Division of Pharmaceutical Sciences Arnold & Marie Schwartz College of Pharmacy & Health Sciences, Long Island University, Brooklyn, NY, USA.
Fairleigh Dickinson University School of Pharmacy and Health Sciences, Teaneck, NJ, USA.
Purinergic Signal. 2020 Sep;16(3):415-426. doi: 10.1007/s11302-020-09697-z. Epub 2020 Aug 13.
Animal models of asthma have shown that limonene, a naturally occurring terpene in citrus fruits, can reduce inflammation and airway reactivity. However, the mechanism of these effects is unknown. We first performed computational and molecular docking analyses that showed limonene could bind to both A and A receptors. The pharmacological studies were carried out with A adenosine receptor knock-out (AKO) and wild-type (WT) mice using ovalbumin (OVA) to generate the asthma phenotype. We investigated the effects of limonene on lung inflammation and airway responsiveness to methacholine (MCh) and NECA (nonselective adenosine analog) by administering limonene as an inhalation prior to OVA aerosol challenges in one group of allergic mice for both WT and KO. In whole-body plethysmography studies, we observed that airway responsiveness to MCh in WT SEN group was significantly lowered upon limonene treatment but no effect was observed in AKO. Limonene also attenuated NECA-induced airway responsiveness in WT allergic mice with no effect being observed in AKO groups. Differential BAL analysis showed that limonene reduced levels of eosinophils in allergic WT mice but not in AKO. However, limonene reduced neutrophils in sensitized AKO mice, suggesting that it may activate A receptors as well. These data indicate that limonene-induced reduction in airway inflammation and airway reactivity occurs mainly via activation of AAR but A receptors may also play a supporting role.
哮喘的动物模型表明,柠檬烯是柑橘类水果中一种天然存在的萜烯,可以减轻炎症和气道反应性。然而,这些作用的机制尚不清楚。我们首先进行了计算和分子对接分析,表明柠檬烯可以与 A 和 A 受体结合。使用卵清蛋白 (OVA) 生成哮喘表型,在 A 腺苷受体敲除 (AKO) 和野生型 (WT) 小鼠中进行了药理学研究。我们通过在一组 WT 和 KO 过敏小鼠的 OVA 气溶胶挑战前进行柠檬烯吸入,研究了柠檬烯对肺炎症和气道对乙酰甲胆碱 (MCh) 和 NECA (非选择性腺苷类似物) 反应性的影响。在全身生理记录仪研究中,我们观察到 WT SEN 组对 MCh 的气道反应性在用柠檬烯处理后显著降低,但在 AKO 中未观察到。柠檬烯还可减弱 WT 过敏小鼠中 NECA 诱导的气道反应性,但在 AKO 组中未观察到。差异 BAL 分析表明,柠檬烯降低了过敏 WT 小鼠中嗜酸性粒细胞的水平,但在 AKO 中没有观察到。然而,柠檬烯减少了致敏 AKO 小鼠中的中性粒细胞,表明它可能也激活了 A 受体。这些数据表明,柠檬烯诱导的气道炎症和气道反应性降低主要通过激活 AAR 发生,但 A 受体也可能发挥支持作用。