Open Access
Standardized Brazilian Green Propolis Extract Attenuates Isoproterenol-Induced Cardiac Fibrosis Through Modulation of TGF-β1/Smad, NF-κB, PI3K/Akt, and Nrf2/HO-1 Signaling in Rats
¹ Department of Physiology, Faculty of Medicine, University of São Paulo, São Paulo, Brazil.
² Laboratory of Cardiovascular Research, Federal University of Minas Gerais, Belo Horizonte, Brazil.
³ Department of Pharmacology, Federal University of Rio Grande do Sul, Porto Alegre, Brazil.
DOI: 10.18081/ajbm.2026.2.150
ABSTRACT
Background
Cardiac fibrosis is a major pathological feature of chronic cardiovascular diseases and heart failure, characterized by excessive extracellular matrix deposition, persistent inflammation, oxidative stress, and progressive ventricular remodeling. Despite advances in cardiovascular therapeutics, effective pharmacological strategies capable of directly attenuating myocardial fibrosis remain limited. Brazilian green propolis contains numerous bioactive compounds with potent antioxidant and anti-inflammatory properties, although its molecular effects on cardiac fibrosis have not been comprehensively elucidated.
Objective
This study investigated the cardioprotective effects of standardized Brazilian green propolis extract (EPP-AF®) against isoproterenol-induced cardiac fibrosis in rats and explored the underlying molecular mechanisms involving the TGF-β1/Smad, NF-κB, PI3K/Akt, and Nrf2/HO-1 signaling pathways.
Methods
Forty adult male Wistar rats were randomly assigned to four groups (n = 10/group): Control, Cardiac Fibrosis (isoproterenol), Isoproterenol + EPP-AF® (100 mg/kg/day), and Isoproterenol + EPP-AF® (200 mg/kg/day). Cardiac fibrosis was induced by subcutaneous administration of isoproterenol (5 mg/kg/day) for seven consecutive days. Following fibrosis induction, EPP-AF® was administered orally for 28 days. Cardiac function was evaluated using transthoracic echocardiography. Histopathological alterations were assessed by hematoxylin and eosin, Masson's Trichrome, and Picrosirius Red staining. Immunohistochemistry, ELISA, quantitative real-time PCR, and Western blot analyses were performed to evaluate fibrosis-related proteins, inflammatory cytokines, oxidative stress biomarkers, and intracellular signaling pathways.
Results
EPP-AF® significantly improved cardiac function, increasing left ventricular ejection fraction from 48.9 ± 3.8% in untreated fibrotic animals to 67.5 ± 4.2% in the high-dose group (P < 0.001). Histological analysis demonstrated a marked reduction in myocardial collagen deposition, with collagen volume fraction decreasing from 27.3 ± 3.1% to 8.4 ± 1.8% (P < 0.001). Immunohistochemical analysis revealed significant reductions in TGF-β1, α-SMA, Collagen I, Collagen III, and Fibronectin expression following EPP-AF® treatment. ELISA demonstrated substantial suppression of TNF-α, IL-1β, IL-6, MCP-1, and TGF-β1, accompanied by restoration of IL-10 levels. Gene expression analysis confirmed downregulation of COL1A1, COL3A1, CTGF, Smad2, and Smad3, while Western blotting demonstrated inhibition of the TGF-β1/Smad, NF-κB, and PI3K/Akt signaling pathways together with activation of the Nrf2/HO-1 antioxidant pathway. Correlation analysis showed that collagen volume fraction was strongly associated with impaired cardiac function and activation of profibrotic molecular markers.
Conclusion
Standardized Brazilian green propolis extract (EPP-AF®) significantly attenuated experimental cardiac fibrosis by suppressing inflammation, oxidative stress, fibroblast activation, and extracellular matrix remodeling through coordinated modulation of the TGF-β1/Smad, NF-κB, PI3K/Akt, and Nrf2/HO-1 signaling pathways. These findings identify Brazilian green propolis as a promising multitarget therapeutic candidate for preventing pathological myocardial remodeling and provide a strong preclinical foundation for future translational and clinical investigations.
