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| PHARMACOLOGICAL STUDY |
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| Year : 2014 | Volume
: 35
| Issue : 2 | Page : 211-217 |
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Therapeutic potency of saponin rich aqueous extract of Scoparia dulcis L. in alloxan induced diabetes in rats
P Saravana Perumal1, PV Anaswara1, A Muthuraman2, S Krishan3
1 Department of Biotechnology, Udaya School of Engineering, Kanyakumari, Tamil Nadu, India
2 Akal Pharmacology and Toxicology Research Centre, A unit of Akal College of Pharmacy and Technical Education, Sangrur, India
3 Department of Pharmaceutical Sciences and Drug Research, Pharmacology Division, Council for Scientific and Industrial Research, Punjabi University, Patiala, Punjab, India
| Date of Web Publication | 5-Dec-2014 |
Correspondence Address:
A Muthuraman
HOD, Akal Pharmacology and Toxicology Research Centre, A unit of Akal College of Pharmacy and Technical Education (ACPTE), Mastunana Sahib, Sangrur - 148 001, Punjab
India
 Source of Support: None, Conflict of Interest: None  | Check |
DOI: 10.4103/0974-8520.146261
 Abstract | | |
Background: Diabetes mellitus is major metabolic disorders of carbohydrate metabolism. This leads to alter the multiple organ system. Aims: To investigate the antidiabetic and antioxidant effects of the saponin rich aqueous extract of Scoparia dulcis (SRE-SD) using alloxan-induced hyperglycemic rat model. Material and Methods: The single dose of alloxan was injected for the induction of diabetes in rats. The SRE-SD and glibenclamide were administered for 15 consecutive days from the 3 rd day of alloxan administration. Quantity of food and water intake was measured at day 0, and 18. Further, body weight was recorded and blood samples were collected at different time intervals that is, day 0, 3, 8, 13, and 18. The oxidative biomarkers (i.e. thiobarbituric acid reactive substances (TBARS), reduced glutathione (GSH) and nitrite (NO 2−) levels were also estimated in the serum sample. Results: The SRE-SD showed a remarkable dose and time-dependent changes in alloxan-induced rise in the level of food consumption and water intake, serum glucose level, TBARS, NO 2− and fall in the level of GSH. Further, significant attenuation was observed at 20 and 30 mg/kg of SRE-SD treated group. Conclusions: These findings demonstrate that SRE-SD has both antidiabetic and antioxidant effects on the experimental model of diabetes in rat. Keywords: Alloxan, diabetes mellitus, oxidative stress, saponin, Scoparia dulcis
How to cite this article:
Perumal P S, Anaswara P V, Muthuraman A, Krishan S. Therapeutic potency of saponin rich aqueous extract of Scoparia dulcis L. in alloxan induced diabetes in rats. AYU 2014;35:211-7 |
How to cite this URL:
Perumal P S, Anaswara P V, Muthuraman A, Krishan S. Therapeutic potency of saponin rich aqueous extract of Scoparia dulcis L. in alloxan induced diabetes in rats. AYU [serial online] 2014 [cited 2023 Jun 4];35:211-7. Available from: https://www.ayujournal.org/text.asp?2014/35/2/211/146261 |
| Introduction | |  |
Diabetes mellitus is one of the most common long lasting metabolic disorders. [1] The World Health Organization (WHO) reported that 171 million people worldwide suffer from diabetes in year 2000. [2] The expected total number of people with diabetes will be about 300 million by year 2025; this number would be double by the year 2030. [2],[3] The use of Indian and Chinese ethno-botanicals has a long folkloric history for the treatment of diabetes mellitus. [4],[5] The WHO has estimated that 80% of the world population use herbal medicine for their primary healthcare needs and also they are totally dependent on traditional medicine. [4],[6] The use of complementary and alternative medicine, especially the consumption of botanicals have been increasing rapidly worldwide because of the less side-effects when compared with modern medicine. [7]
