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