Research Articles
Vol. 11 No. 2 (2024)
Assessing Oral Acute Toxicity and Histopathological Effects of Strelitzia reginae Aiton Leaf Extracts in Zebrafish (Danio rerio Hamilton)
Department of Life Sciences, CHRIST (Deemed to be University), Bengaluru 560029 University, Karnataka, India
Department of Life Sciences, CHRIST (Deemed to be University), Bengaluru 560029 University, Karnataka, India
Department of Life Sciences, CHRIST (Deemed to be University), Bengaluru 560029 University, Karnataka, India
Abstract
Strelitzia reginae, commonly known as the Bird of Paradise, is a decorative shrub endemic to southern Africa. This study marks the first comprehensive investigation into the safety of S. reginae leaf extract through oral acute toxicity assessments and histopathological examinations in Zebrafish (Danio rerio). The interest in this research arises from the historical use of S. reginae components by various indigenous South African societies to treat conditions like swollen glands and sexual problems. GC-MS analysis was used along with traditional methods to look at the phytochemical parts of S. reginae. The results showed the presence of several substances, such as eicosane, hexacosane, 1-octadecene, and neophytadiene. Notably, the analysis also identified certain chemicals with potential cytotoxic properties, such as octacosane and bis (2-ethylhexyl) phthalate. Drawing upon the biological similarities between Zebrafish and humans, who share a majority of their genes, this study represents the first attempt to evaluate the toxicity and histopathology of S. reginae using D. rerio as the test model, aligning with the OECD recommendations outlined in Article 203. The oral acute toxicity tests were done using ethanolic leaf powdered extracts of S. reginae. Higher concentrations (1200 mg/L) were toxic, but lower doses were less harmful to D. rerio. As observed in the histopathology examination, exposure to higher concentrations of S. reginae extract induced severe histological abnormalities in the Zebrafish's gills, liver, kidneys, intestines, and brain. This work contributes greatly to our understanding of S. reginae's safety profile and its potential therapeutic applications for enhancing well-being.
References
- Wannes WA, Mhamdi B, Sriti J, Jemia MB, Ouchikh O, Hamdaoui G. Antioxidant activities of the essential oil and methanol extracts from myrtle (Myrtus communis var. italica L.) leaf, stem and flower. Food and Chemical Toxicology. 2010;48(5):1362-70. https://doi.org/10.1016/j.fct.2010.03.002
- Yu XL, Li YN, Zhang H, Su YJ, Zhou WW, Zhang ZP et al. Rutin inhibits amylin-induced neurocytotoxicity and oxidative stress. Food Funct. 2015;6(10):3296-306. https://doi.org/10.1039/c5fo00500k
- Thiagarajan SK, Rama Krishnan K, Ei T, Husna Shafie N,Arapoc DJ, Bahari H. Evaluation of the effect of aqueous Momordica charantiaLinn. extract on zebrafish embryo model through acute toxicity assay assessment.Evidence-Based Complementary and Alternative Medicine. 2019;Article ID 9152757:pp.9. https://doi.org/10.1155/2019/9152757
- Arome D, Chinedu E. The importance of toxicity testing. Journal of Pharmaceutical and BioScience.2014;vol. 4:pp. 146-48.
- Okoye, TheophineChinwuba, Collins, Phillip FUzor, Okereke,Emeka K.Toxicological survey on African medicinal plants. 2014;pp.535-55. https://doi.org/10.1016/B978-0-12-800018-2.00018-2
- Borges RS, Pereira ACM, de Souza GC, Carvalho JCT. Histopathology of zebrafish (Danio rerio) in nonclinical toxicological studies of new drugs. In (Ed.), Zebrafish in Biomedical Research. IntechOpen.2019;.https://doi.org/10.5772/intechopen.88639
- dos Santos VF, Duarte JL, Pinho Fernandes C, Keita H, Rafael Rodríguez Amado J, Arturo Velázquez-Moyado J et al. Use of zebrafish (Danio rerio) in experimental models for biological assay with natural products. African Journal of Pharmacy and Pharmacology. 2016;10(42):883-91. https://doi.org/10.1201/9780203718896
- Howe K, Clark MD, Torroja CF, Torrance J, Berthelot C, Muffato M et al. The zebrafish reference genome sequence and its relationship to the human genome. Nature. 2013;496(7446):498-503. https://doi.org/10.1038/nature12111
- Heath AG. Water pollution and fish physiology. Boca Raton: CRC Press. 2018. https://doi.org/10.1201/9780203718896
- Van Der Ven LTM, Van Denn Brandhof EJ, Vos JH, Power DM, Wester PW. Effects of the antithyroid agent propylthiouracil in a partial life cycle assay with zebrafish. Environmental Science & Technology. 2006;40(1):74-81. https://doi.org/10.1021/es050972c
- Mele E, Girardo S, Pisignano D. Strelitzia reginae leaf as a natural template for anisotropic wetting and superhydrophobicity. Langmuir: The ACS Journal of Surfaces and Colloids. 2012;28(11):5312-17. DOI: https://doi.org/10.1021/la300243x
- Pooley E. A field guide to wild flowers of KwaZulu-Natal and the Eastern region. Natal Flora Publications Trust, Durban. 1998.