Scoparia dulcis L. commonly known as "Sweet Broomweed" is widely used in Indian folk and Ayurvedic medicine for the treatment of diabetes mellitus. [8] Often this plant is considered as one of the source plant of Pashanabheda (Bergenia ligulata) of Ayurveda. It is a perennial herb widely distributed in tropical and sub-tropical regions. In these regions, fresh or dried S. dulcis plants have been traditionally used as remedies for various ailments such as stomach problems that is, peptic ulcer, [9] hypertension, [10] hyperlipidemia, [11] hepatic injury, [12] algesia, and inflammation. [13],[14] It has various biologically active secondary metabolites such as carbohydrates, coumarins, phenols, saponins, glycosides, tannins, amino acids, flavonoids, terpenoids, catecholamine, noradrenaline, and adrenaline. [15],[16] Moreover, it has also possess the various active chemical constituents that is, scoparic acid A, scoparic acid B, scoparic acid C, scopadulcic acid A and B, scopadiol, scopadulciol, dulcinol, scopadulin etc. [16],[17] It has been documented to possess the various pharmacological actions such as antitumor, anticancer, antibacterial, antiviral, antifungal, antileukemia and antiaging. [16],[18] Moreover, experimental reports suggest that it has potential antidiabetic action. [19],[20]
Various antidiabetic agents from natural products including saponins, flavonoids, alkaloids, anthraquinones, terpenes, coumarins, phenolics, polysaccharides have been promised to possess the antidiabetic action. [21] Saponins are a class of chemical compounds, it is one of major secondary metabolites has found in natural sources and it has found particular abundance in various plant species. Further, saponins have been documented that, it can be serving as major antihyperglycemic components. [22] S. dulcis is reported to possess the antidiabetic potential, [19],[20] whereas there is no report for the responsible phytoconstituents for this activity. Therefore, our works is focused to investigate the therapeutic potency of saponin rich extract of Scoparia dulcis (SRE-SD) in alloxan-induced diabetes in rats.
| Materials and Methods | | |
Drugs and chemicals
Alloxan monohydrate was purchased from Explicit Chemical Pvt. Limited, Pune, India. 5,5'- dithio, bis (2-nitrobenzoic acid), bovine serum albumin, reduced glutathione (GSH) were purchased from Sisco Research Laboratories, Mumbai. Thiobarbituric acid was purchased from Loba Chemie, Mumbai. Glibenclamide was procured from Sun Pharmaceuticals, India. The glibenclamide (GLUCOVANCE® ) has been used as a positive control in this study.
Plant material
Scoparia dulcis plants were collected from the paddy fields of Kalkurichy, Kanyakumari District. The plant was identified and authenticated. The specimen was deposited in the same department for future reference (No. SD/158/06/2013).
Preparation of aqueous extracts
Whole plants of S. dulcis materials were washed individually with clean sterile water and oven dried for 1 h at 16°C. Three hundred grams of S. dulcis material was made into a fine powder and soaked in 150 ml of distilled water (aqueous extract) for 24 h. The slurry was placed in a clean, sterile glass container and shaken vigorously to allow for proper extraction. The slurry was filtered using a Whatman filter paper no 42, the extract was air dried and stored at 4°C for further preparation. The yield of aqueous extract of S. dulcis was obtained 11.36% w/w, dry weight basis.
Preparation of saponin rich extracts Scoparia dulcis
Saponins rich extract was prepared from aqueous extract of S. dulcis as described method in previous study.[23] with some modification. Briefly, the aqueous extract of S. dulcis (300 g) was refluxed with n-butanol for 2 h and n-butanol soluble constituents were separated by filtration. The n-butanol layer was sequentially washed with distilled water, alkali (2% KOH) and distilled water again. The n-butanol layer was evaporated and dried under vacuum to obtain a clear powder of crude saponin. The yield of crude saponin of S. dulcis was obtained 25.3% w/w, dry weight basis.
