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首页> 外文期刊>Neurogastroenterology and motility >Preclinical evaluation of the effects on the gastrointestinal tract of the antineoplastic drug vincristine repeatedly administered to rats
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Preclinical evaluation of the effects on the gastrointestinal tract of the antineoplastic drug vincristine repeatedly administered to rats

机译:对大鼠反对施用抗肿瘤药物血管内胃肠道胃肠道影响的临床前评价

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Abstract Background Vincristine is a commonly used chemotherapeutic agent. It is associated with undesirable digestive side effects. However, the impact of vincristine on gastrointestinal structure and motility or its long‐term effects have not been deeply studied in animal models. This could be useful in order to develop therapeutic or preventive strategies for cancer patients. The aim of this study was to analyze such effects. Methods Rats received saline or vincristine (0.1?mg?kg ?1 , ip) daily for 10?days. Evaluations were performed during treatment and 2‐6?weeks after. Somatic mechano‐sensitivity was assessed using von Frey hairs. Gastrointestinal motor function was studied by means of radiographic still images and colonic propulsion of fecal pellets using fluoroscopy videos. Histological assessment of the gut morphology and immunohistochemistry for HuC/D and nNOS were performed in whole‐mount myenteric plexus preparations. Key Results Peripheral sensitivity was increased in animals treated with vincristine and did not subside 2?weeks after treatment finalization. Vincristine treatment inhibited gastrointestinal motility although this was recovered to normal values with time. Damage in the digestive wall after vincristine treatment was greater in the ileum than in the colon. Villi shortening (in ileum) and large inflammatory nodules still remained 2?weeks after treatment finalization. Finally, the proportion of nNOS ‐immunoreactive neurons was increased with vincristine and continued to be increased 2?weeks after treatment finalization. Conclusions and Inferences Vincristine alters gastrointestinal motility, peripheral sensitivity and mucosal architecture. Vincristine‐induced neuropathy (somatic and enteric), intestinal mucosa damage and inflammatory infiltrations are relatively long‐lasting.
机译:摘要背景血管酮是一种常用的化学治疗剂。它与不期望的消化副作用有关。然而,在动物模型中没有深入研究了血管内对胃肠道结构和运动或其长期效应的影响。这可能是有用的,以便为癌症患者制定治疗或预防策略。本研究的目的是分析这种影响。方法每天10次接受大鼠的盐水或血管内(0.1×mg?kgα1,IP)。在治疗期间进行评估,2-6周后进行。使用von毛细毛发评估躯体机械敏感性。通过使用荧光透视视频通过射线照相静止图像和粪便颗粒的结肠推进来研究胃肠道发器功能。 HUC / D和NNOS对HUC / D和免疫组织化学的组织学评估在全山神经丛制剂中进行。通过长春新碱治疗的动物增加了关键效应差异敏感性,并且在治疗完成后没有消退2?周数。长春肾治疗抑制胃肠动机,尽管随着时间的推移,将其回收到正常值。在复合中的血管内治疗后的消化壁损伤比结肠在结肠中更大。别墅缩短(在回肠)和大型炎症结节仍然留在待遇后2个星期。最后,NNOS -immunoreActive神经元的比例随高潮增加,并在治疗完成后持续增加2个。结论和推迟维克里汀改变了胃肠运动,外周敏感性和粘膜架构。血管内诱导的神经病变(体细胞和肠道),肠粘膜损伤和炎症渗透相对持久。

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