Fortschr Neurol Psychiatr 2015; 83(04): 221-231
DOI: 10.1055/s-0034-1399307
Originalarbeit
© Georg Thieme Verlag KG Stuttgart · New York

Synthetische Cannabinoide: Verbreitung, Suchtbiologie & aktuelle Perspektive der persönlichen Gesundheitsgefährdung

Synthetic Cannabinoids: Spread, Addiction Biology & Current Perspective of Personal Health Hazard
U. Bonnet
1   Klinik für Psychiatrie, Psychotherapie und Psychosomatik, Evangelisches Krankenhaus Castrop-Rauxel, Akademisches Lehrkrankenhaus der Universität Duisburg-Essen, Castrop-Rauxel
,
H. Mahler
2   Kriminalwissenschaftliches und -technisches Institut, Landeskriminalamt Nordrhein-Westfalen, Düsseldorf
› Author Affiliations
Further Information

Publication History

Publication Date:
20 April 2015 (online)

Zusammenfassung

Unter den neuartigen psychoaktiven Stoffen (NPS, engl. new psychoactive substances) werden in Europa am häufigsten synthetische Cannabinoide (SCBs) gefunden. Diese werden z. B. dotiert zu pflanzlicher Matrix in sogenannten „Kräutermischungen“ verkauft. Neben Intoxikationssymptomen, wie sie auch bei starkem Cannabiskonsum auftreten können (z. B. Tachykardie, Herzinfarkt, Verwirrtheit, Halluzinationen, Panikattacken und Paranoia), fallen nach dem Konsum solcher Mischungen weitere toxische Wirkungen auf (schwere Erregung, Koma, katatoner Stupor, Hypertension, Herzrhythmusstörungen, Atemnot, epileptische Anfälle, Myoklonien, Rhabdomyolyse, Hyperthermie, starkes Schwitzen, akutes Nierenversagen, Erbrechen, Kopfschmerzen und Hypokaliämie), die zumindest zum Teil für den Cannabiskonsum unbekannt sind. Darüber hinaus sind bereits erste Abhängigkeits- und Todesfälle in Verbindung mit SCBs beschrieben. Anhand eines Algorithmus mit zwei Hauptkriterien (Abhängigkeitspotenzial und Toxizität) und unter Berücksichtigung der neuesten medizinischen und pharmakologischen Erkenntnisse wird hier erstmals versucht, das persönliche Gesundheitsrisiko durch SCBs im Vergleich zu dem durch den Konsum von anderen psychoaktiven Substanzen einzuschätzen. Demnach wird das relative Gesundheitsrisiko durch SCBs von den Autoren höher als das durch Cannabis und etwas geringer als das durch synthetische Cathinone („Badesalze“) eingeschätzt, wobei die Toxizität von SCBs deutlich über der von Cannabis und somit in etwa auf dem Niveau von synthetischen Cathinonen und Benzodiazepinen liegt. Das Abhängigkeitspotenzial von SCBs erscheint geringer als das von synthetischen Cathinonen, Benzodiazepinen oder Cannabis. Herstellung, Vertrieb und Besitz von SCBs zu kontrollieren erweist sich als äußerst schwierig. Aufgrund der hohen Fluktuation von SCBs auf dem Drogenmarkt und der infolge des Internets neuartigen Beschaffungswege steht die Legislative vor bislang nicht gekannten Herausforderungen, die sich vor allem in einem „Hase-Igel“-Problem äußern.

