|Year : 2015 | Volume
| Issue : 1 | Page : 92-99
Anti-diabetic effects of ethanol extract of Bryonia laciniosa seeds and its saponins rich fraction in neonatally streptozotocin-induced diabetic rats
Sandip B Patel1, Devdas Santani2, Veena Patel3, Mamta Shah4
1 Department of Pharmacology, Indukaka Ipcowala College of Pharmacy, New Vallbh Vidyanagar, Anand, India
2 Department of Clinical Pharmacy, Rofel Shri G.M. Bilakhia College of Pharmacy, Vapi, India
3 Department of Pharmacognosy, Anand College of Pharmacy, Anand, India
4 Department of Pharmacognosy, L. M. College of Pharmacy, Navrangpura, Ahmedabad, Gujarat, India
|Date of Submission||11-Feb-2014|
|Date of Acceptance||18-Aug-2014|
|Date of Web Publication||17-Dec-2014|
Dr. Sandip B Patel
Indukaka Ipcowala College of Pharmacy, New Vallbhvidyanagar, Anand, Guajrat - 388 121
Source of Support: None, Conflict of Interest: None
| Abstract|| |
Context: Bryonia laciniosa Linn. (Cucurbitaceae) seed is used in traditional medicine for a number of ailments including metabolic disorders. Aim: This study evaluated the anti-diabetic action of the ethanol extract of B. laciniosa seeds and saponin fraction of it through its effect on hyperglycemia, dyslipidaemia and oxidative stress in neonatally streptozotocin (n-STZ)-induced diabetic rats (n-STZ diabetic rats). Materials and Methods: Ethanol extract (250 and 500 mg/kg; p.o.), saponin fraction (100 and 200 mg/kg; p.o.) and standard drug glibenclamide (3 mg/kg; p.o.) were administered to diabetic rats when the rats were 6 weeks old and continued for 10 consecutive weeks. Effects of ethanol extract and saponin fraction on various biochemical parameters were studied in diabetic rats. Results: The treatment with ethanol extract and saponin fraction for 10 weeks decrease in the levels of glucose, triglycerides, cholesterol, high-density lipoprotein, low-density lipoprotein, very low-density lipoprotein, serum urea, serum creatinine and diminished activities of aspartate transaminase, and alanine transaminase. The anti-hyperglycemic nature of B. laciniosa is probably brought about by the extra- the pancreatic mechanism as evidenced from unchanged levels of plasma insulin. B. laciniosa modulated effect of diabetes on the liver malondialdehyde, reduced glutathione (GSH), superoxide dismutase (SOD), and catalase (CAT) activity. Administration of ethanol extract and saponin fraction to diabetic rats showed a significant reversal of disturbed antioxidant status. Significant increase in SOD, CAT, and levels of GSH was observed in treated n-STZ diabetic rats. Conclusion: The present study reveals the efficacy of B. laciniosa seed extract and its saponin fraction in the amelioration of n-STZ diabetic rats.
Keywords: Diabetes mellitus, dyslipidemia, hyperglycemia, oxidative stress
|How to cite this article:|
Patel SB, Santani D, Patel V, Shah M. Anti-diabetic effects of ethanol extract of Bryonia laciniosa seeds and its saponins rich fraction in neonatally streptozotocin-induced diabetic rats. Phcog Res 2015;7:92-9
|How to cite this URL:|
Patel SB, Santani D, Patel V, Shah M. Anti-diabetic effects of ethanol extract of Bryonia laciniosa seeds and its saponins rich fraction in neonatally streptozotocin-induced diabetic rats. Phcog Res [serial online] 2015 [cited 2019 May 26];7:92-9. Available from: http://www.phcogres.com/text.asp?2015/7/1/92/147217
| Introduction|| |
Type 2 diabetes mellitus is one of the most common metabolic disorders with increasing prevalence during recent years. Type 2 diabetes mellitus is characterized by the progression of diminishing insulin sensitivity and impaired pancreatic function. Lifestyle modifications or appropriately prescribed drugs such as metformin, sulfonylureas or thiazolidinediones as monotherapy or add-on treatment are essential to tackle the disease; however, many patients still cannot achieve satisfactory glycemic control. Therefore, searching for alternative protective strategies is of great interest. 
