Antidepressant-like activity and safety profile evaluation of 1H-imidazo[2,1-f]purine-2,4(3H,8H)-dione derivatives as 5-HT1A receptor partial agonists.
Anna PartykaAgnieszka ZagórskaMagdalena KotańskaMaria WalczakMagdalena Jastrzębska-WięsekJoanna KnutelskaMarek BednarskiMonika Głuch-LutwinBarbara MordylPaulina JaniszewskaAnna WesołowskaPublished in: PloS one (2020)
Current antidepressant therapy has several disadvantages related to the properties of antidepressants. Considering their unfavourable features, the process of searching for new antidepressant drugs with better safety and tolerability requires consistent efforts and many complementary studies. Serotonin 5-HT1A receptor is considered as an interesting target of antidepressant therapy. In the present study, the intrinsic activity at different signaling pathways coupled to serotonin 5-HT1A receptor, antidepressant-like and pharmacokinetic properties, and the safety profile of two novel imidazopurine-2,4-dione derivatives, namely compounds AZ-853 (8-(4-(4-(2-fluorophenyl)piperazin-1-yl)butyl)-1,3-dimethyl-1H- imidazo[2,1-f]purine-2,4(3H,8H)-dione) and AZ-861 (1,3-dimethyl-8-(4-(4-(3-(trifluoromethyl)phenyl)piperazin-1-yl)butyl)-1H-imidazo[2,1-f]purine-2,4(3H,8H)-dione), were studied in animal models through in vitro and in vivo experiments. We demonstrated that AZ-853 and AZ-861, which structurally differ by one substituent and its placement in the phenyl ring, showed varied functional, pharmacological, and pharmacokinetic properties as well as side effect profiles. AZ-861 exhibited stronger agonistic action in all functional assays. After acute and repeated administration in mice, both compounds showed antidepressant-like activity in the forced swim test, which was partially mediated by 5-HT1A receptor activation. AZ-853 showed a more potent antidepressant-like effect, presumably due to its better penetration into brain structures. Both compounds did not show anticholinergic properties, but after repeated administration, they induced weak sedation and lipid metabolism disturbances without affecting serum glucose level. The stronger α1-adrenolytic effect of AZ-853 is responsible for decreased systolic blood pressure, and in contrast to AZ-861, AZ-853 induced weight gain in mice. The interesting comparative pharmacological profiles of AZ-853 and AZ-861 encourage to conduct further experiments to fully understand their mechanisms and differences in action.
Keyphrases
- major depressive disorder
- blood pressure
- weight gain
- bipolar disorder
- body mass index
- signaling pathway
- heart failure
- magnetic resonance
- stem cells
- metabolic syndrome
- randomized controlled trial
- multiple sclerosis
- drug induced
- magnetic resonance imaging
- high glucose
- weight loss
- binding protein
- type diabetes
- physical activity
- intensive care unit
- computed tomography
- clinical trial
- atrial fibrillation
- acute respiratory distress syndrome
- high throughput
- open label
- bone marrow
- ultrasound guided
- blood glucose
- insulin resistance
- preterm birth
- fatty acid
- resting state
- skeletal muscle
- gestational age
- case control