Abstract

Among the new psychoactive substances (NPS), most frequently synthetic cannabinoids (SCBs) have been found in Europe. These are sold as active compounds in e. g. so-called “herbal blends”. When inhaled or ingested, besides intoxication symptoms, as they occur with heavy cannabis use (e. g., tachycardia, myocardial infarction, confusion, hallucinations, panic attacks, and paranoia), harmful effects (severe agitation, coma, catatonic stupor, hypertension, cardiac arrhythmia, dyspnoea, seizures, myoclonus, rhabdomyolysis, hyperthermia, diaphoresis, acute kidney injury, vomiting, headache, and hypokalemia) arise, which are mostly unusual about cannabis use. In addition, the first cases of addiction and death related to SCBs have been reported. Taking into account the newest literature and using an algorithm with two main criteria (addiction potential, toxicity), the authors made a first attempt to rank the personal health hazard of SCBs in comparison to that of other psychoactive drugs. Accordingly, the relative health hazard of SCBs is found to be somewhat higher than that of cannabis and lower than that of synthetic cathinones (“bath salts”). However, the toxicity of SCBs, is significantly greater than the toxicity of cannabis, thus being similar to that of synthetic cathinones and benzodiazepines. The addiction potential appears to be lower than that of synthetic cathinones, benzodiazepines, or cannabis. Due to the fluctuation of substances and the availability in internet resources, legislation is facing a serious “hare-hedgehog” problem to control the manufacture, trade and possession of SCBs.

 
  • Literatur

  • 1 UNDOC. World Drug Report 2013 – new psychoactive substances (NPS). Im Internet: http://www.unodc.org/wdr/en/nps.html Stand: 08.02.2015
  • 2 UNDOC. World Drug Report 2014 – amphetamine-type substances (ATS) and new psychoactive substances (NPS). Im Internet: http://www.unodc.org/documents/wdr2014 / ATS_NPS_2014_web.pdf Stand: 08.02.2015
  • 3 Schneir AB, Cullen J, Ly BT. “Spice” girls: synthetic cannabinoid intoxication. J Emerg Med 2011; 40: 296-299
  • 4 Harris CR, Brown A. Synthetic cannabinoid intoxication: a case series and review. J Emerg Med 2013; 44: 360-366
  • 5 Helander A, Bäckberg M, Hultén P et al. Detection of new psychoactive substance use among emergency room patients: Results from the Swedish STRIDA project. Forensic Sci Int 2014; 243: 23-29
  • 6 Seely KA, Patton AL, Moran CL et al. Forensic investigation of K2, Spice, and “bath salt” commercial preparations: a three-year study of new designer drug products containing synthetic cannabinoid, stimulant, and hallucinogenic compounds. Forensic Sci Int 2013; 233: 416-422
  • 7 Auwärter V, Dresen S, Weinmann W et al. “Spice” and other herbal blends: harmless incense or cannabinoid designer drugs?. J Mass Spectrom 2009; 44: 832-837
  • 8 Atwood BK, Huffman J, Straiker A et al. JWH018, a common constituent of “Spice” herbal blends, is a potent and efficacious cannabinoid CB receptor agonist. Br J Pharmacol 2010; 160: 585-593
  • 9 Spaderna M, Addy PH, D’Souza DC. Spicing things up: synthetic cannabinoids. Psychopharmacology (Berl) 2013; 228: 525-540
  • 10 Huffman JW, Zengin G, Wu MJ et al. Structure-activity relationships for 1-alkyl-3-(1-naphthoyl)indoles at the cannabinoid CB(1) and CB(2) receptors: steric and electronic effects of naphthoyl substituents. New highly selective CB(2) receptor agonists. Bioorg Med Chem 2005; 13: 89-112
