Cyclophosphamide (CP) is a frequently used drug for its anticancer and immunosuppressive potential. However metabolism of CP in the body results into toxic chemical compounds (to the liver itself and other non-target vital organs) via oxidative stress, apoptosis induction and finally necrosis. Since there is no escaping of using such medications in spite of their harms this study was designed to access the ability to alleviate the side-effects of CP by using peach seed methanolic extract, due to its nutritional value and therapeutic properties. The peach seed extract has bioactive constituents such as phenols and carotenoids. Methanoloic extract is the most widely used since it offers a high recovery of antioxidant compounds. Mice were divided into five major groups: negative control (untreated group), positive control, was injected (IP) with CP in dose 75mg/kg b. wt., Third group received peach seed extract only in a dose of 500 mg/kg b.w., and the fourth and fifth groups received two doses of Peach seeds extract 500 and 250 mg/kg b.wt. after receiving a single dose of CP intraperitoneally. Assessment of the extract was performed using micronucleus test, mitotic chromosomal aberration assay using bone marrow cells, and liver samples were collected for histopathology. Our results demonstrated that CP induced highly significant e genotoxicity, which recorded 9.49% PE's with micronuclei, comparing to 1.03% as control, while the induction of chromosomal aberrations was recorded as 67.6% against 4.4% as negative control. The histological study on the liver cells recorded noticeable damage with liver cells treated with CP. After peach treatment a significant reduction in CP- induced damage was observed and those groups treated with both extract and CP became nearly similar to the untreated group in all tested parameters. peach methanolic seed extract has the potential to ameliorate the damaging effect of cyclophosphamide at both the genetic and histological levels.
Published in | International Journal of Genetics and Genomics (Volume 7, Issue 4) |
DOI | 10.11648/j.ijgg.20190704.19 |
Page(s) | 136-147 |
Creative Commons |
This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited. |
Copyright |
Copyright © The Author(s), 2019. Published by Science Publishing Group |
Cyclophosphamide Genotoxicity, Prunus Persica, Peach Methanolic Seed Extract, Antioxidant, Mice, Micronucleus Assay, Mitotic Chromosomal Aberration Assay, Liver Histopathology
[1] | BERTOLINI, F., PAUL, S., MANCUSO, P., MONESTIROLI, S., GOBBI, A., SHAKED, Y., and KERBEL, R. S., 2003. Maximum tolerable dose and low-dose metronomic chemotherapy have opposite effects on the mobilization and viability of circulating endothelial progenitor cells. Cancer Research 63, (15), 4342-4346. https://www.ncbi.nlm.nih.gov/pubmed/12907602. |
[2] | BROCK, N. and HOHORST, H. J., 1967. Metabolism of cyclophosphamide. Cancer 20, (5), 900-904. https://www.ncbi.nlm.nih.gov/pubmed/6024299. |
[3] | GULIA, S. and KUMAR KATARIA, S., 2017. Histological alterations induced due to malathion and cyclophosphamide exposure in mice 5. https://www.researchgate.net/publication/320977844_Histological_alterations_induced_due_to_malathion_and_cyclophosphamide_exposure_in_mice. |
[4] | ABDELLA, E. M., 2012. Short-term comparative study of the cyclophosphamide genotoxicity administered free and liposome-encapsulated in mice. Iranian journal of cancer prevention 5, (2), 51. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4299619/. |
