Abstract
Arsenic being a toxic metalloid ubiquitously persists in environment and causes several health complications including female reproductive anomalies. Epidemiological studies documented birth anomalies due to arsenic exposure. Augmented reactive oxygen species (ROS) generation and quenched antioxidant pool are foremost consequences of arsenic threat. On the contrary, Vitamin E (VE) and C (VC) are persuasive antioxidants and conventionally used in toxicity management. Present study was designed to explore the extent of efficacy of combined VE and VC (VEC) against Sodium arsenite (NaAsO2) mediated ovarian damage. Thirty-six female Wistar rats were randomly divided into three groups (Grs) and treated for consecutive 30 days; Gr I (control) was vehicle fed, Gr II (treated) was gavaged with NaAsO2 (3 mg/kg/day), Gr III (supplement) was provided with VE (400 mg/kg/day) & VC (200 mg/kg/day) along with NaAsO2. Marked histological alterations were evidenced by disorganization in oocyte, granulosa cells and zona pellucida layers in treated group. Considerable reduction of different growing follicles along with increased atretic follicles was noted in treated group. Altered activities ofΔ5 3β-Hydroxysteroid dehydrogenase and 17β-Hydroxysteroid dehydrogenase accompanied by reduced luteinizing hormone, follicle-stimulating hormone and estradiol levels were observed in treated animals. Irregular estrous cyclicity pattern was also observed due to NaAsO2 threat. Surplus ROS production affected ovarian antioxidant strata as evidenced by altered oxidative stress markers. Provoked oxidative strain further affects DNA status of ovary. However, supplementation with VEC caused notable restoration from such disparaging effects of NaAsO2 toxicities. Antioxidant and antiapoptotic attributes of those vitamins might be liable for such restoration.
![](http://media.springernature.com/m312/springer-static/image/art%3A10.1007%2Fs00210-023-02491-9/MediaObjects/210_2023_2491_Fig1_HTML.png)
![](http://media.springernature.com/m312/springer-static/image/art%3A10.1007%2Fs00210-023-02491-9/MediaObjects/210_2023_2491_Fig2_HTML.png)
![](http://media.springernature.com/m312/springer-static/image/art%3A10.1007%2Fs00210-023-02491-9/MediaObjects/210_2023_2491_Fig3_HTML.png)
![](http://media.springernature.com/m312/springer-static/image/art%3A10.1007%2Fs00210-023-02491-9/MediaObjects/210_2023_2491_Fig4_HTML.png)
![](http://media.springernature.com/m312/springer-static/image/art%3A10.1007%2Fs00210-023-02491-9/MediaObjects/210_2023_2491_Fig5_HTML.png)
![](http://media.springernature.com/m312/springer-static/image/art%3A10.1007%2Fs00210-023-02491-9/MediaObjects/210_2023_2491_Fig6_HTML.png)
![](http://media.springernature.com/m312/springer-static/image/art%3A10.1007%2Fs00210-023-02491-9/MediaObjects/210_2023_2491_Fig7_HTML.png)
![](http://media.springernature.com/m312/springer-static/image/art%3A10.1007%2Fs00210-023-02491-9/MediaObjects/210_2023_2491_Fig8_HTML.png)
![](http://media.springernature.com/m312/springer-static/image/art%3A10.1007%2Fs00210-023-02491-9/MediaObjects/210_2023_2491_Fig9_HTML.png)
![](http://media.springernature.com/m312/springer-static/image/art%3A10.1007%2Fs00210-023-02491-9/MediaObjects/210_2023_2491_Fig10_HTML.png)
Similar content being viewed by others
Data availability
The data sets generated and or analyzed during the study are included in the manuscript. The data that support this study will be shared upon reasonable request to the corresponding author.
