Membrane-stabilizing and clot lysis activities of (±) citronellal: In-vitro studies

Showkoth Akbor , Mst. Farjanamul Haque , Shoyaeb Ahammed , Sakib Al Hasan , Sabbir Hosain , Rokibul Islam Chowdhury , Cassio Rocha Medeiros , Sloana Giesta Lemos Florencio , Henrique Douglas Melo Coutinho , Muhammad Torequl Islam
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Abstract

Numerous plants and their phytochemicals have been identified as having potential medicinal values and are used to treat different ailments worldwide. (±) Citronellal (CTL) is a monoterpene phytochemical with potential therapeutic benefits including anti-inflammatory, antioxidant, antifungal, and antibacterial actions.

Aim

The present study aimed to evaluate the membrane-stabilizing and clot-lysis activities of CTL through in vitro studies. For this, we performed hypotonic solution-induced erythrocyte lysing and human blood clot lysis methods to check the membrane-stabilizing and clot lysis capacities of CTL using acetylsalicylic acid (ASA) and streptokinase (STK) as standards, respectively. CTL exhibited concentration-dependent membrane-stabilizing activity with an IC50 = 28.83 ± 1.19 µg/mL. In the clot lysis test, CTL also showed a concentration-dependent clot lysing capacity, where it exhibited 50.46 ± 3.81 % clot lysis at a concentration of 160 μg/mL. In the latter case, the IC50 value was I158.22 ± 2.21 µg/mL. CTL exhibit potent membrane-stabilizing and moderate clot-lysis activity. We suppose that CTL may exert these effects, possibly through its capacity to inhibit inflammatory mediators. Further in vivo and in silico studies are required to elucidate CTL’s exact molecular mechanisms behind these biological effects.

(±)香茅醛的膜稳定和凝块裂解活性:体外研究
许多植物及其植物化学物质已被确认具有潜在的药用价值,并被用于治疗世界各地的不同疾病。(±)香茅醛(CTL)是一种单萜植物化学物质,具有潜在的治疗功效,包括抗炎、抗氧化、抗真菌和抗菌作用。为此,我们分别以乙酰水杨酸(ASA)和链激酶(STK)为标准,采用低渗溶液诱导红细胞裂解法和人血凝块裂解法检测 CTL 的膜稳定能力和凝块裂解能力。CTL 具有浓度依赖性膜稳定活性,IC50 = 28.83 ± 1.19 µg/mL。在血凝块溶解试验中,CTL 也表现出浓度依赖性血凝块溶解能力,当浓度为 160 μg/mL 时,血凝块溶解度为 50.46 ± 3.81%。在后一种情况下,IC50 值为 I158.22 ± 2.21 µg/mL。CTL 具有强大的膜稳定活性和适度的凝块分解活性。我们推测 CTL 可能是通过抑制炎症介质的能力来发挥这些作用的。要阐明 CTL 这些生物效应背后的确切分子机制,还需要进一步的体内和硅学研究。
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