A Review of Coumarins and Coumarin-Related Compounds for Their Potential Antidiabetic Effect

Abstract

Background and aims:

Worldwide, type 2 diabetes mellitus accounts for a considerable burden of disease, with an estimated global cost of >800 billion USD annually. For this reason, the search for more effective and efficient therapeutic anti-diabetic agents is continuing. Coumarins are naturally derived and synthetic molecules with a wide variety of biological actions. The most common application of these molecules in medicine is for their thrombostatic activity. This study aims to give an overview of the current knowledge about the applicability of these chemical products in the therapeutic strategy against diabetes and its complications.

Methods:

For this purpose, we searched internet databases for publications and abstracts in English that investigated the effects of coumarins or coumarin-like agents with potential anti-diabetic activity.

Results:

The result is that a variety of these agents have proven in in vitro, in silico, and simple animal models to possess properties that may reduce the glucose absorption rate in the intestines, increase the level of insulin, increase the cellular uptake of glucose or reduce the gluconeogenesis. In addition, some of these agents also reduced the level of glycation of peptides in diabetic animal models and showed antioxidant properties.

Conclusion:

In conclusion, we can summarize that coumarins and their related derivatives may be potential antidiabetic agents. Useful formulations with appropriate pharmacokinetic and pharmacodynamic properties must be developed and tested for their efficacy and toxicity in comprehensive animal models before they can enter clinical trials.

Introduction

Type 2 diabetes mellitus is a chronic disease characterized by the heterogeneous disturbance of mainly glucose metabolism in the body, ultimately leading to chronic hyperglycemia. ¹ The disorder is caused mostly through impaired insulin action, followed frequently by impaired insulin secretion. ¹ According to a recent comprehensive review of epidemiological data, in 2017 almost 500 million people suffered worldwide from this disorder, reflecting a global prevalence rate of >6% and with some regions showing figures above 20%. ² The International Diabetes Federation estimated that the total cost of people suffering from this disease was about 850 billion USD for the same year. ³ Finally, the disease and its complications annually account for a mortality rate of up to 10%, ⁴ with more than 7 million reported deaths in the period of 2000 to 2016 in 108 countries. ⁵

The general opinion now is that a high postprandial blood glucose level ⁶ is an important risk factor for the development and progression of type 2 diabetes mellitus and its complications and that lowering this level should be one of the targets of treatment. ⁷ This level depends on the amount and rate of glucose absorbed in the intestine and the uptake by the liver and skeletal muscles. ⁸ The rate of absorption in the intestines can be limited through an inhibition of the digestion of the polysaccharides and disaccharides as well as limiting epithelial transport through specific glucose transporters in the intestinal epithelial cell membranes. ⁸

Transepithelial glucose transport in the intestines is facilitated by a sodium glucose cotransporter (SGLT)1 at the apical cell membrane and a glucose transporter (GLUT)2 at the basolateral membrane. ⁹ Inhibition of these could lead to colonic discomfort due to a higher than normal glucose availability to the microorganisms in the colon. ¹⁰ Nevertheless, a mild inhibition may slow the absorption of glucose in the intestines and hence flatten the postprandial glucose curve. ¹¹

Studies show that a number of synthetic as well as naturally occurring coumarins can inhibit the enzymes α-glucosidase or α-maltase, which convert the disaccharides into simple monosaccharides like glucose. The inhibitory effect on α-glucosidase can be described to the structure of coumarin-like compounds especially the C-C or C-O-C biaryl, terpene sidechain linkage, or the cyclobutane ring. ¹² Several in silico docking experiments have confirmed this hypothesis.^13-15 However, the abundance of studies have been performed in in vitro and animal models, while research on human subjects is not available and the applicability as true antidiabetic agents has yet to be confirmed.