Streptozotocin (STZ) is a chemical substance specifically toxic to pancreatic β-cells. It is taken into the pancreatic β-cells by glucose transporter-2. When injected into adult rats, STZ can cause type 1 diabetes with severely elevated blood glucose level. However, when STZ is administered to neonatal rats, the neonates experience acute hyperglycemia within the first few days, and the blood glucose gradually decreases thereafter. The surviving rats exhibit decreased β-cell mass and developed type 2 diabetes with the features described in type 2 diabetes patients (hyperglycemia, polyphagia, polydipsia, polyuria, insulin resistance and abnormal glucose tolerance) after 6 weeks. Therefore, this model provides an ideal platform for β-cell regeneration study and new anti-diabetic drug screening. ,,
Concurrently, phyto-chemicals identified from traditional medicinal plants are providing exciting opportunities for the development of the new type of therapies.  There are many compounds isolated from traditional medicinal plants with anti-diabetic activity  of which saponins are promising compounds with the potential to be developed into new drugs as anti-diabetic.  Many studies have demonstrated that saponins significantly decreased the plasma glucose level and plasma triglyceride level. It was previously reported that saponins possess anti-lipid peroxidation activity to protect the vascular endothelium, and to prevent diabetic complications. 
In the present study, we have selected a plant which is used as a hypoglycemic herb by native people of Porbandar region. Bryonia laciniosa Linn. syn Bryonopsis laciniosa Linn. (Cucurbitaceae) Syn Diplocyclos palmatus (Linn.) Jeffrey (Cucurbitaceae) locally known as 'Shivlingi' and 'Gargumaru' is distributed throughout India. It is an annual climber with bright red fruits and is reported to be highly medicinal.  Locally in India its seeds are being used for promoting conception in women. Ayurvedic literature survey indicated the use of the entire plant is a bitter tonic, hepatoprotective, anti-pyretic, laxative and used to correct the metabolic abnormalities. ,, From leaves, a bitter principle bryonin has been reported. From seeds, Saponin molecules are identified by thin layer chromatography and antibacterial, antifungal, anti-inflammatory and diuretic activities were investigated.  Occurrence of punicic acid, goniothalamine, and glucomannan has been reported in this plant. ,, Antimicrobial, larvicidal, anti-inflammatory, cytotoxic, analgesic, anti-pyretic and anti-diabetic activities have been reported for various extracts of this plant. ,, There are other two species of Bryonia reported earlier in the literature. One of the species Bryonia alba possess antidiabetic activity.  We also investigated the anti-diabetic potential of seeds of B. laciniosa in STZ induced type-1 diabetic rats.  Therefore, the present study was designed to evaluate the anti-diabetic effects of B. laciniosa seeds in neonatally streptozotocin (n-STZ) induced diabetic rat (n-STZ diabetic rats).
| Materials and Methods|| |
Streptozotocin was purchased from Sisco Research Laboratory Pvt. Ltd., India. All other standard chemicals were obtained from common commercial suppliers.
Collection of plant material and extraction
The fruits of B. laciniosa were collected in October 2009 to December 2009 from Anand and Jamnagar region of Gujarat, India. The plant was identified and authenticated by Dr. A.S. Reddy of department of Bioscience by comparison with voucher specimen No. VSM502 and ARM 2174 at the Prof. G.L. Shah Herbarium of Sardar Patel. University, Vallabh Vidyanagar, Anand, Gujarat, India. The fruits were macerated in a large amount of water and passed through large pore size sieve to separate seeds. The seeds were grinded mechanically to make powder. The powdered seeds were extracted with ethanol by Soxhlet to give B. laciniosa ethanol extract (BLEE). The alcohol extract was concentrated, suspended in distilled water and then partitioned with n-butanol saturated with water. The upper n-butanol layer was collected in a glass flask, and lower aqueous extract was collected and further extracted with n-butanol two more times to increase the yield. The n-butanol extract was pooled and evaporated using a rotary evaporator at 60°C to yield B. laciniosa saponin rich fraction (BLSF).
