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Antidiabetic and hypolipidemic activities of hydroethanolic root extract of Uvaria chamae in streptozotocin induced diabetic albino rats
© The Author(s). 2016
Received: 26 December 2015
Accepted: 8 November 2016
Published: 15 November 2016
Diabetes mellitus is a metabolic disorder of multiple aetiology characterised by hyperglycemia resulting from defects in insulin secretion, insulin action or both. It is a global epidemic ravaging both developed and developing countries. The situation will worsen if nothing is done urgently. In fact, the need to identify natural products with antidiabetic potentials is of great importance as supported by several research efforts all over the world, in search of antidiabetic plant based products that are safe and efficacious. Available literatures show that several phytochemicals with antidiabetic properties have been identified in certain plants amongst which include Uvaria chamae. The potentials of Uvaria chamae as an antidiabetic and hypolipidemic drug-candidate are thus tested.
Diabetes mellitus was experimentally induced after the rats were fasted overnight by administering intraperitoneally, 60 mg/kg streptozotocin. After 72 h, the rats with plasma glucose levels >200 mg/dl were classified as diabetic. A total of six groups containing five rats per group were used. One group of diabetic rats was untreated. Three diabetic groups, each were treated orally with 100, 250 and 400 mg/kg body weight of the extract. Another diabetic group was treated with insulin (0.5 IU/kg) subcutaneously. The control received 0.5 ml (2% solution) of acacia orally. The treatment was for 8 days. The effects of the extract on weight, plasma glucose and other biochemical parameters were evaluated using standard procedures.
The diabetic rats treated with the extract showed significant reductions (p < 0.05) in weight, plasma glucose levels, low density lipoprotein and cholesterol compared with the control. The 100, 250 and 400 mg/kg body weight of the extract showed maximum glucose reduction of 85.16, 81.50 and 86.02% respectively. Histologically the pancreas of the diabetic rats treated with the extract, showed clusters of variably sized regenerated islet of Langerhans within sheets of normal exocrine pancreas, while the pancreas of diabetic rats treated with insulin showed no islet of Langerhans.
The study showed that Uvaria chamae caused weight loss and has good hypoglycemic and hypolipidemic activities that may reduce the risk of developing cardiovascular diseases.
Diabetes mellitus has been described as a metabolic disorder of multiple aetiology, and characterized by chronic hyperglycemia with disturbances of carbohydrate, fat, and protein metabolism, resulting from defects in insulin secretion, insulin action or both [1, 2]. It is one of the oldest diseases of mankind that affects millions of people worldwide . The number of people living with the disease is expected to double with major impact on the population of the developing countries due to increased rate of industrialization [3, 4]. It is a major risk factor for the development of cardiovascular disease . Hence, the need to reduce the risk of vascular complications by securing adequate glycemic, lipidemic, blood pressure and weight control . Currently diabetes is controlled by diet, exercise, oral hypoglycemic agents and insulin therapy . The high level of treatment failures, unpleasant side effects and enormous cost associated with diabetic therapy have generated an urgent need and desire for alternative treatments . However, the preferred choice of plant medicine by many might not be unconnected with the historical successes recorded in the use of herbal products in traditional system of medicine in the management of diabetes mellitus . One of such plants used traditionally in the management of diabetes mellitus is Uvaria chamae.
Uvaria chamae is a medicinal plant that belongs to the family, Annonaceae. It is a climbing plant commonly found in West Africa . In this region of the world, it is identified by numerous names such as: Ogholo by the Esan people of Edo state, Ayiloko by the Igalas, Kaskaifi by the Hausas, Oko oja by the Yorubas, Mmimi ohia by the Igbos in Nigeria and Akotompo by the Akan-fante people of Ghana . The health benefits of medicinal plants are attributed in part to their unique phytochemical composition . The phytochemical analysis of the leaves and roots of Uvaria chamae revealed the presence of alkaloids, glycosides, saponin, tannins, flavonoids, terpenoids and phenols [11, 12]. Our previous study on the preliminary phytochemical screening and evaluation of hypoglycemic properties of Uvaria chamae also revealed that the extract has secondary metabolites such as alkaloids, flavonoids, tannins and terpenoids which corroborate earlier works done on the phytochemical screening of this plant. The study showed that the hypoglycemic properties of Uvaria chamae may be accounted for by the presence of the phytochemicals . The anti-fungal, anti-malarial and anti-inflammatory activities of Uvaria chamae have also been reported [11, 13, 14]. However, no scientific study has been conducted on the antidiabetic activity of this plant. The present study therefore was designed to evaluate the antidiabetic and hypolipidemic activities of the hydroethanolic root extract of Uvaria chamae in streptozotocin induced diabetic rats.
