Mohamed M M Elnasharty, Azhar M Elwan, Mohamed E Elhadidy, Mona A Mohamed, Abeer H Abd El-Rahim, Naglaa A Hafiz, Omaima M Abd-El-Moneim, Kamilia B Abd El-Aziz, Aboelfetoh M Abdalla, Ibrahim M Farag
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The results confirmed that AM treatment induced significant elevation of DNA damage, cytogenetic aberrations, and MDA content in brain, liver, and testis tissues and sperm-shape anomalies. ASE treatment significantly minimized the genetic changes, sperm-shape anomalies, and MDA generation. These enhancements were more pronounced by protective ASE and increased by increasing the dose level. In histopathological examinations, AM treatment caused neurotoxicity in brain tissue. ASE treatment, partially, minimized these damages and the positive effects of therapeutic ASE were more noticeable. Biophysical parameters showed that therapeutic ASE was better for relaxation time, permittivity, and free energy change. 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引用次数: 0
摘要
多项研究表明,阿莫西林会对人体各器官产生不良影响。因此,本研究旨在评估芦荟籽提取物(ASE)对阿莫西林(AM)毒性的调节作用。用 AM(90 毫克/千克)治疗大鼠,用 ASE 剂量(100、200 和 300 毫克/千克)保护大鼠,并以相同的三种剂量用 ASE 治疗大鼠。实验结束时,对大鼠进行了 DNA 彗星试验、细胞遗传学检查、精子形态分析、丙二醛(MDA)百分比评估、组织病理学检查和生物物理测试(脑的模量、弛豫时间、介电常数、熵和内能变化)。结果证实,AM 处理会导致大脑、肝脏和睾丸组织中 DNA 损伤、细胞遗传畸变和 MDA 含量显著升高,以及精子形状异常。ASE 处理能明显减少遗传变化、精子形状异常和 MDA 的产生。保护性 ASE 对这些方面的改善更为明显,并且随着剂量水平的增加而增加。在组织病理学检查中,AM 处理会对脑组织造成神经毒性。ASE 治疗在一定程度上减少了这些损害,治疗性 ASE 的积极作用更加明显。生物物理参数显示,治疗性 ASE 在弛豫时间、介电常数和自由能变化方面更胜一筹。保护性和治疗性 ASE 能够在不同程度上恢复熵和内能的变化。
Various investigations of ameliorative role of Ashwagandha seeds (Withania somnifera) against amoxicillin toxicity.
Several studies showed the adverse effects of amoxicillin on various body organs. So, this research has been designed to evaluate the modulatory role of Ashwagandha seed extract (ASE) against amoxicillin (AM) toxicity. Rats treated with AM (90 mg/kg), protected by ASE doses (100, 200 and 300 mg/kg), and treated by ASE at the same three doses. At the end of the experimental period, DNA comet assay, cytogenetic examinations, sperm-shape analysis, evaluation of the malondialdehyde (MDA) percentages, histopathological examinations, and biophysical tests (modulus, relaxation time, permittivity, entropy, and internal energy change of brain) were documented. The results confirmed that AM treatment induced significant elevation of DNA damage, cytogenetic aberrations, and MDA content in brain, liver, and testis tissues and sperm-shape anomalies. ASE treatment significantly minimized the genetic changes, sperm-shape anomalies, and MDA generation. These enhancements were more pronounced by protective ASE and increased by increasing the dose level. In histopathological examinations, AM treatment caused neurotoxicity in brain tissue. ASE treatment, partially, minimized these damages and the positive effects of therapeutic ASE were more noticeable. Biophysical parameters showed that therapeutic ASE was better for relaxation time, permittivity, and free energy change. Protective and therapeutic ASE were able to recover entropy and internal energy changes in variant degrees.