Determination of saponin contents by high-performance liquid chromatography analysis
The saponin content of SRE-SD was determined by using high-performance liquid chromatography (HPLC). [24] The extracts were filtered through a 0.45 μm membrane filter (Millipore, Bedford, USA) before injection into the column and analyzed by HPLC. Determination of saponin was carried out using a C 18 column (4.6 × 150 mm, ID; particle size 5 μm). The mobile phase consisted of methanol, water, and acetic acid in the ratio of 60:34:6 (v/v/v) at a flow rate of 1.5 ml/min. The mobile phase was filtered and degassed prior to use. The injection volume was 20 μl and the detection wavelength was set at 254 nm and 25°C. A total of 5 mg of ursolic acid (Sigma-Aldrich) was weighed into a 100 ml volumetric flask and diluted to volume with triple deionized water for a final concentration of 0.05 mg/ml for using as a saponin standard. The compounds appearing in chromatograms were identified on retention times and spectral data by comparison with standards. All analyses were performed on triplicate of the extracts. The values were expressed as mean ± standard deviation (SD).
Animals
Male Wistar rats (200-220 g, purchased from Animal Husbandary, Kanyakumari) were used in the present investigation. The rats were allowed free access to feed and tap water under strictly controlled pathogen free conditions with room temperature 25°C ± 2°C, relative humidity (30-70%) on 12 h light and dark cycle, lighted between time intervals of 6:00 AM and 6:00 PM. The rats were fed on standard rodent pellet chow and acclimatization to their environment for 2 weeks before the commencement of the experiment. The study protocol was duly approved by Institutional Animal Ethical Committee (193/98/CPCSEA; dated April 15, 2005) of the department and care of the animals was carried out as per the guidelines of the committee for the purpose of Committee for the Control and Supervision of Experiments on Animals (CPCSEA), Ministry of Environment and Forest, Government of India.
Induction of diabetes
Diabetes was induced by a single intra-venous administration of freshly prepared alloxan monohydrate (40 mg/kg; dissolved in 1 ml normal saline) on overnight fasted rats (i.e. day 0) as described method of Ahmed. [25] After 48 h, blood samples were collected from the rat tail vein puncture method and rats fasting glucose levels were checked by commercial diagnostic device method in alloxan treated animals. The fasting glucose above 210 mg/dl along with showing clear signs of diabetes that is, polyuria, polyphagia and polydipsia were considered and selected for further study. Animals with fasting serum glucose <200 mg/dl were rejected.
Experimental protocol
This study consists of seven groups, each group comprised of six Wistar rats (n = 6). After the development of hyperglycaemic (>210 mg/dl) rats were randomly allotted in Group 2-7.
Group 1 (Normal control): Rats were subjected without administration of the vehicle and drugs in this study.
Group 2 (Alloxan control).
Group 3 (Vehicle control): Diabetic rats were treated orally with 5 ml/kg of distilled water for 18 consecutive days from the 3 rd day of alloxan administration.
Group 4-6 (SRE-SD-10, 20 and 30 mg/kg respectively): Diabetic rats were treated orally with SRE-SD at the dose of 10, 20, 30 mg/kg of body weight/day for 18 consecutive days from the 3 rd day of alloxan administration.
Group 7 (Glibenclamide 1.25 mg/kg): Diabetic rats were treated orally with glibenclamide at the dose of 1.25 mg/kg of body weight/day for 18 consecutive days from the 3 rd day of alloxan administration. [25] The graphical study design was expressed in [Figure 1]. | Figure 1: The study design of alloxan induced diabetes mellitus. Glibenclamide has been used as a reference drug. Saponin rich aqueous extract of Scoparia dulcis (20 and 30 mg/kg, p.o.) and glibenclamide (1.25 mg/kg, p.o.) were administered once a day for 18 days and blood samples were collected at different time intervals (i.e., day 0, 2, 3, 8, 14 and day 20)
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The dose was suspended in 1% w/v of carboxy methyl cellulose and it was administered through a gastric gavage by using oral cannula. Further, measurement of body weight, food and water consumption as well as blood sample analysis were performed different time intervals that is, day 0, 2, 8, 14, and 20. In serum glucose level was determined using one touch electronic glucometer (Life Scan, Johnson and Johnson Limited, Mumbai, India) and blood biomarkers that is, thiobarbituric acid reactive substances (TBARS), [26] reduced GSH, [27] nitrite (NO 2− ) [28] and total protein [29] levels were also estimated by spectrophotometric method.