The roots of Uvaria chamae were obtained from a farm in Uromi, Edo State, Nigeria during the rainy season. They were authenticated by a taxonomist, Mr T. K. Odewo, of Department of Botany, University of Lagos, Nigeria. The voucher specimen with number LUH 3572 was deposited in the University herbarium.
Preparation of the plant material for extraction
The roots were washed with clean water to remove foreign materials, chopped into small pieces and dried in an oven at 45° centigrade for 4 days. They were ground to coarse powder with electric grinder. The root powder, 500 g, was extracted with 93.3% hydroethanol by maceration with frequent stirring for 5 days. The extract was filtered using Whatman filter paper number 4 and concentrated with a rotary evaporator at a reduced pressure. The concentrated extract was dried in an oven at 40° centigrade to obtain 22.41 g dry residue (4.48% yields).
Albino rats (160 ± 20 g) of both sexes were obtained from the Laboratory Animal Center, College of Medicine, University of Lagos, Idi-Araba and kept under standard environmental condition of 12/12 h light/dark cycle. They were housed in cages (5 animals per cage), maintained on standard animal pellets (Pfizer Feeds Plc, Nigeria), and provided with water ad libitum. They were allowed to acclimatize for 7 days to the laboratory conditions before the experiment. The use and care of the animals, and the experimental protocol were in strict compliance with the National Research Council guidelines on the care and use of laboratory animals . The experimental protocol (with Protocol ID: RGEEC/21/2015) was approved by the research grants and experimentation Ethics committee of the College of Medicine, University of Lagos, Nigeria.
The dose selection for the diabetic study was guided by the result obtained from the oral acute toxicity study done in our previous work which showed that the median lethal dose was 7.08 g/kg body weight .
Group I: control given 0.5 ml (2% solution) of acacia
Group II: Induced diabetic rats treated daily subcutaneously with (soluble) insulin 0.5 I.U / kg body weight
Group III: Induced diabetic rats treated daily with 400 mg/kg of the extract
Group IV: Induced diabetic rats treated daily with 250 mg/kg of the extract
Group V: Induced diabetic rats treated daily with 100 mg/kg of the extract
Group VI: Induced diabetic rats untreated
The rats were weighed and blood samples were collected from the tail vein for fasting blood glucose levels from the beginning of the treatment, the 5th day and at the end of the treatment (the 8th day). On the 8th day, blood was obtained via ocular puncture into heparinised containers for biochemical profile.
The heparinised blood was centrifuged within 5 min of collection at 4000 g for 10 min to obtain plasma, that was analysed for total cholesterol (Chol), triglyceride (TG), and High density lipoprotein-cholesterol (HDL-cholesterol) levels by modified enzymatic procedures from Sigma Diagnostics . Low density lipoprotein-cholesterol (LDL-cholesterol) levels were calculated using the Friedwald equation . Plasma was analysed for alanine aminotransferase (ALT), aspartate aminotransferase (AST), alkaline phosphatase (ALP) and creatinine by standard enzymatic assay analysis . The plasma protein contents and plasma glucose contents were determined using enzymatic spectroscopic methods .
The pancreatic tissue harvested from each group was fixed in 10% buffered formalin for 7 days before subjecting the tissues to routine histological processing techniques as described by Grizzle et al.  and staining with Haematoxylin and Eosin (H and E). Each section was examined under light microscope at high power magnification (×100 and x400) for structural changes. Photomicrographs were taken using an attached digital camera.
Data analysis was done using Graph Pad Prism 6. One way analysis of variance (ANOVA) was used to compare means. One–way ANOVA was done followed by Dunnett’s multiple comparisons test of treated groups with control. The results were expressed as Mean ± SEM. Level of significance was set at p < 0.05.