Determination of total saponins
The total saponins content of each extract was determined approximately using the method described by Hiai et al. Briefly, the extracts (50 μL) were mixed with the vanillin (8% w/v, 0.5 mL) and sulfuric acid (72% w/v, 5 mL). The mixture was incubated at 60°C for 10 min, cooled in an ice water bath for 15 min and the absorbance read at 538 nm. Oleanolic acid was used as a reference standard, and the content of total saponins was expressed as oleanolic acid equivalents (μg/mg extract).
Sprague Dawley rats from an inbred colony were bred under well-controlled conditions of temperature, humidity and 12 h/12 h light-dark cycle with diet and water provided ad libitum. 2-day-old neonates of either sex were injected intraperitoneally with 90 mg/kg STZ (Sisco, Mumbai, USA) in a 0.1 M citrate buffer (pH 4.5). Control neonates received an equivalent amount of isotonic saline alone. Site of injection was controlled to be under the inguinal fat of the neonates to prevent any leakage of the liquids. All procedures were performed on ice and in darkness to avoid the degradation of STZ. The pups were weaned when 4 weeks old and 6 weeks after the injection of STZ, animals were checked for fasting glucose levels using a commercially available kit (Span Diagnostics Ltd., India). The animals with fasting glucose levels >140 mg/dl were considered diabetic. 
In the experiment, a total of 54 rats (42 diabetic rats,
12 normal rats) were used. Study of the effect of BLEE and BLSF on type 2 diabetic rats involved 2 sets of experiments. The groups of animals in two different set were as follows:
- Set 1: Effect of BLEE on n-STZ diabetic rats (n = 6 animals per group)
- Group 1: Normal control rats were administered vehicle
- Group 2: Diabetic control rats were administered vehicle
- Group 3: Diabetic rats were administered BLEE (250 mg/kg)
- Group 4: Diabetic rats were administered BLEE (500 mg/kg).
- Set 2: Effect of BLSF on n-STZ diabetic rats (n = 6 animals per group)
- Group 1: Normal control rats were administered vehicle
- Group 2: Diabetic control rats were administered vehicle
- Group 3: Diabetic rats were administered BLSF (100 mg/kg)
- Group 4: Diabetic rats were administered BLSF (200 mg/kg)
- Group 5: Diabetic rats were administered glipizide (10 mg/kg).
All the treatments were administered and given orally (once a day) by gavage syringe at 8:30 a.m. when the rats were 6 weeks of age and continued for 10 consecutive weeks. The rats in control and diabetic groups were administered the same volume of vehicle.
The protocol of this experiment was approved by our institutional animal ethical committee as per the guidance of the Committee for the Purpose of Control and Supervision of Experiments on Animals, the Ministry of Social Justice and Empowerment, Government of India (Protocol No.: IICP/PH/2009-06/02).
Oral glucose tolerance test
At the end of the 10 weeks study, rats were subjected to an oral glucose tolerance test (OGTT). Glucose (1.5 g/kg) was administered to 18 h fasted rats. Blood samples were collected from retro-orbital plexus vein at 0, 30, 60 and 120 min. Serum was analyzed for glucose and insulin. The results were expressed as an integrated area under the curve (AUC) for glucose that was calculated by the trapezoid rule (AUC = C1 + C2/2 × [t1 - t2]) and changes in glucose concentrations during OGTT were expressed as AUCglucose (mg/dl/min).
Blood collection and serum analysis
At the end of 10 weeks of treatment, body weight, food intake and water intake were determined. Thereafter, animals were fasted for 12 h, and blood samples were collected from the retro-orbital plexuses of each rat under light ether anesthesia. The serum was separated and analyzed spectrophotometrically for glucose, cholesterol, triglycerides, high-density cholesterol, creatinine, urea, aspartate amino transferase (AST) and alanine amino transferase (ALT) (Shimadzu, UV-1701E, Japan) using commercially available biochemical diagnostic kits (Bayer Diagnostics Ltd., India). Serum insulin was estimated by radioimmunoassay using kits from Rat Insulin RIA Kit, Linco Research, Inc., St. Charles, MO and g-counter (Packard, USA). Low-density lipoprotein cholesterol (LDL-C), very low-density lipoprotein cholesterol (VLDL-C) and atherogenic index were calculated.