  • 11 Europäische Beobachtungsstelle für Drogen und Drogensucht: Drogenangebot in Europa (EMCDDA). Perspectives on drugs. Synthetic cannabinoids in Europe, update 16.5. 2014. Im Internet: http://www.emcdda.europa.eu/attachements.cfm/att_212361_EN_EMCDDA_POD_2013_Synthetic%20cannabinoids.pdf Stand: 08.02.2015
  • 12 Uchiyama N, Matsuda S, Kawamura M et al. The new-type cannabimimetic quinolinyl carboxylates, QUPIC and QUCHIC, two new cannabimimetic carboxamide derivates, ADP-FUBINACA and ADBICA, and five cannabinoids detected with thiophene derivate α-PVT and an opioid agonist AH-7921 identified in illegal products. Forensic Toxicol 2013; 31: 223-230
  • 13 Europäische Beobachtungsstelle für Drogen und Drogensucht: Drogenangebot in Europa (EMCDDA). In: Europäischer Drogenbericht 2013: Trends und Entwicklungen. Luxemburg: Amt für Veröffentlichungen der Europäischen Union; 2013: 28-29
  • 14 Europäische Beobachtungsstelle für Drogen und Drogensucht: Drogenangebot in Europa (EMCDDA). Europäischer Drogenbericht 2014: Trends und Entwicklungen. Im Internet: http://www.emcdda.europa.eu/attachements.cfm/att_228272_DE_TDAT14001DEN.pdf Stand: 08.02.2015
  • 15 Gunderson EW, Haughey HM, Ait-Daoud N et al. A survey of synthetic cannabinoid consumption by current cannabis users. Subst Abus 2014; 35: 184-189
  • 16 Pabst A, Kraus L, Gomes de Matos E et al. Substanzkonsum und substanzbezogene Störungen in Deutschland im Jahr 2012. Sucht 2013; 59: 321-331
  • 17 Reid MJ, Baz-Lomba JA, Ryu Y et al. Using biomarkers in wastewater to monitor community drug use: a conceptual approach for dealing with new psychoactive substances. Sci Total Environ 2014; 487: 651-658
  • 18 Brents LK, Prather PL. The K2/Spice phenomenon: emergence, identification, legislation and metabolic characterization of synthetic cannabinoids in herbal incense products. Drug Metab Rev 2014; 46: 72-85
  • 19 Fadda P, Scherma M, Spano MS et al. Cannabinoid self-administration increases dopamine release in the nucleus accumbens. Neuroreport 2006; 17: 1629-1632
  • 20 Maldonado R, Berrendero F, Ozaita A et al. Neurochemical basis of cannabis addiction. Neuroscience 2011; 181: 1-17
  • 21 Flores Á, Maldonado R, Berrendero F. The hypocretin/orexin receptor-1 as a novel target to modulate cannabinoid reward. Biol Psychiatry 2014; 75: 499-507
  • 22 Fantegrossi WE, Moran JH, Radominska-Pandya A et al. Distinct pharmacology and metabolism of K2 synthetic cannabinoids compared to Δ(9)-THC: mechanism underlying greater toxicity?. Life Sci 2014; 97: 45-54
  • 23 Järbe TU, Gifford RS. “Herbal incense”: designer drug blends as cannabimimetics and their assessment by drug discrimination and other in vivo bioassays. Life Sci 2014; 97: 64-71
  • 24 Franklin JM, Mathew M, Carrasco GA. Cannabinoid-induced upregulation of serotonin 2A receptors in the hypothalamic paraventricular nucleus and anxiety-like behaviors in rats. Neurosci Lett 2013; 548: 165-169
  • 25 EMCDDA. Molekülstrukturen. Im Internet: http://www.emcdda.europa.eu/topics/pods/synthetic-cannabinoids#panel2
  • 26 Bundesministeriums der Justiz und für Verbraucherschutz. Gesetz über den Verkehr mit Betäubungsmitteln (Betäubungsmittelgesetz – BtMG). Letzte Änderung am 5.12.2014. http://www.gesetze-im-internet.de/bundesrecht/btmg_1981/gesamt.pdf Stand: 08.02.2015
  • 27 Tomiyama K, Funada M. Cytotoxicity of synthetic cannabinoids on primary neuronal cells of the forebrain: the involvement of cannabinoid CB1 receptors and apoptotic cell death. Toxicol Appl Pharmacol 2014; 274: 17-23
