropofol: Clinical and Forensic Interpretative Aspects. BioMed Res. Int., 2018, 20186852857
[22]
Dinis-Oliveira, R.J. Metabolomics of cocaine: Implications in toxicity. Toxicol. Mech. Methods, 2015, 25, 494-500.
[23]
Dinis-Oliveira, R.J. Metabolomics of Delta9-tetrahydrocannabinol: Implications in toxicity. Drug Metab. Rev., 2016, 48, 80-87.
[24]
Dinis-Oliveira, R.J. Metabolomics of methadone: Clinical and forensic toxicological implications and variability of dose response. Drug Metab. Rev., 2016, 48, 568-576.
[25]
Dinis-Oliveira, R.J. Metabolomics of Methylphenidate and Ethylphenidate: Implications in Pharmacological and Toxicological Effects. Eur. J. Drug Metab. Pharmacokinet., 2017, 42, 11-16.
[26]
Nobrega, L.; Dinis-Oliveira, R.J. The synthetic cathinone alpha-pyrrolidinovalerophenone (alpha-PVP): Pharmacokinetic and pharmacodynamic clinical and forensic aspects. Drug Metab. Rev., 2018, 50, 125-139.
[27]
Dinis-Oliveira, R.J. Metabolism and metabolomics of ketamine: A toxicological approach. J. Forensic Sci., 2017, 2(1), 2-10.
[28]
Ogunbodede, O.; McCombs, D.; Trout, K.; Daley, P.; Terry, M. New mescaline concentrations from 14 taxa/cultivars of Echinopsis spp. (Cactaceae) (“San Pedro”) and their relevance to shamanic practice. J. Ethnopharmacol., 2010, 131, 356-362.
[29]
Aragane, M.; Sasaki, Y.; Nakajima, J.; Fukumori, N.; Yoshizawa, M.; Suzuki, Y.; Kitagawa, S.; Mori, K.; Ogino, S.; Yasuda, I.; Nagumo, S. Peyote identification on the basis of differences in morphology, mescaline content, and trnL/trnF sequence between Lophophora williamsii and L. diffusa. J. Nat. Med., 2011, 65, 103-110.
[30]
Carod-Artal, F.J.; Vazquez-Cabrera, C.B. Mescaline and the San Pedro cactus ritual: Archaeological and ethnographic evidence in northern Peru. Rev. Neurol., 2006, 42, 489-498.
[31]
Dasgupta, A. Challenges in Laboratory Detection of Unusual Substance Abuse: Issues with Magic Mushroom, Peyote Cactus, Khat, and Solvent Abuse. Adv. Clin. Chem., 2017, 78, 163-186.
[32]
Crosby, D.M.; McLaughlin, J.L. Cactus alkaloids. XIX. Crystallization of mescaline HCl and 3-methoxytyramine HCl from Trichocereus pachanoi. Lloydia, 1973, 36, 416-418.
[33]
Anderson, E.F. The cactus family; Timber Press: Oregon, 2001.
[34]
Pinto Nde, C.; Duque, A.P.; Pacheco, N.R.; Mendes Rde, F.; Motta, E.V.; Bellozi, P.M.; Ribeiro, A.; Salvador, M.J.; Scio, E. Pereskia aculeata: A plant food with antinociceptive activity. Pharm. Biol., 2015, 53, 1780-1785.
[35]
Schlumpberger, B.O.; Renner, S.S. Molecular phylogenetics of Echinopsis (Cactaceae): Polyphyly at all levels and convergent evolution of pollination modes and growth forms. Am. J. Bot., 2012, 99, 1335-1349.
[36]
Clement, B.A.; Goff, C.M.; Forbes, T.D.A. Toxic amines and alkaloids from Acacia berlandieri. Phytochemistry, 1997, 46, 249-254.
[37]
Neal, J.M.; Sato, P.T.; Howald, W.N.; McLaughlin, J.L. yote Alkaloids: Identification in the Mexican ictus Pelecyphora aselliformis Ehrenberg. Science, 1972, 176, 1131-1133.
