Antidiabetic activity, glucose uptake stimulation and α-glucosidase inhibitory effect of Chrysophyllum cainito L. stem bark extract

BMC Complementary and Alternative Medicine

Volumn 18, Issue 1, 2018, Pages

  Doan, Hau Van ^a   Riyajan, Siriporn ^a   Iyara, Roongtip ^a   Chudapongse, Nuannoi ^a  

^a SURANAREE UNIVERSITY OF TECHNOLOGY   (Thailand)

Author keywords

Alloxan; Antidiabetic activity; Chrysophyllum cainito; Glucose uptake; glucosidase

Indexed keywords

ACARBOSE; ALLOXAN; ALPHA GLUCOSIDASE; ANTIDIABETIC AGENT; ANTIOXIDANT; ASCORBIC ACID; BUTYLCRESOL; CHRYSOPHYLLUM CAINITO EXTRACT; GLIBENCLAMIDE; GLUCOSE; INSULIN; PLANT EXTRACT; UNCLASSIFIED DRUG; GLYCOSIDASE INHIBITOR;

ABDOMINAL WALL MUSCULATURE; ABTS RADICAL SCAVENGING ASSAY; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ANTIDIABETIC ACTIVITY; ANTIOXIDANT ACTIVITY; AREA UNDER THE CURVE; ARTICLE; BARK; CHRYSOPHYLLUM CAINITO; CONTROLLED STUDY; DPPH RADICAL SCAVENGING ASSAY; ENZYME INHIBITION; FERRIC REDUCING ANTIOXIDANT POWER ASSAY; GLUCOSE ABSORPTION; GLUCOSE BLOOD LEVEL; GLUCOSE TRANSPORT; IC50; IN VITRO STUDY; JEJUNUM; MALE; MOUSE; NON INSULIN DEPENDENT DIABETES MELLITUS; NONHUMAN; ORAL GLUCOSE TOLERANCE TEST; PHYTOCHEMISTRY; PLANT STEM; SAPOTACEAE; TRADITIONAL MEDICINE; ANIMAL; CHEMISTRY; DRUG EFFECT; ENZYMOLOGY; EXPERIMENTAL DIABETES MELLITUS; HUMAN; INSTITUTE FOR CANCER RESEARCH MOUSE; METABOLISM; PHYTOTHERAPY; TRANSPORT AT THE CELLULAR LEVEL;

ALPHA-GLUCOSIDASES; ANIMALS; BIOLOGICAL TRANSPORT; BLOOD GLUCOSE; DIABETES MELLITUS, EXPERIMENTAL; GLYCOSIDE HYDROLASE INHIBITORS; HUMANS; HYPOGLYCEMIC AGENTS; INSULIN; MALE; MICE; MICE, INBRED ICR; PHYTOTHERAPY; PLANT BARK; PLANT EXTRACTS; SAPOTACEAE;

EID: 85054251898     PISSN: None     EISSN: 14726882     Source Type: Journal    
DOI: 10.1186/s12906-018-2328-0     Document Type: Article

References (54)

