Abstract
Objectives
Annona squamosa has beneficial properties. However, its cytotoxicity and antioxidative effects on human promyelocytic leukemia cells (HL60) deserve investigation. Therefore, the efficacy of its crude extracts in offsetting damage in HL60 cells subjected to oxidative stress was studied.
Methods
Crude extracts at different concentrations were incubated with HL60 cells. The beneficial properties of the plant extract against oxidative damage were evaluated post-induction of oxidative stress utilizing hydrogen peroxide.
Results
Extracts at concentrations 600 and 800 μg/mL were most effective at increasing the viability of damaged cells compared to the control group after 48 h of incubation. Significant increases in lipid peroxidation were observed in exposed cells treated with 600 μg/mL extract after 72 h of incubation. Superoxide dismutase (SOD) and catalase activities significantly increased in exposed cells after 24 h of incubation at all extract concentrations. Exposed cells treated with 600 and 1,000 μg/dL of the extract showed significantly increased catalase activity after 48 h, and a similar profile was maintained after 72 h of exposure. SOD activity in exposed cells remained significantly increased at all treatment concentrations after 48 and 72 h of incubation. Treatment with 400, 600, and 800 μg/mL of the extract resulted in significantly increased reduced glutathione levels compared to the other groups after 24 and 72 h of incubation. However, after 48 h of incubation, significant increases were noted in glutathione levels in exposed cells incubated with either 400, 800, or 1,000 μg/mL extract.
Conclusions
The findings suggest that A. squamosa might effectively protect against oxidative damage in a time and extract concentration-dependent manner.
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Research funding: None declared.
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Author contributions: All the authors have contributed and accepted responsibility for the entire content of this manuscript and have also approved submission.
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Competing interests: Authors declare no conflict of interest.
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Informed consent: Not applicable.
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Ethical approval: The local Institutional Review Board deemed the study exempt from review.
References
1. Saha, R. Pharmacognosy and pharmacology of Annona squamosa: a review. IJPLS 2011;2:1183–9.Suche in Google Scholar
2. Shehata, MG, Abu-Serie, MM, Abd El-Aziz, NM, El-Sohamimy, SA. Nutritional, phytochemical, and in vitro anticancer potential of sugar apple (Annona squamosa) fruits. Sci Rep 2021;11:6224. https://doi.org/10.1038/s41598-021-85772-8.Suche in Google Scholar PubMed PubMed Central
3. Gajalakshmi, S, Divya, R, Deepika, VD, Mythili, S. Pharmacological activities of Annona squamosa: a review. Int J Pharmaceut Sci Rev Res 2011;10:004.Suche in Google Scholar
4. Safira, A, Widayani, P, An-Najaaty, D, Rani, CAM, Septiani, M, Putra, YAS, et al.. A review of an important plants: Annona squamosa leaf. Pharm J 2022;14:456–63. https://doi.org/10.5530/pj.2022.14.58.Suche in Google Scholar
5. Simon, KN, Santhoshkumar, R, Neethu, SK. Phytochemical analysis and antimicrobial activities of Annona squamosa (L) leaf extracts. J Pharmacogn Phytochem 2016;5:128–31.Suche in Google Scholar
6. Kumari, N, Prakash, S, Kumar, M, Radha, Zhang, B, Sheri, V, et al.. Seed waste from custard apple (Annona squamosa L.): a comprehensive insight on bioactive compounds, health promoting activity and safety profile. Processes 2022;10:2119. https://doi.org/10.3390/pr10102119.Suche in Google Scholar
