American Journal of Public Health Research
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American Journal of Public Health Research. 2025, 13(5), 208-223
DOI: 10.12691/ajphr-13-5-2
Open AccessArticle

Protective Effects of Lady’s Mantle (Alchemilla vulgaris L.) against Hepatotoxicity in a Rat Model: Insights into Active Compounds and Underlying Mechanisms

Yousif A. Elhassaneen1, , Amira H. Darwish1 and Alaa A. Mosa1

1Department of Nutrition and Food Science, Faculty of Home Economics, Menoufia University, Shebin El-Kom, Egypt

Pub. Date: October 17, 2025

Cite this paper:
Yousif A. Elhassaneen, Amira H. Darwish and Alaa A. Mosa. Protective Effects of Lady’s Mantle (Alchemilla vulgaris L.) against Hepatotoxicity in a Rat Model: Insights into Active Compounds and Underlying Mechanisms. American Journal of Public Health Research. 2025; 13(5):208-223. doi: 10.12691/ajphr-13-5-2

Abstract

Alchemilla vulgaris (Lady’s mantle) has shown various therapeutic properties, yet its liver-protective potential remains underexplored. This study aimed to evaluate its hepatoprotective effects in a rat model of CCl₄-induced liver toxicity and to characterize its bioactive compounds. Thirty rats were divided into five groups: a negative control, a CCl₄-induced positive control, and three treatment groups receiving ethanol extract of Lady’s mantle (AVE) at doses of 150, 300, and 450 mg/kg body weight/day. Proximate analysis of the aerial parts revealed 39.86% carbohydrates, 30.92% crude fiber, 15.94% protein, 10.83% ash, and 2.45% fat. The ethanol extract was rich in bioactive compounds, including phenolics (621.67 µg GAE/g), terpenoids (411.52 µg/g), anthocyanins (214.66 µg/g), flavonoids (181.45 µg/g), and triterpenoids (129.34 µg/g). AVE exhibited strong antioxidant activity (87.34%), with an IC50 of 14.42 µg/mL. In the biological study, AVE treatment dose-dependently improved body weight gain, food intake, and feed efficiency ratio in hepatotoxic rats. Liver function markers also improved, with glycogen content increasing by 128.64%, G6PD activity by 95.78%, and G6Pase activity decreasing by 53.25% at the highest dose. Serum lipid profiles were corrected, with HDL-c increasing by up to 65.06%, LDL-c decreasing by 32.52%, and total cholesterol dropping by up to 9.42%. Antioxidant defenses were restored as reduced glutathione increased by 89.49%, while oxidative stress markers such as ROS and MDA decreased by up to 53.61% and 26.01%, respectively. Histopathological analysis confirmed reduced liver damage and inflammation in treated groups. In conclusion, Alchemilla vulgaris ethanol extract demonstrates potent antioxidant and hepatoprotective properties. Further investigation may support its use as a natural therapeutic agent for liver disorders.

Keywords:
Antioxidant activity scavenging activity liver functions serum lipid profile glutathione fractions reactive oxygen species malonaldehyde

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References:

[1]  Crawford, J. M. (1999). The Liver and the Biliary Tract. In R. S. Cotran, V. Kumar, & T. Collins (Eds.), Pathologic Basis of Disease (pp. 1-15). W. B. Saunders Company.
 
[2]  Trefts, E., Gannon, M., & Wasserman, D. H. (2017). The liver. Current Biology, 27(21), R1147-R1151.
 
[3]  Elhassaneen, Y. A. (1996). Biochemical and technological studies on pollution of fish with pesticides and polycyclic aromatic hydrocarbons [Unpublished doctoral dissertation]. Mansoura University, Egypt.
 
[4]  Sayed-Ahmed, S. A., Shehata, N. A., & Elhassaneen, Y. A. (2020). Potential protective effects of Ganoderma lucidum powder against carbon tetrachloride-induced liver disorders in rats: Biological, biochemical, and immunological studies. Egyptian Bulletin of the National Nutrition Institute of the Arab Republic of Egypt, 56(2), 99-132.
 
[5]  Yuan, Y., Liu, Z., & Yu, L. (2020). Impact of dietary fiber on human health. Food & Function, 11(7), 6598-6610.
 
[6]  Elhassaneen, Y., Abd El-Rahman, A., & El-Samouny, S. (2021a). Potential protective effects of cauliflower leaves and prickly pear fruits skin on liver disorders induced by carbon tetrachloride in rats. Journal of Home Economics, 32(1), 19-42.
 
[7]  Lawrence, S. F., & Emmet, B. K. (2012). Handbook of Liver Disease (3rd ed.). Elsevier Saunders.
 
[8]  Ng, C. H., Huang, D. Q., & Nguyen, M. H. (2022). Nonalcoholic fatty liver disease versus metabolic-associated fatty liver disease: Prevalence, outcomes and implications of a change in name. Clinical and Molecular Hepatology, 28(4), 790-801.
 