In addition, type 2 diabetes mellitus is generally characterized as a condition with a disturbed action of insulin on the cellular uptake of glucose with or without a diminished insulin availability. ¹⁶ Insulin release by the pancreas is predominately nutrient triggered. ¹⁷ Advanced research has also identified other molecular mechanisms that may initiate insulin release. These are, among others, the release of glucagon-like peptide (GLP)-1 during meals ¹⁸ and the inhibition of K_ATP channels by sulfonyl(thio)urea derivatives that are used as oral antidiabetics. ¹⁹ Glucagon-like peptide 1 augments the release of insulin by the pancreas after meals through a separate mechanism (i.e., not yet fully understood),^20,21 but may involve an increased sensitivity of the beta-cells of the pancreas for glucose. ²² The glucose lowering effect of insulin is mainly through the promotion of peripheral cellular uptake of glucose with the aid of GLUT4 transporters.^23,24

The complications of diabetes are mostly the consequence of advanced glycation end products ²⁵ or oxidative processes.^26,27 Examples of these are the cataract found in the eyes of diabetics, which is predominantly the consequence of glycation of the normally highly transparent lens proteins ²⁸ and the diabetic retinopathy and nephropathy, which are more the consequence of oxidative damage to the blood vessels in these organs.^29,30

Consequently, therapeutic strategies for this metabolic disorder include inhibition of glucose processing and absorption in the intestines, ³¹ stimulation of hepatic and muscle uptake of glucose by insulin,^32,33 supplementing insulin, ³⁴ stimulating insulin release, ³⁵ decreasing peripheral insulin resistance, ³⁶ inhibition of glucose reabsorption in the kidneys, ³⁷ and prevention of the glycation and oxidation of biologically active proteins.^26,38 Up till now, no single best agent for therapy has been found, so the search for effective and more efficient pharmacological agents is continuing.

Coumarin (Figure 1) is a 1, 2-benzopyrone class of molecule that is abundantly found in many plants. ³⁹ The molecule and its related compounds have been evaluated for a variety of pharmacological properties such as antimicrobial, ⁴⁰ anti-inflammatory, ⁴¹ antidiabetic, ⁴² and antioxidant ⁴³ activity, as well as a significant influence on physiological processes like enzyme inhibitory activity. ⁴⁴ In plants, coumarins are often found in the form of glycosides and esters. Most of the time they are in a free form and many of them can sublimate. Coumaric compounds are lactones of 2-coumaric acid (2-hydroxy-Z-cinnamic acid) and are constructed by a benzene ring fused to an α-pyrone ring (Figure 1). ⁴⁵ Based on their chemical diversity and complexity, natural coumarins are subdivided in various classes like, but not limited to, simple coumarins, isocoumarins, furanocoumarins, pyranocoumarins (angular and linear), biscoumarins, and phenylcoumarins. ⁴⁶

Figure 1.

Basic structure of coumarin.

For the determination of coumarin in drugs, colorimetric, fluorometric, and liquid chromatographic methods are used. Preparative liquid chromatography and gel filtration are methods of isolating and purifying coumarins and their heterosides. They are photosensitive and when they are characterized by UV light absorption (320-380 nm), they can result in blue, green, and yellow fluorescence. ⁴⁶ The smell of coumarin is specific, sweet, and spicy, often like vanilla. Generally, they may have a bitter taste. ⁴⁵

The International Union of Pure and Applied Chemistry name of Coumarin is 2H-chromen-2-one. ⁴⁷ The general molecular formula of the molecule is C₉H₆O₂ and it has a relatively low molecular weight of 146.6 g/mol (Figure 1). ⁴⁵ The melting point of the substance is 71°C (344 K), the boiling point is 301.71°C (574.86 K), and its density is 0.935 g/cm³. The molecule is soluble in hot water, methanol, ethanol, ether, chloroform, and other organic reagents. ⁴⁶

Despite the wide availability of coumarins and their lead compounds and metabolites in natural products, ⁴⁸ their medical application until now has been mostly limited to the anticoagulant activity of warfarin derived from dicoumarol and its analogs. ⁴⁹ Warfarin (Figure 2) and its derivatives acenocoumarol (Figure 3) and fenprocoumon (Figure 4) are widely known for their thrombostatic properties. ⁵⁰

Figure 2.

Warfarin.

Figure 3.

Acenocoumarol.

Figure 4.

Fenprocoumon.

