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Research Articles

Lagerstroemia speciosa (L.) Pers., ethanolic leaves extract attenuates dapsone-induced liver inflammation in rats

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References

  • Abdelkader, N.F., et al., 2020. Ellagic acid attenuates liver toxicity induced by valproic acid in rats. Journal of Pharmacological Sciences, 143 (1), 23–29.
  • Akbulut, S., et al., 2014. Cytoprotective effects of amifostine, ascorbic acid and N-acetylcysteine against methotrexate-induced hepatotoxicity in rats. World Journal of Gastroenterology, 20 (29), 10158–10165.
  • Asrani, S.K., et al., 2019. Burden of liver diseases in the world. Journal of Hepatology, 70 (1), 151–171.
  • Bancroft, J. D., and Cook, B. C., 1984. Manual of histological techniques. Edinburgh: Churchill Livingstone, 49–51.
  • Chougule, M., Padhi, B., and Misra, A., 2008. Development of spray dried liposomal dry powder inhaler of Dapsone. AAPS PharmSciTech, 9 (1), 47–53.
  • Coleman, M.D., 1993. Dapsone: modes of action, toxicity and possible strategies for increasing patient tolerance. British Journal of Dermatology, 129 (5), 507–513.
  • Coleman, M.D., 2001. Dapsone-mediated agranulocytosis: risks, possible mechanisms and prevention. Toxicology, 162 (1), 53–60.
  • Das, A.K., and Jawed, Q., 2014. Drug-induced acute pancreatitis: a rare manifestation of an incomplete "dapsone syndrome". Indian Journal of Pharmacology, 46 (4), 455–457.
  • Devaraj, E., et al., 2020. β-Sitosterol attenuates carbon tetrachloride-induced oxidative stress and chronic liver injury in rats. Naunyn-Schmiedeberg's Archives of Pharmacology, 393 (6), 1067–1075.
  • Devarbhavi, H., et al., 2010. Single-center experience with drug-induced liver injury from India: causes, outcome, prognosis, and predictors of mortality. The American Journal of Gastroenterology, 105 (11), 2396–2404.
  • Devarbhavi, H., et al., 2017. Features and treatment of dapsone-induced hepatitis, based on analysis of 44 cases and literature review. Clinical Gastroenterology and Hepatology, 15 (11), 1805–1807.
  • Devarbhavi, H., et al., 2018. Drug-induced acute liver failure in children and adults: results of a single-centre study of 128 patients. Liver International, 38 (7), 1322–1329.
  • Devarbhavi, H., et al., 2019. Drug-induced acute-on-chronic liver failure in Asian patients. American Journal of Gastroenterology, 114 (6), 929–937.
  • East, J., and Blanton, L.S., 2012. Symptomatic hyperbilirubinemia secondary to dapsone-induced hemolysis and atazanavir therapy. Antimicrobial Agents and Chemotherapy, 56 (2), 1081–1083.
  • Ezhilarasan, D., 2018. Oxidative stress is bane in chronic liver diseases: clinical and experimental perspective. Arab Journal of Gastroenterology, 19 (2), 56–64.
  • Ezhilarasan, D., 2021. Dapsone-induced hepatic complications: it's time to think beyond methemoglobinemia. Drug and Chemical Toxicology, 44 (3), 330–333.
  • Ezhilarasan, D., and Karthikeyan, S., 2016. Silibinin alleviates N-nitrosodimethylamine-induced glutathione dysregulation and hepatotoxicity in rats. Chinese Journal of Natural Medicines, 14 (1), 40–47.
  • Ezhilarasan, D., Karthikeyan, S., and Vivekanandan, P., 2012. Ameliorative effect of silibinin against N-nitrosodimethylamine-induced hepatic fibrosis in rats. Environmental Toxicology and Pharmacology, 34 (3), 1004–1013.
  • Ezhilarasan, D., Sokal, E., Karthikeyan, S., and Najimi, M., 2014. Plant derived antioxidants and antifibrotic drugs: past, Present and Future. Journal of Coastal Life Medicine, 2 (9), 738–745.
  • Ezhilarasan, D., Sokal, E., and Najimi, M., 2018. Hepatic fibrosis: it is time to go with hepatic stellate cell-specific therapeutic targets. Hepatobiliary & Pancreatic Diseases International, 17 (3), 192–197.
  • Ezhilarasan, D., Srilekha, S., and Raghu, R., 2017. HAART and hepatotoxicity. Journal of Applied Pharmaceutical Science, 7 (04), 220–226.
