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Association of Vitamin B12, Lactate Dehydrogenase, and Regulation of NF-κB in the Mitigation of Sodium Arsenite-Induced ROS Generation in Uterine Tissue by Commercially Available Probiotics

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Abstract

Managing arsenic intoxication with conventional metal chelators is a global challenge. The present study demonstrated the therapeutic role of probiotics against arsenic-induced oxidative stress and female reproductive dysfunction. Sodium arsenite-treated (1.0 mg/100 g body weight) Wistar female rats were followed up by a post-treatment of commercially available probiotic mixture in powder form (0.25 mg/100 g body weight) orally. Rats that experienced arsenic ingestion showed a significant lessening in the activities of uterine superoxide dismutase (SOD), catalase activities, and the level of non-protein soluble thiol (NPSH) with a concomitant increase in malondialdehyde (MDA) and conjugated dienes (CD). Exposure to arsenic significantly lowered the levels of vitamin B12 and estradiol. Exposure to arsenic highly expressed the inflammatory marker and transcription factor NF-κB. Arsenic-mediated instability of these above parameters was controlled by the probiotics with a rebuilding of better function of anti-oxidant components. Besides its function in regulating endogenous anti-oxidant system, probiotics were able to augment the protection against mutagenic uterine DNA-breakage, necrosis, and ovarian-uterine tissue damages in arsenicated rats.

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References

  1. Erlenkeuser HE, Willkomm SH (1974) Industrialization affects heavy metal and carbon isotope concentrations in recent Baltic Sea sediments. Geochim Cosmochim Acta 38:823–842

    CAS  Google Scholar 

  2. Tseng CH, Tseng CP, Chiou HY, Hsueh YM, Chong CK, Chen CJ (2002) Epidemiologic evidence of diabetogenic effect of arsenic. Toxicol Lett 133:69–76

    CAS  PubMed  Google Scholar 

  3. Goebel HH, Schmidt PF, Bohl J, Tettenborn B, Kramer G, Gutmann L (1990) Polyneuropathy due to acute arsenic intoxication: biopsy studies. J Neuropathol Exp Neurol 49:137–149

    CAS  PubMed  Google Scholar 

  4. Neiger RD, Osweiler GD (1989) Effect of sub-acute low level dietary sodium arsenite on dogs. Fundam Appl Toxicol 13:439–451

    CAS  PubMed  Google Scholar 

  5. Pant N, Shankar R, Srivastava SP (1997) In utero and lactational exposure of carbofuran to rats: effect on testes and sperm. Hum ExpToxicol 16:267–272

    CAS  Google Scholar 

  6. Pant N, Murthy RC, Srivastava SP (2004) Male reproductive toxicity of sodium arsenite in mice. Hum ExpToxicol 23:399–403

    CAS  Google Scholar 

  7. Biswas R, Poddar S, Mukherjee A (2007) Investigation on the genotoxic effects of long-term administration of sodium arsenite in bone marrow and testicular cells in vivo using the comet assay. J Environ Pathol Toxicol Oncol 26:29–37

    CAS  PubMed  Google Scholar 

  8. Sarkar M, Chaudhuri GR, Chattopadhyay A, Biswas NM (2003) Effect of sodium arsenite on spermatogenesis, plasma gonadotrophins and testosterone in rats. Asian J Androl 5:27–31

    CAS  PubMed  Google Scholar 

  9. Helleday T, Nilsson R, Jenssen D (2000) Arsenic [III] and heavy metal ions induce intrachromosomal homologous recombination in the hprt gene V79 Chinese hamster cells. Environ Mol Mutage 35:114–122

    CAS  Google Scholar 

  10. Zadorozhnaja TD, Little RE, Miller RK, Mendel NA, Taylor RJ, Presley BJ, Gladen BC (2000) Concentrations of arsenic, cadmium, copper, lead, mercury, and zinc in human placentas from two cities in Ukraine. J Toxicol Environ Health A 61:255–263

    CAS  PubMed  Google Scholar 

  11. Yang CY, Chang CC, Tsai SS, Chuang HY, Ho CK, TN W (2003) Arsenic in drinking water and adverse pregnancy outcome in an arseniasis-endemic area in northeastern Taiwan. Environ Res 91:29–34

