THE EFFECT OF ALOIN ADMINISTRATION ON FOAM CELL FORMATION IN THE KIDNEYS OF MALE MICE (MUS MUSCULUS) WITH DYSLIPIDEMIA-INDUCED OBESITY
DOI:
https://doi.org/10.59003/nhj.v6i1.2255Keywords:
Aloin; Aloe vera; dyslipidemia; obesity; foam cells; kidney; oxidative stress; histopathologyAbstract
Dyslipidemia and obesity are major metabolic disorders characterized by abnormal lipid metabolism, chronic inflammation, and oxidative stress, all of which contribute to progressive renal injury. Excessive accumulation of oxidized low-density lipoprotein (ox-LDL) promotes macrophage infiltration and foam cell formation within renal tissue, accelerating glomerular damage and increasing the risk of chronic kidney disease. Aloin, the principal anthraquinone glycoside isolated from Aloe vera, possesses potent antioxidant and anti-inflammatory properties that may attenuate oxidative injury and inhibit foam cell formation. This study aimed to investigate the effect of oral aloin administration on renal foam cell formation in male Mus musculus with dyslipidemia-induced obesity. A true experimental study employing a posttest-only control group design was conducted using male mice with experimentally induced dyslipidemia and obesity. Animals were randomly allocated into control and treatment groups. The treatment group received oral aloin for 28 consecutive days following dyslipidemia induction. Kidney tissues were collected for histopathological examination using Hematoxylin–Eosin staining. Foam cell formation was evaluated microscopically, and differences between groups were analyzed using the Independent Samples t-test with a significance level of p < 0.05. Histopathological analysis demonstrated that aloin administration reduced renal foam cell formation compared with the untreated control group. The treatment group exhibited approximately 25% foam cell formation, whereas the control group demonstrated approximately 93.8%. These findings suggest that aloin suppresses lipid accumulation and inflammatory responses within renal tissue through its antioxidant activity. Nevertheless, the therapeutic effect remained lower than that reported for atorvastatin, indicating that aloin is more appropriately considered a complementary rather than a replacement therapy. Oral administration of aloin effectively reduced foam cell formation in the kidneys of dyslipidemia-induced obese male mice. The protective effect is likely mediated through antioxidant activity, inhibition of lipid peroxidation, and attenuation of inflammatory processes.
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Abdel-Moniem, M. M. et al. (2022) ‘Iron supplementation ameliorates aloin-induced iron deficiency anemia in rats’, Experimental and Molecular Pathology, 124. doi: 10.1016/j.yexmp.2021.104740.
Aman, A. M. et al. (2021) Panduan Pengelolaan Dislipidemia di Indonesia-2021. PB Perkeni.
Bonilha, I. et al. (2021) ‘The reciprocal relationship between LDL metabolism and type 2 diabetes mellitus’, Metabolites, 11(12).
Burmistrova, N. A., Krivets, O. O. and Monakhova, Y. B. (2020) ‘UV Spectroscopic Determination of Aloin in Aloe vera (A. vera) Samples Based on Chemometric Data Processing’, Journal of Analytical Chemistry, 75(9). doi: 10.1134/S1061934820070047.
Dewi, N. P. et al. (2024) ‘Effect Of Aloin Extract On The Increase Of Fibroblast Cell Expression On Healing Of Wound Of Male White Rats (Rattus norvegicus) By The Aging Process’, Majority Science Journa, 1, pp. 171–179. doi: https://doi.org/10.61942/msj.v1i4.92.
Hua, H. et al. (2021) ‘The intervention and mechanism of action for aloin against subchronic aflatoxin b1 induced hepatic injury in rats’, International Journal of Molecular Sciences, 22(21). doi: 10.3390/ijms222111620.
Jing, Y. et al. (2020) ‘Aloin Protects Against Blood–Brain Barrier Damage After Traumatic Brain Injury in Mice’, Neuroscience Bulletin, 36(6). doi: 10.1007/s12264-020-00471-0.
Li, L. J. et al. (2017) ‘Evaluation of efficacy of aloin in treating acute trauma in vitro and in vivo’, Biomedicine & Pharmacotherapy, 88, pp. 1211–1219. doi: 10.1016/J.BIOPHA.2017.01.174.
Ma, Y. et al. (2018) ‘Aloin suppresses lipopolysaccharide-induced inflammation by inhibiting JAK1-STAT1/3 activation and ROS production in RAW264.7 cells’, International Journal of Molecular Medicine, 42(4). doi: 10.3892/ijmm.2018.3796.
Malbos, D. (2025) ‘Management of dyslipidemia’, Actualites Pharmaceutiques, 64(651). doi: 10.1016/j.actpha.2025.09.009.
Nussbaumerova, B. and Rosolova, H. (2023) ‘Obesity and Dyslipidemia’, Current Atherosclerosis Reports. doi: 10.1007/s11883-023-01167-2.
Saleh Al-Sowayan, N. and Mohammad AL-Sallali, R. (2023a) ‘The effect of aloin in blood glucose and antioxidants in male albino rats with Streptozoticin-induced diabetic’, Journal of King Saud University - Science, 35(4). doi: 10.1016/j.jksus.2023.102589.
Saleh Al-Sowayan, N. and Mohammad AL-Sallali, R. (2023b) ‘The effect of aloin in blood glucose and antioxidants in male albino rats with Streptozoticin-induced diabetic’, Journal of King Saud University - Science, 35(4). doi: 10.1016/j.jksus.2023.102589.
Santosa, B. et al. (2023) ‘Effect of Biotin Treatment on the improvement of Lipid Profile and Foam Cells in Dyslipidemia rats’, Research Journal of Pharmacy and Technology, 16(6). doi: 10.52711/0974-360X.2023.00457.
Vani, ade teti (2022) GEL ALOE VERA - Google Play Books. 1st edn. Edited by M. Silpi, D. hasbi Rahman, and B. Anggreno. Indramayu: Adab. Available at: https://play.google.com/books/reader?id=cmBZEAAAQBAJ&pg=GBS.PR2&lr=&printsec=frontcover (Accessed: 2 February 2022).
Vekic, J. et al. (2023) ‘Oxidative Stress, Atherogenic Dyslipidemia, and Cardiovascular Risk’, Biomedicines. doi: 10.3390/biomedicines11112897.
Wan, L. et al. (2017) ‘Aloin promotes A549 cell apoptosis via the reactive oxygen species-mitogen activated protein kinase signaling pathway and p53 phosphorylation’, Molecular Medicine Reports, 16(5). doi: 10.3892/mmr.2017.7379.
Wang, Y., Wang, H. and Yang, F. (2020) ‘Barbaloin Treatment Contributes to the Rebalance of Glucose and Lipid Homeostasis of Gestational Diabetes Mellitus Mice’, Dose-Response, 18(4). doi: 10.1177/1559325820984910.
Xu, D. et al. (2024) ‘Triglyceride-rich lipoproteins and cardiovascular diseases’, Frontiers in Endocrinology. doi: 10.3389/fendo.2024.1409653.
Zhang, C. et al. (2020) ‘Inhibition of PI3K/Akt/NF-κB signaling by Aloin for ameliorating the progression of osteoarthritis: In vitro and in vivo studies’, International Immunopharmacology, 89. doi: 10.1016/j.intimp.2020.107079.
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