THE PROTECTIVE EFFECT OF EXTRA VIRGIN OLIVE OIL ON ARSENIC INDUCED CARDIOMYOPATHY IN ALBINO RATS
Main Article Content
Keywords
Arsenic toxicity, Cardiomyopathy, Extra virgin olive oil, Oxidative stress.
Abstract
Background: Arsenic contamination of drinking water is a major public health concern in Pakistan and globally. Chronic exposure induces oxidative stress, inflammation, and structural cardiac damage leading to cardiomyopathy. Extra virgin olive oil (EVOO), rich in polyphenols and antioxidants, has shown protective effects in various organs, but its role in arsenic-induced cardiac injury is not well established.
Objective: To evaluate the protective effect of EVOO against arsenic-induced gross and histological alterations in the heart of albino rats.
Methods: Forty-five adult male albino rats were divided into three groups (n = 15 each): Group I (control, distilled water), Group II (arsenic, 40 mg/kg sodium arsenate), and Group III (arsenic + EVOO, 0.2 ml/day). After four weeks, hearts were excised, weighed, and examined histologically for congestion, inflammatory infiltration, edema and myocyte hypertrophy. Data were analyzed using ANOVA, post hoc Tukey, and Chi-square tests, with p ≤ 0.05 considered significant.
Results: Arsenic significantly increased heart weight (1.77 ± 0.04 g) and myocyte diameter (36.9 ± 1.0 µm) compared with controls (1.32 ± 0.03 g; 22.0 ± 0.9 µm; p < 0.001). EVOO prevented these changes, with values (1.38 ± 0.02 g; 24.4 ± 1.1 µm) comparable to controls (p > 0.05). Edema and inflammatory infiltration were absent in controls, but present in 80% and 93% of arsenic-exposed rats, respectively. EVOO reduced these to 60% each (p < 0.0001). Congestion was observed in 27% of arsenic-only and 33% of arsenic + EVOO rats, with no significant difference (p = 0.054).
Conclusion: EVOO confers significant cardioprotection against arsenic-induced cardiomyopathy by normalizing heart weight and myocyte size and reducing histological damage.
References
2. Crucean A, Spicer DE, Tretter JT, Mohun TJ, Anderson RH. Revisiting the anatomy of the right ventricle in the light of knowledge of its development. J Anat. 2024;244(2):297–311.
3. ghonimi W. Left Ventricles of the Mature Camel Heart (Camelus dromedaries) with Special References to the Structure and Distribution of the Purkinje Cardiomyocytes: Microanatomy. J Vet Sci Technol. 2014;05(03).
4. Ramadan NA, Mahmood EM, Mohammed SA. Morphometric Study of Epicardium and Myocardium Thickness in Adult Human Hearts. J Angiother. 2024;8(3):1–5.
5. Shah A, Arjunan A, Baroutaji A, Zakharova J. A review of physicochemical and biological contaminants in drinking water and their impacts on human health. Water Sci Eng [Internet]. 2023;16(4):333–44. Available from: http://dx.doi.org/10.1016/j.wse.2023.04.003
6. Huq ME, Fahad S, Shao Z, Sarven MS, Khan IA, Alam M, et al. Arsenic in a groundwater environment in Bangladesh: Occurrence and mobilization. J Environ Manage [Internet]. 2020;262(January 2019):110318. Available from: https://doi.org/10.1016/j.jenvman.2020.110318
7. Higgins MA, Metcalf MJ, Robbins GA. Nonpoint source arsenic contamination of soil and groundwater from legacy pesticides. J Environ Qual. 2022;51(1):66–77.
8. Nahar K, Rhaman MS, Parvin K, Bardhan K, Marques DN, García-Caparrós P, et al. Arsenic-Induced Oxidative Stress and Antioxidant Defense in Plants. Stresses. 2022;2(2):179–209.