References
Abercrombie M (1946) Estimation of nuclear population from microtome sections. Anat Rec 94:239–247. https://doi.org/10.1002/ar.1090940210
Abuja PM, Albertini R (2001) Methods for monitoring oxidative stress, lipid peroxidation and oxidation resistance of lipoproteins. Clin Chim Acta 306:1–17
Aguilar TAF, Navarro BCH, Pérez JAM (2016) Endogenous Antioxidants: A Review of their Role in Oxidative Stress. In: A Master Regulator of Oxidative Stress - The Transcription Factor Nrf2. pp 3–14
Allan AM, Hafez AK, Labrecque MT et al (2015) Sex-dependent effects of developmental arsenic exposure on methylation capacity and methylation regulation of the glucocorticoid receptor system in the embryonic mouse brain. Toxicol Reports 2:1376–1390. https://doi.org/10.1016/j.toxrep.2015.10.003
Almeida DAT, Braga CP, Novelli ELB, Fernandes AAH (2012) Evaluation of lipid profile and oxidative stress in STZ-induced rats treated with antioxidant vitamin. Brazilian Arch Biol Technol 55:527–536. https://doi.org/10.1590/S1516-89132012000400007
Aritonang TR, Rahayu S, Sirait LI et al (2017) The Role of FSH, LH, Estradiol and Progesterone Hormone on Estrus Cycle of Female Rats. Int J Sci Basic Appl Res 35:92–100
Asadi E, Jahanshahi M, Golalipour MJ (2012) Effect of Vitamin E on Oocytes Apoptosis in nicotine-treated Mice. Iran J Basic Med Sci 15:880–884
Ayinde OC, Ogunnowo S, Ogedegbe RA (2012) Influence of Vitamin C and Vitamin E on testicular zinc content and testicular toxicity in lead exposed albino rats. BMC Pharmacol Toxicol 13:3–8. https://doi.org/10.1186/2050-6511-13-17
Barai M, Ahsan N, Paul N et al (2017) Amelioration of arsenic-induced toxic effects in mice by dietary supplementation of Syzygium cumini leaf extract. Nagoya J Med Sci 79:167–177. https://doi.org/10.18999/nagjms.79.2.167
Baxley MN, Hood RD, Vedel GC et al (1981) Prenatal toxicity of orally administered sodium arsenite in mice. Bull Environ Contam Toxicol 26:749–756. https://doi.org/10.1007/BF01622166
Beers RF, Sizer IW (1952) A spectrophotometric method for measuring the breakdown of hydrogen peroxide by catalase. J Biol Chem 195:133–140. https://doi.org/10.1093/jxb/48.2.181
Bhardwaj, Jitender Kumar; Mittal, Meenu; Saraf, Priyanka; Sharma S (2022) Ameliorative potential of vitamin C and E against Roundup-glyphosate induced genotoxicity triggering apoptosis in caprine granulosa cells. Env Mol Mutagen. https://doi.org/10.1002/em.22497
Bhardwaj JK, Sharma RK (2011) Scanning electron microscopic changes in granulosa cells during follicular atresia in Caprine ovary. Scanning 33:21–24. https://doi.org/10.1002/sca.20217
Biswas S, Kumar Mukhopadhyay P (2020) Casein- and pea-enriched high-protein diet can take care of the reprotoxic effects of arsenic in male rats. Andrologia 52:e13560. https://doi.org/10.1111/and.13560
Biswas P, Mukhopadhyay A, Kabir SN, Mukhopadhyay PK (2019) High-Protein Diet Ameliorates Arsenic-Induced Oxidative Stress and Antagonizes Uterine Apoptosis in Rats. Biol Trace Elem Res 192:222–233. https://doi.org/10.1007/s12011-019-1657-2
Biswas B, Chakraborty A, Chatterjee D et al (2021) Arsenic exposure from drinking water and staple food (rice): A field scale study in rural Bengal for assessment of human health risk. Ecotoxicol Environ Saf 228:2–8. https://doi.org/10.1016/j.ecoenv.2021.113012