At the end of the experiment, Liver tissue was excised, rinsed in ice-cold saline and then homogenized in Tris-HCl buffer (pH 7.4) using a Teflon homogenizer. The liver homogenate was then centrifuged in a cooling centrifuge at 5000 × g to remove the debris, and the supernatant was used for the analysis of nonenzymatic antioxidants according to the method of Mihara and Uchiyama for malondialdehyde (MDA)  and Sedlak and Lindsay for reduced glutathione (GSH).  The enzymatic antioxidants such as superoxide dismutase (SOD) and catalase (CAT) were assayed. ,
Results are presented as the mean ± standard error of the mean statistical differences between the means of the various groups were evaluated using one-way analysis of variance, followed by Tukey's test. Data were considered statistically significant at P < 0.05.
| Results|| |
Rats which received STZ showed a significant reduction in body weight, increase in food intake, and water intake at the end of 10 weeks when compared with nondiabetic control rats. Noninsulin-dependent diabetes mellitus diabetic rats when treated with BLEE (500 mg/kg, p.o.) and BLSF (200 mg/kg, p.o.) significantly (P < 0.05) reduced the food intake and the water intake when compared with diabetic control rats. Further, Treatment with BLEE and BLSF failed to show any changes in the body weight [Table 1] and [Table 2].
Serum glucose, insulin and oral glucose tolerance test
Rats which received STZ showed a significant hyperglycemia associated with hyperinsulinemia in rats. Treatment with BLEE (250 and 500 mg/kg, p.o.) and BLSF (100 and 200 mg/kg, p.o.) significantly decreased fasting glucose, but not the insulin levels when compared with diabetic control groups. The result of OGTT revealed that AUCglucose significantly increased in diabetic control rats when compared with normal control rats. Treatment with BLEE (250 and 500 mg/kg, p.o.) and BLSF (100 and 200 mg/kg, p.o.) significantly reduced elevated AUCglucose levels [Table 3] and [Table 4].
|Table 3: Effect of BLEE on glucose, serum insulin, AUCglucose lipid profiles, renal function tests and liver function tests in n-STZ diabetic rats|
Click here to view
|Table 4: Effect of BLSF on glucose, serum insulin, AUCglucose lipid profiles, renal function tests and liver function tests in n-STZ diabetic rats|
Click here to view
Diabetic control rats showed significant rise in serum lipid levels when compared with normal control rats. Diabetic control rats produced significant rise in serum cholesterol, triglycerides, VLDL, LDL, decrease in high-density lipoprotein (HDL) levels when compared with control rats. Treatment of diabetic rats with BLEE (250 and 500 mg/kg, p.o.) and BLSF (100 and 200 mg/kg, p.o.) produced significant decrease in serum cholesterol, triglycerides, and VLDL and LDL while no significant change in serum HDL levels when compared with diabetic control group [Table 3] and [Table 4].
Kidney and liver function tests
Diabetic control rats exhibited significant rise in serum creatinine and urea levels when compared with normal control rats. Treatment of diabetic rats with BLEE (250 and 500 mg/kg, p.o.) and BLSF (100 and 200 mg/kg, p.o.) produced significant decrease in urea and creatinine levels when compared with diabetic control group. Diabetic control rats exhibited significantly higher AST and ALT levels when compared with normal control rats. Treatment of diabetic rats with
BLEE (250 and 500 mg/kg, p.o.) and BLSF (100 and 200 mg/kg, p.o.) failed to exhibit significant changes in elevated AST and ALT levels when compared with diabetic control group [Table 3] and [Table 4].
