Giannini L, Nistri S, Mastroianni R, Cinci L, Vannacci A, Mariottini C, Passani M B, Mannaioni P F, Bani D, Masini E
Department of Preclinical and Clinical Pharmacology, University of Florence, Florence, Italy.
J Cell Mol Med. 2008 Dec;12(6A):2381-94. doi: 10.1111/j.1582-4934.2008.00258.x. Epub 2008 Feb 4.
In this study we evaluated the effects of the CB1/CB2 cannabinoid receptor agonist CP55, 940 (CP) on antigen-induced asthma-like reaction in sensitized guinea pigs and we tested the ability of the specific CB2 receptor antagonist SR144528 (SR) and CB1 receptor antagonist AM251 (AM) to interfere with the effects of CP. Ovalbumin-sensitized guinea pigs placed in a respiratory chamber were challenged with the antigen given by aerosol. CP (0.4 mg/kg b.wt.) was given i.p. 3 hrs before ovalbumin challenge. Sixty minutes before CP administration, some animals were treated i.p. with either AM, or SR, or both (0.1 mg/kg b.wt.). Respiratory parameters were recorded and quantified. Lung tissue specimens were then taken for histopathological and morphometric analyses and for eosinophilic major basic protein immunohistochemistry. Moreover, myeloperoxidase activity, 8-hydroxy-2-deoxyguanosine, cyclic adenosine monophosphate (cAMP) and guanosine monophosphate (cGMP) levels, and CB1 and CB2 receptor protein expression by Western blotting were evaluated in lung tissue extracts. In the bronchoalveolar lavage fluid, the levels of prostaglandin D2 and tumour necrosis factor-alpha TNF-alpha were measured. Ovalbumin challenge caused marked abnormalities in the respiratory, morphological and biochemical parameters assayed. Treatment with CP significantly reduced these abnormalities. Pre-treatment with SR, AM or both reverted the protective effects of CP, indicating that both CB1 and CB2 receptors are involved in lung protection. The noted treatments did not change the expression of cannabinoid receptor proteins, as shown by Western blotting. These findings suggest that targeting cannabinoid receptors could be a novel preventative therapeutic strategy in asthmatic patients.
在本研究中,我们评估了CB1/CB2大麻素受体激动剂CP55,940(CP)对致敏豚鼠抗原诱导的哮喘样反应的影响,并测试了特异性CB2受体拮抗剂SR144528(SR)和CB1受体拮抗剂AM251(AM)干扰CP作用的能力。将置于呼吸舱中的卵清蛋白致敏豚鼠通过气雾剂给予抗原进行激发。在卵清蛋白激发前3小时腹腔注射CP(0.4mg/kg体重)。在给予CP前60分钟,一些动物腹腔注射AM、或SR、或两者(0.1mg/kg体重)。记录并量化呼吸参数。然后取肺组织标本进行组织病理学和形态计量学分析以及嗜酸性粒细胞主要碱性蛋白免疫组织化学分析。此外,还评估了肺组织提取物中的髓过氧化物酶活性、8-羟基-2-脱氧鸟苷、环磷酸腺苷(cAMP)和环磷酸鸟苷(cGMP)水平,以及通过蛋白质印迹法检测的CB1和CB2受体蛋白表达。在支气管肺泡灌洗液中,测量前列腺素D2和肿瘤坏死因子-α(TNF-α)的水平。卵清蛋白激发导致所检测的呼吸、形态和生化参数出现明显异常。CP治疗显著减轻了这些异常。用SR、AM或两者预处理可逆转CP的保护作用,表明CB1和CB2受体均参与肺保护。如蛋白质印迹法所示,上述处理并未改变大麻素受体蛋白的表达。这些发现表明,靶向大麻素受体可能是哮喘患者一种新的预防性治疗策略。