- Dyer RA. Strelitzia of the Eastern cape. The Eastern Cape Naturalist. 1977;(61):10-12.
- Anilakumar KR, Kumar GP, Ilaiyaraja N. Nutritional, pharmacological and medicinal properties of Momordica charantia. International Journal of Nutrition and Food Sciences.2015;4:75.https://doi.org/10.11648/J.IJNFS.20150401.21
- Xavier J, Kripasana K. Acute toxicity of leaf extracts of Enydra fluctuans Lour. in zebrafish (Danio rerio Hamilton). Scientifica. 2020;2020:3965376.https://doi.org/10.1155/2020/3965376
- Xavier J, Jose J. Study of mineral and nutritional composition of some seaweeds found along the coast of Gulf of Mannar, India. Plant Science Today. 2020;7. https//doi.org/10.14719/pst.2020.7.4.912
- Suresh A, Xavier J. Comprehensive phytochemical, anti-oxidant and GC-MS analysis of Strobilanthesjomyi P. Biju, Josekutty, Rekha & J.R.I.Wood. Asian Journal of Plant Sciences. 2023;22:227-38. https//doi.org/10.3923/ajps.2023.227.238
- OECD.Test No. 203: Fish, acute toxicity test, OECD guidelines for the testing of chemicals. Section 2, OECDPublishing, Paris, France. 1992.
- Jobi Xavier, Jayaram Reddy. Acute toxicity study of ethanolic extracts of leaf and fruit of two different varieties of M. Charantia in Danio Rerio. J Pharm Chem Biol Sci. 2019;7(2):102-09.
- Indrayan AK, Kumar N, Tyagi DK, Gaur A. Nutritive value of rhizome of the ginger resembling Alpinia allughas Rose. and characteristics of various extracted materials from the rhizome. J Indian Chern Soc. 2012;89:pp. 557-61.
- Clapham DE. Calcium signaling. Cell. 2007;131(6):1047-58.https//doi.org/10.1016/j.cell.2007.11.028
- Bailey RL, Fulgoni VL, Keast DR, Dwyer JT. Dietary supplement use is associated with higher intakes of minerals from food sources. Am J Clin Nutr. 2011;94(5):1376-81.https//doi.org/10.3945/ajcn.111.020289
- Sloup V, Jankovská I, Nechybová S, Pe?inková P, Langrova I. Zinc in the animal organism: A review. Scientia AgriculturaeBohemica. 2017;48. 10.1515/sab-2017-0003. https//doi.org/10.1515/sab-2017-0003
- Benson K. Zinc toxicosis in animals. Pet Poison Helpline & Safety Call International, LLC, Bloomington, MN. Merck Veterinary Manual. 2022.
- Harris ED. Basic and clinical aspects of copper. Critical Reviews in Clinical Laboratory Sciences.2003;40:547-86.https//doi.org/10.1080/10408360390250649
- Wang ZY, He N, Wang YJ, Zhang J. Effects of copper on organisms: A review. AMR. 2013;340(3):726-31.https://doi.org/10.4028/www.scientific.net/AMR.726-731.340
- Longman Li, Xiaobo Yang. The essential element manganese, oxidative stress and metabolic diseases: Links and interactions. Oxidative Medicine and Cellular Longevity. 2018; Article ID 7580707:pp.11. https://doi.org/10.1155/2018/7580707
- Nkpaa KW et al. Ethanol via regulation of NF-kB/p53 signaling pathway increases manganese-induced inflammation and apoptosis in hypothalamus of rats. Biol Trace Elem Res. 2018;1:1-8. https://doi.org/10.1007/s12011-018-1535-3
- He WL, Feng Y, Li XL, Wei YY, Yang XE. Availability and toxicity of Fe (II) and Fe (III) in Caco-2 cells. J Zhejiang Univ Sci B. 2008;9(9):707-12. https//doi.org/10.1631/jzus.B0820023
- Assi MA, Hezmee MN, Haron AW, Sabri MY, Rajion MA. The detrimental effects of lead on human and animal health. Veterinary World. 2016;9(6):660-71. https//doi.org/10.14202/vetworld.2016.660-671
- Genchi G, Sinicropi MS, Lauria G, Carocci A, Catalano A. The effects of cadmium toxicity. International Journal of Environmental Research and Public Health. 2020;17(11):3782. https://doi.org/10.3390/ijerph17113782
- Singh N et al. Biochemical and molecular bases of lead-induced toxicity in mammalian systems and possible mitigations. Chem Res Toxicol. 2018;31:1009-21. https//doi.org/10.1021/acs.chemrestox.8b00193
- Yu S et al. Immunological dysfunction in chronic arsenic exposure: From subclinical condition to skin cancer. J Dermatol. 2018;45:1271-77.https//doi.org/10.1111/1346-8138.14620
- Swamy MK, Arumugam G, Kaur R, Ghasemzadeh A, Yusoff MM, Sinniah UR. GC-MS based metabolite profiling, antioxidant and antimicrobial properties of different solvent extracts of Malaysian Plectranthusamboinicus leaves. Evid Based Complement Altern Med.2017.https://doi.org/10.1155/2017/1517683.