1. Ogurtsova K, da Rocha Fernandes JD, Huang Y, Linnenkamp U, Guariguata L, Cho NH, et al. IDF diabetes atlas: global estimates for the prevalence of diabetes for 2015 and 2040. Diabetes Res Clin Pract. 2017;128:40-50.
2. Fowler MJ. Microvascular and macrovascular complications of diabetes. Clin Diabetes. 2008;26:77-82.
3. Johansen JS, Harris AK, Rychly DJ, Ergul A. Oxidative stress and the use of antioxidants in diabetes: linking basic science to clinical practice. Cardiovasc Diabetol. 2005;4:5.
4. Pietta P, Simonetti P, Mauri P. Antioxidant activity of selected medicinal plants. J Agric Food Chem. 1998;46:4487-90.
5. Krishnaiah D, Sarbatly R, Nithyanandam R. A review of the antioxidant potential of medicinal plant species. Food Bioprod Process. 2011;89:217-33.
6. Yashwant Kumar A, Nandakumar K, Handral M, Talwar S, Dhayabaran D. Hypoglycaemic and anti-diabetic activity of stem bark extracts Erythrina indica in normal and alloxan-induced diabetic rats. Saudi Pharm J. 2011;19:35-42.
7. Meira NA, Klein LCJ, Rocha LW, Quintal ZM, Monache FD, Cechinel Filho V, et al. Anti-inflammatory and anti-hypersensitive effects of the crude extract, fractions and triterpenes obtained from Chrysophyllum cainito leaves in mice. J Ethnopharmacol. 2014;151:975-83.
8. Shailajan S, Gurjar D. Wound healing activity of Chrysophyllum cainito L. leaves: evaluation in rats using excision wound model. J Young Pharm. 2016;8:96-103.
9. Oranusi SU, Braide W, Umeze RU. Antimicrobial activities and chemical compositions of Chrysophyllum cainito (star apple) fruit. Ambit J. 2015;1:8-24.
10. Koffi N, Ernest AK, Marie-Solange T, Beugre K, Noeuml ZG. L. Effect of aqueous extract of Chrysophyllum cainito leaves on the glycaemia of diabetic rabbits. African J Pharm Pharmacol. 2009;3:501-6.
11. Hegde K, Arathi A, Mathew A. Evaluation of antidiabetic activity of hydro alcoholic extract of Chrysophyllum cainito fruits. Int J Pharm Sci Res. 2016;7:4422-8.
12. Morton JF. The star apple. In: Fruits of Warm Climates. Miami: Julia F. Morton; 1987. p. 408-10.
13. Koffi N, Konan Édouard K, Kouassi K. Ethnobotanical study of plants used to treat diabetes, in traditional medicine, by Abbey and Krobou people of Agboville (Côte-d'Ivoire). Am J Sci Res. 2009;2009:45-58.
14. Yadav RNS, Agarwala M. Phytochemical analysis of some medicinal plants. J Phytol. 2011;3:10-4.
15. Sharma V, Paliwal R. Preliminary phytochemical investigation and thin layer chromatography profiling of sequential extracts of Moringa oleifera pods. Int J Green Pharm. 2013;7:41-5.
16. Kumkrai P, Weeranantanapan O, Chudapongse N. Antioxidant, α-glucosidase inhibitory activity and sub-chronic toxicity of Derris reticulata extract: its antidiabetic potential. BMC Complement Altern Med. 2015;15:35.
17. Abdennacer B, Karim M, Yassine M, Nesrine R, Mouna D, Mohamed B. Determination of phytochemicals and antioxidant activity of methanol extracts obtained from the fruit and leaves of Tunisian Lycium intricatum Boiss. Food Chem. 2015;174:577-84.
18. Sudan R, Bhagat M, Gupta S, Singh J, Koul A. Iron (FeII) chelation, ferric reducing antioxidant power, and immune modulating potential of Arisaema jacquemontii (Himalayan cobra lily). Biomed Res Int. 2014;2014:179865.
19. Ibrahim MA, Islam MS. Butanol fraction of Khaya senegalensis root modulates beta-cell function and ameliorates diabetes-related biochemical parameters in a type 2 diabetes rat model. J Ethnopharmacol. 2014;154:832-8.
20. Alam MM, Meerza D, Naseem I. Protective effect of quercetin on hyperglycemia, oxidative stress and DNA damage in alloxan induced type 2 diabetic mice. Life Sci. 2014;109:8-14.
21. Shahid S, Bukhari I, Abbasi MH, Ahmad MK. Dose optimization of alloxan for diabetes in albino mice. Biologica. 2015;61:301-5.
22. Parra-Naranjo A, Delgado-Montemayor C, Fraga-López A, Castañeda-Corral G, Salazar-Aranda R, Acevedo-Fernández JJ, et al. Acute hypoglycemic and antidiabetic effect of teuhetenone a isolated from Turnera diffusa. Molecules. 2017;22:559.
23. Widyawati T, Yusoff AN, Asmawi ZM, Ahmad M. Antihyperglycemic effect of methanol extract of Syzygium polyanthum (Wight.) leaf in streptozotocin-induced diabetic rats. Nutrients. 2015;7(9):7764-80.
24. Hassan Z, Yam MF, Ahmad M, Yusof APM. Antidiabetic properties and mechanism of action of Gynura procumbens water extract in streptozotocin-induced diabetic rats. Molecules. 2010;15:9008-23.
25. Fowler MJ. Diabetes treatment, part 2: Oral agents for glycemic management. Clin Diabetes. 2007;25:131-4.
26. Groop LC, Pelkonen R, Koskimies S, Bottazzo GF, Doniach D. Secondary failure to treatment with oral antidiabetic agents in non-insulin-dependent diabetes. Diabetes Care. 1986;9:129-33.
27. Grover JK, Yadav S, Vats V. Medicinal plants of India with anti-diabetic potential. J Ethnopharmacol. 2002;81:81-100.
