145
Views
0
CrossRef citations to date
0
Altmetric
Research Articles

Effects of catechin hydrate in benzo[a]pyrene-induced lung toxicity: roles of oxidative stress, apoptosis, and DNA damage

, , & ORCID Icon
Pages 467-475 | Received 14 Dec 2020, Accepted 08 Apr 2021, Published online: 23 May 2021

References

  • Aebi H. 1984. Catalase in vitro. Methods Enzymol. 105:121–126.
  • Ali R, Shahid A, Ali N, Hasan SK, Majed F, Sultana S. 2017. Amelioration of Benzo[a]pyrene-induced oxidative stress and pulmonary toxicity by Naringenin in Wistar rats: a plausible role of COX-2 and NF-κB. Hum Exp Toxicol. 36(4):349–364.
  • Almatroodi SA, Alrumaihi F, Alsahli MA, Alhommrani MF, Khan A, Rahmani AH. 2020. Curcumin, an active constituent of turmeric spice: implication in the prevention of lung injury induced by Benzo(a) Pyrene (BaP) in rats. Molecules. 25(3):724.
  • Alshatwi AA. 2010. Catechin hydrate suppresses MCF-7 proliferation through TP53/caspase-mediated apoptosis. J Exp Clin Cancer Res. 29(1):1–9.
  • Alvarez-Gonzalez I, Mojica R, Madrigal-Bujaidar E, Camacho-Carranza R, Escobar- García D, Espinosa-Aguirre J. 2011. The antigenotoxic effects of grapefruit juice on the damage induced by benzo (a) pyrene and evaluation of its interaction with hepatic and intestinal Cytochrome P450 (Cyp) 1a1. Food Chem Toxicol. 49(4):807–811.
  • Anandakumar P, Kamaraj S, Jagan S, Ramakrishnan G, Devaki T. 2013. Capsaicin provokes apoptosis and restricts benzo(a)pyrene induced lung tumorigenesis in Swiss albino mice. Int Immunopharmacol. 17(2):254–259.
  • Arisha AH, Ahmed MM, Kamel MA, Attia YA, Hussein MMA. 2019. Morin ameliorates the testicular apoptosis, oxidative stress, and impact on blood–testis barrier induced by photo-extracellularly synthesized silver nanoparticles. Environ Sci Pollut Res. 26(28):28749–28762.
  • Arisha AH, Moustafa A. 2019. Potential inhibitory effect of swimming exercise on the Kisspeptin-GnRH signaling pathway in male rats. Theriogenology. 133:87–96.
  • Arjumand W, Seth A, Sultana S. 2011. Rutin attenuates cisplatin induced renal inflammation and apoptosis by reducing NFκB, TNF-α and caspase-3 expression in Wistar rats. Food Chem Toxicol. 49(9):2013–2021.
  • Audra P, Dangle Z, Julius K, Saule U. 2007. Evaluation of the combined effect of cadmium, benzo(a)pyrene and pyrene in general toxicity studies on Wistar rats. MedycynaWeterynaryjn. 63(1):51–55.
  • Babich H, Krupka ME, Nissim HA, Zuckerbraun HL. 2005. Differential in vitro cytotoxicity of (-)-epicatechingallate (ECG) to cancer and normal cells from the human oral cavity. Toxicol in Vitro. 19(2):231–242.
  • Bancroft J, Gamble A. 2002. Theory and practice of histological techniques. Vol. 15, 1st ed. New York and London: Churchill, Living Stone. p. 165–180.
  • Baybutt RC, Rosales C, Brady H, Molteni A. 2002. Dietary fish oil protects against lung and liver inflammation and fibrosis in monocrotaline treated rats. Toxicology. 175(1–3):1–13.
  • Buffone GJ, Darlington GJ. 1985. Isolation of DNA from biological specimens without extraction with phenol. Clin Chem. 31(1):164–165.