Statistical analysis
The data were analyzed by two-way analysis of variance followed by Bonferonni's post-hoc test by using Graph-Pad prism software, California, USA. Values were expressed as mean standard deviation (mean ± SD). P < 0.05 was considered to be statistically significant.
| Results | | |
Total saponin content level in aqueous extract of Scoparia dulcis
The aqueous extract of S. dulcis contained 38.64% of total saponins when compared to ursolic acid (100%). The triplicate value of total saponin value has shown to possess the 0.350 ± 0.011 mg of ursolic acid equivalent per ml. The chromatogram of SRE-SD and standard saponin that is, ursolic acid (real time value is 19.93 [Figure 2]). | Figure 2: High-performance liquid chromatography (HPLC) chromatogram of saponin rich aqueous extract of Scoparia dulcis (SRE-SD) and standard compounds HPLC peak in a and b indicates saponin contents of SRE-SD and reference samples, that is, ursolic acid respectively (real time value is 19.93). The peaks in HPLC chromatogram represent saponin concentrations which were expressed as ursolic acid equivalent
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Effect of saponin rich aqueous extract of Scoparia dulcis on serum glucose level
Administration of alloxan resulted in significant rise serum glucose level when compared to normal control group. The administration of SRE-SD have shown to possess the attenuating effect on alloxan-induced diabetes in dose-dependent manner. Moreover, the significant ameliorative effect has been observed in 20 and 30 mg/kg of SRE-SD treated group. The vehicle treated group did not produce the any significant changes when compared to alloxan treated group. Further, the administration of glibenclamide has also been produced the significant (P < 0.05) ameliorative effect when compared to alloxan treated groups [Figure 3]. | Figure 3: Effect of saponin rich aqueous extract of Scoparia dulcis on alloxan-induced serum glucose levels F (6, 41) = 4331.053; P < 0.001. Digits in parentheses indicate dose in mg/kg. (*P < 0.05 vs. normal control group, †P <0.05 vs. alloxan control group)
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Effect of saponin rich aqueous extract of Scoparia dulcis on bodyweight, food and water consumption levels
Administration of alloxan resulted in significant rise in food and water consumption and decrease in bodyweight levels when compared to normal control group. The administration of SRE-SD shown to possess the attenuating effect on alloxan-induced above changes in a dose-dependent manner. Moreover, the significant ameliorative effect has been observed in 20 and 30 mg/kg of SRE-SD treated group. The vehicle treated group did not produce the any significant changes when compared to alloxan treated group. Further, the administration of glibenclamide has also been produced the significant (P < 0.05) ameliorative effect on bodyweight, fluid intake, and food consumption levels when compared to alloxan treated groups [Table 1]. | Table 1: Effect of SRE-SD on body weight, fluid intake and food consumption changes in alloxan-induced diabetic rats
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Effect of saponin rich aqueous extract of Scoparia dulcis on oxidative stress marker levels
Administration of alloxan resulted in significant rise in TBARS, NO 2− and decrease in GSH levels when compared to normal control group. The administration SRE-SD shown to possess the attenuating effect on alloxan-induced oxidative stress marker changes in a dose-dependent manner. Moreover, the significant ameliorative effect has been observed in 20 and 30 mg/kg of SRE-SD treated group. The vehicle treated group did not produce the any significant changes when compared to alloxan treated group. Further, the administration of glibenclamide has also been produced the significant (P < 0.05) ameliorative effect on TBARS, GSH, and NO 2− levels when compared to alloxan treated groups [Table 2]. | Table 2: Effect of SRE-SD on oxidative stress marker levels in alloxan-induced diabetic rats