However, recent studies support the search for coumarins or related compounds with potential blood glucose lowering properties. For instance, several Structure-Activity Relationship studies showed that coumarins have the potential structure to bind to the active site of the enzymes α-glucosidase,^13,46,51 a key step in the digestion of disaccharides and absorption of glucose by the intestines, and aldose reductase ⁵² which is involved in the synthesis of advanced glycation end products, leading to complications in diabetes mellitus.

Furthermore, investigators successfully bound a coumarin to glucagon-like peptide (GLP)-1, with the result that the half-life of this intestinal peptide with insulin release stimulating properties increased significantly in rats. ⁵³ As mentioned earlier, GLP-1 augments the release of insulin by the pancreas after meals. The protein normally has a very short half life of only a few minutes. ²² In addition, coumarins reduced the glycation of peptides, ⁵⁴ a metabolic step leading to most of the complications in diabetes.^26,38 However, all available evidence has been derived from in vitro, in silico, and some animal studies.

The aim of this review is to present an overview of possible applications of coumarins or related compounds in the therapeutic strategies against type 2 diabetes mellitus and its complications. For this purpose, we reviewed the literature from the year 2000 onward. Preliminary searches revealed that before 2000, very few or no investigations were performed in this area. Despite this, older reports containing a clear lead toward the applicability of compounds were also included. The reported articles present examples of coumarins or their derivatives with different possible mechanisms of action against diabetes.

Methods

An extensive search of the PubMed, Medline, and Google Scholar databases was conducted to identify relevant reports concerning coumarins and different pathogenetic aspects of diabetes mellitus including intestinal processing of glucose, absorption of glucose, regulation of glucose metabolism, insulin secretion, insulin sensitivity, and complications of diabetes. The search strings included “coumarin AND glucose,” “coumarin AND diabetes mellitus,” “coumarin AND nephropathy,” “coumarin AND neuropathy,” and “coumarin AND retinopathy.” A preliminary search was performed in November 2020. The actual search was performed from 18th to 25th December 2020. Additional searches were performed in April and June 2021. We reviewed all publications in English and those having English abstracts. Articles reporting coumarin or coumarin related compounds with a possible antidiabetic activity in in vitro, in vivo, and in silico models were included. Articles cited in the reference lists of identified publications were considered as a potential source of information. Studies of raw material with a possible coumarin content that did not mention the exact (groups of) molecules or a specific mechanism of action were excluded. The compounds have been grouped according to their possible mechanisms in 3 categories, carbohydrate digestion and glucose absorption, cellular glucose uptake, and complications of Diabetes Mellitus. All figures were drawn with Chem Office 2016—ChemDraw.

Results

Results have been grouped by their possible mechanism of action. Table 1 gives an overview of the reported compounds, their possible mechanism of action, their source and the references citing them. Figures 5 to 14 show the chemical structures of the most cited and promising compounds.

Table 1.

Examples of coumarins with effects hinting toward a possible antidiabetic action.

