Department of Pharmacology, Graduate School of Biomedical and Health Sciences, Hiroshima University, 1-2-3 Kasumi Minami-ku, Hiroshima, 734-8553, Japan.
Department of Pharmacology, Graduate School of Biomedical and Health Sciences, Hiroshima University, 1-2-3 Kasumi Minami-ku, Hiroshima, 734-8553, Japan.
Eur J Pharmacol. 2022 Jun 15;925:174986. doi: 10.1016/j.ejphar.2022.174986. Epub 2022 Apr 28.
Connexin 43 (Cx43) expression is decreased in the prefrontal cortex of patients with depression, but its significance is still unknown. Neurotrophic factors, such as brain-derived neurotrophic factor (BDNF), are involved in the effects of antidepressant. However, the relationship between Cx43 expression and induction of brain-derived neurotrophic factor production by antidepressants is unknown. On the basis of our previous study, which showed that adrenergic receptors stimulation results in potentiation of BDNF expression in astrocytes with downregulated Cx43 expression, we investigated the induction of BDNF expression by amitriptyline, a tricyclic antidepressant, in Cx43-knockdown astrocytes. Amitriptyline treatment potentiated BDNF expression in Cx43-knockdown astrocytes compared with those treated with non-targeting small interfering RNA (siRNA). Using a pharmacological approach, we revealed that the potentiating effect of amitriptyline on BDNF expression was mediated by lysophosphatidic acid (LPA) receptor (LPA) stimulation and subsequent activation of Src-extracellular signal-regulated kinase (ERK) signaling. These findings suggest that downregulation of Cx43 in patients with depression might contribute to the therapeutic efficacy of antidepressants rather than the pathogenesis of depression.
缝隙连接蛋白 43(Cx43)在抑郁症患者的前额叶皮层中的表达降低,但其意义尚不清楚。神经营养因子,如脑源性神经营养因子(BDNF),参与了抗抑郁药的作用。然而,Cx43 表达与抗抑郁药诱导脑源性神经营养因子产生之间的关系尚不清楚。基于我们之前的研究表明,肾上腺素能受体的刺激导致下调 Cx43 表达的星形胶质细胞中 BDNF 表达的增强,我们研究了三环类抗抑郁药阿米替林在 Cx43 敲低星形胶质细胞中诱导 BDNF 表达的情况。与用非靶向小干扰 RNA(siRNA)处理的星形胶质细胞相比,阿米替林处理增强了 Cx43 敲低星形胶质细胞中的 BDNF 表达。通过药理学方法,我们揭示了阿米替林对 BDNF 表达的增强作用是通过溶血磷脂酸(LPA)受体(LPA)刺激和随后的Src-细胞外信号调节激酶(ERK)信号通路的激活介导的。这些发现表明,抑郁症患者中 Cx43 的下调可能有助于抗抑郁药的治疗效果,而不是抑郁症的发病机制。