Spondias tuberosa inner bark extract exert antidiabetic effects in streptozotocin-induced diabetic rats

Journal of Ethnopharmacology

Volumn 227, Issue , 2018, Pages 248-257

  de Moura Barbosa, Humberto ^a   Amaral, Dionísio ^a   do Nascimento, Jailson Nunes ^a   Machado, Dijanah Cota ^a   de Sousa Araújo, Thiago Antônio ^a   de Albuquerque, Ulysses Paulino ^a   Guedes da Silva Almeida, Jackson Roberto ^b   Rolim, Larissa Araújo ^b   Lopes, Norberto Peporine ^c   Gomes, Dayane Aparecida ^a   Lira, Eduardo Carvalho ^a  

^a FEDERAL UNIVERSITY OF PERNAMBUCO   (Brazil)

^b University of San Francisco Valley   (Brazil)

^c UNIVERSITY OF SÃO PAULO   (Brazil)

Author keywords

Diabetes mellitus; Ethnopharmacology; Medicinal plants; Spondias tuberosa

Indexed keywords

ALANINE AMINOTRANSFERASE; ALBUMIN; ANTIDIABETIC AGENT; ASPARTATE AMINOTRANSFERASE; CATALASE; CHOLESTEROL; GALLIC ACID; GLUCOSE; GLUTATHIONE; GLUTATHIONE DISULFIDE; HIGH DENSITY LIPOPROTEIN CHOLESTEROL; NITRITE; PLANT EXTRACT; PROTEIN; QUERCETIN; SPONDIAS TUBEROSA EXTRACT; STREPTOZOCIN; SUPEROXIDE DISMUTASE; THIOBARBITURIC ACID REACTIVE SUBSTANCE; TRIACYLGLYCEROL; UNCLASSIFIED DRUG; UREA; VERY LOW DENSITY LIPOPROTEIN; ANTIOXIDANT;

ADULT; ALANINE AMINOTRANSFERASE BLOOD LEVEL; ALBUMIN BLOOD LEVEL; ANACARDIACEAE; ANIMAL EXPERIMENT; ANTIDIABETIC ACTIVITY; ARTICLE; ASPARTATE AMINOTRANSFERASE BLOOD LEVEL; BARK; BODY WEIGHT GAIN; CHOLESTEROL BLOOD LEVEL; CONTROLLED STUDY; DIABETES CONTROL; ETHNOPHARMACOLOGY; FLUID INTAKE; GLUCOSE BLOOD LEVEL; GLUCOSE TOLERANCE; GLYCOGEN LIVER LEVEL; GLYCOGEN MUSCLE LEVEL; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; INSULIN TOLERANCE TEST; LIVER TOXICITY; MALE; MUSCLE MASS; NONHUMAN; ORAL GLUCOSE TOLERANCE TEST; PLANT STEM; PROTEIN BLOOD LEVEL; RAT; SPONDIAS TUBEROSA; STREPTOZOTOCIN-INDUCED DIABETES MELLITUS; TRIACYLGLYCEROL BLOOD LEVEL; UREA BLOOD LEVEL; URINARY EXCRETION; URINE VOLUME; WHITE ADIPOSE TISSUE; ANALYSIS; ANIMAL; DRUG EFFECT; EXPERIMENTAL DIABETES MELLITUS; LIPID METABOLISM; LIVER; METABOLISM; PHYTOTHERAPY; WISTAR RAT;

ANACARDIACEAE; ANIMALS; ANTIOXIDANTS; BLOOD GLUCOSE; DIABETES MELLITUS, EXPERIMENTAL; GLUTATHIONE; HYPOGLYCEMIC AGENTS; LIPID METABOLISM; LIVER; MALE; PHYTOTHERAPY; PLANT BARK; PLANT EXTRACTS; RATS, WISTAR;

