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气管内注射罂粟碱诱导的闭塞性细支气管炎:一种新型动物模型。

Bronchiolitis obliterans induced by intratracheal papaverine: a novel animal model.

作者信息

Svetlecic J, Molteni A, Herndon B

机构信息

University of Missouri-Kansas City School of Medicine, Pulmonary Research Laboratory, Gold 5 Lab of Pulmonary Research, M5-210, 2411 Holmes St., Kansas City, Missouri 64108, USA.

出版信息

Lung. 2004;182(2):119-34. doi: 10.1007/s00408-003-1049-3.

Abstract

Constrictive bronchiolitis obliterans (CBO), a highly fatal syndrome seen following toxicant exposure and lung transplantation, is in need of mechanistic study. This report creates an animal model of toxicant induced CBO, validates its pathology and suggests a physiologic mechanism for its origin. Papaverine, the alkaloid in Sauropus plants and responsible for human toxicant-induced CBO, was used to create the rat model. A mini-osmotic pump delivered papaverine intratracheally for up to 28 days (0.25 microL/hr, totaling 6.4 mg). Bronchoalveolar lavage (BAL) was measured. Lung tissue was evaluated for signs of CBO (H&E and Trichrome staining). Cytokines deregulated in human CBO were also measured (TGF-beta and eNOS). Peribronchial inflammation, extensive denudation and destruction of bronchial mucosa, as well as increased peribronchial collagen (all classic signs of CBO) were observed as early as 7 days in papaverine treated animals, with more extensive damage after 28 days. Significant elevations of TGF-beta and eNOS were seen in lung homogenates. Our toxicant induced model of CBO via a novel delivery method of intratracheal papaverine accurately reproduces pathology and cytokine profiles of human CBO. Papaverine has potential for producing CBO by multiple routes. This model introduces a vehicle for both understanding and development of innovative treatment for CBO.

摘要

闭塞性细支气管炎(CBO)是一种在接触毒物和肺移植后出现的高度致命综合征,需要进行机制研究。本报告建立了毒物诱导的CBO动物模型,验证了其病理学特征,并提出了其发病的生理机制。用罂粟碱(一种存在于守宫木属植物中的生物碱,可导致人类毒物诱导的CBO)建立大鼠模型。通过微型渗透泵经气管内给予罂粟碱,持续28天(0.25微升/小时,总量6.4毫克)。测量支气管肺泡灌洗(BAL)。对肺组织进行CBO体征评估(苏木精-伊红染色和三色染色)。还测量了在人类CBO中失调的细胞因子(转化生长因子-β和内皮型一氧化氮合酶)。在罂粟碱处理的动物中,早在7天就观察到了支气管周围炎症、支气管黏膜广泛剥脱和破坏,以及支气管周围胶原增加(所有CBO经典体征),28天后损伤更广泛。在肺匀浆中观察到转化生长因子-β和内皮型一氧化氮合酶显著升高。我们通过经气管内给予罂粟碱的新给药方法建立的毒物诱导CBO模型准确再现了人类CBO的病理学特征和细胞因子谱。罂粟碱有可能通过多种途径产生CBO。该模型为理解和开发CBO的创新治疗方法提供了一个载体。

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