[
Almeida IM, Rodrigues F, Sarmento B, Alves RC, Oliveira MB. Isoflavones in food supplements: chemical profile, label accordance and permeability study in Caco-2 cells. Food Funct 6, 938–946, 2015.10.1039/C4FO01144A
]Search in Google Scholar
[
Atlante A, Bobba A, Paventi G, Pizzuto R, Passarella S. Genistein and daidzein prevent low potassium-dependent apoptosis of cerebellar granule cells. Biochem Pharmacol 79, 758–767, 2010.10.1016/j.bcp.2009.10.00519822130
]Search in Google Scholar
[
Banu SK, Stanley JA, Sivakumar KK, Arosh JA, Burghardt RC. Resveratrol protects the ovary against chromium-toxicity by enhancing endogenous antioxidant enzymes and inhibiting metabolic clearance of estradiol. Toxicol Appl Pharmacol 303, 65–78, 2016.10.1016/j.taap.2016.04.016583008527129868
]Search in Google Scholar
[
Baranowska-Wojcik E, Szwajgier D, Oleszczuk P, Winiarska-Mieczan A. Effects of titanium dioxide nanoparticles exposure on human health - a review. Biol Trace Elem Res 193, 118–129, 2020.10.1007/s12011-019-01706-6691471730982201
]Search in Google Scholar
[
Beazley KE, Nurminskaya M. Effects of dietary quercetin on female fertility in mice: implication of transglutaminase 2. Reprod Fertil Dev 28, 974–981, 2016.10.1071/RD14155479443525557047
]Search in Google Scholar
[
Bodis J, Sulyok E, Koszegi T, Godony K, Premusz V, Varnagy A. Serum and follicular fluid levels of sirtuin 1, sirtuin 6, and resveratrol in women undergoing in vitro fertilization: an observational, clinical study. J Int Med Res 47, 772–782, 2019.10.1177/0300060518811228638145330556451
]Search in Google Scholar
[
Brohi RD, Wang L, Talpur HS, Wu D, Khan FA, Bhattarai D, Rehman ZU, Farmanullah F, Huo LJ. Toxicity of nanoparticles on the reproductive system in animal models: a review. Front Pharmacol 8, 606, 2017.10.3389/fphar.2017.00606559188328928662
]Search in Google Scholar
[
De Matteis V, Cascione M, Toma CC, Leporatti S. Silver nanoparticles: synthetic routes, in vitro toxicity and theranostic applications for cancer disease. Nanomaterials (Basel) 8, 319, 2018.10.3390/nano8050319597733329748469
]Search in Google Scholar
[
Di Virgilio AL, Reigosa M, Arnal PM, Fernandez Lorenzo de Mele M. Comparative study of the cytotoxic and genotoxic effects of titanium oxide and aluminium oxide nanoparticles in Chinese hamster ovary (CHO-K1) cells. J Hazard Mater 177, 711–718, 2010.10.1016/j.jhazmat.2009.12.08920079968
]Search in Google Scholar
[
Feranchak AP, Kilic G, Wojtaszek PA, Qadri I, Fitz JG. Volume-sensitive tyrosine kinases regulate liver cell volume through effects on vesicular trafficking and membrane Na+ permeability. J Biol Chem 278, 44632–44638, 2003.10.1074/jbc.M30195820012939281
]Search in Google Scholar
[
Flores-Lopez LZ, Espinoza-Gomez H, Somanathan R. Silver nanoparticles: Electron transfer, reactive oxygen species, oxidative stress, beneficial and toxicological effects. Mini review. J Appl Toxicol 39, 16–26, 2019.10.1002/jat.365429943411
]Search in Google Scholar
[
Gao G, Ze Y, Li B, Zhao X, Zhang T, Sheng L, Hu R, Gui S, Sang X, Sun Q, Cheng J, Cheng Z, Wang L, Tang M, Hong F. Ovarian dysfunction and gene-expressed characteristics of female mice caused by long-term exposure to titanium dioxide nanoparticles. J. Hazard. Mater 243, 19–27, 2012.10.1016/j.jhazmat.2012.08.04923131501
]Search in Google Scholar
[
Grande F, Tucci P. Titanium dioxide nanoparticles: a risk for human health? Mini Rev Med Chem 16, 762–769, 2016.10.2174/138955751666616032111434126996620
]Search in Google Scholar
[
Han JW, Jeong JK, Gurunathan S, Choi YJ, Das J, Kwon DN, Cho SG, Park C, Seo HG, Park JK, Kim JH. Male-and female-derived somatic and germ cell-specific toxicity of silver nanoparticles in mouse. Nanotoxicology 10, 361–373, 2016.10.3109/17435390.2015.107339626470004
]Search in Google Scholar
[
Hill EK, Li J. Current and future prospects for nanotechnology in animal production. J Animal Sci Biotechnol 8, 26, 2017.10.1186/s40104-017-0157-5535105428316783
]Search in Google Scholar
[
Hong F, Wang L. Nanosized titanium dioxide-induced premature ovarian failure is associated with abnormalities in serum parameters in female mice. Int J Nanomedicine 13, 2543–2549, 2018.10.2147/IJN.S151215592735429731629
]Search in Google Scholar
[