    PubMed  Google Scholar 

  12. Ahmad SA, Sayed MH, Barua S, Khan MH, Faruquee MH, Jalil A, Hadi SA, Talukder HK (2001) Arsenic in drinking water and pregnancy outcomes. Environ Health Perspect 109:629–631

    CAS  PubMed  PubMed Central  Google Scholar 

  13. Chattopadhyay S, Ghosh D (2010) The involvement of hypophyseal-gonadal and hypophyseal-adrenal axes in arsenic-mediated ovarian and uterine toxicity modulation by hCG. J BiochemMolToxicol 24:29–41

    CAS  Google Scholar 

  14. Vahter M (2009) Effects of arsenic on maternal and fetal health. Annu Rev Nutr 29:381–399

    CAS  PubMed  Google Scholar 

  15. He W, Greenwell RJ, Brooks DM, Calderón-Garcidueñas L, Beall HD, Coffin JD (2007) Arsenic exposure in pregnant mice disrupts placental vasculogenesis and causes spontaneous abortion. Toxicol Sci 99:244–253

    CAS  PubMed  Google Scholar 

  16. Ahmed S, Mahabbat-e Khoda S, Rekha RS, Gardner RM, Ameer SS, Moore S, Ekström EC, Vahter M, Raqib R (2011) Arsenic-associated oxidative stress, inflammation, and immune disruption in human placenta and cord blood. Environ Health Perspect 119:258–264

    CAS  PubMed  Google Scholar 

  17. Parajuli RP, Umezaki M, Fujiwara T, Watanab C (2013) Association of cord blood levels of lead, arsenic, and zinc with neurodevelopmental indicators in newborns: a birth cohort study in Chitwan Valley, Nepal. Environ Res 121:45–51

    CAS  PubMed  Google Scholar 

  18. Chattopadhyay S, Ghosh D (2010) Role of dietary GSH in the amelioration of sodium arsenite-induced ovarian and uterine disorders. Reprod Toxicol 30:481–488

    CAS  PubMed  Google Scholar 

  19. Xie Y, Liu J, Tallaa LB, Ward JM, Logsdon D, Diwan BA (2007) Aberrant DNA methylation and gene expression in livers of newborn mice transplacentally exposed to a hepatocarcinogenic dose of inorganic arsenic. Toxicology 236:7–15

    CAS  PubMed  Google Scholar 

  20. Alarifi S, Ali D, Alkahtani S, Siddiqui MA, Ali BA (2013) Arsenic trioxide-mediated oxidative stress and genotoxicity in human hepatocellular carcinoma cells. Onco Targets Ther 6:75–84

    CAS  PubMed  PubMed Central  Google Scholar 

  21. Inns RH, Rice P, Bright JE, Marrs TC (1990) Evaluation of the efficacy of dimercapto chelating agents for the treatment of systemic organic arsenic poisoning in rabbits. Hum ExpToxicol 9:215–220

    CAS  Google Scholar 

  22. Flora SJ, Bhadauria S, Kannan GM, Singh N (2007) Arsenic induced oxidative stress and the role of antioxidant supplementation during chelation: a review. J Environ Biol 28:333–347

    CAS  PubMed  Google Scholar 

  23. Maiti S, Chattopadhyay S, Acharyya N, Deb B, Hati A (2013) Emblica officinalis (amla) ameliorates arsenic-induced liver damage via DNA protection by antioxidant systems. Mol Cell Toxicology 9:000–000

    Google Scholar 

  24. Bhattacharjee S, Pal S (2014) Additive protective effects of selenium and vitamin E against arsenic induced lipidemic and cardiotoxic effects in mice. Int J Pharm Pharm Sci 4:406–413

    Google Scholar 

  25. Chattopadhyay S, Misro M, Debnath J, Ghosh D (2000) Supplementary effect of Α-tocopherol succinate (vitamin e) on sodium arsenite-induced ovarian steroidogenic function and plasma levels of gonadotrophins in mature albino rats. Toxic Substance Mechanisms 19:137–150

    CAS  Google Scholar 

  26. Chattopadhyay S, Pal S, Ghosh D, Debnath J (2003) The 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

    CAS  PubMed  Google Scholar 

  27. Perveen H, Dash M, Khatun S, Maity M, Islam SS, Chattopadhyay S (2017) Electrozymographic evaluation of the attenuation of arsenic induced degradation of hepatic SOD, catalase in an in vitro assay system by pectic polysaccharides of Momordica charantia in combination with curcumin. Biochemistry and Biophysics Reports 11:64–71