EID: 85053415458     PISSN: 03788741     EISSN: 18727573     Source Type: Journal    
DOI: 10.1016/j.jep.2018.08.038     Document Type: Article

References (45)

1. Adefegha, S.A., Oboh, G., Adefegha, O.M., Boligon, A.A., Athayde, M.L., Antihyperglycemic, hypolipidemic, hepatoprotective and antioxidative effects of dietary clove (Szyzgium aromaticum) bud powder in a high-fat diet/streptozotocininduced diabetes rat model. J. Sci. Food Agric. 94 (2014), 2726–2737.
2. Aguilar-Barajas, E., Sork, V.L., González-Zamora, A., Rocha_Ramírez, V., Arroyo-Rodríguez, V., Oyama, K., Isolation and characterization of polymorphic microsatellite loci in Spondias radlkoferi (Anacardiaceae). Appl. Plant Sci. 2 (2014), 1–3.
3. Albuquerque, U.P., Medeiros, P.M., Almeida, A.L.S., Monteiro, J.M., Lins Neto, E.M.F., Melo, J.G., Santos, J.P., Medicinal plants of the caatinga (semi-arid) vegetation of NE Brazil: a quantitative approach. J. Ethnopharmacol. 3 (2007), 325–354.
4. Barbosa, H.M., Nascimento, J.N., Araújo, T.A., Duarte, F.S., Albuquerque, U.P., Vieira, J.R., et al. Acute toxicity and citotoxity effect of ethanolic extract of Spondias tuberosas Arruda Bark: hematological, biochemical and histopathological evaluation. An. Acad. Bras. Cienc. 88 (2016), 1993–2004.
5. Beers, R.F. Jr., Sizer, I.W., A spectrophotometric method for measuring breakdown of hydrogen peroxide by catalase. J. Biol. Chem. 195 (1952), 133–140.
6. Bonora, E., Moghetti, P., Zancanaro, C., Cigolini, M., Querena, M., Cacciatrori, V., et al. Estimates of in vivo insulin action in man: comparison of insulin tolerance test with euglycemic and hyperglycemic glucose clamp studies. J. Clin. Endocrinol. Metab. 68 (1989), 374–378.
7. Bradford, M.M., A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal. Biochem. 72 (1976), 248–254.
8. Brady, M.J., Allosteric trumps covalent in the control of glycogen synthesis. Cell Metab. 12 (2010), 428–430.
9. Carroll, N.V., Longley, R.W., Roe, J.H., The determination of glycogen in liver and muscle by use of anthrone reagente. J. Biol. Chem. 220 (1956), 586–593.
10. Cavan, D., Fernandes, J.C., Makaroff, L., Ogurtsova, K., Webber, S., 2015. IDF Diabetes Atlas. Seventh, Belgium.
11. Chandran, R., Parimelazhagan, T., Shanmugam, S., Thankarajan, S., Antidiabetic activity of Syzygium calophyllifolium in streptozotocin-nicotinamide induced Type-2 diabetic rats. Biomed. Pharmacother. 82 (2016), 547–554.
12. Chaudhury, A., Duvoor, C., Dendi, V.R.S., Kraleti, S., Chada, A., Ravilla, R., Marco, A., Clinical review of antidiabetic drugs: implications for Type 2 diabetes mellitus management. Front. Endocrinol. (Lausanne) 24 (2017), 1–12.
13. Da Silva Siqueira, E.M., Félix-Silva, J., de Araújo, L.M., Fernandes, J.M., Cabral, B., Gomes, J.A., et al. Spondias tuberosa (Anacardiaceae) leaves: profiling phenolic compounds by HPLC-DAD and LC-MS/MS and in vivo anti-inflammatory activity. Biomed. Chromatogr. 30 (2016), 1656–1665.