[38]
Gomez-Coronado, N.; Walker, A.J.; Berk, M.; Dodd, S. Current and Emerging Pharmacotherapies for Cessation of Tobacco Smoking. Pharmacotherapy, 2018, 38, 235-258.
[39]
Tutka, P.; Zatonski, W. Cytisine for the treatment of nicotine addiction: from a molecule to therapeutic efficacy. Pharmacol. Rep., 2006, 58(6), 777-798.
[40]
Walker, N.; Howe, C.; Glover, M.; McRobbie, H.; Barnes, J.; Nosa, V.; Parag, V.; Bassett, B.; Bullen, C. Cytisine versus nicotine for smoking cessation. N. Engl. J. Med., 2014, 371, 2353-2362.
[41]
Terry, M.; Mauseth, J.D. Root-shoot anatomy and post-harvest
vegetative clonal development in Lophophora williamsii (Cactaceae:
Cacteae): Implications for conservation. 2006, 22, 565-592.
[42]
Spinella, M. The psychopharmacology of herbal medicine: Plant drugs that alter mind, brain, and behavior; MIT Press: Massachusetts, 2001.
[43]
Kapadia, G.J.; Fayez, M.B. Peyote constituents: chemistry, biogenesis, and biological effects. J. Pharm. Sci., 1970, 59, 1699-1727.
[44]
Štarha, R.; Kuchiňa, J. Analysis of Mexican Populations of Lophophora (Cactaceae). Universitas Ostraviensis Acta Facultatis Rerum Naturalium. Physica-Chemia, 1996, 156, 67-70.
[45]
Heffter, A. Ueber Pellote. Ein Betrag zur pharmakologischen Kenntnis der Cacteen. Naunyn Schmiedebergs Arch. Pharmacol., 1894, 34, 65-86.
[46]
Lundstrom, J.; Agurell, S. Biosynthesis of mescaline and anhalamine in peyote. IIa. Tetrahedron Lett., 1968, 9, 4437-4440.
[47]
Klein, M.T.; Kalam, M.; Trout, K.; Fowler, N.; Terry, M. Mescaline concentrations in three principal tissues of Lophophora Williamsii (Cactaceae): Implications for sustainable harvesting practices. Haseltonia, 2015, 2015(20), 34-42.
[48]
Steiner, I.; Brauers, G.; Temme, O.; Daldrup, T. A sensitive method for the determination of hordenine in human serum by ESI(+) UPLC-MS/MS for forensic toxicological applications. Anal. Bioanal. Chem., 2016, 408, 2285-2292.
[49]
Frank, M.; Weckman, T.J.; Wood, T.; Woods, W.E.; Tai, C.L.; Chang, S.L.; Ewing, A.; Blake, J.W.; Tobin, T. Hordenine: Pharmacology, pharmacokinetics and behavioural effects in the horse. Equine Vet. J., 1990, 22, 437-441.
[50]
Ghansah, E.; Kopsombut, P.; Maleque, M.A.; Brossi, A. Effects of mescaline and some of its analogs on cholinergic neuromuscular transmission. Neuropsychopharmacol., 1993, 32, 169-174.
[51]
Bruhn, J.G.; El-Seedi, H.R.; Stephanson, N.; Beck, O.; Shulgin, A.T. Ecstasy analogues found in cacti. J. Psychoactive Drugs, 2008, 40, 219-222.
[52]
da Silva, D.D.; Silva, E.; Carvalho, F.; Carmo, H. Mixtures of 3,4-methylenedioxymethamphetamine (ecstasy) and its major human metabolites act additively to induce significant toxicity to liver cells when combined at low, non-cytotoxic concentrations. J. Appl. Toxicol., 2014, 34, 618-627.
[53]
Millan, M.J.; Marin, P.; Bockaert, J.; Mannoury la Cour, C. Signaling at G-protein-coupled serotonin receptors: Recent advances and future research directions. Trends Pharmacol. Sci., 2008, 29, 454-464.