[5] | BROCK, N., 1989. Oxazaphosphorine cytostatics: past-present-future: seventh cain memorial award lecture. Cancer Research 49, (1), 1-7. https://cancerres.aacrjournals.org/content/49/1/1.article-info. |
[6] | HICKMAN, J. A., 1992. Apoptosis induced by anticancer drugs. Cancer Metastasis Rev 11, (2), 121-139. DOI https://doi.org/10.1007/BF00048059. |
[7] | O'CONNOR, P. M., WASSERMANN, K., SARANG, M., MAGRATH, I., BOHR, V. A., and KOHN, K. W., 1991. Relationship between DNA cross-links, cell cycle, and apoptosis in Burkitt's lymphoma cell lines differing in sensitivity to nitrogen mustard. Cancer Research 51, (24), 6550-6557. https://www.ncbi.nlm.nih.gov/pubmed/1742728. |
[8] | DIPLOCK, A., CHARULEUX, J.-L., CROZIER-WILLI, G., KOK, F., RICE-EVANS, C., ROBERFROID, M., STAHL, W., and VINA-RIBES, J., 1998. Functional food science and defence against reactive oxidative species. British Journal of Nutrition 80, (S1), S77-S112. DOI https://doi.org/10.1079/BJN19980106. |
[9] | VALKO, M., LEIBFRITZ, D., MONCOL, J., CRONIN, M., MAZUR, M., and TELSER, J., 2007. Free radicals and antioxidants in normal physiological functions and human disease. Int. J. Biochem. Cell. Biol. DOI 10.1016/j.biocel.2006.07.001. |
[10] | PRATHEESHKUMAR, P. and KUTTAN, G., 2010. Ameliorative action of Vernonia cinerea L. on cyclophosphamide-induced immunosuppression and oxidative stress in mice. Inflammopharmacology 18, (4), 197-207. DOI 10.1007/s10787-010-0042-8. |
[11] | WATERS, M. D., STACK, H. F., JACKSON, M. A., BROCKMAN, H. E., and DE FLORA, S., 1996. Activity profiles of antimutagens: in vitro and in vivo data. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis 350, (1), 109-129. DOI https://doi.org/10.1016/0027-5107(95)00097-6. |
[12] | KAUR, S., ARORA, S., KAUR, K., and KUMAR, S., 2002. The in vitro antimutagenic activity of Triphala—an Indian herbal drug. Food and Chemical Toxicology 40, (4), 527-534. DOI https://doi.org/10.1016/S0278-6915(01)00101-6. |
[13] | NOH, J.-R., KIM, Y.-H., GANG, G.-T., HWANG, J.-H., KIM, S.-K., RYU, S.-Y., KIM, Y.-S., LEE, H.-S., and LEE, C.-H., 2011. Hepatoprotective effect of Platycodon grandiflorum against chronic ethanol-induced oxidative stress in C57BL/6 mice. Annals of Nutrition and Metabolism 58, (3), 224-231. DOI 10.1159/000330117. |
[14] | NEMA, G. F., LOCATELLI, J., FREITASAND, P. C., and SILVA, G. L., 2000. Antibacterial activity of plant extracts and phytochemicals on antibiotic-resistant bacteria. Brazilian Journal of Microbiology 31, 247-256. DOI http://dx.doi.org/10.1590/S1517-83822000000400003. |
[15] | SOURI, E., AMIN, G., FARSAM, H., JALALIZADEH, H., and BAREZI, S., 2010. Screening of thirteen medicinal plant extracts for antioxidant activity. Iranian Journal of Pharmaceutical Research, 149-154. DOI 10.22037/IJPR.2010.758. |
[16] | KIM, D.-O., CHUN, O. K., KIM, Y. J., MOON, H.-Y., and LEE, C. Y., 2003. Quantification of polyphenolics and their antioxidant capacity in fresh plums. Journal of Agricultural and Food Chemistry 51, (22), 6509-6515. DOI https://doi.org/10.1021/jf0343074. |
[17] | TOMÁS-BARBERÁN, F. A., GIL, M. I., CREMIN, P., WATERHOUSE, A. L., HESS-PIERCE, B., and KADER, A. A., 2001. HPLC− DAD− ESIMS analysis of phenolic compounds in nectarines, peaches, and plums. Journal of Agricultural and Food Chemistry 49, (10), 4748-4760. DOI https://doi.org/10.1021/jf0104681. |
