Histopatologi Hati Mencit (Mus Musculus) yang Diberikan Minuman Ringan Berkarbonasi dan Ekstrak Daun Kersen (Muntingia Calabura L.)
Liver Histopathology of Mice (Mus Musculus) Induced by Carbonated Soft Drink and Kersen Leaves Extract (Muntingia Calabura L.)
DOI:
https://doi.org/10.25026/jsk.v6i2.1886Abstract
High consumption of carbonated soft drinks (CSD) has caused risks of metabolic syndrome, obesity, various chronic diseases, and organ damage. Kersen has the potential to prevent and reduce damage to the liver caused by CSD. The study aimed to analyze the liver histopathological of mice given CSD and the effect of Kersen leaf extract. This experimental study used a completely randomized design with 25 male white mice divided into 5 groups, namely control grup (K), negative control (N), treatment 1, 2, and 3 with doses (35 mg/30g BW, 45 mg/30g BW, 65 mg/30g BB) for 30 days. The sample was terminated on the 31st day, and the liver organs were prepared to observe the microscopic of the liver. The analytical test used the ANOVA test with Duncan's multiple-range test. The results showed that the negative control group had significantly lower numbers of liver cell damage than the positive controls who were given CSD (p<0.05), and the treatment groups 2 and 3 also had significantly less cell damage than the positive control group and did not significantly different from the negative control group. Kersen leaf extract can prevent and reduce liver cell damage in carbonated soft drink-induced mice.
Keywords: Liver, Histopathology, Kersen, Mice, Soft drink
Abstrak
Konsumsi minuman berkarbonasi/ carbonated soft drink (CSD) yang berlebih berisiko menyebabkan terjadinya sindrom metabolik, obesitas, berbagai penyakit kronis, dan kerusakan organ. Kersen berpotensi mencegah dan mengurangi kerusakan pada hati yang disebabkan oleh CSD. Penelitian ini bertujuan untuk melihat gambaran histopatologi hati mencit yang diberikan minuman CSD dan efek pemberian ekstrak daun kersen. Penelitian experimental ini menggunakan rancangan acak lengkap dengan 25 mencit putih jantan yang dibagi 5 kelompok yaitu kelompok kontrol (K), kontrol negatif (N), perlakuan 1, 2, dan 3 dengan dosis (35 mg/30g BB, 45 mg/30g BB, 65 mg/30g BB) selama 30 hari. Sampel diterminasi pada hari ke 31 dan organ hepar dibuat preparat untuk diamati gambaran mikroskopis hati. Uji analisis menggunakan uji beda ANOVA dengan uji lanjut Duncan’s multiple-range test. Hasil pengamatan menunjukkan bahwa kelompok kontrol negatif memiliki jumlah kerusakan sel hati yang signifikan lebih rendah dibandingkan dengan kontrol positif yang diberikan CSD (p<0.05) dan kelompok perlakuan 2 dan 3 juga signifikan memiliki jumlah kerusakan sel yang lebih sedikit dibandingkan kelompok kontrol positif serta tidak berbeda signifikan dengan kelompok kontrol negatif. Ekstrak daun kersen memberikan pengaruh terhadap pencegahan dan mengurangi kerusakan sel hati pada mencit putih yang diberikan CSD.
Kata Kunci: Hepar, Histopatologi, Kersen, Mencit, Carbonated Soft Drink
References
Ferretti F, Mariani M, dan Sarti E. 2021. Is the development of obesogenic food environments a self-reinforcing process? Evidence from soft drink consumption. Global. Health, vol. 17, no. 1, pp. 1–13, 2021, doi: 10.1186/s12992-021-00735-y.
Yang L, Bovet P, Liu Y, Zhao M, Ma C, Liang Y, dan Xi B. 2017. Consumption of carbonated soft drinks among young adolescents aged 12 to 15 years in 53 low-and middle-income countries. Am. J. Public Health, vol. 107, no. 7, pp. 1095–1100, doi: 10.2105/AJPH.2017.303762.
Crichton G, Alkerwi A, dan Elias M. 2015. Diet soft drink consumption is associated with the metabolic syndrome: A two sample comparison. Nutrients, vol. 7, no. 5, pp. 3569–3586, doi: 10.3390/nu7053569.
