Assessment of hepatorenal biochemical indices in male Sprague Dawley rats preceding concurrent oral administration of Ghana alcoholic bitters and natural cocoa powder
DOI:
https://doi.org/10.15584/ejcem.2024.1.23Keywords:
biochemistry, Ghanaian alcoholic bitters, hepatorenal indices, natural cocoa powder, Sprague Dawley ratAbstract
Introduction and aim. There has been a surge in the consumption of Ghanaian alcoholic bitters. Ghanaian alcoholic bitters are formulated from a maceration of not less than three plant parts making the organic composition very complex. There appear to be no studies on the effect of Ghanaian alcoholic bitters on the hepatorenal biochemistry indices. The study aimed to assess the effects of alcoholic bitters and cocoa powder on the liver and kidney serum biochemistry.
Material and methods. Twenty-four healthy male Sprague Dawley rats, age 11–12 weeks, weighing 150–250 g were used. The rats were randomly assigned to four groups (n=6). At the end of the experimentation, a blood sample was taken by cardiac puncture and centrifuged to obtain the serum for biochemical assays and analysis.
Results. The liver enzymes showed no significant difference between the treatment and control groups. There were higher mean values for total bilirubin and direct bilirubin for alcoholic bitters and natural cocoa powder groups respectively than the control group and the co-administration of alcoholic bitters and natural cocoa powder group.
Conclusion. The study concludes that alcoholic bitters consumption might cause injury to the liver and kidney resulting in anomaly of the hepatorenal indices from rat blood serum biochemistry.
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Kouassi GK, Kouakou LK, Oussou JBN, Malan FD, Yapo PA. Acute toxicity and effect of subacute administration of “4 heures du matin” bitters on anthropometric and hematological parameters in Wistar rats. GSC Biological and Pharmaceutical Sciences. 2022;19(02):121-130. doi: 10.5281/zenodo.6627500
Kyeremeh K, Agbemafo FW, Appiah-Opong R. Quantitative analysis of chemical contaminants in Ghanaian herbal alcoholic bitters. International Journal of Chemistry and Applications. 2013;5(2):153-167.
Vandebroek I, Balick MJ, Ososki AL, et al. The importance of botellas and other plant mixtures in Dominican traditional medicine. J Ethnopharmacol. 2010;128(1):20-41. doi: 10.1016/j.jep.2009.12.013
Kouassi KG, Malan DF, Kouakou KL, Diop AL, Litta AL. Trade and consumption of bitters, alcoholic macerates, in the district of Abidjan (southern Côte d'Ivoire). Journal of Medicinal Plants. 2023;11(1):113-125.
Baydilli N, Can Akınsal E, Doğanyiğit Z, Ekmekçioğlu O, Silici S. Protective role of poplar propolis against alcohol-induced biochemical and histological changes in liver and testes tissues of rats. J Clin Pract Res. 2020;42(2):132-138. doi: 10.14744/etd.2020.83097
Odey MO, Ofonime ME, Ogar I, et al. Biochemical and Haematological Responses to Chronic Consumption of some Herbalized Nigerian Alcoholic Drinks. Nigerian Journal of Biochemistry and Molecular Biology. 2022;37(3):181-187.