Keywords: Cardiac fibrosis; Brazilian green propolis; EPP-AF®; Heart failure; TGF-β1/Smad; NF-κB; PI3K/Akt; Nrf2/HO-1; Oxidative stress.
Recommended Citation
Ferreira LA, Oliveira MC, Santos RM, Costa AP. Standardized Brazilian Green Propolis Extract Attenuates Isoproterenol-Induced Cardiac Fibrosis Through Modulation of TGF-β1/Smad, NF-κB, PI3K/Akt, and Nrf2/HO-1 Signaling in Rats. Advanced Journal of Biomedicine & Medicine. 2026;14(2):150-175. doi:10.18081/ajbm.2026.2.150
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This work is licensed under a Creative Commons Attribution 4.0 International License.
Citations
- Frangogiannis NG. Cardiac fibrosis. Cardiovasc Res. 2021;117(6):1450-1488. doi:10.1093/cvr/cvaa324
- Frangogiannis NG. Cardiac fibrosis: cell biological mechanisms, molecular pathways and therapeutic opportunities. Mol Aspects Med. 2019;65:70-99. doi:10.1016/j.mam.2018.07.001
- Travers JG, Kamal FA, Robbins J, Yutzey KE, Blaxall BC. Cardiac fibrosis: the fibroblast awakens. Circ Res. 2016;118(6):1021-1040. doi:10.1161/CIRCRESAHA.115.306565
- Fan D, Takawale A, Lee J, Kassiri Z. Cardiac fibroblasts, fibrosis and extracellular matrix remodeling in heart disease. Fibrogenesis Tissue Repair. 2012;5(1):15. doi:10.1186/1755-1536-5-15
- Souders CA, Bowers SLK, Baudino TA. Cardiac fibroblast: the renaissance cell. Circ Res. 2009;105(12):1164-1176. doi:10.1161/CIRCRESAHA.109.209809
- Humeres C, Frangogiannis NG. Fibroblasts in the infarcted, remodeling, and failing heart. JACC Basic Transl Sci. 2019;4(3):449-467. doi:10.1016/j.jacbts.2019.02.006
- Shinde AV, Frangogiannis NG. Fibroblasts in myocardial infarction: a role in inflammation and repair. J Mol Cell Cardiol. 2014;70:74-82. doi:10.1016/j.yjmcc.2013.11.015
- Kong P, Christia P, Frangogiannis NG. The pathogenesis of cardiac fibrosis. Cell Mol Life Sci. 2014;71(4):549-574. doi:10.1007/s00018-013-1349-4
- Ma ZG, Yuan YP, Wu HM, Zhang X, Tang QZ. Cardiac fibrosis: new insights into the pathogenesis. Int J Biol Sci. 2018;14(12):1645-1657. doi:10.7150/ijbs.28103
- González A, Schelbert EB, Díez J, Butler J. Myocardial interstitial fibrosis in heart failure: biological and translational perspectives. J Am Coll Cardiol. 2018;71(15):1696-1706. doi:10.1016/j.jacc.2018.02.021
- López B, Ravassa S, Moreno MU, et al. Diffuse myocardial fibrosis: mechanisms, diagnosis and therapeutic approaches. Nat Rev Cardiol. 2021;18(7):479-498. doi:10.1038/s41569-020-00504-1
- Rockey DC, Bell PD, Hill JA. Fibrosis—a common pathway to organ injury and failure. N Engl J Med. 2015;372(12):1138-1149. doi:10.1056/NEJMra1300575
- Tallquist MD, Molkentin JD. Redefining the identity of cardiac fibroblasts. Nat Rev Cardiol. 2017;14(8):484-491. doi:10.1038/nrcardio.2017.57
- Ivey MJ, Tallquist MD. Defining the cardiac fibroblast. Circ J. 2016;80(11):2269-2276. doi:10.1253/circj.CJ-16-1003
- Kurose H, Mangmool S. Myofibroblasts and inflammatory cells as players of cardiac fibrosis. Arch Pharm Res. 2016;39(8):1100-1113. doi:10.1007/s12272-016-0809-6