Streptozotocin-induced type 2 diabetic rats exhibited higher lipid peroxidation in liver tissue when compared with normal control rats. Treatments with BLEE (250 and 500 mg/kg, p.o.) and BLSF (100 and 200 mg/kg, p.o.) decreased lipid peroxidation at significantly extent when compared with diabetic control animals [Table 5] and [Table 6].
|Table 5: Effect of BLEE on oxidative stress parameters in n-STZ diabetic rats|
Click here to view
|Table 6: Effect of BLSF on oxidative stress parameters in n-STZ diabetic rats|
Click here to view
Effect on antioxidant parameters
Streptozotocin-induced type 2 diabetic rats showed significant reduction in SOD, CAT and GSH content in liver tissue as compared to normal control rats. Treatment with BLEE (250 and 500 mg/kg, p.o.) and BLSF (100 and 200 mg/kg, p.o.) elevates the SOD and CAT level to a significant extent when compared with diabetic control rats. However, treatment with extract (500 mg/kg), significantly raise the level of GSH when compared with diabetic control rats [Table 5] and [Table 6].
| Discussion|| |
In the present study, we investigated the anti-diabetic effects of ethanol extract of seeds of B. laciniosa and its saponin fraction in n-STZ diabetic rats. It has been established previously that the anti-diabetic activity of B. laciniosa in STZ-induced type 1 diabetic rats.  Herein, we showed for the 1 st time that, ethanol extract of seeds of B. laciniosa and its saponin fraction significantly attenuated hyperglycemia and improved glucose homeostasis in experimentally induced n-STZ induced diabetic rats.
The development and progression of type 2 diabetes first manifests itself as glucose intolerance and postprandial hyperglycemia, and eventually fasting hepatic glucose production increases,  leading to the elevated fasting glucose levels characteristic of symptomatic diabetes. Furthermore, dyslipidemia is often associated with hyperglycemia in type 2 diabetes due to the close relationship between glucose and lipid metabolism. The n-STZ diabetic rat model experienced the classical pathogenesis of type 2 diabetes from merely glucose intolerance to elevated fasting glucose levels in the current study, along with a significant increase in lipid levels. Chronic administration of BLEE and BLSF dose-dependently lowered postprandial glucose and lipid levels, attenuated the glucose intolerance and prevented the onset of overt diabetes in n-STZ diabetic rats.
The n-STZ diabetic rats show significant glucose intolerance when 1.5 g/kg glucose is orally administered, and they also have high levels of insulin.  Hyperinsulinemia with low hepatic excretion and the hypersecretion of β-cells are also reported in mildly glucose intolerant obese subjects.  In the present study, STZ produced a significant increase in glucose levels that was associated with a significant increase in insulin levels in diabetic rats. Treatment with BLEE and BLSF significantly reduced the serum glucose and but failed to alter the insulin levels of the diabetic rats. Although we did not determine the insulin sensitivity of the cells, the unchanged insulin profile and improved glucose response during OGTT suggest that the extract may have improved glucose tolerance via increased insulin sensitivity.  In considering this, the anti-hyperglycemic activity of the B. laciniosa may be due to an improved glucose uptake, insulin resistance in cells or inhibiting the glucose absorption through gastrointestinal tract. Our study suggests that the hypoglycemic activity of B. laciniosa is not related to the insulin secretion and that post prandial glucose reduction is probably effected without any extra load on pancreatic β-cells and/or stimulation of glucose uptake by peripheral tissues. Hence, the hypoglycemic effect may be probably brought about by an extra pancreatic mechanism. There are medicinal plants, which are known to exert antidiabetic activity without the stimulation of insulin secretion. ,, In vitro studies on Hep G2 cell lines have shown that berberine is able to exert an insulin independent glucose lowering effect glucose lowering effect in hepatocytes similar to that of metformin. 
Circulating levels of free fatty acids are elevated in diabetes.  Free fatty acids may impair endothelial function through several mechanisms, including the increased production of oxygen-derived free radicals, the activation of protein kinase c, and the exacerbation of dyslipidemia.  In the present study, diabetic animals showed elevated triglyceride, cholesterol, LDL, and VLDL levels and decreased HDL levels, compared with control animals. Serum cholesterol, triglyceride, LDL, and VLDL levels were significantly decreased by treatment with BLEE and BLSF in diabetic rats. The reduction in cholesterol and triglyceride levels by extract and its saponin fraction suggests a beneficial effect on coronary heart diseases.