    PubMed  PubMed Central  Google Scholar 

  28. Chattopadhyay S, Maiti S, Maji J, Deb B, Pan B, Ghosh D (2011) Protective role of Moringa oleifera (Sajina) seed on arsenic-induced hepatocellular degeneration in female albino rats. Biol Trace Elem Res 142:200–212

    CAS  PubMed  Google Scholar 

  29. Maity M, Perveen H, Dash M, Jana S, Khatun S, Dey A, Mandal AK, Chattopadhyay S (2017) Arjunolic acid improves the serum level of vitamin B12 and folate in the process of the attenuation of arsenic induced 6 uterine oxidative stress. Biol Trace Elem Res

  30. O’Sullivan MG, Thornton G, O’Sullivan GC, Collins JK (1992) Probiotic bacteria: myth or reality. Trends Food Sci Technol 3:309–314

    Google Scholar 

  31. Cammarota M, De Rosa M, Stellavato A, Lamberti M, Marzaioli I, Giuliano M (2009) In vitro evaluation of Lactobacillus plantarum (DSMZ) 12028 as a probiotic: emphasis on innate immunity. Int J Food Microbiol 135:90–98

    CAS  PubMed  Google Scholar 

  32. Amara A (2012) In: Amara A (ed) Toward healthy genes. Germany, Schuling Verlage

    Google Scholar 

  33. Marteau P, Seksik P, Jian R (2002) Probiotics and intestinal health effects: a clinical perspective. Br J Nutr 88:S51–S57

    CAS  PubMed  Google Scholar 

  34. He T, Priebe M, Zhong Y, Huang C, Harmsen H, Raangs G, Antoine J, Wellingand G, Vonk R (2008) Effects of yogurt and bifidobacteria supplementation on the colonic microbiota in lactose-intolerant subjects. J Appl Microbiol 104:595–604

    CAS  PubMed  Google Scholar 

  35. De Vrese M, Stegelmann A, Richter B, Fenselau S, Laue C, Schrezenmeir J (2001) Probiotics-compensation for lactase insufficiency. The American Journal of Clinical Nutrition 73:421–429

    Google Scholar 

  36. Jain S, Yadav H, Sinha P, Kapila S, Naito Y, Marotta F (2010) Anti-allergic effects of probiotic Dahi through modulation of the gut immune system. Turkish Journal of Gastroenterology 21:244–250

    Google Scholar 

  37. Chen X, Fruehauf J, Goldsmith J, Xu H, Katchar K, Koon H, Zhao D, Kokkotou E, Pothoulakis C, Kelly C (2009) Saccharomyces boulardii inhibits EGF receptor signaling and intestinal tumor growth in Apc(min) mice. Gastroenterology 137:914–923

    CAS  PubMed  Google Scholar 

  38. Baroutkoub A, Mehdi R, Beglarian R, Hassan J, Zahra S, Mohammad M, Mohammad hadi E (2010) Effects of probiotic yoghurt consumption on the serum cholesterol levels in hypercholestromic cases in Shiraz, Southern Iran. Sci Res Essays 5:2206–2209

    Google Scholar 

  39. Koller VJ, Marian B, Stidl R, Nersesyan A, Winter H, Simić T, Sontag G, Knasmüller S (2008) Impact of lactic acid bacteria on oxidative DNA damage in human derived colon cells. Food Chem Toxicol 46:1221–1229

    CAS  PubMed  Google Scholar 

  40. Bhakta JN, Ohnishi K, Munekage Y, Iwasaki K, Wei MQ (2012) Minireview characterization of lactic acid bacteria-based probiotics as potential heavy metal sorbents. J Appl Microbiol 112:1193–1206

    CAS  PubMed  Google Scholar 

  41. Stidl R, Sontag G, Koller V, Knasmüller S (2008) Binding of heterocyclic aromatic amines by lactic acid bacteria: results of a comprehensive screening trial. Mol Nutr Food Res 52:322–329

