کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
2564785 1561037 2015 15 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Purinergic system dysfunction in mood disorders: a key target for developing improved therapeutics
موضوعات مرتبط
علوم زیستی و بیوفناوری علم عصب شناسی روانپزشکی بیولوژیکی
پیش نمایش صفحه اول مقاله
Purinergic system dysfunction in mood disorders: a key target for developing improved therapeutics
چکیده انگلیسی


• Purines and their metabolites regulate mood, cognition, and behavior.
• P1 and P2 receptor function and SNPs play a role in mood disorders.
• We review purinergic pathophysiology in mood disorders.
• We review the potential therapeutic role of purinergic agents in mood disorders.

Uric acid and purines (such as adenosine) regulate mood, sleep, activity, appetite, cognition, memory, convulsive threshold, social interaction, drive, and impulsivity. A link between purinergic dysfunction and mood disorders was first proposed a century ago. Interestingly, a recent nationwide population-based study showed elevated risk of gout in subjects with bipolar disorder (BD), and a recent meta-analysis and systematic review of placebo-controlled trials of adjuvant purinergic modulators confirmed their benefits in bipolar mania. Uric acid may modulate energy and activity levels, with higher levels associated with higher energy and BD spectrum. Several recent genetic studies suggest that the purinergic system – particularly the modulation of P1 and P2 receptor subtypes – plays a role in mood disorders, lending credence to this model. Nucleotide concentrations can be measured using brain spectroscopy, and ligands for in vivo positron emission tomography (PET) imaging of adenosine (P1) receptors have been developed, thus allowing potential target engagement studies. This review discusses the key role of the purinergic system in the pathophysiology of mood disorders. Focusing on this promising therapeutic target may lead to the development of therapies with antidepressant, mood stabilization, and cognitive effects.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Progress in Neuro-Psychopharmacology and Biological Psychiatry - Volume 57, 3 March 2015, Pages 117–131
نویسندگان
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