Kocak Mehmet Nuri, Ates Orhan, Hacımuftuoglu Ahmet, Ates Irem, Tekin Erdal, Ceylan Onur, Okkay Ufuk
Department of Neurology, Atatürk University School of Medicine, Erzurum, Turkey.
Department of Ophthalmology, Atatürk University School of Medicine, Erzurum, Turkey.
Eurasian J Med. 2022 Feb;54(1):54-60. doi: 10.5152/eurasianjmed.2022.21288.
There might be dopaminergic connections between the retina and the brain. In this context, the study was aimed to investigate the possible interaction between the retina and basal ganglia through the dopaminergic system.
In total, 32 healthy rats were randomized into 4 groups: healthy, Sham, dopamine antagonist injected group (risperidone, 0.04 mg/kg intravitreally), and dopamine agonist injected group (apomorphine, 0.4 mg/kg intravitreally). The locomotor activity and Morris water maze tests were applied to all rats twice, before the injection and 28 days after, to detect changes in movement, memory, and attention. Histopathologically, the basal ganglia and hippocampus regions were removed and examined.
In the locomotor activity test, a statistical significance was found between the first and last measurement values of the apomorphine group and a decrease in activities and an increase in resting times (P < .05). In the Morris water maze test, a statistical significance was detected between the first and last tests of the control group and the apomorphine groups and showed significantly shorter learning times (P < .05). Histological analyses of the substantia nigra and hippocampus were noteworthy in that the number of damaged neurons in the risperidone group was considerably higher than the other groups. The number of damaged neurons in the apomorphine group was significantly lower than in the healthy group.
Intravitreal administration of dopamine agonists and antagonists has given rise to alterations in the cerebral dopaminergic system, leading to changes in locomotor activity and memory and histopathological changes.
视网膜与大脑之间可能存在多巴胺能连接。在此背景下,本研究旨在通过多巴胺能系统研究视网膜与基底神经节之间可能的相互作用。
总共32只健康大鼠被随机分为4组:健康组、假手术组、多巴胺拮抗剂注射组(利培酮,玻璃体内注射0.04mg/kg)和多巴胺激动剂注射组(阿扑吗啡,玻璃体内注射0.4mg/kg)。在注射前和注射后28天,对所有大鼠进行两次运动活动和莫里斯水迷宫测试,以检测运动、记忆和注意力的变化。组织病理学上,切除基底神经节和海马区域并进行检查。
在运动活动测试中,阿扑吗啡组第一次和最后一次测量值之间存在统计学显著性差异,活动减少,休息时间增加(P < 0.05)。在莫里斯水迷宫测试中,对照组和阿扑吗啡组第一次和最后一次测试之间存在统计学显著性差异,学习时间显著缩短(P < 0.05)。黑质和海马的组织学分析值得注意的是,利培酮组受损神经元数量明显高于其他组。阿扑吗啡组受损神经元数量明显低于健康组。
玻璃体内注射多巴胺激动剂和拮抗剂导致大脑多巴胺能系统改变,进而导致运动活动和记忆变化以及组织病理学改变。