7. Ashokkumar, S, Elanthiraiyan, A, Shagu, S, Srinivasan, S, Deepan, KB. Comparison and analysis of custard apple seed oil with engine lubricant (bio lubricant). IOP Conf Ser Mater Sci Eng 2020;993:012008. https://doi.org/10.1088/1757-899x/993/1/012008.Suche in Google Scholar
8. Singh, Y, Bhatnagar, P, Thakur, N. A review on insight of immense nutraceutical and medicinal potential of custard apple (Annona squamosa Linn). Int J Chem Sci 2019;7:1237–45.Suche in Google Scholar
9. Vikas, B, Anil, S, Remani, P. Cytotoxicity profiling of Annona squamosa in cancer cell lines. Asian Pac J Cancer Prev 2019;20:2831–40. https://doi.org/10.31557/APJCP.2019.20.9.2831.Suche in Google Scholar PubMed PubMed Central
10. Fadholly, A, Proboningrat, A, Iskandar, RPD, Rantam, FA, Sudjarwo, SA. In vitro anticancer activity Annona squamosa extract nanoparticle on WiDr cells. J Adv Pharm Technol Res 2019;10:149–54. https://doi.org/10.4103/japtr.JAPTR_10_19.Suche in Google Scholar PubMed PubMed Central
11. Qi, Y, Chen, X, Chan, CY, Li, D, Yuan, C, Yu, F, et al.. Two-dimensional differential gel electrophoresis/analysis of diethylnitrosamine induced rat hepatocellular carcinoma. Int J Cancer 2008;122:2682–8. https://doi.org/10.1002/ijc.23464.Suche in Google Scholar PubMed
12. Hayes, JD, Dinkova-Kostova, AT, Tew, KD. Oxidative stress in cancer. Cancer Cell 2020;38:167–97. https://doi.org/10.1016/j.ccell.2020.06.001.Suche in Google Scholar PubMed PubMed Central
13. Dehshahri, S, Wink, M, Afsharypuor, S, Asghari, G, Mohagheghzadeh, A. Antioxidant activity of methanolic leaf extract of Moringa peregrina (Forssk.) Fiori. Res Pharm Sci 2012;7:111–8.Suche in Google Scholar
14. Campos, LM, Souza, LF, Souza, MAS, Souza, SM, Fabri, RL. Effects of methanolic extract of Annona squamosa L. leaves on germination, root development and cell cycle of Lactuca sativa L. Rev Bras Pl Med São Paulo 2017;19:37–41.Suche in Google Scholar
15. Nguyen, K, Sparks, J, Omoruyi, F. Effects of Ligusticum porteri (osha) root extract on human promyelocytic leukemia cells. Pharmacogn Res 2017;9:156–60. https://doi.org/10.4103/0974-8490.204641.Suche in Google Scholar PubMed PubMed Central
16. Chkhikvishvili, I, Sanikidze, T, Gogia, N, Mchedlishvili, T, Enukidze, M, Machavariani, M, et al.. Rosmarinic acid-rich extracts of summer savory (Satureja hortensis L.) protect Jurkat T cells against oxidative stress. Oxid Med Cell Longev 2013;2013:456253. https://doi.org/10.1155/2013/456253.Suche in Google Scholar PubMed PubMed Central
17. Nguyen, MT, Nguyen, T, Le, VM, Trieu, LH, Lam, TD, Bui, LM, et al.. Assessment of preliminary phytochemical screening, polyphenol content, flavonoid content, and antioxidant activity of custard apple leaves (Annona squamosa Linn). IOP Conf Ser Mater Sci Eng 2020;736:062012. https://doi.org/10.1088/1757-899x/736/6/062012.Suche in Google Scholar
18. Dilworth, L, Stennett, DK, Omoruyi, FO. Effects of moringa oleifera leaf extract on human promyelocytic leukemia cells subjected to oxidative stress. J Med Food 2019;23:728–34. https://doi.org/10.1089/jmf.2019.0192.Suche in Google Scholar PubMed
19. Genet, S, Kale, RK, Baquer, NZ. Alterations in antioxidant enzymes and oxidative damage in experimental diabetic rat tissues: effect of vanadate and fenugreek (Trigonellafoenum graecum). Mol Cell Biochem 2002;236:7–12. https://doi.org/10.1023/a:1016103131408.10.1023/A:1016103131408Suche in Google Scholar PubMed
20. Nawaz, SK, Hasnain, S. Effects of noise exposure on catalase activity of growing lymphocytes. Bosn J Basic Med Sci 2011;11:219–22. https://doi.org/10.17305/bjbms.2011.2550.Suche in Google Scholar PubMed PubMed Central
