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大麻素(CB)在变应原诱导的气道炎症的小鼠模型中的有益作用:CB1/CB2 受体的作用。

Beneficial effects of cannabinoids (CB) in a murine model of allergen-induced airway inflammation: role of CB1/CB2 receptors.

机构信息

ZAUM - Center for Allergy and Environment, Division of Environmental Dermatology and Allergy, Helmholtz Zentrum München/Technische Universität München (TUM), Ingolstädter Landstrasse 1, 85764 Neuherberg, Germany.

出版信息

Immunobiology. 2011 Apr;216(4):466-76. doi: 10.1016/j.imbio.2010.09.004. Epub 2010 Sep 18.

Abstract

The endocannabinoid system (ECS) consists of two cannabinoid (CB) receptors, namely CB(1) and CB(2) receptor, and their endogenous (endocannabinoids) and exogenous (cannabinoids, e.g. delta-9-tetrahydrocannabinol (THC)) ligands which bind to these receptors. Based on studies suggesting a role of THC and the ECS in inflammation, the objective of this study was to examine their involvement in type I hypersensitivity using a murine model of allergic airway inflammation. THC treatment of C57BL/6 wildtype mice dramatically reduced airway inflammation as determined by significantly reduced total cell counts in bronchoalveolar lavage (BAL). These effects were greatest when mice were treated during both, the sensitization and the challenge phase. Furthermore, systemic immune responses were significantly suppressed in mice which received THC during sensitization phase. To investigate a role of CB(1/2) receptors in this setting, we used pharmacological blockade of CB(1) and/or CB(2) receptors by the selective antagonists and moreover CB(1)/CB(2) receptor double-knockout mice (CB(1)(-/-)/CB(2)(-/-)) and found neither significant changes in the cell patterns in BAL nor in immunoglobulin levels as compared to wildtype mice. Our results indicate that the activation of the ECS by applying the agonist THC is involved in the development of type I allergies. However, CB(1)/CB(2) receptor-independent signalling seems likely in the observed results.

摘要

内源性大麻素系统 (ECS) 由两种大麻素 (CB) 受体,即 CB(1) 和 CB(2) 受体,以及它们的内源性 (内源性大麻素) 和外源性 (大麻素,如 δ-9-四氢大麻酚 (THC)) 配体组成,这些配体与这些受体结合。基于研究表明 THC 和 ECS 在炎症中的作用,本研究的目的是使用过敏性气道炎症的小鼠模型研究它们在 I 型超敏反应中的作用。用 THC 治疗 C57BL/6 野生型小鼠,通过显著减少支气管肺泡灌洗液 (BAL) 中的总细胞计数,可显著减轻气道炎症。当在致敏和挑战阶段均对小鼠进行治疗时,这些效果最大。此外,在致敏阶段接受 THC 治疗的小鼠的全身免疫反应也受到显著抑制。为了研究 CB(1/2) 受体在此环境中的作用,我们使用选择性拮抗剂对 CB(1)和/或 CB(2)受体进行药理学阻断,此外还使用 CB(1)/CB(2)受体双敲除小鼠 (CB(1)(-/-)/CB(2)(-/-)),与野生型小鼠相比,在 BAL 中的细胞模式或免疫球蛋白水平均未发现明显变化。我们的结果表明,应用激动剂 THC 激活 ECS 参与了 I 型过敏的发生。然而,在观察到的结果中,CB(1)/CB(2)受体非依赖性信号传递似乎很可能。

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