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Therapeutic Potential of Persea americana Stem Bark in Lipopolysaccharide (LPS) Induced Hepatic Inflammation and Oxidative Stress in Mice

Received: 29 January 2024     Accepted: 12 February 2024     Published: 2 April 2024
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Abstract

This study investigated the potential of Persea americana stem bark for the treatment of inflammation and oxidation in mice. Oxidative stress occurs in the body when there is serious imbalance between the generation of free radicals and the antioxidant defense system, inflammation is a natural defense mechanism against pathogens and it is associated with many pathogenic diseases such as microbial and viral infections, exposure to allergens, radiation and toxic chemicals, autoimmune and chronic diseases, obesity, consumption of alcohol, tobacco use, and a high-calorie diet. Plants offer significant potentials for development of new anti-inflammatory therapies and treatment of diseases associated with inflammation and Oxidation. Stem bark of Persea ameriacna was extracted using EtOH/H2O (80:20 v/v), the extract obtained was subjected to maceration using 3 different solvents, hexane fraction (PAHF), Ethyl-acetate fraction (PAEF) and methanol fraction (PAMF). The methanol fraction came out with the highest yield and was used for the animal study, 30 male mice was divided into 3 different groups, LPS was introduced in one of the groups, PAMF was later administered to the same group, The experiment shows that the extract was able to demonstrate significant reduction in inflammation and also ameliorate oxidation in mice. In conclusion the methanolic fraction of Persea americana stem bark might contain beneficial phytochemicals that can be explored as potential anti-inflammatory and oxidative therapy.

Published in International Journal of Biomedical Science and Engineering (Volume 12, Issue 1)
DOI 10.11648/j.ijbse.20241201.11
Page(s) 1-9
Creative Commons

This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited.

