Doğan Murat, Albayrak Yakup, Erbaş Oytun
Hekim Medical Company, İstanbul, Turkey.
Department of Psychiatry, Tekirdağ Namık Kemal University Faculty of Medicine, Tekirdağ, Turkey.
Alpha Psychiatry. 2023 Jan 1;24(1):22-31. doi: 10.5152/alphapsychiatry.2023.22975. eCollection 2023 Jan.
Autism spectrum disorder is a neurodevelopmental disease in which impaired social behaviors, impaired sociality, and restricted and repetitive behaviors are seen. Bumetanide is a loop diuretic that inhibits Na-K-2Cl cotransporter 1 and it is currently used in clinical phase studies in patients with autism spectrum disorder. In present research, it is purposed to demonstrate the beneficial effects of torasemide which is another Na-K-2Cl cotransporter 1 inhibitor on an experimental autism model induced with propionic acid by providing imaging and brain tissue investigations.
Male Wistar rats were used in the present study (n = 30). Propionic acid of 250 mg/kg/day was administrated intraperitoneally in rats to induce autism for 5 days. Three groups were created for present study as follows: group 1, normal control (n = 10); group 2, propionic acid and saline given group (n = 10); group 3, propionic acid + tora-semide-administrated group (n = 10).
Torasemide group scored higher on behavioral tests compared to saline group. The brain levels of malondialdehyde, tumor necrosis factor-alpha, interleukin-2, interleukin-17, and Nuclear Factor kappa B (NF-κB), Glial fibrillary acidic protein (GFAP) were remarkably higher in propionic acid + saline group. In histopathology assessments, torasemide group had higher neuronal count of Cornu Ammonis 1, neuronal count of Cornu Ammonis 2 in hippocampus, and Purkinje cells in cerebellum. GFAP immunostaining index (Cornu Ammonis 1) and cerebellum were lower in torasemide group. Magnetic resonance spectroscopy revealed that mean lactate value was higher in propionic acid + saline group compared to torasemide group.
Our experimental results showed that torasemide might enhance gamma-aminobutyric acid activity. Torasemide can be considered another promising Na-K-2Cl cotransporter 1 inhibitor in the treatment of autism with a longer half-life and less side effects after further studies.
自闭症谱系障碍是一种神经发育疾病,其特征为社交行为受损、社交能力障碍以及存在受限和重复行为。布美他尼是一种袢利尿剂,可抑制钠-钾-2氯协同转运蛋白1,目前正用于自闭症谱系障碍患者的临床阶段研究。在本研究中,旨在通过影像学和脑组织研究,证明托拉塞米(另一种钠-钾-2氯协同转运蛋白1抑制剂)对丙酸诱导的实验性自闭症模型的有益作用。
本研究使用雄性Wistar大鼠(n = 30)。以250 mg/kg/天的丙酸腹腔注射大鼠5天以诱导自闭症。本研究分为三组:第1组,正常对照组(n = 10);第2组,丙酸加生理盐水给药组(n = 10);第3组,丙酸+托拉塞米给药组(n = 10)。
与生理盐水组相比,托拉塞米组在行为测试中得分更高。丙二酸、肿瘤坏死因子-α、白细胞介素-2、白细胞介素-17和核因子κB(NF-κB)、胶质纤维酸性蛋白(GFAP)的脑水平在丙酸+生理盐水组中显著更高。在组织病理学评估中,托拉塞米组海马中角回1的神经元计数、海马中角回2的神经元计数以及小脑中的浦肯野细胞数量更高。托拉塞米组GFAP免疫染色指数(角回1)和小脑更低。磁共振波谱显示,与托拉塞米组相比,丙酸+生理盐水组的平均乳酸值更高。
我们的实验结果表明,托拉塞米可能增强γ-氨基丁酸活性。经过进一步研究,托拉塞米可被视为另一种有前景的钠-钾-2氯协同转运蛋白1抑制剂,用于治疗自闭症,其半衰期更长且副作用更少。