Sifeddine Wahiba, Ba-M'hamed Saadia, Landry Marc, Bennis Mohamed
Laboratory of Pharmacology, Neurobiology, Anthropobiology, and Environment, Faculty of Sciences, Cadi Ayyad University, Avenue Prince My Abdellah, B.P. 2390, 40000, Marrakesh, Morocco.
University of Bordeaux, CNRS, Institute of Neurodegenerative Diseases, UMR 5293, Bordeaux, France.
Pharmacol Rep. 2023 Apr;75(2):342-357. doi: 10.1007/s43440-023-00459-3. Epub 2023 Feb 14.
Methylphenidate and atomoxetine are used for the treatment of attention-deficit/hyperactivity disorder (ADHD). Our previous studies established the validity of the 6-hydroxydopamine (6-OHDA) mouse model of ADHD and demonstrated hypersensitivity to pain, in line with clinical reports in ADHD patients. Acute methylphenidate treatment reduces hyperactivity and increases attention, but does not affect pain behaviors in this mouse model. Whereas atomoxetine has been shown to be effective against some symptoms of ADHD, nothing is known about its possible action on comorbid pain hypersensitivity. The objectives of the present research are (1) to investigate the effects of acute and chronic treatment with atomoxetine on ADHD-like symptoms and nociceptive thresholds, and (2) to explore the catecholaminergic systems underlying these effects.
Sham and 6-OHDA cohorts of male mice were tested for hyperactivity (open field), attention and impulsivity (5-choice serial reaction time task test), and thermal (hot plate test) and mechanical (von Frey test) thresholds after acute or repeated treatment with vehicle or atomoxetine (1, 3 or 10 mg/kg).
Acute administration of atomoxetine (10 mg/kg) reduced the hyperactivity and impulsivity displayed by 6-OHDA mice, without affecting attention or nociception. However, atomoxetine administered at 3 mg/kg/day for 7 days alleviated the ADHD-like core symptoms and attenuated the hyperalgesic responses. Furthermore, hyperlocomotion and anti-hyperalgesic activity were antagonized with phentolamine, propranolol, and sulpiride pre-treatments.
These findings demonstrated that when administered chronically, atomoxetine has a significant effect on ADHD-associated pain hypersensitization, likely mediated by both α- and β-adrenergic and D2/D3 dopaminergic receptors, and suggest new indications for atomoxetine that will need to be confirmed by well-designed clinical trials.
哌甲酯和托莫西汀用于治疗注意力缺陷多动障碍(ADHD)。我们之前的研究证实了ADHD的6-羟基多巴胺(6-OHDA)小鼠模型的有效性,并证明该模型对疼痛过敏,这与ADHD患者的临床报告一致。急性哌甲酯治疗可减少多动并提高注意力,但对该小鼠模型的疼痛行为没有影响。虽然托莫西汀已被证明对ADHD的某些症状有效,但其对合并的疼痛过敏可能产生的作用尚不清楚。本研究的目的是:(1)研究急性和慢性托莫西汀治疗对ADHD样症状和痛觉阈值的影响;(2)探索这些作用背后的儿茶酚胺能系统。
雄性小鼠假手术组和6-OHDA组在给予溶剂或托莫西汀(1、3或10mg/kg)急性或重复治疗后,进行多动(旷场试验)、注意力和冲动性(5选串行反应时任务测试)以及热(热板试验)和机械(von Frey试验)阈值测试。
急性给予托莫西汀(10mg/kg)可减少6-OHDA小鼠表现出的多动和冲动性,而不影响注意力或痛觉感受。然而,以3mg/kg/天的剂量连续给予托莫西汀7天可减轻ADHD样核心症状并减弱痛觉过敏反应。此外,酚妥拉明、普萘洛尔和舒必利预处理可拮抗运动亢进和抗痛觉过敏活性。
这些发现表明,长期给药时,托莫西汀对ADHD相关的疼痛过敏有显著作用,可能由α和β肾上腺素能受体以及D2/D3多巴胺能受体介导,并提示托莫西汀有新的适应证,这需要通过精心设计的临床试验来证实。