The mechanisms involved in the long‐lasting neuroprotective effect of fluoxetine against MDMA (‘ecstasy’)‐induced degeneration of 5‐HT nerve endings in rat brain
British Journal of Pharmacology – September 01, 2001
Source: OpenAlex
Summary
Fluoxetine, at a dose of 10 mg/kg, provides significant protection against MDMA-induced neurotoxicity in rats, preventing degeneration of serotonin nerve endings. Co-administering fluoxetine with MDMA or administering it days prior resulted in complete neuroprotection. In contrast, fluvoxamine only offered protection when given concurrently with MDMA. Notably, fluoxetine maintained elevated cerebral levels for seven days, while fluvoxamine concentrations dropped significantly within 24 hours. These findings suggest fluoxetine's enduring protective effects are linked to its inhibition of the serotonin transporter without altering MDMA metabolism.
Abstract
It has been reported that co‐administration of fluoxetine with 3,4‐methylenedioxymethamphetamine (MDMA, ‘ecstasy’) prevents MDMA‐induced degeneration of 5‐HT nerve endings in rat brain. The mechanisms involved have now been investigated. MDMA (15 mg kg −1 , i.p.) administration produced a neurotoxic loss of 5‐HT and 5‐hydroxyindoleacetic acid (5‐HIAA) in cortex, hippocampus and striatum and a reduction in cortical [ 3 H]‐paroxetine binding 7 days later. Fluoxetine (10 mg kg −1 , i.p., ×2, 60 min apart) administered concurrently with MDMA or given 2 and 4 days earlier provided complete protection, and significant protection when given 7 days earlier. Fluvoxamine (15 mg kg −1 , i.p., ×2, 60 min apart) only produced neuroprotection when administered concurrently. Fluoxetine (10 mg kg −1 , ×2) markedly increased the K D and reduced the B max of cortical [ 3 H]‐paroxetine binding 2 and 4 days later. The B max was still decreased 7 days later, but the K D was unchanged. [ 3 H]‐Paroxetine binding characteristics were unchanged 24 h after fluvoxamine (15 mg kg −1 , ×2). A significant cerebral concentration of fluoxetine plus norfluoxetine was detected over the 7 days following fluoxetine administration. The fluvoxamine concentration had decreased markedly by 24 h. Pretreatment with fluoxetine (10 mg kg −1 , ×2) failed to alter cerebral MDMA accumulation compared to saline pretreated controls. Neither fluoxetine or fluvoxamine altered MDMA‐induced acute hyperthermia. These data demonstrate that fluoxetine produces long‐lasting protection against MDMA‐induced neurodegeneration, an effect apparently related to the presence of the drug and its active metabolite inhibiting the 5‐HT transporter. Fluoxetine does not alter the metabolism of MDMA or its rate of cerebral accumulation. British Journal of Pharmacology (2001) 134 , 46–57; doi: 10.1038/sj.bjp.0704230