[9]  Teng, M. L., Ng, C. H., Huang, D. Q., Chan, K. E., Tan, D. J., Lim, W. H., Yang, J. D., Tan, E., & Muthiah, M. D. (2023). Global incidence and prevalence of nonalcoholic fatty liver disease. Clinical and Molecular Hepatology, 29(Suppl), S32-S42.
 
[10]  Zheng, S., Xue, C., Li, S., Zao, X., Li, X., Liu, Q., Cao, X., Wang, W., Qi, W., Du, H., Zhang, P., & Ye, Y. (2024). Liver cirrhosis: current status and treatment options using western or traditional Chinese medicine. Frontiers in Pharmacology, 15, 1381476.
 
[11]  Wang, Y., Li, J., & Xia, L. (2023). Plant-derived natural products and combination therapy in liver cancer. Frontiers in Oncology, 13, 1116532.
 
[12]  Fan, Y., Xue, H., & Zheng, H. (2022). Systemic Therapy for Hepatocellular Carcinoma: Current Updates and Outlook. Journal of Hepatocellular Carcinoma, 9, 233-263.
 
[13]  Hamzawy, M. A., El-Denshary, E. S. M., & Abdel-Wahhab, M. A. (2015). Effects of natural compounds in treatment and prevention of hepatotoxicity and hepatocellular carcinoma. Hepatoma Research, 1(4), 111-118.
 
[14]  Prajapati, J., Bhatt, N., & Rawal, R. (2025). Hepatoprotective effects of phytochemicals and plant extracts against chemotherapy-induced liver damage in animal models: a systematic review. Archives of Toxicology, 99(3), 887-914.
 
[15]  Li, Z., Wu, J., Zhao, Y., Song, J., Wen, Y. (2024). Natural products and dietary interventions on liver enzymes: an umbrella review and evidence map. Frontiers in Nutrition, 11, 1300860.
 
[16]  Erfanian, S. S., Ansari, H., Javanmard, S. H., Amini, Z., & Hajigholami, A. (2024). The hepatorenal protective effects of silymarin in cancer patients receiving chemotherapy: a randomized, placebo-controlled trial. BMC Complementary Medicine and Therapies, 24, 329.
 
[17]  Gibbons, S. (2003). An Overview of Plant Extracts as Potential Therapeutics. Expert Opinion on Therapeutic Patents, 13(4), 489-497.
 
[18]  Redzić, S. S. (2007). The Ecological Aspect of Ethnobotany and Ethnopharmacology of Population in Bosnia and Herzegovina. Coll. Antropol., 31(3), 869-890.
 
[19]  Bradley, P. (2006). British Herbal Compendium: A Handbook of Scientific Information on Widely Used Plant Drugs (Vol. 2). British Herbal Medicine Association.
 
[20]  Gehrke, B., Bräuchler, C., Romoleroux, K., Lundberg, M., Heubl, G., & Eriksson, T. (2008). Molecular Phylogenetics of Alchemilla, Aphanes and Lachemilla (Rosaceae) Inferred from Plastid and Nuclear Intron and Spacer DNA Sequences, with Comments on Generic Classification. Molecular Phylogenetics and Evolution, 47(3), 1030-1044.
 
[21]  Sepp, S., Bobrova, V. K., Troitsky, A. K., & Glazunova, K. P. (2000). Genetic Polymorphism Detected with RAPD Analysis and Morpho-logical Variability in Some Microspecies of Apomictic Alchemilla. Annales Botanici Fennici, 37(2), 105–123.
 
[22]  Ergene, B., Acikara, Ö. B., Bakar, F., Saltan, G., & Nebioǧlu, S. (2010). Antioxidant Activity and Phytochemical Analysis of Alchemilla persica Rothm. Ankara Üniversitesi Eczacılık Fakültesi Dergisi, 39(2), 145-154.
 
[23]  Ghedira, K., Goetz, P., & Le Jeune, R. (2012). Alchemilla vulgaris L.: Alchémille (Rosaceae). Phytothérapie, 10(3), 263-266.
 
[24]  Šavikin, K., Zdunić, G., Menković, N., Živković, J., Ćujić, N., Tereščenko, M., & Bigović, D. (2013). Ethnobotanical Study on Traditional Use of Medicinal Plants in South-Western Serbia, Zlatibor District. Journal of Ethnopharmacology, 146(2), 803-810.
 
[25]  Filippova, E. I. (2017). Antiviral Activity of Lady’s Mantle (Alchemilla vulgaris L.) Extracts against Orthopoxviruses. Bulletin of Experimental Biology and Medicine, 163(3), 374-377.
 
[26]  Tadić, V., & Žugić, A. (2020). Multi-Target Herbal Preparation. In R. Edward (Ed.), Supercritical CO2 Extractions and Its Application (pp. 99-121). Polish Foundations of the Opportunities Industrialization Centers "OIC Poland."
 