21. Ellman, GL. Tissue sulfhydryl groups. Arch Biochem Biophys 1959;82:70–7. https://doi.org/10.1016/0003-9861(59)90090-6.Suche in Google Scholar PubMed
22. Arlt, S, Beisiegel, U, Kontush, A. Lipid peroxidation in neurodegeneration: new insights into Alzheimer’s disease. Curr Opin Lipidol 2002;13:289–94. https://doi.org/10.1097/00041433-200206000-00009.Suche in Google Scholar PubMed
23. Chang, KH, Chen, CM. The role of oxidative stress in Parkinson’s disease. Antioxidants 2020;9:597. https://doi.org/10.3390/antiox9070597.Suche in Google Scholar PubMed PubMed Central
24. Polidori, MC, Praticó, D, Savino, K, Rokach, J, Stahl, W, Mecocci, P. Increased F2 isoprostane plasma levels in patients with congestive heart failure are correlated with antioxidant status and disease severity. J Card Fail 2004;10:334–8. https://doi.org/10.1016/j.cardfail.2003.11.004.Suche in Google Scholar PubMed
25. Rodrigo, R, Libuy, M, Feliú, F, Hassan, D. Oxidative stress-related biomarkers in essential hypertension and ischemia-reperfusion myocardial damage. Dis Markers 2013;35:18. https://doi.org/10.1155/2013/974358.Suche in Google Scholar PubMed PubMed Central
26. Steinberg, D. Low density lipoprotein oxidation and its pathobiological significance. J Biol Chem 1997;272:20963–6. https://doi.org/10.1074/jbc.272.34.20963.Suche in Google Scholar PubMed
27. Garrido, MA, Griendling, KK. NADPH oxidases and angiotensin II receptor signaling. Mol Cell Endocrinol 2009;302:148–58. https://doi.org/10.1016/j.mce.2008.11.003.Suche in Google Scholar PubMed PubMed Central
28. Park, HS, Kim, SR, Lee, YC. Impact of oxidative stress on lung diseases. Respirology 2009;14:27–38. https://doi.org/10.1111/j.1440-1843.2008.01447.x.Suche in Google Scholar PubMed
29. Drost, EM, Skwarski, KM, Sauleda, J, Soler, N, Roca, J, Agusti, A, et al.. Oxidative stress and airway inflammation in severe exacerbations of COPD. Thorax 2005;60:293–300. https://doi.org/10.1136/thx.2004.027946.Suche in Google Scholar PubMed PubMed Central
30. Özcan, O, Erdal, H, Çakırca, G, Yonden, Z. Oxidative stress and its impacts on intracellular lipids, proteins and DNA. J Clin Exp Invest 2015;6:331–6. https://doi.org/10.5799/ahinjs.01.2015.03.0545.Suche in Google Scholar
31. Das, K, Roychoudhury, A. Reactive oxygen species (ROS) and response of antioxidants as ROS-scavengers during environmental stress in plants. Front Environ Sci 2014;2:1–13. https://doi.org/10.3389/fenvs.2014.00053.Suche in Google Scholar
32. Rabinovitch, RC, Samborska, B, Faubert, B, Ma, EH, Gravel, SP, Andrzejewski, S, et al.. AMPK maintains cellular metabolic homeostasis through regulation of mitochondrial reactive oxygen species. Cell Rep 2017;21:1–9. https://doi.org/10.1016/j.celrep.2017.09.026.Suche in Google Scholar PubMed
33. Forni, C, Facchiano, F, Bartoli, M, Pieretti, S, Facchiano, A, D’Arcangelo, D, et al.. Beneficial role of phytochemicals on oxidative stress and age-related diseases. BioMed Res Int 2019;7:8748253. https://doi.org/10.1155/2019/8748253.Suche in Google Scholar PubMed PubMed Central
34. Li, C, Tang, Y, Gu, F, Wang, X, Yang, W, Han, Y, et al.. Phytochemical analysis reveals an antioxidant defense response in Lonicera japonica to cadmium-induced oxidative stress. Sci Rep 2022;12:6840. https://doi.org/10.1038/s41598-022-10912-7.Suche in Google Scholar PubMed PubMed Central
35. Engwa, GA. Free radicals and the role of plant phytochemicals as antioxidants against oxidative stress-related diseases. In: Phytochemicals – source of antioxidants and role in disease prevention. London England: BoD–Books on Demand; 2018, vol. 7:49–74 pp.10.5772/intechopen.76719Suche in Google Scholar