Copyright

Copyright © The Author(s), 2024. Published by Science Publishing Group

Keywords

P. americana, Methanolic Extract, LPS, Anti-inflammation

References
[1] Edewor-Kuponiyi T. I. (2013). Spectroscopic determination of total phenolic and flavonoid contents, and antioxidant activities of leaves P. Americana. Int. J. Pharm. Sci. vol. 5, issues 3, p. 598-603.
[2] Owolabi M A, Coker H A B, Jaja S I, (2000). Flavonoid metabolites in urine after oral administration of the aqueous extract of P. Americana to rats. J. Nat. Med., 61; p. 200-204.
[3] Owolabi M. O (2010). What are the consistent predictors of generic and specific post stroke health- related quality of life? Cerebrovasc Dis. 29(2), 105-10.
[4] Amuda M. O., Edewor T. I., Ogunyemi O. (2023). Antimicrobial analysis of Persea americana leaf. Am. J. Pharmtech. Res. 13 (01).
[5] Oelrichs P. B, Ng J. C, Seawright A. A, Ward A, Schaffeler L, MacLeod J. K. (1995). Isolation and identification of a compound from avocado (Persea americana) leaves which causes necrosis of the acinar epithelium of the lactating mammary gland and the myocardium. Nat Toxins; 3: 344-9.
[6] Edewor T. I., Agboola P. O., Amuda M. O.,. Mmuo A. I., Owa S. O (2023). Total phenolic, flavonoid and mineral contents of the methanolic leaf extract of Parinari curatellifolia planch, ex benth.
[7] Igbal S., Farooq A. (2005). Anti oxidant properties and components of some commercially available varieties of rice bran in Pakistan. Food chemistry 93: 265-272.
[8] Sivanandham V., (2011). Free radicals in health and diseases-a mini review. Pharmacologyonline. 1: 1062-1077.
[9] Juranek I., Bezek S. (2005). Controversy of free radical hypothesis: reactive oxygen specie-cause or consequence of tissue injury? Gen Physiol. Biophys. 24: 263-278.
[10] Halliwell B. (2008). Are polyphenols antioxidants or pro-oxidants? What do we learn from cell culture and in vivo studies? Arch Biochem Biophys. 476: 107-12.
[11] Hyun P. K., Kan H. S., Hyeun W. C., Sam S. K. (2004). Anti-inflammatory plant flavonoids and cellular action mechanisms. J. Pharmacol. Sci. 96, 229-245.
[12] Shen. S. C., Lee W. R., Lin H. Y., Huang H. C., Ko C. H., Yang L. L. (2002). In vitro and in vivo inhibitory activities of rutin, wogonin, and quecetin on LPS induced nitric oxide and postagladin E2 production. Eur. J. Pharmacol. 446: 187-194.
[13] Annika W., Thomas L. M., Kristen M. D, Steve T. (2012). Creatinine inhibit bacteria replication. J. Antibiotic 65(3): 153-156.
[14] Adeyemi O. O, Okpo S. O, Ogunti O. O. (2002). Analgesic and antiinfl ammatory effects of the aqueous extract of leaves of Persea americana Mill (Lauraceae). Fitoterapia; 73: 375-80.
[15] Ore Ayokanmiand Oluseyi A. A (2019). Oxidative stress and biomarkers in clinical and experimental models of non-alcoholic fatty liver diseases Medicinal (Kaunas). 55(2): 26.
[16] Jollow D. J., Mitchell J. R., Zampaglione N., Gillete J. R. (1974). Bromobenzene induced liver necrosis. Protective role of glutathione and evidence for 3,4-bromobenzene oxide as a hepatotoxic metabolite. Pharmacology. 1: 151-169.
[17] Sun M. and Zigman S. (1978). An improved spectrophotometric assay for superoxide dismutate based on epinephrine autoxidation. Anal. Biochem. 90, 81-89.
[18] Kim H. J., Wei Y., Wojtkiewicz G. R, Lee J. Y., Moskowitz M. A., and Chen J. W (2019). Reducing myeloperoxidase activity decreases inflammation and increases cellular protection in ischemic stroke. J. Cereb. Blood flow metab. 39, 1964-1877.
[19] Iqbal A. J., Fisher E. A., Grease D. R. (2016). Inflammation- a critical appreciation of the role of myeloid cells. Microbial. Spectr. 4:
[20] Canan C. H., Gokhale N. S., Caruthers B., Lafuse W. P., Schlesinger L. S., Torrelles J. B., Turner J. (2014). Characterisation of lung inflammation and its impact on macrophage function in aging. J. Leukoc. Biol. 96: 473-487.
[21] Juskewitch J. E., Knudsen B. E., Platt J. L., Nath K. A, Knutson K. L, Brunn G. J., Grande J. P. (2012). LPS induced murine systemic inflammation is driven by parenchymal cell activation and exclusively predicted by early MCP-1 plasma level. Am. J. Phatol. 180: 32-40.
[22] Palsson-McDermott E. M. and Oneill L. A. (2004). Signal transduction by the LPS receptor, Toll- like receptor -4. Immunology. 113: 153-162.
[23] Tarique Hussain, Bie Tan, Yulong Yin, Francois Blachier, Myrlene C. B. Tossou, and Najma Rahu, (2016). Oxidative Stress and Inflammation: What PolyphenolsCan Do for Us? Hindawi Publishing Corporation Oxidative Medicine and Cellular Longevity Volume 2016, Article ID 7432797, 9 pages
[24] Balavione G. G., Geletti Y. V. (1999). Peroxynitrite scavenging by different antioxidants. Part 1: convenient study. Nitric oxide. 3: 40-54.
[25] Josiah and Bartholomew (2015). In-vitrp antioxidant capacity and free radical scavenging evaluation of active metabolite constituents of newbouldia laevis ethanolic leaf extract. Bio. Res. 48(1): 16.
[26] Yuan L. and Kaplowitz N. (2008). Gluthathione in inner disease and hepatocity. Mol. Aspect Med. In press.
[27] Kim H. W, Murakami A, Nakamura Y, Ohigashi H. (2002). Screening of edible Japanese plants for suppressive effects on phorbol esterinduced superoxide generation in differentiated HL-60 cells and AS52 cells. Cancer Lett; 176: 7-16.
[28] Daniel C., Chihhao C., Ting-chieh H. (2005). Free radical the body killer. National Taichung second high school. Pp 1-7. Retrieved from www.pdffactory.com
[29] Fu X., Kassim S. Y., Park W. C., Heinecke J. W (2001). Hypochlorus acid oxygenated the cysteine switch domain of pro-matilysm (MMP-7). J. Biochem. 276: 41279-41287.
[30] Tavora F., Mary R., Ling Li, Allen P. B (2009). Monocytes and neutrophils expressing myeloperoxidase occur in fibrous caps and thumbl in unstable coronary plaques. BMC cardiovascular disorder 9(1): 27.
[31] Anderson M. M., Hzan S. L., Hsu F. F., Heinecke J. W (1997). Human neutrophils employs the myeloperoxidase-hydrogen peroxide-chloride system to convert hydroxyl-amino acid into glycolaldehyde, 2-hydroxy-propanal and acrolein. J. clinical investigation. 99, 424-432.
[32] Benson-bard A., Courtiuos C., Gauthier A. (2008). Nitric acid in plants. production and cross-take with Ca2+ signaling. Mol. Plant. 1: 218-228.
[33] Rice-Evans (2001). Flavonoid antioxidants. Curr. Med. Chem. 8(7): 797-807.
Cite This Article
  • APA Style

    Oluwatoyin, B., Olasunkanmi, A. M., Ayokanmi, O. (2024). Therapeutic Potential of Persea americana Stem Bark in Lipopolysaccharide (LPS) Induced Hepatic Inflammation and Oxidative Stress in Mice. International Journal of Biomedical Science and Engineering, 12(1), 1-9. https://doi.org/10.11648/j.ijbse.20241201.11