Chronic metabolic disorders in type 2 diabetes are reported to cause varied forms of complications, including liver or kidney diseases. ,, Blood ALT and AST levels are considered to be liver function markers, and ALT value has been reported to increase significantly in STZ-induced diabetic rats. , Moreover, in n-STZ diabetic rats, chronic hyperglycemia and polyuria symptoms lead to further deterioration of kidney function and the ultimate occurrence of diabetic nephropathy. Renal hypertrophy and abnormal extracellular matrix deposition were reported to be the hallmarks of diabetic nephropathy, and glomerular hyperfiltration occurred at the early phase of diabetic nephropathy.  In the present study, n-STZ diabetic rats exhibited significantly elevated creatinine and urea levels, and chronic BLEE and BLSF administration dose-dependently reversed the renal and liver function parameters induced by diabetes, suggesting that B. laciniosa is capable of protecting the peripheral target organs from damages induced by chronic hyperglycemia in type 2 diabetes.
The accumulation of reactive oxygen species is a characteristic feature of oxidative stress, and a relationship between oxidative stress and the vascular complications in diabetes was suggested previously.  Oxidative stress is associated with complications of diabetes and has been linked to insulin resistance in vitro and in vivo. When glucose and free fatty acids increase; they cause oxidative stress and the activation of stress sensitive signaling pathways. The activation of these pathways, in turn, worsens both insulin action and secretion, which leads to overt type 2 diabetes.  In our study, there was a high level of serum MDA and a low level of SOD, CAT, GSH in the diabetic group, compared with levels in normal animals. Chronic BLEE and BLSF treatment reduced the elevated level of MDA and increased the levels of SOD, CAT, GSH, which indicates a decrease in oxidative stress.
| Conclusion|| |
Taken together, we conclude that B. laciniosa treatment is effective to significantly enhance glucose homeostasis in n-STZ diabetic rats. As such, B. laciniosa may be considered as a candidate anti-diabetic drug in diabetic patients. However, further studies are needed to address more detailed information regarding the action mechanisms for B. laciniosa in treating diabetes.
| References|| |
Wang Y, Xin X, Jin Z, Hu Y, Li X, Wu J, et al.
Anti-diabetic effects of pentamethylquercetin in neonatally streptozotocin-induced diabetic rats. Eur J Pharmacol 2011;668:347-53.
Andrade-Cetto A, Revilla-Monsalve C, Wiedenfeld H. Hypoglycemic effect of Tournefortia hirsutissima
L. on n-streptozotocin diabetic rats. J Ethnopharmacol 2007;112:96-100.
Li L, Yi Z, Seno M, Kojima I. Activin A and betacellulin: Effect on regeneration of pancreatic beta-cells in neonatal streptozotocin-treated rats. Diabetes 2004;53:608-15.
Thyssen S, Arany E, Hill DJ. Ontogeny of regeneration of beta-cells in the neonatal rat after treatment with streptozotocin. Endocrinology 2006;147:2346-56.
Tiwari AK, Rao JM. Diabetic mellitus and multiple therapeutic approaches of phytochemicals: Present status and future prospects. Curr Sci 2002;83:30-7.
Zhang LH, Xiao PG. Recent advances in studies of antihyperlipaemic and antihyperglycaemic compounds from Chinese traditional and herbal medicines. Phytother Res 1993;7:217-26.
Xu R, Zhao W, Xu J, Shao B, Qin G. Studies on bioactive saponins from Chinese medicinal plants. Adv Exp Med Biol 1996;404:371-82.
Xi M, Hai C, Tang H, Chen M, Fang K, Liang X. Antioxidant and antiglycation properties of total saponins extracted from traditional Chinese medicine used to treat diabetes mellitus. Phytother Res 2008;22:228-37.
Kirtikar K, Basu B. Indian Medicinal Plants. 2 nd
ed. Allahabad: The Indian Press; 1987.