Boyland E, Chasseaud LF (1969) The role of glutathione and glutathione S-transferases in mercapturic acid biosynthesis. Adv Enzymol Relat Areas Mol Biol 32:173–219
Chaineau E, Binet S, Pol D et al (1990) Embryotoxic effects of sodium arsenite and sodium arsenate on mouse embryos in culture. Teratology 41:105–112. https://doi.org/10.1002/tera.1420410111
Channing CP, Kammerman S (1973) Characteristics of gonadotropin receptors of porcine granulosa cells during follicle maturation. Endocrinology 92:531–540. https://doi.org/10.1210/endo-92-2-531
Chatterjee A, Chatterji U (2010) Arsenic abrogates the estrogen-signaling pathway in the rat uterus. Reprod Biol Endocrinol 2:80. https://doi.org/10.1186/1477-7827-8-80
Chattopadhyay S, Ghosh S, Chaki S et al (1999) Effect of sodium arsenite on plasma levels of gonadotrophins and ovarian steroidogenesis in mature albino rats: Duration-dependent response. J Toxicol Sci 24:425–431. https://doi.org/10.2131/jts.24.5_425
Chattopadhyay S, Pal Ghosh S, Ghosh D, Debnath J (2003) Effect of dietary co-administration of sodium selenite on sodium arsenite-induced ovarian and uterine disorders in mature albino rats. Toxicol Sci 75:412–422
Chow CK, Reddy K, Tappel AL (1973) Effect of dietary vitamin E on the activities of the glutathione peroxidase system in rat tissues. J Nutr 103:618–624. https://doi.org/10.1093/jn/103.4.618
Chun SY, Eisenhauer KM, Minami S et al (1996) Hormonal Regulation of Apoptosis in Early Antral Follicles: Follicle-Stimulating Hormone as a Major Survival Factor. Endocrinology 137:1447–1456. https://doi.org/10.1210/endo.137.4.8625923
Das PC, Das KP, Bagchi K, Dey CD (1993) Evaluation of tissue ascorbic acid status in different hormonal states of female rat. Life Sci 52:1493–1498. https://doi.org/10.1016/0024-3205(93)90111-F
Das J, Ghosh J, Manna P, Sil PC (2010) Protective role of taurine against arsenic-induced mitochondria-dependent hepatic apoptosis via the inhibition of PKCδ-JNK pathway. PLoS One 5:e12602. https://doi.org/10.1371/journal.pone.0012602
Dash M, Dey A, Chattopadhyay S (2020) Mitigation of arsenic driven utero-ovarian malfunction and changes of apoptotic gene expression by dietary NAC. Ecotoxicol Environ Saf 199:110675. https://doi.org/10.1016/j.ecoenv.2020.110675
Deneke SM, Fanburg BL (1989) Regulation of cellular glutathione. Am J Physiol - Lung Cell Mol Physiol 257:163–173
Eruslanov E, Kusmartsev S (2010) Identification of ROS using oxidized DCFDA and flow-cytometry. Methods Mol Biol 594:57–72. https://doi.org/10.1007/978-1-60761-411-1_4
FAO) (2017) About FAO | Food and Agriculture Organization of the United Nations. In: Food Agric. Organ. United Nations
Fitzgerald MJT (1987) Anatomy and embryology of the laboratory rat. J Anat 153:256
Flora SJS, Pachauri V (2010) Chelation in metal intoxication. Int J Environ Res Public Health 7:2745–2788
Flora SJ, Kannan GM, Pant BP, Jaiswal DK (2002) Combined administration of oxalic acid, succimer and its analogue for the reversal of gallium arsenide-induced oxidative stress in rats. Arch Toxicol 76:269–276. https://doi.org/10.1007/s00204-002-0347-5