Compound	Observed effect	Source	Research method	References
3-(5′-Methyl-2′-aryl-3′-[thiazol-2′-yl amino] thiazolidin-4′-one) coumarin	Hypoglycemic	Synthetic	In vivo/animal	Kini and Ghate 73
3-coumarincarbohydrazides	Inhibition of α-glucosidase and pancreatic lipase	Synthetic	In vitro/in silico	Xu et al 51
3-coumarincarbohydrazones	Inhibition of α-glucosidase	Synthetic	In vitro/in silico	Taha et al 13
4-hydroxy Pd-C-III coumarin	Inhibition of α-glucosidase Inhibition of Protein Tyrosine Phosphatase 1B	Semi-synthetic	In vitro	Ali et al 63
Coumarin	Prolonging half life of GLP1 Enhanced glycolysis and decreased gluconeogenesis Increasing insulin and decreasing glucose in diabetic rats Reduced protein glycation	Natural/semisynthetic	In vitro/in vivo/animals	Han et al 53 , Abul Qais and Ahmad 54 , Pari and Rajarajeswari 74
Coumarin diglycoside	Stimulation of insulin release	Natural	In vitro/cell culture	Cao et al 72
Coumarin-3-carboxylic acid derivatives	Decreased gluconeogenesis	Semi-synthetic	In vitro/cell culture	Ji et al 95
Coumarin-cyclic imide conjugates	Increased cellular uptake of glucose	Synthetic	In vitro/cell culture	Reddy et al 82
Decursinol	Inhibition of α-glucosidase	Natural	In vitro	Ali et al 63
Esculin	Increased cellular uptake of glucose	Natural	In vitro/cell culture/in vivo/animals	Mo et al 87
Ficusin	Increased cellular uptake of glucose	Natural	In vivo/animals/in silico	Irudayaraj et al 83
Flavonoid-coumarin hybrids	Inhibition of α-glucosidase/Increased glucose uptake by hepatic cellular cells	Synthetic	In vitro/cell culture	Sun et al 56
Fraxetin	Increased cellular uptake of glucose	Natural/semisynthetic	In vitro/cell culture/in vivo/animals	Mo et al 87
Isofraxidin	Lowers triglyceride and total cholesterol content of liver cells. Possible enhanced sensitivity for insulin	Natural	In vitro/cell culture/animals	Li et al 76
Isorutarine	Inhibition of α-glucosidase	Natural	In silico	Mishra et al 67
Osthole	Increased cellular uptake of glucose Increased bone fromation	Natural	In vitro/cell culture/in vivo/animals	Lee et al 85 , Alabi et al 86 , Mo et al 87 , Gao et al 97
Praeruptori	Inhibition of SGLT1	Natural	In vitro/cell culture	Oranje et al 69
Pteryxin	Selective inhibition of SGLT1 and Lowering of intracellular triglyceride content	Natural	In vitro/cell culture	Oranje et al 69
Quinazolinone-coumarin hybrids	Inhibition of α-glucosidase	Natural	In vitro/in silico	Menteşe et al 55
Scoparone	Inhibition of glucose induced proliferation of mesangial cells	Natural	In vitro/cell culture	Wang et al 100
Scopoletin	Inhibition of α-glucosidase and reducing the postprandial glucose level Increased sensitivity for insulin	Natural	In vitro/in vivo/animal	Jang et al 60 , Jang et al 61
Selaginolide A	Inhibition of Protein Tyrosine Phosphatase 1B	Natural	In vitro/cell culture	Nguyen et al 80
Skimming	Decreased glomerulosclerosis	Natural	In vivo/animals	Sen et al 101
Umbelliferone	Increased cellular uptake of glucose	Semi -Synthetic	In vivo/animals	Naowaboot et al 84 , Ramesh and Pugalendi 94
	Decreased gluconeogenesis

Figure 5.

Scopoletin.

Figure 14.

Scoparone.

Coumarins and intestinal carbohydrate digestion and absorption of glucose

Investigators synthesized about 17 coumarin derivatives that showed varying degrees of inhibition on α-glucosidase with IC₅₀ values ranging between 1.10 ± 0.01 and 36.46 ± 0.70 μM compared with acarbose having IC₅₀ values 39.45 ± 0.10 μM in an in vitro assay. ¹³ In another study, synthetic coumarin derivatives inhibited α-glucosidase in a reversible fashion. The study further showed that the coumarins formed hydrogen bonds with LYS293 on the enzyme to lower the binding affinity for the saccharose in silico. ⁵¹ Furthermore, coumarin derivatives like N′-{2-(2-[3,4-dichlorobenzyl]-4-oxoquinazolin-3[4H]-yl)acetyl}-2-oxo-2H-chromene-3-carbohydrazide and N′-{2-(2-[4-bromobenzyl]-4-oxoquinazolin-3[4H]-yl)acetyl}-2-oxo-2H-chromene-3-carbohydrazide showed pancreatic lipase and α-glucosidase inhibition properties. ⁵⁵ In other studies, synthesized coumarin hybrids showed inhibition of the activity of α-glucosidase, α-amylase, and α-galactosidase, while some of them stimulated glucose uptake by cultured hepatic cells. ⁵⁶ Other coumarin hybrids showed a higher affinity for α-glucosidase than the standard acarbose. ⁵⁷ Molecular docking and in silico studies revealed, as mentioned earlier in the introduction, that the mechanism of action was probably based on the reversible binding on the active sites of the enzymes.^46,51,57-59

