Sanches Eliane S, Boia Raquel, Leitão Ricardo A, Madeira Maria H, Fontes-Ribeiro Carlos A, Ambrósio António Francisco, Fernandes Rosa, Silva Ana Paula
Institute of Pharmacology and Experimental Therapeutics, Faculty of Medicine, University of Coimbra, 3000-548 Coimbra, Portugal.
Coimbra Institute for Clinical and Biomedical Research (iCBR), Faculty of Medicine, University of Coimbra, 3000-548 Coimbra, Portugal.
Antioxidants (Basel). 2023 Apr 15;12(4):937. doi: 10.3390/antiox12040937.
Attention-Deficit/Hyperactivity Disorder (ADHD) is one of the most prevalent neurodevelopmental disorders. Interestingly, children with ADHD seem to experience more ophthalmologic abnormalities, and the impact of methylphenidate (MPH) use on retinal physiology remains unclear. Thus, we aimed to unravel the retina's structural, functional, and cellular alterations and the impact of MPH in ADHD versus the control conditions. For that, spontaneously hypertensive rats (SHR) and Wistar Kyoto rats (WKY) were used as animal models of ADHD and the controls, respectively. Animals were divided into four experimental groups as follows: WKY vehicle (Veh; tap water), WKY MPH (1.5 mg/kg/day), SHR Veh, SHR MPH. Individual administration was performed by gavage between P28-P55. Retinal physiology and structure were evaluated at P56 followed by tissue collection and analysis. The ADHD animal model presents the retinal structural, functional, and neuronal deficits, as well as the microglial reactivity, astrogliosis, blood-retinal barrier (BRB) hyperpermeability and a pro-inflammatory status. In this model, MPH had a beneficial effect on reducing microgliosis, BRB dysfunction, and inflammatory response, but did not correct the neuronal and functional alterations in the retina. Curiously, in the control animals, MPH showed an opposite effect since it impaired the retinal function, neuronal cells, and BRB integrity, and also promoted both microglia reactivity and upregulation of pro-inflammatory mediators. This study unveils the retinal alterations in ADHD and the opposite effects induced by MPH in the retina of ADHD and the control animal models.
注意缺陷多动障碍(ADHD)是最常见的神经发育障碍之一。有趣的是,患有ADHD的儿童似乎更容易出现眼科异常,而使用哌甲酯(MPH)对视网膜生理的影响仍不清楚。因此,我们旨在揭示ADHD与对照条件下视网膜的结构、功能和细胞改变以及MPH的影响。为此,分别将自发性高血压大鼠(SHR)和Wistar Kyoto大鼠(WKY)用作ADHD及其对照的动物模型。动物分为以下四个实验组:WKY溶剂组(Veh;自来水)、WKY MPH组(1.5 mg/kg/天)、SHR Veh组、SHR MPH组。在P28 - P55期间通过灌胃进行个体给药。在P56评估视网膜生理和结构,随后进行组织采集和分析。ADHD动物模型呈现出视网膜结构、功能和神经元缺陷,以及小胶质细胞反应性、星形胶质细胞增生、血视网膜屏障(BRB)高通透性和促炎状态。在该模型中,MPH对减少小胶质细胞增生、BRB功能障碍和炎症反应具有有益作用,但未纠正视网膜中的神经元和功能改变。奇怪的是,在对照动物中,MPH显示出相反的效果,因为它损害了视网膜功能、神经元细胞和BRB完整性,还促进了小胶质细胞反应性和促炎介质的上调。这项研究揭示了ADHD中的视网膜改变以及MPH在ADHD和对照动物模型视网膜中诱导的相反作用。