Adeyemi MM, Afolabi OM, Balogun N. Hepatorenal function of Wistar rats treated with Alamo and Jekomo, an alcoholic herbal bitters in Nigeria. Journal of Phytomedicine and Therapeutics. 2022;21(2):992-1002. doi: 10.4314/jopat.v21i2.18
Aidoo E, Addai FK, Ahenkorah J, Hottor BA, Bugyei KA, Gyan B. Natural cocoa ingestion reduced liver damage in mice infected with Plasmodium berghei (NK65). Res Rep Trop Med. 2012;3:107-116. doi: 10.2147/RRTM.S33149
Khwaldeh A, Shraideh Z, Badran DH, et al. Ameliorative Effect of Turmeric and Cocoa Extract against Acute Second hand Exposure of Tobacco Smoking on Hepatocytes and Enterocytes in Albino Rats: Ultra structural Study. Biomedical and Pharmacology Journal. 2021;14(1):199-206. doi: 10.13005/bpj/2114
Andersen ML, Winter LMF. Animal models in biological and biomedical research - experimental and ethical concerns. Anais Da Academia Brasileira De Ciencias. 2019;91(1):e20170238. doi: 10.1590/0001-3765201720170238
Kayode OT, Kayode AAA, Nwonuma CO. Alcoholic bitters modulates sex hormones and some biochemical parameters of testicular function in male Wistar rats. F1000Research. 2018;7:1838. doi: 10.12688/f1000research.16648.1
Sokpor G, Addai FK, Gyasi RK, Bugyei KA, Ahenkorah J, Hottor BA. Voluntary Ingestion of Natural Cocoa Extenuated Hepatic Damage in Rats with Experimentally Induced Chronic Alcoholic Toxicity. Functional Foods in Health and Disease. 2012;2(5):166. doi: 10.31989/ffhd.v2i5.91
Srikanth V, Malini T, Govindarajulu P, Balasubramanian K. Effects of ethanol ingestion on epididymal glycosidases and fertility in the rat. Int J Androl. 1998;21(6):343-351. doi: 10.1046/j.1365-2605.1998.00134.x
Siervo GE, Vieira HR, Ogo FM, et al. Spermatic and testicular damages in rats exposed to ethanol: influence of lipid peroxidation but not testosterone. Toxicology. 2015;330:1-8. doi: 10.1016/j.tox.2015.01.016
Jt J, Eo O, Od I. Effects of various alcoholic bitters on the haematological parameters of albino wistar rats. Asian Journal of Biomedical and Pharmaceutical Sciences. 2021;11(80):1-5.
Adias TC, Egerton E, Erhabor O. Evaluation of coagulation parameters and liver enzymes among alcohol drinkers in Port Harcourt, Nigeria. Int J Gen Med. 2013;6:489-494. doi: 10.2147/IJGM.S43472
Quaye I, Nyame PK, Dodoo D, Gyan B, Adjei AA. Biochemical and haematological markers of alcohol intake in Ghanaians. West Afr J Med. 1992;11(3):199-202.
Shair RM, Maskat MY, Ayob MK, Kasran R. Protective effect of cocoa extract on ethanol induced liver injury in sprague-dawley rats. Sains Malaysiana. 2020;49(1):93-101. doi: 10.17576/jsm-2020-4901-11
Iluz-Freundlich D, Zhang M, Uhanova J, Minuk GY. The relative expression of hepatocellular and cholestatic liver enzymes in adult patients with liver disease. Ann Hepatol. 2020;19(2):204-208. doi: 10.1016/j.aohep.2019.08.004
Sato KK, Hayashi T, Nakamura Y, et al. Liver enzymes compared with alcohol consumption in predicting the risk of type 2 diabetes: the Kansai Healthcare Study. Diabetes Care. 2008;31(6):1230-1236. doi: 10.2337/dc07-2184
Stranges S, Freudenheim JL, Muti P, et al. Differential effects of alcohol drinking pattern on liver enzymes in men and women. Alcohol Clin Exp Res. 2004;28(6):949-956. doi: 10.1097/01.alc.0000128229.23396.42
Hashimoto E, Riederer P, Hesselbrock V, et al. Consensus paper of the WFSBP task force on biological markers: Biological markers for alcoholism. World J Biol Psychiatry. 2013;14(8):549-564. doi: 10.3109/15622975.2013.838302
Mostafa H, Amin AM. Arif NH, Ibrahim B. Nuclear magnetic resonance spectroscopy-based metabolomics to identify novel biomarkers of alcohol-dependence. Songklanakarin Journal of Science and Technology. 2017;39(2):153-162.