9. Wen A, Wang J, Deng Q, Ren T, Yang J, Wen G, et al. The anti-inflammatory effect of arsenic trioxide effectively mitigates the pathogenic process in local chickens with avian leukosis. Poult Sci. 2024;104288.
10. Li J, Guo C, Liu Y, Han B, Lv Z, Jiang H, et al. Chronic arsenic exposure-provoked biotoxicity involved in liver-microbiota-gut axis disruption in chickens based on multi-omics technologies. J Adv Res [Internet]. 2024;(600). Available from: https://doi.org/10.1016/j.jare.2024.01.019
11. Duker AA, Carranza EJM, Hale M. Arsenic geochemistry and health. 2004;
12.Longnecker MP, Daniels JL. Environmental contaminants as etiologic factors for diabetes. Environ Health Perspect. 2001 Dec;871–6.
13. Tseng CH, Tseng CP, Chiou HY, Hsueh YM, Chong CK, Chen CJ. Epidemiologic evidence of diabetogenic effect of arsenic. Toxicol Lett. 2002;133:69–76.
14. Tseng CH, Tai TY, Chong CK, Tseng CP, Lai MS, Lin BJ, et al. Long-term arsenic exposure and incidence of non-insulin-dependent diabetes mellitus: a cohort study in arseniasis-hyperendemic villages in Taiwan. Environ Health Perspect. 2000 Sep;108(9):847–51.
15. KAPAJ S, PETERSON H, LIBER K, BHATTACHARYA P. Human Health Effects From Chronic Arsenic Poisoning–A Review. J Environ Sci Heal Part A. 2006 Oct;41(10):2399–428.
16. RAVAL D, NERELLA B, RATHOD V, YOUNG M, KANAKANNAVAR SS, ORING J. MULTISYSTEM IMPACT: COPD, INFILTRATIVE CARDIOMYOPATHY SECONDARY TO CHRONIC ARSENIC POISONING FROM WELL CONTAMINATION. Chest [Internet]. 2024 Oct;166(4):A4938–9. Available from: https://linkinghub.elsevier.com/retrieve/pii/S0012369224037322
17. Das D, Pamia J, Kumar D, Panda SK, Jenna G. Histopathological Grading of Induced Cardiotoxicity Due to Arsenic and its Alleviation by Allium sativum in Ducks. Indian J Anim Res. 2021 Oct 14;(Of).
18. Singh V. the Anatomical Society. 2019;2019–22.
19. Hira Waqas Cheema SA. The Protective Effect of Olive Oil on Arsenic Induced Histological Changes in the Liver of Albino Rats. J Islam Int Med Coll [Internet]. 2018;13(4):200–5. Available from: https://journals.riphah.edu.pk/index.php/jiimc/article/view/1057
20. Khaleda L, Begum SK, Apu MAR, Chowdhury RH, Alam MJ, Datta A, et al. Arsenic-Induced Cardiovascular Diseases and their Correlation with Mitochondrial DNA Copy Number, Deletion, and Telomere Length in Bangladeshi Population. Cardiovasc Toxicol. 2024 Jan 1;24(1):27–40.
21. Souza ACF, de Paiva Coimbra JL, Ervilha LOG, Bastos DSS, Cossolin JFS, Santos EC, et al. Arsenic induces dose-dependent structural and ultrastructural pathological remodeling in the heart of Wistar rats. Life Sci. 2020 Sep 15;257.
22. Azam MT, Ahmad A, Ahmed A, Khalid A, Saleem S. Health risk assessment of arsenic and lead contamination in drinking water: A study of Islamabad and Rawalpindi, Pakistan. Water Supply. 2024;24(6):2055–65.
23. Das S, Pradhan GK, Das S, Nath D, Das Saha K. Enhanced protective activity of nano formulated andrographolide against arsenic induced liver damage. Chem Biol Interact [Internet]. 2015;242:281–9. Available from: http://dx.doi.org/10.1016/j.cbi.2015.10.011
24. Genchi G, Lauria G, Catalano A, Carocci A, Sinicropi MS. Arsenic: A Review on a Great Health Issue Worldwide. Appl Sci. 2022;12(12).
