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Tetrapleura tetraptera fruit phenolics fraction protects against the impact of ischemic stroke-induced hippocampal distortions and memory deficits in Wistar rats

机译:四翅目果实酚类成分可防止缺血性中风诱导的 Wistar 大鼠海马扭曲和记忆缺陷的影响

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摘要

Stroke is the most significant cause of disability worldwide. Despite mounting data supporting memory deficit after stroke, dysfunction and treatment effect mechanisms remain unknown. Phenolics can be found in a variety of fruits and vegetables. There is, however, a scarcity of research on the therapeutic potential of the phenolics fraction of Tetrapleura tetraptera (PTT) fruit against ischemic stroke-induced abnormalities in hippocampal tissue. The rats were divided into five groups: Group I, vehicle; group II, ischemia/reperfusion (I/R)+vehicle; group III, I/R+50 mg/kg minocycline (MNC); group IV, I/R+100 mg/kg PTT; and group V, I/R+200 mg/kg PTT. Ischemia was induced via bilateral common carotid artery occlusion for 30 minutes followed by reperfusion. PTT and MNC were intraorally administered daily for 7 days. Neurodegenerative changes, cornu ammonis 1 (CA1) and cornu ammonis 3 (CA3) pyramidal cell count, levels of oxidative stress indicators, and memory functions were assessed. Rats treated with PTT, as well as MNC compared to untreated I/R rats, showed a substantial (P<0.05) rise in catalase, superoxide dismutase, glutathione levels, as well as decreased lipid peroxidation and improved memory. I/R resulted in histoarchitectural distortions, a marked decrease (P<0.05) in the intensity of the Nissl substance, and a striking decrease (P<0.05) in the number of pyramidal cells in the CA1 and CA3. PTT and MNC-treated groups showed significant attenuation in all the above parameters. Taking together, these findings revealed that PTT attenuated oxidative stress, histologic alterations and substantially restored memory impairment in the I/R rat model.
机译:中风是全世界导致残疾的最重要原因。尽管越来越多的数据支持中风后记忆缺陷,但功能障碍和治疗效果机制仍然未知。酚类物质存在于各种水果和蔬菜中。然而,关于四翅目四胸膜 (PTT) 果实的酚类成分对缺血性中风诱导的海马组织异常的治疗潜力的研究很少。将大鼠分为 5 组:I 组,载体;II 组,缺血/再灌注 (I/R)+ 载体;III 组,I/R +50 mg/kg 米诺环素 (MNC);IV 组,I/R+100 mg/kg PTT;和 V 组,I/R+200 mg/kg PTT。通过双侧颈总动脉闭塞 30 分钟,然后再灌注诱导缺血。PTT 和 MNC 每天口服给药,持续 7 天。评估神经退行性变化、山茱萸 1 (CA1) 和山茱萸 3 (CA3) 锥体细胞计数、氧化应激指标水平和记忆功能。与未治疗的 I/R 大鼠相比,用 PTT 和 MNC 治疗的大鼠显示过氧化氢酶、超氧化物歧化酶、谷胱甘肽水平显着升高 (P<0.05),脂质过氧化降低和记忆力改善。I/R 导致组织结构扭曲,Nissl 物质强度显着降低 (P<0.05),CA1 和 CA3 中锥体细胞的数量显着减少 (P<0.05)。PTT 和 MNC 处理组在上述所有参数中均表现出显着衰减。综上所述,这些发现揭示了 PTT 减轻了 I/R 大鼠模型中的氧化应激、组织学改变并显着恢复了记忆障碍。

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