Nadkarni K. Indian Materia Medica. Bombay, India: Popular Book Depot; 1927.
Gabrielian SE, Gevorgovich A. Bryonia
, as novel plant adoptogen, for prevention and treatment of stress induced disorders. Promising Res Abstr PRA 1997;(5003):1-8.
Acharya D. Shivlingi: A common but important twine in Patalkot. Am Chron 2007.
Saxena N, Balyari N, Srivastva A. Pharmacological studies of novel pharmaceutical saponin molecules of seeds of Bryonia laciniosa
. New Delhi, India: IUPAC. Internationational Conference on Biodiversity, Natural Product Chemistry and Medicinal Applications; 2004. p. 368.
Gowrikumar G, Mani VV, Chandrasekhararao T, Kaimal TN, Lakshminarayana G. Diplocyclos palmatus
L: A new seed source of punicic acid. Lipids 1981;116:558-9.
Mosaddik MA, Ekramul Haque M, Abdur Rashid M. Goniothalamin from Bryonopsis laciniosa
Linn (Cucurbiataceae). Biochem Syst Ecol 2000;28:1039-040.
Singh V, Malviya T, Tripathi DN, Naraian U. An escherichia coli
antimicrobial effect of arabinoglucomannan from fruit of Bryonia lacinosa
. Carbohydr Polym 2009;75:534-37.
Mosaddik MA, Haque ME. Cytotoxicity and antimicrobial activity of goniothalamin isolated from Bryonopsis laciniosa
. Phytother Res 2003;17:1155-7.
Gupta M, Mazumdar UK, Sivakumar T, Vamsi ML, Karki SS, Sambathkumar R, et al.
Evaluation of anti-inflammatory activity of chloroform extract of Bryonia laciniosa
in experimental animal models. Biol Pharm Bull 2003;26:1342-4.
Karageuzyan K, Vartanyan G, Agadjanov M. Restoration of disordered glucose-fatty acid cycle in alloxan-diabetic rats by trihydrixyoctadecdienoic acids from Bryonia alba
- A native americal plant. Planta Med 1998;64:417-22.
Patel S, Santani D, Shah M, Patel V. Anti-hyperglycemic and Anti-hyperlipidemic Effects of Bryonia Laciniosa
Seed Extract and its saponin fraction in streptozotocin-induced Diabetes in Rats. J Young Pharm 2012;4:171-6.
Hiai S, Oura H, Nakajima T. Color reaction of some sapogenins and saponins with vanillin and sulfuric acid. Planta Med 1976;29:116-22.
Mihara M, Uchiyama M. Determination of malonaldehyde precursor in tissues by thiobarbituric acid test. Anal Biochem 1978;86:271-8.
Sedlak J, Lindsay RH. Estimation of total, protein-bound, and nonprotein sulfhydryl groups in tissue with Ellman's reagent. Anal Biochem 1968;25:192-205.
Misra HP, Fridovich I. The role of superoxide anion in the autoxidation of epinephrine and a simple assay for superoxide dismutase. J Biol Chem 1972;247:3170-5.
Takahara S, Hamilton HB, Neel JV, Kobara TY, Ogura Y, Nishimura ET. Hypocatalasemia: A new genetic carrier state. J Clin Invest 1960;39:610-9.
Weyer C, Bogardus C, Mott DM, Pratley RE. The natural history of insulin secretory dysfunction and insulin resistance in the pathogenesis of type 2 diabetes mellitus. J Clin Invest 1999;104:787-94.
Portha B, Picon L, Rosselin G. Chemical diabetes in the adult rat as the spontaneous evolution of neonatal diabetes. Diabetologia 1979;17:371-7.
Bonora E, Zavaroni I, Coscelli C, Butturini U. Decreased hepatic insulin extraction in subjects with mild glucose intolerance. Metabolism 1983;32:438-46.
Carnevale Schianca GP, Rossi A, Sainaghi PP, Maduli E, Bartoli E. The significance of impaired fasting glucose versus impaired glucose tolerance: Importance of insulin secretion and resistance. Diabetes Care 2003;26:1333-7.