Gaeini AA, Rahnama N, Hamedinia MR (2006) Effects of vitamin E supplementation on oxidative stress at rest and after exercise to exhaustion in athletic students. J Sports Med Phys Fitness 46:458–461
Galmés S, Serra F, Palou A (2018) Vitamin E metabolic effects and genetic variants: A challenge for precision nutrition in obesity and associated disturbances. Nutrients 10:1919
Gao J, Lin H, Wang XJ et al (2010) Vitamin E supplementation alleviates the oxidative stress induced by dexamethasone treatment and improves meat quality in broiler chickens. Poult Sci 89:318–327. https://doi.org/10.3382/ps.2009-00216
Goralczyk K (2021) A review of the impact of selected anthropogenic chemicals from the group of endocrine disruptors on human health. Toxics 9:146. https://doi.org/10.3390/toxics9070146
Han SS, Rajaniemi HJ, Cho MI et al (1974) Gonadotropin receptors in rat ovarian tissue. II. Subcellular localization of lh binding sites by electron microscopic radioautography1. Endocrinology 95:589–598. https://doi.org/10.1210/endo-95-2-589
Handali S, Rezaei M (2021) Arsenic and weight loss: At a crossroad between lipogenesis and lipolysis. J Trace Elem Med Biol 68:126836. https://doi.org/10.1016/j.jtemb.2021.126836
He L, He T, Farrar S et al (2017) Antioxidants Maintain Cellular Redox Homeostasis by Elimination of Reactive Oxygen Species. Cell Physiol Biochem 44:532–553
Hemalatha P, Reddy AG, Reddy YR, Shivakumar P (2013) Evaluation of protective effect of N-acetyl cysteine on arsenic-induced hepatotoxicity. J Nat Sci Biol Med 4:393–395. https://doi.org/10.4103/0976-9668.116986
Holesh JE, Bass AN, Lord M (2022) Physiology, ovulation. In: StatPearls. StatPearls Publishing, Treasure Island
Hood RD (1972) Effects of sodium arsenite on fetal development. Bull Environ Contam Toxicol 7:216–222. https://doi.org/10.1007/BF01684401
Ishfaq Ahmad H, Bilal Bin Majeed M, Jabbar A et al (2021) Reproductive toxicity of arsenic: what we know and what we need to know? Environ Health. IntechOpen. https://doi.org/10.5772/intechopen.95379
Jain N, Chandramani S (2018) Arsenic poisoning- An overview. Indian J Med Spec 9:143–145. https://doi.org/10.1016/j.injms.2018.04.006
Jarabak J, Adams JA, Williams-Ashman HG, Talalay P (1962) Purification of a 17beta-hydroxysteroid dehydrogenase of human placenta and studies on its transhydrogenase function. J Biol Chem 237:345–357. https://doi.org/10.1016/s0021-9258(18)93926-8
Jaturakan O, Dissayabutra T, Chaiyabutr N et al (2017) Combination of vitamin E and vitamin C alleviates renal function in hyperoxaluric rats via antioxidant activity. J Vet Med Sci 79:896–903. https://doi.org/10.1292/jvms.17-0083
Jomova K, Jenisova Z, Feszterova M et al (2011) Arsenic: Toxicity, oxidative stress and human disease. J Appl Toxicol 31:95–107
Kadirvel R, Sundaram K, Mani S et al (2007) Supplementation of ascorbic acid and α-tocopherol prevents arsenic-induced protein oxidation and DNA damage induced by arsenic in rats. Hum Exp Toxicol 26:939–946. https://doi.org/10.1177/0960327107087909
Kang H-G, Jeong P-S, Kim MJ et al (2022) Arsenic exposure during porcine oocyte maturation negatively affects embryonic development by triggering oxidative stress-induced mitochondrial dysfunction and apoptosis. Toxicology 480. https://doi.org/10.1016/j.tox.2022.153314.