  • 28 Koller VJ, Auwärter V, Grummt T et al. Investigation of the in vitro toxicological properties of the synthetic cannabimimetic drug CP-47,497-C8. Toxicol Appl Pharmacol 2014; 277: 164-171
  • 29 Dhopeshwarkar A, Mackie K. CB2 cannabinoid receptors as a therapeutic target – What does the future hold?. Mol Pharmacol 2014; 86: 430-437
  • 30 Shanks KG, Behonick GS, Dahn T et al. Identification of novel third-generation synthetic cannabinoids in products by ultra-performance liquid chromatography and time-of-flight mass spectrometry. J Anal Toxicol 2013; 37: 517-525
  • 31 Castaneto MS, Gorelick DA, Desrosiers NA et al. Synthetic cannabinoids: epidemiology, pharmacodynamics, and clinical implications. Drug Alcohol Depend 2014; 144: 12-41
  • 32 Martin BR, Compton DR, Thomas BF et al. Behavioral, biochemical, and molecular modeling evaluations of cannabinoid analogs. Pharmacol Biochem Behav 1991; 40: 471-478
  • 33 Cha HJ, Lee KW, Song MJ et al. Dependence Potential of the Synthetic Cannabinoids JWH-073, JWH-081, and JWH-210: In Vivo and In Vitro Approaches. Biomol Ther. (Seoul) 2014; 22: 363-369
  • 34 Ginsburg BC, Schulze DR, Hruba L et al. JWH-018 and JWH-073: Δ⁹-tetrahydrocannabinol-like discriminative stimulus effects in monkeys. J Pharmacol Exp Ther 2012; 340: 37-45
  • 35 Hruba L, Ginsburg BC, McMahon LR. Apparent inverse relationship between cannabinoid agonist efficacy and tolerance/cross-tolerance produced by Δ⁹-tetrahydrocannabinol treatment in rhesus monkeys. J Pharmacol Exp Ther 2012; 342: 843-849
  • 36 Hyatt WS, Fantegrossi WE. Δ9-THC exposure attenuates aversive effects and reveals appetitive effects of K2/'Spice' constituent JWH-018 in mice. Behav Pharmacol 2014; 25: 253-257
  • 37 Gronewold A, Skopp G. A preliminary investigation on the distribution of cannabinoids in man. Forensic Sci Int 2011; 210: e7-e11
  • 38 Chimalakonda KC, Seely KA, Bratton SM et al. Cytochrome P450-mediated oxidative metabolism of abused synthetic cannabinoids found in K2/Spice: identification of novel cannabinoid receptor ligands. Drug Metab Dispos 2012; 40: 2174-2184
  • 39 Chimalakonda KC, Bratton SM, Le VH et al. Conjugation of synthetic cannabinoids JWH-018 and JWH-073, metabolites by human UDP-glucuronosyltransferases. Drug Metab Dispos 2011; 39: 1967-1976
  • 40 De Brabanter N, Esposito S, Tudela E et al. In vivo and in vitro metabolism of the synthetic cannabinoid JWH-200. Rapid Commun Mass Spectrom 2013; 27: 2115-2126
  • 41 Teske J, Weller JP, Fieguth A et al. Sensitive and rapid quantification of the cannabinoid receptor agonist naphthalen-1-yl-(1-pentylindol-3-yl)methanone (JWH-018) in human serum by liquid chromatography-tandem mass spectrometry. J Chromatogr B Analyt Technol Biomed Life Sci 2010; 878: 2659-2663
  • 42 Gandhi AS, Zhu M, Pang S et al. First characterization of AKB-48 metabolism, a novel synthetic cannabinoid, using human hepatocytes and high-resolution mass spectrometry. AAPS J 2013; 15: 1091-1098
  • 43 Krasowski MD, Ekins S. Using cheminformatics to predict cross reactivity of “designer drugs” to their currently available immunoassays. J Cheminform 2014; 6: 22
  • 44 Arntson A, Ofsa B, Lancaster D et al. Validation of a novel immunoassay for the detection of synthetic cannabinoids and metabolites in urine specimens. J Anal Toxicol 2013; 37: 284-290
  • 45 Castaneto MS, Desrosiers NA, Ellefsen K et al. Method validation of the biochip array technology for synthetic cannabinoids detection in urine. Bioanalysis 2014; 21: 2919-2930
