Protective effect of grape seed and skin extract against diabetes-induced oxidative stress and renal dysfunction in virgin and pregnant rat

Biomedicine and Pharmacotherapy

Volumn 83, Issue , 2016, Pages 584-592

  Oueslati, Nourhene ^a,b   Charradi, Kamel ^a,b   Bedhiafi, Takwa ^a,b   Limam, Ferid ^b   Aouani, Ezzedine ^a,b  

^a University of Carthage   (Tunisia)

^b CENTRE DE BIOTECHNOLOGIE DE BORJ CÉDRIA   (Tunisia)

Author keywords

Diabetes; Grape seed and skin extract; Kidney protection; Oxidative stress; Rat

Indexed keywords

ACETYLCHOLINESTERASE; BIOLOGICAL MARKER; CALPAIN; CATALASE; COPPER; CREATININE; GLUTATHIONE PEROXIDASE; GRAPE SEED EXTRACT; IRON; LACTATE DEHYDROGENASE; MANGANESE; MONOPHENOL MONOOXYGENASE; SELENIUM; SUPEROXIDE DISMUTASE; TRANSITION ELEMENT; ZINC; ANTIOXIDANT; METAL; PHENOL DERIVATIVE; PLANT EXTRACT; PROTECTIVE AGENT;

ADULT; ALLOXAN-INDUCED DIABETES MELLITUS; ANALYTICAL PARAMETERS; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CONTROLLED STUDY; DIABETES MELLITUS; DRUG MEGADOSE; DRUG POTENCY; DRUG SAFETY; FEMALE; KIDNEY DYSFUNCTION; KIDNEY FUNCTION; LIPID PEROXIDATION; NONHUMAN; OXIDATION; OXIDATIVE STRESS; PRIORITY JOURNAL; PROTEINURIA; RAT; RENAL PROTECTION; UREMIA; ANIMAL; BODY WEIGHT; CHEMISTRY; DIABETES MELLITUS, EXPERIMENTAL; DRUG EFFECTS; INTRACELLULAR SPACE; KIDNEY; LIQUID CHROMATOGRAPHY; METABOLISM; PATHOLOGY; PATHOPHYSIOLOGY; PLANT SEED; PREGNANCY; PROTEIN CARBONYLATION; TANDEM MASS SPECTROMETRY; VITIS;

ANIMALS; ANTIOXIDANTS; BIOMARKERS; BODY WEIGHT; CHROMATOGRAPHY, LIQUID; DIABETES MELLITUS, EXPERIMENTAL; FEMALE; INTRACELLULAR SPACE; KIDNEY; LIPID PEROXIDATION; METALS; OXIDATIVE STRESS; PHENOLS; PLANT EXTRACTS; PREGNANCY; PROTECTIVE AGENTS; PROTEIN CARBONYLATION; SEEDS; TANDEM MASS SPECTROMETRY; VITIS;

EID: 84989951477     PISSN: 07533322     EISSN: 19506007     Source Type: Journal    
DOI: 10.1016/j.biopha.2016.07.024     Document Type: Article

References (53)