Karanth S, Yu WH, Walczewska A et al (2001) Ascorbic acid stimulates gonadotropin release by autocrine action by means of NO. Proc Natl Acad Sci U S A 98:11783–11788. https://doi.org/10.1073/pnas.191369398
Karvinen S, Juppi HK, Le G et al (2021) Estradiol deficiency and skeletal muscle apoptosis: Possible contribution of microRNAs. Exp Gerontol 147:111267. https://doi.org/10.1016/j.exger.2021.111267
Levine RL, Williams JA, Stadtman EP, Shacter E (1994) Carbonyl assays for determination of oxidatively modified proteins. Methods Enzymol 233:346–357. https://doi.org/10.1016/S0076-6879(94)33040-9
Lima AC, Jung M, Rusch J et al (2017) A standardized approach for multispecies purification of mammalian male germ cells by mechanical tissue dissociation and flow cytometry. J Vis Exp 2017:55913. https://doi.org/10.3791/55913
Lin JY, Selim MA, Shea CR et al (2003) UV photoprotection by combination topical antioxidants vitamin C and vitamin E. J Am Acad Dermatol 48:866–874. https://doi.org/10.1067/mjd.2003.425
Liu Y, Liu C, Li J (2020) Comparison of vitamin c and its derivative antioxidant activity: Evaluated by using density functional theory. ACS Omega 5:25467–25475. https://doi.org/10.1021/acsomega.0c04318
Liu P, Li R, Tian X et al (2021) Co-exposure to fluoride and arsenic disrupts intestinal flora balance and induces testicular autophagy in offspring rats. Ecotoxicol Environ Saf 222:1–10. https://doi.org/10.1016/j.ecoenv.2021.112506
Lopez SG, Luderer U (2004) Effects of cyclophosphamide and buthionine sulfoximine on ovarian glutathione and apoptosis. Free Radic Biol Med 36:1366–1377. https://doi.org/10.1016/j.freeradbiomed.2004.02.067
Luderer U, Kavanagh TJ, White CC, Faustman EM (2001) Gonadotropin regulation of glutathione synthesis in the rat ovary. Reprod Toxicol 15:495–504. https://doi.org/10.1016/S0890-6238(01)00157-5
Mahapatra D, Chandra AK (2017) Biphasic action of iodine in excess at different doses on ovary in adult rats. J Trace Elem Med Biol 39:210–220. https://doi.org/10.1016/j.jtemb.2016.10.006
Martin JP, Dailey M, Sugarman E (1987) Negative and positive assays of superoxide dismutase based on hematoxylin autoxidation. Arch Biochem Biophys 255:329–336. https://doi.org/10.1016/0003-9861(87)90400-0
Martínez-Castillo M, García-Montalvo EA, Arellano-Mendoza MG et al (2021) Arsenic exposure and non-carcinogenic health effects. Hum Exp Toxicol 40:S826–S850. https://doi.org/10.1177/09603271211045955
Meng L, Jan SZ, Hamer G et al (2018) Preantral follicular atresia occurs mainly through autophagy, while antral follicles degenerate mostly through apoptosis. Biol Reprod 99:853–863. https://doi.org/10.1093/biolre/ioy116
Min YN, Niu ZY, Sun TT et al (2018) Vitamin E and Vitamin C supplementation improves antioxidant status and immune function in oxidative-stressed breeder roosters by up-regulating expression of GSH-Px gene. Poult Sci 97:1238–1244. https://doi.org/10.3382/ps/pex417
Mitra K, Kundu SN, KhudaBukhsh AR (1999) Efficacy of a potentized homoeopathic drug (Arsenicum Album-30) in reducing toxic effects produced by arsenic trioxide in mice: II. On alterations in body weight, tissue weight and total protein. Complement Ther Med 7:157–165. https://doi.org/10.1016/S0965-2299(99)80055-7
Mondal S, Mukherjee S, Chaudhuri K et al (2013) Prevention of arsenic-mediated reproductive toxicity in adult female rats by high protein diet. Pharm Biol 51:1363–1371. https://doi.org/10.3109/13880209.2013.792846
Mondal R, Biswas S, Chatterjee A et al (2016) Protection against arsenic-induced hematological and hepatic anomalies by supplementation of Vitamin C and vitamin e in adult male rats. J Basic Clin Physiol Pharmacol 27:643–652. https://doi.org/10.1515/jbcpp-2016-0020