  • Fabregat, I., et al., 2016. TGF-β signalling and liver disease. The FEBS Journal, 283 (12), 2219–2232.,
  • Fromm, E., and Wittmann, J., 1908. Derivate des p-nitrothiophenols. Berichte Der Deutschen Chemischen Gesellschaft, 41 (2), 2264–2273.
  • Ghaoui, N., et al., 2020. Update on the use of dapsone in dermatology. International Journal of Dermatology, 59 (7), 787–795.
  • Gupta, A., Agrawal, V.K., and Rao, C.V., 2017. Exploration of analgesic and antiinflammatory potential of Lagerstroemia speciosa. Journal of Applied Pharmaceutical Science, 7 (02), 156–161.
  • Hassan, H.M., et al., 2020. Suppression of cisplatin-induced hepatic injury in rats through alarmin high-mobility group box-1 pathway by Ganoderma lucidum: theoretical and experimental study. Drug Design, Development and Therapy, 14, 2335–2353.
  • Hoofnagle, J.H., and Björnsson, E.S., 2019. Drug-induced liver injury - types and phenotypes. Reply. The New England Journal of Medicine, 381 (14), 1396.
  • Ikeda, Y., Chen, J.T., and Matsuda, T., 1999. Effectiveness and safety of banabamin tablet containing extract from banaba in patients with mild type-2 diabetes. Japanese Pharmacology & Therapeitics, 27, 829–835.
  • Irshaid, Y., et al., 1994. Monoacetyldapsone inhibition of dapsone N-hydroxylation by human and rat liver microsomes. Drug Metabolism and Disposition: The Biological Fate of Chemicals, 22 (1), 161–164.
  • Itha, S., et al., 2003. Dapsone induced cholangitis as a part of dapsone syndrome: a case report. BMC Gastroenterology, 3, 21.
  • Jayakumar, K.S., et al., 2014. Corosolic acid content and SSR markers in Lagerstroemia speciosa (L.) Pers.: a comparative analysis among populations across the Southern Western Ghats of India. Phytochemistry, 106, 94–103.
  • Keerty, D., Eaton, K., and Haynes, E., 2020. Dapsone-induced hypoxia. Cureus, 12 (7), e9334.
  • Kirby, B., et al., 1999. Abnormal liver function tests induced by dapsone in a patient with dermatitis herpetiformis and primary sclerosing cholangitis. The British Journal of Dermatology, 141 (1), 172–173.
  • Lee, H.C., et al., 2019. Escin protects against acetaminophen-induced liver injury in mice via attenuating inflammatory response and inhibiting ERK signaling pathway. American Journal of Translational Research, 11 (8), 5170–5182.
  • Lewis, J.S., and Jacobs, Z.G., 2020. Subtle case of dapsone-induced methaemoglobinaemia. BMJ Case Reports, 13 (8), e235403.
  • Licata, A., 2016. Adverse drug reactions and organ damage: the liver. European Journal of Internal Medicine, 28, 9–16.
  • Liu, T., et al., 2017. NF-κB signaling in inflammation. Signal Transduction and Targeted Therapy, 2 (1), 17023.
  • Luedde, T., and Schwabe, R.F., 2011. NF-κB in the liver-linking injury, fibrosis and hepatocellular carcinoma. Nature Reviews. Gastroenterology & Hepatology, 8 (2), 108–118.
  • Misra, H.P., and Fridovich, I., 1972. The role of superoxide anion in the autoxidation of epinephrine and a simple assay for superoxide dismutase. Journal of Biological Chemistry, 247 (10), 3170–3175.
  • Moron, M.S., Depierre, J.W., and Mannervik, B., 1979. Levels of glutathione, glutathione reductase and glutathione S-transferase activities in rat lung and liver. Biochimica et Biophysica Acta, 582 (1), 67–78.
  • Mosedale, M., and Watkins, P.B., 2017. Drug-induced liver injury: advances in mechanistic understanding that will inform risk management. Clinical Pharmacology and Therapeutics, 101 (4), 469–480.
  • Mousa, A.M., et al., 2019. Lagerstroemia speciosa (L.) Pers leaf extract attenuates lung tumorigenesis via alleviating oxidative stress. Biomolecules, 9 (12), 871.
  • Norman, B.H., 2020. Drug Induced Liver Injury (DILI). Mechanisms and medicinal chemistry avoidance/mitigation strategies. Journal of Medicinal Chemistry, 63 (20), 11397–11419.
  • Ohkawa, H., Ohishi, N., and Yagi, K., 1979. Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Analytical Biochemistry, 95 (2), 351–358.