36. Akuru, U, Amadi, B. Phytochemicals and antioxidant properties of some selected medicinal plants. J Pharmacogn Phytochem 2018;7:283–5.Suche in Google Scholar
37. Cui, Y, Li, F, Zhu, X, Muhammad, A, Chen, Y, Li, D, et al.. Alfalfa saponins inhibit oxidative stress-induced cell apoptosis through the MAPK signaling pathway. Redox Rep 2022;27:1–8. https://doi.org/10.1080/13510002.2021.2017681.Suche in Google Scholar PubMed PubMed Central
38. Salehi, B, Azzini, E, Zucca, P, Varoni, EM, Kumar, NVA, Dini, L, et al.. Plant-derived bioactives and oxidative stress-related disorders: a key trend towards healthy aging and longevity promotion. Appl Sci 2020;10:947. https://doi.org/10.3390/app10030947.Suche in Google Scholar
39. Wang, QH, Kuang, N, Hu, WY, Yin, D, Wei, YY, Hu, TJ. The effect of Panax notoginseng saponins on oxidative stress induced by PCV2 infection in immune cells: in vitro and in vivo studies. J Vet Sci 2020;21:e61. https://doi.org/10.4142/jvs.2020.21.e61.Suche in Google Scholar PubMed PubMed Central
40. Gaweł, S, Wardas, M, Niedworok, E, Wardas, P. Malondialdehyde (MDA) as a lipid peroxidation marker. Wiad Lek 2004;57:453–5.Suche in Google Scholar
41. Cheng, Y, Lu, C, Yen, G. Phytochemicals enhance antioxidant enzyme expression to protect against NSAID-induced oxidative damage of the gastrointestinal mucosa. Mol Nutr Food Res 2017;61:1600659. https://doi.org/10.1002/mnfr.201600659.Suche in Google Scholar PubMed
42. Abd El-Aal, HAHMA. Lipid peroxidation end-products as a key of oxidative stress: effect of antioxidant on their production and transfer of free radicals. In: Lipid Peroxidation; 2012.Suche in Google Scholar
43. Pigeolet, E, Corbisier, P, Houbion, A, Lambert, D, Michiels, C, Zachary, MD, et al.. Glutathione peroxidase, superoxide dismutase, and catalase inactivation by peroxides and oxygen derived free radicals. Mech Ageing Dev 1990;51:283–97. https://doi.org/10.1016/0047-6374(90)90078-tSuche in Google Scholar PubMed
44. Pizzorno, J. Glutathione!. Integr Med (Encinitas) 2014;13:8–12.Suche in Google Scholar
45. Le Gal, K, Schmidt, EE, Sayin, VI. Cellular redox homeostasis. Antioxidants 2021;10:1377, https://doi.org/10.3390/antiox10091377.Suche in Google Scholar PubMed PubMed Central
© 2023 Walter de Gruyter GmbH, Berlin/Boston
Artikel in diesem Heft
- Frontmatter
- Reviews
- The effect of lavender on mothers sleep quality in the postpartum period: a systematic review and meta-analysis
- The effect of Salvia officinalis on blood glycemic indexes and blood lipid profile in diabetic patients: a systematic review and meta-analysis
- Neuroprotective potential of Celastrus paniculatus seeds against common neurological ailments: a narrative review
- Intuitive and mindful eating to improve physiological health parameters: a short narrative review of intervention studies
- Research Articles
- Vitamin C supplementation modulates crude oil contaminated water induced gravid uterine impaired contractile mechanism and foetal outcomes in Wistar rats
- Acute and sub acute toxicity of Amirdha Gandhi Kukkil Vallathy an effective Siddha herbo mineral formulation used in the treatment of rheumatoid arthritis in wistar albino rat model
- Anti-hyperplastic effects of the Dacryodes edulis (Burseraceae) leaves aqueous extract on tamoxifen-induced endometrium hyperplasia on Wistar rat
- Vitamin A and vitamin D3 protect the visual apparatus during the development of dopamine-2 receptor knockout mouse model of Parkinsonism