[54]
Landolt, H.P.; Wehrle, R. Antagonism of serotonergic 5-HT2A/2C receptors: Mutual improvement of sleep, cognition and mood? Eur. J. Neurol., 2009, 29, 1795-1809.
[55]
Urbán, L.; Patel, V.F.; Vaz, R.J. Antitargets and drug safety; Wiley-VCH: Weinheim, 2015.
[56]
Aghajanian, G.K.; Marek, G.J. Serotonin and hallucinogens. Neuropsychopharmacology, 1999, 21, 16s-23s.
[57]
Monte, A.P.; Waldman, S.R.; Marona-Lewicka, D.; Wainscott, D.B.; Nelson, D.L.; Sanders-Bush, E.; Nichols, D.E. Dihydrobenzofuran analogues of hallucinogens. 4. Mescaline derivatives. J. Med. Chem., 1997, 40, 2997-3008.
[58]
Freedman, D.X.; Gottlieb, R.; Lovell, R.A. Psychotomimetic drugs and brain 5-hydroxytryptamine metabolism. Biochem. Pharmacol., 1970, 19, 1181-1188.
[59]
Tilson, H.A.; Sparber, S.B. Studies on the concurrent behavioral and neurochemical effects of psychoactive drugs using the push-pull cannula. J. Pharmacol. Exp. Ther., 1972, 181, 387-398.
[60]
Trulson, M.E.; Crisp, T.; Henderson, L.J. Mescaline elicits behavioral effects in cats by an action at both serotonin and dopamine receptors. Eur. J. Pharmacol., 1983, 96, 151-154.
[61]
Freedman, D.X. The psychopharmacology of hallucinogenic agents. Annu. Rev. Med., 1969, 20, 409-418.
[62]
van Amsterdam, J.; Opperhuizen, A.; van den Brink, W. Harm potential of magic mush2room use: A review. Regul. Toxicol. Pharmacol., 2011, 59, 423-429.
[63]
Dasgupta, A. Chapter Five - Challenges in Laboratory Detection of
Unusual Substance Abuse: Issues with Magic Mushroom, Peyote
Cactus, Khat, and Solvent Abuse. In: Advances in clinical chemistry,
Makowski,; G.S., Ed. Elsevier:, 2017; 78, pp. 63-186.
[64]
Mokrasch, L.C.; Stevenson, I. The metabolism of mescaline with a note on correlations between metabolism and psychological effects. J. Nerv. Ment. Dis., 1959, 129, 177-183.
[65]
Cochin, J.; Woods, L.A.; Seevers, M.H. The absorption, distribution and urinary excretion of mescaline in the dog. J. Pharmacol. Exp. Ther., 1951, 101, 205-209.
[66]
Palenicek, T.; Balikova, M.; Bubenikova-Valesova, V.; Horacek, J. Mescaline effects on rat behavior and its time profile in serum and brain tissue after a single subcutaneous dose. Psychopharmacology, 2008, 196, 51-62.
[67]
Halpern, J.H. Hallucinogens and dissociative agents naturally growing in the United States. Pharmacol. Ther., 2004, 102, 131-138.
[68]
Charalampous, K.D.; Walker, K.E.; Kinross-Wright, J. Metabolic fate of mescaline in man. Psychopharmacology, 1966, 9, 48-63.
[69]
Harley-Mason, J.; Laird, A.H.; Smythies, J.R. The metabolism of mescalin in the human; Delayed clinical reactions to mescalin. Confin. Neurol., 1958, 18, 152-155.
[70]
Shah, N.S.; Green, C. Tissue levels of mescaline in mice: Influence of chlorpromazine on repeated administration of mescaline. Eur. J. Pharmacol., 1973, 24, 334-340.
[71]
Seiler, N.; Demisch, L. Oxidative metabolism of mescaline in the central nervous system-III: Side chain degradation of mescaline and formation of 3,4,5-trimethoxy-benzoic acid In vivo. Biochem. Pharmacol., 1974, 23, 259-271.