  • 46 Smith DL, Roberts C. Synthetic marijuana use and development of catatonia in a 17-year-old male. Minn Med 2014; 97: 38
  • 47 Buser GL, Gerona RR, Horowitz BZ et al. Acute kidney injury associated with smoking synthetic cannabinoid. Clin Toxicol (Phila) 2014; 52: 664-673
  • 48 Mir A, Obafemi A, Young A. Myocardial infarction associated with use of the synthetic cannabinoid K2. Pediatrics 2011; 128: e1622-e1627
  • 49 Gunderson EW, Haughey HM, Ait-Daoud N et al. “Spice” and “K2” herbal highs: a case series and systematic review of the clinical effects and biopsychosocial implications of synthetic cannabinoid use in humans. Am J Addict 2012; 21: 320-326
  • 50 Every-Palmer S. Synthetic cannabinoid JWH-018 and psychosis: an explorative study. Drug Alcohol Depend 2011; 117: 152-157
  • 51 Hermanns-Clausen M, Kneisel S, Szabo B et al. Acute toxicity due to the confirmed consumption of synthetic cannabinoids: clinical and laboratory findings. Addiction 2013; 108: 534-544
  • 52 Hopkins CY, Gilchrist BL. A case of cannabinoid hyperemesis syndrome caused by synthetic cannabinoids. J Emerg Med 2013; 45: 544-546
  • 53 Nacca N, Vatti D, Sullivan R et al. The synthetic cannabinoid withdrawal syndrome. J Addict Med 2013; 7: 296-298
  • 54 Zimmermann US, Winkelmann PR, Pilhatsch M et al. Withdrawal phenomena and dependence syndrome after the consumption of “spice gold”. Dtsch Arztebl Int 2009; 106: 464-467
  • 55 Rominger A, Cumming P, Xiong G et al. Effects of acute detoxification of the herbal blend “Spice Gold” on dopamine D2/3 receptor availability: a [18F]fallypride PET study. Eur Neuropsychopharmacol 2013; 23: 1606-1610
  • 56 Behonick G, Shanks KG, Firchau DJ et al. Four Postmortem Case Reports with Quantitative Detection of the Synthetic Cannabinoid, 5F-PB-22. J Anal Toxicol 2014; 38: 559-562
  • 57 Schaefer N, Peters B, Bregel D et al. A fatal case involving several synthetic cannabinoids. Toxichem Krimtech 2013; 80 (Special Issue): 248-251
  • 58 Ibrahim S, Al-Saffar F, Wannenburg T. A Unique Case of Cardiac Arrest following “K2” Abuse. Case Rep Cardiol 2014; 2014: 120607
  • 59 Patton A, Chimalakonda KC, Moran CL et al. K2 toxicity: fatal case of psychiatric complications following AM2201 exposure. J Forensic Sci 2013; 58: 1676-1680
  • 60 Saito T, Namara A, Miura N et al. A fatal case of MAM-2201 poisoning. Forensic Toxicol 2013; 31: 333-337
  • 61 Kronstrand R, Roman M, Andersson M et al. Toxicological findings of synthetic cannabinoids in recreational users. J Anal Toxicol 2013; 37: 534-541
  • 62 Wikström M, Thelander G, Dahlgren M et al. An accidental fatal intoxication with methoxetamine. J Anal Toxicol 2013; 37: 43-46
  • 63 Ware MA, St Arnaud-Trempe E. The abuse potential of the synthetic canabinonid nabilone. Addiction 2010; 105: 494-503
  • 64 Winstock AR, Barratt MJ. Synthetic cannabis: a comparison of patterns of use and effect profile with natural cannabis in a large global sample. Drug Alcohol Depend 2013; 131: 106-111
  • 65 Winstock AR, Barratt MJ. The 12-month prevalence and nature of adverse experiences resulting in emergency medical presentations associated with the use of synthetic cannabinoid products. Hum Psychopharmacol 2013; 28: 390-393
  • 66 Musshoff F, Madea B, Kernbach-Wighton G et al. Driving under the influence of synthetic cannabinoids (“Spice”): a case series. Int J Legal Med 2014; 128: 59-64
  • 67 Bonar EE, Ashrafioun L, Ilgen MA. Synthetic cannabinoid use among patients in residential substance use disorder treatment: prevalence, motives, and correlates. Drug Alcohol Depend 2014; 143: 268-271