    CAS  PubMed  Google Scholar 

  42. Lin MY, Yen CL (1999) Antioxidative ability of lactic acid bacteria. J Agric Food Chem 47:1460–1466

    CAS  PubMed  Google Scholar 

  43. Wang J, Tang H, Zhang C, Zhao Y, Derrien M, Rocher E, van-Hylckama Vlieg JE, Strissel K, Zhao L, Obin M et al (2015) Modulation of gut microbiota during probiotic-mediated attenuation of metabolic syndromein high fat diet-fed mice. ISME J 9:1–15

    PubMed  Google Scholar 

  44. Rad AH, Sahhaf F, Hassanalilou T, Ejtahed HS, Motayagheni N, Soroush AR, Javadi M, Mortazavian AM, Khalili L (2016) Diabetes management by probiotics: current knowledge and future perspectives. Curr Diabetes Rev

  45. Gomes AC, Bueno AA, de Souza RG, Mota JF (2014) Gut microbiota, probiotics and diabetes. Nutr J 13:60

    PubMed  PubMed Central  Google Scholar 

  46. Stecchini ML, Del Torre M, Munari M (2001) Determination of peroxy radical-scavenging of lactic acid bacteria. Int J Food Microbiol 64:183–188

    CAS  PubMed  Google Scholar 

  47. Kullisaar T, Zilmer M, Mikelsaar M, Vihalemm T, Annuk H, Kairane C, Kilk A (2002) Two antioxidative lactobacilli strains as promising probiotics. Int J Food Microbial 72:215–224

    CAS  Google Scholar 

  48. Martarelli D, Verdenelli MC, Scuri S, Cocchioni M, Silvi S, Cecchini C, Pompei P (2011) Effect of aprobiotic intake on oxidant and antioxidant parameters in plasma of athletes during intense exercise training. Curr Microbiol 62:1689–1696

    CAS  PubMed  Google Scholar 

  49. Devasagayam TPA, Boloor KK (2003) Methods for estimating lipid peroxidation: an analysis of merits and demerits. Ind. J Bioche Biophys 40:300–308

    CAS  Google Scholar 

  50. Kumar A (2012) Effect of simuastation on paraxonase 1 (PON1) activity and oxidation stress. In: Kumar A (ed) Significance of lipid profile assay as diagnostic and prognostic tool. CreateSpace Independent Publishing Platform, California, pp 105–109

    Google Scholar 

  51. Pattichis KI, Louca LL, Glover V (1994) Quantitation of soluble superoxide dismutase in rat striata, based on the inhibition of nitrite formation from hydroxylammonium chloride. Anal Biochem 221:428–431

    CAS  PubMed  Google Scholar 

  52. Hadwan MH (2016) New method for assessment of serum catalase activity. Indian Journal of Science and Technology 9:1–5

    CAS  Google Scholar 

  53. Sadasivan S, Manickam A (1966) Peroxidase. In: Sadasivan S, Manickam A (eds) Methods in biochemistry. New Age International Publishers, New Delhi, pp 108–110

    Google Scholar 

  54. Forman HJ (2009) Critical methods in free radical biology & medicine. Free Radic Biol Med 47:207

    Google Scholar 

  55. Mieyal JJ, Gallogly MM, Qanungo S, Sabens EA, Shelton MD (2008) Molecular mechanisms and clinical implications of reversible protein S-glutathionylation. Antioxid Redox Signal 10:1941–1988

    CAS  PubMed  PubMed Central  Google Scholar 

  56. Weydert CJ, Cullen JJ (2010) Measurement of superoxide dismutase, catalase and glutathione peroxidase in cultured cells and tissue. Nat Protoc 5:51–66

    CAS  PubMed  Google Scholar 

  57. Lewis A, Du J, Liu J, Ritchie JM, Oberley LW, Cullen JJ (2006) Metastatic progression of pancreatic cancer: zhanges in antioxidant enzymes and cell growth. Clin Exp Metastasis 22:523–532

    Google Scholar 

  58. Hasan HR, Aburahma NA (2012) Electrophoresis profile of total peroxidases in sera and saliva of patients with different oral tumors. Orient J Chem 30:81–86

    Google Scholar 

  59. Brandt RB, Laux JE, Spainhour SE, Kline ES (1987) Lactate dehydrogenase in rat mitochondria. Arch Biochem Biophys 259:412–422