[72]
Daly, J.; Axelrod, J.; Witkop, B. Methylation and demethylation in relation to the in vitro metabolism of mescaline. Ann. N. Y. Acad. Sci., 1962, 96, 37-43.
[73]
Kovacic, P.; Somanathan, R. Novel, unifying mechanism for mescaline in the central nervous system: Electrochemistry, catechol redox metabolite, receptor, cell signaling and structure activity relationships. Oxid. Med. Cell. Longev., 2009, 2, 181-190.
[74]
Shah, N.S.; Himwich, H.E. Study with mescaline-8-C14 in mice: Effect of amine oxidase inhibitors on metabolism. Neuropsychopharmacol., 1971, 10, 547-556.
[75]
Hilliker, K.S.; Roth, R.A. Prediction of mescaline clearance by rabbit lung and liver from enzyme kinetic data. Biochem. Pharmacol., 1980, 29, 253-255.
[76]
Scheline, R.R. Handbook of mammalian metabolism of plant compounds (1991); CRC Press: Boca Raton, 2017.
[77]
Friedhoff, A.J.; Goldstein, M. New developments in metabolism of mescaline and related amines. Ann. N. Y. Acad. Sci., 1962, 96, 5-13.
[78]
Seiler, N.; Demisch, L. Oxidative metabolism of mescaline in the central nervous system. II. Oxidative deamination of mescaline and 2,3,4-trimethoxy-beta-phenylethylamine by different mouse brain area in vitro. Biochem. Pharmacol., 1971, 20, 2485-2493.
[79]
Steensholt, G. On an amine oxidase in rabbit’s liver. Acta Physiol. Scand., 1947, 14, 356-362.
[80]
Demisch, L.; Seiler, N. Oxidative metabolism of mescaline in the central nervous system-V: In vitro deamination of mescaline to 3,4,5-trimethoxy-benzoic acid. Biochem. Pharmacol., 1975, 24, 575-580.
[81]
Carvalho, M.; Carmo, H.; Costa, V.M.; Capela, J.P.; Pontes, H.; Remiao, F.; Carvalho, F.; Bastos Mde, L. Toxicity of amphetamines: An update. Arch. Toxicol., 2012, 86, 1167-1231.
[82]
Demisch, L.; Seiler, N. Oxidative metabolism of mescaline in the central nervous system-V. In vitro deamination of mescaline to 3,4,5-trimethoxy-benzoic acid. Biochem. Pharmacol., 1975, 24, 575-580.
[83]
Musacchio, J.; Goldstein, M. The metabolism of mescaline-14C in rats. Biochem. Pharmacol., 1967, 16, 963-970.
[84]
Axelrod, J. The enzymic cleavage of aromatic ethers. Biochem. J., 1956, 63, 634-639.
[85]
Friedhoff, A.J.; Hollister, L.E. Comparison of the metabolism of 3,4-dimethoxyphenylethylamine and mescaline in humans. Biochem. Pharmacol., 1966, 15, 269-273.
[86]
Wu, D.; Otton, S.V.; Inaba, T.; Kalow, W.; Sellers, E.M. Interactions of amphetamine analogs with human liver CYP2D6. Biochem. Pharmacol., 1997, 53, 1605-1612.
[87]
Demisch, L.; Kaczmarczyk, P.; Seiler, N. 3,4,5-Trimethoxybenzoic acid, a new mescaline metabolite in humans. Drug Metab. Dispos., 1978, 6, 507-509.
[88]
Goldstein, M.; Contrera, J.F. The substrate specificity of phenylamine-beta-hydroxylase. J. Biol. Chem., 1962, 237, 1898-1902.
[89]
Hermle, L.; Funfgeld, M.; Oepen, G.; Botsch, H.; Borchardt, D.; Gouzoulis, E.; Fehrenbach, R.A.; Spitzer, M. Mescaline-induced psychopathological, neuropsychological, and neurometabolic effects in normal subjects: Experimental psychosis as a tool for psychiatric research. Biol. Psychiatry, 1992, 32, 976-991.
