Amelioration of Cadmium-Induced Biochemical Alterations in Heart Tissues of Wistar Rats Using Bee Honey

Main Article Content

Ovovwe Diakparomre
Onyeka B. Onyeukwu
Samuel O. Asagba

Abstract

The hunt for potential remedies for cadmium (Cd) toxicity is an exciting topic of research that is now being investigated globally. This study investigated amelioration of cadmium-induced biochemical alterations in heart tissues of Wistar rats using bee honey. Six groups (1–6) of thirty adult Wistar rats were used for the study: control, sub-chronic Cd exposure, sub-chronic Cd exposure plus honey, acute Cd exposure, acute Cd exposure plus honey, and honey only. For the sub-chronic investigation, Cd chloride (CdCl2) was injected intraperitoneally (IP) at a dose of 2mg/kg body weight every two days for a period of four weeks, and for the acute trial, a dose of 4
mg/kg body weight was injected IP 12 hours prior to sacrifice. 1 ml/kg of body weight of honey was given orally once every day for four weeks. According to the study, groups 2 and 4 had substantially greater levels of lipid peroxidation and acid phosphatase (ACP) activity in the heart tissues compared to group 1. Catalase (CAT), superoxide dismutase (SOD), alanine aminotransferase (ALT), aspartate aminotransferase (AST), and alkaline phosphatase (ALP) enzyme activity were also significantly decreased. This study shows that honey treatment significantly ameliorates Cd-induced toxicities in heart tissues by suppressing lipid peroxidation and normalizing antioxidant enzyme activity. Further work should be done to identify specific phytochemical antioxidants and its mode of action in ameliorating Cd-induced toxicities in heart tissues.

Article Details

How to Cite
Diakparomre, O., Onyeukwu, O. B., & Asagba, S. O. (2024). Amelioration of Cadmium-Induced Biochemical Alterations in Heart Tissues of Wistar Rats Using Bee Honey. Tropical Journal of Natural Product Research (TJNPR), 8(7), 7855-7860. https://doi.org/10.26538/tjnpr/v8i7.32
Section
Articles

References

Quddus A, Yimer N, Basit MA, Khan S, Amir M. Review of antioxidant-rich natural dietary products as protective and therapeutic factors against cadmium toxicity in living organisms. Pertanika J. Tropic Agric Sci.2021; 44(1):83–105. Doi:10.47836/pjtas.44.1.05

Vardhan KH, Kumar PS, Panda RC. A review on heavy metal pollution, toxicityand remedial measures: Current trends and future perspectives. J. Mol Liquids. 2019; 290: 111197. Doi: 10.1016/J.Molliq.2019.111197

Omotoso OD, Olorunnado SE, Onoja-Alexander MO, Ayodeji OS. Evaluation of the therapeutic effects of Moringa oleifera seed oil on cadmium and herbal alcoholic beverage–induced prefrontal cortex damage in Wistar rats. Asian J. Med Health. 2022; 20(12):179-187. Doi: 10.9734/AJMAH/2022/v20i12

Araujo-Padilla X, Briseño-Bugarín J, López-Luna A, Flores de la Torre JA. Effects ofcadmium exposure on lactatingmice and rats: A systematic reviewof breastfeeding experiments. Appl Sci. 2022; 12: 11412. Doi: 10.3390/app122211412

Li C, Wang B, Lu X, Huang Y, Wang H, Xu D, Zhang J. Maternal exposure to cadmium from puberty through lactation induces abnormal reproductive development in female offspring. Ecotoxicol Environ Safety. 2022; 242: 113927.

Unsal V, Dalkıran T, Çiçek M, Kölükçü E. The role of natural antioxidants against reactive oxygen species produced by cadmium toxicity: A review. Adv Pharmaceu Bull. 2020; 10(2): 184-202. Doi: 10.34172/apb.2020.023

Nasiadek M, Skrzypińska-Gawrysiak M, Daragó A, Zwierzyńska E, Kilanowicz A. Involvement of oxidative stress in the mechanism of cadmium–induced toxicity on rat uterus. Environ ToxicolPharmacol. 2014; 38(2): Doi: 10.1016/j.etap.2014.07.007

Sarkar A, Ravindran G, Krishnamurthy V. A brief review on the effect of cadmium toxicity: from cellular to organ level. Intl J.Biotechnol Res.2013;3(1): 17-36.

Eze CE and Asomugha AL. Neurotoxicity and oxidative stress prevention by honey and garlic in adult male Wistar rats exposed to lead. Intl J.Innov Sci Res Technol. 2022; 7(1): 1011-1018.