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| Discussion | | |
In the present investigation, administration of alloxan-induced a significant development of diabetic changes that is, fasting blood glucose, bodyweight, food as well as water consumption levels and oxidative stress marker changes that is, TBARS, reduced GSH, as well as NO 2− levels in rats. Moreover, treatment of SRE-SD has shown to produce significant attenuating effect on alloxan-induced diabetic and antioxidant changes. These observations are in line with others research reports, that is suggested, crude extract of S. dulcis has possess the ameliorative effect in streptozotocin-induced of diabetic changes. [20],[30],[31]
Alloxan monohydrate is a pyrimidine derivative has been commonly used as a pharmacological tool for induction of diabetes mellitus in experimental animals. The pathogenesis of alloxan-induced diabetes is mainly through the ability of destroying the insulin-producing beta cells of the pancreas. [32],[33] In vitro studies have also shown that alloxan is selectively toxic to pancreatic beta cells, causing cell necrosis. [34] The cytotoxic action of alloxan is mediated through rise in oxidative stress by free radical (reactive oxygen species and reactive nitrogen species) generations along with a massive increase of cytosolic calcium concentration, leading to a rapid destruction of beta cells. [35] Oxidative stress has been reported to be the most common and important mechanism in diabetes mellitus and their complications. [36],[37]
Many natural products, especially plants-derived medicines have been promised to treat and management of diabetes mellitus in experimental animal and human trials via antioxidative mechanism. [21],[38],[39] The research report from literature and this study has been revealed that, the S. dulcis has antidiabetic and antioxidant potential. [20],[31] Numerous studies has been reported that herbal constituents such as saponins, tannins, flavonoids, phenolic compounds, terpenoids, glycosides alkaloids etc., shown to possess the free radical scavenging role in vitro as well as in biological systems and also ameliorated the oxidative injury and disease progress. [40] However, among the all-natural compounds, saponins and flavonoids are reported to possess the potential antidiabetic action. [41],[42]
Saponins has been documented to possess the ameliorate effects from disease progress by various number cellular mechanisms such as reduction in the lipid peroxidation, cytokines, chemokines, pro-apoptotic, and pro-inflammatory mediators, cellular calcium accumulation, and oxidation of 2'- deoxyribose; increased in the levels of reduced GSH, antiinflammatory and antiapoptotic mediators as well as physiological process that is, rise in the activity of myeloperoxidase, superoxide dismutase and GSH peroxidase; decreased in the levels creatine kinase, catalase levels. [43],[44],[45] Moreover, it has been reported that, saponins are possess the potential free radical scavenging action on hydroxyl and superoxide radicals along with suppression of inducible nitric oxide synthase, cyclooxygenase-2, and tumor necrosis factor-alpha expression. [44],[46] Soponins have also been demonstrated that, it possesses the inhibitory action on opening of the potassium adenosine-triphosphate (K ATP ) channel. [44] Glibenclamide inhibits the opening of ATP-sensitive K ATP channels, which represents a protective mechanism in type-II diabetes mellitus in experimental animal as well as human. [47],[48],[49] It also possesses the potential antioxidant and antiinflammatory actions. [48],[50] Therefore, glibenclamide has been selected as a positive control in this investigation.
