Effects of the local purple sticky rice bran extract on antioxidant activity and calcium oxalate crystal formation and aggregation in vitro
Main Article Content
Abstract
Introduction: Kidney stone disease is a common urological disorder affecting human health. Inhibition of calcium oxalate (CaOx) formation and aggregation can prevent the recurrence of kidney stones. Pigmented rice has been studied for various functions including antioxidant activity, anti-inflammation, antidiabetic, anticancer, and antiaging. However, the function of purple rice bran on the antioxidant activity related to the kidney stone disease is limited.
Objective: To investigate the effect of the purple sticky rice bran (PSB) extract obtained from the local strain at Songkhla province on its antioxidant activity and subsequent in vitro inhibition of CaOx crystal formation and aggregation.
Methodology: The PSB ethanol extract was prepared at different concentrations (0.025–1.4 mg/mL). The levels of anthocyanin and total phenolic compounds were analyzed using pH differential and the Folin–Ciocalteu reagent methods. The antioxidant activity of PSB extract was determined using the DPPH assay and FRAP. The formed CaOx crystals were incubated with the PSB extract at different concentrations (20 - 400 µg/mL). The number of CaOx crystals and their aggregation forms were determined and compared with the control.
Results: The levels of anthocyanin and total phenolic compounds in PSB extract were 18.67 ± 1.50 µg/g and 34.70 ± 1.64 mg gallic acid equivalent/g of rice bran, respectively. The DPPH free radical scavenging antioxidant activity and ferric-reducing antioxidant power increased after the concentration of the PSB extract was increased. The IC50 of ascorbic acid and PSB extract were 0.016 and 0.07 mg/ml, respectively. The PSB extract significantly decreased the formation and the number of CaOx crystals. Moreover, the high concentration of PSB extract augmented the calcium oxalate dihydrate (COD) crystal formation rather than the monohydrate crystal formation. Furthermore, it inhibited the CaOx crystal aggregation in a dose-dependent manner.
Conclusion: PSB extract contained substances with high antioxidative activity and could suppress the CaOx crystal formation and aggregation. This study can be helpful to the researchers in the development of strategies for the prevention of kidney stones.
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References
Romero V, Akpinar H, Assimos DG. Kidney stones: a global picture of prevalence, incidence, and associated risk factors. Rev Urol. 2010 Spring;12(2-3):e86-96. PMID: 20811557.
Coe F, Evan A, Worcester E. Pathogenesis and Treatment of Nephrolithiasis, Seldin and Geibisch's. The Kidney. 2013, 2311-2349, 2.
Kok DJ, Khan SR. Calcium oxalate nephrolithiasis, a free or fixed particle disease. Kidney Int. 1994 Sep;46(3):847-54. doi:10.1038/ki.1994.341.
Wiessner JH, Mandel GS, Mandel NS. Membrane interactions with calcium oxalate crystals: variation in hemolytic potentials with crystal morphology. J Urol. 1986 Apr;135(4):835-9. doi:10.1016/s0022-5347(17)45871-x.
Ratkalkar VN, Kleinman JG. Mechanisms of Stone Formation. Clin. Rev. Bone Miner. Metab. 2011 Dec; 9(3-4), 187–197. doi: 10.1007/s12018-011-9104-8.
Semangoen T, Sinchaikul S, Chen ST, Thongboonkerd V. Proteomic analysis of altered proteins in distal renal tubular cells in response to calcium oxalate monohydrate crystal adhesion: Implications for kidney stone disease. Proteomics Clin Appl. 2008 Jul;2(7-8):1099-109. doi:10.1002/prca.200780136.
Thongboonkerd V, Semangoen T, Sinchaikul S, Chen ST. Proteomic analysis of calcium oxalate monohydrate crystal-induced cytotoxicity in distal renal tubular cells. J Proteome Res. 2008 Nov;7(11):4689-700. doi:10.1021/pr8002408.
Nirumand MC, Hajialyani M, Rahimi R, Farzaei MH, Zingue, S, Nabavi SM, et al. Dietary Plants for the Prevention and Management of Kidney Stones: Preclinical and Clinical Evidence and Molecular Mechanisms. Int J Mol Sci. 2018 Mar;19(3):765. doi: 10.3390/ijms19030765.
Butterweck V, Khan SR. Herbal medicines in the management of urolithiasis: alternative or complementary? Planta Med. 2009 Aug;75(10),1095–1103. doi:10.1055/s-0029-1185719.
Ahuja U, Ahuja SC, Chaudhary, N, Thakrar R. 2007. Red rices – past, present and future. Asian Agri-History. 2007;11:291–304.
Sookwong P, Nakagawa K, Murata K, Kojima Y, Miyazawa T. Quantitation of tocotrienol and tocopherol in various rice brans. J Agric Food Chem. 2007 Jan;55(2):461-466. doi:10.1021/jf0621572.
Jariwalla RJ. Rice-bran products: phytonutrients with potential applications in preventive and clinical medicine. Drugs Exp Clin Res. 2001;27(1):17-26. PMID: 11276826.
Oki T, Masuda M, Kobayashi M, Nishiba Y, Furuta S, Suda I, et al. Polymeric procyanidins as radical-scavenging components in red-hulled rice. J Agric Food Chem. 2002 Dec;50(26):7524-7529. doi:10.1021/jf025841z.
