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植物蛋白酶抑制剂在控制小鼠哮喘反应中起作用。

The Plant Proteinase Inhibitor Plays a Role in Controlling Asthma Response in Mice.

机构信息

Departamento de Clínica Médica, Faculdade de Medicina da Universidade de São Paulo, 01246-903 São Paulo, SP, Brazil.

Universidade Cidade de São Paulo, São Paulo, SP, Brazil.

出版信息

Biomed Res Int. 2018 Oct 1;2018:9274817. doi: 10.1155/2018/9274817. eCollection 2018.

DOI:10.1155/2018/9274817
PMID:30364003
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6188594/
Abstract

is a protein isolated from bark. It has been shown to exhibit several biological properties, including anti-inflammatory, analgesic, antitumor, and insecticidal activities. There are no studies evaluating the role of in experimental asthma models. . To evaluate the effects of on lung mechanics, inflammation, remodeling, and oxidative stress activation of mice with allergic pulmonary inflammation. . BALB/c mice (6-7 weeks old, 25-30g) were divided into four groups: nonsensitized and nontreated mice (C group, n=8); ovalbumin- (OVA-) sensitized and nontreated mice (OVA group, n=8); nonsensitized and -treated mice (C+CR group, n=8); OVA-sensitized and -treated mice (OVA+CR group, n=8). We evaluated hyperresponsiveness to methacholine, bronchoalveolar lavage fluid (BALF), pulmonary inflammation, extracellular matrix remodeling, and oxidative stress markers. treatment in OVA-sensitized mice (OVA+CR group) attenuated the following variables compared to OVA-sensitized mice without treatment (OVA group) (all p<0.05): (1) respiratory system resistance (Rrs) and elastance (Ers) after methacholine challenge; (2) total cells, macrophages, polymorphonuclear cells, and lymphocytes in BALF; (3) eosinophils and volume fraction of collagen and elastic fibers in the airway and alveolar wall according to histopathological and morphometry analysis; (4) IL-4-, IL-5-, IL-13-, IL-17-, IFN--, MMP-9-, TIMP-1-, TGF--, iNOS-, and NF-kB-positive cells and volume of 8-iso-PGF2 in airway and alveolar septa according to immunohistochemistry; and (5) IL-4, IL-5, and IFN- according to an ELISA. contributes to the control of hyperresponsiveness, pulmonary inflammation, extracellular matrix remodeling, and oxidative stress responses in an animal model of chronic allergic pulmonary inflammation.

摘要

是从树皮中分离得到的一种蛋白质。已证实其具有多种生物学特性,包括抗炎、镇痛、抗肿瘤和杀虫活性。目前尚无研究评估 在实验性哮喘模型中的作用。 。评估 在过敏性肺炎症小鼠模型中对肺力学、炎症、重塑和氧化应激激活的影响。 。将 BALB/c 小鼠(6-7 周龄,25-30g)分为四组:未致敏且未治疗的小鼠(C 组,n=8);卵清蛋白致敏且未治疗的小鼠(OVA 组,n=8);未致敏且给予 的小鼠(C+CR 组,n=8);OVA 致敏且给予 的小鼠(OVA+CR 组,n=8)。我们评估了对乙酰甲胆碱的高反应性、支气管肺泡灌洗液(BALF)、肺炎症、细胞外基质重塑和氧化应激标志物。与未治疗的 OVA 致敏小鼠(OVA 组)相比,在 OVA 致敏小鼠中给予 (OVA+CR 组)可减轻以下变量(均 p<0.05):(1)乙酰甲胆碱激发后呼吸系统阻力(Rrs)和弹性阻力(Ers);(2)BALF 中的总细胞、巨噬细胞、多形核细胞和淋巴细胞;(3)根据组织病理学和形态计量学分析,气道和肺泡壁中的嗜酸性粒细胞和胶原及弹性纤维体积分数;(4)气道和肺泡隔中根据免疫组织化学的 IL-4-、IL-5-、IL-13-、IL-17-、IFN--、MMP-9-、TIMP-1-、TGF--、iNOS-和 NF-kB-阳性细胞和 8-iso-PGF2 体积;(5)ELISA 法测定气道和肺泡隔中的 IL-4、IL-5 和 IFN-。 有助于控制慢性过敏性肺炎症动物模型中的高反应性、肺炎症、细胞外基质重塑和氧化应激反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4537/6188594/4de92d9126ae/BMRI2018-9274817.007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4537/6188594/b9ca5b1b2b13/BMRI2018-9274817.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4537/6188594/01c819c90c88/BMRI2018-9274817.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4537/6188594/b794d917230d/BMRI2018-9274817.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4537/6188594/83f78d0d4215/BMRI2018-9274817.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4537/6188594/56b7158c7b75/BMRI2018-9274817.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4537/6188594/90c3fbd6b3ea/BMRI2018-9274817.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4537/6188594/4de92d9126ae/BMRI2018-9274817.007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4537/6188594/b9ca5b1b2b13/BMRI2018-9274817.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4537/6188594/01c819c90c88/BMRI2018-9274817.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4537/6188594/b794d917230d/BMRI2018-9274817.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4537/6188594/83f78d0d4215/BMRI2018-9274817.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4537/6188594/56b7158c7b75/BMRI2018-9274817.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4537/6188594/90c3fbd6b3ea/BMRI2018-9274817.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4537/6188594/4de92d9126ae/BMRI2018-9274817.007.jpg

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