Adedosu OT, Jacob AG, Alabi ZO. Protective effect of ethanol extract of Senna occidentalis leaf against cadmiuminduced hepatotoxicity in rats. Trop J. Nat Prod Res. 2017; 1(1):17-21. Doi: 10.26538/tjnpr/v1i1.4

Tian X, Zhang K, Zhang Y, Wang N, Wang H, Xu H, Guang S. Preparation and mechanism study of hydrogen bond induced enhanced composited gelatin microsphereprobe. Intl J. Biol Macromol.2024; 266(2):130752. Doi: 10.1016/j.ijbiomac.2024.130752.

Ekakitie LI and Orororo OC. Changes in haematological parameters of aluminium-exposed rats treated with natural bee honey. OSR J. Environ Sci Toxicol Food Technol. 2021; 15(5): 22-25.

Khleifat KM, Qaralleh H, Al-limoun MO, Al-khlifeh EM, Aladaileh SA, Tawarah N, Almajali IS. Antibacterial and antioxidant activities of local honey from Jordan. Trop J. Nat Prod Res. 2021; 5(3):470-477. Doi: 10.26538/tjnpr/v5i3.10

Suliman RS. Efficacy of white honey in attenuating histological changes resulting from multivitamin-induced hepatotoxicity in Albino rats. Trop J. Nat Prod Res. 2021; 5(1):84-87. Doi.org/10.26538/tjnpr/v5i1.10

Atagana OS and Asagba SO. Protective Effects of Honey against Cadmium-Induced Alteration of some Biochemical Parameters in Rats. Toxicol Environ Chem. 2015; 96(10):1-7.

Diakparomre O, Onyeukwu OB, Asagba SO. Effect of honey on some biochemical parameters in the brain tissues of Wistar rats exposed to cadmium. Uniport J. Eng Sci Res. 2023; 8(1):1-8.

National Institute of Health (NIH). Guide for the care and use of laboratory animals. Maryland: NIH. 1985.

Varshney R and Kale RK. Effects of Calmodulin Antagonists on Radiation-Induced Lipid Peroxidation. Intl J. Rad Biol.1990; 58(5):733-743.

Reitman S and Frankel S. A colorimetric method for determination of serum glutamate oxaloacetate and glutamic pyruvate transaminase. Am J. Clin Pathol. 1957; 28:56-58.

Roy AV. Rapid method for determining alkaline phosphatase activity in serum with thymolphthalein monophosphate. Clin Chem. 1970; 16:431.

Hillman GZ. Continuous photometric measurement of acid phosphatase activity. Zeitschrift fur KlinischeChemie und KlinischeBiochemie. 1971; 3:273-274.

Misra HP and Fridovich I. The role of superoxide anion in the autoxidation of epinephrine and a simple assay for superoxide dismutase. J Biol Chem. 1972;247(10): 3170-3175.

Kaplan A, Dembiec D, Cohen G, Marcus J. Measurement of catalase activity in tissue extracts. Anal Biochem. 1972; 34:30-38.

Arbi S, Bester MJ, Pretorius L, Oberholzer HM. Adverse cardiovascular effects of exposure tocadmium and mercury alone and in combinationon the cardiac tissue and aorta of Sprague–Dawley rats. J. Environ Sci Health. 2021; 56(6):609–624. Doi: 10.1080/10934529.2021.1899534

Singh A, Kukreti R, Saso L, Kukreti S. Oxidativestress: a key modulator in neurodegenerative diseases. Molecule. 2019; 24(8):1583. Doi: 10.3390/molecules24081583

Ekayoda O, Kadiri HE, Ohwokevwo OA. Combined effects of cadmium- andcyanide-contaminated diet on oxidative stressbiomarkers in different tissues of rats. Gal Med J. 2022; 29(4): E202244. Doi: 10.21802/gmj.2022.4.4

Kadiri HE and Apiamu A. Aframomummelegueta: a stimulator of liver function enzymes and a downregulatorof cyanide-mediated oxidative injuries in rats. Sci World J. 2022; 17(3):375-337.

Al-Kafaween MA, Alwahsh M, MohdHilmi, AB, Abulebdah DH. Physicochemical characteristics and bioactive compounds of different types of honey and their biological and therapeutic properties: A comprehensive review. Antibio. 2023; 12:337. Doi: 10.3390/antibiotics12020337

Shalaby KA and Saleh EM. Ameliorative effect of honey bee propolis on the nonylphenol-induced reproductive toxicity in male albino rats. Aust J Basic Appl Sci. 2011;5(11): 918-927.