    CAS  PubMed  Google Scholar 

  60. Sing NP, McCoy MT, Tice RR, Schneider EL (1988) A simple technique for quantitation of low levels of DNA damage in individual cells. Exp Cells Res 175:184–191

    Google Scholar 

  61. Zar JH (2010) One sample hypothesis. In: Zar JH (ed) Biostatistical analysis, 5th edn. Prentice Hall, New Jersey, pp 93–98

    Google Scholar 

  62. Kirkman HN, Gaetani GF (1984) Catalase: a tetrameric enzyme with four tightly bound molecules of NADPH. Proc Natl Acad Sci USA 81:4343–4347

    CAS  PubMed  PubMed Central  Google Scholar 

  63. Kono Y, Fridovich I (1982) Superoxide radical inhibits catalase. J Biol Chem 257:5751–5754

    CAS  PubMed  Google Scholar 

  64. Maiti S, Chattopadhyay S, Deb B, Samanta T, Maji G, Pan B, Ghosh A, Ghosh D (2012) Antioxidant and metabolic impairment result in DNA damage in arsenic-exposed individuals with severe dermatological manifestations in Eastern India. Environ Toxicol 27:342–350

    CAS  PubMed  Google Scholar 

  65. Rana T, Bera AK, Das S, Bhattacharya D, Pan D, Das SK (2012) Metabolic adaptations to arsenic-induced oxidative stress in male Wistar rats. J Biochem MolToxicol 26:109–116

    CAS  Google Scholar 

  66. Christine J, Weydert J, Cullen J (2010) Measurement of superoxide dismutase, catalase, and glutathione peroxidase in cultured cells and tissue. Nat Protoc 5: 51–66

  67. Zhang J, Yao YH, Li BG, Yang Q, Zhang PY, Wang HT (2015) Prognostic value of pretreatment serum lactate dehydrogenase level in patients with solid tumors, a systematic review and meta-analysis. Sci Rep 5:9800

    CAS  PubMed  PubMed Central  Google Scholar 

  68. Corsini E, Luster MI, Mahler J, Craig WA, Blazka ME, Rosenthal GJ (1994) A protective role for T lymphocytes in asbestos-induced pulmonary inflammation and collagen deposition. Am J Respir Cell Mol Biol 11:531–539

    CAS  PubMed  Google Scholar 

  69. Kottmann RM, Kulkarni AA, Smolnycki KA, Lyda E, Dahanayake T, Salibi R, Honnons S, Jones C, Isern NG, JZ H, Nathan SD, Grant G, Phipps RP, Sime PJ (2012) Lactic acid is elevated in idiopathic pulmonary fibrosis and induces myofibroblast differentiation via pH-dependent activation of transforming growth factor-β. Am J Respir Crit Care Med 186:740–751

    CAS  PubMed  PubMed Central  Google Scholar 

  70. Keskin EY, Keskin M (2015) Severe vitamin B12 deficiency in a 15-year-old boy, presentation with haemolysis and pancytopenia. BMJ Case Rep. https://doi.org/10.1136/bcr-2015-209718

  71. Edman CD (1983) The effect of steroid on endometrium. Semin Reprod Endocrinol 1:179–187

    Google Scholar 

  72. Kulin HE, Reiter EO (1973) Gonadotrophins during childhood and adolescence. A review. Pediatrics 51:260–271

    CAS  PubMed  Google Scholar 

  73. Chatterjee A, Chatterji U (2010) Arsenic abrogates the estrogen-signaling pathway in the rat uterus. Reprod Biol Endocrinol 8:80–90

    PubMed  PubMed Central  Google Scholar 

  74. Acharyya N, Deb B, Chattopadhyay S, Maiti S (2015) Arsenic induced antioxidant depletion, oxidative DNA breakage, and tissue damages are prevented by the combined action of folate and vitamin B12. Biol Trace Elem 168:122–132

    CAS  Google Scholar 

  75. Manna P, Sinha M, Sil PC (2007) Protection of arsenic-induced hepatic disorder by arjunolic acid. Basic Clin Pharmacol Toxicol 101:333–338

    CAS  PubMed  Google Scholar 

  76. 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

    CAS  PubMed  Google Scholar 

  77. Felix K, Manna SK, Wise K, Barr J, Ramesh GT (2005) Low levels of arsenite activates nuclear factor-κB and activator protein-1 in immortalized mesencephalic cells. J Biochem Mol Toxicol 19:67–77