[27]  Atef, N. M., Shanab, S. M., Negm, S. I., & Abbas, Y. A. (2019). Evaluation of Antimicrobial Activity of Some Plant Extracts Against Antibiotic Susceptible and Resistant Bacterial Strains Causing Wound Infection. Bulletin of the National Research Centre, 43, 144.
 
[28]  Shilova, I. V., Suslov, N. I., Samylina, I. A., Baeva, V. M., Lazareva, N. B., & Mazin, E. V. (2020). Neuroprotective Properties of Common Lady’s Mantle Infusion. Pharmaceutical Chemistry Journal, 53(11), 1059-1062.
 
[29]  Neagu, E., Paun, G., Albu, C., & Radu, G.-L. (2015). Assessment of Acetylcholinesterase and Tyrosinase Inhibitory and Antioxidant Activity of Alchemilla vulgaris and Filipendula Ulmaria Extracts. Journal of the Taiwan Institute of Chemical Engineers, 52, 1-6.
 
[30]  Vlaisavljević, S., Jelača, S., Zengin, G., Mimica-Dukić, N., Berežni, S., Miljić, M., & Stevanović, Z. D. (2019). Alchemilla vulgaris Agg. (Lady’s Mantle) from Central Balkan: Antioxidant, Anticancer and Enzyme Inhibition Properties. RSC Advances, 9(64), 37474-37483.
 
[31]  Ibrahim, O. H. M., Abo-Elyousr, K. A. M., Asiry, K. A., Alhakamy, N. A., & Mousa, M. A. A. (2022). Phytochemical Characterization, Antimicrobial Activity and In Vitro Antiproliferative Potential of Alchemilla vulgaris Auct Root Extract against Prostate (PC-3), Breast (MCF-7) and Colorectal Adenocarcinoma (Caco-2) Cancer Cell Lines. Plants, 11(16), 2140.
 
[32]  Association of Official Analytical Chemists (AOAC). (1995). Official methods of the Association of Official Analytical Chemists (16th ed.). AOAC.
 
[33]  Singleton, V. L., & Rossi, J. A., Jr. (1965). Colorimetry of total phenolics with phosphomolybdic-phosphotungstic acid reagents. American Journal of Enology and Viticulture, 16, 144-158.
 
[34]  Wolfe, K., Wu, X., & Liu, R. H. (2003). Antioxidant activity of apple peels. Journal of Agricultural and Food Chemistry, 51, 609–614.
 
[35]  Lichtenthaler, H. K. (1987). Chlorophylls and carotenoids, the pigments of photosynthetic biomembranes. In R. Douce & L. Packer (Eds.), Methods in Enzymology (Vol. 148, pp. 350-382). Academic Press Inc.
 
[36]  Zhishen, J., Mengcheng, T., & Jianming, W. (1999). The determination of flavonoid contents in mulberry and their scavenging effects on superoxide radicals. Food Chemistry, 64(4), 555–559.
 
[37]  Giusti, M. M., & Wrolstad, R. E. (2001). Characterization and Measurement of Anthocyanins by UV-Visible Spectroscopy. In R. E. Wrolstad (Ed.), Current Protocols in Food Analytical Chemistry. John Wiley & Sons.
 
[38]  Vazirian, M., Dianat, S., Manayi, A., Ziari, R., Mousazadeh, A., Emran, H., Saeidnia, S., & Amanzadeh, Y. (2014). Anti-inflammatory effect, total polysaccharide, total phenolics content and antioxidant activity of the aqueous extract of three basidiomycetes. Research Journal of Pharmacognosy, 1(1), 13-19.
 
[39]  Ghorai, N., Chakraborty, S., Guchhait, S., Saha, S., & Biswas, S. (2012). Estimation of total terpenoids concentration in plant tissues using a monoterpene, Linalool as standard reagent: Protocol Exchange. Protocol Exchange, 1-6.
 
[40]  Schneider, P., Hosseiny, S. S., Szczotka, M., Jordan, V., & Schlitter, K. (2009). Rapid solubility determination of the triterpenes oleanolic acid and ursolic acid by UV-spectroscopy in different solvents. Phytochemistry Letters, 2(2), 85-87.
 
[41]  Van-Burden, T. P., & Robinson, W. C. (1981). Formation of complexes between protein and tannic acid. Journal of Agricultural and Food Chemistry, 1(1), 77.
 
[42]  Fouda, W., Wael, M., Ibrahim, A., Ellamie1, M., & Gamal, R. (2019). Biochemical and mineral compositions of six brown seaweeds collected from Red Sea at Hurghada Coast. Indian Journal of Geo Marine Sciences, 48(04), 484-491.
 
[43]  Zhao, J., & Wang, M. Y. (2010). Colorimetric determination of total alkaloids in plant extracts. Journal of Analytical Methods in Chemistry, 2010, 482476.
 
[44]  Marco, G. (1968). A rapid method for evaluation of antioxidants. Journal of the American Oil Chemists' Society, 45(10), 594-598.
 
