• Seth P, Scholl L, Rudd RA, Bacon S. Overdose deaths involving opioids, cocaine, and psychostimulants—United States, 2015–2016. Am J Transplant. 2018;18(6):1556-68. https://doi.org/10.1111/ajt.14905
• Jalili C, Ahmadi S, Roshankhah S, Salahshoor M. Effect of Genistein on reproductive parameter and serum nitric oxide levels in morphine-treated mice. Int J Reprod Biomed. 2016;14:95. https://doi.org/10.29252/ijrm.14.2.95
• Pert CB, Snyder SH. Opiate receptor: demonstration in nervous tissue. Science. 1973;179(4077):1011-4. https://doi.org/10.1126/science.179.4077.1011 PMid:4687585
• Salahshoor MR. Protective effect of crocin on liver toxicity induced by morphine. Res Pharm Sci. 2016;11:120.
• Desmedt S, Spinewine A, Jadoul M, Henrard S, Wouters D, Dalleur O. Impact of a clinical decision support system for drug dosage in patients with renal failure. Int J Clin Pharm. 2018;21:1-9. https://doi.org/10.1007/s11096-018-0612-1 PMid:29785684
• Ahmadnia H, Ghanbari M, Moradi MR, Khaje-Dalouee M. Effect of cigarette smoke on spermatogenesis in rats. J Urol. 2009;4(3):159-63.
• Mercadante S, Arcuri E. Opioids and renal function. The Journal of Pain 2004;5(1):2-19. https://doi.org/10.1016/j.jpain.2003.09.007 PMid:14975374
• Jalili C, Tabatabaei H, Kakaberiei S, Roshankhah S, Salahshoor MR. Protective role of Crocin against nicotine induced damages on male mice liver. Int J Prev Med. 2015;6:92. https://doi.org/10.4103/2008-7802.165203 PMid:26442615 PMCid:PMC4593238
• Gibanananda RS. Oxidants, antioxidants and carcinogenesis. Indian J Exp Biol 2002;40:1213-32.
• Zarrindast M, Delphi L. Morphine-induced Nitric Oxide Production in PC12 Cells. Arch Iran Med. 2012;15:404-8.
• Dolinoy DC, Weidman JR, Waterland RA, Jirtle RL. Maternal genistein alters coat color and protects A vy mouse offspring from obesity by modifying the fetal epigenome. Environ Health Perspect. 2006:567-72. https://doi.org/10.1289/ehp.8700 PMid:16581547 PMCid:PMC1440782
• Salahshoor MR, Roshankhah S, Hosseni P, Jalili C. Genistein Improves Liver Damage in Male Mice Exposed to Morphine. Chin Med J 2018;131:1598-604. https://doi.org/10.4103/0366-6999.235117 PMid:29941714 PMCid:PMC6032674
• Choi M, Jung U, Yeo J, Kim M, Lee M. Genistein and daidzein prevent diabetes onset by elevating insulin level and altering hepatic gluconeogenic and lipogenic enzyme activities in non‐obese diabetic (NOD) mice. Diabetes Metab Res Rev. 2008;24(1):74-81. https://doi.org/10.1002/dmrr.780 PMid:17932873
• Rajaram S. The effect of vegetarian diet, plant foods, and phytochemicals on hemostasis and thrombosis. Am J Clin Nutr. 2003;78(3):552S-8S. https://doi.org/10.1093/ajcn/78.3.552S PMid:12936949
• Dattner AM. From medical herbalism to phytotherapy in dermatology: back to the future. Dermatologic therapy. 2003;16(2):106-13. https://doi.org/10.1046/j.1529-8019.2003.01618.x PMid:12919112
• Jalili C, Salahshoor MR, Hoseini M, Roshankhah S, Sohrabi M, Shabanizadeh A. Protective Effect of Thymoquinone Against Morphine Injuries to Kidneys of Mice. Iran J Kidney Dis. 2017;11(2).142-150
• Salahshoor M, Mohamadian S, Kakabaraei S, Roshankhah S, Jalili C. Curcumin improves liver damage in male mice exposed to nicotine. J Tradit Complement Med. 2016;6:176-83. https://doi.org/10.1016/j.jtcme.2014.11.034 PMid:27114942 PMCid:PMC4833467
• Roshankhah Sh, Salahshoor MR, Jalili F, Karimi F, Sohrabi M, Jalili C. Crocin effects on the nicotine-induce ovary injuries in female rat. Int J Life Sci. Pharma 2017;7:1-8.
• Lei L, Liu S, Li Y, Song H, He L, Liu Q, et al. The potential role of glucokinase activator SHP289-04 in anti-diabetes and hepatic protection. European journal of pharmacology. 2018 May 5;826:17-23. https://doi.org/10.1016/j.ejphar.2018.02.036 PMid:29477658
• Muangman V, Cherdshewasart W. Clinical trial of the phytoestrogen-rich herb, Pueraria mirifica as a crude drug in the treatment of symptoms in menopausal women. Siriraj Medical Journal. 2018;53(5):300-9.