[18] | KIM, Y.-K., KOO, B.-S., GONG, D.-J., LEE, Y.-C., KO, J.-H., and KIM, C.-H., 2003. Comparative effect of Prunus persica L. BATSCH-water extract and tacrine (9-amino-1, 2, 3, 4-tetrahydroacridine hydrochloride) on concentration of extracellular acetylcholine in the rat hippocampus. Journal of ethnopharmacology 87, (2-3), 149-154. DOI 10.1016/S0378-8741(03)00106-5. |
[19] | MIYAZAWA, M. and HISAMA, M., 2003. Antimutagenic activity of phenylpropanoids from clove (Syzygium aromaticum). Journal of Agricultural and Food Chemistry 51, (22), 6413-6422. DOI https://doi.org/10.1021/jf030247q. |
[20] | KAMEI, H., KOJIMA, T., HASEGAWA, M., KOIDE, T., UMEDA, T., YUKAWA, T., and TERABE, K., 1995. Suppression of tumor cell growth by anthocyanins in vitro. Cancer Investigation 13, (6), 590-594. DOI https://doi.org/10.3109/07357909509024927. |
[21] | ABIDI, W., CANTÍN, C. M., JIMÉNEZ, S., GIMÉNEZ, R., MORENO, M. Á., and GOGORCENA, Y., 2015. Influence of antioxidant compounds, total sugars and genetic background on the chilling injury susceptibility of a non-melting peach (Prunus persica (L.) Batsch) progeny. Journal of the Science of Food and Agriculture 95, (2), 351-358. DOI 10.1002/jsfa.6727. |
[22] | LOIZZO, M. R., PACETTI, D., LUCCI, P., NÚÑEZ, O., MENICHINI, F., FREGA, N. G., and TUNDIS, R., 2015. Prunus persica var. platycarpa (Tabacchiera Peach): bioactive compounds and antioxidant activity of pulp, peel and seed ethanolic extracts. Plant foods for human nutrition 70, (3), 331-337. DOI 10.1007/s11130-015-0498-1. |
[23] | WANG, N., QINGYUN, L., DAIYIN, P., LAN, W., and SHENGXIANG, W., 2002. Experimental Study on Anti-thrombus Effect of Different Extracts from Semen Persicae [J]. Journal of Chinese Medicinal Materials 6. http://en.cnki.com.cn/Article_en/CJFDTotal-ZYCA200206017.htm. |
[24] | XU, L., LIU, P., LIU, C., HONG, J., LU, G., XUE, H., ZHU, J., and HU, Y., 1994. Observation on the action of extractum semen Persicae on anti-fibrosis of liver. Zhongguo Zhong yao za zhi= Zhongguo zhongyao zazhi= China journal of Chinese materia medica 19, (8), 491-494, 512. https://europepmc.org/abstract/med/7980864. |
[25] | ARICHI, S., KUBO, M., TANI, T., NAKAMURA, H., IMAZU, C., KADOKAWA, T., NAGAMOTO, N., NANBA, K., and NISHIMURA, H., 1985. Studies on Persicae semen. III. Oxygen radical scavenging activity of PR-B, an anti-inflammatory protein of Persicae semen. Yakugaku zasshi: Journal of the Pharmaceutical Society of Japan 105, (9), 895-901. DOI 10.1248/yakushi1947.105.9_895. |
[26] | EDENHARDER, R., KRIEG, H., KÖTTGEN, V., and PLATT, K., 2003. Inhibition of clastogenicity of benzo [a] pyrene and of its trans-7, 8-dihydrodiol in mice in vivo by fruits, vegetables, and flavonoids. Mutation Research/Genetic Toxicology and Environmental Mutagenesis 537, (2), 169-181. DOI 10.1016/S1383-5718(03)00078-0. |
[27] | ABOUL-ELA, E. I. and OMARA, E. A., 2014. Genotoxic and histopathological aspects of treatment with grape seed extract on cancer induced with cyclophosphamide in mice. J Cell Biol 2, 18-27. DOI 10.11648/j.cb.20140203.11. |
[28] | CHO, H.-B., PARK, J.-H., SEO, B.-I., CHO, S.-Y., PARK, K.-R., CHOI, S.-H., HAN, C.-K., SONG, C.-H., PARK, S.-J., and KU, S.-K., 2013. Single Oral Dose Toxicity Test of Persicae Semen Aqueous Extracts in Mice. The Korea Journal of Herbology 28, (3), 17-24. http://citeseerx.ist.psu.edu/viewdoc/download?doi=10.1.1.885.1805&rep=rep1&type=pdf. |
