Biphasic effect of limonene on contraction of isolated rat aorta

IF 4.7 2区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Renata Evaristo Rodrigues da Silva , Luís Pereira-de-Morais , Andressa de Alencar Silva , Carla Mikevely de Sena Bastos , Emanuel Kennedy-Feitosa , Irwin Rose Alencar de Menezes , Daniel Weinreich , José Henrique Leal-Cardoso , Roseli Barbosa
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Abstract

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 Ba2+. Limonene has complex effects on aortic tone, amplifying or inhibiting contractions, suggesting that the therapeutic window should be carefully studied to optimize clinical results.

Abstract Image

柠檬烯对离体大鼠主动脉收缩的双相效应
柠檬烯是精油中的一种单萜,具有抗真菌、抗氧化、神经保护、胃肠保护和血管舒张等多种活性。然而,在临床前研究中观察到的柠檬烯的双相效应提供了有关其剂量依赖性作用的重要信息。在临床试验之前,了解这种行为对于优化治疗剂量和预测可能出现的副作用至关重要。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力的作用机制。实验对象是从大鼠身上分离出的主动脉环,对其环状平滑肌进行等距收缩记录,并暴露于不同浓度的柠檬烯。实验发现,柠檬烯能阻止氯化钾(60 mM)引起的收缩,但对苯肾上腺素(0.1 μM)引起的收缩有双相作用。在较低浓度下,柠檬烯能放大苯肾上腺素诱导的收缩,而在较高浓度下,它则能抑制收缩。一氧化氮合酶阻断剂 L-NAME 和 TRP 离子通道阻断剂钌红对柠檬烯的双相特性没有明显干扰。然而,花生四烯酸衍生物阻断剂吲哚美辛完全阻断了苯肾上腺素诱导的收缩放大作用。此外,在钙通道激动剂 BAY-K 8644 和 Ba2+ 诱导的收缩中,柠檬烯能促进松弛。柠檬烯对主动脉张力有复杂的影响,可放大或抑制收缩,这表明应仔细研究治疗窗口,以优化临床效果。
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来源期刊
CiteScore
7.70
自引率
3.90%
发文量
410
审稿时长
36 days
期刊介绍: Chemico-Biological Interactions publishes research reports and review articles that examine the molecular, cellular, and/or biochemical basis of toxicologically relevant outcomes. Special emphasis is placed on toxicological mechanisms associated with interactions between chemicals and biological systems. Outcomes may include all traditional endpoints caused by synthetic or naturally occurring chemicals, both in vivo and in vitro. Endpoints of interest include, but are not limited to carcinogenesis, mutagenesis, respiratory toxicology, neurotoxicology, reproductive and developmental toxicology, and immunotoxicology.
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