1. Khodaie S-A, Razavi R, Nikkhah H, Namiranian N, Kamalinejad M. Topical Remedy for Diabetic Neuropathy in Persian Medicine and Modern Phytotherapy: A Narrative Review. J Adv Med Biomed Res. 2025;33(158):172-8. [
DOI:10.30699/jambr.33.158.172]
2. Heidari H, Kamalinejad M, Noubarani M, Rahmati M, Jafarian I, Adiban H, et al. Protective mechanisms of Cucumis sativus in diabetes-related modelsof oxidative stress and carbonyl stress. Bioimpacts. 2016;6(1):33-9. [
DOI:10.15171/bi.2016.05] [
PMID] [
PMCID]
3. Chong K, Chang JK, Chuang LM. Recent advances in the treatment of type 2 diabetes mellitus using new drug therapies. Kaohsiung J Med Sci. 2024;40(3):212-20. [
DOI:10.1002/kjm2.12800] [
PMID] [
PMCID]
4. Shayesteh R, Kamalinejad M, Adiban H, Kardan A, Keyhanfar F, Eskandari MR. Cytoprotective Effects of Pumpkin (Cucurbita Moschata) Fruit Extract against Oxidative Stress and Carbonyl Stress. Drug Res (Stuttg). 2017;67(10):576-82. [
DOI:10.1055/s-0043-110484] [
PMID]
5. Panjeshahin MR, Azadbakht M, Akbari N. Antidiabetic activity of different extracts of Myrtus communis in streptozotocin induced diabetic rats. Rom J Diabetes Nutr Metab Dis. 2016;23(2):183-90. [
DOI:10.1515/rjdnmd-2016-0022]
6. Kesari AN, Kesari S, Singh SK, Gupta RK, Watal G. Studies on the glycemic and lipidemic effect of Murraya koenigii in experimental animals. J Ethnopharmacol. 2007;112(2):305-11. [
DOI:10.1016/j.jep.2007.03.023] [
PMID]
7. Aleksic V, Knezevic P. Antimicrobial and antioxidative activity of extracts and essential oils of Myrtus communis L. Microbiol Res. 2014;169(4):240-54. [
DOI:10.1016/j.micres.2013.10.003] [
PMID]
8. Elfellah MS, Akhter MH, Khan MT. Anti-hyperglycaemic effect of an extract of Myrtus communis in streptozotocin-induced diabetes in mice. J Ethnopharmacol. 1984;11(3):275-81. [
DOI:10.1016/0378-8741(84)90073-4] [
PMID]
9. Djenane D, Yangüela J, Amrouche T, Boubrit S, Boussad N, Roncalés P. Chemical composition and antimicrobial effects of essential oils of Eucalyptus globulus, Myrtus communis and Satureja hortensis against Escherichia coli O157:H7 and Staphylococcus aureus in minced beef. Food Sci Technol Int. 2011;17(6):505-15. [
DOI:10.1177/1082013211398803] [
PMID]
10. Hosseinzadeh H, Khoshdel M, Ghorbani M. Antinociceptive, anti-inflammatory effects and acute toxicity of aqueous and ethanolic extracts of Myrtus communis L. Aerial parts in mice. J Acupunct Meridian Stud. 2011;4(4):242-7. [
DOI:10.1016/j.jams.2011.09.015] [
PMID]
11. Alipour G, Dashti S, Hosseinzadeh H. Review of pharmacological effects of Myrtus communis L. and its active constituents. Phytother Res. 2014;28(8):1125-36. [
DOI:10.1002/ptr.5122] [
PMID]
12. Sepici A, Gürbüz I, Cevik C, Yesilada E. Hypoglycaemic effects of myrtle oil in normal and alloxan-diabetic rabbits. J Ethnopharmacol. 2004;93(2-3):311-8. [
DOI:10.1016/j.jep.2004.03.049] [
PMID]
13. Tas S, Tas B, Bassalat N, Jaradat N. In-vivo, hypoglycemic, hypolipidemic and oxidative stress inhibitory activities of Myrtus communis L. fruits hydroalcoholic extract in normoglycemic and streptozotocin-induced diabetic rats. Biomed Res. 2018;29(13):2727-34. [
DOI:10.4066/biomedicalresearch.29-18-708]
14. Talebianpoor MS, Talebianpoor MS, Mansourian M, Vafaiee‑Nejad T. Antidiabetic activity of hydroalcoholic extract of Myrtus communis (Myrtle) fruits in streptozotocin‑induced and dexamethasone‑induced diabetic rats. Pharmacogn Res. 2019;11(2):115-20. [
DOI:10.4103/pr.pr_160_18]
15. Colvin DM. A review on comparison of the extraction methods used in licorice root: Their principle, strength and limitation. Med Aromat Plants. 2018;7(6):323. [
DOI:10.4172/2167-0412.1000323]
16. Amereh Z, Hatami N, Shirazi FH, Gholami S, Hosseini SH, Noubarani M, et al. Cancer chemoprevention by oleaster (Elaeagnus angustifoli L.) fruit extract in a model of hepatocellular carcinoma induced by diethylnitrosamine in rats. EXCLI J. 2017;16:1046-56.