| Conclusion | | |
Saponin rich aqueous extract of S. dulcis has potent antidiabetic and antioxidant effects thus might be a potential therapeutic agent for the management of diabetes mellitus. However, the more elaborative and mechanistic studies are required to explore their possible therapeutic action.
| References | | |
| 1. | Swinnen SG, Simon AC, Holleman F, Hoekstra JB, Devries JH. Insulin detemir versus insulin glargine for type 2 diabetes mellitus. Cochrane Database Syst Rev 2011;7:CD006383-447.  |
| 2. | Wild S, Roglic G, Green A, Sicree R, King H. Global prevalence of diabetes: Estimates for the year 2000 and projections for 2030. Diabetes Care 2004;27:1047-53. |
| 3. | Sone H. Diabetes mellitus and metabolic syndrome in epidemiological studies. Nihon Rinsho 2011;69 Suppl 1:93-100. [ PUBMED] |
| 4. | Chen W, Zhang Y, Liu JP. Chinese herbal medicine for diabetic peripheral neuropathy. Cochrane Database Syst Rev 2013;10;CD007796-932. |
| 5. | Prabhakar PK, Doble M. Mechanism of action of natural products used in the treatment of diabetes mellitus. Chin J Integr Med 2011;17:563-74. |
| 6. | Srinivasan K. Spices as influencers of body metabolism: An overview of three decades of research. Food Res Int 2005;38:77-86. |
| 7. | Hu X, Sato J, Oshida Y, Xu M, Bajotto G, Sato Y. Effect of Gosha-jinki-gan (Chinese herbal medicine: Niu-Che-Sen-Qi-Wan) on insulin resistance in streptozotocin-induced diabetic rats. Diabetes Res Clin Pract 2003;59:103-11. |
| 8. | Zulfiker A, Siddiqua M, Nahar L, Habib MR, Uddin N, Hasan N, et al. In vitro antibacterial, antifungal and cytotoxic activity of Scoparia dulcis L. Int J Pharm Pharm Sci 2011;3:198203. |
| 9. | Babincová M, Schronerová K, Sourivong P. Antiulcer activity of water extract of Scoparia dulcis. Fitoterapia 2008;79:587-8. |
| 10. | Esume C, Opajobi A, Osasuyi A, Ebong O, Osakwe A. Hypertensive and sympathomimetic effects of the methanol and aqueous extracts of Scoparia dulcis in anaesthetized male wistar rats. Biomed Pharma J 2011;4:11-9. |
| 11. | Pari L, Latha M. Antihyperlipidemic effect of Scoparia dulcis (sweet broomweed) in streptozotocin diabetic rats. J Med Food 2006;9:102-7. |
| 12. | Tsai JC, Peng WH, Chiu TH, Huang SC, Huang TH, Lai SC, et al. Hepatoprotective effect of Scoparia dulcis on carbon tetrachloride induced acute liver injury in mice. Am J Chin Med 2010;38:761-75. |
| 13. | Ahmed M, Shikha HA, Sadhu SK, Rahman MT, Datta BK. Analgesic, diuretic, and antiinflammatory principle from Scoparia dulcis. Pharmazie 2001;56:657-60. |
| 14. | Tsai JC, Peng WH, Chiu TH, Lai SC, Lee CY. Antiinflammatory effects of Scoparia dulcis L. and betulinic acid. Am J Chin Med 2011;39:943-56. |
| 15. | Yisa J. Phytochemical analysis and antimicrobial activity of Scoparia dulcis and nymphaea lotus. Aust J Basic App Sci 2009;3:3975-9. |
| 16. | Okhale SE, Amanabo MO, Jegede IA, Egharevba HO, Muazzam IW, Kunle OF. Phytochemical and pharmacognostic investigation of antidiabetic Scoparia dulcis Linn Scrophulariaceae whole plant grown in nigeria. Researcher 2010;2:7-16. |
| 17. | Yamamoto Y, Gaynor RB. Therapeutic potential of inhibition of the NF-kappaB pathway in the treatment of inflammation and cancer. J Clin Invest 2001;107:135-42. |
| 18. | Fulda S. Betulinic acid for cancer treatment and prevention. Int J Mol Sci 2008;9:1096-107. [ PUBMED] |
| 19. | Pari L, Latha M. Protective role of Scoparia dulcis plant extract on brain antioxidant status and lipidperoxidation in STZ diabetic male Wistar rats. BMC Complement Altern Med 2004;4:16. |
