Pharmacy research at URI: mining red maple (Acer rubrum) trees for novel therapeutics to manage diabetes.
Journal: 2012/December - Medicine and health, Rhode Island
ISSN: 1086-5462
PUBMED: 23094425
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Med Health R I 95(9): 283-284

Mining Red Maple (<em>Acer rubrum</em>) Trees for Novel Therapeutics to Manage Diabetes

Plant polyphenols as α-glucosidase inhibitors

Dietary carbohydrates are hydrolyzed by pancreatic α-amylase with absorption aided by α-glucosidases and thus, inhibition of the activities of these enzymes is a promising approach for managing T2DM. In fact, the clinical α-glucosidase inhibitor, acarbose, has been shown to effectively reduce glycated hemoglobin levels when given as monotherapy or as an add-on to other antidiabetic drug treatment1. Additionally, a fixed dose combination of acarbose and metformin was reported to be superior to metformin alone in controlling HbA1C, fasting blood glucose, and post prandial blood glucose levels in T2DM patients2, as well as, enhances the blood glucose control in patients with T2DM3. Multiple plant-derived polyphenols have been investigated as α-glucosidase inhibitors. Extracts from grape seeds and green tea been demonstrated to exert inhibition on α-glucosidase activity4. We recently have shown a similar activity for phenolic-enriched extracts from the bark of Acer rubrum, commonly known as red maple.

Study of maple for novel therapeutics

The sugar maple (Acer saccharum) and red maple plant species are native to eastern North America and highly regarded for their sap which is used to produce the natural sweetener, maple syrup. Our laboratory has recently identified a number of phenolic compounds native in maple plant parts that are also present in maple syrup5.

Here we report a case study in which the ability of red maple bark extract (MBE) to decrease elevation of blood glucose levels was investigated. Male adult C57BL/6 mice were administered MBE in combination with a bolus sucrose challenge to evaluate the effect of MBE or acarbose on α-glucosidase activity in vivo according to described methods6. As expected, mice receiving a bolus sucrose challenge increased blood glucose concentration 30, 60, and 90 minutes after administration compared to initial blood glucose concentration (Figure 1). Both MBE and acarbose significantly lowered blood glucose concentrations at these time intervals after the sucrose challenge. Compared to acarbose, MBE was less effective, but did impart a significant inhibitory effect. We now hope to further purify and evaluate individual phytochemicals of MBE to evaluate for activity against sucrose-induced glucose elevation.

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Adult male C57BL/6 mice were administered sucrose (3g/kg BW), sucrose and acarbose (3g/kg BW + 3 mg/kg BW), or 3) sucrose and maple bark extract (3g/kg BW+150mg/kg BW) by oral gavage. Blood glucose levels were determined by tail bleed at 0, 30, 60, 90, and 120 minutes post sucrose administration. An asterisk (*) denotes statistical significance (p<0.05) from the sucrose treatment group.

We have demonstrated previously that phenolic glycosides are present in various maple constituents. The isolated compounds and extracts inhibit α-glucosidase activity in vitro7,8. Recently, multiple gallotannins, named maplexins A-E, were isolated from red maple stems and bark7,8. These maplexin compounds were shown in vitro to possess more inhibitory activity than acarbose for inhibition of α-glucosidase activity (IC50= 8 vs. 160 µM; maplexin E vs. acarbose, respectively). These interesting maplexin compounds, that are as effective as acarbose in vitro, will be further evaluated and developed to determine whether they impart beneficial properties in preventing blood glucose elevations in vivo. Overall, we report that MBE contains bioactive constituents that can potentially aid in the regulation of blood glucose control after carbohydrate challenge

Going forward as collaborators, we will continue to explore how bioactive extracts and molecules isolated from plants can impart beneficial effects on metabolic syndrome. As metabolic syndrome encompasses T2DM, dyslipidemia, systemic inflammation, and Non-alcoholic fatty liver disease, the potential therapeutics isolated will be tested in various cell-based and in vivo models. We are currently exploring anti-inflammatory effects of maple-derived extracts and compounds, as well as, the potential for plant-derived extracts to augment weight loss and T2DM therapies. Ultimately, we hope that identification of beneficial components in foods commonly consumed can arm the consumer with information to make better food choices that can be synergistic with drug therapies used to treat T2DM. We also will continue to mine botanicals for potential therapies to treat T2DM or enhance activity of commonly prescribed anti-diabetes therapies.

Acknowledgments

FUNDING SOURCES. This project was supported by funding provided by Agriculture and Agri-Food Canada through the Developing Innovative Agri Products (DIAP) initiative and, in part, by The National Institute of Health (R01ES-016042-03 and 3R-01ES-016042-2S2). The authors would like to thank Mr. J. Peter Morgan for assistance with plant authentication.

Corresponding author.

Type 2 diabetes mellitus (T2DM) accounts for about 90% of all diagnosed cases of diabetes in adults with over 200 million people suffering from this disease worldwide. In the United States alone, in 2007, 10% of American adults had diabetes and the cost to manage diabetes was $174 billion and this figure is expected to skyrocket (Centers for Disease Control and Prevention, 2010). Plants and their derived products have been used for centuries by various cultures as traditional medicines for the management of diabetes. Plants contain secondary metabolites (known as phytochemicals; 'phyto' means plant), which are implicated in the prevention and treatment of several chronic human diseases, including diabetes. Among these natural products, polyphenols and phenolic glycosides, have attracted significant interests for their anti-diabetic properties.

References

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