[45]  Al-Saikhan, M. S., Howard, L. R., & Miller, J. C., Jr. (1995). Antioxidant activity and total phenolics in different genotypes of potato (Solanum tuberosum L.). Journal of Food Science, 60(2), 341-343.
 
[46]  Desmarchelier, C., Bermudez, M. J. N., Coussio, J., Ciccia, G., & Boveris, A. (1997). Antioxidant and prooxidant activities in aqueous extract of Argentine plants. International Journal of Pharmacognosy, 35, 116-120.
 
[47]  Reeves, P. G., Nielsen, F., & Fahey, G. (1993). AIN-93 Purified Diets for Laboratory Rodents: Final Report of the American Institute of Nutrition AdHoc Writing Committee on the Reformulation of the AIN-76A Rodent Diet. Journal of Nutrition, 123(11), 1939-1951.
 
[48]  Jayasekhar, P., Mohan, P. V., & Rahinam, K. (1997). Hepatoprotective activity of ethylacetate extract of Acacia catechu. Indian Journal of Pharmacology, 29(6), 426-428.
 
[49]  National Research Council (NRC). (1996). Guide for the Care and Use of Laboratory Animals. National Academy Press.
 
[50]  Saad, B., Azaizeh, H., Abu-Hijleh, G., & Said, O. (2006). Safety of Traditional Arab Herbal Medicine. Evidence-Based Complementary and Alternative Medicine, 3(4), 433-439.
 
[51]  Chapman, D. G., Castilla, R., & Champbell, J. A. (1959). Evaluation of protein in food. I. A. Method for the determination of protein efficiency ratio. Canadian Journal of Biochemistry and Physiology, 37, 679-686.
 
[52]  Drury, R. A., & Wallington, E. A. (1980). Carlton's Histological Technique (5th ed.). Oxford University Press.
 
[53]  El-Khawaga, O. Y., Abou-Seif, M. A., El-Waseef, A., & Negm, A. A. (2010). Hypoglycemic, Hypolipidemic and Antioxidant Activities of Cleome droserifolia in Streptozotocin-Diabetic Rats. Journal of Stress Physiology & Biochemistry, 6(4), 28-41.
 
[54]  Damsbo, P., Vaag, A., Hother-Nielsen, O., & Beck-Nielsen, H. (1991). Reduced glycogen synthase activity in skeletal muscle from obese patients with and without type 2 diabetes mellitus. Diabetologia, 34(4), 239-245.
 
[55]  Chan, T. K., Todd, D., & Wong, C. C. (1965). Tissue levels in erythrocyte glucose-6-phosphate dehydrogenase deficiency. Journal of Laboratory and Clinical Medicine, 6, 936-940.
 
[56]  Rossetti, L., Lee, Y. T., Ruiz, J., Aldridge, S., Shamoon, H., & Boden, G. (1993). Quantitation of glycolysis and skeletal muscle glycogen synthesis in humans. American Journal of Physiology, 295, 761-769.
 
[57]  Ahmadi, S. A., Boroumand, M., Gohari-Moghaddam, K., Tajik, P., & Dibaj, S. (2008). The impact of low serum triglyceride on LDL-cholesterol estimation. Archives of Iranian Medicine, 11, 318-321.
 
[58]  Fossati, P., & Prencipe, L. (1982). Serum triglycerides determined colorimetrically with an enzyme that produces hydrogen peroxide. Clinical Chemistry, 28, 2077–2080.
 
[59]  Lopes-Virella, M. F., Stone, P., Ellis, S., & Colwell, J. A. (1977). Cholesterol determination in high-density lipoproteins separated by three different methods. Clinical Chemistry, 23(5), 882-884.
 
[60]  Richmond, W. (1973). Preparation and Properties of a Cholesterol Oxidase from Nocardia sp. and its Application to the Enzymatic Assay of Total Cholesterol in Serum. Clinical Chemistry, 19, 1350-1356.
 
[61]  Ellman, G. L. (1959). Tissue sulfhydryl groups. Archives of Biochemistry and Biophysics, 82(1), 70-77.
 
[62]  Buege, J. A., & Aust, S. D. (1978). Microsomal lipid peroxidation. In S. Fleischer & L. Packer (Eds.), Methods in Enzymology (Vol. 52, pp. 302-310). Academic Press.
 
[63]  Jambunathan, N. (2010). Determination and detection of reactive oxygen species (ROS), lipid peroxidation, and electrolyte leakage in plants. In T. N. H. T. T. H. T. E. B. S. J. (Ed.), Methods in Molecular Biology (Vol. 639, pp. 292-298). Humana Press.
 
[64]  Carleton, H. (1978). Histological Techniques (4th ed.). London, Oxford, New York, Tornoto.
 
[65]  Snedecor, G. W., & Cochran, W. G. (1967). Statistical Methods (6th ed.). Lowa State University Press.
 
