INVESTIGAÇÃO DO POSSÍVEL EFEITO PROTETOR DA FOLHA DE Smilax fluminensis STEUD. EM CAMUNDONGOS SUBMETIDOS AO ESTRESSE OXIDATIVO PELO PARACETAMOL
DOI:
https://doi.org/10.14393/BJ-v37n0a2021-53862Palavras-chave:
Acetaminophen, Free Radicals, Hepatotoxicity, Smilax fluminensis.Resumo
Paracetamol (PCM), um fármaco amplamente utilizado pela população como antipirético e analgésico. Se administrado em altas doses pode causar dano hepático, levando a hepatoxicidade. O gênero Smilax, encontradas em regiões temperadas e tropicais, é tradicionalmente utilizado pela população através do extrato das folhas e raízes para diversas afecções, como no tratamento da sífilis, diabetes, asma e como ação diurética. Através disto, utilizaram-se os extratos das folhas da Smilax fluminensis para avaliar o efeito protetor frente ao estresse oxidativo induzido através de uma alta dose de PCM em camundongos que receberam o medicamento e após receberam o tratamento com extrato bruto e frações. Foram realizadas análise do plasma através da aspartato aminotransferase (AST), alanina aminotransferase (ALT), glicose, triglicérides e colesterol, além de técnicas bioquímicas como, catalase (CAT), glutationa-S-transferase (GST), glutationa reduzida (GSH), ácido ascórbico (ASA), substâncias reativas ao ácido tiobarbitúrico (TBARS) e proteínas carboniladas (CARBONIL) de fígado, cérebro e rins. A fração 1 do extrato foi a mais promissora, diminuindo os níveis plasmáticos da AST e ALT, os níveis de CAT e GST do fígado, juntamente com a GSH e no tecido renal e cerebral houve uma diminuição das proteínas carboniladas (PCM+F1 versus PCM). Além disso, a fração 1 mostrou-se hipoglicêmica e hipocolesterolêmica. Conclui-se que a fração 1 das folhas da Smilax fluminensis possui boa atividade antioxidante frente aos danos causados pela alta dose de paracetamol.
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Referências
ADAM, G.O., et al. Hepatoprotective effects of Nigella sativa seed extract against acetaminophen-induced oxidative stress. Asian Pacific Journal of Tropical Medicine. 2016, 9(3), 221–227. https://doi.org/10.1016/j.apjtm.2016.01.039
AJIBOYE, T.O. Standardized extract of Vitex doniana Sweet stalls protein oxidation, lipid peroxidation and DNA fragmention in acetaminopheninduced hepatotoxicity. Journal of Ethnopharmacology. 2015, 164(22), 273–282. https://doi.org/10.1016/j.jep.2015.01.026
AJIBOYE, T.O., et al. Hepatoprotective potential of Phyllanthus muellarianus leaf extract: studies on hepatic, oxidative stress and inflammatory biomarkers. Pharmaceutical Biology. 2017, 55(1), 1662-1670. https://doi.org/10.1080/13880209.2017.1317819
AMARO, C.A.B., et al. Hypoglycemic and hypotensive activity of a root extract of Smilax aristolochiifolia, standardized on n-trans-feruloyl-tyramine. Molecules. 2014, 19(8), 11366–11384. https://doi.org/10.3390/molecules190811366
ANAND-DAVID, A.V., ARULMOLI, R. and PARASURAMAN, S. Overviews of Biological Importance of Quercetin: A Bioactive Flavonoid. Pharmacognosy Reviews. 2016, 10(20), 84–89.
BAHADORAN, Z., MIRMIRAN, P. and AZIZI, F. Dietary polyphenols as potential nutraceuticals in management of diabetes: a review. Journal of Diabetes Metabolic Disorders. 2013, 12(43), 1-9.