Semangoen T, Khawsuk W, Simanon N, Soiphet T, Homjai W, Boonchaleaw B, et al. Antioxidant effects of unpolished Sung-Yod sticky rice on prevention of ethylene glycol-induced renal pathology in rats. Chula Med J. 2018 May – Jun; 62(3):451 – 64.
Khawsuk W, Semangoen T, Nuurai P, Mepan W, Wingworn K. Antioxidant activity of unpolished Riceberry (Oryza sativa) and the inhibition of calcium oxalate crystal growth and aggregation. Chula Med J. 2018 May - Jun; 62(3):419 – 34.
Ebisuno S, Morimoto S, Yasukawa S, Ohkawa T. Results of long-term rice bran treatment on stone recurrence in hypercalciuric patients. Br J Urol. 1991 Mar;67(3):237-40. doi:10.1111/j.1464-410x.1991.tb15125.x.
Jun HI, Song GS, Yang EI, Youn Y, Kim YS. Phenolic compounds of pigmented rice bran extracts. J Food Sci. 2012 Jul; 77:759-64. doi:10.1111/j.1750-3841.2012.02763.x.
Vijayalakshmi M, Ruckmani K. Ferric reducing anti-oxidant power assay in plant extract. Bangladesh J Pharmacol. 2016 Jun;11:570-2. doi:10.3329/bjp.v11i3.27663.
Thongboonkerd V, Semangoen T, Chutipongtanate S. Factors determining types and morphologies of calcium oxalate crystals: molar concentrations, buffering, pH, stirring and temperature. Clin Chim Acta. 2006 May;367(1-2):120-31. doi:10.1016/j.cca.2005.11.033.
Jang S, Xu Z. Lipophilic and Hydrophilic Antioxidants and Their Antioxidant Activities in Purple Rice Bran. J. Agric. Food Chem. 2009 Jan;57(3):858–62. doi: 10.1021/jf803113c.
Srisawat U, Panunto W, Kaendee N, Tanuchit S, Itharat A, Lerdvuthisopon N, et al. 2010. Determination of Phenolic Compounds, Flavonoids, and Antioxidant Activities in Water Extracts of Thai Red and White Rice Cultivars. J Med Assoc Thai. 2010;93(Suppl.7):S83-S91.
Hu C, Zawistowski J, Ling W, Kitts DD. Black rice (Oryza sativa L. indica) pigmented fraction suppresses both reactive oxygen species and nitric oxide in chemical and biological model systems. J Agric Food Chem. 2003 Aug 27;51(18):5271-7. doi:10.1021/jf034466n.
Atmani F, Khan SR Effects of an extract from Herniaria hirsuta on calcium oxalate crystallization in vitro. BJU Int. 2000 Apr;85(6):621-5. doi: 10.1046/j.1464-410x.2000.00485.x.
Bashir S, Gilani AH. Antiurolithic effect of Bergenia ligulata rhizome: an explanation of the underlying mechanisms J Ethnopharmacol. 2009 Feb 25;122(1):106-16. doi:10.1016/j.jep.2008.12.004.
Khan A, Bashir S, Khan SR, Gilani AH. Antiurolithic activity of Origanum vulgare is mediated through multiple pathways. BMC Complement Altern Med. 2011 Oct 17;11:96. doi: 10.1186/1472-6882-11-96.
Wesson JA, Worcester EM, Wiessner JH, Mandel NS, Kleinman JG. Control of calcium oxalate crystal structure and cell adherence by urinary macromolecules. Kidney Int. 1998 Apr;53(4):952-7. doi:10.1111/j.1523-1755.1998.00839.x.
Hess, B., Kok, D.J., 1996. Nucleation growth and aggregation of crystals. In: Coe, F.L., Favus, M.J., Pak, C.Y., Parks, J.H., Preminger, G.M. (Eds.), Kidney Stones, Medical and Surgical Management. Lippincott-Raven, Philadelphia, PA, USA, pp. 3–32.
Kok DJ, Papapoulos SE, Bijvoet OLM. Crystal agglomeration is a major element in calcium oxalate urinary stone formation. Kidney Int. 1990 Jan;37(1):51-6. doi:10.1038/ki.1990.7.
Kumar MS, Selvam R. Supplementation of vitamin E and selenium prevents hyperoxaluria in experimental urolithic rats. J Nutr Biochem. 2003 Jun;14(6):306-13. doi:10.1016/s0955-2863(03)00033-0.
Thamilselvan S, Menon M. Vitamin E therapy prevents hyperoxaluria-induced calcium oxalate crystal deposition in the kidney by improving renal tissue antioxidant status. BJU Int. 2005 Jul;96(1):117-26. doi:10.1111/j.1464-410X.2005.05579.x.
Itoh Y, Yasui T, Okada A, Tozawa K, Hayashi Y, Kohri K. Preventive effects of green tea on renal stone formation and the role of oxidative stress in nephrolithiasis. J Urol. 2005 Jan;173(1):271-5. doi:10.1097/01.ju.0000141311.51003.87.
Byahatti VV, Pat KV, D’Souza MG. Effect of Phenolic Compounds from Bergenia ciliata (Haw.) Sternb.leaves on Experimental kidney stones. Anc Sci Life. 2010 Jul;30(1):14-7. PMID: 22557418.