Cone Neurosurgical Research Laboratory, Department of Neurology and Neurosurgery, Montreal Neurological Institute, McGill University, Montreal, Quebec, Canada.
Neurochem Int. 2012 Dec;61(8):1417-23. doi: 10.1016/j.neuint.2012.10.006. Epub 2012 Oct 22.
Antidepressant treatments, including those that increase serotonin (5-HT) neurotransmission, require several weeks or months until the onset of the therapeutic effect in depressed patients. The negative feedback on 5-HT transmission exhibited by the 5-HT(1A) and 5-HT(1B) autoreceptors has been postulated as a possible delaying factor. The aim of the present study was to assess the effect of the acute and subchronic treatment with pindolol, a 5-HT(1A/1B,) β₁ and β₂ adrenoceptor antagonist, on 5-HT synthesis, one of the key parameters of 5-HT neurotransmission. Male Sprague-Dawley (SPD) rats (180-220 g) were treated with pindolol or an adequate volume of saline, administered either acutely (15 mg/kg i.p.; SPD-AC-SAL, SPD-AC-TR) or subchronically (15 mg/kg day i.p. for 7 days; SPD-SUBCHR-SAL, SPD-SUBCHR-TR). Thirty minutes following the single i.p. injection (acute experiment) or at the 8th day following the commencement of the subchronic treatment (subchronic experiment), 5-HT synthesis was measured using α-[¹⁴C]methyl-L-tryptophan autoradiography. The analysis of variance (ANOVA), followed by the Benjamini-Hochberg correction for multiple comparisons, revealed: (1) a significant increase of 5-HT synthesis in the SPD-AC-TR rats, relative to the SPD-AC-SAL rats in all brain regions examined except the substantia nigra--pars reticularis, dorsal subiculum, inferior olive, raphe magnus and raphe obscurus and (2) a significant increase of 5-HT synthesis in the SPD-SUBCHR-TR rats, relative to the SPD-SUBCHR-SAL rats in all brain regions except the median raphe, hypothalamus and raphe pontine. On the basis of these results, we hypothesized that the antagonism of the 5-HT(1A/1B) receptors prevents the negative feedback mediated by these receptors on 5-HT synthesis, resulting in a persistent increase of 5-HT synthesis. The results accord with clinical reports on the utility of pindolol in the augmentation of antidepressant treatment.
抗抑郁药物治疗,包括那些增加 5-羟色胺(5-HT)神经传递的药物,需要数周或数月才能在抑郁患者中开始产生治疗效果。5-HT(1A)和 5-HT(1B)自身受体表现出的 5-HT 传递的负反馈作用,被认为是可能的延迟因素。本研究的目的是评估急性和亚慢性给予匹哚洛尔(一种 5-HT(1A/1B)、β₁和 β₂肾上腺素能受体拮抗剂)对 5-HT 合成的影响,5-HT 合成是 5-HT 神经传递的关键参数之一。雄性 Sprague-Dawley(SPD)大鼠(180-220g)用匹哚洛尔或适量的生理盐水处理,分别急性(15mg/kg 腹腔注射;SPD-AC-SAL、SPD-AC-TR)或亚慢性(15mg/kg 天腹腔注射,共 7 天;SPD-SUBCHR-SAL、SPD-SUBCHR-TR)。单次腹腔注射后 30 分钟(急性实验)或亚慢性治疗开始后第 8 天(亚慢性实验),用 α-[¹⁴C]甲基-L-色氨酸放射自显影测量 5-HT 合成。方差分析(ANOVA),随后进行贝叶斯-霍赫伯格多重比较校正,结果显示:(1)与 SPD-AC-SAL 大鼠相比,除黑质网状部、背侧海马下托、下橄榄核、中缝大核和中缝隐核外,所有研究脑区的 SPD-AC-TR 大鼠 5-HT 合成均显著增加;(2)与 SPD-SUBCHR-SAL 大鼠相比,除中缝核、下丘脑和桥脑中缝核外,所有研究脑区的 SPD-SUBCHR-TR 大鼠 5-HT 合成均显著增加。基于这些结果,我们假设 5-HT(1A/1B)受体的拮抗作用阻止了这些受体对 5-HT 合成的负反馈作用,导致 5-HT 合成持续增加。这些结果与匹哚洛尔在增强抗抑郁治疗中的应用的临床报告一致。