    CAS  PubMed  PubMed Central  Google Scholar 

  78. Gong X, Ivanov VN, Davidson MM, Hei TK (2014) Tetramethylpyrazine (TMP) protects against sodium arsenite-induced nephrotoxicity by suppressing ROS production, mitochondrial dysfunction, pro-inflammatory signaling pathways and programmed cell death. Arch. Toxicology 89:1–14

    Google Scholar 

  79. Nishi T, Shimizu N, Hiramoto M (2002) Spatial redox regulation of a critical cysteine residue of NF-κB in vivo. J Biol Chem 277:44548–44556

    CAS  PubMed  Google Scholar 

  80. Chen F, Castranova V, Shi X (2001) New insights into the role of nuclear factor-κB in cell growth regulation. Am J Pathol 159:387–397

    CAS  PubMed  PubMed Central  Google Scholar 

  81. Baldwin AS Jr (1996) The NF-κB and IκB proteins: new discoveries and insights. Annu Rev Immunol 14:649–683

  82. Li M, Cai JF, Chiu JF (2002) Arsenic induces oxidative stress and activates stress gene expressions in cultured lung epithelial cells. J Cell Biochem 87:29–38

    CAS  PubMed  Google Scholar 

  83. Kligerman AD, Doerr CL, Tennant AH, Harrington Brock K, Allen JW, Winkfield E, Poorman Allen P, Kundu B, Funasaka K, Roop BC, Mass MJ, De Marini DM (2003) Methylated trivalent arsenicals as candidate ultimate genotoxic forms of arsenic, induction of chromosomal mutations but not gene mutations. Environ Mol Mutagen 42:192–205

    CAS  PubMed  Google Scholar 

  84. Salnikow K, Zhitkovich A (2008) Genetic and epigenetic mechanisms in metal carcinogenesis and cocarcinogenesis, nickel, arsenic, and chromium. Chem Res Toxicol 21:28–44

    PubMed  Google Scholar 

  85. Jomova K, Jenisova Z, Feszterova M, Baros S, Liska J, Hudecova D, Rhodes CJ, Valko M (2011) Arsenic toxicity, oxidative stress and human disease. J Appl Toxicol 31:95–107

    CAS  PubMed  Google Scholar 

  86. Zamora PL, Rockenbauer A, Villamena FA (2014) Radical model of arsenic III toxicity, theoretical and EPR spin trapping studies. Chem Res Toxicol 27:765–774

    CAS  PubMed  Google Scholar 

  87. Hey T, Filipic M (2004) Role of oxidative damage in the genotoxicity of arsenic. Free Radic Bio Med 37:574–581

    Google Scholar 

  88. Horst NL, Marques RG, Diestel CF, Matzke BD, Caetano CE, Simões FC, Andrade AF, Lobão WI, Vaz LC, Portela MC, Braga JU, Melo PA (2009) Effects of probiotic supplementation on markers of acute pancreatitis in rats. Curr Ther Res Clin Exp 70:136–148

    PubMed  PubMed Central  Google Scholar 

  89. Shen Q, Shang N, Li P (2011) In vitro and in vivo antioxidant activity of Bifidobacterium animalis 01 isolated from centenarians. Curr Microbiol 62:1097–1103

    CAS  PubMed  Google Scholar 

  90. Wang Y, Wu Y, Wang Y, Fu A, Gong L, Li W, Li Y (2016) Bacillus amyloliquefaciens SC06 alleviates the oxidative stress of IPEC-1 via modulating Nrf2/Keap1 signaling pathway and decreasing ROS production. Appl Microbiol Biotechnol 101:1–12

    CAS  Google Scholar 

  91. Petrof EO, Kojima K, Ropeleski MJ, Musch MW, Tao Y, De Simone C, Chang EB (2004) Probiotics inhibit nuclear factor-κB and induce heat shock proteins in colonic epithelial cells through proteasome inhibition. Gastroenterology 127:1474–1487

    CAS  PubMed  Google Scholar 

  92. Candela M et al (2008) Interaction of probiotic Lactobacillus and Bifidobacteriumstrains with human intestinal epithelial cells: adhesion properties, competition against enteropathogens and modulation of IL-8 production. Int. J Food Microbiol 125:286–292