Antidiabetic activity of the root extract of Uvaria chamae
Effect of Uvaria chamae on Fasting Blood Glucose (FBG) Levels (mg/dl) and % Reduction (% R) of FBG levels
%R in Day5
%R in Day8
74.33 ± 0.88
75.66 ± 2.19
86.00 ± 3.22
90.67 ± 6.17
59.33 ± 2.91
363.00 ± 50.5*
270.70 ± 33.17*
133.30 ± 10.04*
63.33 ± 0.67
303.00 ± 7.10*
44.00 ± 7.00*
42.37 ± 0.52*
54.67 ± 1.45
263.30 ± 3.84*
52.67 ± 7.27*
48.70 ± 1.04*
66.67 ± 3.93
325.70 ± 17.85*
46.00 ± 2.08*
48.33 ± 0.88*
60.00 ± 4.36
242.30 ± 3.93*
256.30 ± 1.86*
300.30 ± 2.03*
Effect of Uvaria chamae on plasma lipid profile
Effect of Uvaria chamae on Plasma Lipid Profile (mg/dl)
126.3 ± 2.3
78.0 ± 0.6*
72.3 ± 0.9*
70.0 ± 14.4*
89.33 ± 0.9*
107.0 ± 0.6
43.2 ± 0.6
42.3 ± 1.9
57.3 ± 8.2
34.7 ± 0.3
61.3 ± 1.9
73.7 ± 0.9*
24.4 ± 0.4
25.3 ± 1.9
36.3 ± 4.1
31.7 ± 0.9
30.7 ± 0.7
29.7 ± 1.5
93.3 ± 0.6
44.2 ± 1.9 *
24.5 ± 7.8*
31.36 ± 7.13*
46.37 ± 1.53*
62.56 ± 2.52
Effect of Uvaria chamae on other biochemical parameters
Effect of Uvaria chamae on other biochemical parameters on the 8th Day
34.9 ± 0.1
25.7 ± 0.9
20.0 ± 2.3*
35.0 ± 1.2
23.7 ± 0.3
15.0 ± 2.0*
43.9 ± 0.3
25.3 ± 1.5*
16.3 ± 1.5*
37.3 ± 0.9
27.0 ± 0.6
33.3 ± 1.2
0.6 ± 0.01
1.0 ± 0.03
1.0 ± 0.1
1.03 ± 0.2
0.8 ± 0.1
1.13 ± 0.1*
27.7 ± 0.9
56.0 ± 0.6*
64.0 ± 0.6*
43.3 ± 0.9*
31.0 ± 0.6
46.3 ± 2.3*
12.6 ± 0.2
27.2 ± 0.2*
13.3 ± 2.2
16.3 ± 0.3
13.8 ± 0.2
31.1 ± 1.8*
10.8 ± 0.5
22.3 ± 1.3*
11.3 ± 2.2
14.8 ± 0.4
12.8 ± 0.4
27.7 ± 0.7*
13.0 ± 0.3
30.7 ± 0.7*
14.7 ± 2.3
23.7 ± 5.7
16.7 ± 1.2
17.8 ± 0.03
Effect of Uvaria chamae on the body weight
Effect of Uvaria chamae on the body weight (g)
130.7 ± 17.9
135.7 ± 20.5
159.0 ± 2.1
137.7 ± 5.8
127.3 ± 16.8
167.0 ± 3.5
133.7 ± 5.6
140.0 ± 6.1
122.7 ± 9.3*
121.0 ± 4.4
107.7 ± 4.1
102.3 ± 1.5*
124.0 ± 7.2
118.3 ± 7.1
120.0 ± 2.9*
135.0 ± 6.4
124.0 ± 2.7
118.3 ± 3.5*
Diabetes mellitus is a disease that affects the quality of life and life expectancy of its victim’s worldwide . Many deaths of diabetic subjects have been attributed to hyperglycemia and its accompanied vascular diseases. Hyperglycemia in particular, is the primary clinical manifestation of diabetes  and is thought to contribute to diabetic complications by altering vascular cellular metabolism, vascular matrix and circulating lipoproteins . The major goal in the treatment of diabetes has been to keep both short-term and long-term glucose levels within acceptable limits, thereby reducing the risk of long term complications .
The result of this study showed that there was a significant reduction in the blood glucose levels of all the diabetic rats treated with the extract compared with the control. The 100, 250 and 400 mg/kg body weight of the Uvaria chamae extract achieved diabetic control at the 5th day of treatment with a glucose reduction of 85.88, 80.00 and 85.48% respectively. This diabetic control was maintained till the end of the experiment. This marked reduction in plasma glucose concentration may be as a result of increased release of insulin from regenerated beta cells of the pancreas (Figs. 3, 4 and 5). The presence of phytochemicals such as flavonoids, alkaloids and tannins in the extract as reported in our previous study  may also have contributed to its antidiabetic activity.
Besides hyperglycemia, diabetes mellitus is highly characterized by elevated levels of triglycerides and cholesterol in the blood associated with a modern lifestyle and increased consumption of a high fat diet . The reduced absorption of free fatty acids and free cholesterol by inhibition of pancreatic lipase and pancreatic cholesterol esterase reduces hyperlipidemia associated with diabetes mellitus [28, 29]. This study revealed that the extract lowered the plasma total cholesterol and LDL-cholesterol levels significantly in the treated diabetic rats. This clearly demonstrated the presence of hypolipidemic agents in the extract. The hypolipidemic activity of the extract may be due to the inhibition of pancreatic lipase and pancreatic cholesterol esterase. The reduced plasma LDL-cholesterol reduces the risk of developing cardiovascular disease .