Mondal R, Mukhopadhyay A, Chattopadhyay A et al (2022) Ovarian follicular atresia and uterine toxicity after subchronic oral exposure of postpubertal rats to sodium arsenite. Comp Clin Path 31:597–612. https://doi.org/10.1007/s00580-022-03358-w
Murugesan P, Muthusamy T, Balasubramanian K, Arunakaran J (2007) Effects of vitamins C and E on steroidogenic enzymes mRNA expression in polychlorinated biphenyl (Aroclor 1254) exposed adult rat Leydig cells. Toxicology 232:170–182. https://doi.org/10.1016/j.tox.2007.01.008
Nath Barbhuiya S, Barhoi D, Giri S (2021) Impact of arsenic on reproductive health. Environ Health. IntechOpen. https://doi.org/10.5772/intechopen.101141
Navarro PAAS, Liu L, Keefe DL (2004) In Vivo Effects of Arsenite on Meiosis, Preimplantation Development, and Apoptosis in the Mouse. Biol Reprod 70:980–985. https://doi.org/10.1095/biolreprod.103.020586
Ohkawa H, Ohishi N, Yagi K (1979) Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Anal Biochem 95:351–358. https://doi.org/10.1016/0003-2697(79)90738-3
Ojo OA, Ojo AB, Awoyinka O et al (2018) Aqueous extract of Carica papaya Linn. roots potentially attenuates arsenic induced biochemical and genotoxic effects in Wistar rats. J Tradit Complement Med 8:324–334. https://doi.org/10.1016/j.jtcme.2017.08.001
Oliveira CPMS, Da Costa Gayotto LC, Tatai C et al (2003) Vitamin C and vitamin E in prevention of Nonalcoholic Fatty Liver Disease (NAFLD) in choline deficient diet fed rats. Nutr J 2:1–5. https://doi.org/10.1186/1475-2891-2-9
Ommati MM, Shi X, Li H et al (2020) The mechanisms of arsenic-induced ovotoxicity, ultrastructural alterations, and autophagic related paths: An enduring developmental study in folliculogenesis of mice. Ecotoxicol Environ Saf 204:110973. https://doi.org/10.1016/j.ecoenv.2020.110973
Paccola CC, Resende CG, Stumpp T et al (2013) The rat estrous cycle revisited: a quantitative and qualitative analysis. Anim Reprod 10:677–683
Pacier C, Martirosyan DM (2015) Vitamin C: Optimal dosages, supplementation and use in disease prevention. Funct Foods Heal Dis 5:89–107
Paglia DE, Valentine WN (1967) Studies on the quantitative and qualitative characterization of erythrocyte glutathione peroxidase. J Lab Clin Med 70:158–169
Pal P, De A, TaritRoychowdhury PKM (2022) Vitamin C and E supplementation can ameliorate NaF mediated testicular and spermatozoal DNA damages in adult Wistar rats. Biomarkers. https://doi.org/10.1080/1354750X.2022.2048891
Pinchoff J, Monseur B, Desai S et al (2022) Is living in a region with high groundwater arsenic contamination associated with adverse reproductive health outcomes? An analysis using nationally representative data from India. Int J Hyg Environ Health 239:113883. https://doi.org/10.1016/j.ijheh.2021.113883
Raghu HM, Nandi S, Reddy SM (2002) Follicle size and oocyte diameter in relation to developmental competence of buffalo oocytes in vitro. Reprod Fertil Dev 14:55–61. https://doi.org/10.1071/RD01060
Rahman I, Kode A, Biswas SK (2007) Assay for quantitative determination of glutathione and glutathione disulfide levels using enzymatic recycling method. Nat Protoc 1:3159–3165. https://doi.org/10.1038/nprot.2006.378
Ramanathan K, Balakumar BS, Panneerselvam C (2002) Effects of ascorbic acid and α-tocopherol on arsenic-induced oxidative stress. Hum Exp Toxicol 21:675–680
Rizvi S, Raza ST, Ahmed F et al (2014) The role of Vitamin E in human health and some diseases. Sultan Qaboos Univ Med J 14:e157-165
Rössig L, Hoffmann J, Hugel B et al (2001) Vitamin C inhibits endothelial cell apoptosis in congestive heart failure. Circulation 104:2182–2187. https://doi.org/10.1161/hc4301.098284
