skip to main content

The Effect of Chronic Exposure Between Ascorbic Acid-Based Vape and Tobacco Cigarette Towards Oxidative Stress Level and Tracheal Histopathology in White Rats (Rattus Norvegicus)

*Levina Athaya Anarizta  -  Department of Biomedical Science, Faculty of Medicinie, Universitas Diponegoro, Semarang, Indonesia, Indonesia
Udadi Sadhana orcid scopus  -  Department of Biomedical Science, Faculty of Medicinie, Universitas Diponegoro, Semarang, Indonesia, Indonesia
Awal Prasetyo orcid scopus  -  Department of Biomedical Science, Faculty of Medicinie, Universitas Diponegoro, Semarang, Indonesia, Indonesia
Hermawan Istiadi orcid  -  Department of Anatomic Pathology, Faculty of Medicine, Universitas Diponegoro- Dr. Kariadi Hospital, Semarang, Indonesia, Indonesia

Citation Format:
Abstract

Background: Nicotine-based vape has gained popularity as an alternative to cigarette use. Numerous studies have proven the dangers of smoking, including the elevation of oxidative stress and tracheal structure alteration. Ascorbic acid (AA) is a potential nicotine replacement in vape's e-liquid. Publications about AA as nicotine alternative in vape’s e-liquid are still scarce.

Objective: This research aimed to analyze the effects of oxidative stress and tracheal histopathology in white rats (Rattus norvegicus) exposed to cigarette smoke and aerosol generated from AA-based e-liquid.

Methods: True experimental research design was conducted using a post-test only control group design approach with 21 white rats (Rattus norvegicus). Rats were randomly distributed into three groups: K1= non-exposed group; K2= exposed to smoke from three cigarettes/day; and K3= exposed with 0.5mL/day of AA-based vape aerosol. The exposure period lasted 12 weeks; then, the blood samples and the trachea were collected after termination. SOD-3 and MDA were measured in blood serum as oxidative stress biomarkers, while goblet cell count and mucosal epithelium thickness were measured through trachea histopathology slide. The data were statistically analyzed using a One-Way ANOVA test, followed by Post Hoc Bonferroni test and Games-Howell test.

Results: Statistical analysis significant result (p<0.05) was found in SOD-3 level on K1&K3 and K2&K3, goblet cell count on K1&K3, and mucosal epithelial thickness on K1&K2. MDA level did not show any significant difference between groups. Tracheal histopathology revealed damages, K2 had the highest average of goblet cells (3.93±2.67) and the smallest average mucosal epithelial thickness in K2 (34.65±6.55), likely due to regeneration dysfunction in trachea.

Conclusion: Cigarette smoke exposure and AA-based vape aerosol showed significant differences in SOD-3 level, the number of goblet cells, and mucosal epithelial thickness. MDA level did not show any significant difference. AA as vape e-liquid base alternative is not significantly lower the stress oxidative level and require further investigations.

Keywords: Ascorbic acid, Cigarette, E-cigarette, Oxidative stress, Tracheal histopathology

Article Metrics:

Article Info
Section: Original Research Article
Language : EN
  1. A. Famiglietti, J. W. Memoli, and P. G. Khaitan, “Are electronic cigarettes and vaping effective tools for smoking cessation? Limited evidence on surgical outcomes: A narrative review,” J. Thorac. Dis., vol. 13, no. 1, pp. 384–395, 2021, doi: 10.21037/jtd-20-2529
  2. T. Jerzyński and G. V. Stimson, “Estimation of the global number of vapers: 82 million worldwide in 2021,” Drugs, Habits Soc. Policy, vol. 24, no. 2, pp. 91–103, 2023, doi: 10.1108/DHS-07-2022-0028
  3. A. Ghosali, “Rokok elektrik dan tuberkulosis paru : sebuah tinjauan pustaka,” vol. 15, no. 1, pp. 201–209, 2024, doi: 10.15562/ism.v15i1.1963
  4. R. Florentika and W. Kurniawan, “Analisis Kuantitatif Tar dan Nikotin Terhadap Rokok Kretek Yang Beredar di Indonesia,” Erud. Indones. J. Food Drug Saf., vol. 2, no. 2, pp. 22–32, 2022, doi: 10.54384/eruditio.v2i2.118
  5. D. Nuryunarsih, S. Lewis, and T. Langley, “Health Risks of Kretek Cigarettes: A Systematic Review,” Nicotine Tob. Res., vol. 23, no. 8, pp. 1274–1282, 2021, doi: 10.1093/ntr/ntab016
  6. P. Marques, L. Piqueras, and M. J. Sanz, “An updated overview of e-cigarette impact on human health,” Respir. Res., vol. 22, no. 1, pp. 1–14, 2021, doi: 10.1186/s12931-021-01737-5
  7. A. Mishra, P. Chaturvedi, S. Datta, S. Sinukumar, P. Joshi, and A. Garg, “Harmful effects of nicotine,” Indian J. Med. Paediatr. Oncol., vol. 36, no. 1, pp. 24–31, 2015, doi: 10.4103/0971-5851.151771
  8. A. W. Caliri, S. Tommasi, and A. Besaratinia, “Relationships among smoking, oxidative stress, inflammation, macromolecular damage, and cancer,” Mutat. Res. Mutat. Res., vol. 787, 2021
  9. N. H. Nguyen, G. B. Tran, and C. T. Nguyen, “Anti-oxidative effects of superoxide dismutase 3 on inflammatory diseases,” J. Mol. Med., vol. 98, no. 1, pp. 59–69, 2020, doi: 10.1007/s00109-019-01845-2
  10. M. Passi, S. Shahid, S. Chockalingam, I. K. Sundar, and G. Packirisamy, “Conventional and nanotechnology based approaches to combat chronic obstructive pulmonary disease: Implications for chronic airway diseases,” Int. J. Nanomedicine, vol. 15, pp. 3803–3826, 2020, doi: 10.2147/IJN.S242516
  11. M. Morales and S. Munné-Bosch, “Malondialdehyde: Facts and artifacts,” Plant Physiol., vol. 180, no. 3, pp. 1246–1250, 2019, doi: 10.1104/pp.19.00405
  12. A. Toto et al., “Urinary Malondialdehyde (MDA) Concentrations in the General Population—A Systematic Literature Review and Meta-Analysis,” Toxics, vol. 10, no. 4, 2022, doi: 10.3390/toxics10040160
  13. Z. H. Saeed, M. A. E. A. El Hakim, and N. R. Mohamed, “Chronic obstructive pulmonary disease in non-smokers: role of oxidative stress,” Egypt. J. Bronchol., vol. 15, no. 1, 2021, doi: 10.1186/s43168-021-00088-5
  14. E. S. Son et al., “Effects of antioxidants on oxidative stress and inflammatory responses of human bronchial epithelial cells exposed to particulate matter and cigarette smoke extract,” Toxicol. Vitr., vol. 67, no. May, 2020, doi: 10.1016/j.tiv.2020.104883
  15. N. J. Ahmed et al., “The effects of smoking on IgE, oxidative stress and haemoglobin concentration,” Asian Pacific J. Cancer Prev., vol. 21, no. 4, pp. 1069–1072, 2020, doi: 10.31557/APJCP.2020.21.4.1069
  16. S. Ziad, A.-A. Wajdy, and B. Darwish, “Effects of cigarette smoking on histology of trachea and lungs of albino rat,” J. Res. Opin. Anim. Vet. Sci., vol. 3, no. 10, pp. 356–362, 2013, [Online]. Available: www.roavs.com
  17. N. W. S. Antari, “The Activity Test of Dewandaru Fruit (Eeugenia uniflora L.) in Trachea of Male Mice (Mus musculus L.) Which Exposed to Cigarette Smoke,” J. Pijar Mipa, vol. 19, no. 1, pp. 125–130, 2024, doi: 10.29303/jpm.v19i1.6385
  18. A. Prasetyo, U. Sadhana, and J. Budiman, “Nasal mucociliary clearance in smokers: A systematic review,” Int. Arch. Otorhinolaryngol., vol. 25, no. 1, pp. 160–169, 2021, doi: 10.1055/s-0040-1702965
  19. K. Syal, S. Chakraborty, R. Bhattacharyya, and D. Banerjee, “Combined inhalation and oral supplementation of Vitamin A and Vitamin D: A possible prevention and therapy for tuberculosis,” Med. Hypotheses, vol. 84, no. 3, pp. 199–203, 2015, doi: 10.1016/j.mehy.2014.12.022
  20. D. Banerjee and D. Kaul, “Combined inhalational and oral supplementation of ascorbic acid may prevent influenza pandemic emergency: A hypothesis,” Nutrition, vol. 26, no. 1, pp. 128–132, 2010, doi: 10.1016/j.nut.2009.09.015