14. Draper, H.H., Squires, E.J., Mahmoodi, H., Wu, J., Agarwal, S., Hadley, M., A comparative evaluation of thiobarbituric acid methods for the determination of malondialdehyde in biological materials. Free Radic. Biol. Med. 15 (1993), 353–363.
15. Dubowski, K.M., An o-toluidine method for body-fluid glucose determination. Clin. Chem. 8 (1962), 215–235.
16. Ezuruike, U.F., Prieto, J.M., The use of plants in the traditional management of diabetes in Nigeria: pharmacological and toxicological considerations. J. Ethonopharmacol. 155 (2014), 857–924.
17. Fred-Jaiyesimi, A.A., Wilkins, M.R., Abo, K.A., Hypoglicemic and amylase inhibitory activity of leaves of Spondias mombin Linn. Afr. J. Med. Med. Sci. 38 (2009), 343–349.
18. Hissin, P.J., Hilf, R., A fluorometric method for determination of oxidized and reduced glutathione in tissues. Anal. Biochem. 74 (1976), 214–216.
19. Hu, X.F., et al. Evaluation of in vitro/in vivo anti-diabetic effects and identification of compounds from Physalis alkekengi. Fitoterapia 127 (2018), 129–137, 10.1016/j.fitote.2018.02.015 (Jun, Epub 2018 Feb 12).
20. Kabir, M.S.H., Uddin, M.M.N., Hosen, S.M.Z., Investigation on hypoglycemic effects of ethanol extract of Alpinia nigra (Gaertn.) in animal model. J. Intercult. Ethnopharmacol. 5 (2016), 131–136.
21. Kalyanaraman, B., Teaching the basics of redox biology to medical and graduate students: oxidants, antioxidants and disease mechanisms. Redox Biol. 1 (2013), 244–257.
22. Karan, S.K., Mondal, A., Mishra, S.K., Pal, D., Rout, K.K., 2013. Antidiabetic Effect of Streblus asper in Streptozotocin-Induced Diabetic Rats.
23. Katz, S.R., Newman, R.A., Lansky, E.P., Punica granatum: heuristic treatment for diabetes mellitus. J. Med. Food 10 (2007), 213–217.
24. Malmstrom, R., Packard, C.J., Caslake, M., Bedford, D., Stewart, P., YkiJarvinen, H., et al. Effects of insulin and acipimox on VLDL1 and VLDL2 apolipoprotein B production in normal subjects. Diabetes 47 (1998), 779–787.
25. Marin-Peñalver, J.J., Martín-Timón, I., Sevillano-Collantes, C., Cañizo-Gómez, F.J., Update on the treatment of type 2 diabetes mellitus. World J. Diabetes 7 (2016), 354–395.
26. Miranda, K.M., Espey, M.G., Wink, D.A., A rapid, simple spectrophotometric method for simultaneous detect ion of nitrate and nitrite. Nitric Oxide 5 (2001), 62–71.
27. Misra, H.P., Fridovich, I., The role of superoxide anion in the autoxidation of epinephrine and a simple assay for superoxide dismutase. J. Biol. Chem. 247 (1972), 3170–3175.
28. Moodley, K., Joseph, K., Naidoo, Y., Islam, S., Mackraj, I., Antioxidant, antidiabetic and hypolipidemic effects of Tulbaghia violacea Harv. (wild garlic) rhizome methanolic extract in a diabetic rat model. BMC Complement. Altern. Med. 15 (2015), 1–13.
29. Nurdiana, S., Goh, U.M., Ahmad, H., Dom, S.M., Symal'ain Azmi, N., Noor Mohamda zin, N.S., et al. Changes in pancreatic histology, insulin secretion and oxidative status in diabetic rats following treatment with Ficus deltoidea and vitexin. BMC Complement. Altern. Med. 17 (2017), 1–17.
30. Ojewole, J.A., Antiinflamatory, analgesic and hypoglicemic effects of Mangifera indica Linn (Anacardiaceae) stem-bark aqueous extract. Methods Find. Exp. Clin. Pharmacol. 27 (2005), 547–554.