[66]  Hekal, H. A. (2012). Nutritional, biochemical and microbiological studies on mulberry [Unpublished master's thesis]. Minoufiya University, Egypt.
 
[67]  Abd El-Mageed, L. S. M. (2012). Magnification of Using Berries (Leaves and Fruits) on Food in Food Technology and Therapeutic Nutrition [Unpublished doctoral dissertation]. Minoufiya University, Egypt.
 
[68]  El-Nassag, D., Ghamry, H., & Elhassaneen, Y. (2019). Stevia (Stevia rebaudiana) leaves: Chemical composition, bioactive compounds, antioxidant activities, antihyperglycemic and antiatherogenic effects. Journal of Studies and Searches of Specific Education, 5(1), 157-180.
 
[69]  Elhassaneen, Y. A., Nour El-Deen, A. A., & Nasef, A. Z. (2023). Ultraviolet-c radiation induced changes on bioactive compounds content, antioxidant capacity and microbial quality of minimally processed molokhia (Corchorus olitorius L.) leaves. Journal of Agriculture and Crops, 9(3), 309–322.
 
[70]  Elhassaneen, Y. A., ElBassouny, G. M., Emam, O. A., & Ammar, H. E. (2024a). Strawberry and cauliflower leaves are rich in bioactive compounds and antioxidant activity: Application on obese rats. American Journal of Public Health Research, 12(4), 64–80.
 
[71]  Elhassaneen, Y. A., ElBassouny, G. M., Emam, O. A., & Aram, E. I. (2024b). Nutrients and nutraceuticals content and in vitro biological activities of formulae from plant parts commonly spread in Egyptian markets. American Journal of Food and Nutrition, 12(5), 134–151.
 
[72]  Jakimiuk, K., & Tomczyk, M. (2024). A review of the traditional uses, phytochemistry, pharmacology, and clinical evidence for the use of the genus Alchemilla (Rosaceae). Journal of Ethnopharmacology, 320, 117439.
 
[73]  Bouba, A. A., Yanou Njintang, N., Foyet, H. S., Scher, J., Montet, D., & Mbofung, C. M. F. (2012). Proximate composition, mineral and vitamin content of some wild plants used as spices in Cameroon. Food and Nutrition Sciences, 3(4), 423–432.
 
[74]  El-Hadidy, E. M., Refat, O. G., Halaby, M. S., Elmetwaly, E. M., & Omar, A. A. (2018). Effect of Lion’s Foot (Alchemilla vulgaris) on Liver and Renal Functions in Rats Induced by CCl4. Food and Nutrition Sciences, 9(1), 46-62.
 
[75]  Nour ElDeen, A. A. (2023). Potential effects of refrigeration processes on bioactive compounds content and biological activities of leafy vegetables [Master's thesis]. Minoufiya University, Shebin El-Kom, Egypt.
 
[76]  Elhassaneen, Y. A., ElBassouny, G., & Moharem, E. (2022). Preservation of leafy vegetables by co-treatment with refrigeration process and ultraviolet radiation (UV-c) and its potential effects on bioactive compounds content and antioxidant activity. Journal of the College of Specific Education for Educational and Specific Studies (SJSE), 7(22), 584–615.
 
[77]  Elhassaneen, Y. A., Hassab El-Nabi, S. I., Khalil, N. A., & Abd ElMaksoud, S. A. (2025a). Investigating the protective roles of mulberry (Morus alba L.) leaves in alleviating benzo[a]pyrene-induced liver damage in rats. American Journal of Public Health Research, 13(3), 117–132.
 
[78]  Gupta, M., Sasmal, S., Majumdar, S., & Mukherjee, A. (2012). HPLC Profiles of Standard Phenolic Compounds Present in Medicinal Plants. International Journal of Pharmacognosy and Phytochemical Research, 4(2), 162-167.
 
[79]  Jelača, S., Dajić-Stevanović, Z., Vuković, N., Kolašinac, S., Trendafilova, A., Nedialkov, P., Stanković, M., Tanić, N., Acović, A., Mijatović, S., & Maksimović-Ivanić, D. (2022). Beyond traditional use of Alchemilla vulgaris: Genoprotective and antitumor activity in vitro. Molecules, 27(23), 8113.
 
[80]  El-Barbary, A. K. M. Z. (2019). Evaluation of bioactive compounds of stevia (Stevia rebaudiana) leaves and their antihyperglycemic effects in alloxan-induced diabetic rats [Unpublished master's thesis]. Minoufiya University, Egypt.
 
[81]  Vanja, T., Krgović, N., & Zugić, A. (2020). Lady’s mantle (Alchemilla vulgaris L., Rosaceae): A review of traditional uses, phytochemical profile, and biological properties. Natural Medicinal Materials, 40, 66–74.
 
[82]  Jakimiuk, K., Kruk, A., Lemieszek, M. K., Strawa, J. W., Granica, S., Wiater, A., & Tomczyk, M. (2025). Ex vivo biotransformation of lady's mantle extracts via the human gut microbiota: the formation of phenolic metabolites and their impact on human normal and colon cancer cell lines. Frontiers in Pharmacology, 16, 1504787.
 