[90]
Hardman, H.F.; Haavik, C.O.; Seevers, M.H. Relationship of the structure of mescaline and seven analogs to toxicity and behavior in five species of laboratory animals. Toxicol. Appl. Pharmacol., 1973, 25, 299-309.
[91]
Schultes, R.E. Hallucinogens of plant origin. Science, 1969, 163, 245-254.
[92]
Bressloff, P.C.; Cowan, J.D.; Golubitsky, M.; Thomas, P.J.; Wiener, M.C. What geometric visual hallucinations tell us about the visual cortex. Neural Comput., 2002, 14, 473-491.
[93]
Golembiowska, K.; Jurczak, A.; Kaminska, K.; Noworyta-Sokolowska, K.; Gorska, A. Effect of Some Psychoactive Drugs Used as ‘Legal Highs’ on Brain Neurotransmitters. Neurotox. Res., 2016, 29, 394-407.
[94]
Shulgin, A.T. Mescaline: The chemistry and pharmacology of its analogs. Lloydia, 1973, 36, 46-58.
[95]
Schultes, R.E. The Appeal of Peyote (Lophophora Williamsii) as a Medicine. Am. Anthropol., 1938, 40, 698-715.
[96]
McLaughlin, J.L. Peyote: An introduction. Lloydia, 1973, 36, 1-8.
[97]
Halpern, J.H. The Use of Hallucinogens in the Treatment of Addiction. Addict. Res., 1996, 4, 177-189.
[98]
Gilmore, H.T. Peyote use during pregnancy. S. D. J. Med., 2001, 54, 27-29.
[99]
Hardaway, R.; Schweitzer, J.; Suzuki, J. Hallucinogen Use Disorders. Child Adolesc. Psychiatr. Clin. N. Am., 2016, 25, 489-496.
[100]
Brown, R.T.; Braden, N.J. Hallucinogens. Pediatr. Clin. North Am., 1987, 34, 341-347.
[101]
Stevenson, I.; Mokrasch, L.C. A further note on the mechanism of the antidotal action of sodium succinate in the mescaline psychosis. Am. J. Psychiatry, 1958, 114, 1038-1039.
[102]
Stevenson, I.; Sanchez, A.J., Jr The antidotal action of sodium succinate in the mescaline psychosis. Am. J. Psychiatry, 1957, 114, 328-332.
[103]
Nolte, K.B.; Zumwalt, R.E. Fatal peyote ingestion associated with Mallory-Weiss lacerations. West. J. Med., 1999, 170, 328.
[104]
Hashimoto, H.; Clyde, V.J.; Parko, K.L. Botulism from peyote. N. Engl. J. Med., 1998, 339, 203-204.
[105]
McCleary, J.A.; Sypherd, P.S.; Walkington, D.L. Antibiotic activity of an extract of peyote (Lophophora Williamii (Lemaire) coulter). Econ. Bot., 1960, 14, 247-249.
[106]
Lumholtz, C. Unknown Mexico; MacMillan and Co., Limited: London, 1903.
[107]
Cassels, B.K.; Saez-Briones, P. Dark classics in chemical neuroscience: mescaline. ACS Chem. Neurosci., 2018, 9(10), 2448-2458.
[108]
Rucker, J.J.H.; Iliff, J.; Nutt, D. J. Psychiatry & the psychedelic drugs. Past, present & future. Neuropsychopharmacol, 2017, 142, 200-218.
[109]
Rickli, A.; Moning, O.D.; Hoener, M.C.; Liechti, M.E. Receptor interaction profiles of novel psychoactive tryptamines compared with classic hallucinogens. Eur. Neuropsychopharmacol., 2016, 26, 1327-1337.
[110]
Shulgin, A.T.; Shulgin, A. PIHKAL: A chemical love story; Transform Press: Berkeley, 1991.