28. Andrikopoulos S, Blair AR, Deluca N, Fam BC, Proietto J. Evaluating the glucose tolerance test in mice. Am J Physiol Endocrinol Metab. 2008;295:E1323-32.
29. Lenzen S. The mechanisms of alloxan- and streptozotocin-induced diabetes. Diabetologia. 2008;51:216-26.
30. Hirsh AJ, Yao SY, Young JD, Cheeseman CI. Inhibition of glucose absorption in the rat jejunum: a novel action of alpha-D-glucosidase inhibitors. Gastroenterology. 1997;113:205-11.
31. Ma X, Iwanaka N, Masuda S, Karaike K, Egawa T, Hamada T, et al. Morus alba leaf extract stimulates 5′-AMP-activated protein kinase in isolated rat skeletal muscle. J Ethnopharmacol. 2009;122:54-9.
32. Kleinert M, Liao Y-H, Nelson JL, Bernard JR, Wang W, Ivy JL. An amino acid mixture enhances insulin-stimulated glucose uptake in isolated rat epitrochlearis muscle. J Appl Physiol. 2011;111:163-9.
33. O'Harte FP, Gray AM, Flatt PR. Gastric inhibitory polypeptide and effects of glycation on glucose transport and metabolism in isolated mouse abdominal muscle. J Endocrinol. 1998;156:237-43.
34. Boyd AC, Abdel-Wahab YH, McKillop AM, McNulty H, Barnett CR, O'Harte FP, et al. Impaired ability of glycated insulin to regulate plasma glucose and stimulate glucose transport and metabolism in mouse abdominal muscle. Biochim Biophys Acta. 2000;1523:128-34.
35. DeFronzo RA, Tripathy D. Skeletal muscle insulin resistance is the primary defect in type 2 diabetes. Diabetes Care. 2009;32:S157-63.
36. Olefsky JM. Treatment of insulin resistance with peroxisome proliferator-activated receptor γ agonists. J Clin Invest. 2000;106:467-72.
37. Ferré P. The biology of peroxisome proliferator-activated receptors. Diabetes. 2004;53:S43-50.
38. Herman MA, Kahn BB. Glucose transport and sensing in the maintenance of glucose homeostasis and metabolic harmony. J Clin Invest. 2006;116:1767-75.
39. Rose AJ, Richter EA. Skeletal muscle glucose uptake during exercise: how is it regulated? Physiology. 2005;20:260-70.
40. Satoh T. Molecular mechanisms for the regulation of insulin-stimulated glucose uptake by small guanosine triphosphatases in skeletal muscle and adipocytes. Int J Mol Sci. 2014;15:18677-92.
41. Röhling M, Herder C, Stemper T, Müssig K. Influence of acute and chronic exercise on glucose uptake. J Diabetes Res. 2016;2016:2868652.
42. Vlavcheski F, Naimi M, Murphy B, Hudlicky T, Tsiani E. Rosmarinic acid, a rosemary extract polyphenol, increases skeletal muscle cell glucose uptake and activates AMPK. Molecules. 2017;22:E1669.
43. Mohamed EAH, Siddiqui MJA, Ang LF, Sadikun A, Chan SH, Tan SC, et al. Potent α-glucosidase and α-amylase inhibitory activities of standardized 50% ethanolic extracts and sinensetin from Orthosiphon stamineus Benth as anti-diabetic mechanism. BMC Complement Altern Med. 2012;12:176.
44. Kedare SB, Singh RP. Genesis and development of DPPH method of antioxidant assay. J Food Sci Technol. 2011;48:412-22.
45. Huang D, Ou B, Prior RL. The chemistry behind antioxidant capacity assays. J Agric Food Chem. 2005;53:1841-56.
46. Abdallah HM, Salama MM, Abd-elrahman EH, El-Maraghy SA. Antidiabetic activity of phenolic compounds from pecan bark in streptozotocin-induced diabetic rats. Phytochem Lett. 2011;4:337-41.
47. Nazaruk J, Borzym-Kluczyk M. The role of triterpenes in the management of diabetes mellitus and its complications. Phytochem Rev. 2015;14:675-90.
48. Piluzza G, Bullitta S. Correlations between phenolic content and antioxidant properties in twenty-four plant species of traditional ethnoveterinary use in the Mediterranean area. Pharm Biol. 2011;49:240-7.
49. Luo XD, Basile MJ, Kennelly EJ. Polyphenolic antioxidants from the fruits of Chrysophyllum cainito L. (star apple). J Agric Food Chem. 2002;50:1379-82.
50. Shailajan S, Gurjar D. Pharmacognostic and phytochemical evaluation of Chrysophyllum cainito Linn. leaves. Int J Pharm Sci Rev Res. 2014;26:106-11.
51. Castro AJG, Frederico MJS, Cazarolli LH, Mendes CP, Bretanha LC, Schmidt ÉC, et al. The mechanism of action of ursolic acid as insulin secretagogue and insulinomimetic is mediated by cross-talk between calcium and kinases to regulate glucose balance. Biochim Biophys Acta. 2015;1850:51-61.
52. Gupta R, Sharma AK, Dobhal MP, Sharma MC, Gupta RS. Antidiabetic and antioxidant potential of beta-sitosterol in streptozotocin-induced experimental hyperglycemia. J Diabetes. 2011;3:29-37.
53. Gupta R, Sharma AK, Sharma MC, Dobhal MP, Gupta RS. Evaluation of antidiabetic and antioxidant potential of lupeol in experimental hyperglycaemia. Nat Prod Res. 2012;26:1125-9.
54. Oboh G, Ogunsuyi OB, Ogunbadejo MD, Adefegha SA. Influence of gallic acid on α-amylase and α-glucosidase inhibitory properties of acarbose. J Food Drug Anal. 2016;24:627-34.