31. Oliveira, H.C., dos Santos, M.P., Grigulo, R., Lima, L.L., Martins, D.T., Lima, J.C., et al. Antidiabetic activity of Vatairea macrocarpa extract in rats. J. Ethnopharmacol. 115 (2008), 515–519.
32. Oloyede, H.O.B., Bello, T.O., Ajiboye, T.O., Salawu, M.O., Antidiabetic and antidyslipidemic activities of aqueous leaf extract of Dioscoreophyllum cumminsii (Stapf) Diels in alloxan-induced diabetic rats. J. Ethnopharmacol. 166 (2015), 313–322.
33. Parmar, H.S., Kar, A., Antidiabetic potential of Citrus sinensis and Punica granatum peel extracts in alloxan treated male mice. Biofactors 31 (2007), 17–24.
34. Rashid, U., Khan, M.R., Sajid, M., Hepatoprotetive potential of Fagonia olivieri DC against acetaminophen induced toxicity in rats. BMC Complement. Altern. Med. 161 (2016), 449–662 467.
35. Rivera-Ramírez, F., Escalona-Cardoso, G.N., Garduño-Siciliano, L., Galaviz-Hernández, C., Paniagua-Castro, N., Antiobesity and hypoglycaemic effects of aqueous extract of Ibervillea sonorae in mice fed a high-fat diet with fructose. J. Biomed. Biotechnol. 2011 (2011), 1–6.
36. Seino, S., Sugawara, K., Yokoi, N., Takahashi, H., β-cell signalling and insulin secretagogues A path for improved diabetes therapy. Diabetes Obes. Metab. 19 (2017), 22–29.
37. Shah, N.A., Khan, M.R., Antidiabetic effect of Sida cordata in alloxan induced diabetic rats. Biomed. Res. Int. 2014 (2014), 1–15.
38. Sharma, S., Pathak, S., Gupta, G., Sharma, S.K., Singh, L., Sharma, R.K., et al. Pharmacological evaluation of aqueous extract of Syzigium cumini for its antihyperglucemic and antidyslipidemic properties in diabetic rats fed a high cholesterol diet – role of PPARγ and PPARα. Biomed. Pharmacother. 89 (2017), 447–453.
39. Szkudelski, T., The mechanism of alloxan and streptozotocin action in beta cells of the rat pancreas. Physiol. Res. 50 (2001), 537–546.
40. Taskinen, M.R., Lipoprotein lipase in diabetes. Diabetes Metab. Rev. 3 (1987), 551–570.
41. Wang, M., Carver, J.J., Phelan, V.V., Sanchez, L.M., Garq, N., Peng, Y., et al. Sharing and community curation of mass spectrometry data with global natural products social molecular networking. Nat. Biotechnol. 34 (2016), 828–837.
42. Wang, Y.H., Liu, Y.H., He, G.R., Ly, Y., Du, G.H., Esculin improves dyslipidemia, inflammation and renal damage in streptozotocin-induced diabetic rats. BMC Complement. Altern. Med. 15 (2015), 1–8.
43. Wang, Z., Wang, J., Chan, P., Treating type 2 diabetes mellitus with traditional Chinese and Indian medicinal herbs. Evid.-Based Complem. Altern. Med. 7 (2013), 1–17.
44. Widyawati, T., Yusoff, N.A., Asmawi, M.Z., Ahmad, M., Antihyperglycemic effect of methanol extract of Syzygium polyanthum(Wight.) leaf in streptozotocin-induced diabetic rats. Nutrients 7 (2015), 7764–7780.
45. Yusoff, N.A., Ahmad, M., Al-Hindi, B., Widyawati, T., Mahmud, M.F.Y.R., Razak, K.N.A., Asmawi, M.Z., Aqueous extract of Nypa fruticans Wurmb. vinegar alleviates postprandial hyperglycemia in normoglycemic rats. Nutrients 7 (2015), 7012–7026.