- Rukaiyat M, Garba S, Labaran S. Antimicrobial activities of hexacosane isolated from Sanseveria liberica (Gerome and Labroy) plant. Advancement in Medicinal Plant Research.2015;3(3):pp. 120-25.
- Karanja E, Boga H, Muigai A, Wamunyokoli F, Kinyua J, Nonoh J. Growth characteristics and production of secondary metabolites from selected novel Streptomyces species isolated from selected Kenyan national parks. In: Scienti?c Conference Proceeding. 2012.
- Samarasinghe BA, Kaliyadasa E, Marasinghe PA. Physicochemical properties and bioactivities of six Alpiniaspecies in Sri Lanka. International Journal of Ayurvedic Medicine. 2020.https//doi.org/10.47552/ijam.v11i4.1717
- Yuandani, Jantan I, Rohani AS, Sumantri IB. Immunomodulatory effects and mechanisms of Curcuma species and their bioactive compounds: A review. Frontiers in Pharmacology. 2021;12:643119.https//doi.org/10.3389/fphar.2021.643119
- Batista-Silva H, Dambrós BF, Rodrigues K, Cesconetto PA, Zamoner A, Sousa de Moura KRet al. Acute exposure to bis(2-ethylhexyl) phthalate disrupts calcium homeostasis, energy metabolism and induces oxidative stress in the testis of Danio rerio. Biochimie. 2020. https//doi.org/10.1016/j.biochi.2020.05.002
- Kakalis A, Tsekouras V, Mavrikou S, Moschopoulou G, Kintzios S, Evergetis E et al. Farm or lab? A comparative study of oregano's leaf and callus volatile isolates chemistry and cytotoxicity. Plants. 2023;12(7):1472. https://doi.org/10.3390/plants12071472
- Zakaria F, Ibrahim WN, Ismail IS, Ahmad H, Manshoor N, Ismail Net al. LCMS/MS metabolite profiling and analysis of acute toxicity effect of the ethanolic extract of Centella asiatica on zebrafshmodel. Pertanika Journal of Science & Technology. 2019;27(2).
- Satpathy L, Parida SP. Acute toxicity assessment and behavioral responses induced by Kandhamalhaladi in adult zebrafish (Danio rerio). Biointerface Research in Applied Chemistry. 2020. https//doi.org/10.33263/briac111.73687381
- Carvalho JCT, Keita H, Santana GR, de Souza GC, dos Santos IVF, Amado JRR et al. Effects of Bothropsalternatus venom in zebrafish: A histopathological study. Inflammopharmacology. 2018;26(1):273-84. https//doi.org/10.1007/s10787-017-0362-z
- Saeidnia S, Abdollahi M. Are medicinal plants polluted with phthalates? Daru. 2013 May 29;21(1):43. https//doi.org/10.1186/2008-2231-21-43
- Herr C, Nieden A, Koch HM, Schuppe HC, Fieber C, Angerer Jet al. Urinary di (2-ethylhexyl) phthalate (DEHP) metabolites and male human markers of reproductive function. Int J Hyg Env Health. 2009;212:648-53. https//doi.org/10.1007/s00204-003-0522-3
- Mazon AF, Cerqueira CCC, Fernandes MN. Gill cellular changes induced by copper exposure in the South American tropical freshwater fish Prochilodus scrofa. Environmental Research. 2002;88(1):52-63. https://doi.org/10.1006/enrs.2001.4315
- Seth PK. Hepatic effects of phthalate esters. Environmental health perspectives. 1982;45:27-34. https//doi.org/10.1289/ehp.824527
- Borges RS, Keita H, Ortiz BLS, dos Santos Sampaio TI, Ferreira IM, Lima ES et al. Anti- inflammatory activity of nanoemulsions of essential oil from Rosmarinusofficinalis L.: in vitro and in zebrafish studies. Inflammopharmacology. 2018;26(4):1057-80. https//doi.org/10.1007/s10787-017-0438-9
- Menke AL, Spitsbergen JM, Wolterbeek APM, Woutersen RA. Normal anatomy and histology of the adult zebrafish. Toxicologic Pathology. 2011;39(5):759-75. https//doi.org/10.1177/0192623311409597
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