• Yoshida S, Tajiri T, Yahara T, Yoshizumi T, Tanaka K, Muraoka T, et al. Administration of opiate receptor antagonist inhibits mucosal atrophy of the gut in fasting rats. J Surg Res. 2000;93(1):177-81. https://doi.org/10.1006/jsre.2000.5970 PMid:10945961
• Heim M, Frank O, Kampmann G, Sochocky N, Pennimpede T, Fuchs P, et al. The phytoestrogen genistein enhances osteogenesis and represses adipogenic differentiation of human primary bone marrow stromal cells. Endocrinology. 2004;145(2):848-59. https://doi.org/10.1210/en.2003-1014 PMid:14605006
• King TJ, Shandala T, Lee AM, Foster BK, Chen K-M, Howe PR, et al. Potential effects of phytoestrogen genistein in modulating acute methotrexate chemotherapy-induced osteoclastogenesis and bone damage in rats. Int J Mol Sci. 2015;16(8):18293-311. https://doi.org/10.3390/ijms160818293 PMid:26258775 PMCid:PMC4581246
• Santell RC, Chang YC, Nair MG, Helferich WG. Dietary genistein exerts estrogenic effects upon the uterus, mammary gland and the hypothalamic/pituitary axis in rats. Int J Nutr. 1997 Feb 1;127(2):263-9. https://doi.org/10.1093/jn/127.2.263 PMid:9039826
• Rezazadeh H, Kahnouei MH, Hassanshahi G, Allahtavakoli M, Shamsizadeh A, Roohbakhsh A, et al. Regulatory effects of chronic low-dose morphine on nitric oxide level along with baroreflex sensitivity in two-kidney one-clip hypertensive rats. Iran J Kidney Dis. 2014;8(3):194.
• Liu D, Homan LL, Dillon JS. Genistein acutely stimulates nitric oxide synthesis in vascular endothelial cells by a cyclic adenosine 5’-monophosphate-dependent mechanism. Endocrinology. 2004;145(12):5532-9. https://doi.org/10.1210/en.2004-0102 PMid:15319357
• Leffel EK, Wolf C, Poklis A, White KL. Drinking water exposure to cadmium, an environmental contaminant, results in the exacerbation of autoimmune disease in the murine model. Toxicology. 2003;188(2):233-50. https://doi.org/10.1016/S0300-483X(03)00092-1
• Atici S, Cinel I, Cinel L, Doruk N, Eskandari G, Oral U. Liver and kidney toxicity in chronic use of opioids: an experimental long term treatment model. Journal of biosciences. 2005;30(2):245-252. https://doi.org/10.1007/BF02703705 PMid:15886461
• Javanbakht MH, Sadria R, Djalali M, Derakhshanian H, Hosseinzadeh P, Zarei M, et al. Soy protein and genistein improves renal antioxidant status in experimental nephrotic syndrome. Nefrologia. 2014;34(4):483-90.
• Santell RC, Chang YC, Nair MG, Helferich WG. Dietary genistein exerts estrogenic effects upon the uterus, mammary gland and the hypothalamic/pituitary axis in rats. The Journal of nutrition. 1997;127(2):263-9. https://doi.org/10.1093/jn/127.2.263 PMid:9039826
• Sung MJ, Kim DH, Jung YJ, Kang KP, Lee AS, Lee S, et al. Genistein protects the kidney from cisplatin-induced injury. Kidney international. 2008;74(12):1538-47. https://doi.org/10.1038/ki.2008.409 PMid:18716605
• Loei MA, Mami S, Parviz SA. The effect of the opium addiction on histological structure of liver and kidney in rabbits. 2013:32-45.
• Lyman J. Blood urea nitrogen and creatinine. Emergency medicine clinics of North America. 1986;4(2):223-33.
• Hall AM, Unwin RJ. The not so ‘mighty chondrion’: emergence of renal diseases due to mitochondrial dysfunction. Nephron Physiology. 2006;105(1):p1-p10. https://doi.org/10.1159/000096860 PMid:17095876
• Zaragoza A, Andrés D, Sarrión D, Cascales Ma. Potentiation of thioacetamide hepatotoxicity by phenobarbital pretreatment in rats. Inducibility of FAD monooxygenase system and age effect. Chemico-Biological Interactions. 2000;124(2):87-101. https://doi.org/10.1016/S0009-2797(99)00147-7
• Khodadadi S, Naghsh N, Mashayekh A. Effects of Silver Nanoparticle on Phosphocreatine kinase and Histological Changes of Skeletal Muscle Tissue in Male Wistar Rat. J Mazand Univ Med Sci. 2013;23(97):36-41.
• Samarghandian S, Afshari R, Farkhondeh T. Effect of long-term treatment of morphine on enzymes, oxidative stress indices and antioxidant status in male rat liver. Int J Clin Exp Med. 2014;7(5):1449-53.
• Shahsavar F, Ghanadi K, Jafarzadeh M, Nasiri B, Forutani SH. Opium addiction decreases T3 uptake amount. Life Science Journal. 2013; 10(5s):608-10.