Alkhedaide A, Soliman M.M, Salah-Eldin A.E, Ismail T.A, Alshehiri Z.S, dan Attia H.F. 2016. Chronic effects of soft drink consumption on the health state of Wistar rats: A biochemical, genetic and histopathological study. Mol. Med. Rep., vol. 13, no. 6, pp. 5109–5117, doi: 10.3892/mmr.2016.5199.
Lebda M.A, Tohamy H.G, dan El-Sayed YS. 2017. Long-term soft drink and aspartame intake induces hepatic damage via dysregulation of adipocytokines and alteration of the lipid profile and antioxidant status. Nutr. Res., vol. 41, pp. 47–55. doi: 10.1016/j.nutres.2017.04.002.
Halegoua-De Marzio DL dan Fenkel JM. 2014. Concepts and Treatment Approaches in Nonalcoholic Fatty Liver Disease. Adv. Hepatol., vol. 2014, pp. 1–7, doi: 10.1155/2014/357965.
Meng, X., Tang, GY., Liu, PH., Liu, Q., Bin Li, H., dan Zhao CJ. 2020. Antioxidant activity and hepatoprotective effect of 10 medicinal herbs on CCl4-induced liver injury in mice. World J. Gastroenterol., vol. 26, no. 37, pp. 5629–5645, doi: 10.3748/wjg.v26.i37.5629.
Z. Akar, M. Küçük, dan H. Do?an. 2017. A new colorimetric DPPH• scavenging activity method with no need for a spectrophotometer applied on synthetic and natural antioxidants and medicinal herbs. J. Enzyme Inhib. Med. Chem., vol. 32, no. 1, pp. 640–647, doi: 10.1080/14756366.2017.1284068.
D. Triswaningsih, S. Kumalaningsih, Wignyanto, dan Pratikto. 2017. Estimation of chemical compounds and antioxidant activity of Muntingia Calabura extract. Int. J. ChemTech Res., vol. 10, no. 3, pp. 17–23.
Singh, R., Iye, S., Prasad, S., Deshmukh N., Gupta, U., Zanje, A., Patil, S., dan Joshi, S. 2017. Phytochemical Analysis of Muntingia calabura Extracts Possessing Anti-Microbial and Anti-Fouling Activities. Int. J. Pharmacogn. Phytochem. Res., vol. 9, no. 6, pp. 826–832, 2017, doi: 10.25258/phyto.v9i6.8186.
Al-Sayed, E., Martiskainen, O., Seif El-Din, SH., Sabra, Abdel Nasser A., Hammam, Olfat A., El-Lakkany, Naglaa M., Abdel-Daim, Mohamed M. 2014. Hepatoprotective and antioxidant effect of bauhinia hookeri extract against carbon tetrachloride-induced hepatotoxicity in mice and characterization of its bioactive compounds by HPLC-PDA-ESI-MS/MS. Biomed Res. Int., vol. 2014, 2014, doi: 10.1155/2014/245171.
Milei, J., Loasda, MO., Llambi HG., Grana, DR., Suarez, D., Azzato, F., dan Ambrosio, G. 2011. Chronic cola drinking induces metabolic and cardiac alterations in rats,” World J. Cardiol., vol. 3, no. 4, p. 111, doi: 10.4330/wjc.v3.i4.111.
T. H. Yamashita N, Miyagi Y, Maekawa M. 2022. A patient with rheumatoid arthritis who developed liver cirrhosis after increased soft drinks intake. Nihon Ronen Igakkai Zasshi, vol. 59, no. 2, pp. 244–248, 2022, doi: 10.3143/geriatrics.59.244. PMID: 35650059.
F. K. Murti, S. Amarwati, dan N. Wijayahadi. 2016. Pengaruh Ekstrak Daun Kersen (Muntingia calabura) Terhadap Gambaran Mikroskopis Hepar Tikus Wistar. Kedokt. Diponegoro, vol. 5, no. 4, pp. 871–883.
N. D. Mahmood, S.S. Mamat, F.H. Kamisan, F. Yahya, M.F.F. Kamarolzaman, N. Nasir, N. Mohtaruddin, S.F.Md. Tohid, dan Z.A. Zakaria. 2014. Amelioration of paracetamol-induced hepatotoxicity in rat by the administration of methanol extract of Muntingia calabura L. Leaves,” Biomed Res. Int., vol. 2014, doi: 10.1155/2014/695678.