- Dobaczewski M, de Haan JJ, Frangogiannis NG. The extracellular matrix modulates fibroblast phenotype and function in the infarcted myocardium. J Cardiovasc Transl Res. 2012;5(6):837-847. doi:10.1007/s12265-012-9406-3
- Frangogiannis NG. Transforming growth factor-β in tissue fibrosis. J Exp Med. 2020;217(3):e20190103. doi:10.1084/jem.20190103
- Frangogiannis NG. TGF-β as a therapeutic target in the infarcted and failing heart. Expert Opin Ther Targets. 2024;28(3):217-231. doi:10.1080/14728222.2024.2316655
- Humeres C, Shinde AV, Hanna A, et al. Smad-dependent pathways in the infarcted and failing heart. 2022;11(7):1147. doi:10.3390/cells11071147
- Biernacka A, Cavalera M, Wang J, et al. Smad3 signaling promotes fibrosis while preserving cardiac and aortic geometry in obese diabetic mice. Circ Heart Fail. 2015;8(4):788-798. doi:10.1161/CIRCHEARTFAILURE.114.001963
- Khalil H, Kanisicak O, Prasad V, et al. Fibroblast-specific TGF-β-Smad2/3 signaling underlies cardiac fibrosis. J Clin Invest. 2017;127(10):3770-3783. doi:10.1172/JCI94753
- Dobaczewski M, Chen W, Frangogiannis NG. Transforming growth factor-β signaling in cardiac remodeling. J Mol Cell Cardiol. 2011;51(4):600-606. doi:10.1016/j.yjmcc.2010.10.033
- Leask A. Getting to the heart of the matter: new insights into cardiac fibrosis. Circ Res. 2015;116(7):1269-1276. doi:10.1161/CIRCRESAHA.116.305381
- Meng XM, Nikolic-Paterson DJ, Lan HY. TGF-β: the master regulator of fibrosis. Nat Rev Nephrol. 2016;12(6):325-338. doi:10.1038/nrneph.2016.48
- Wynn TA, Ramalingam TR. Mechanisms of fibrosis: therapeutic translation for fibrotic disease. Nat Med. 2012;18(7):1028-1040. doi:10.1038/nm.2807
- Prabhu SD, Frangogiannis NG. The biological basis for cardiac repair after myocardial infarction: from inflammation to fibrosis. Circ Res. 2016;119(1):91-112. doi:10.1161/CIRCRESAHA.116.303577
- Turner NA. Inflammatory and fibrotic responses of cardiac fibroblasts to myocardial damage associated molecular patterns. J Mol Cell Cardiol. 2016;94:189-200. doi:10.1016/j.yjmcc.2015.11.002
- Gordon JW, Shaw JA, Kirshenbaum LA. Multiple facets of NF-κB in the heart: to be or not to NF-κB. Circ Res. 2011;108(9):1122-1132. doi:10.1161/CIRCRESAHA.110.226928
- Liu T, Zhang L, Joo D, Sun SC. NF-κB signaling in inflammation. Signal Transduct Target Ther. 2017;2:17023. doi:10.1038/sigtrans.2017.23
- Zhang QJ, He Y, Li Y, et al. Matricellular protein CIP regulates cardiac fibrosis through the TGF-β/Smad pathway. J Mol Cell Cardiol. 2022;168:1-14. doi:10.1016/j.yjmcc.2022.03.006
- Bugger H, Pfeil K. Mitochondrial ROS in myocardial ischemia reperfusion and remodeling. Biochim Biophys Acta Mol Basis Dis. 2020;1866(7):165768. doi:10.1016/j.bbadis.2020.165768
- Münzel T, Camici GG, Maack C, Bonetti NR, Fuster V, Kovacic JC. Impact of oxidative stress on the heart and vasculature: part 2 of a 3-part series. J Am Coll Cardiol. 2017;70(2):212-229. doi:10.1016/j.jacc.2017.05.035
- Ma Q. Role of Nrf2 in oxidative stress and toxicity. Annu Rev Pharmacol Toxicol. 2013;53:401-426. doi:10.1146/annurev-pharmtox-011112-140320