  • Prasad, P., 2000. A study of dapsone syndrome at a rural teaching hospital in South India. Indian Journal of Dermatology, Venereology, 66 (3), 136–138.
  • Priya, T.T., Sabu, M.C., and Jolly, C.I., 2008. Free radical scavenging and anti-inflammatory properties of Lagerstroemia speciosa (L). Inflammopharmacology, 16 (4), 182–187.
  • Quaresma, M.V., et al., 2015. Dapsone in the treatment of pemphigus vulgaris: adverse effects and its importance as a corticosteroid sparing agent. Anais Brasileiros de Dermatologia, 90 (3 Suppl 1), 51–54.
  • Rohit Singh, T., and Ezhilarasan, D., 2020. Ethanolic extract of Lagerstroemia speciosa (L.) Pers., induces apoptosis and cell cycle arrest in HepG2 cells. Nutrition and Cancer, 72 (1), 146–156.
  • Saumya, S.M., and Basha, P.M., 2011. Antioxidant effect of Lagerstroemia speciosa Pers (banaba) leaf extract in streptozotocin-induced diabetic mice. Indian Journal of Experimental Biology, 49 (2), 125–131.
  • Schwabe, R.F., and Brenner, D.A., 2006. Mechanisms of Liver Injury. I. TNF-alpha-induced liver injury: role of IKK, JNK, and ROS pathways. American Journal of Physiology. Gastrointestinal and Liver Physiology, 290 (4), G583–G589.
  • Semira , Wafai, Z.A., et al., 2014. Livedo reticularis associated with dapsone therapy in a patient with chronic urticaria. Indian Journal of Pharmacology, 46 (4), 438–440.
  • Sharmin, T., Rahman, M.S., and Mohammadi, H., 2018. Investigation of biological activities of the flowers of Lagerstroemia speciosa, the Jarul flower of Bangladesh. BMC Complementary and Alternative Medicine, 18 (1), 231.
  • Stohs, S.J., Miller, H., and Kaats, G.R., 2012. A review of the efficacy and safety of banaba (Lagerstroemia speciosa L.) and corosolic acid. Phytotherapy Research : PTR, 26 (3), 317–324.
  • Takahara, S., et al., 1960. Hypocatalasemia: a new genetic carrier state. The Journal of Clinical Investigation, 39, 610–619.
  • Thakur, R.S., and Devaraj, E., 2020. Lagerstroemia speciosa (L.) Pers. triggers oxidative stress mediated apoptosis via intrinsic mitochondrial pathway in HepG2 cells. Environmental Toxicology, 35 (11), 1225–1233.
  • Tiwary, B.K., et al., 2017. Radical Scavenging Activities of Lagerstroemia speciosa (L.) Pers. Petal Extracts and its hepato-protection in CCl4-intoxicated mice. BMC Complementary and Alternative Medicine, 17 (1), 55.
  • Unno, T., et al., 1997. Antioxidative activity of water extracts of Lagerstroemia speciosa leaves. Bioscience, Biotechnology, and Biochemistry, 61 (10), 1772–1774.
  • Veggi, L.M., et al., 2002. Dapsone-induced cholestasis and impairment of bile salt output in the rat. Biochemical Pharmacology, 63 (8), 1553–1563.
  • Veggi, L.M., et al., 2005. Dapsone impairs the bile salt-independent fraction of bile flow in rats: possible involvement of its N-hydroxylated metabolite. Toxicology, 211 (1–2), 97–106.
  • Veggi, L. M., et al., 2008. Dapsone induces oxidative stress and impairs antioxidant defenses in rat liver. Life Sciences, 83 (5-6), 155–163.
  • Vinod, K.V., Arun, K., and Dutta, T.K., 2013. Dapsone hypersensitivity syndrome: a rare life threatening complication of dapsone therapy. Journal of Pharmacology & Pharmacotherapeutics, 4 (2), 158–160.
  • Wozel, G., and Blasum, C., 2014. Dapsone in dermatology and beyond. Archives of Dermatological Research, 306 (2), 103–124.
  • Zhang, J.X., et al., 2020. Corosolic acid attenuates hepatic lipid accumulation and inflammatory response via AMPK/SREBPs and NF-κB/MAPK signaling pathways. The American Journal of Chinese Medicine, 48 (3), 579–595.
  • Zhu, Y.I., and Stiller, M.J., 2001. Dapsone and sulfones in dermatology: overview and update. Journal of the American Academy of Dermatology, 45 (3), 420–434.

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