  • Chen J, Qian C, Duan H, Cao S, Yu X, Li J, Gu C, Yan F, Wang L, Chen G. 2015. Melatonin attenuates neurogenic pulmonary edema via the regulation of inflammation and apoptosis after subarachnoid hemorrhage in rats. J Pineal Res. 59(4):469–477.
  • Chung SY, Hong W, Jayson XC, Jinsong Z. 2014. Effects of tea catechins on cancer signaling pathways. Enzymes. 36:195–221.
  • Clere N, Faure S, Carmen Martinez M, Andriantsitohaina R. 2011. Anticancer properties of flavonoids: roles in various stages of carcinogenesis. Cardiovasc Hematol Agents Med Chem. 9:62–77.
  • Cory S, Adams JM. 2002. The Bcl2 family: regulators of the cellular life-or-death switch. Nat Rev Cancer. 2(9):647–656.
  • Delgado ME, Haza AI, Arranz N, García A, Morales P. 2008. Dietary polyphenols protect against N-nitrosamines and benzo (a) pyrene-induced DNA damage (strand breaks and oxidized purines/pyrimidines) in HepG2 human hepatoma cells. Eur J Nutr. 47(8):479–490.
  • Deng C, Dang F, Gao J, Zhao H, Qi S, Gao M. 2018. Acute benzo[a]pyrene treatment causes different antioxidant response and DNA damage in liver, lung, brain, stomach and kidney. Heliyon. 4(11):e00898.
  • Erika D, Angela S. 2007. Occurence of benzo[a]pyrene in some foods of animal origin in the Slovak Republic. J Food Nutr Res. 46(4):181–185.
  • Fang AH, Smith WA, Vouros P, Gupta RC. 2001. Identification and characterization of a novel benzo [a] pyrene-derived DNA adduct. Biochem Biophys Res Commun. 281(2):383–389.
  • Fatma GU, Yusuf K. 2013. Chlorpyrifos induced hepatotoxic and hematologic changes in rats: the role of quercetin and catechin. Food Chem Toxicol. 55:549–556.
  • Fu Z, Zhen W, Yuskavage J, Liu D. 2011. Epigallocatechingallate delays the onset of type 1 diabetes in spontaneous non-obese diabetic mice. Br J Nutr. 105(8):1218–1225.
  • Fujii M, Sherchan P, Soejima Y, Doycheva D, Zhang JH. 2016. Subarachnoid hemorrhage-triggered acute hypotension is associated with left ventricular cardiomyocyte apoptosis in a rat model. Acta Neurochir Suppl. 121:145–150.
  • Fukuda I, Tsutsui M, Sakane I, Ashida H. 2009. Suppression of cytochrome P4501A1 expression induced by 2, 3, 7, 8-tetrachlorodibenzo-p-dioxin in mouse hepatoma hepa-1c1c7 cells treated with serum of epigallocatechin-3-gallate-and green tea extract-administered rats. Biosci Biotechnol Biochem. 73(5):1206–1208.
  • Gelboin HV. 1980. Benzo [alpha] pyrene metabolism, activation and carcinogenesis: role and regulation of mixed-function oxidases and related enzymes. Physiol Rev. 60(4):1107–1166.
  • Harborne JB, Williams CA. 2000. Advantages in flavonoid research since 1992. Phytochemistry. 55(6):481–504.
  • Hassan AM, Alam SS, Abdel-Aziem SH, Ahmed KA. 2011. Benzo-a-pyrene induced genotoxicity and cytotoxicity in germ cells of mice: intervention of radish and cress. J Genet Eng Biotechnol. 9(1):65–72.
  • Hodek P, Koblihova J, Kizek R, Frei E, Arlt VM, Stiborova M. 2013. The relationship between DNA adduct formation by benzo [a] pyrene and expression of its activation enzyme cytochrome P450 1A1 in rat. Environ Toxicol Pharmacol. 36(3):989–996.
