α-Amylase, α-glucosidase and aldose reductase inhibitory and molecular docking studies on Tinospora cordifolia (Guduchi) leaf extract

IF 3.4 Q2 PHARMACOLOGY & PHARMACY
Hemlata Janardhan Bhosale, Shailesh Vaijeenath Mamdapure, Ramdas Balaji Panchal, Umesh Pravin Dhuldhaj
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引用次数: 0

Abstract

Background

Type II diabetes mellitus is posing a severe health threat throughout the globe due to its associated pathophysiological risks and high mortality rate. Carbohydrate catabolic enzymes, including α-amylase, α-glucosidase and aldose reductase, play an important role in the development of diabetes. The natural or synthetic inhibitors of these enzymes are crucial in reducing diabetes and its related complications. Tinospora cordifolia is a plant of great significance in Ayurveda due to its unique biological activities, including anti-diabetic properties. The present study aims to identify the active constituents of T. cordifolia leaves and evaluate the in vitro inhibitory potential of its ethanol extract constituents against α-amylase, α-glucosidase and aldose reductase activities.

Results

The ethanolic leaf extract of T. cordifolia inhibited the activities of α-amylase, α-glucosidase and aldose reductase in a dose-dependent manner. It was on par  with the standard inhibitors acarbose and quercetin. At 5 mg/ml, the noted % inhibition values of extract were 69.27 ± 0.17, 67.8 ± 0.26 and 62.55 ± 0.24, respectively, for α-amylase, α-glucosidase and aldose reductase. Using GC-MS analysis, neophytadiene, γ-sitosterol, phytol, phytyl palmitate, and phytyl acetate were identified as prominent constituents of the ethanolic extract. Based on molecular docking and ADME analysis, γ-sitosterol was found as the major reactive phytoconstituent, which showed the highest inhibitory potential against α-amylase, α-glucosidase and aldose reductase activities.

Conclusions

The present study identified γ-sitosterol as triplet inhibitor of α-amylase, α-glucosidase and aldose reductase and affirmed the ethno-medicinal significance of T. cordifolia leaves in the development of new anti-diabetic leads.

天竺葵叶提取物对α-淀粉酶、α-葡萄糖苷酶和醛糖还原酶的抑制作用及分子对接研究
背景II型糖尿病由于其相关的病理生理风险和高死亡率,正在对全球健康构成严重威胁。碳水化合物分解酶,包括α-淀粉酶、α-葡萄糖苷酶和醛糖还原酶,在糖尿病的发病过程中起着重要作用。这些酶的天然或合成抑制剂对减少糖尿病及其相关并发症至关重要。Tinospora cordifolia 是一种在阿育吠陀中具有重要意义的植物,因为它具有独特的生物活性,包括抗糖尿病特性。本研究旨在确定 T. cordifolia 叶子的活性成分,并评估其乙醇提取物成分对 α-淀粉酶、α-葡萄糖苷酶和醛糖还原酶活性的体外抑制潜力。它与标准抑制剂阿卡波糖和槲皮素的效果相当。在 5 毫克/毫升的浓度下,提取物对 α-淀粉酶、α-葡萄糖苷酶和醛糖还原酶的抑制率分别为 69.27 ± 0.17、67.8 ± 0.26 和 62.55 ± 0.24。通过气相色谱-质谱(GC-MS)分析,确定乙醇提取物的主要成分为新茶二烯、γ-谷甾醇、植醇、棕榈酸植脂酯和乙酸植脂酯。结论本研究发现γ-谷甾醇是α-淀粉酶、α-葡萄糖苷酶和醛糖还原酶的三重抑制剂,并肯定了T. cordifolia叶片在开发新的抗糖尿病药物方面的民族药用价值。
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来源期刊
自引率
0.00%
发文量
44
审稿时长
23 weeks
期刊介绍: Future Journal of Pharmaceutical Sciences (FJPS) is the official journal of the Future University in Egypt. It is a peer-reviewed, open access journal which publishes original research articles, review articles and case studies on all aspects of pharmaceutical sciences and technologies, pharmacy practice and related clinical aspects, and pharmacy education. The journal publishes articles covering developments in drug absorption and metabolism, pharmacokinetics and dynamics, drug delivery systems, drug targeting and nano-technology. It also covers development of new systems, methods and techniques in pharmacy education and practice. The scope of the journal also extends to cover advancements in toxicology, cell and molecular biology, biomedical research, clinical and pharmaceutical microbiology, pharmaceutical biotechnology, medicinal chemistry, phytochemistry and nutraceuticals.
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