Rodrigues da Silva Renata Evaristo, Pereira-de-Morais Luís, Alencar Silva Andressa de, Sena Bastos Carla Mikevely de, Kennedy-Feitosa Emanuel, Menezes Irwin Rose Alencar de, Weinreich Daniel, Leal-Cardoso José Henrique, Barbosa Roseli
Department of Biological Chemistry, Regional University of Cariri, 63105-000, Crato, CE, Brazil.
Department of Biological Chemistry, Regional University of Cariri, 63105-000, Crato, CE, Brazil.
Chem Biol Interact. 2025 Jan 5;405:111313. doi: 10.1016/j.cbi.2024.111313. Epub 2024 Nov 15.
Limonene, a monoterpene found in essential oils, has various activities, such as antifungal, antioxidant, neuroprotective, gastroprotective and vasorelaxant. However, the observation of limonene's biphasic effect in preclinical studies provides crucial information about its dose-dependent actions. Understanding this behavior is essential for optimizing therapeutic doses and anticipating possible side effects prior to clinical trials. The objective of this study is to provide a more detailed characterization and investigation of the mechanisms of action of limonene on the contractile tonus of isolated aorta.The experiments were carried out on aortic rings isolated from rats, subjected to isometric recording of contractions in their circular smooth muscle and exposed to different concentrations of limonene. It was found that limonene blocked the contraction induced by KCl (60 mM), but had a biphasic effect on the contraction induced by phenylephrine (0.1 μM). At lower concentrations, limonene was able to amplify the contraction induced by phenylephrine, while at higher concentrations, it inhibited it. The nitric oxide synthase blockers L-NAME and ruthenium red, a TRP ion channel blocker, did not significantly interfere with the biphasic character of limonene. However, indomethacin, a blocker of arachidonic acid derivatives, completely blocked the amplification of contraction induced by phenylephrine. In addition, limonene promoted relaxation in contractions induced by BAY-K 8644, a calcium channel agonist and by Ba. Limonene has complex effects on aortic tone, amplifying or inhibiting contractions, suggesting that the therapeutic window should be carefully studied to optimize clinical results.
柠檬烯是一种存在于香精油中的单萜,具有多种活性,如抗真菌、抗氧化、神经保护、胃保护和血管舒张作用。然而,临床前研究中对柠檬烯双相效应的观察为其剂量依赖性作用提供了关键信息。了解这种行为对于优化治疗剂量以及在临床试验前预测可能的副作用至关重要。本研究的目的是更详细地描述和研究柠檬烯对离体主动脉收缩张力的作用机制。实验在从大鼠分离的主动脉环上进行,对其环形平滑肌的收缩进行等长记录,并使其暴露于不同浓度的柠檬烯。结果发现,柠檬烯可阻断由氯化钾(60 mM)诱导的收缩,但对由去氧肾上腺素(0.1 μM)诱导的收缩具有双相效应。在较低浓度下,柠檬烯能够增强去氧肾上腺素诱导的收缩,而在较高浓度下则抑制该收缩。一氧化氮合酶阻滞剂L - 精氨酸甲酯(L - NAME)和钌红(一种瞬时受体电位离子通道阻滞剂)并未显著干扰柠檬烯的双相特性。然而,花生四烯酸衍生物阻滞剂吲哚美辛完全阻断了去氧肾上腺素诱导的收缩增强。此外,柠檬烯可促进由钙通道激动剂BAY - K 8644和钡诱导的收缩舒张。柠檬烯对主动脉张力具有复杂的影响,可增强或抑制收缩,这表明应仔细研究治疗窗口以优化临床效果。