| 20. | Latha M, Pari L, Ramkumar KM, Rajaguru P, Suresh T, Dhanabal T, et al. Antidiabetic effects of scoparic acid D isolated from Scoparia dulcis in rats with streptozotocin-induced diabetes. Nat Prod Res 2009;23:1528-40. |
| 21. | Qi LW, Liu EH, Chu C, Peng YB, Cai HX, Li P. Antidiabetic agents from natural products - An update from 2004 to 2009. Curr Top Med Chem 2010;10:434-57. |
| 22. | Yang CY, Wang J, Zhao Y, Shen L, Jiang X, Xie ZG, et al. Antidiabetic effects of Panax notoginseng saponins and its major antihyperglycemic components. J Ethnopharmacol 2010;130:231-6. |
| 23. | Sivaramakrishna C, Rao CV, Trimurtulu G, Vanisree M, Subbaraju GV. Triterpenoid glycosides from Bacopa monnieri. Phytochemistry 2005;66:2719-28. |
| 24. | Sezgin AEC, Artik N. Determination of saponin content in Turkish tahini halvah by using HPLC. Adv J Food Sci Technol 2010;2:109-15. |
| 25. | Ahmed N. Alloxan diabetes-induced oxidative stress and impairment of oxidative defense system in rat brain: Neuroprotective effects of cichorium intybus. Int J Diabetes Metab 2009;17:105-9. |
| 26. | Yagi K. A simple fluorometric assay for lipoperoxide in blood plasma. Biochem Med 1976;15:212-6. [ PUBMED] |
| 27. | Ellman GL. Tissue sulfhydryl groups. Arch Biochem Biophys 1959;82:70-7. [ PUBMED] |
| 28. | Green LC, Wagner DA, Glogowski J, Skipper PL, Wishnok JS, Tannenbaum SR. Analysis of nitrate, nitrite, and [15N] nitrate in biological fluids. Anal Biochem 1982;126:131-8. [ PUBMED] |
| 29. | Lowry OH, Rosebrough NJ, Farr AL, Randall RJ. Protein measurement with the Folin phenol reagent. J Biol Chem 1951;193:265-75. [ PUBMED] |
| 30. | Pari L, Latha M, Rao CA. Effect of Scoparia dulcis extract on insulin receptors in streptozotocin induced diabetic rats: Studies on insulin binding to erythrocytes. J Basic Clin Physiol Pharmacol 2004;15:223-40. |
| 31. | Pari L, Latha M. Antidiabetic effect of Scoparia dulcis: Effect on lipid peroxidation in streptozotocin diabetes. Gen Physiol Biophys 2005;24:13-26. |
| 32. | Jörns A, Munday R, Tiedge M, Lenzen S. Comparative toxicity of alloxan, N-alkylalloxans and ninhydrin to isolated pancreatic islets in vitro. J Endocrinol 1997;155:283-93. |
| 33. | Dahech I, Belghith KS, Hamden K, Feki A, Belghith H, Mejdoub H. Oral administration of levan polysaccharide reduces the alloxan-induced oxidative stress in rats. Int J Biol Macromol 2011;49:942-7. |
| 34. | Yang W, Wang S, Li L, Liang Z, Wang L. Genistein reduces hyperglycemia and islet cell loss in a high-dosage manner in rats with alloxan-induced pancreatic damage. Pancreas 2011;40:396-402. |
| 35. | Sudheesh NP, Ajith TA, Janardhanan KK, Krishnan CV. Palladium-a-lipoic acid complex attenuates alloxan-induced hyperglycemia and enhances the declined blood antioxidant status in diabetic rats. J Diabetes 2011;3:293-300. |
| 36. | Sekar N, Kanthasamy A, William S, Subramanian S, Govindasamy S. Insulinic actions of vanadate in diabetic rats. Pharmacol Res 1990;22:207-17. |
| 37. | Vincent AM, Callaghan BC, Smith AL, Feldman EL. Diabetic neuropathy: cellular mechanisms as therapeutic targets. Nat Rev Neurol 2011;7:573-83. |
| 38. | Jung M, Park M, Lee HC, Kang YH, Kang ES, Kim SK. Antidiabetic agents from medicinal plants. Curr Med Chem 2006;13:1203-18. |
| 39. | Mollace V, Sacco I, Janda E, Malara C, Ventrice D, Colica C, et al. Hypolipemic and hypoglycaemic activity of bergamot polyphenols: From animal models to human studies. Fitoterapia 2011;82:309-16. |
| 40. | Firuzi O, Miri R, Tavakkoli M, Saso L. Antioxidant therapy: Current status and future prospects. Curr Med Chem 2011;18:3871-88. |
| 41. | Han C, Hui Q, Wang Y. Hypoglycaemic activity of saponin fraction extracted from Momordica charantia in PEG/salt aqueous two-phase systems. Nat Prod Res 2008;22:1112-9. |
