Elgamal Mariam A, Khodeer Dina M, Abdel-Wahab Basel A, Ibrahim Ibrahim Abdel Aziz, Alzahrani Abdullah R, Moustafa Yasser M, Ali Azza A, El-Sayed Norhan M
Egypt Healthcare Authority, Comprehensive Health Insurance, Port-Said, Egypt.
Department of Pharmacology and Toxicology, Faculty of Pharmacy, Suez Canal University, Ismailia, Egypt.
Front Pharmacol. 2023 Feb 22;14:1113966. doi: 10.3389/fphar.2023.1113966. eCollection 2023.
Autism is complex and multifactorial, and is one of the fastest growing neurodevelopmental disorders. Canagliflozin (Cana) is an antidiabetic drug that exhibits neuroprotective properties in various neurodegenerative syndromes. This study investigated the possible protective effect of Cana against the valproic acid (VPA)-induced model of autism. VPA was injected subcutaneously (SC) into rat pups at a dose of 300 mg/kg, twice daily on postnatal day-2 (PD-2) and PD-3, and once on PD-4 to induce an autism-like syndrome. Graded doses of Cana were administered (5 mg/kg, 7.5 mg/kg, and 10 mg/kg, P.O.) starting from the first day of VPA injections and continued for 21 days. At the end of the experiment, behavioral tests and histopathological alterations were assessed. In addition, the gene expression of peroxisome proliferator-activated receptor γ (PPAR γ), lactate dehydrogenase A (LDHA), pyruvate dehydrogenase kinase (PDK), cellular myeloctomatosis (c-Myc) with protein expression of glucose transporter-1 (GLUT-1), phosphatase and tensin homolog (PTEN), and level of acetylcholine (ACh) were determined. Treatment with Cana significantly counteracted histopathological changes in the cerebellum tissues of the brain induced by VPA. Cana (5 mg/kg, 7.5 mg/kg, and 10 mg/kg) improved sociability and social preference, enhanced stereotypic behaviors, and decreased hyperlocomotion activity, in addition to its significant effect on the canonical Wnt/β-catenin pathway the downregulation of gene expression of LDHA (22%, 64%, and 73% in cerebellum tissues with 51%, 60%, and 75% in cerebrum tissues), PDK (27%, 50%, and 67% in cerebellum tissues with 34%, 66%, and 77% in cerebrum tissues), c-Myc (35%, 44%, and 72% in cerebellum tissues with 19%, 58%, and 79% in cerebrum tissues), protein expression of GLUT-1 (32%, 48%, and 49% in cerebellum tissues with 30%, 50%, and 54% in cerebrum tissues), and elevating gene expression of PPAR-γ (2, 3, and 4 folds in cerebellum tissues with 1.5, 3, and 9 folds in cerebrum tissues), protein expression of PTEN (2, 5, and 6 folds in cerebellum tissues with 6, 6, and 10 folds in cerebrum tissues), and increasing the ACh levels (4, 5, and 7 folds) in brain tissues. The current study confirmed the ameliorating effect of Cana against neurochemical and behavioral alterations in the VPA-induced model of autism in rats.
自闭症复杂且具有多因素性,是发展最快的神经发育障碍之一。卡格列净(Cana)是一种抗糖尿病药物,在各种神经退行性综合征中表现出神经保护特性。本研究调查了Cana对丙戊酸(VPA)诱导的自闭症模型可能的保护作用。在出生后第2天(PD - 2)和PD - 3,以300 mg/kg的剂量每天两次皮下注射(SC)VPA给幼鼠,在PD - 4注射一次以诱导类似自闭症的综合征。从VPA注射的第一天开始给予不同剂量的Cana(5 mg/kg、7.5 mg/kg和10 mg/kg,口服),持续21天。实验结束时,评估行为测试和组织病理学改变。此外,还测定了过氧化物酶体增殖物激活受体γ(PPARγ)、乳酸脱氢酶A(LDHA)、丙酮酸脱氢酶激酶(PDK)、细胞性骨髓细胞瘤(c - Myc)的基因表达以及葡萄糖转运蛋白1(GLUT - 1)、磷酸酶和张力蛋白同源物(PTEN)的蛋白表达,以及乙酰胆碱(ACh)水平。Cana治疗显著抵消了VPA诱导的大脑小脑组织的组织病理学变化。Cana(5 mg/kg、7.5 mg/kg和10 mg/kg)改善了社交能力和社交偏好,增强了刻板行为,并减少了过度活动,此外,它对经典Wnt/β - 连环蛋白通路有显著影响——下调LDHA的基因表达(小脑组织中分别下调22%、64%和73%,大脑组织中分别下调51%、60%和75%)、PDK的基因表达(小脑组织中分别下调27%、50%和67%,大脑组织中分别下调34%、66%和77%)、c - Myc的基因表达(小脑组织中分别下调35%、44%和72%,大脑组织中分别下调19%、58%和79%)、GLUT - 1的蛋白表达(小脑组织中分别下调32%、48%和49%,大脑组织中分别下调30%、50%和54%),并上调PPAR - γ的基因表达(小脑组织中分别上调2、3和4倍,大脑组织中分别上调1.5、3和9倍)、PTEN的蛋白表达(小脑组织中分别上调2、5和6倍,大脑组织中分别上调6、6和10倍),并增加脑组织中ACh水平(分别增加4、5和7倍)。本研究证实了Cana对VPA诱导的大鼠自闭症模型中神经化学和行为改变的改善作用。