Persistent hyperglycemia causes increase in cellular glucose level in tissues undergoing insulin-independent glucose uptake such as eye lens, retina, kidney, and peripheral nerves, leading to secondary late stage diabetic complications. Influx of excess glucose into polyol pathway causes accumulation of sorbitol in the tissues, resulting in hyperosmotic stress to the cells. This is postulated to be the primary cause of diabetic complications which include nephropathy, retinopathy, cataract, and neuropathy . Creatinine is the most commonly used indicator of renal function. A raised plasma level of creatinine is a recognised marker of renal dysfunction . The significant increase in the plasma creatinine levels of the diabetic rats’ untreated indicated renal impairment in this group of rats. Therefore, persistent hyperglycemia due to poorly controlled diabetes mellitus may lead to diabetic nephropathy. A number of extra renal factors influence the circulating urea concentration limiting its value as a test of kidney function. For example plasma urea concentration is increased by high protein diet, increased protein catabolism and dehydration. In the above pre-renal situations, the plasma creatinine concentration is usually normal . The raised plasma urea seen in the diabetic rats treated with insulin and the extract could be as a result of dehydration or induced diabetic state from streptozotocin. This assertion is corroborated by Parvizi et al. , who reported that streptozotocin induced diabetes caused a significant increase in serum blood urea nitrogen level in type1 diabetes mellitus. ALT, AST and ALP are part of the liver enzymes . They are frequently used to diagnose or screen for hepatobiliary disease, examine the progression of a disease as well as to monitor or detect the hepatotoxicity that may arise from the use of drugs or substances [36, 37]. The heart also releases AST and ALT, and an elevation in their plasma concentrations is an indicator of liver and heart damage . The results in this study showed that the activities of AST and ALT in the plasma of diabetic rats untreated were markedly elevated. These enzymes are usually found in large quantities in the liver where they play an important role in the metabolism of amino acid . However, as a result of damage or toxicity to the liver, these enzymes may leak from the hepatocytes into the circulation where their levels become elevated . Therefore, the elevated plasma levels of AST and ALT in the diabetic untreated rats suggested liver and heart damage. Administration of the root extract of Uvaria chamae considerably reduced the elevated levels of AST and ALT in the diabetic rats. This showed that the extract is hepatocellular and cardio-protective. However, the elevated levels of AST, ALT and ALP in the diabetic rats treated with insulin during the period of the experiment could be as a result of damage to the liver and the heart from poorly controlled diabetes mellitus. Elevations of transaminases and alkaline phosphatase are common in diabetes mellitus . Weight loss is considered an important aspect of therapy for patients with diabetes. Excess weight places greater direct demand on the beta-cell and also aggravates insulin resistance. Numerous studies have shown that weight loss in patients with diabetes can result in improvement in glucose levels . The results of this study revealed that there was a significant weight reduction in the diabetic rats treated with the extract compared with the control. The weight loss may be due to suppression of appetite.
This study showed that Uvaria chamae has antidiabetic and hypolipidemic activities. From the study the extract not only improved glycemic and lipidemic control but also caused weight loss, making it beneficial for diabetic patients that are overweight. These findings reduce the risk of developing cardiovascular disease and give credence to the use of the extract traditionally in the treatment of diabetes mellitus. The study also revealed that the extract is hepatocellular and cardio-protective.
The authors wish to thank Mr M.E Idemudia of Idumu-une Quarters, Uromi, Edo State, Nigeria, for his assistance in plant collection. Authors also wish to thank Dr A.O. Nwaopara, Head of Department, Anatomy, Ambrose Alli University, for his technical assistance. Authors want to specially thank Dr T.A. Azeke, consultant Histopathologist, Irrua Specialist Teaching Hospital for reviewing the histology slides.
The research was funded by the authors.
Availability of data and materials
All the data are contained in the manuscript.
EJE, AEO and OIA conceived this study. The experiments were carried out by EJE and IOI. EJE and IOI performed the statistical analysis. EJE drafted the manuscript. The authors read and approved the final manuscript.
The authors declare that they have no competing interests.
Consent for publication
Authors gave their consent to the publication of this manuscript.
Ethics approval and consent to participate
The experimental protocol (with Protocol ID: RGEEC/21/2015) was approved by the research grants and experimentation Ethics committee of the College of Medicine, University of Lagos, Nigeria.
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