Royack GA, Nguyen MP, Tong DC et al (2000) Response of human oral epithelial cells to oxidative damage and the effect of vitamin E. Oral Oncol 36:37–41. https://doi.org/10.1016/S1368-8375(99)00047-0
Ryan RJ, Lee CY (1976) The role of membrane bound receptors. Biol Reprod 14:16–29. https://doi.org/10.1095/biolreprod14.1.16
Sahin K, Kucuk O (2001) Effects of vitamin C and vitamin E on performance, digestion of nutrients and carcass characteristics of Japanese quails reared under chronic heat stress (34 °C). J Anim Physiol Anim Nutr (berl) 85:335–341. https://doi.org/10.1046/j.1439-0396.2001.00339.x
Seif M, Abd El-Aziz T, Sayed M, Wang Z (2021) Zingiber officinale ethanolic extract attenuates oxidative stress, steroidogenic gene expression alterations, and testicular histopathology induced by sodium arsenite in male rats. Environ Sci Pollut Res 28:19783–19798. https://doi.org/10.1007/s11356-020-11509-1
Sezer Z, EkizYilmaz T, Gungor ZB et al (2020) Effects of vitamin E on nicotine-induced lipid peroxidation in rat granulosa cells: Folliculogenesis. Reprod Biol 20:63–74. https://doi.org/10.1016/j.repbio.2019.12.004
Shaji E, Santosh M, Sarath KV et al (2021) Arsenic contamination of groundwater: A global synopsis with focus on the Indian Peninsula. Geosci Front 12:101079. https://doi.org/10.1016/j.gsf.2020.08.015
Shen J, Griffiths PT, Campbell SJ et al (2021) Ascorbate oxidation by iron, copper and reactive oxygen species: review, model development, and derivation of key rate constants. Sci Rep 11:7417. https://doi.org/10.1038/s41598-021-86477-8
Shih YH, Islam T, Hore SK et al (2017) Associations between prenatal arsenic exposure with adverse pregnancy outcome and child mortality. Environ Res 158:456–461. https://doi.org/10.1016/j.envres.2017.07.004
Sinha M, Manna P, Sil PC (2008) Protective effect of arjunolic acid against arsenic-induced oxidative stress in mouse brain. J Biochem Mol Toxicol 22:15–26. https://doi.org/10.1002/jbt.20209
Singh NP (1998) A rapid method for the preparation of single-cell suspensions from solid tissues. Cytometry 31:229–32. https://doi.org/10.1002/(SICI)1097-0320(19980301)31:3<229::AID-CYTO10>3.0.CO;2-T
Srinivasan M, Sabarinathan A, Geetha A et al (2017) Pharmacology & Clinical Research A Comparative Study on Staining Techniques for Vaginal Exfoliative Cytology of Rat. J Pharmacol Clin Res 3:55615. https://doi.org/10.19080/JPCR.2017.03.555615r
Susko ML, Bloom MS, Neamtiu IA et al (2017) Low-level arsenic exposure via drinking water consumption and female fecundity - A preliminary investigation. Environ Res 154:120–125. https://doi.org/10.1016/j.envres.2016.12.030
Tam LM, Price NE, Wang Y (2020) Molecular Mechanisms of Arsenic-Induced Disruption of DNA Repair. Chem Res Toxicol 33:709–726
Tazari M, Baghshani H, Moosavi Z (2018) Effect of betaine versus arsenite-induced alterations of testicular oxidative stress and circulating androgenic indices in rats. Andrologia 50:e13091. https://doi.org/10.1111/and.13091
Tian Y, Shen W, Lai Z et al (2015) Isolation and identification of ovarian theca-interstitial cells and granulose cells of immature female mice. Cell Biol Int 39:584–590. https://doi.org/10.1002/cbin.10426
Traber MG (2004) Vitamin E, nuclear receptors and xenobiotic metabolism. Arch Biochem Biophys 423:6–11
Traber MG (2013) Mechanisms for the prevention of vitamin e excess. J Lipid Res 54:2295–2306
Traber MG, Stevens JF (2011) Vitamins C and E: Beneficial effects from a mechanistic perspective. Free Radic Biol Med 51:1000–1013
Underwood BR, Imarisio S, Fleming A et al (2010) Antioxidants can inhibit basal autophagy and enhance neurodegeneration in models of polyglutamine disease. Hum Mol Genet 19:3413–3429. https://doi.org/10.1093/hmg/ddq253