- Dodson M, de la Vega MR, Cholanians AB, Schmidlin CJ, Chapman E, Zhang DD. Modulating NRF2 in disease: timing is everything. Annu Rev Pharmacol Toxicol. 2019;59:555-575. doi:10.1146/annurev-pharmtox-010818-021856
- Chen QM, Maltagliati AJ. Nrf2 at the heart of oxidative stress and cardiac protection. Physiol Genomics. 2018;50(2):77-97. doi:10.1152/physiolgenomics.00041.2017
- Zhang Q, Wang L, Wang S, et al. Signaling pathways and targeted therapy for myocardial fibrosis. Signal Transduct Target Ther. 2022;7(1):78. doi:10.1038/s41392-022-00916-0
- Qin W, Cao L, Massey IY. Role of PI3K/Akt signaling pathway in cardiac fibrosis. Mol Cell Biochem. 2021;476(11):4045-4059. doi:10.1007/s11010-021-04219-w
- Benjamin IJ, Jalil JE, Tan LB, Cho K, Weber KT, Clark WA. Isoproterenol-induced myocardial fibrosis in relation to myocyte necrosis. Circ Res. 1989;65(3):657-670. doi:10.1161/01.RES.65.3.657
- George JC, Liner A, Hoit BD. Isoproterenol-induced myocardial injury: a systematic comparison of subcutaneous versus intraperitoneal delivery in a rat model. 2010;27(6):716-721. doi:10.1111/j.1540-8175.2009.01107.x
- Dai H, Jia G, Lu M, et al. Phosphocreatine attenuates isoproterenol-induced cardiac fibrosis and inhibits TGF-β1/Smad signaling in rats. Sci Rep. 2019;9(1):1443. doi:10.1038/s41598-018-38239-8
- Slimani H, Zhai Y, Yousif NG, et al. Enhanced monocyte chemoattractant protein-1 production in aging mice exaggerates cardiac depression during endotoxemia. Critical Care, 2014; 18:527. doi: 1186/s13054-014-0527-8
- Sforcin JM, Bankova V. Propolis: is there a potential for the development of new drugs? J Ethnopharmacol. 2011;133(2):253-260. doi:10.1016/j.jep.2010.10.032
- Daleprane JB, Abdalla DS. Emerging roles of propolis: antioxidant, cardioprotective, and antiangiogenic actions. Evid Based Complement Alternat Med. 2013;2013:175135. doi:10.1155/2013/175135
- Pahlavani N, Malekahmadi M, Firouzi S, et al. Molecular and cellular mechanisms of the effects of propolis in inflammation, oxidative stress and glycemic control. Phytother Res. 2020;34(9):2184-2202. doi:10.1002/ptr.6664
- Alvarenga L, Cardozo LFMF, Lindholm B, Stenvinkel P, Mafra D. To bee or not to bee? The bee extract propolis as a bioactive compound in chronic kidney disease. Food Funct. 2021;12(8):3203-3215. doi:10.1039/D0FO03170A
- Baptista BG, Chermut TR, Barbeiro DF, et al. Effects of standardized Brazilian green propolis extract on inflammation in patients with chronic kidney disease: a randomized double-blind controlled clinical trial. Clin Nutr. 2023;42(5):677-685. doi:10.1016/j.clnu.2023.03.003
- Chermut TR, Baptista BG, Barbeiro DF, et al. Effects of propolis on inflammatory markers in patients undergoing hemodialysis: a randomized, double-blind, placebo-controlled study. 2023;15(3):721. doi:10.3390/nu15030721
- Salatino A, Fernandes-Silva CC, Righi AA, Salatino MLF. Propolis research and the chemistry of plant products. Nat Prod Rep. 2011;28(5):925-936. doi:10.1039/C0NP00072H
2026 Vol 14, Issue 2 Pages 150-175
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