1. [1] Ferrara, A., Increasing prevalence of gestational diabetes mellitus: a public health perspective. Diabetes Care 30 (2007), 141–146.
2. [2] West, I.C., Radicals and oxidative stress in diabetes. Diabetes Med. 17 (2000), 171–180.
3. [3] Khanal, R.C., Howard, L.R., Prior, R.L., Procyanidin composition of selected fruits and fruit byproducts is affected by extraction method and variety. J. Agric. Food Chem. 57 (2009), 8839–8843.
4. [4] Sarkaki, A., Farbood, Y., Badavi, M., The effect of grape seed extract (GSE) on spatial memory in aged male rats. Pak. J. Med. Sci. 23 (2007), 561–565.
5. [5] Bagchi, D., Bagchi, M., Stohs, S.J., et al. Kuszynski, free radicals and grape seed proanthocyanidin extract: importance in human health and disease prevention. Toxicology 148 (2000), 187–197.
6. [6] Nassiri-Asl, M., Hosseinzadeh, H., Review of the pharmacological effects of Vitis vinifera (grape) and its bioactive compounds. Phytother. Res. 23 (2009), 1197–1204.
7. [7] Singleton, V.L., Rossi, J., Colorimetry of total phenolics with phospho-molybdic-phosphotungstic acid reagents. Am. J. Enol. Vitic. 16 (1965), 144–158.
8. [8] Dewanto, V., Wu, X., Adom, K.K., Liu, R.H., Thermal processing enhance the nutritional value of tomatoes by increasing total antioxidant activity. J. Agric. Food Chem. 50 (2002), 3010–3014.
9. [9] Sun, B., Richardo da Silva, J.M., Spranger, I., Critical factors of vanillin assay for catechin and proanthocyanidins. J. Agric. Food Chem. 46 (1998), 4267–4274.
10. [10] National Research council, Guide for the Care and the Use of Laboratory Animals, 20, National Institute of Health, Bethesda (1985) pp. 85–123.
11. [11] Beach, J.E., Miles, D.J., Lukes, Y.G., Vigersky, R.A., Microplate solid-phase radioimmunoassay for rat prolactin. J. Lab. Clin. Med. 105 (1985), 294–298.
12. [12] Folch, J., Lees, M., Sloane Stanley, G.H., A simple method for the isolation and purification of total lipids from animal tissues. J. Biol. Chem. 226 (1957), 497–509.
13. [13] Humbert, G., Guingamp, M.F., Linden, G., Method for the measurement of lipase activity in milk. J. Dairy Res. 64 (1997), 465–469.
14. [14] Draper, H.H., Hadley, M., Malondialdehyde determination as index of lipid peroxidation. Methods Enzymol. 186 (1990), 421–431.
15. [15] Levine, R.L., Garland, D., Oliver, C.N., et al. Determination of carbonyl content in oxidatively modified proteins. Methods Enzymol. 186 (1990), 464–478.
16. [16] Ohnishi, S.T., Barr, J.K., A simplified method of quantitating protein using the biuret and phenol reagents. Anal. Biochem. 86 (1978), 193–200.
17. [17] Ellman, G.L., Tissue sulfhydryl groups. Arch. Biochem. Biophys. 82 (1959), 70–77.
18. [18] Nakamura, K., Hosada, S., Hayashi, K., Purification and properties of rat liver glutathione peroxidase. Biochem. Biophys. Acta 358 (1974), 251–261.
19. [19] Aebi, H., Methods of Enzymatic Analysis. 2nd ed., 1974, Chemia Weinheium, New York, N. Y., USA.
20. [20] 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.
21. [21] Leardi, A., Caraglia, M., Selleri, C., et al. Desferioxamine increases iron depletion and apoptosis induced by ara-C of human myeloid leukaemic cells. Br. J. Haematol. 102 (1998), 746–752.
22. [22] Stern, J., Lewis, W.H., The colorimetric estimation of calcium in serum with ocresolphthalein complexone. Clin. Chim. Acta 2 (1957), 576–580.
23. 2 release by the treatment of human blood polymorphonuclear leucocytes with myristate. J. Biochem. 86 (1979), 87–95.
24. [24] Santoro, J.C., Harris, G., Sitlani, A., Colorimetric detection of glutamine synthetase-catalyzed transferase activity in glucocorticoid-treated skeletal muscle cells. Anal. Biochem. 289 (2001), 18–25.
25. [25] Bergmeyer, H.U., New values for the molar extinction coefficients of NADH and NADPH for the use in routine laboratories (author's transl). Z. Klin. Chem. Klin. Biochem. 13 (1975), 507–508.
26. [26] Worthington Biochemical Corporation, Worthington Enzyme Manual Worthington Biochemical Corp., Freehold, NJ, USA (1977) 74–75.
27. [27] Sasaki, T., Kikuchi, T., Yumoto, N., Yoshimura, N., Murachi, T., Comparative specificity and kinetic studies on porcine calpain I and calpain II with naturally occurring peptides and synthetic fluorogenic substrates. J. Biol. Chem. 259 (1984), 12489–12494.
28. [28] Ellman, G.L., Courtney, K.D., Andres, V. Jr., Feather-Stone, R.M., A new and rapid colorimetric determination of acetylcholinesterase activity. Biochem. Pharmacol. 7 (1961), 88–95.
29. [29] Gao, W., Li, X., Gao, Z., Li, H., Iron increases diabetes-induced kidney injury and oxidative stress in rats. Biol. Trace Elem. Res. 160 (2014), 368–375.
30. [30] Zhuang, T., Han, H., Yang, Z., Iron, oxidative stress and gestational diabetes. Nutrients 6 (2014), 3968–3980.
31. [31] Akhlaghi, F., Bagheri, S.M., Rajabi, O., A comparative study of relationship between micronutrients and gestational diabetes. ISRN Obstet. Gynecol., 2012, 2012, 470419.