  • 68 Papanti D, Schifano F, Botteon G et al. Spiceophrenia": a systematic overview of “spice”-related psychopathological issues and a case report. Hum Psychopharmacol 2013; 28: 379-389
  • 69 Hodcroft CJ, Rossiter MC, Buch AN. Cannabis-associated Myocardial Infarction in a Young Man with Normal Coronary Arteries. J Emerg Med 2014; 47: 277-281
  • 70 Bernson-Leung ME, Leung LY, Kumar S. Synthetic cannabis and acute ischemic stroke. J Stroke Cerebrovasc Dis 2014; 23: 1239-1241
  • 71 Hohmann N, Mikus G, Czock D. Wirkungen und Risiken neuartiger psychoaktiver Substanzen. Dtsch Arztebl 2014; 111: 139-147
  • 72 Derungs A, Schwaninger AE, Mansella G et al. Symptoms, toxicities, and analytical results for a patient after smoking herbs containing the novel synthetic cannabinoid MAM-2201. Forensic Toxicol 2013; 31: 164-171
  • 73 McQuade D, Hudson S, Dargan PI et al. First European case of convulsions related to analytically confirmed use of the synthetic cannabinoid receptor agonist AM-2201. Eur J Clin Pharmacol 2013; 69: 373-376
  • 74 Monte AA, Bronstein AC, Cao DJ et al. An outbreak of exposure to a novel synthetic cannabinoid. N Engl J Med 2014; 370: 389-390
  • 75 Tofighi B, Lee JD. Internet highs – seizures after consumption of synthetic cannabinoids purchased online. J Addict Med 2012; 6: 240-241
  • 76 Lapoint J, James LP, Moran CL et al. Severe toxicity following synthetic cannabinoid ingestion. Clin Toxicol (Phila) 2011; 49: 760-764
  • 77 Seely KA, Lapoint J, Moran JH et al. Spice drugs are more than harmless herbal blends: a review of the pharmacology and toxicology of synthetic cannabinoids. Prog Neuropsychopharmacol Biol Psychiatry 2012; 39: 234-243
  • 78 APA (American Psychiatric Association). Diagnostic And Statistical Manual Of Mental Disorders, Fifth Edition (DSM-5TM). Cannabis Withdrawal (292.0/F12.88). Washington, DC: APA; 2013: 517-519
  • 79 Alhadi S, Tiwari A, Vohra R et al. High times, low sats: diffuse pulmonary infiltrates associated with chronic synthetic cannabinoid use. J Med Toxicol 2013; 9: 199-206
  • 80 Swift W, Wong A, Li KM et al. Analysis of cannabis seizures in NSW, Australia: cannabis potency and cannabinoid profile. PLoS One 2013; 8: e70052
  • 81 Nutt DJ, King LA, Phillips LD. Independent Scientific Committee on Drugs. Drug harms in the UK: a multicriteria decision analysis. Lancet 2010; 376: 1558-1565
  • 82 van Amsterdam J, Opperhuizen A, Koeter M et al. Ranking the harm of alcohol, tobacco and illicit drugs for the individual and the population. Eur Addict Res 2010; 16: 202-207
  • 83 Griffiths RR, Johnson MW. Relative abuse liability of hypnotic drugs: a conceptual framework and algorithm for differentiating among compounds. J Clin Psychiatry 2005; 66 (Suppl. 09) 31-41
  • 84 Halpin LE, Collins SA, Yamamoto BK. Neurotoxicity of methamphetamine and 3,4-methylenedioxymethamphetamine. Life Sci 2014; 97: 37-44
  • 85 Miotto K, Striebel J, Cho AK et al. Clinical and pharmacological aspects of bath salt use: a review of the literature and case reports. Drug Alcohol Depend 2013; 132: 1-12
  • 86 Musselman ME, Hampton JP. “Not for human consumption”: a review of emerging designer drugs. Pharmacotherapy 2014; 34: 745-757
  • 87 German CL, Fleckenstein AE, Hanson GR. Bath salts and synthetic cathinones: an emerging designer drug phenomenon. Life Sci 2014; 97: 2-8
  • 88 Paillet-Loilier M, Cesbron A, Le Boisselier R et al. Emerging drugs of abuse: current perspectives on substituted cathinones. Subst Abuse Rehabil 2014; 5: 37-52
