Abstract
Ivacaftor-lumacaftor and ivacaftor are two new breakthrough cystic fibrosis transmembrane conductance modulators. The interactions of ivacaftor and its two metabolites hydroxymethylivacaftor (iva-M1) and ivacaftorcarboxylate (iva-M6) with neurotransmitter receptors were investigated in radioligand binding assays. Ivacaftor displayed significant affinity to the 5-hydroxytryptamine (5-HT; serotonin) 5-HT(2C) receptor (pK(i)=6.06±0.03), β(3)-adrenergic receptor (pK(i)=5.71±0.07), δ-opioid receptor (pK(i)=5.59±0.06) and the dopamine transporter (pK(i)=5.50±0.20); iva-M1 displayed significant affinity to the 5-HT(2C) receptor (pK(i)=5.81±0.04) and the muscarinic M3 receptor (pK(i)=5.70±0.10); iva-M6 displayed significant affinity to the 5-HT(2A) receptor (pK(i)=7.33±0.05). The in vivo central nervous system activity of ivacaftor (40 mg·kg(-1) intraperitoneally for 21 days) was assessed in a chronic mouse model of depression. In the forced swim test, the ivacaftor-treated group displayed decreased immobility (52.8±7.6 s), similarly to fluoxetine (33.8±11.0 s), and increased climbing/swimming activity (181.5±9.2 s). In the open field test, ivacaftor produced higher locomotor activity than the fluoxetine group, measured both as mean number of paw touches (ivacaftor 81.1±9.6 versus fluoxetine 57.9±9.5) and total distance travelled (ivacaftor 120.6±16.8 cm versus fluoxetine 84.5±16.0 cm) in 600 s. Treatment of 23 cystic fibrosis patients with ivacaftor-lumacaftor resulted in significant improvements in quality of life (including anxiety) in all five domains of the AweScoreCF questionnaire (p=0.092-0.096). Our findings suggest ivacaftor displays potential clinical anxiolytic and stimulating properties, and may have beneficial effects on mood.