[29] | ATTIA, S. M., AL-ANTEET, A. A., AL-RASHEED, N. M., ALHAIDER, A. A., and AL-HARBI, M. M., 2009. Protection of mouse bone marrow from etoposide-induced genomic damage by dexrazoxane. Cancer Chemotherapy and Pharmacology 64, (4), 837-845. DOI https://doi.org/10.1007/s00280-009-0934-8. |
[30] | SCHMID, W., 1976. The micronucleus test for cytogenetic analysis. In Chemical mutagens Springer, 31-53. DOI: http://dx.doi.org/DOI https://doi.org/10.1007/978-1-4684-0892-8_2. |
[31] | YOSIDA, H. T. and AMANO, K. H., 1965. Autosomal polymorphism in laboratory bred and wild Norway rats, Rattus norvegicus, found in Misima. |
[32] | FRAISER, L. H., KANEKAL, S., and KEHRER, J. P., 1991. Cyclophosphamide toxicity. Drugs 42, (5), 781-795. DOI 0012-6667/91/0011-0781/$07.50/0. |
[33] | DAS, U. B., MALLICK, M., DEBNATH, J. M., and GHOSH, D., 2002. Protective effect of ascorbic acid on cyclophosphamide-induced testicular gametogenic and androgenic disorders in male rats. Asian journal of andrology 4, (3), 201-208. http://www.asiaandro.com/archive/1008-682X/4/201.htm?rgwzfkuotmfihfbc?frpegdgdnhojsrio?ywjzynrgtmpvqezf?fumiotmwjzpeihmy?cesiqqnynrplufri?skbzahydxsbcojsr. |
[34] | GHOSH, D., DAS, U., GHOSH, S., MALLICK, M., and DEBNATH, J., 2002. Testicular gametogenic and steroidogenic activities in cyclophosphamide treated rat: a correlative study with testicular oxidative stress. Drug and chemical toxicology 25, (3), 281-292. DOI https://doi.org/10.1081/DCT-120005891. |
[35] | ANDERSON, D., BISHOP, J. B., GARNER, R. C., OSTROSKY-WEGMAN, P., and SELBY, P. B., 1995. Cyclophosphamide: Review of its mutagenicity for an assessment of potential germ cell risks. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis 330, (1), 115-181. DOI https://doi.org/10.1016/0027-5107(95)00039-L. |
[36] | MURATA, M., SUZUKI, T., MIDORIKAWA, K., OIKAWA, S., and KAWANISHI, S., 2004. Oxidative DNA damage induced by a hydroperoxide derivative of cyclophosphamide. Free Radical Biology and Medicine 37, (6), 793-802. DOi https://doi.org/10.1016/j.freeradbiomed.2004.05.009. |
[37] | DKHIL, M. A., TOHAMY, A., and GABRY, M. S., 2011. Chromosomal aberrations induced in bone marrow cells of mice due to the administration of the non-steroidal anti-inflammatory drug, Piroxicam. African Journal of Pharmacy and Pharmacology 5, (1), 93-103. DOI 10.5897/AJPP10.267. |
[38] | DOLARA, P., TORRICELLI, F., and ANTONELLI, N., 1994. Cytogenetic effects on human lymphocytes of a mixture of fifteen pesticides commonly used in Italy. Mutation Research Letters 325, (1), 47-51. DOI https://doi.org/10.1016/0165-7992(94)90026-4. |
[39] | DE HONDT, H., FAHMY, A., and ABDELBASET, S., 1984. Chromosomal and biochemical studies on the effect of kat extract on laboratory rats. Environmental mutagenesis 6, (6), 851-860. DOI https://doi.org/10.1002/em.2860060611. |
[40] | ITO, D. and MATSUMOTO, T., 2010. Molecular Mechanisms and Function of the Spindle Checkpoint, a Guardian of the Chromosome Stability. In Polyploidization and Cancer, R. Y. C. POON Ed. Springer New York, New York, NY, 15-26. DOI: http://dx.doi.org/DOI 10.1007/978-1-4419-6199-0_2. |
[41] | GOLDBERG, M. T., BLAKEY, D. H., and BRUCE, W. R., 1983. Comparison of the effects of 1, 2-dimethylhydrazine and cyclophosphamide on micronucleus incidence in bone marrow and colon. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis 109, (1), 91-98. DOI https://doi.org/10.1016/0027-5107(83)90098-2. |
[42] | STEVENS, J. F. and MAIER, C. S., 2008. Acrolein: sources, metabolism, and biomolecular interactions relevant to human health and disease. Molecular nutrition & food research 52, (1), 7-25. DOI https://doi.org/10.1002/mnfr.200700412. |