Vancouver

Jalili C, Rashidi I, Roshankhah S, Jalili F, Salahshoor MR. Protective Effect of Genistein on the Morphine-Induced Kidney Disorders in Male Mice. Electron J Gen Med. 2020;17(3):em213. https://doi.org/10.29333/ejgm/7874

APA

Jalili, C., Rashidi, I., Roshankhah, S., Jalili, F., & Salahshoor, M. R. (2020). Protective Effect of Genistein on the Morphine-Induced Kidney Disorders in Male Mice. Electronic Journal of General Medicine, 17(3), em213. https://doi.org/10.29333/ejgm/7874

AMA

Jalili C, Rashidi I, Roshankhah S, Jalili F, Salahshoor MR. Protective Effect of Genistein on the Morphine-Induced Kidney Disorders in Male Mice. Electron J Gen Med. 2020;17(3), em213. https://doi.org/10.29333/ejgm/7874

Chicago

Jalili, Cyrus, Iraj Rashidi, Shiva Roshankhah, Faramarz Jalili, and Mohammad Reza Salahshoor. "Protective Effect of Genistein on the Morphine-Induced Kidney Disorders in Male Mice". Electronic Journal of General Medicine 2020 17 no. 3 (2020): em213. https://doi.org/10.29333/ejgm/7874

Harvard

Jalili, C., Rashidi, I., Roshankhah, S., Jalili, F., and Salahshoor, M. R. (2020). Protective Effect of Genistein on the Morphine-Induced Kidney Disorders in Male Mice. Electronic Journal of General Medicine, 17(3), em213. https://doi.org/10.29333/ejgm/7874

MLA

Jalili, Cyrus et al. "Protective Effect of Genistein on the Morphine-Induced Kidney Disorders in Male Mice". Electronic Journal of General Medicine, vol. 17, no. 3, 2020, em213. https://doi.org/10.29333/ejgm/7874