Hou J, Wan XY, Wang F, Xu GF, Liu Z [Effects of titanium dioxide nanoparticles on development and maturation of rat preantral follicle in vitro]. Acad J Second Mil Med Univ 30, 869–873, 2009.10.3724/SP.J.1008.2009.00869
]Search in Google Scholar
[
Jahan S, Abid A, Khalid S, Afsar T, Qurat-Ul-Ain, Shaheen G, Almajwal A, Razak S. Therapeutic potentials of Quercetin in management of polycystic ovarian syndrome using Letrozole induced rat model: a histological and a biochemical study. J Ovarian Res 11, 26, 2018.10.1186/s13048-018-0400-5588360729615083
]Search in Google Scholar
[
Jozkowiak M, Hutchings G, Jankowski M, Kulcenty K, Mozdziak P, Kempisty B, Spaczynski RZ, Piotrowska-Kemp-isty H. The stemness of human ovarian granulosa cells and the role of resveratrol in the differentiation of MSCs-A review based on cellular and molecular knowledge. Cells 9, 1418, 2020.10.3390/cells9061418734918332517362
]Search in Google Scholar
[
Jungbauer A, Medjakovic S. Phytoestrogens and the metabolic syndrome. J Steroid Biochem Mol Biol 139, 277–289, 2014.10.1016/j.jsbmb.2012.12.00923318879
]Search in Google Scholar
[
Kim S, Lim YT, Soltesz EG, De Grand AM, Lee J, Nakayama A, Parker JA, Mihaljevic T, Laurence RG, Dor DM, Cohn LH, Bawendi MG, Frangioni JV. Near-infrared fluorescent type II quantum dots for sentinel lymph node mapping. Nat Biotechnol 22, 93–97, 2004.10.1038/nbt920234661014661026
]Search in Google Scholar
[
Li N, Sun C, Zhou B, Xing H, Ma D, Chen G, Weng D. Low concentration of quercetin antagonizes the cytotoxic effects of anti-neoplastic drugs in ovarian cancer. PLoS One 9, e100314, 2014.10.1371/journal.pone.0100314408506624999622
]Search in Google Scholar
[
Liu Y, Wang YL, He SW, Chen MH, Zhang Z, Fu XP, Fu BB, Liao BQ, Lin YH, Qi ZQ, Wang HL. Protective effects of resveratrol against mancozeb induced apoptosis damage in mouse oocytes. Oncotarget 8, 6233–6245, 2017.10.18632/oncotarget.14056535162728031523
]Search in Google Scholar
[
Mikhailov OV, Mikhailova EO. Elemental Silver nanoparticles: biosynthesis and bio applications. Materials (Basel) 12, 3177, 2019.10.3390/ma12193177680399431569794
]Search in Google Scholar
[
Nawaz W, Zhou Z, Deng S, Ma X, Ma X, Li C, Shu X. Therapeutic versatility of resveratrol derivatives. Nutrients 9, 1188, 2017.10.3390/nu9111188570766029109374
]Search in Google Scholar
[
Ortega I, Villanueva JA, Wong DH, Cress AB, Sokalska A, Stanley SD, Duleba AJ. Resveratrol reduces steroidogenesis in rat ovarian theca-interstitial cells: the role of inhibition of Akt/PKB signaling pathway. Endocrinology 153, 4019–4029, 2012.10.1210/en.2012-1385340435422719052
]Search in Google Scholar
[
Ozatik FY, Ozatik O, Yigitaslan S, Kaygisiz B, Erol K. Do resveratrol and dehydroepiandrosterone increase diminished ovarian reserve? Eurasian J Med 52, 6–11, 2020.10.5152/eurasianjmed.2019.19044705123132158305
]Search in Google Scholar
[
Podolak I, Galanty A, Sobolewska D. Saponins as cytotoxic agents: a review. Phytochem Rev 9, 425–474, 2010.10.1007/s11101-010-9183-z292844720835386
]Search in Google Scholar
[
Rietjens IMCM, Louisse J, Beekmann K. The potential health effects of dietary phytoestrogens. Br J Pharmacol 174, 1263–1280, 2017.10.1111/bph.13622542933627723080
]Search in Google Scholar
[
Said RS, El-Demerdash E, Nada AS, Kamal MM. Resveratrol inhibits inflammatory signaling implicated in ionizing radiation-induced premature ovarian failure through antagonistic crosstalk between silencing information regulator 1 (SIRT1) and poly(ADP-ribose) polymerase 1 (PARP-1). Biochem Pharmacol 103, 140–150, 2016.10.1016/j.bcp.2016.01.01926827941
]Search in Google Scholar
[
Said RS, Mantawy EM, El-Demerdash E. Mechanistic perspective of protective effects of resveratrol against cisplatin-induced ovarian injury in rats: emphasis on anti-inflammatory and anti-apoptotic effects. Naunyn Schmiedebergs Arch Pharmacol 392, 1225–1238, 2019.10.1007/s00210-019-01662-x31129703
]Search in Google Scholar
[
Santini SE, Basini G, Bussolati S, Grasselli F. The phytoestrogen quercetin impairs steroidogenesis and angiogenesis in swine granulosa cells in vitro. J Biomed Biotechnol 2009, 419891, 2009.10.1155/2009/419891269393219704917
]Search in Google Scholar
[
Sirotkin AV. Regulators of ovarian functions, second ed., Nova Science Publishers, Inc New York, 2014.
