Institute of Psychiatry, King's College London, PO Box 63, De Crespigny Park, Denmark Hill, London SE5 8AF, UK.
Ther Adv Psychopharmacol. 2013 Jun;3(3):163-76. doi: 10.1177/2045125312471963.
Lithium has been used for the treatment of mood disorders for over 60 years, yet the exact mechanisms by which it exerts its therapeutic effects remain unclear. Two enzymatic chains or pathways emerge as targets for lithium: inositol monophosphatase within the phosphatidylinositol signalling pathway and the protein kinase glycogen synthase kinase 3. Lithium inhibits these enzymes through displacing the normal cofactor magnesium, a vital regulator of numerous signalling pathways. Here we provide an overview of evidence, supporting a role for the inhibition of glycogen synthase kinase 3 and inositol monophosphatase in the pharmacodynamic actions of lithium. We also explore how inhibition of these enzymes by lithium can lead to downstream effects of clinical relevance, both for mood disorders and neurodegenerative diseases. Establishing a better understanding of lithium's mechanisms of action may allow the development of more effective and more tolerable pharmacological agents for the treatment of a range of mental illnesses, and provide clearer insight into the pathophysiology of such disorders.
锂已被用于治疗情绪障碍超过 60 年,但它发挥治疗作用的确切机制仍不清楚。两种酶链或途径成为锂的作用靶点:磷脂酰肌醇信号通路中的肌醇单磷酸酶和蛋白激酶糖原合酶激酶 3。锂通过取代正常辅助因子镁来抑制这些酶,镁是许多信号通路的重要调节剂。在这里,我们提供了抑制糖原合酶激酶 3 和肌醇单磷酸酶在锂的药效作用中的证据综述。我们还探讨了锂对这些酶的抑制如何导致情绪障碍和神经退行性疾病等具有临床相关性的下游效应。更好地了解锂的作用机制可能有助于开发更有效和更耐受的药物来治疗一系列精神疾病,并更清楚地了解这些疾病的病理生理学。