Department of Pharmacobiology, Jagiellonian University Medical College, Medyczna 9, PL 30-688 Krakow, Poland.
Department of Pharmacobiology, Jagiellonian University Medical College, Medyczna 9, PL 30-688 Krakow, Poland.
Pharmacol Ther. 2021 Sep;225:107842. doi: 10.1016/j.pharmthera.2021.107842. Epub 2021 Mar 19.
At present most of the evidence for the relevance of oligomerization for the pharmacology of depression comes from in vitro studies which identified oligomers, and from neuropsychopharmacological studies of receptors which participate in oligomerization. For example, behavioural and biochemical studies in knockout animals suggest that GPR39 may mediate the antidepressant action of monoaminergic antidepressants. We have recently found long-lasting antidepressant-like effects of GPR39 agonist, thus suggesting GPR39 as a target for the development of novel antidepressant drugs. In vitro studies have shown that GPR39 oligomerizes with other GPCRs. Oligomerization of GPR39 should thus be considered in relation to the development of new antidepressants targeting this receptor as well as antidepressants targeting other receptors that may form complexes with GPR39. Here, we summarize recent data suggestive of the importance of oligomerization for the pharmacology of depression and discuss approaches for validation of this phenomenon.
目前,大多数关于寡聚化与抑郁症药理学相关性的证据来自体外研究,这些研究鉴定了寡聚体,以及参与寡聚化的神经精神药理学研究受体。例如,敲除动物的行为和生化研究表明,GPR39 可能介导单胺能抗抑郁药的抗抑郁作用。我们最近发现了 GPR39 激动剂的持久抗抑郁样作用,因此提示 GPR39 是开发新型抗抑郁药物的靶点。体外研究表明,GPR39 与其他 GPCR 寡聚化。因此,应该考虑 GPR39 的寡聚化与针对该受体的新型抗抑郁药物以及可能与 GPR39 形成复合物的其他受体的抗抑郁药物的开发有关。在这里,我们总结了最近表明寡聚化对抑郁症药理学重要性的数据,并讨论了验证这一现象的方法。