]Search in Google Scholar
[
Sirotkin AV, Harrath AH. Phytoestrogens and their effects. Eur J Pharmacol 741, 230–236, 2014.10.1016/j.ejphar.2014.07.05725160742
]Search in Google Scholar
[
Sirotkin AV, Alexa R, Alwasel S, Harrath AH. The phytoestrogen, diosgenin, directly stimulates ovarian cell functions in two farm animal species. Domest Anim Endocrinol 69, 35–41, 2019.10.1016/j.domaniend.2019.04.00231280024
]Search in Google Scholar
[
Tarko A, Stochmalova A, Hrabovszka S, Vachanova A, Harrath AH, Alwasel S, Grossman R, Sirotkin AV. Can xylene and quercetin directly affect basic ovarian cell functions? Res Vet Sci 119, 308–312, 2018.10.1016/j.rvsc.2018.07.01030086515
]Search in Google Scholar
[
Tarko A, Stochmalova A, Jedlickova K, Hrabovszka S, Vachanova A, Harrath AH, Alwasel S, Alrezaki A, Kotwica J, Balazi A, Sirotkin AV. Effects of benzene, quercetin, and their combination on porcine ovarian cell proliferation, apoptosis, and hormone release. Arch Anim Breed 62, 345–351, 2019.10.5194/aab-62-345-2019685286231807645
]Search in Google Scholar
[
van Duursen MBM. Modulation of estrogen synthesis and metabolism by phytoestrogens in vitro and the implications for women‘s health. Toxicol Res (Camb) 6, 772–794, 2017.10.1039/c7tx00184c606238230090542
]Search in Google Scholar
[
Volkovova K, Handy RD, Staruchova M, Tulinska J, Kebis A, Pribojova J, Ulicna O, Kucharska J, Dusinska M. Health effects of selected nanoparticles in vivo: liver function and hepatotoxicity following intravenous injection of titanium dioxide and Na-oleate-coated iron oxide nanoparticles in rodents. Nanotoxicology 9 (Suppl 1), 95–105, 2015.10.3109/17435390.2013.81528523763576
]Search in Google Scholar
[
Wu M, Ma L, Xue L, Ye W, Lu Z, Li X, Jin Y, Qin X, Chen D, Tang W, Chen Y, Hong Z, Zhang J, Luo A, Wang S. Resveratrol alleviates chemotherapy-induced oogonial stem cell apoptosis and ovarian aging in mice. Aging (Albany NY) 11, 1030–1044, 2019.10.18632/aging.101808638241830779707
]Search in Google Scholar
[
Zhang J, Chen Q, Du D, Wu T, Wen J, Wu M, Zhang Y, Yan W, Zhou S, Li Y, Jin Y, Luo A, Wang S. Can ovarian aging be delayed by pharmacological strategies? Aging (Albany NY) 11, 817–832, 2019.10.18632/aging.101784636695630674710
]Search in Google Scholar
[
Zhao X, Ze Y, Gao G, Sang X, Li B, Gui S, Sheng L, Sun Q, Cheng J, Cheng Z, Hu R, Wang L, Hong F. Nanosized TiO2-induced reproductive system dysfunction and its mechanism in female mice. PLoS One 8, e59378, 2013.10.1371/journal.pone.0059378361500823565150
]Search in Google Scholar