Usoh IF, Akpan EJ, Etim EO, Farombi EO (2005) Antioxidant Actions of Dried Flower Extracts of Hibiscus sabdariffa L. On Sodium Arsenite - Induced Oxidative Stress in Rats. Pakistan J Nutr 4:135–141. https://doi.org/10.3923/pjn.2005.135.141
Vahter M, Concha G (2008) Role of Metabolism in Arsenic Toxicity. Pharmacol Toxicol 89:1–5. https://doi.org/10.1111/j.1600-0773.2001.890101.x
Valk EEJ, Hornstra G (2000) Relationship between vitamin E requirement and polyunsaturated fatty acid intake in man: A review. Int J Vitam Nutr Res 70:31–42
Wang X, Quinn PJ (2000) The location and function of vitamin E in membranes (Review). Mol Membr Biol 17:143–156
Wang W, Gong Y, Greenfield BK et al (2021) Relative contribution of rice and fish consumption to bioaccessibility-corrected health risks for urban residents in eastern China. Environ Int 155:106682. https://doi.org/10.1016/j.envint.2021.106682
WHO (2011) Arsenic in drinking-water. Background document for development of WHO Guidelines for Drinking-water Quality. WHO/SDE/WSH/03.04/75/Rev/1 Arsenic
Wyllie AH, Kerr JFR, Currie AR (1980) Cell Death: The Significance of Apoptosis. Int Rev Cytol 68:251–306. https://doi.org/10.1016/S0074-7696(08)62312-8
Zhang X, Zhou C, Li W, et al (2020) Vitamin C Protects Porcine Oocytes From Microcystin-LR Toxicity During Maturation. Front Cell Dev Biol 8. https://doi.org/10.3389/fcell.2020.582715
Acknowledgements
The authors would like to acknowledge Dr. Souryadeep Mukherjee, Department of Life Sciences, Presidency University and Dr. Sumit Mandal, Department of Life Sciences, Presidency University for their help.
Funding
This work was supported by the grant received from Department of Higher Education, Science & Technology and Biotechnology, Government of West Bengal (No. 265(Sanc.) / ST/ P/ S&T/1G-44/2017 dated 25.03.2018). Authors also would like to acknowledge the DST-FIST and DBT BUILDERS grant of the Government of India and FRPDF grant of Presidency University.
Author information
Authors and Affiliations
Contributions
The authors declare that all data were generated in-house and that no paper mill was used. All authors contributed to the study design and experiments. Conceived and designed the experiments: RM, AM, and PKM. Performed the experiments: RM, PP and SB. Analysed the data: RM, PP, SB, AC, AB, AM, and PKM. Wrote the paper: RM. Overall manuscript checked: RM, PP, SB, AC, AB, AM, and PKM. Manuscript critically checked: RM, PP, PKM. Final approval was given by all the authors.
Corresponding author
Ethics declarations
Competing interests
The authors declare no competing interests.
Ethics approval
The experiments were performed following the national guidelines implemented by the Committee for the Purpose of Control and Supervision of Experiments on Animals, India, with approval from the Animal Ethics Committee of Presidency University (Sanction number: PU/IAEC/PM/12).
Consent to participate
Not applicable.
Consent for publication
Not applicable.
Conflict of interest
The authors declare no competing interests.
Additional information
Publisher's note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.
About this article
Cite this article
Mondal, R., Pal, P., Biswas, S. et al. Attenuation of sodium arsenite mediated ovarian DNA damage, follicular atresia, and oxidative injury by combined application of vitamin E and C in post pubertal Wistar rats. Naunyn-Schmiedeberg's Arch Pharmacol 396, 2701–2720 (2023). https://doi.org/10.1007/s00210-023-02491-9
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00210-023-02491-9