  • Hollman PC, Katan MB. 1999. Dietary flavonoids: intake, health effects and bioavailability. Food Chem Toxicol. 37(9–10):937–942.
  • Igney FH, Krammer PH. 2002. Death and anti-death: tumour resistance to apoptosis. Nat Rev Cancer. 2(4):277–288.
  • Johirul I, Alpa S, Shekh MA, Abul V, Sarwat S. 2020. Protective effect of Diosmin against benzo(a)pyrene‐induced lung injury in Swiss Albino Mice. Environ Toxicol. 35(9):652–664.
  • Johnstone RW, Ruefli AA, Lowe SW. 2002. Apoptosis: a link between cancer genetics and chemotherapy. Cell. 108(2):153–164.
  • Joslin J. 2009. Blood collection: techniques in exotic small mammals. J Exotic Pet Med. 18(2):117–139.
  • Kasala ER, Bodduluru LN, Madana RM, V AK, Gogoi R, Barua CC. 2015. Chemopreventive and therapeutic potential of chrysin in cancer: mechanistic perspectives. Toxicol Lett. 233(2):214–225.
  • Khamis T, Abdelalim AF, Abdallah SH, Saeed AA, Edress NM, Arisha AH. 2020. Early intervention with breast milk mesenchymal stem cells attenuates the development of diabetic-induced testicular dysfunction via hypothalamic Kisspeptin/Kiss1r-GnRH/GnIH system in male rats. BiochimicaetBiophysicaActa (BBA) – Mol Basis Disease. 1866(1):165577.
  • Khan N, Mukhtar H. 2008. Multitargeted therapy of cancer by green tea polyphenols. Cancer Lett. 269(2):269–280.
  • Livak KJ, Schmittgen TD. 2001. Analysis of relative gene expression data using real-time quantitative PCR and the 2− ΔΔCT method. Methods. 25(4):402–408.
  • Lobo V, Patil A, Phatak A, Chandra N. 2010. Free radicals, antioxidants and functional foods: impact on human health. Phcog Rev. 4(8):118–126.
  • Marie S, Helena D, Lucie B-D, Zuzana K, Jana H, Markéta M, Heinz HS, Volker MA. 2018. Exposure to endocrine disruptors 17alpha-ethinylestradiol and estradiol influences cytochrome P450 1A1-mediated genotoxicity of benzo[a]Pyrene and expression of this enzyme in rats. Toxicology. 400–401:48–56.
  • Martinvalet D, Zhu P, Lieberman J. 2005. Granzyme A induces caspase-independent mitochondrial damage, a required first step for apoptosis. Immunity. 22(3):355–370.
  • Molinari M, Watt KD, Kruszyna T, Nelson R, Walsh M, Huang WY, Nashan B, Peltekian K. 2006. Acute liver failure induced by green tea extracts: case report and review of the literature. Liver Transpl. 12(12):1892–1895.
  • Mostafa HES, Allithy ANA, Abdellatif NA, Anani M, Fareed SA, El-Shafei DA, El-Din EAA. 2021. Amelioration of pulmonary aflatoxicosis by green tea extract: an in vivo study. Toxicon. 189:48–55.
  • Newman DJ, Cragg GM. 2007. Natural products as sources of new drugs over the last 25 Years. J Nat Prod. 70(3):461–477.
  • Nishikimi M, Appaji Rao N, Yagi K. 1972. The occurrence of superoxide anion in the reaction of reduced phenazine methosulfate and molecular oxygen. Biochem Biophys Res Common. 46(2):849–854.
  • Ohkawa H, Ohishi W, Yagi K. 1979. Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Anal Biochem. 95(2):351–358.
  • Pervin M, Unno K, Ohishi T, Tanabe H, Miyoshi N, Nakamura Y. 2018. Beneficial effects of green tea catechins on neurodegenerative diseases. Molecules. 23(6):1297.
