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从诺丽(Morinda citrifolia L.)种子中分离出的脂质转移蛋白对伊立替康诱导的小鼠肠道黏膜炎的治疗作用。

Therapeutic effects of a lipid transfer protein isolated from Morinda citrifolia L. (noni) seeds on irinotecan-induced intestinal mucositis in mice.

机构信息

Department of Physiology and Pharmacology, Federal University of Ceará, Campus do Porangabuçu, Fortaleza, Ceará, 60430-275, Brazil.

Department of Biochemistry and Molecular Biology, Federal University of Ceará, Campus do Pici Prof. Prisco Bezerra, Fortaleza, Ceará, 60440-900, Brazil.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 2022 Sep;395(9):1097-1107. doi: 10.1007/s00210-022-02267-7. Epub 2022 Jul 1.

DOI:10.1007/s00210-022-02267-7
PMID:35776167
Abstract

This work aimed to evaluate the activity of a lipid transfer protein isolated from Morinda citrifolia L. seeds, McLTP, on the development of intestinal mucositis following irinotecan administration. McLTP (0.5, 2, and 8 mg/kg, i.v.) was injected into mice 1h before irinotecan administration (75 mg/kg, i.p.; 4 days), and then for additional 6 days. Seven days after the first dose of irinotecan, diarrhea was assessed, and the intestine was removed for histological evaluation, assessment of intestinal over-contractility, measurement of myeloperoxidase (MPO), proinflammatory cytokines and chemokine (IL-1, IL-6, and KC levels - a murine homolog of human IL-8 chemokine), analysis of cyclooxygenase 2 (COX-2), nuclear factor kappa B (NF-κB), and nitric oxide synthase (iNOS) expression. At the two highest doses, McLTP administration decreased mortality and diarrhea. McLTP (8 mg/kg, i.v.) significantly prevented irinotecan-induced intestinal damage and led to a reduction in over-contractility of the intestinal muscle (p < 0.05). Moreover, McLTP decreased the MPO, IL-1β, IL-6, and KC levels by 74.7%, 42%, 92.9%, and 95.9%, respectively. Also, the expression of COX-2, NF-κB, and iNOS was reduced. Our study provides a potential new therapeutic for preventing irinotecan-induced mucositis, improved clinical parameters, and reduced inflammation.

摘要

本研究旨在评估从桑黄子中分离得到的脂转移蛋白(McLTP)对伊立替康给药后肠道黏膜炎发展的活性。McLTP(0.5、2 和 8mg/kg,iv)在伊立替康给药前 1 小时(75mg/kg,ip;4 天)注射入小鼠体内,然后再注射 6 天。伊立替康首次给药后 7 天,评估腹泻情况,并取出肠道进行组织学评估、肠过度收缩性评估、髓过氧化物酶(MPO)、促炎细胞因子和趋化因子(IL-1、IL-6 和 KC 水平-人类 IL-8 趋化因子的鼠类同源物)、环氧化酶 2(COX-2)、核因子 kappa B(NF-κB)和一氧化氮合酶(iNOS)表达分析。在两个最高剂量下,McLTP 给药可降低死亡率和腹泻。McLTP(8mg/kg,iv)可显著预防伊立替康引起的肠道损伤,并导致肠道肌肉过度收缩性降低(p<0.05)。此外,McLTP 使 MPO、IL-1β、IL-6 和 KC 水平分别降低了 74.7%、42%、92.9%和 95.9%。同时,COX-2、NF-κB 和 iNOS 的表达也减少了。本研究为预防伊立替康诱导的黏膜炎提供了一种新的潜在治疗方法,改善了临床参数并减少了炎症。

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