Z. A. Zakaria, N. D. Mahmood, M. H. Omar, M. Taher, dan R. Basir. 2019. Methanol extract of Muntingia calabura leaves attenuates CCl4-induced liver injury: possible synergistic action of flavonoids and volatile bioactive compounds on endogenous defence system. Pharm. Biol., vol. 57, no. 1, pp. 335–344, doi: 10.1080/13880209.2019.1606836.
B. A. V. Maran, M. Iqbal, P. Gangadaran, B. Ahn, P. V. Rao, dan M. D. Shah. 2022. Hepatoprotective Potential of Malaysian Medicinal: A Review on Phytochemicals, Oxidative Stress, and Antioxidant Mechanisms. Molecules, vol. 27, p. 1533, doi: doi.org/10.3390/molecules27051533.
E. P. Hestiana, N. Hidayat, dan S. Koesdarto. 2010. Addition Time Interval effect og Temu Ireng (Curcuma aeruginosa Roxb.) Extract to Male Mice (Mus Musculus) Liver Histopathological Description. Vet. Med., vol. 3, no. 1, pp. 1–23, 2010.
Z. A. Zakaria, N. D. Mahmood, S. S. Mamat, N. Nasir, dan M. H. Omar. 2018. Endogenous antioxidant and LOX-mediated systems contribute to the hepatoprotective activity of aqueous partition of methanol extract of Muntingia calabura L. leaves against paracetamol intoxication. Front. Pharmacol., vol. 8, no. FEB, pp. 1–14, doi: 10.3389/fphar.2017.00982.
?. Tóthová, J. Hodosy, K. Mattenburg, H. Fabryova, A. Wagnerova, J. Babickova, M. Okuliarova, M. Zeman, dan P. Celec. 2013. No harmful effect of different Coca-cola beverages after 6months of intake on rat testes. Food Chem. Toxicol., vol. 62, pp. 343–348, doi: 10.1016/j.fct.2013.08.073.
E. E. Ventura, J. N. Davis, dan M. I. Goran. 2015. Sugar Content of Popular Sweetened Beverages Based on Objective Laboratory Analysis?: Focus on Fructose Content. Obesity, vol. 19, no. 4, pp. 868–874, 2009, doi: 10.1038/oby.2010.255.
S. Zakaria, R. A. Hasan, M. F. Mahmoud, H. M. El Fayoumi, dan A. A. A. Mahmoud. 2020. The concurrent exposure to aluminium and fructose induces liver injury in rats: Protection by monoammonium glycyrrhizinate. Clin. Exp. Pharmacol. Physiol., vol. 47, no. 5, pp. 809–820, doi: 10.1111/1440-1681.13257.
Z. A. Zakaria, T. Balan, A.K. Azemi, M.A. Omar, N. Mohtarrudin, Z. Ahmad, M. N. H. Abdullah, M.N.M. Desa, L.K.S, Teh, dan M.S. Zaki. 2016. Mechanism(s) of action underlying the gastroprotective effect of ethyl acetate fraction obtained from the crude methanolic leaves extract of Muntingia calabura. BMC Complement. Altern. Med., vol. 16, no. 1, pp. 1–17, doi: 10.1186/s12906-016-1041-0.
V. S. Panda dan P. D. Khambat. 2014. Antiulcer activity of Garcinia indica fruit rind (kokum berry) in rats. Biomed. Aging Pathol., vol. 4, no. 4, pp. 309–316, doi: 10.1016/j.biomag.2014.07.008.
[S. Li, H. Tan, N. Wang, Z. Zhang, L. Lao, C. Wong, dan Y. Feng. 2015. The Role of Oxidative Stress and Antioxidants in Liver Diseases. International Journal of Molecular Science. no. November, pp. 26087–26124. doi: 10.3390/ijms161125942.
A. Li, S. Li, Y. Zhang, X. Xu, Y. Chen, dan H. Li. 2014. Resources and Biological Activities of Natural Polyphenols. Nutrients. pp. 6020–6047, doi: 10.3390/nu6126020.
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