  • Petrie A, Sabin C. 2005. Basic techniques for analysing data. In: Sugden M, Moore K, editors. Medical statistics at a glance. 2nd ed. New York, NY: Blackwell Publishing Ltd; p. 55–56.
  • Phillips DH, Venitt S. 2012. DNA and protein adducts in human tissues resulting from exposure to tobacco smoke. Int J Cancer. 131(12):2733–2753.
  • Pisani C, Ramella M, Boldorini R. 2020. Apoptotic and predictive factors by Bax, Caspases 3/9, Bcl-2, p53 and Ki-67 in prostate cancer after 12 Gy single-dose. Sci Rep. 10:70–50.
  • Ramos S. 2007. Effects of dietary flavonoids on apoptotic pathways related to cancer chemoprevention. J Nutr Biochem. 18(7):427–442.
  • Sakthivel R, Sheeja Malar D, Archunan G, Pandima Devi K. 2019. Phytol ameliorated benzo(a)pyrene induced lung carcinogenesis in Swiss albino mice via inhibition of oxidative stress and apoptosis. Environ Toxicol. 34(4):355–363.
  • Sang EK, Jong HK, Sang WL, Moon JL. 2013. A study of roasting conditions on benzo[a]pyrene content in coffee beans. J Korean Soc Food Sci Nutr. 42(1):134.
  • Savitha S, Panneerselvam C. 2007. Mitigation of age-dependent oxidative damage to DNA in rat heart by carnitine and lipoic acid. Mech Ageing Dev. 128(2):206–212.
  • Shahid A, Ali R, Ali N, Hasan SK, Bernwal P, Afzal SM, Vafa A, Sultana S. 2016. Modulatory effects of catechin hydrate against genotoxicity, oxidative stress, inflammation and apoptosis induced by benzo(a)pyrene in mice. Food Chem Toxicol. 92:64–74.
  • Sikdar S, Mukherjee A, Khuda-Bukhsh AR. 2014. Ethanolic extract of Marsdenia condurango ameliorates benzo[a]pyrene-induced lung cancer of rats: Condurango ameliorates BaP-induced lung cancer in rats. J Pharmacopuncture. 17(2):7–17.
  • Sunil KD, Manoj K, Priti B, Dhawan DK. 2019. White tea – a cost effective alternative to EGCG in fight against benzo(a)pyrene (BaP) induced lung toxicity in SD rats. Food Chem Toxicol. 131:110551.
  • Suzuki T, Pervin M, Goto S, Isemura M, Nakamura Y. 2016. Beneficial effects of tea and the green tea catechin epigallocatechin-3-gallate on obesity. Molecules. 21(10):1305.
  • Takami S, Imai T, Hasumura M, Cho Y-M, Onose J, Hirose M. 2008. Evaluation of toxicity of green tea catechins with 90-day dietary administration to F344 rats. Food Chem Toxicol. 46(6):2224–2229.
  • US EPA. 2013. United States Environmental Protection Agency. http://www.epa.gov/.
  • Wlodek D, Banath J, Olive PL. 1991. Comparison between pulsed-field and constant-field gel electrophoresis for measurement of DNA double-strand breaks in irradiated Chinese hamster ovary cells. Int J Radiat Biol. 60(5):779–790.
  • Xia L, Xinwei J, Jianxia S, Cuijuan Z, Xiaoling L, Lingmin T, Liu L, Weibin B. 2017. Cytoprotective effects of dietary flavonoids against cadmium‐induced toxicity. Ann NY Acad Sci. 1398(1):5–19.
  • Yan Y, Griffiths WJ, Nordling M, Nygren J, M€Oller L, Bergman J, Liepinsh E, Otting G, Gustafsson JA, Rafter J, et al. 2000. Ring opening of benzo[a]pyrene in the germ-free rat is a novel pathway for formation of potentially genotoxic metabolites. Biochemistry. 39:15585–15591.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.