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    ACS Style

    Oluwatoyin, B.; Olasunkanmi, A. M.; Ayokanmi, O. Therapeutic Potential of Persea americana Stem Bark in Lipopolysaccharide (LPS) Induced Hepatic Inflammation and Oxidative Stress in Mice. Int. J. Biomed. Sci. Eng. 2024, 12(1), 1-9. doi: 10.11648/j.ijbse.20241201.11

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    AMA Style

    Oluwatoyin B, Olasunkanmi AM, Ayokanmi O. Therapeutic Potential of Persea americana Stem Bark in Lipopolysaccharide (LPS) Induced Hepatic Inflammation and Oxidative Stress in Mice. Int J Biomed Sci Eng. 2024;12(1):1-9. doi: 10.11648/j.ijbse.20241201.11

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  • @article{10.11648/j.ijbse.20241201.11,
      author = {Babatunde Oluwatoyin and Amuda Mutiu Olasunkanmi and Ore Ayokanmi},
      title = {Therapeutic Potential of Persea americana Stem Bark in Lipopolysaccharide (LPS) Induced Hepatic Inflammation and Oxidative Stress in Mice
    },
      journal = {International Journal of Biomedical Science and Engineering},
      volume = {12},
      number = {1},
      pages = {1-9},
      doi = {10.11648/j.ijbse.20241201.11},
      url = {https://doi.org/10.11648/j.ijbse.20241201.11},
      eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.ijbse.20241201.11},
      abstract = {This study investigated the potential of Persea americana stem bark for the treatment of inflammation and oxidation in mice. Oxidative stress occurs in the body when there is serious imbalance between the generation of free radicals and the antioxidant defense system, inflammation is a natural defense mechanism against pathogens and it is associated with many pathogenic diseases such as microbial and viral infections, exposure to allergens, radiation and toxic chemicals, autoimmune and chronic diseases, obesity, consumption of alcohol, tobacco use, and a high-calorie diet. Plants offer significant potentials for development of new anti-inflammatory therapies and treatment of diseases associated with inflammation and Oxidation. Stem bark of Persea ameriacna was extracted using EtOH/H2O (80:20 v/v), the extract obtained was subjected to maceration using 3 different solvents, hexane fraction (PAHF), Ethyl-acetate fraction (PAEF) and methanol fraction (PAMF). The methanol fraction came out with the highest yield and was used for the animal study, 30 male mice was divided into 3 different groups, LPS was introduced in one of the groups, PAMF was later administered to the same group, The experiment shows that the extract was able to demonstrate significant reduction in inflammation and also ameliorate oxidation in mice. In conclusion the methanolic fraction of Persea americana stem bark might contain beneficial phytochemicals that can be explored as potential anti-inflammatory and oxidative therapy.
    },
     year = {2024}
    }
    

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  • TY  - JOUR
    T1  - Therapeutic Potential of Persea americana Stem Bark in Lipopolysaccharide (LPS) Induced Hepatic Inflammation and Oxidative Stress in Mice
    
    AU  - Babatunde Oluwatoyin
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    JF  - International Journal of Biomedical Science and Engineering
    JO  - International Journal of Biomedical Science and Engineering
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    PB  - Science Publishing Group
    SN  - 2376-7235
    UR  - https://doi.org/10.11648/j.ijbse.20241201.11
    AB  - This study investigated the potential of Persea americana stem bark for the treatment of inflammation and oxidation in mice. Oxidative stress occurs in the body when there is serious imbalance between the generation of free radicals and the antioxidant defense system, inflammation is a natural defense mechanism against pathogens and it is associated with many pathogenic diseases such as microbial and viral infections, exposure to allergens, radiation and toxic chemicals, autoimmune and chronic diseases, obesity, consumption of alcohol, tobacco use, and a high-calorie diet. Plants offer significant potentials for development of new anti-inflammatory therapies and treatment of diseases associated with inflammation and Oxidation. Stem bark of Persea ameriacna was extracted using EtOH/H2O (80:20 v/v), the extract obtained was subjected to maceration using 3 different solvents, hexane fraction (PAHF), Ethyl-acetate fraction (PAEF) and methanol fraction (PAMF). The methanol fraction came out with the highest yield and was used for the animal study, 30 male mice was divided into 3 different groups, LPS was introduced in one of the groups, PAMF was later administered to the same group, The experiment shows that the extract was able to demonstrate significant reduction in inflammation and also ameliorate oxidation in mice. In conclusion the methanolic fraction of Persea americana stem bark might contain beneficial phytochemicals that can be explored as potential anti-inflammatory and oxidative therapy.
    
    VL  - 12
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Author Information
  • Department of Physical Sciences, Ajayi Crowther University, Oyo, Nigeria

  • Department of Pure and Applied Chemistry, Ladoke Akintola University of Technology, Ogbomoso, Nigeria

  • Department of Physical Sciences, Ajayi Crowther University, Oyo, Nigeria

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