Department of Parasitology, Theodor Bilharz Research Institute, Imbaba, Giza, Egypt.
Department of Parasitology, Theodor Bilharz Research Institute, Imbaba, Giza, Egypt.
Exp Parasitol. 2022 Jul;238:108260. doi: 10.1016/j.exppara.2022.108260. Epub 2022 Apr 18.
This study aimed to evaluate the efficacy of gamma-aminobutyric acid (GABA) alone or combined with praziquantel (PZQ) against Schistosoma (S) mansoni infection in a murine model.
Five groups, 8 mice each, were studied; GI served as normal controls; GII: S. mansoni-infected control group and the other three S. mansoni-infected groups received drug regimens for 5 consecutive days as follows GIII: Infected-PZQ treated group (200 mg/kg/day); GIV: Infected-GABA treated group (300 mg/kg/day) and GV: Infected-PZQ-GABA treated group (100 mg/kg/day for each drug). All animal groups were sacrificed two weeks later and different parasitological, histopathological and biochemical parameters were assessed.
Combined GABA-PZQ treated group recorded the highest significant reduction in all parasitological, histopathological and biochemical parameters followed by PZQ and finally GABA groups. Combined GABA-PZQ treatment led to the complete disappearance of immature eggs and marked reduction of deposited eggs in liver tissues and improved liver pathology. Significant improvement in hepatic oxidative stress levels, serum albumin and total protein in response to GABA treatment alone or combined with PZQ.
GABA had schistosomicidal, hepatoprotective and antioxidant activities against S. mansoni infection, GABA disrupted parasite pairing and activity, reduced the total number of worms recovered and the number of ova in the tissues. GABA may be considered an adjuvant therapy to potentiate PZQ antiparasitic activity and eradicate infection-induced liver damage and oxidative stress.
本研究旨在评估γ-氨基丁酸(GABA)单独或联合吡喹酮(PZQ)对曼氏血吸虫(S)感染的疗效。
研究了 5 组 8 只小鼠;GI 为正常对照组;GII:曼氏血吸虫感染对照组,另外三组曼氏血吸虫感染组连续 5 天接受药物治疗,如下:GIII:感染-PZQ 治疗组(200mg/kg/天);GIV:感染-GABA 治疗组(300mg/kg/天)和 GV:感染-PZQ-GABA 治疗组(每种药物 100mg/kg/天)。两周后,所有动物组均被处死,评估不同的寄生虫学、组织病理学和生化参数。
联合 GABA-PZQ 治疗组记录的所有寄生虫学、组织病理学和生化参数的降低最显著,其次是 PZQ 组,最后是 GABA 组。联合 GABA-PZQ 治疗导致不成熟卵完全消失,并显著减少肝组织中沉积的卵,改善肝病理。GABA 单独或联合 PZQ 治疗可显著改善肝氧化应激水平、血清白蛋白和总蛋白。
GABA 对曼氏血吸虫感染具有杀血吸虫、保肝和抗氧化作用,GABA 破坏寄生虫配对和活性,减少回收的总蠕虫数量和组织中的卵数。GABA 可被认为是一种辅助治疗方法,增强 PZQ 的抗寄生虫活性,消除感染引起的肝损伤和氧化应激。