[83]  Del Prado-Audelo, M. L., Cortés, H., Caballero-Florán, I. H., González-Torres, M., Escutia-Guadarrama, L., Bernal-Chávez, S. A., Giraldo-Gomez, D. M., Magaña, J. J., & Leyva-Gómez, G. (2021). Therapeutic applications of terpenes on inflammatory diseases. Frontiers in Pharmacology, 12, 704197.
 
[84]  Zhao, M., Wu, F., Tang, Z., Yang, X., Liu, Y., Wang, F., & Chen, B. (2023). Anti-inflammatory and antioxidant activity of ursolic acid: A systematic review and meta-analysis. Frontiers in Pharmacology, 14, 1256946.
 
[85]  Mattioli, R., Francioso, A., Mosca, L., & Silva, P. (2020). Anthocyanins: A comprehensive review of their chemical properties and health effects on cardiovascular and neurodegenerative diseases. Molecules, 25(17), 3809.
 
[86]  Pedrosa, L. F., & Fabi, J. P. (2024). Polysaccharides from medicinal plants: Bridging ancestral knowledge with contemporary science. Plants, 13(13), 1721.
 
[87]  Khoneem, A. (2009). Antioxidant activity of some vegetables, spices, and herbs distributed in Egyptian local markets [Unpublished master's thesis]. Minoufiya University, Egypt.
 
[88]  Jaggi, L. (2012). Turmeric, curcumin, and our life: A review. Bulletin of Environmental Pharmacology and Life Sciences, 1(7), 11-17.
 
[89]  Elhassaneen, Y., Sherif, R., Alaa, E., & Emad, A. (2013). Mango peel powder: A potential source of phenolics, carotenoids, and dietary fiber in biscuit preparations. In Journal of Home Economics (Special Issue), 23(4), 1-16. Presented at the 2nd International-16th Arab Conference of Home Economics "Home Economics in the Service of Industry", Minoufiya University, Egypt.
 
[90]  Aly, A., Elbassyouny, G., & Elhassaneen, Y. (2017). Studies on the antioxidant properties of vegetables processing by-products extract and their roles in the alleviation of health complications caused by diabetes in rats. In Proceeding of the 1st International Conference of the Faculty of Specific Education, Kafrelsheikh University, "Specific Sciences, their Developmental Role and Challenges of Labor Market” (pp. 1-24). Sharm El-Sheikh, Egypt.
 
[91]  Elhassaneen, Y. A., Gharib, M. A., Abd El-Rahman, T. M., & Abd El-Moez, O. S. (2025b). Bioactive colored extracts from agro-industrial food wastes: Functional ingredients to improve food quality and health. American Journal of Food Science and Technology, 13(3), 53-69.
 
[92]  Elhassaneen, Y. A., El-khateeb, B. A., & Abd El-Aty, E. S. (2025c). Bioactive components and antioxidant properties of Acacia nilotica seeds: Exploring their potential as a cholesterol-lowering agent in rats. American Journal of Food and Nutrition, 13(4), 138-153.
 
[93]  Elhassaneen, Y. A., Saad, H. H., & Meharm, E. B. (2025d). Effect of solvents with different polarity on the extraction of bioactive compounds from reishi mushroom (Ganoderma lucidum) and their antioxidant and free radicals. Egyptian Journal of Chemistry, 68(6), 113-128.
 
[94]  Stagos, D. (2019). Antioxidant activity of polyphenolic plant extracts. Antioxidants, 9(1), 19.
 
[95]  Khalighi-Sigaroodi, F., Ahvazi, M., Hadjiakhoondi, A., Taghizadeh, M., Yazdani, D., Khalighi-Sigaroodi, S., & Bidel, S. (2012). Cytotoxicity and antioxidant activity of 23 plant species of Leguminosae family. Iranian Journal of Pharmaceutical Research, 11(1), 295-302.
 
[96]  Abd-ElAziz, Y. E. (2024). Effect of delonix regia seeds on liver injuries induced by carbon tetrachloride in rats: technological, chemical, biological, histopathological studies [Unpublished doctoral dissertation]. Minoufiya University, Shebin El-Kom, Egypt.
 
[97]  El-Tarabily, H. M. E. (2024). Bioactive compounds content and antioxidant activities of brown algae extracts and their effects on obesity complications in rats [Unpublished doctoral dissertation]. Port Said University, Port Said, Egypt.
 
[98]  Gouda, D. O., Elhassaneen, Y. A., & Saad, H. H. (2024). Date (Phoenix dactylifera var. Khalas) seed extracts rich in bioactive compounds and antioxidant activities: Potential preventive effects against atherosclerosis and lipid oxidation in model systems. Alexandria Science Exchange Journal, 45(3), 535-550.
 