  21. N. RS, M. V. N. J. Reddy, S. Batra, S. K. Srivastava, and K. Syal, “Vitamin C and its therapeutic potential in the management of COVID19,” Clin. Nutr. ESPEN, vol. 50, no. January, pp. 8–14, 2022, doi: 10.1016/j.clnesp.2022.05.026
  22. M. Arumugam, R. L. Sundaram, V. Jayajothi, M. Arul, J. A. Suresh, and S. K. Kesavan, “Recirculating bioavailable nicotine metabolite using ascorbic acid: A pragmatic approach for treating nicotine dependence,” Adv. Redox Res., vol. 10, no. October 2023, 2024, doi: 10.1016/j.arres.2023.100089
  23. Ranjit Ambad, Saurabh Hadke, Pradip Jain, and Ashish Anjankar, “Role of Serum Malondialdehyde (MDA) and Vitmin- C Level in Non-Smokers and Chronic Smokers with Acute Myocardial Infarction (AMI) in Male,” Indian J. Forensic Med. Toxicol., vol. 15, no. 2, pp. 4363–4367, 2021, doi: 10.37506/ijfmt.v15i2.15049
  24. A. Prasetyo and N. Irawati, “Inhalation of Ascorbic Acid Modulates Sinonasal Immune System,” Ascorbic Acid - Biochem. Funct., no. March, pp. 1–53, 2024, doi: 10.5772/intechopen.110891
  25. R. Emma, M. Caruso, D. Campagna, R. Pulvirenti, and G. Li Volti, “The Impact of Tobacco Cigarettes, Vaping Products and Tobacco Heating Products on Oxidative Stress,” Antioxidants, vol. 11, no. 9, pp. 1–28, 2022, doi: 10.3390/antiox11091829
  26. H. B. Jebur et al., “Lung Histo-Pathological Changes and Sods Gene Expression in Wister Rats Exposed To Conventional and Electronic Cigarettes,” Bull. Pharm. Sci. Assiut, vol. 46, no. 2, pp. 1429–1440, 2023, doi: 10.21608/BFSA.2023.327634
  27. F. S. Bezerra et al., " Oxidative Stress and Inflammation in Acute and Chronic Lung Injuries" Antioxidants, vol. 12, pp. 548, 2023, doi: https://doi.org/10.3390/antiox12030548
  28. K. Sakaguchi et al., “Serum Free Radical Scavenging Capacity Profiles of Patients with Chronic Obstructive Pulmonary Disease,” Int. J. COPD, vol. 18, pp. 615–624, 2023, doi: 10.2147/COPD.S385780
  29. C. Grazioli et al., “A colorimetric paper-based smart label soaked with a deep-eutectic solvent for the detection of malondialdehyde,” Sensors Actuators, B Chem., vol. 329, no. July 2020, 2021, doi: 10.1016/j.snb.2020.129174
  30. A. Ali et al., “Potential of ascorbic acid in human health against different diseases: an updated narrative review,” Int. J. Food Prop., vol. 27, no. 1, pp. 493–515, 2024, doi: 10.1080/10942912.2024.2327335
  31. E. N. Indasari, A. P. W. Marhendra, and A. W. Wardhana, “Extract Bee Propolis (Trigona sp) for Preventive Increase Protease Activity and Defect of Trachea Histology in Rats (Rattus norvegicus) Exposed to Cigarette Smoke,” IOP Conf. Ser. Earth Environ. Sci., vol. 391, no. 1, pp. 0–11, 2019, doi: 10.1088/1755-1315/391/1/012048
  32. M. D. Kim et al., “The combination of propylene glycol and vegetable glycerin e-cigarette aerosols induces airway inflammation and mucus hyperconcentration,” Sci. Rep., vol. 14, no. 1, pp. 1–14, 2024, doi: 10.1038/s41598-024-52317-8
  33. M. Bodas et al., “Cigarette Smoke Activates NOTCH3 to Promote Goblet Cell Differentiation in Human Airway Epithelial Cells,” vol. 64, no. 4, pp. 426–440, 2021, doi: 10.1165/rcmb.2020-0302OC
  34. J. Jiao and L. Zhang, “Influence of intranasal drugs on human nasal mucociliary clearance and ciliary beat frequency,” Allergy, Asthma Immunol. Res., vol. 11, no. 3, pp. 306–319, 2019, doi: 10.4168/aair.2019.11.3.306
  35. M. Schnoor, L. M. Yin, and S. Sun, Cell movement in health and disease. Academic Press, 2022
  36. R. M. Jagirdar et al., “Short Term Exposure of Sheep Tracheal Epithelium to Cigarette Smoke Extract Reduces ENaC Current: A Pilot Study,” In Vivo (Brooklyn)., vol. 38, no. 5, pp. 2294–2299, 2024, doi: 10.21873/invivo.13694
  37. C. Jiang, Q. Chen, and M. Xie, “Smoking increases the risk of infectious diseases: A narrative review,” Tob. Induc. Dis., vol. 18, pp. 1–17, 2020, doi: 10.18332/tid/123845
  38. H. Brody, “Chronic obstructive pulmonary disease,” Nature, vol. 489, no. 7417, 2012, doi: 10.1038/489S1a
  39. M. Manevski et al., “Increased Expression of LASI lncRNA Regulates the Cigarette Smoke and COPD Associated Airway Inflammation and Mucous Cell Hyperplasia,” Front. Immunol., vol. 13, no. June, pp. 1–16, 2022, doi: 10.3389/fimmu.2022.803362
  40. R. Chethana, P. Mishra, M. Kaushik, R. Jadhav, and A. Dehadaray, “Effect of Smoking on Nasal Mucociliary Clearance,” Indian J. Otolaryngol. Head Neck Surg., vol. 74, no. s2, pp. 956–959, 2022, doi: 10.1007/s12070-020-02026-1

Last update:

No citation recorded.

Last update:

No citation recorded.