Mephedrone does not damage dopamine nerve endings of the striatum, but enhances the neurotoxicity of methamphetamine, amphetamine, and MDMA. (8th January 2013)

• Record Type: Journal Article
• Authors: Angoa‐Pérez, Mariana; Kane, Michael J.; Briggs, Denise I.; Francescutti, Dina M.; Sykes, Catherine E.; Shah, Mrudang M.; Thomas, David M.; Kuhn, Donald M.
• Is Part Of: Journal of neurochemistry. Volume 125:Number 1(2013:Apr.)
• Page Start: 102
• Page End: 110
• Publication Date: 2013-01-08
• Subjects: amphetamine -- dopamine -- MDMA -- mephedrone -- methamphetamine -- neurotoxicity; Neurochemistry -- Periodicals; 616.8042
• DOI: 10.1111/jnc.12114
• Languages: English
• ISSNs: 0022-3042

Abstract

Abstract: Mephedrone (4‐methylmethcathinone) is a β‐ketoamphetamine stimulant drug of abuse with close structural and mechanistic similarities to methamphetamine. One of the most powerful actions associated with mephedrone is the ability to stimulate dopamine (DA) release and block its re‐uptake through its interaction with the dopamine transporter (DAT). Although mephedrone does not cause toxicity to DA nerve endings, its ability to serve as a DAT blocker could provide protection against methamphetamine‐induced neurotoxicity like other DAT inhibitors. To test this possibility, mice were treated with mephedrone (10, 20, or 40 mg/kg) prior to each injection of a neurotoxic regimen of methamphetamine (four injections of 2.5 or 5.0 mg/kg at 2 h intervals). The integrity of DA nerve endings of the striatum was assessed through measures of DA, DAT, and tyrosine hydroxylase levels. The moderate to severe DA toxicity associated with the different doses of methamphetamine was not prevented by any dose of mephedrone but was, in fact, significantly enhanced. The hyperthermia caused by combined treatment with mephedrone and methamphetamine was the same as seen after either drug alone. Mephedrone also enhanced the neurotoxic effects of amphetamine and 3, 4‐methylenedioxymethamphetamine on DA nerve endings. In contrast, nomifensine protected against methamphetamine‐induced neurotoxicity. As mephedrone increases methamphetamine neurotoxicity, the present results suggest that it interacts with the DAT in a manner unlike that of other typical DAT inhibitors. The relatively innocuous effects of mephedrone alone on DA nerve endings mask a potentially dangerous interaction with drugs that are often co‐abused with it, leading to heightened neurotoxicity. Abstract : Mephedrone is a psychoactive component of 'bath salts'. Despite its remarkable structural similarity to the neurotoxic amphetamines, mephedrone is not neurotoxic. Mephedrone is often co‐abused with amphetamines, and data presented here show that when combined with methamphetamine, amphetamine, or MDMA, mephedrone significantly increases the neurotoxicity of the latter drugs. These findings focus much needed attention on the dangers associated with this designer drug of abuse.