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圆锥花榄仁树皮的体内外抗糖尿病活性:对糖尿病血糖控制可能的植物成分及机制的评估

In Vivo and In Vitro Antidiabetic Activity of Terminalia paniculata Bark: An Evaluation of Possible Phytoconstituents and Mechanisms for Blood Glucose Control in Diabetes.

作者信息

Ramachandran Subramaniam, Rajasekaran Aiyalu, Adhirajan Natarajan

机构信息

KMCH College of Pharmacy, Kovai Estate, Kalapatti Road, Coimbatore-641048, Tamil Nadu, India.

出版信息

ISRN Pharmacol. 2013 Jul 14;2013:484675. doi: 10.1155/2013/484675. Print 2013.

DOI:10.1155/2013/484675
PMID:23936668
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3725811/
Abstract

The present study was aimed to investigate in vivo, in vitro antidiabetic activity of aqueous extract of Terminalia paniculata bark (AETPB) and characterize its possible phytoconstituents responsible for the actions. Type 2 diabetes was induced in rats by streptozotocin-nicotinamide (65 mg/kg-110 mg/kg; i.p.) administration. Oral treatment of AETPB using rat oral needle at 100 and 200 mg/kg doses significantly (P < 0.001) decreased blood glucose and glycosylated haemoglobin levels in diabetic rats than diabetic control rats. AETPB-treated diabetic rats body weight, total protein, insulin, and haemoglobin levels were increased significantly (P < 0.001) than diabetic control rats. A significant (P < 0.001) reduction of total cholesterol and triglycerides and increase in high-density lipoprotein levels were observed in type 2 diabetic rats after AETPB administration. Presence of biomarkers gallic acid, ellagic acid, catechin, and epicatechin in AETPB was confirmed in HPLC analysis. AETPB and gallic acid showed significant (P < 0.001) enhancement of glucose uptake action in presence of insulin in muscle cells than vehicle control. Also AETPB inhibited pancreatic α -amylase and α -glucosidase enzymes. In conclusion, the above actions might be responsible for the antidiabetic activity of AETPB due to presence of gallic acid and other biomarkers.

摘要

本研究旨在考察榄仁树树皮水提取物(AETPB)的体内外抗糖尿病活性,并对其可能产生作用的植物成分进行表征。通过腹腔注射链脲佐菌素-烟酰胺(65mg/kg - 110mg/kg)诱导大鼠患2型糖尿病。以100和200mg/kg剂量用大鼠口服针剂对AETPB进行口服治疗,与糖尿病对照大鼠相比,显著(P < 0.001)降低了糖尿病大鼠的血糖和糖化血红蛋白水平。与糖尿病对照大鼠相比,AETPB治疗的糖尿病大鼠的体重、总蛋白、胰岛素和血红蛋白水平显著增加(P < 0.001)。在给予AETPB后,2型糖尿病大鼠的总胆固醇和甘油三酯显著降低(P < 0.001),高密度脂蛋白水平升高。高效液相色谱分析证实AETPB中存在生物标志物没食子酸、鞣花酸、儿茶素和表儿茶素。与溶媒对照相比,AETPB和没食子酸在肌肉细胞中胰岛素存在的情况下显著增强(P < 0.001)葡萄糖摄取作用。此外,AETPB抑制胰腺α -淀粉酶和α -葡萄糖苷酶。总之,由于没食子酸和其他生物标志物的存在,上述作用可能是AETPB抗糖尿病活性的原因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb72/3725811/e7dd9605b186/ISRN.PHARMACOLOGY2013-484675.007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb72/3725811/b6bc728ea877/ISRN.PHARMACOLOGY2013-484675.001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb72/3725811/8640c287b8d1/ISRN.PHARMACOLOGY2013-484675.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb72/3725811/e7dd9605b186/ISRN.PHARMACOLOGY2013-484675.007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb72/3725811/b6bc728ea877/ISRN.PHARMACOLOGY2013-484675.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb72/3725811/35aa4545ebb4/ISRN.PHARMACOLOGY2013-484675.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb72/3725811/f23d398c455c/ISRN.PHARMACOLOGY2013-484675.003.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb72/3725811/5ca0726e0849/ISRN.PHARMACOLOGY2013-484675.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb72/3725811/8640c287b8d1/ISRN.PHARMACOLOGY2013-484675.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb72/3725811/e7dd9605b186/ISRN.PHARMACOLOGY2013-484675.007.jpg

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