In addition to these (semi) synthetic coumarins, naturally occurring compounds also showed in vitro inhibition activity on the above-mentioned enzymes. Scopoletin (Figure 5) is a coumarin that is widespread in the plant world. Investigators showed that this compound inhibited α-glucosidase in vitro and reduced the postprandial glucose level in mice. ⁶⁰ The latter effect is possibly the result of phosphatidylinositol-3-kinase induced expression of the plasma membrane GLUT4. ⁶¹

Coumarins extracted from the flowers of Edgeworthia gardneri significantly inhibited the in vitro activity of both α-amylase and α-glucosidase. ⁶² At least 2 coumarins, 4-hydroxy Pd-C-III, and decursinol (Figure 6) isolated from Angelica decursiva also showed α-glucosidase enzyme inhibition, ⁶³ while a cinnamon extract with abundant coumarin derivatives inhibited the enzyme in vitro and lowered the postprandial glucose excursion in diabetic rats. ⁶⁴ Recent reports also confirmed the α-glucosidase inhibition properties of other plant-derived pyranocoumarins.^65,66 With computer aided drug design technology, researchers identified the best active coumarin derivatives to inhibit lysosomal α-glucosidase. They found that isorutarine, among a few others, showed a good in silico inhibition of the enzyme. In addition they showed that substitution with hydrophobic groups at the C4 and C5 positions of the coumarin ring increased the activity, while substitutions at the C1, C2, C3, C6, C7, and C8 on the contrary showed a decreased activity of the compounds. ⁶⁷

Figure 6.

Decursinol.

A relatively early investigation already showed the inhibitory activity of coumarin-like compounds on sodium-dependent glucose absorption in brush border membrane vesicles isolated from rat small intestine. ⁶⁸ Moreover, in a well-carried out comprehensive in vitro study, several naturally derived pyranocoumarin compounds like pteryxin (Figure 7) and praeruptorin showed significant and selective SGLT1 inhibition in cultured adapted Chinese Hamster Ovary and Caco-2 intestinal cells, ⁶⁹ with a potential effect on transepithelial intestinal glucose absorption. It is noteworthy that pteryxin also demonstrates favorable effects on fat metabolism, since it suppressed the triglyceride content in both cultured adipocytes and hepatocytes, ⁷⁰ a factor that could reduce resistance to insulin action.

Figure 7.

Pteryxin.

Finally, in a study carried out with an extract of various herbs containing an abundance of coumarin, an inhibition of transepithelial glucose transport was observed in a cell culture model of the intestine. ⁷¹ Unfortunately, it was not determined whether this effect could be specifically ascribed to the action of the coumarins, but the mechanism hinted toward interference with the SGLT-1 and GLUT-2 transporters.

Possible effects of coumarins on glucose uptake

Lately, coumarins stimulating or prolonging the release of insulin have been identified. The 6-Prenylcoumarin-7-O-b-D-apiofuranosyl-(1!6)-b-D-glucopyranoside coumarin derivative induced at least 2 times more insulin release from cultured pancreatic islet cells compared to glucose alone, ⁷² but the study did not reveal any mechanism of action. Synthetic 3-(5′-Methyl-2′-aryl-3′-[thiazol-2ʺ-yl amino] thiazolidin-4′-one) coumarin derivatives led to hypoglycemic effects in diabetic Wistar rats. ⁷³ However, it is not entirely clear from the report whether this could be ascribed to an increased insulin activity. Moreover, researchers conjugated glucagon-like peptide 1 with coumarin and achieved a longer half-life for the peptide and consequently prolonged the insulin increasing effect ⁵³ with this molecular binding. In another study, investigators showed that coumarin itself increased the insulin level and reduced the level of glucose in plasma of diabetic rats possibly through increased activity of the glycolytic enzyme hexokinase and the hepatic shunt enzyme glucose-6-phophate dehydrogenase or decreased activity of the gluconeogenic enzymes glucose-6-phosphatase and fructose-1,6-biphosphatase. ⁷⁴

