PMID- 21060995 OWN - NLM STAT- MEDLINE DCOM- 20110714 LR - 20211020 IS - 1432-2072 (Electronic) IS - 0033-3158 (Linking) VI - 214 IP - 3 DP - 2011 Apr TI - Determining the subjective and physiological effects of BZP combined with TFMPP in human males. PG - 761-8 LID - 10.1007/s00213-010-2081-7 [doi] AB - RATIONALE: 'Party Pills' containing benzylpiperazine (BZP) and trifluoromethylphenylpiperazine (TFMPP) have been used in a recreational context since the 1990s and, prior to April 2008, were legally available in New Zealand. Taken together, they have been reported to produce a 'high' similar to that produced by 3,4-methylenedioxymethamphetamine (MDMA). OBJECTIVES: There has been little research on the subjective effects of piperazines in humans. The purpose of this study is to further investigate the subjective and physiological responses following an oral dose of BZP combined with TFMPP in males. METHODS: In a randomised, double-blind, placebo-controlled study the subjective and physiological effects of BZP/TFMPP were investigated in 36 healthy, non-smoking males (mean age 22 +/- 4 years). Participants were tested before and approximately 120 min after administration of a single dose of placebo (n = 16) or 100/30 mg BZP/TFMPP (n = 20). Participants were required to comment on the subjective effects using three rating scales-the Addiction Research Centre Inventory (ARCI), the Visual Analogue Scale (VAS) and the Profile of Mood States (POMS). Participants' blood pressure, heart rate and body temperature were also measured. RESULTS: Statistical analysis using repeated-measures analysis of variance (ANOVA) and planned comparisons revealed that BZP/TFMPP significantly increases blood pressure and heart rate (p < 0.05). Likewise, the subjective rating scales revealed that BZP/TFMPP has significant dexamphetamine-like effects, increases dysphoria and feelings of self-confidence (p < 0.05). CONCLUSION: These physiological and subjective data reflect clear similarities between the effects of BZP/TFMPP and commonly known stimulants such as dexamphetamine and MDMA. FAU - Lin, Joanne C AU - Lin JC AD - School of Pharmacy, Faculty of Medical and Health Sciences, University of Auckland, Private Bag, 92019 Auckland, New Zealand. joanne.lin@auckland.ac.nz FAU - Jan, Reem K AU - Jan RK FAU - Lee, HeeSeung AU - Lee H FAU - Jensen, Maree-Ann AU - Jensen MA FAU - Kydd, Rob R AU - Kydd RR FAU - Russell, Bruce R AU - Russell BR LA - eng PT - Clinical Trial PT - Journal Article PT - Randomized Controlled Trial PT - Research Support, Non-U.S. Gov't PL - Germany TA - Psychopharmacology (Berl) JT - Psychopharmacology JID - 7608025 RN - 0 (Drug Combinations) RN - 0 (Illicit Drugs) RN - 0 (Piperazines) RN - 25R3ONU51C (1-(3-trifluoromethylphenyl)piperazine) RN - 3UG152ZU0E (1-benzylpiperazine) SB - IM MH - Adolescent MH - Adult MH - Affect/*drug effects MH - Analysis of Variance MH - Blood Pressure/drug effects MH - Body Temperature/drug effects MH - Dose-Response Relationship, Drug MH - Double-Blind Method MH - Drug Combinations MH - Heart Rate/drug effects MH - Humans MH - Illicit Drugs/*pharmacology MH - Male MH - New Zealand MH - Pain Measurement MH - Physiological Phenomena/*drug effects MH - Piperazines/*pharmacology MH - Psychiatric Status Rating Scales MH - Young Adult EDAT- 2010/11/10 06:00 MHDA- 2011/07/16 06:00 CRDT- 2010/11/10 06:00 PHST- 2010/09/13 00:00 [received] PHST- 2010/10/27 00:00 [accepted] PHST- 2010/11/10 06:00 [entrez] PHST- 2010/11/10 06:00 [pubmed] PHST- 2011/07/16 06:00 [medline] AID - 10.1007/s00213-010-2081-7 [doi] PST - ppublish SO - Psychopharmacology (Berl). 2011 Apr;214(3):761-8. doi: 10.1007/s00213-010-2081-7.