17. Gholami S, Hosseini MJ, Jafari L, Omidvar F, Kamalinejad M, Mashayekhi V, et al. Mitochondria as a Target for the Cardioprotective Effects of Cydonia oblonga Mill. and Ficus carica L. in Doxorubicin-Induced Cardiotoxicity. Drug Res (Stuttg). 2017;67(6):358-65. [
DOI:10.1055/s-0043-101824] [
PMID]
18. Mousavi M, Abedimanesh N, Mohammadnejad K, Sharini E, Nikkhah M, Eskandari MR, et al. Betanin alleviates oxidative stress through the Nrf2 signaling pathway in the liver of STZ-induced diabetic rats. Mol Biol Rep. 2022;49(10):9345-54. [
DOI:10.1007/s11033-022-07781-8] [
PMID]
19. Kurylo K, Budniak L, Volska A, Zablotskyy B, Klishch I. Influence of Phytocompositions on Dynamics of Changes in Basal Glycemia and Glycemia In Oral Glucose Tolerance Test In Rats With Streptozotocin-Nicotinamide-Induced Diabetes Mellitus Type 2. Georgian Med News. 2020(300):112-6.
20. Yu Z, Xu H, Yu X, Sui D, Lin G. Hypolipidemic effects of total flavonoide extracted from the leaves of Actinidiakolomikta in rats fed a high-fat diet. Iran J Basic Med Sci. 2017;20(10):1141-8.
21. Consultation WHO. Definition, diagnosis and classification of diabetes mellitus and its complications. 1999.
22. Patel DK, Prasad SK, Kumar R, Hemalatha S. An overview on antidiabetic medicinal plants having insulin mimetic property. Asian Pac J Trop Biomed. 2012;2(4):320-30. [
DOI:10.1016/S2221-1691(12)60032-X] [
PMID]
23. Bouaoudia-Madi N, Boulekbache-Makhlouf L, Kadri N, Dahmoune F, Remini H, Dairi S, et al. Phytochemical analysis of Myrtus communis plant: Conventional versus microwave assisted-extraction procedures. J Complement Integr Med. 2017;14(4):20160098. [
DOI:10.1515/jcim-2016-0098] [
PMID]
24. Giampieri F, Cianciosi D, Forbes‐Hernández TY. Myrtle (Myrtus communis L.) berries, seeds, leaves, and essential oils: New undiscovered sources of natural compounds with promising health benefits. Food Frontiers. 2020;1(3):276-95. [
DOI:10.1002/fft2.37]
25. Sarian MN, Ahmed QU, Mat So'ad SZ, Alhassan AM, Murugesu S, Perumal V, et al. Antioxidant and Antidiabetic Effects of Flavonoids: A Structure-Activity Relationship Based Study. Biomed Res Int. 2017;2017:8386065. [
DOI:10.1155/2017/8386065] [
PMID] [
PMCID]
26. Sepici-Dincel A, Açikgöz S, Cevik C, Sengelen M, Yeşilada E. Effects of in vivo antioxidant enzyme activities of myrtle oil in normoglycaemic and alloxan diabetic rabbits. J Ethnopharmacol. 2007;110(3):498-503. [
DOI:10.1016/j.jep.2006.10.015] [
PMID]
27. Mirmohammadlu M, Hosseini SH, Kamalinejad M, Esmaeili Gavgani M, Noubarani M, Eskandari MR. Hypolipidemic, Hepatoprotective and Renoprotective Effects of Cydonia Oblonga Mill. Fruit in Streptozotocin-Induced Diabetic Rats. Iran J Pharm Res. 2015;14(4):1207-14.
28. Karimlar S, Naderi A, Mohammadi F, Moslehishad M, Delrish E, Aghajanpour L, et al. Hypoglycemic and Hypolipidemic Effects of Myrtus communis, Trachyspermum copticum and Ferula gummosa Essential Oils on Streptozotocin Induced Diabetic Rats. Nutr Food Sci Res. 2019;6(1):1-8. [
DOI:10.29252/nfsr.6.1.1]
29. Khan RA, Feroz Z, Jamil M, Ahmed M. Hypolipidemic and antithrombotic evaluation of Myrtus communis L. in cholesterol-fed rabbits. Afr J Pharm Pharmacol. 2014;8(8):235-9. [
DOI:10.5897/AJPP2013.3488]
30. Salvamani S, Gunasekaran B, Shaharuddin NA, Ahmad SA, Shukor MY. Antiartherosclerotic effects of plant flavonoids. Biomed Res Int. 2014;2014:480258. [
DOI:10.1155/2014/480258] [
PMID] [
PMCID]
31. Murase T, Nagasawa A, Suzuki J, Hase T, Tokimitsu I. Beneficial effects of tea catechins on diet-induced obesity: stimulation of lipid catabolism in the liver. Int J Obes Relat Metab Disord. 2002;26(11):1459-64. [
DOI:10.1038/sj.ijo.0802141] [
PMID]
32. Kumar MR, Phaneendra P, Bodhanapu S, Rahiman OMF, Niyas KM, Tamizmani T. Antioxidant and hepatoprotective activity of the aqueous extract of Myrtus communis (Myrtle) Linn. leaves. Pharmacologyonline. 2011;1(1):1083-90.
33. Hsouna AB, Dhibi S, Dhifi W, Mnif W, Hfaiedh N. Chemical composition and hepatoprotective effect of essential oil from Myrtus communis L. flowers against CCL 4-induced acute hepatotoxicity in rats. RSC Adv. 2019;9(7):3777-87. [
DOI:10.1039/C8RA08204A] [
PMID] [
PMCID]
34. Namdar F, Bahrami F, Bahari Z, Ghanbari B, Elahi SA, Mohammadi MT. Evaluation of the Effects of Fullerene C60 Nanoparticles on Oxidative Stress Parameters at Liver and Brain of Normal Rats. J Adv Med Biomed Res. 2019;27(124):8-15. [
DOI:10.30699/jambs.27.124.8]