- Leaf paste of Telfairia occidentalis favourably modulates deleterious effects associated with exposure to diethylnitrosamine in male Wistar rats
- Chemical composition, antioxidant, and enzyme inhibitory properties of Rauwolfia vomitoria extract
- Intra-stromal injection of honey-treated keratocytes as a cell-based therapy for experimental corneal laceration
- Effect of Annona squamosa leaf extract on human promyelocytic leukemia cells subjected to oxidative stress
- Cinnamic acids as promising bioactive compounds for cancer therapy by targeting MAPK3: a computational simulation study
- Cowanin induces apoptosis in breast cancer cells via Bcl-2 signaling pathway
- Arq Ajīb – a wonder Unani formulation for inhibiting SARS-CoV-2 spike glycoprotein and main protease – an in silico approach
- Immediate effect of a meditation technique on blood glucose, state anxiety and relaxation in patients with type 2 diabetes: a pilot randomized crossover study
- Effect of moderate intensity resistance training with blood flow restriction on muscle strength and girth in young adults – a randomized control trial
- Short Communication
- Icosapent ethyl (VASCEPA®) as treatment for post-acute sequelae of SARS CoV-2 (PASC) vaccine induced injury and infection
Artikel in diesem Heft
- Frontmatter
- Reviews
- The effect of lavender on mothers sleep quality in the postpartum period: a systematic review and meta-analysis
- The effect of Salvia officinalis on blood glycemic indexes and blood lipid profile in diabetic patients: a systematic review and meta-analysis
- Neuroprotective potential of Celastrus paniculatus seeds against common neurological ailments: a narrative review
- Intuitive and mindful eating to improve physiological health parameters: a short narrative review of intervention studies
- Research Articles
- Vitamin C supplementation modulates crude oil contaminated water induced gravid uterine impaired contractile mechanism and foetal outcomes in Wistar rats
- Acute and sub acute toxicity of Amirdha Gandhi Kukkil Vallathy an effective Siddha herbo mineral formulation used in the treatment of rheumatoid arthritis in wistar albino rat model
- Anti-hyperplastic effects of the Dacryodes edulis (Burseraceae) leaves aqueous extract on tamoxifen-induced endometrium hyperplasia on Wistar rat
- Vitamin A and vitamin D3 protect the visual apparatus during the development of dopamine-2 receptor knockout mouse model of Parkinsonism
- Leaf paste of Telfairia occidentalis favourably modulates deleterious effects associated with exposure to diethylnitrosamine in male Wistar rats
- Chemical composition, antioxidant, and enzyme inhibitory properties of Rauwolfia vomitoria extract
- Intra-stromal injection of honey-treated keratocytes as a cell-based therapy for experimental corneal laceration
- Effect of Annona squamosa leaf extract on human promyelocytic leukemia cells subjected to oxidative stress
- Cinnamic acids as promising bioactive compounds for cancer therapy by targeting MAPK3: a computational simulation study
- Cowanin induces apoptosis in breast cancer cells via Bcl-2 signaling pathway
- Arq Ajīb – a wonder Unani formulation for inhibiting SARS-CoV-2 spike glycoprotein and main protease – an in silico approach
- Immediate effect of a meditation technique on blood glucose, state anxiety and relaxation in patients with type 2 diabetes: a pilot randomized crossover study
- Effect of moderate intensity resistance training with blood flow restriction on muscle strength and girth in young adults – a randomized control trial
- Short Communication
- Icosapent ethyl (VASCEPA®) as treatment for post-acute sequelae of SARS CoV-2 (PASC) vaccine induced injury and infection