  • 89 Hawley LA, Auten JD, Matteucci MJ et al. Cardiac complications of adult methamphetamine exposures. J Emerg Med 2013; 45: 821-827
  • 90 Panenka WJ, Procyshyn RM, Lecomte T et al. Methamphetamine use: a comprehensive review of molecular, preclinical and clinical findings. Drug Alcohol Depend 2013; 129: 167-179
  • 91 Carvalho M, Carmo H, Costa VM et al. Toxicity of amphetamines: an update. Arch Toxicol 2012; 86: 1167-1231
  • 92 Cottencin O, Rolland B, Karila L. New designer drugs (synthetic cannabinoids and synthetic cathinones): review of literature. Curr Pharm Des 2014; 20: 4106-4111
  • 93 McNabb CB, Russell BR, Caprioli D et al. Single chemical entity legal highs: assessing the risk for long term harm. Curr Drug Abuse Rev 2012; 5: 304-319
  • 94 Liechti M. Novel psychoactive substances (designer drugs): overview and pharmacology of modulators of monoamine signaling. Swiss Med Wkly 2015; 145: w14043
  • 95 Bonnet U. Einschätzung des Abhängigkeitsrisikos von Propofol. Fortschr Neurol Psychiatr 2011; 79: 442-452
  • 96 Brennan R, Van Hout MC. Gamma-Hydroxybutyrate (GHB): A Scoping Review of Pharmacology, Toxicology, Motives for Use, and User Groups. J Psychoactive Drugs 2014; 46: 243-251
  • 97 Brunt TM, van Amsterdam JG, van den Brink W. GHB, GBL and 1,4-BD addiction. Curr Pharm Des 2014; 20: 4076-4085
  • 98 Corazza O, Assi S, Schifano F. From “Special K” to “Special M”: the evolution of the recreational use of ketamine and methoxetamine. CNS Neurosci Ther 2013; 19: 454-460
  • 99 Kalsi SS, Wood DM, Dargan PI. The epidemiology and patterns of acute and chronic toxicity associated with recreational ketamine use. Emerg Health Threats J 2011; 4: 7107
  • 100 Bonnet U, Scherbaum N. Cannabisbezogene Störungen. Teil I: Pharmakologie, Epidemiologie und Therapieverfahren. Fortschr Neurol Psychiat 2010; 78: 297-305
  • 101 Bonnet U, Scherbaum N. Cannabisbezogene Störungen. Teil II: Psychiatrische und somatische Folgestörungen und Komorbiditäten. Fortschr Neurol Psychiat 2010; 78: 360-370
  • 102 Brown SD, Melton TC. Trends in bioanalytical methods for the determination and quantification of club drugs: 2000-2010. Biomed Chromatogr 2011; 25: 300-321
  • 103 Ernst L, Krüger K, Lindigkeit R et al. Synthetic cannabinoids in “spice-like” herbal blends: first appearance of JWH-307 and recurrence of JWH-018 on the German market. Forensic Sci Int 2012; 222: 216-222
  • 104 Info Curia. Rechtsprechung des Gerichtshofs. Im Internet: http://curia.europa.eu/juris/document/document.jsf;jsessionid=9ea7d2dc30d6686695f92d2b4b5d94a6c225f2d2b8f0.e34KaxiLc3qMb40Rch0SaxuOa310?text=&docid=154827&pageIndex=0&doclang=de&mode=req&dir=&occ=first&part=1&cid=214760 Stand: 08.02.2015
  • 105 Bonnet U, Specka M, Stratmann U et al. Abstinence phenomena of chronic cannabis-addicts prospectively monitored during controlled inpatient detoxification: Cannabis withdrawal syndrome and its correlation with delta-9-tetrahydrocannabinol and -metabolites in serum. Drug Alcohol Depend 2014; 143: 189-197
  • 106 Drug and Chemical Evaluation Section, Office of Diversion Control, Drug Enforcement Administration, Washington, DC 20537, December 2014. http://www.grassley.senate.gov/sites/default/files/news/upload/3-factor%20analysis%20AB-CHMINACA%20AB-PINACA%20THJ2201%2012172014.pdf Stand: 14.03.2015
  • 107 Werse B, Morgenstern C. Der Trend geht zur Reinsubstanz – Entwicklungen im Konsum von „Legal highs“/neuen psychoaktiven Substanzen (NPS) auf Basis zweier Online-Befragungen. Suchttherapie 2015; 16: 36-41