Kadiri HE. The ameliorating effects of honey on some biochemical parameters on rats exposed to cyanide. Biokem. 2018; 30(1):13-20.

Wang Y., Branicky R, Noё A, Hekimi S. Superoxide dismutases: dual roles in controlling ROS damage and regulating ROS signaling. J. Cell Biol. 2018; 217(6):1915–1928. Doi: 10.1083/jcb.201708007.

Ezedom T, Asagba SO, Tonukari NJ. Toxicological effects of the concurrent administration of cadmium and arsenic through the food chain on the liver and kidney of rats. J. Basic Appl Zoolog. 2020; 81:16. Doi: 10.1186/s41936-020-00146-2.

Zayed Mohamed N, Farouk Aly H, El-Mezayen HA, ElSalamonya HE. Effect of co-administration of bee honey and some chemotherapeutic drugs on dissemination of hepatocellular carcinoma in rats. Toxicol Rep. 2019; 6(2019): 875–888.

Cheng N, Wu L, Zheng J, Cao W. Buckwheat honey attenuates carbon tetrachloride-induced liver and DNA damage in mice, evidence-based complement. Altern Med. 2015; 987385. Doi: 10.1155/2015/987385.

Nordin A, Bin Saim A, Bt Hj Idrus R. Honey ameliorate negative effects in neurodegenerative diseases: An evidence-based review. SainsMalaysiana. 2021; 50(3):791-801. Doi: 10.17576/Jsm-2021-5003-20.

Yaman T, Yener Z, Celik I. Histopathological and biochemical investigations ofprotective role of honey in rats with experimental aflatoxicosis, BMC Complement Altern Med. 2016; 16:232. Doi: 10.1186/S12906-016-1217-7.

Yildirim S, Celikezen FC, Oto G, Sengul E, Bulduk M, Tasdemir M, Ali Cinar D. An investigation ofprotective effects of litium borate on blood and histopathological parameters in acute cadmium-induced rats. Biol Trace Elem Res. 2018; 182:287–294.

Cobbina SJ, Chen Y, Zhou Z, Wu X, Zhao T, Zhang Z, Feng W, Wang W, Li Q, Wu X, Yang L. Toxicity assessment due to sub-chronic exposure to individual and mixtures of four toxic heavy metals. J. Hazard Mater. 2015; 294:109–120.

Yuan G, Dai S, Yin Z, Lu H, Jia R, Xu J, Song X, Li L, Shu Y, Zhao X. Toxicological assessment of combined lead and cadmium: Acute and sub-chronic toxicity study in rats. Food Chem Toxicol. 2014; 65:260–268.

Andjelkovic M, Djordjevic AB, Antonijevic E, Antonijevic B, Stanic M, Kotur-Stevuljevic J, Spasojevic-Kalimanovska V, Jovanovic M, Boricic N, Wallace D, Bulat Z. Toxic effect of acute cadmium and lead exposure in rat blood, liver, and kidney. Intl J. Environ Res Pub Health. 2019; 16(274):1-21. Doi:10.3390/ijerph16020274

Zhu H, Jia Y, Cao H, Meng F, Liu X. Biochemical and histopathological effects of subchronic oral exposure of rats to a mixture of five toxic elements. Food Chem Toxicol. 2014; 71:166–175.

Asagba SO, Adaikpoh MA, Kadiri H, Obi FO. Influence of aqueous extract of Hibiscus sabdariffa l. petals on cadmium toxicity in rats. Biol Trace Elem Res. 2007; 125: 47-57.

Abdel-Moneim WM and Ghafeer HH. The potential protective effect of natural honey against cadmium-induced hepatotoxicity and nephrotoxicity. Mansoura J.Foren Med Clin Toxicol. 2007; 15:75-98.

Ciriolo MR, Palamara AT, Incerpi S, Lafavia E, Bue MC, De Vito P, Garaci E, Rotilio G. Loss of GSH, Oxidative stress and decrease in intracellular pH as sequential steps in viral infection.J. Biol Chem.1997; 272(5):2700-2708.

Oladele JO, Adewale OO, Oyewole O, Salami MO, Owoade G, Oyeleke OM. Annona muricata protects against cadmium-mediated oxidative damage in the brain and liver of rats. Acta Facultatis Medicae Naissensis. 2020; 37(3): 252-260.

Onwuka FC, Erhabor O, Eteng MU, Umoh IB. Ameliorative effect of cabbage extract on cadmium-induced changes on hematology and biochemical parameters of albino rats. J. Toxicol Environ Health Sci.2010; 2(2): 11-16.