    CAS  PubMed  Google Scholar 

  93. Lin PW, Myers LE, Ray L, Song SC, Nasr TR, Berardinelli AJ, Kundu K, Murthy N, Hansen JM, Neish AS (2009) Lactobacillus rhamnosus blocks inflammatory signaling in vivo via reactive oxygen species generation. Free Radic Biol Med 47:1205–1211

    CAS  PubMed  PubMed Central  Google Scholar 

  94. Kelly D, Campbell JI, King TP, Grant G, Jansson EA, Coutts AG, Pettersson S, Conway S (2004) Commensal anaerobic gut bacteria attenuate inflammation by regulating nuclear–cytoplasmic shuttling of PPAR-γ and RelA. Nat Immunol 5:104–112

    CAS  PubMed  Google Scholar 

  95. Kumar A, Wu H, Collier-Hyams LS, Hansen JM, Li T, Yamoah K, Pan ZQ, Jones DP, Neish AS (2007) Commensal bacteria modulate cullin-dependent signaling via generation of reactive oxygen species. EMBO J 26:4457–4466

    CAS  PubMed  PubMed Central  Google Scholar 

  96. Kumar M, Kumar A, Nagpal R, Mohania D, Behare P, Verma V, Kumar P, Poddar D, Aggarwal PK, Henry CJ, Jain S, Yadav H (2010) Cancer-preventing attributes of probiotics: an update. Int J Food Sci Nutr 61:473–496

    CAS  PubMed  Google Scholar 

  97. Nardone G, Compare D, Liguori E, Di Mauro V, Rocco A, Barone M, Napoli A, Lapi D, Iovene MR, Colantuoni A (2010) Protective effects of Lactobacillus paracasei F19 in a rat model of oxidative and metabolic hepatic injury. Am J Physiol Gastrointest Liver Physiol 299:G669–G676

    CAS  PubMed  Google Scholar 

  98. Azcárate-Peril MA, Sikes M, Bruno-Bárcena JM (2011) The intestinal microbiota, gastrointestinal environment and colorectal cancer: a putative role for probiotics in prevention of colorectal cancer? Am J Physiol Gastr L 301:G401–G424

    Google Scholar 

  99. Albert MJ, Mathan VI, Baker SJ (1980) Vitamin B12 synthesis by human small intestinal bacteria. Nature 283:781–782

    CAS  PubMed  Google Scholar 

  100. Taranto MP, Vera JL, Hugenholtz J, de Valdez GF, Sesma F (2003) Lactobacillus reuteri CRL1098 produces cobalamin. J Bacteriol 185:5643–5647

    CAS  PubMed  PubMed Central  Google Scholar 

  101. Lukic J, Strahinic I, Jovcic B, Filipic B, Topisirovic L, Kojic M, Begovic J (2012) Different roles of lactococcal aggregation factor and mucin binding protein in adhesion to gastrointestinal mucosa. Appl Environ Microbiol

  102. Tsirtsikos P, Fegeros K, Balaskas C, Kominakis A, Mountzouris KC (2012) Dietary probiotic inclusion level modulates intestinal mucin composition and mucosal morphology in broilers. Poult Sci 91:1860–1868

    CAS  PubMed  Google Scholar 

  103. Howarth GS (2010) Probiotic-derived factors: probiotaceuticals? J Nutr 140:229–230

    CAS  PubMed  Google Scholar 

  104. Ejtahed HS, Mohtadi-Nia J, Homayouni-Rad A, Niafar M, Asghari-Jafarabadi M, Mofid V (2012) Probiotic yogurt improves antioxidant status in type 2 diabetic patients. Nutrition 28:539–543

    CAS  PubMed  Google Scholar 

  105. Choi SS, Kim Y, Han KS, You S, Oh S, Kim SH (2006) Effects of Lactobacillus strains on cancer cell proliferation and oxidative stress in vitro. Lett Appl Microbiol 42:452–458

    CAS  PubMed  Google Scholar 

  106. Lee J, Hwang KT, Heo MS, Lee JH, Park KY (2005) Resistance of Lactobacillus plantarum KCTC 3099 from Kimchi to oxidative stress. J Med Food 8:299–304