| 42. | Misra M. Opportunities for the exploration, investigation and utilization for biological activity of novel medicinal plants. J Med Plants Res 2009;3:1-9. |
| 43. | Desai SD, Desai D, Kaur H. Saponins and their biological activities. Pharma Times 2009;41:13-6. |
| 44. | He L, Zhou G, Zhang H, He Y. Chemical constituents and biological activities of saponin from the seed of Camellia oleifera. Sci Res Essays 2010;5:4088-92. |
| 45. | An HJ, Kim IT, Park HJ, Kim HM, Choi JH, Lee KT. Tormentic acid, a triterpenoid saponin, isolated from Rosa rugosa, inhibited LPS-induced iNOS, COX-2, and TNF-a expression through inactivation of the nuclear factor-?b pathway in RAW 264.7 macrophages. Int Immunopharmacol 2011;11:504-10. |
| 46. | Rajput ZI, Hu SH, Xiao CW, Arijo AG. Adjuvant effects of saponins on animal immune responses. J Zhejiang Univ Sci B 2007;8:153-61. |
| 47. | Fravel MA, McDanel DL, Ross MB, Moores KG, Starry MJ. Special considerations for treatment of type 2 diabetes mellitus in the elderly. Am J Health Syst Pharm 2011;68:500-9. |
| 48. | Stephens JW, Bodvarsdottir TB, Wareham K, Prior SL, Bracken RM, Lowe GD, et al. Effects of short-term therapy with glibenclamide and repaglinide on incretin hormones and oxidative damage associated with postprandial hyperglycaemia in people with type 2 diabetes mellitus. Diabetes Res Clin Pract 2011;94:199-206. |
| 49. | Tahara A, Matsuyama-Yokono A, Shibasaki M. Effects of antidiabetic drugs in high-fat diet and streptozotocin-nicotinamide-induced type 2 diabetic mice. Eur J Pharmacol 2011;655:108-16. |
| 50. | Schmid D, Svoboda M, Sorgner A, Moravcevic I, Thalhammer T, Chiba P, et al. Glibenclamide reduces proinflammatory cytokines in an ex vivo model of human endotoxinaemia under hypoxaemic conditions. Life Sci 2011;89:725-34. |
[Figure 1], [Figure 2], [Figure 3]
[Table 1], [Table 2]
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| Dora Dayu Rahma Turista, Qurrotu A’yunin Lathifah, Arif Nur Muhammad Ansori, Yulanda Antonius, Gabrielle Ann Villar Posa, Wahyu Choirur Rizky, Tim Godefridus Antonius Dings, Galiya Kazhibayeva, Karina Omarova, Irina Anikina | | Research Journal of Pharmacy and Technology. 2022; : 3879 | | [Pubmed] | [DOI] | | | 4 |
Antidiabetic Activity, Phytochemical and Proximate Compositions of Different Extracts of Tephrosia bracteolata Leaves |
|
| Precious Adejoh Ida,Parker Elijah Jos,Rita Onyekachukwu Asomadu,Obioma Uzoma Njoku,Okwesili Fred Chiletugo | | Asian Journal of Plant Sciences. 2021; 20(2): 291 | | [Pubmed] | [DOI] | | | 5 |
Medicinal plants utilized in Thai Traditional Medicine for diabetes treatment: Ethnobotanical surveys, scientific evidence and phytochemicals |
|
| Catarina Andrade,Nelson G.M. Gomes,Sutsawat Duangsrisai,Paula B. Andrade,David M. Pereira,Patrícia Valentão | | Journal of Ethnopharmacology. 2020; 263: 113177 | | [Pubmed] | [DOI] | | | 6 |
In vitro
therapeutic properties of different fractions of Phaseolus vulgaris
seeds as affected by the distribution of phytochemicals |
|
| Usha Rani Telikicherla,Mahadeva Naika,Anilakumar Kandangath Raghavan,Sashikala Vadakkoot Balakrishnan | | Journal of Food Biochemistry. 2017; : e12485 | | [Pubmed] | [DOI] | | | 7 |
Sensitive quantification of coixol, a potent insulin secretagogue, in Scoparia dulcis
extract using high-performance liquid chromatography combined with tandem mass spectrometry and UV detection |
|
| Arslan Ali,Faraz Ul Haq,Qamar ul Arfeen,Khaga Raj Sharma,Achyut Adhikari,Syed Ghulam Musharraf | | Biomedical Chromatography. 2017; : e3964 | | [Pubmed] | [DOI] | | | 8 |
Experimental diabetes induced by alloxan and streptozotocin: The current state of the art |
|
| Miroslav Radenkovic,Marko Stojanovic,Milica Prostran | | Journal of Pharmacological and Toxicological Methods. 2016; 78: 13 | | [Pubmed] | [DOI] | |
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