Administration of low doses of the 5-HT1A receptor agonist 8-OH-DPAT attenuates the discriminative signal of amphetamine in the conditioned taste aversion procedure

• Published in: Pharmacology, biochemistry and behavior Vol. 193; p. 172932
• Main Authors: Sandoval-Sánchez, Alma R., Cedillo Zavaleta, Laura N., Jiménez, Juan C., Ruíz-García, Isela, Miranda, Florencio
• Format: Journal Article
• Language: English
• Published: Elsevier Inc 01-06-2020
• Subjects: 5-HT1A receptors; Addiction; Amphetamine; Dopamine; Drug discrimination; Drug discrimination; Amphetamine; Dopamine; Addiction; 5-HT1A receptors
• ISSN: 0091-3057; 1873-5177
• DOI: 10.1016/j.pbb.2020.172932

Several studies have reported that low doses of the 5-HT1A receptor agonist 8-OH-DPAT reduce cocaine-induced locomotor activity. However, it has also been reported that high doses of 8-OH-DPAT do not substitute for or alter the discriminative signal of cocaine (COC) or amphetamine (AMPH). This study aimed to evaluate the effects of low and high doses of the 5-HT1A agonist 8-OH-DPAT on the discriminative signal of AMPH using conditioned taste aversion as a drug discrimination procedure. Additionally, to establish a correlation between the behavioral effects in drug discrimination and changes in dopamine (DA) and gamma-aminobutyric acid (GABA) concentrations, we evaluated the effect of systemic administration of low or high doses of the 5-HT1A receptor agonist 8-OH-DPAT and of the 5-HT1A receptor antagonist WAY100135 on DA and GABA extracellular concentrations in the nucleus accumbens (nAcc) and ventral tegmental area (VTA), respectively, using cerebral microdialysis. The behavioral results showed that low but not high doses of 8-OH-DPAT produced a reduction in the AMPH-induced discriminative signal, while WAY100135 administration prevented such effects. The microdialysis results showed that a low dose of 8-OH-DPAT decreased extracellular DA concentrations in the nAcc and increased GABA concentrations in the VTA. Pretreatment with WAY100135 prevented these effects. These data support the hypothesis that 5-HT1A receptors modulate the behavioral effects of psychostimulant drugs, such as AMPH, through somatodendritic 5-HT1A autoreceptors in the raphe nucleus indicating that 5-HT1A receptors may be an important target for the development of pharmacological treatments for psychostimulant addiction.
•Low doses of the 5-HT1A receptor agonist 8-OH-DPAT on the discriminative signal of AMPH were evaluated.•Low doses of 8-OH-DPAT decreased the discriminative signal of AMPH.•Low dose of 8-OH-DPAT decreased extracellular DA levels in the nAcc and increased extracellular GABA levels in the VTA.•The observed results may be due to the activation of presynaptic 5-HT1A receptors.•5-HT1A receptors play an important role in drug addiction-associated behaviors.