Unnikrishnan P S, Suthindhiran K, Jayasri M A
Marine Biotechnology and Bioproducts Laboratory, School of Biosciences and Technology VIT University, Vellore, Tamil Nadu, India.
Pharmacogn Mag. 2015 Oct;11(Suppl 4):S511-5. doi: 10.4103/0973-1296.172954.
In the continuing search for safe and efficient antidiabetic drug, marine algae become important source which provide several compounds of immense therapeutic potential. Alpha-amylase, alpha-glucosidase inhibitors, and antioxidant compounds are known to manage diabetes and have received much attention recently. In the present study, four green algae (Chaetomorpha aerea, Enteromorpha intestinalis, Chlorodesmis, and Cladophora rupestris) were chosen to evaluate alpha-amylase, alpha-glucosidase inhibitory, and antioxidant activity in vitro.
The phytochemical constituents of all the extracts were qualitatively determined. Antidiabetic activity was evaluated by inhibitory potential of extracts against alpha-amylase and alpha-glucosidase by spectrophotometric assays. Antioxidant activity was determined by 2,2-diphenyl-1-picrylhydrazyl, hydrogen peroxide (H2O2), and nitric oxide scavenging assay. Gas chromatography-mass spectrometry (GC-MS) analysis was carried out to determine the major compound responsible for its antidiabetic action.
Among the various extracts screened, chloroform extract of C. aerea (IC50 - 408.9 μg/ml) and methanol extract of Chlorodesmis (IC50 - 147.6 μg/ml) showed effective inhibition against alpha-amylase. The extracts were also evaluated for alpha-glucosidase inhibition, and no observed activity was found. Methanol extract of C. rupestris showed notable free radical scavenging activity (IC50 - 666.3 μg/ml), followed by H2O2 (34%) and nitric oxide (49%). Further, chemical profiling by GC-MS revealed the presence of major bioactive compounds. Phenol, 2,4-bis (1,1-dimethylethyl) and z, z-6,28-heptatriactontadien-2-one were predominantly found in the methanol extract of C. rupestris and chloroform extract of C. aerea.
Our results demonstrate that the selected algae exhibit notable alpha-amylase inhibition and antioxidant activity. Therefore, characterization of active compounds and its in vivo assays will be noteworthy.
Four green algae were chosen to evaluate alpha-amylase, alpha-glucosidase inhibitory, and antioxidant activity in vitro C. aerea and Chlorodesmis showed significant inhibition against alpha-amylase, and C. rupestris showed notable free radical scavenging activityNo observed activity was found against alpha-glucosidaseGC-MS analysis of the active extracts reveals the presence of major compounds which gives an insight on the antidiabetic and antioxidant activity of these algae. Abbreviations used: DPPH: 2,2-diphenyl-1-picrylhydrazyl, BHT: Butylated hydroxytoluene, GC-MS: Gas chromatography-mass spectrometry.
在持续寻找安全有效的抗糖尿病药物的过程中,海藻成为了重要来源,它能提供多种具有巨大治疗潜力的化合物。已知α-淀粉酶、α-葡萄糖苷酶抑制剂和抗氧化化合物可用于控制糖尿病,且最近受到了广泛关注。在本研究中,选取了四种绿藻(铜藻、肠浒苔、绿管浒苔和石莼)来评估其体外α-淀粉酶、α-葡萄糖苷酶抑制活性和抗氧化活性。
对所有提取物的植物化学成分进行定性测定。通过分光光度法检测提取物对α-淀粉酶和α-葡萄糖苷酶的抑制潜力来评估抗糖尿病活性。通过2,2-二苯基-1-苦基肼自由基清除法、过氧化氢(H2O2)清除法和一氧化氮清除法测定抗氧化活性。采用气相色谱-质谱联用(GC-MS)分析来确定其抗糖尿病作用的主要化合物。
在筛选的各种提取物中,铜藻的氯仿提取物(IC50 - 408.9 μg/ml)和绿管浒苔的甲醇提取物(IC50 - 147.6 μg/ml)对α-淀粉酶表现出有效抑制作用。还对提取物进行了α-葡萄糖苷酶抑制活性评估,但未观察到活性。石莼的甲醇提取物表现出显著的自由基清除活性(IC50 - 666.3 μg/ml),其次是对H2O2(清除率34%)和一氧化氮(清除率49%)的清除活性。此外,GC-MS化学分析揭示了主要生物活性化合物的存在。在石莼的甲醇提取物和铜藻的氯仿提取物中主要发现了2,4-双(1,1-二甲基乙基)苯酚和z,z-6,28-三十七碳二烯-2-酮。
我们的结果表明,所选藻类表现出显著的α-淀粉酶抑制和抗氧化活性。因此,对活性化合物进行表征及其体内试验将值得关注。
选取四种绿藻评估其体外α-淀粉酶、α-葡萄糖苷酶抑制活性和抗氧化活性。铜藻和绿管浒苔对α-淀粉酶表现出显著抑制作用,石莼表现出显著的自由基清除活性。未观察到对α-葡萄糖苷酶的抑制活性。对活性提取物的GC-MS分析揭示了主要化合物的存在,这为这些藻类的抗糖尿病和抗氧化活性提供了深入了解。使用的缩写:DPPH:2,2-二苯基-1-苦基肼,BHT:丁基羟基甲苯,GC-MS:气相色谱-质谱联用。