BUEGE, J.A. and AUST, S.D. Microsomal lipid peroxidation. Methods in Enzymolog. 1978, 52, 302-309. https://doi.org/10.1016/S0076-6879(78)52032-6
BRADFORD, M.M. A rapid and sensitive method for the quantification of microgram quantities of protein utilizing the principle of protein-dye binding. Analytical Biochemistry. 1976, 72(1-2), 248-254. https://doi.org/10.1016/0003-2697(76)90527-3
CAROCHO, M. and FERREIRA, I.C.F.R. A review on antioxidants, prooxidants and related controversy: Natural and synthetic compounds, screening and analysis methodologies and future perspectives. Food and Chemical Toxicology. 2013, 51, 15-25. https://doi.org/10.1016/j.fct.2012.09.021
CHEN, L., et al. Anti-hyperuricemic and nephroprotective effects of Smilax china L. Journal of Ethnopharmacology. 2011, 135(2), 399–405. https://doi.org/10.1016/j.jep.2011.03.033
COURAD, J.P., et al. Acetaminophen distribution in the rat central nervous system. Life Sciences. 2001, 69(12), 1455-1464. https://doi.org/10.1016/S0024-3205(01)01228-0
DAI, J. and MUMPER, R.J. Plant phenolics: extraction, analysis, and their antioxidant and anticancer properties. Molecules. 2010, 15(10), 7313-7352, 2010. https://doi.org/10.3390/molecules15107313
DESANMI, S.O., LAWAL, O.R.A. and OJOKUKU, S.A. Effects of ethanolic extract of Tetrapleura tetraptera on liver function profile andhistopathology in male Dutch white rabbits. International Journal of Tropical Medicine. 2009, 4(4), 136–139.
FERNÁNDEZ-IGLESIAS, A., et al. Combination of grape seed proanthocyanidin extract and docosahexaenoic acid-rich oil increases the hepatic detoxification by GST mediated GSH conjugation in a lipidic postprandial state. Food Chemistry. 2014, 165(15), 14-20. https://doi.org/10.1016/j.foodchem.2014.05.057
GHANEM, C.I., et al. Acetaminophen from liver to brain: New insights into drug pharmacological action and toxicity. Pharmacological Research. 2016, 109, 119-131. https://doi.org/10.1016/j.phrs.2016.02.020
GHOSH, J., et al. Acetaminophen induced renal injury via oxidative stress and TNF-alpha production: therapeutic potential of arjunolic acid. Toxicology. 2010, 268(1-2), 8-18. https://doi.org/10.1016/j.tox.2009.11.011
GULCIN, I. Antioxidant activity of food constituents: an overview. Archives of Toxicology. 2012, 86, 345–391. https://link.springer.com/content/pdf/10.1007/s00204-011-0774-2.pdf
GOPIA, S., VADDEA, R. and SETTYA, O.H. Protective effect of aqueous extract of Phyllanthus fraternus against bromobenzene induced changes on cytosolic glutathione S-transferase isozymes in rat liver. Biochemistry and Biophysics Reports. 2017, 10, 208–214. https://doi.org/10.1016/j.bbrep.2017.04.001
HABIG, W.H., PABST, M.J. and JAKOBY, W.B. Glutathione S-transferase, the first enzymatic step in mercapturic acid formation. The Journal of Biological Chemistry. 1974, 249, 7130-7139.
HINSON, J.A., ROBERTS, D.W. and JAMES, L. P. Mechanisms of acetaminophen-induced liver necrosis. Handbook of Experimental Pharmacology. 2010, 196, 369-405. https://doi.org/10.1007/978-3-642-00663-012
HODGMAN, M.J., GARRARD, A.R. A Review of Acetaminophen Poisoning. Critical Care Clinics. 2012, 28(4), 499-516. https://doi.org/10.1016/j.ccc.2012.07.006
HURKADALE, P.J., et al. Hepatoprotective activity of Amorphophallus paeoniifolius tubers against paracetamol-induced liver damage in rats. Asian Pacific Journal of Tropical Biomedicine. 2012, 2(1), S238-S242. https://doi.org/10.1016/S2221-1691(12)60167-1
HUSSAIN, L., et al. Hepatoprotective effects of Malva sylvestris L. against paracetamol-induced hepatotoxicity. Turkish Journal of Biology. 2014, 38, 396–402.
JUDD, W.S., et al. Sistemática vegetal: um enfoque filogenético. 3ª ed. Porto Alegre: Artmed, 2009.
KHALIGH, P., et al. Bioactive compounds from Smilax excelsa L. Journal of the Iranian Chemical Society. 2016, 13, 1055–1059. https://doi.org/10.1007/s13738-016-0819-9
KHANDELWAL, N., et al. Unrecognized acetaminophen toxicity as a cause of indeterminate acute liver failure. Hepatology. 2011, 53, 567-576. https://doi.org/10.1002/hep.24060
KOZŁOWSKA, A. and SZOSTAK-WĘGIEREK, D. Flavonoids - food sources and health benefits. Roczniki Panstwowego Zakladu Higieny. 2014, 65(2), 79-85.