[99]  Ismail, N. S., Elhassaneen, Y. A., & El Kholey, H. M. (2024). Effect of mixing date seed powder with wheat flour on the rheological parameters, nutrients, bioactive compounds content, and antioxidant activity of the Egyptian Balady bread. Alexandria Science Exchange Journal, 45(3), 455-477.
 
[100]  Elhassaneen, Y. A., ElBassouny, G. M., Emam, O. A., & Aram, E. I. (2024c). Nutrients and nutraceuticals content and in vitro biological activities of formulae from plant parts commonly spread in Egyptian markets. American Journal of Food and Nutrition, 12(5), 134-151.
 
[101]  Chaitanya, K. V., Pathan, A. A. K., Mazumdar, S. S., Charavarthi, G. P., Parine, N., & Bobbarala, V. (2010). Role of oxidative stress in human health: An overview. Journal of Pharmacy Research, 3, 1330-1333.
 
[102]  Elmaadawy, A., Arafa, R., & Elhassaneen, Y. (2016). Oxidative Stress and antioxidant defense systems status in obese rats feeding some selected food processing by-products applied in bread. Journal of Home Economics, 26(1), 1-37.
 
[103]  El-Harby, E.N.A. (2019). Nutritional and Technological Studies on some Plant Parts and their fects on Obesity Complications Induced in Experimental Animals [Unpublished master's thesis]. Benha University, Benha, Egypt.
 
[104]  Elhassaneen, Y., Youssef, H., & Mansour, Z. (2016). Hepatoprotective activity and antioxidant effects of avocado peels (Persea americana) on rats hepatotoxicity induced by carbon tetrachloride. Journal of Home Economics, 26(4), 1-12.
 
[105]  Sayed Ahmed, S. (2016). Nutritional and technological studies on the effect of phytochemicals on obesity injuries and their related diseases using experimental animals [Unpublished doctoral dissertation]. Port Said University, Egypt.
 
[106]  Elbasouny, G., Shehata, N., & Elhassaneen, Y. (2019). Feeding of some selected food industries by-products induced changes in oxidants/antioxidant status, lipids profile, glucose, and immunological parameters of blood obese rats. In The 6th Scientific and 4th International Conference: "The Future of Specific Education and People with Special Needs in Light of the Concept of Quality". El-Ain El-Soghna, Egypt.
 
[107]  Mater, E. N. A. (2019). Effect of Papaya (Leaves and Seeds) on Rat Liver Disorders Induced by Carbon Tetrachloride [Unpublished master's thesis]. Minoufiya University, Egypt.
 
[108]  Darwish, D. H. A. (2020). Potential Therapeutic Applications of Persimmon (Diospyros kaki-Virginiana) fruits and Leaves as Evaluated on Diabetic and Hepatopathic Male Albino Rats [Unpublished doctoral dissertation]. Minoufiya University, Egypt.
 
[109]  Abd El-Rahman, N. A. (2021). Potential effect of olive and mango leaves in diabetic rats induced by aloxane [Unpublished doctoral dissertation]. Minoufiya University, Shebin El-Kom, Egypt.
 
[110]  Badawy, E. Z. M. (2022). Study on the effect of strawberry leaves on diabetic rats induced by alloxan [Unpublished master's thesis]. Minoufiya University, Shebin El-Kom, Egypt.
 
[111]  Elhassaneen, Y., Badran, H., Abd El-Rahman, A., & Badawy, N. (2021b) Tetrachloride. Journal of Home Economics, 31(1), 83-93.
 
[112]  Elhassaneen, Y. A., Emam, O., El-Bassouny, G., & El-Qalaaf, G. (2022). Effect of cabbage and radish leaves on obesity biological changes induced in rats. Journal of the College of Specific Education for Educational and Specific Studies, 7(19), 1-33.
 
[113]  Al-Qarawi, A. A., Al-Damegh, M. A., & El-Mougy, S. A. (2002). Effect of Freeze Dried Extract of Olea europaea on the Pituitary thyroidaxis in Rats. Phytotherapy Research, 16(3), 286-287.
 
[114]  Platzer, M., Kiese, S., Tybussek, T., Herfellner, T., Schneider, F., Schweiggert-Weisz, U., & Eisner, P. (2022). Radical scavenging mechanisms of phenolic compounds: A quantitative structure-property relationship (QSPR) study. Frontiers in Nutrition, 9, 882458.
 
[115]  Elhassaneen, Y., Sayed Ahmed, S. A., & Fayez, S. A. (2021). Bioactive compounds and antioxidant activities of brown algae collected from the shores of the Egyptian seas. Port Saied Specific Research Journal (PSSRJ), 14(2), 645-665.
 
[116]  Antwi-Baffour, S., Adjei, J. K., Forson, P. O., Akakpo, S., Kyeremeh, R., & Seidu, M. A. (2019). Comorbidity of Glucose-6-Phosphate Dehydrogenase Deficiency and Sickle Cell Disease Exert Significant Effect on RBC Indices. BioMed Research International, 1-8.
 