Most of the identified compounds work through enhancement of the sensitivity to insulin on a cellular level in fat, liver, or muscle tissue. Free fatty acids among other factors contribute to the development of insulin resistance. ⁷⁵ The coumarin Isofraxidin altered lipid metabolism in cultured hepatic cells and mice with induced liver steatosis and decreased plasma free fatty acids through enhanced phosphorylation of adenosine monophosphate (AMP)-activated protein kinase among other actions. ⁷⁶ Researchers also synthesized several coumarins which antagonized aldehyde dehydrogenase 1A1 that improved palmitic acid-induced impairment of glucose consumption in cultured hepatic cells, ⁷⁷ a process that may result in a possible increased sensitivity for insulin. The observed glucose lowering activity of coumarin that has been previously mentioned, might be partly the result of an enhanced sensitivity to insulin since apart from the increased insulin level, a significant increase in the levels of the glycolytic enzyme hexokinase and the hepatic shunt enzyme glucose-6-phophate dehydrogenase was observed in the liver of the animals treated with the compound. ⁷⁴

Currently, Protein Tyrosine Phosphatase 1B inhibitors are being considered as potential antidiabetic agents. This enzyme has a negative feedback on the insulin signaling pathway, hence inhibition of this phosphatase may result in an increased sensitivity for insulin.^78,79 The coumarin selaginolide A demonstrated inhibitory activity on this enzyme as well as on α-glucosidase ⁸⁰ and in this way may have a beneficial effect on diabetes. Docking studies with dihydroxanthyletin-type coumarins—(+)-trans-decursidinol showed that they preferably bound with the active site of Protein Tyrosine Phosphatase 1B. ⁸¹

Coumarin-cyclic imide conjugates increased the glucose absorption rate to a level that is comparable to metformin in cultured hepatic carcinoma and kidney cells. ⁸² The furanocoumarin ficusin significantly improved the cellular uptake through the translocation and activation of GLUT4 in the plasma membranes of adipose tissue of diabetic rats. ⁸³ In addition to this, it also lowered serum fat and demonstrated antioxidant activity, 2 processes that enhance the sensitivity to insulin. ⁸³ A 7-hydroxycoumarin, also known as Umbelliferone (Figure 12), significantly reduced the elevated blood glucose level and insulin resistance, and increased liver glycogen in diabetic rats, probably due to increased mobilization of GLUT4. ⁸⁴ The naturally occurring coumarins osthole (Figure 10) and scopoletin (Figure 5) significantly induced AMP-activated protein kinase, which is favorable for preventing and treating type 2 diabetes mellitus. They also increased the level of translocation of GLUT4 to plasma membranes, increased the glucose uptake in skeletal muscle and fat cells, and reduced the plasma glucose level in diabetic mice.^61,85 Furthermore, osthole increased the absorption of glucose in cultured fibroblasts. ⁸⁶ A similar effect was observed in dexamethasone induced diabetic mice with the coumarin esculin. ⁸⁷ Esculin (Figure 8), fraxetin (Figure 9), and osthole (Figure 10) also were able to promote glucose uptake in cultured normal and insulin resistance-induced myotubes. ⁸⁷ Moreover, coumarins demonstrate antioxidant activity, an action that increases the sensitivity for insulin.^88,89

Figure 12.

Umbelliferone.

Figure 10.

Osthole.

Figure 8.

Esculin.

Figure 9.

Fraxetin.

Novel production of glucose ⁹⁰ in the liver ⁹¹ and other organs like the kidney ⁹² may also contribute to an increased glucose level in plasma. ⁹³ Coumarin itself significantly reduced the hepatic gluconeogenic enzymes glucose-6-phosphatase and fructose-1,6-bisphosphatase in diabetic rats. ⁷⁴ Umbelliferone decreased blood glucose and HbA1c, as well as the activities of glucose-6-phosphatase and fructose-1,6-bisphosphatase. ⁹⁴ In addition, it elevated plasma insulin and liver glycogen as well as glucokinase and glucose-6-phosphate dehydrogenase in diabetic rats. ⁹⁴ Coumarin-3-carboxylic acid derivatives inhibited the uptake of lactate by several tumoral cell lines. ⁹⁵ Hepatic conversion of lactate is one of the known mechanisms for gluconeogenesis. ⁹⁶