25. Ebrahimi Y, AL-Baghdady HFA, Hameed NM, Iswanto A, Shnain Ali M, Hammoodi HA, et al. Common fatty acids and polyphenols in olive oil and its benefits to heart and human health. Casp J Environ Sci. 2022;1–7.
26. Garcia AR, Filipe SB, Fernandes C, Estevão C, Ramos G. No 主観的健康感を中心とした在宅高齢者における 健康関連指標に関する共分散構造分析Title. 1(443).
27. Lu Y, Zhao J, Xin Q, Yuan R, Miao Y. Food Science and Human Wellness Protective effects of oleic acid and polyphenols in extra virgin olive oil on cardiovascular diseases. Food Sci Hum Wellness. 2024;13(2):529–40.
28. Ramadan O, Abuamara T, Taha R, Awad M, Mohammed M, Omar N. Alleviation of the arsenic induced hepatotoxicity in rats by ginger or omega-3 : a histological and biochemical study. 2024;(4):221–32.
29. Sassi HS, Eldresi SM, Elharabi TA, Amer AH. Olive Oil ’ s protective potential against cyclophosphamide-induced nephrotoxicity in Swiss albino rats Olive Oil ’ s protective potential against cyclophosphamide-induced nephrotoxicity in Swiss albino rats. 2024;(October).
30. Ahmed QA, Abdullah KK, Saber H, Hassan K. The Effect Of Olive Oil ( Oo ) And Hydroxytyrosol ( Hxt ) In Improving The Level Of Sex Hormones And Suppressing Oxidative Stress And Histopathological Of The Testes Caused By Hyperlipidemia In Male Rats. 2021;8(4):13072–86.
31. Review S. Association between arsenic exposure and inflammatory cytokines and C-reaction protein. 2022;50(November).
32. Ibrahim G, Kawkab F. Curcumin Ameliorates Doxorubicin ‑ Induced Cardiotoxicity and Hepatotoxicity Via Suppressing Oxidative Stress and Modulating iNOS , NF ‑ κB , and TNF ‑ α in Rats. Cardiovasc Toxicol. 2022;22(2):152–66.
33. Fahad T, Ali S, Qureshi T, Khan NF. Maternal Hypothyroidism-Induced Impaired Development of Neurons in Rat Offspring: Insights for Antenatal Care. Life Sci. 2024;5(1):07.
34. Khuntia G, Dash JR, Jena B, Mishra UK, Parija SC. Hesperidin attenuates arsenic trioxide-induced cardiac toxicity in rats. Asian Pac J Trop Biomed. 2023;13(4):156–64.
35. Al-allaf L, Alnuaeimy W. A Histologic Study of Imatinib Cardiotoxicity in Adult Male Rats. 2023;11:105–10.
36. Attia AA, Sorour JM, Mohamed NA, Mansour TT, Al-eisa RA. Biochemical , Histological , and Ultrastructural Studies of the Protective Role of Vitamin E on Cyclophosphamide-Induced Cardiotoxicity in Male Rats. 2023;
37. Orgil B ochir, Xu ÃF, Munkhsaikhan ÃU, Alberson NR, Bajpai AK, Johnson JN, et al. Echocardiography phenotyping in murine genetic reference population of BXD strains reveals signi fi cant QTLs associated with cardiac function and morphology. 2025;(August 2022):51–66.
38. Shahidi S, Ramezani-aliakbari K, Sarihi A, Heshmati A, Shiri E. Olive oil protects against cardiac hypertrophy in D-galactose induced aging rats. 2024;
39. Wang Y, Zhang S, Ma Y, Xiang A, Sun H, Song J, et al. Melatonin protected against myocardial infarction injury in rats through a Sirt6 -dependent antioxidant pathway. 2022;1–8.

