首页> 美国卫生研究院文献>Cancer Biology Therapy >Protective effects of alanyl-glutamine supplementation against nelfinavir-induced epithelial impairment in IEC-6 cells and in mouse intestinal mucosa
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Protective effects of alanyl-glutamine supplementation against nelfinavir-induced epithelial impairment in IEC-6 cells and in mouse intestinal mucosa

机译:补充丙氨酰谷氨酰胺对奈非那韦诱导的IEC-6细胞和小鼠肠粘膜上皮损伤的保护作用

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摘要

Purpose: Human Immunodefiency Virus (HIV) protease inhibitors (PI) remain a crucial component of highly active therapy (HAART) and recently have been demonstrated to have potent antitumor effect on a wide variety of tumor cell lines. However, discontinuation of therapy is an important issue, which may be related to various side-effects, especially diarrhea. The aim of this study was to evaluate the effects of nelfinavir (NFV), an HIV PI, and of alanyl-glutamine (AQ) supplementation, on intestinal cell migration, proliferation, apoptosis and necrosis, using IEC-6 cells and on intestinal crypt depth, villus length, villus area, mitotic index and apoptosis in Swiss mice. Methods: Migration was evaluated at 12 and 24 h after injury using a wound healing assay. Cellular proliferation was measured indirectly at 24 and 48 h using tetrazolium salt WST-1. Apoptosis and necrosis were measured by flow cytometry using the Annexin V assay. Intestinal morphometry and mitotic index in vivo were assessed following a seven-day treatment with 100 mg/kg of NFV, given orally. In vivo proliferation and apoptosis were evaluated by intestinal crypt mitotic index and immunohistochemistry, respectively. Results: In vitro, AQ supplementation enhanced IEC-6 cell migration and proliferation, following challenge with NFV. In vivo, AQ increased intestinal villus length, villus area, crypt depth and cell proliferation and cell migration, following treatment with NFV. AQ did not decrease cell death induced by NFV both in vivo and in vitro. Conclusions: AQ supplementation is potentially beneficial in preventing the effects of PIs, such as NFV, in the intestinal tract.
机译:目的:人类免疫缺陷病毒(HIV)蛋白酶抑制剂(PI)仍然是高活性疗法(HAART)的重要组成部分,最近已被证明对多种肿瘤细胞系具有有效的抗肿瘤作用。但是,中止治疗是一个重要问题,可能与各种副作用有关,尤其是腹泻。这项研究的目的是评估使用IEC-6细胞和肠隐窝对纳非那韦(NFV),HIV PI和丙氨酰谷氨酰胺(AQ)的补充对肠道细胞迁移,增殖,凋亡和坏死的影响。瑞士小鼠的深度,绒毛长度,绒毛面积,有丝分裂指数和细胞凋亡。方法:使用伤口愈合试验评估受伤后12和24小时的迁移情况。使用四唑盐WST-1在24和48小时间接测量细胞增殖。使用膜联蛋白V测定法通过流式细胞术测量细胞凋亡和坏死。在口服给予100 mg / kg NFV 7天后,评估了体内肠道形态和有丝分裂指数。分别通过肠隐窝有丝分裂指数和免疫组织化学评估体内增殖和凋亡。结果:在体外,AQ补充剂在受到NFV攻击后增强了IEC-6细胞的迁移和增殖。在体内,用NFV治疗后,AQ会增加肠道绒毛长度,绒毛面积,隐窝深度以及细胞增殖和细胞迁移。在体内和体外,AQ均未降低NFV诱导的细胞死亡。结论:补充AQ可能对预防PIs(例如NFV)在肠道中的作用有益。

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