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Review: Benzylpiperazine: a drug of abuse?
Alice C. Johnstone
Envirogenomics Group, Institute of Environmental Science and Research Ltd, Porirua, New Zealand, Department of Pathology, Christchurch School of Medicine and Health Sciences, University of Otago, Dunedin, New Zealand
Rod A. Lea
Envirogenomics Group, Institute of Environmental Science and Research Ltd, Porirua, New Zealand
Katie A. Brennan
Envirogenomics Group, Institute of Environmental Science and Research Ltd, Porirua, New Zealand
Susan Schenk
Department of Psychology, Victoria University of Wellington, Wellington, New Zealand
Martin A. Kennedy
Department of Pathology, Christchurch School of Medicine and Health Sciences, University of Otago, Dunedin, New Zealand
Paul S. Fitzmaurice
Envirogenomics Group, Institute of Environmental Science and Research Ltd, Porirua, New Zealand, paul.fitzmaurice{at}esr.cri.nz
N-benzylpiperazine (BZP) is the active ingredient in recreational `party' or `p.e.p.' pills, which are used to provide a stimulant, euphoric effect akin to that of methylenedioxymethamphetamine (MDMA, `ecstasy'). BZP predominantly affects dopamine neurotransmission in a similar fashion to known `drugs of abuse', such as methamphetamine and cocaine, which strongly suggests BZP has abuse liability. BZP is illegal in many countries including the United States of America and Australia, yet it remains legal in the United Kingdom, Canada and New Zealand. There has been little research, to date, on the neurological consequences of high dose or chronic exposure of BZP. Here we provide a comprehensive review of the information currently available on BZP and suggest a need for further research into the mechanisms of action, long-term effects and potentially addictive properties of BZP.
Key Words: benzylpiperazine BZP party pills p.e.p. pills TFMPP drugs of abuse
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This version was published on November
1, 2007
Journal of Psychopharmacology, Vol. 21, No. 8,
888-894 (2007)
DOI: 10.1177/0269881107077260

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