[117]  Larit, F., León, F., Benyahia, S., & Cutler, S. J. (2019). Total Phenolic and Flavonoid Content and Biological Activities of Extracts and Isolated Compounds of Cytisus villosus Pourr. Biomolecules, 9(11), 732.
 
[118]  Mazo, V. K., Sidorova, Y. S., Shipelin, V. A., Petrov, N. A., & Kochetkova, A. A. (2016). Polyphenolic plant extracts: Effects on disorders of carbohydrate and lipid metabolism in laboratory animals. Problems of Endocrinology, 62(4), 38-44.
 
[119]  Sun, P., Zhao, L., Zhang, N., Zhou, J., Zhang, L., Wu, W., Ji, B., & Zhou, F. (2021). Bioactivity of dietary polyphenols: The role in LDL-C lowering. Foods, 10(11), 2666.
 
[120]  Singdam, P., Naowaboot, J., Senggunprai, L., Boonloh, K., & Pannangpetch, P. (2022). Pluchea indica leaf extract alleviates dyslipidemia and hepatic steatosis by modifying the expression of lipid metabolism-related genes in rats fed a high fat-high fructose diet. Preventive Nutrition and Food Science, 27(4), 384-398.
 
[121]  Mahran, M. Z., Elbassyouny, G. M., & Elhassaneen, Y. A. (2018). Preventive effects of onion skin powder against hepatotoxicity in rats treated with benzo(a)pyrene. In Proceeding of the Annual Conference (13th Arab; 10th International). Mansoura, Egypt.
 
[122]  Elhassaneen, Y., Ghamry, H., & Lotfy, L. (2018). Potential chemoprevention of liver disorders by dietary curcumin in rats treated with Benzo(a)pyrene. In Proceeding of the 1st Scientific International Conference of the Faculty of Specific Education, Minia University, “Specific Education, innovation and labor market” (pp. 16-17). Minia, Egypt.
 
[123]  Ajami, A. M. A. (2022). Study the effects of Turmeric on Liver disorder induced by Benzo(a)pyrene [Unpublished master's thesis]. Benha University, Benha, Egypt.
 
[124]  Menusy, A. E. M. (2025). Bioactive compound content and biological activities of brown algae and their effect on liver toxicity induced by benzo(a)pyrene in rats [Unpublished master's thesis]. Minoufiya University, Shebin El-Kom, Egypt.
 
[125]  El-Banaa, S. (2014). Phytochemicals in Artichoke and their effects on liver cancer induced by carbon tetrachloride, CCl4 [Unpublished master's thesis]. Minoufiya University, Egypt.
 
[126]  Mansour, Z. M. A. (2017). Hepatoprotective activity and antioxidant effects of avocado (Persea americana) fruits on rat's hepatotoxicity induced by carbon tetrachloride [Unpublished master's thesis]. Minoufiya University, Egypt.
 
[127]  Tahoon, S. R. H. (2019). Hepatoprotective effect of Apricot and Plum kernel on carbon tetrachloride induced hepatic rats [Unpublished master's thesis]. Minoufiya University, Egypt.
 
[128]  Mollazadeh, H., & Hosseinzadeh, H. (2014). The protective effect of Nigella sativa against liver injury: A review. Iranian Journal of Basic Medical Sciences, 17(12), 958-966.
 
[129]  Kanak, S., Krzemińska, B., Celiński, R., Bakalczuk, M., & Dos Santos Szewczyk, K. (2022). Phenolic composition and antioxidant activity of Alchemilla species. Plants (Basel), 11(20), 2709.
 
[130]  Kumar, S., Saxena, J., Srivastava, V. K., Kaushik, S., Singh, H., Abo-El-Sooud, K., Abdel-Daim, M. M., Jyoti, A., & Saluja, R. (2022). The interplay of oxidative stress and ROS scavenging: Antioxidants as a therapeutic potential in sepsis. Vaccines (Basel), 10(10), 1575.
 
[131]  El-Aslouty, M. A. E. (2024). Potential therapeutic effects of Annone Fruit on carbon tetrachloride induced hepatotoxicity in rats [Unpublished master's thesis]. Minoufiya University, Shebin El-Kom, Egypt.
 
[132]  Elhassaneen, Y. A., Khader, S. A., Gharib, M. A., & Abd-ElAziz, Y. E. (2024). Possible protective roles of Poinciana (Delonix regia) seeds against carbon tetrachloride-induced biochemical and histological disorders in rat liver. American Journal of Medical Sciences and Medicine, 12(1), 1-15.
 
[133]  Patel, J., Roy, H., Chintamaneni, P. K., Patel, R., & Bohara, R. (2025). Advanced strategies in enhancing the hepatoprotective efficacy of natural products: Integrating nanotechnology, genomics, and mechanistic insights. ACS Biomaterials Science & Engineering, 11(5), 2528-2549.