Department of Biochemistry, Center of Biological Sciences, Universidade Federal de Santa Catarina, Florianópolis, SC, 88040-900, Brazil.
Division of Medical Sciences, University of Victoria, Victoria, BC, Canada.
Purinergic Signal. 2021 Jun;17(2):285-301. doi: 10.1007/s11302-021-09779-6. Epub 2021 Mar 13.
Guanosine is a purine nucleoside that has been shown to exhibit antidepressant effects, but the mechanisms underlying its effect are not well established. We investigated if the antidepressant-like effect induced by guanosine in the tail suspension test (TST) in mice involves the modulation of α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor, voltage-dependent calcium channel (VDCC), and brain-derived neurotrophic factor (BDNF)/tropomyosin receptor kinase B (TrkB) pathway. We also evaluated if the antidepressant-like effect of guanosine is accompanied by an acute increase in hippocampal and prefrontocortical BDNF levels. Additionally, we investigated if the ability of guanosine to elicit a fast behavioral response in the novelty suppressed feeding (NSF) test is associated with morphological changes related to hippocampal synaptogenesis. The antidepressant-like effect of guanosine (0.05 mg/kg, p.o.) in the TST was prevented by DNQX (AMPA receptor antagonist), verapamil (VDCC blocker), K-252a (TrkBantagonist), or BDNF antibody. Increased P70S6K phosphorylation and higher synapsin I immunocontent in the hippocampus, but not in the prefrontal cortex, were observed 1 h after guanosine administration. Guanosine exerted an antidepressant-like effect 1, 6, and 24 h after its administration, an effect accompanied by increased hippocampal BDNF level. In the prefrontal cortex, BDNF level was increased only 1 h after guanosine treatment. Finally, guanosine was effective in the NSF test (after 1 h) but caused no alterations in dendritic spine density and remodeling in the ventral dentate gyrus (DG). Altogether, the results indicate that guanosine modulates targets known to be implicated in fast antidepressant behavioral responses (AMPA receptor, VDCC, and TrkB/BDNF pathway).
鸟苷是一种嘌呤核苷,已被证明具有抗抑郁作用,但它的作用机制尚未得到很好的确定。我们研究了鸟苷在小鼠悬尾试验(TST)中诱导的抗抑郁样效应是否涉及α-氨基-3-羟基-5-甲基-4-异恶唑丙酸(AMPA)受体、电压依赖性钙通道(VDCC)和脑源性神经营养因子(BDNF)/原肌球蛋白受体激酶 B(TrkB)通路的调制。我们还评估了鸟苷的抗抑郁样效应是否伴随着海马体和前额皮质 BDNF 水平的急性增加。此外,我们研究了鸟苷在新奇性抑制进食(NSF)试验中快速引发行为反应的能力是否与海马突触发生相关的形态变化有关。鸟苷(0.05mg/kg,po)在 TST 中的抗抑郁样作用被 DNQX(AMPA 受体拮抗剂)、维拉帕米(VDCC 阻断剂)、K-252a(TrkB 拮抗剂)或 BDNF 抗体所阻止。鸟苷给药 1 小时后,观察到海马体中 P70S6K 磷酸化增加和突触素 I 免疫含量增加,但前额皮质中没有观察到这种变化。鸟苷给药 1、6 和 24 小时后产生抗抑郁样作用,同时伴有海马体 BDNF 水平增加。在前额皮质中,只有在鸟苷处理 1 小时后才会增加 BDNF 水平。最后,鸟苷在 NSF 试验中有效(在 1 小时后),但不会改变腹侧齿状回的树突棘密度和重塑。总之,这些结果表明,鸟苷调节了已知与快速抗抑郁行为反应有关的靶点(AMPA 受体、VDCC 和 TrkB/BDNF 通路)。