Mood Disorders Psychopharmacology Unit, University Health Network, Toronto, ON, Canada.
Mood Disorders Psychopharmacology Unit, University Health Network, Toronto, ON, Canada; Institute of Medical Science, University of Toronto, Toronto, ON, Canada.
Prog Neuropsychopharmacol Biol Psychiatry. 2021 Jan 10;104:110032. doi: 10.1016/j.pnpbp.2020.110032. Epub 2020 Jul 4.
Numerous pharmacological treatments for mood disorders are currently available; however, rates of treatment resistance, relapse and recurrence remain high. Therefore, novel treatments acting outside of the conventionally targeted monoamine system are urgently needed to improve patient outcomes. Emerging and converging evidence suggests that immune dysfunction, oxidative stress, impaired cerebral blood flow (CBF) and decreased neurotrophic factors all contribute to mood disorder pathophysiology and are therefore treatment targets of interest. Pentoxifylline (PTX) is a phosphodiesterase inhibitor with potent anti-inflammatory and antioxidant effects, with additional pleiotropic effects that lead to improved CBF and increases in brain derived neurotrophic factor (BDNF) levels. The direct effect of non-specific phosphodiesterase inhibition may also improve alertness and cognitive function through enhancing second messenger systems. Replicated preclinical studies have demonstrated antidepressant-like effects in animal models. Small preliminary clinical trials have demonstrated promising results for antidepressant and procognitive effects, however, have yet to be replicated in larger mood disorder samples. Only one randomized clinical trial (RCT) specifically assessed the effects of adjunctive PTX in major depressive disorder (MDD), showing clinically and statistically significant antidepressant effects compared to placebo. No studies have assessed PTX in bipolar disorder (BD), where inflammation and altered CBF have also been strongly implicated. Taken together, PTX presents as a promising pleiotropic agent with several potential novel mechanisms of action meriting further evaluation in clinical trials to evaluate target engagement, antidepressant, procognitive and mood stabilizing effects.
目前有许多治疗情绪障碍的药物;然而,治疗抵抗、复发和再发的比率仍然很高。因此,迫切需要新的治疗方法来改善患者的预后,这些方法作用于传统的靶向单胺系统之外。新出现的和趋同的证据表明,免疫功能障碍、氧化应激、脑血流(CBF)受损和神经营养因子减少都有助于情绪障碍的病理生理学,因此是治疗的关注目标。己酮可可碱(PTX)是一种磷酸二酯酶抑制剂,具有强大的抗炎和抗氧化作用,具有额外的多效作用,可改善 CBF 并增加脑源性神经营养因子(BDNF)水平。非特异性磷酸二酯酶抑制的直接作用也可能通过增强第二信使系统来提高警觉性和认知功能。复制的临床前研究表明,在动物模型中具有抗抑郁样作用。小型初步临床试验表明,PTX 具有抗抑郁和认知促进作用的有希望的结果,但尚未在更大的情绪障碍样本中得到复制。只有一项随机临床试验(RCT)专门评估了辅助性 PTX 在重度抑郁症(MDD)中的作用,与安慰剂相比,显示出临床和统计学上显著的抗抑郁作用。没有研究评估 PTX 在双相情感障碍(BD)中的作用,炎症和 CBF 改变也被强烈牵连。总之,PTX 作为一种有前途的多效药物,具有几种潜在的新作用机制,值得在临床试验中进一步评估,以评估其对目标的影响、抗抑郁、认知促进和稳定情绪的作用。