32. [32] Ye, W., Gong, X., Xie, J., et al. AChE deficiency or inhibition decreases apoptosis and p53 expression and protects renal function after ischemia/reperfusion. Apoptosis 15 (2010), 474–487.
33. [33] Zhu, H., Gao, W., Jiang, H., Wu, J., Shi, Y.F., Zhang, X.J., Calcineurin mediates acetylcholinesterase expression during calcium ionophore A23187-induced HeLa cell apoptosis. Biochim. Biophys. Acta 1773 (2007), 593–602.
34. [34] Jin, Q.H., He, H.Y., Shi, Y.F., Lu, H., Zhang, X.J., Overexpression of acetylcholinesterase inhibited cell proliferation and promoted apoptosis in NRK cells. Acta Pharmacol. Sin. 25 (2004), 1013–1021.
35. [35] Jun, J.G., Maeda, S., Kuwahara-Otani, S., et al. Expression of adrenergic and cholinergic receptors in murine renal intercalated cells. J. Vet. Med. Sci. 76 (2014), 1493–1500.
36. [36] Smith, M.A., Schnellmann, R.G., Calpains mitochondria, and apoptosis. Cardiovasc. Res. 96 (2012), 32–37.
37. [37] Covington, M.D., Schnellmann, R.G., Chronic high glucose downregulates mitochondrial calpain 10 and contributes to renal cell death and diabetes-induced renal injury. Kidney Int. 81 (2012), 391–400.
38. [38] Hawkes, W.C., Alkan, Z., Lang, K., King, J.C., Plasma selenium decrease during pregnancy is associated with glucose intolerance. Biol. Trace Elem. Res. 100 (2004), 19–29.
39. [39] Bomback, A.S., Rekhtman, Y., Whaley-Connell, A.T., Kshirsagar, A.V., Sowers, J.R., Chen, S.C., et al. Gestational diabetes mellitus alone in the absence of subsequent diabetes is associated with microalbuminuria: results from the Kidney Early Evaluation Program (KEEP). Diabetes Care 33 (2010), 2586–2591.
40. [40] Güçlü, A., Yonguç, N., Dodurga, Y., Gündoğdu, G., Güçlü, Z., Yonguç, T., et al. The effects of grape seed on apoptosis-related gene expression and oxidative stress in streptozotocin-induced diabetic rats. Ren. Fail. 37 (2015), 192–197.
41. [41] Gao, Z., Liu, G., Hu, Z., Li, X., Yang, X., Jiang, B., et al. Grape seed proanthocyanidin extract protects from cisplatin-induced nephrotoxicity by inhibiting endoplasmic reticulum stress-induced apoptosis. Mol. Med. Rep. 9 (2014), 801–817.
42. [42] Hamidian Jahromi, A., Roozbeh, J., Bastani, B., Potential protective effect of grape seed proanthocyanidine extract in cold ischemia-reperfusion injury of the transplanted kidney. Iran. J. Kidney Dis. 7 (2013), 327–328.
43. [43] Salem, N.A., Salem, E.A., Renoprotective effect of grape seed extract against oxidative stress induced by gentamicin and hypercholesterolemia in rats. Ren. Fail. 33 (2011), 824–832.
44. [44] Rayman, M.P., Searle, E., Kelly, L., Johnsen, S., Bodman-Smith, K., Bath, S.C., et al. Effect of selenium on markers of risk of pre-eclampsia in UK pregnant women: a randomised controlled pilot trial. Br. J. Nutr. 112 (2014), 99–111.
45. [45] Nair, A.V., Hocher, B., Verkaart, S., van Zeeland, F., Pfab, T., Slowinski, T., et al. Loss of insulin-induced activation of TRPM6 magnesium channels results in impaired glucose tolerance during pregnancy. Proc. Natl. Acad. Sci. U. S. A. 109 (2012), 11324–11329.
46. [46] Lappas, M., Hiden, U., Desoye, G., Froehlich, J., Hauguel-de Mouzon, S., Jawerbaum, A., The role of oxidative stress in the pathophysiology of gestational diabetes mellitus. Antioxid. Redox. Signal. 15 (2011), 3061–3100.
47. [47] Lappas, M., Mitton, A., Lim, R., Barker, G., Riley, C., Permezel, M., SIRT1 is a novel regulator of key pathways of human labor. Biol. Reprod. 84 (2011), 167–178.
48. [48] Charradi, K., Elkahoui, S., Karkouch, I., Limam, F., Hamdaoui, G., Hassine, F.B., et al. Grape seed and skin extract alleviates high-fat diet-induced renal lipotoxicity and prevents copper depletion in rat. Appl. Physiol. Nutr. Metab. 38 (2013), 259–267.
49. [49] Safwen, K., Selima, S., Mohamed, E., Ferid, L., Pascal, C., Mohamed, A., et al. Protective effect of grape seed and skin extract on cerebral ischemia in rat: implication of transition metals. Int. J. Stroke 10 (2015), 415–424.
50. [50] Shafiee, M., Carbonneau, M.A., Urban, N., Descomps, B., Leger, C.L., Grape and grape seed extract capacities at protecting LDL against oxidation generated by Cu2+, AAPH or SIN-1 and at decreasing superoxide THP-1 cell production. A comparison to other extracts or compounds. Free Radic. Res. 37 (2003), 573–584.
51. [51] Du, Y., Guo, H., Lou, H., Grape seed polyphenols protect cardiac cells from apoptosis via induction of endogenous antioxidant enzymes. J. Agric. Food Chem. 55 (2007), 1695–1701.
52. [52] del Bas, J.M., Crescenti, A., Arola-Arnal, A., Oms-Oliu, G., Arola, L., Caimari, A., Grape seed procyanidin supplementation to rats fed a high-fat diet during pregnancy and lactation increases the body fat content and modulates the inflammatory response and the adipose tissue metabolism of the male offspring in youth. Int. J. Obes. (Lond.) 39 (2015), 7–15.
53. [53] FDA agency response letter GRAS notice n° GRN000124, http//www.fda.gov/Food/Food ingredients Packaging/Generally Recognized as Safe GRAS/GRAS Listings/ucm 153940.htm, 2011 (accessed 01.06.11).