KUMPULAINEN, E., et al. Paracetamol (acetaminophen) penetrates readily into the cerebrospinal fluid of children after intravenous administration. Pediatrics. 2007, 119(4), 766-771. https://doi.org/10.1542/peds.2006-3378
LI, P., et al. Evaluating the impacts of osmotic and oxidative stress on common carp (Cyprinus carpio, L.) sperm caused by cryopreservation techniques. Biology of Reproduction. 2010, 83(5), 852–858. https://doi.org/10.1095/biolreprod.110.085852
MAJEWSKA-WIERZBICKA, M. and CZECZOT, H. Flavonoids in the prevention and treatment of cardiovascular diseases. Pol Merkur Lekarski. 2012, 32(187), 50-54.
MOHANRAJ, S., et al. Hepatoprotective effect of leaves of Morinda tinctoria Roxb. Against paracetamol induced liver damage in rats. Drug Invention Today. 2013, 5(3), 223-228. https://doi.org/10.1016/j.dit.2013.06.008
MORAIS, M.I., et al. Antioxidant and antifungal activities of Smilax campestris Griseb. (Smilacaceae). Natural Product Research. 2014, 28(16), 1275–1279. https://doi.org/10.1080/14786419.2014.895728
MURALI, A., ASHOK, P. and MADHAVAN, V. Effect of Smilax zeylanica roots and rhizomes in paracetamol induced hepatotoxicity. Journal of Complementary and Integrative Medicine. 2012, 9(1). https://doi.org/10.1515/1553-3840.1639
MUROTA, K. and TERAO, J. Antioxidative flavonoid quercetin: implications of its intestinal absorption and metabolism. Archives of Biochemistry Biophysics. 2003, 417(1), 12-17. https://doi.org/10.1016/S0003-9861(03)00284-4
MUROTA, K., NAKAMURA, Y. and UEHARA, M. Flavonoid metabolism: The interaction of metabolites and gut microbiota. Bioscience, Biotechnology, and Biochemistry. 2018, 82(4), 600-610. https://doi.org/10.1080/09168451.2018.1444467
NELSON, D.P. and KIESOW, L.A. Enthalphy of decomposition of hydrogen peroxide by catalase at 25 °C (with molar extinction coefficients of H2O2 solution in the UV). Analytical Biochemistry. 1972, 49(2), 474–478. https://doi.org/10.1016/0003-2697(72)90451-4
OLALEYE, M.T. and ROCHA, B.T.J. Acetaminophen-induced liver damage in mice: Effects of some medicinal plants on the oxidative defense system. Experimental and Toxicologic Pathology. 2008, 59(5), 319–327. https://doi.org/10.1016/j.etp.2007.10.003
OZSOY, N., et al. Antioxidant activity of Smilax excelsa L. leaf extracts. Food Chemistry. 2008, 110(3), 571-583. https://doi.org/10.1016/j.foodchem.2008.02.037
PEREIRA, D.L., et al. Antioxidant and hepatoprotective effects of ethanolic and ethyl acetate stem bark extracts of Copaifera multijuga (Fabaceae) in mice. Acta Amazonica. 2018, 48(4), 347-357. https://doi.org/10.1590/1809-4392201704473
PETRICA, E.E.A., et al. First phytochemical studies of japecanga (Smilax fluminensis) leaves: flavonoids analysis. Revista Brasileira de Farmacognosia. 2014, 24(4), 443-445. http://dx.doi.org/10.1016/j.bjp.2014.07.020
PHANIENDRA, A., JESTADI, D.B. and PERIYASAMY, L. Free radicals: properties, sources, targets, and their implication in various diseases. Indian Journal of Clinical Biochemistry. 2015, 30, 11–26. https://doi.org/10.1007/s12291-014-0446-0
POSADAS, I., et al. Acetaminophen Induces Apoptosis in Rat Cortical Neurons. PLoS ONE. 2010, 5(12), e15360. https://doi.org/10.1371/journal.pone.0015360
RADOSAVLJEVI´C, T., et al. The role of oxida-tive/nitrosative stress in pathogenesis of paracetamol-induced toxic hepatitis. Medicinski Pregled. 2010, 63(11-12), 827–832. https://doi.org/10.2298/MPNS1012827R
RAJESH, V. and PERUMAL, P. In vitro cytoprotective activity of Smilax zeylanica leaves against hydrogen peroxide induced oxidative stress in L-132 and BRL 3A cells. Oriental Pharmacy and Experimental Medicine. 2014, 14, 255–268. https://doi.org/10.1007/s13596-014-0154-6
RATNAM, D., et al. Role of antioxidants in prophylaxis and therapy: A pharmaceutical perspective. Journal of Controlled Release. 2006, 113(3), 189-207. https://doi.org/10.1016/j.jconrel.2006.04.015
