α-Glucosidase, Angiotensin-converting Enzyme, and Acetylcholinesterase Inhibitory Activities of a Marine Red Alga Galaxaura oblongata

Kimnard Joseph Magsacay Duat, Chona De Guzman Gelani
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Abstract

Seaweeds have gained interest from the pharmaceutical industry due to their diverse secondary metabolites with potential applications in the prevention and treatment of lifestyle diseases. In spite of the abundance of seaweeds in the coastal area of Iligan Bay in the Philippines, there has been limited investigation into their pharmacological properties. Therefore, this study aimed to evaluate the in vitro α-glucosidase inhibition, angiotensin-converting enzyme (ACE) inhibition, and acetylcholinesterase (AChE) inhibition properties of various fractions obtained from the marine red alga Galaxaura oblongata. The methanol extract of G. oblongata was sequentially partitioned into hexane, dichloromethane, ethyl acetate, butanol, and methanol fractions. All assays were performed in vitro and microplate based. The results of α-glucosidase inhibition activity assay showed that the n-hexane fraction and dichloromethane fraction exhibited greater than 50% inhibitory activity at 200 ppm. Furthermore, ACE inhibition activity assay revealed that dichloromethane fraction, ethyl acetate fraction, and butanol fraction displayed ACE inhibition activity above 50% at 250 ppm. In addition, the hexane fraction, dichloromethane fraction, and ethyl acetate fraction demonstrated potent AChE inhibitory activity at 250 ppm. Overall, the findings show that G. oblongata has antidiabetic, anti-hypertensive, and neuroprotective potentials. This is the first report of the in vitro α-Glucosidase, ACE, and AChE inhibition activities of G. oblongata. Further investigation and purification of the highly potent fractions in each assay is highly suggested to identify and characterize the compounds responsible for the observed bioactivities, which could serve as possible leads for drug discovery efforts in the management of various lifestyle diseases.
海洋红藻α-葡萄糖苷酶、血管紧张素转换酶和乙酰胆碱酯酶抑制活性的研究
由于海藻具有多种次生代谢产物,在预防和治疗生活方式疾病方面具有潜在的应用前景,因此引起了制药行业的兴趣。尽管菲律宾Iligan湾沿海地区有丰富的海藻,但对其药理特性的研究有限。因此,本研究旨在评价海洋红藻不同部位对α-葡萄糖苷酶、血管紧张素转换酶(ACE)和乙酰胆碱酯酶(AChE)的体外抑制作用。将龙葵甲醇提取物依次分为己烷、二氯甲烷、乙酸乙酯、丁醇和甲醇馏分。所有实验均在体外和微孔板基础上进行。α-葡萄糖苷酶抑制活性测定结果表明,正己烷馏分和二氯甲烷馏分在200 ppm时的抑制活性均大于50%。此外,ACE抑制活性测定表明,在250 ppm下,二氯甲烷组分、乙酸乙酯组分和丁醇组分的ACE抑制活性均在50%以上。此外,己烷馏分、二氯甲烷馏分和乙酸乙酯馏分在250 ppm时表现出有效的AChE抑制活性。综上所述,黄芪具有抗糖尿病、抗高血压和神经保护作用。本文首次报道了长叶草α-葡萄糖苷酶、ACE和AChE的体外抑制活性。强烈建议进一步研究和纯化每个测定中的高效组分,以确定和表征导致所观察到的生物活性的化合物,这可能为管理各种生活方式疾病的药物发现工作提供可能的线索。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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