Hannan JM, Rokeya B, Faruque O, Nahar N, Mosihuzzaman M, Azad Khan AK, et al.
Effect of soluble dietary fibre fraction of Trigonella foenum graecum
on glycemic, insulinemic, lipidemic and platelet aggregation status of type 2 diabetic model rats. J Ethnopharmacol 2003;88:73-7.
Maghrani M, Lemhadri A, Jouad H, Michel JB, Eddouks M. Effect of the desert plant Retama raetam
on glycaemia in normal and streptozotocin-induced diabetic rats. J Ethnopharmacol 2003;87:21-5.
Sachdewa A, Khemani LD. Effect of Hibiscus rosa sinensis
Linn. ethanol flower extract on blood glucose and lipid profile in streptozotocin induced diabetes in rats. J Ethnopharmacol 2003;89:61-6.
Yin J, Hu R, Chen M, Tang J, Li F, Yang Y, et al.
Effects of berberine on glucose metabolism in vitro
. Metabolism 2002;51:1439-43.
Fujimoto WY. The importance of insulin resistance in the pathogenesis of type 2 diabetes mellitus. Am J Med 2000;108 Suppl 6a: 9S-14S.
Inoguchi T, Li P, Umeda F, Yu HY, Kakimoto M, Imamura M, et al.
High glucose level and free fatty acid stimulate reactive oxygen species production through protein kinase C-dependent activation of NAD(P)H oxidase in cultured vascular cells. Diabetes 2000;49:1939-45.
Celik S, Erdogan S, Tuzcu M. Caffeic acid phenethyl ester (CAPE) exhibits significant potential as an antidiabetic and liver-protective agent in streptozotocin-induced diabetic rats. Pharmacol Res 2009;60:270-6.
Nosadini R, Tonolo G. Relationship between blood glucose control, pathogenesis and progression of diabetic nephropathy. J Am Soc Nephrol 2004;15 Suppl 1:S1-5.
Shinde UA, Goyal RK. Effect of chromium picolinate on histopathological alterations in STZ and neonatal STZ diabetic rats. J Cell Mol Med 2003;7:322-9.
Thrailkill KM, Clay Bunn R, Fowlkes JL. Matrix metalloproteinases: Their potential role in the pathogenesis of diabetic nephropathy. Endocrine 2009;35:1-10.
Stehouwer CD, Schaper NC. The pathogenesis of vascular complications of diabetes mellitus: One voice or many? Eur J Clin Invest 1996;26:535-43.
Rahimi R, Nikfar S, Larijani B, Abdollahi M. A review on the role of antioxidants in the management of diabetes and its complications. Biomed Pharmacother 2005;59:365-73.
Evans JL, Maddux BA, Goldfine ID. The molecular basis for oxidative stress-induced insulin resistance. Antioxid Redox Signal 2005;7:1040-52.
[Table 1], [Table 2], [Table 3], [Table 4], [Table 5], [Table 6]
|This article has been cited by|
||Chronic saponin treatment attenuates damage to the pancreas in chronic alcohol-treated diabetic rats
| ||Mi Ran Choi,Su Min Kwak,Sol Hee Bang,Jo-Eun Jeong,Dai-Jin Kim |
| ||Journal of Ginseng Research. 2016; |
|[Pubmed] | [DOI]|
||Effect of Streptozotocin on Plasma Insulin Levels of Rats and Mice: A Meta-analysis Study
| ||Burcu Koksal |
| ||Open Access Macedonian Journal of Medical Sciences. 2015; 3(3): 380 |
|[Pubmed] | [DOI]|
||The effect of a preparation of minerals, vitamins and trace elements on the cardiac gene expression pattern in male diabetic rats
| ||Márta Sárközy,Gergo Szucs,Márton Pipicz,Ágnes Zvara,Katalin Éder,Veronika Fekete,Csilla Szucs,Judit Bárkányi,Csaba Csonka,László G. Puskás,Csaba Kónya,Péter Ferdinandy,Tamás Csont |
| ||Cardiovascular Diabetology. 2015; 14(1) |
|[Pubmed] | [DOI]|