α-Glucosidase and α-Amylase Inhibition Activities of Sarcococca coriacea Hook. And Sarcococca wallichii Staph. of Nepalese Origin

J. Baral, D. Shrestha, A. Adhikari
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Abstract

Diabetes mellitus is being severe health problem globally with an increasing number of patients every day. Due to the lack of effective and non-toxic medicine to cure diabetes, plants that are used in ethnomedicine may be a good source for antidiabetic drug discovery.  Plants of the Sarcococca genus are medicinally important and are used by local people for managing many diseases including diabetes. In the course of our continuous search of antidiabetic plants and pure compounds,  in vitro α-glucosidase, and α-amylase inhibition activity along with the antioxidant activity of methanolic extract of S. coriacea leaf ( Sc-A), S. coriacea stem (Sc-B), and dichloromethane fraction of methanolic extract of Sarcococca wallichi (Sw-D) were carried out. The research revealed dicholoromethane fraction of S. wallichii (Sw-D) with good inhibition of α- amylase enzyme (IC50= 53.79 ± 2.50), whereas Sc-B inhibits α-glucosidase (20.97±2.37) effectively. Similarly, Sc-A showed significant antioxidant activity with IC50=24.56±3.3. The total phenolic content on Sc-A and Sc-B was calculated as 151.35±4.42 mg GAE/g and 86.22±1.59 mg GAE/g whereas the total flavonoid content on Sc-A and Sc-B was found to be 21.61±4.88 mg QE/g and 24.09±4.02 mg QE/g respectively. Similarly, total phenolic and total flavonoid content on Sw-D were found to be 85.26±3.16 mg GAE/g and 21.57±1.26 mg QE/g. To the best of our knowledge, this is the first report of α-glucosidase and α-amylase inhibition activity in these plants. This research work has scientifically supported the use of these plants to manage diabetes by local people and has explored new plants for antidiabetic drug discovery research.
麻豆α-葡萄糖苷酶和α-淀粉酶抑制活性研究和疣状葡萄球菌。源自尼泊尔的
糖尿病是全球范围内严重的健康问题,每天都有越来越多的患者。由于目前缺乏有效且无毒的治疗糖尿病的药物,民族医学中使用的植物可能是发现抗糖尿病药物的良好来源。麻豆属植物具有重要的药用价值,被当地人用来治疗包括糖尿病在内的许多疾病。在不断寻找抗糖尿病植物和纯化合物的过程中,我们对山参叶(Sc-A)、山参茎(Sc-B)和山参醇提物(sd - d)的α-葡萄糖苷酶和α-淀粉酶的体外抑制活性以及抗氧化活性进行了研究。研究发现,华氏沙棘二氯甲烷组分(Sw-D)对α-淀粉酶有较好的抑制作用(IC50= 53.79±2.50),Sc-B组分对α-葡萄糖苷酶有较好的抑制作用(IC50= 20.97±2.37)。Sc-A具有显著的抗氧化活性,IC50=24.56±3.3。Sc-A和Sc-B的总酚含量分别为151.35±4.42 mg GAE/g和86.22±1.59 mg GAE/g,而Sc-A和Sc-B的总黄酮含量分别为21.61±4.88 mg QE/g和24.09±4.02 mg QE/g。Sw-D的总酚和总黄酮含量分别为85.26±3.16 mg GAE/g和21.57±1.26 mg QE/g。据我们所知,这是这些植物中α-葡萄糖苷酶和α-淀粉酶抑制活性的首次报道。本研究为当地居民利用这些植物治疗糖尿病提供了科学依据,并为抗糖尿病药物的研发探索了新的植物。
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