Buyco D, Martin J, Jeon S, Hooks R, Lin CY, Carr RM. Experimental models of metabolic and alcoholic fatty liver disease. World J Gastroenterol. 2021;27(1):1-18. doi: 10.3748/wjg.v27.i1.1
Bellentani S, Saccoccio G, Costa GC, et al. Drinking habits as cofactors of risk for alcohol induced liver damage. Gut. 1997;41(6):845-850. doi: 10.1136/gut.41.6.845
Chalmers DM, Rinsler MG, MacDermott S, Spicer CC, Levi AJ. Biochemical and haematological indicators of excessive alcohol consumption. Gut. 1981;22(12):992-996. doi: 10.1136/gut.22.12.992
Petterino C, Argentino-Storino A. Clinical chemistry and haematology historical data in control Sprague-Dawley rats from pre-clinical toxicity studies. Exp Toxicol Pathol. 2006;57(3):213-219. doi: 10.1016/j.etp.2005.10.002
Ola-Davies OE, Olukole SG, Amoo O. Haematological and Serum Biochemical Variables in rats Treated with Ethanol Extract of the Root of Moringa oleifera. African Journal of Biomedical Research. 2014;17(1):31.
O’Malley SS, Gueorguieva R, Wu R, Jatlow P. Acute alcohol consumption elevates serum bilirubin: An endogenous antioxidant. Drug Alcohol Depend. 2015;149:87-92. doi: 10.1016/j.drugalcdep.2015.01.023
Tanaka M, Budhathoki S, Hirata A, et al. Behavioral and clinical correlates of serum bilirubin concentrations in Japanese men and women. BMC Endocr Disord. 2013;13(1):39. doi: 10.1186/1472-6823-13-39
Foti R, Fisher MB. Assessment of UDP-glucuronosyltransferase catalyzed formation of ethyl glucuronide in human liver microsomes and recombinant UGTs. Forensic Sci Int. 2005;153(2-3):109-116. doi: 10.1016/j.forsciint.2004.12.003
Palmer RB. A review of the use of ethyl glucuronide as a marker for ethanol consumption in forensic and clinical medicine. Semin Diagn Pathol. 2009;26(1):18-27. doi: 10.1053/j.semdp.2008.12.005
Perumal E, Sundari BT. Erythrocyte glutathione depletion impairs resistance to haemolysis in women consuming alcohol. J Clin Biochem Nutr. 2008;42(1):14-20. doi: 10.3164/jcbn.2008003
Waribo HA, Edamisan E, Elekima I, Bartimaeus ES. Effect of oral consumption of action bitters on renal indices of apparently healthy subjects in Port Harcourt Metropolis. Asian Journal of Biochemistry, Genetics and Molecular Biology. 2021;9(3):14-19. doi: 10.9734/ajbgmb/2021/v9i330217
Delwatta SL, Gunatilake M, Baumans V, et al. Reference values for selected hematological, biochemical and physiological parameters of Sprague-Dawley rats at the Animal House, Faculty of Medicine, University of Colombo, Sri Lanka. Animal Model Exp Med. 2018;1(4):250-254. doi: 10.1002/ame2.12041
Alemán C, Más R, Rodeiro I, et al. Reference database of the main physiological parameters in Sprague-Dawley rats from 6 to 32 months. Lab Anim. 1998;32(4):457-466. doi: 10.1258/002367798780599802
Ogoun TR. Ogidi OI, Aye T. Toxicity Studies of Yoyo Cleanser Bitters Poly-Herbal Formulation in Albino Rats. World Journal of Pharmaceutical Research. 2022;11(1):1-11.
Fanton S, Cardozo LFMF, Combet E, et al. The sweet side of dark chocolate for chronic kidney disease patients. Clin Nutr. 2021;40(1):15-26. doi: 10.1016/j.clnu.2020.06.039
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