Coumarins and complications of diabetes

In a very recent in vitro study, coumarin showed up to 80% reduction of the glycation of human serum albumin by glucose and methylglyoxal. ⁵⁴ On one hand, this is a favorable action, but we must realize that the monitoring of therapy of diabetes also depends on the amount of glycated hemoglobin (HbA₁C). A lower level of this product induced by coumarin might falsely implicate a successful therapy, when we realize that these molecules are abundant in food and supplements and potentially might lower the glycation of peptides, including hemoglobin and albumin. Like most natural products, coumarins have also proven to possess antioxidative properties. Isofraxidin, ⁷⁶ coumarin, ⁴³ ficusin (Figure 11), ⁸³ umbelliferone, ⁷⁷ and coumarin-3-carboxamides and their hybrids with alpha-lipoic acid (Figure 13) ⁸⁸ are examples of coumarins or their derivatives with antioxidant capability. Investigators demonstrated an increased bone formation effect of the coumarin-like osthole in mice, ⁹⁷ which is possibly capable of reversing the osteolysis found in the periodontal space of diabetics. ⁹⁸ This is a well known complication of the disorder.

Figure 11.

Ficusin.

Figure 13.

Alpha-lipoic acid.

Coumarins derived from the plants Urtica dentata, ⁹⁹ Artemisia capillaries, ¹⁰⁰ and Hydrangea paniculate ¹⁰¹ showed the potency to slow down the progression of diabetic nephropathy. The total coumarin content of Urtica dentata prevented the high glucose-induced proliferation and hypertrophy of a mesangial cell line, a preliminary process in the development of the nephropathy. ⁹⁹ In addition they significantly reduced albuminuria and serum creatinine in streptozotocin-induced diabetic rats. ⁹⁹ The coumarin scoparone, found in Artemisia capillaries, also inhibited the glucose induced proliferation of cultured mesangial cells. ¹⁰⁰ Finally, treatment with the compound skimming found in Hydrangea paniculate, led to a lower degree of glomerulosclerosis compared to losartan treated streptozotocin-induced diabetic rats. ¹⁰¹ The mechanism of this process has not been elucidated yet.

Conclusion

Diabetes is a very disabling disorder and its prevalence is projected to have a considerable burden on the world economy. The current treatment strategies vary from changes in lifestyle to medication, and surgical intervention of complications. However, they all stop short of curing the disease. Consequently, the search for more effective and efficient therapeutic strategies, especially new drug agents, is continuing. In the past decades, a substantial number of natural and (semi)synthetic coumarins have been acquired. Among these, there are a number with proven efficacy in in vitro and in silico studies as well as in some animal models.

The abundance of the coumarins mentioned in this review inhibit the intestinal enzyme α-glucosidase. Examples of these are scopoletin, decursinol, and flavonoid hybrids of coumarin. Inhibition of this enzyme blocks the formation of glucose in the intestines and therefore limits the absorption rate of the carbohydrate. The coumarins pteryxin and praeruptorin inhibit sodium coupled glucose transport across the intestinal epithelium. Several coumarins have been found that are able to increase the secretion of or the sensitivity for insulin. Examples of these are coumarin, ficusin, esculin, fraxetin, and osthole. Some other compounds like coumarin, umbelliferone, and coumarin-3-carboxylic acid derivatives have the potential to inhibit gluconeogenesis. Finally the coumarins scoparone and skimming have demonstrated properties that might be useful in the management of diabetic nephropathy.

Unfortunately, up till now these studies have been limited to in vitro and in silico biochemical and simple animal studies. No clinical trial has yet been performed. The absence of these as well as the absence of detailed studies addressing biochemical or physiological and pharmacological mechanisms in suitable animals still limit the prospect of one of these agents to be developed into a useful drug against type 2 diabetes mellitus. There is thus still a long way to go to formulate clinical applicable agents from this group with high efficiency and low toxicity. However, the future of these compounds as potential antidiabetic agents looks promising.