ROE, J.H. Chemical determination of ascorbic, dehydroascorbic, and diketogulonic acids. Methods of Biochemical Analysis. 1954, 1, 115-139. https://doi.org/10.1002/9780470110171.ch5
ROMO-PÉREZ, A., ESCANDÓN-RIVERA, S.M. and ANDRADE-CETTO, A. Chronic hypoglycemic effect and phytochemical composition of Smilax moranensis roots. Revista Brasileira de Farmacognosia. 2019, 29(2), 246-253. https://doi.org/10.1016/j.bjp.2019.02.007
SABIR, S.M., et al. Antioxidant and hepatoprotective activity of ethanolic extract of leaves of Solidago microglossa containing polyphenolic compounds. Food Chemistry. 2012, 131(3), 741–747. https://doi.org/10.1016/j.foodchem.2011.09.026
SAHU, S., et al. Osmolyte modulated enhanced rice leaf catalase activity under salt-stress. Advances in Bioscience and Biotechnology. 2010, 1(1), 39-46. https://doi.org/10.4236/abb.2010.11006
SALWE, K.J., et al. Hepatoprotective and antioxidant activity of Murraya koenigii leaves extract against paracetamol induced hepatotoxicity in Rats. International Journal of Basic & Clinical Pharmacology. 2017, 6(6), 1274-1281. http://dx.doi.org/10.18203/2319-2003.ijbcp20172044
SEDLACK, J. and LINDSAY, R.H. Estimation of total, protein-bound, and nonprotein sulfhydryl groups in tissue with Ellman’s reagent. Analytical Biochemistry. 1968, 25, 192-205. https://doi.org/10.1016/0003-2697(68)90092-4
SERRA, A., et al. Metabolic pathways of the colonic metabolism of flavonoids (flavonols, flavones and flavanones) and phenolic acids. Food chemistry. 2012, 130(2), 383-393. https://doi.org/10.1016/j.foodchem.2011.07.055
SERBAN, M.C., et al. Effects of quercetin on blood pressure: a systematic review and meta-analysis of randomized controlled trials. Journal of the American Heart Association. 2016, 5(7), e002713. https://doi.org/10.1161/JAHA.115.002713
SHAHRBAF, F.G. and ASSADI, F. Drug-induced renal disorders. Journal of Renal Injury Prevention. 2015, 4(3), 57-60. https://doi.org/10.12861/jrip.2015.12
SOUZA, V.C. and LORENZI, H. Botânica sistemática: guia ilustrado para identificação das famílias de fanerógamas nativas e exóticas no Brasil, baseado em APG II. São Paulo: Instituto Plantarum de Estudos da Flora. 2nd ed. 2008.
TOWNSEND, D.M. and TEW, K.D. The role of glutathione-S-transferase in anti-cancer drug resistance. Oncogene. 2003, 22, 7369-7375. https://doi.org/10.1038/sj.onc.1206940
XIA, D., et al. Protective effect of Smilax glabra extract against lead-induced oxidative stress in rats. Journal of Ethnopharmacology. 2010, 130(2), 414–420. https://doi.org/10.1016/j.jep.2010.05.025
WANG, S., et al. The flavonoid-rich fraction from rhizomes of Smilax glabra Roxb. ameliorates renal oxidative stress and inflammation in uric acid nephropathy rats through promoting uric acid excretion. Biomedicine & Pharmacotherapy. 2019, 111, 162-168. https://doi.org/10.1016/j.biopha.2018.12.050
WU, L., et al. Cytotoxic polyphenols against breast tumor cell in Smilax china L. Journal of Ethnopharmacology. 2010, 130(3), 460-464. https://doi.org/10.1016/j.jep.2010.05.032
WUNGSINTAWEEKUL, B., et al. Estrogenic and anti-estrogenic compounds from the Thai medicinal plant, Smilax corbularia (Smilacaceae). Phytochemistry. 2011, 72(6), 495-502. https://doi.org/10.1016/j.phytochem.2010.12.018
YAN, L.J., TRABER, M.G. and PACKER, L. Spectrophotometric method for determination of carbonyls in oxidatively modified apolipoprotein B of human low-density lipoproteins. Analytical Biochemistry. 1995, 228(2), 349–351. https://doi.org/10.1006/abio.1995.1362
ZHOU, M., et al. New furostanol saponins with anti-inflammatory and cytotoxic activities from the rhizomes of Smilax davidiana. Steroids. 2017, 127, 62-68. https://doi.org/10.1016/j.steroids.2017.08.013
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Copyright (c) 2021 Ana Paula Simões da Cunha, Larissa Scremin Ferreira, Ana Júlia Pasuch Gluzezak, Edith Eunice Arthur Petrica, Adilson Paulo Sinhorin, Valéria Dornelles Gindri Sinhorin
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