    CAS  PubMed  Google Scholar 

  107. Forsyth CB, Farhadia A, Jakate SM, Tang YM, Shaikh M, Keshavarzian A (2009) Lactobacillus GG treatment ameliorates alcohol-induced intestinal oxidative stress, gut leakiness, and liver injury in a rat model of alcoholic steatohepatitis. Alcohol 43:163–172

    CAS  PubMed  PubMed Central  Google Scholar 

  108. Chen P, Zhang Q, Dang H, Liu X, Tian F, Zhao J, Chen Y, Zhang H, Chen W (2014) Screening for potential new probiotic based on probiotic properties and α-glucosidase inhibitory activity. Food Control 35:65–72

    Google Scholar 

  109. Bing SR, Kinouchi T, Kataoka K, Kuwahara T, Ohnishi Y (1998) Protective effects of a culture supernatant of Lactobacillus acidophilus and antioxidants on ileal ulcer formation in rats treated with a nonsteroidal antiinflammatory drug. Microbiol Immunol 42:745–753

    CAS  PubMed  Google Scholar 

  110. Liu H, Gao Y, LR Y, Jones RC, Elkins CA, Hart ME (2011) Inhibition of Staphylococcus aureus by lysostaphin-expressing Lactobacillus plantarum WCFS1 in a modified genital tract secretion medium. Appl Environ Microbiol 77:8500–8508

    CAS  PubMed  PubMed Central  Google Scholar 

  111. Reid G, Buerman D, Heinemann C, Bruce AW (2001) Probiotic Lactobacillus dose required to restore and maintain a normal vaginal flora. FEMS Immunol Med Microbiol 32:37–41

    CAS  PubMed  Google Scholar 

  112. Possemiers S, Verstraete W (2009) Oestrogenicity of prenylflavonoids from hops: activation of pro-oestrogens by intestinal bacteria. Environ Microbiol Rep 1(2):100–109. https://doi.org/10.1111/j.1758-2229.2009.00011.x

    Article  CAS  PubMed  Google Scholar 

  113. Lambert MNT, Thybo CB, Lykkeboe S, LM3 R, Frette X, Christensen LP, Jeppesen PB (2017) Combined bioavailable isoflavones and probiotics improve bone status and estrogen metabolism in postmenopausal osteopenic women: a randomized controlled trial. Am J Clin Nutr 106:909–920. https://doi.org/10.3945/ajcn.117.153353

  114. Anwar H, Rahman ZU (2016) Dynamics of anterior pituitary immunoreactive gonadotrophs in moulted hens supplemented with protein, symbiotic and probiotics. J Anim Physiol Anim Nutr (Berl) 100(3):448–455. https://doi.org/10.1111/jpn.12382

    Article  CAS  Google Scholar 

  115. Lin MY, Yen CL (1999) Antioxidative ability of lactic acid bacteria. Agric Food Chem 47:1460–1466

    CAS  Google Scholar 

  116. Kumar R, Kumari S, Kumari P, Kumar A, Ali M, Niraj PK, Ghosh A (2017) In vitro elimination of arsenic from water through Lactobacillus sporogenes. Eur J Pharma Med Res 4:581–585

    Google Scholar 

  117. Bisanz JE, Enos MK, Mwanga JR, Changalucha J, Burton JP, Gloor GB, Reid G (2014) Randomized open-label pilot study of the influence of probiotics and the gut microbiome on toxic metal levels in Tanzanian pregnant women and school children. MBio 5:e01580-14. https://doi.org/10.1128/mBio.01580-14

    Article  CAS  PubMed  PubMed Central  Google Scholar 

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Funding

This research was partially supported by a grant from UGC Maulana Azad National Fellowship (no. F1-17.1/2014-15/MANF-2014-15-MUS-WES-36088).

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Correspondence to Sandip Chattopadhyay.

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Chattopadhyay, S., Khatun, S., Maity, M. et al. Association of Vitamin B12, Lactate Dehydrogenase, and Regulation of NF-κB in the Mitigation of Sodium Arsenite-Induced ROS Generation in Uterine Tissue by Commercially Available Probiotics. Probiotics & Antimicro. Prot. 11, 30–42 (2019). https://doi.org/10.1007/s12602-017-9333-3

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