[43] | WANG, H.-T., HU, Y., TONG, D., HUANG, J., GU, L., WU, X.-R., CHUNG, F.-L., LI, G.-M., and TANG, M.-S., 2012. Effect of carcinogenic acrolein on DNA repair and mutagenic susceptibility. Journal of Biological Chemistry 287, (15), 12379-12386. DOI 10.1074/jbc.M111.329623. |
[44] | SENTHILKUMAR, S., YOGEETA, S. K., SUBASHINI, R., and DEVAKI, T., 2006. Attenuation of cyclophosphamide induced toxicity by squalene in experimental rats. Chemico-biological interactions 160, (3), 252-260. DOI 10.1016/j.cbi.2006.02.004. |
[45] | OHNO, Y. and ORMSTAD, K., 1985. Formation, toxicity and inactivation of acrolein during biotransformation of cyclophosphamide as studied in freshly isolated cells from rat liver and kidney. Archives of toxicology 57, (2), 99-103. DOI https://doi.org/10.1007/BF00343118. |
[46] | YOUSEFIPOUR, Z., RANGANNA, K., NEWAZ, M., and MILTON, S., 2005. Mechanism of acrolein-induced vascular toxicity. Journal of physiology and pharmacology 56, (3), 337. http://www.jpp.krakow.pl/journal/archive/09_05/pdf/337_09_05_article.pdf. |
[47] | ABDELFATTAH-HASSAN, A., SHALABY, S. I., KHATER, S. I., EL-SHETRY, E. S., ABD EL FADIL, H., and ELSAYED, S. A., 2019. Panax ginseng is superior to vitamin E as a hepatoprotector against cyclophosphamide-induced liver damage. Complementary Therapies in Medicine 46, 95-102. DOI https://doi.org/10.1016/j.ctim.2019.08.005. |
[48] | FOUAD, A. A., QUTUB, H. O., and AL-MELHIM, W. N., 2016. Punicalagin alleviates hepatotoxicity in rats challenged with cyclophosphamide. Environmental Toxicology and Pharmacology 45, 158-162. DOI https://doi.org/10.1016/j.etap.2016.05.031. |
[49] | CUCE, G., ÇETINKAYA, S., KOC, T., ESEN, H. H., LIMANDAL, C., BALCı, T., KALKAN, S., and AKOZ, M., 2015. Chemoprotective effect of vitamin E in cyclophosphamide-induced hepatotoxicity in rats. Chemico-biological interactions 232, 7-11. DOI https://doi.org/10.1016/j.cbi.2015.02.016. |
[50] | ALQAHTANI, S. and MAHMOUD, A. M., 2016. Gamma-Glutamylcysteine ethyl Ester protects against cyclophosphamide-induced liver injury and hematologic alterations via upregulation of PPARγ and attenuation of oxidative stress, inflammation, and apoptosis. Oxidative medicine and cellular longevity 2016. DOI http://dx.doi.org/10.1155/2016/4016209. |
[51] | OYAGBEMI, A. A., OMOBOWALE, O. T., ASENUGA, E. R., AKINLEYE, A. S., OGUNSANWO, R. O., and SABA, A. B., 2016. Cyclophosphamide-induced hepatotoxicity in wistar rats: the modulatory role of gallic acid as a hepatoprotective and chemopreventive phytochemical. International journal of preventive medicine 7. DOI 10.4103/2008-7802.177898. |
[52] | BHAT, N., KALTHUR, S. G., PADMASHALI, S., and MONAPPA, V., 2018. Toxic Effects of Different Doses of Cyclophosphamide on Live. Ethiopian journal of health sciences 28, (6). DOI http://dx.doi.org/10.4314/ejhs.v28i6.5. |
[53] | ADIKWU, E. and BOKOLO, B., 2018. Effect of cimetidine on cyclophosphamide-induced liver toxicity in albino rats. Asian Journal of Medical Sciences 9, (5), 50-56. DOI http://orcid.org/0000-0001-6426-6228. |
[54] | COHEN, S. M., GARLAND, E. M., JOHN, M. S., OKAMURA, T., and SMITH, R. A., 1992. Acrolein initiates rat urinary bladder carcinogenesis. Cancer Research 52, (13), 3577-3581. https://cancerres.aacrjournals.org/content/52/13/3577.full-text.pdf. |
[55] | YOKOYAMA, Y., FUTAGAMI, M., FUKUSHI, Y., SAKAMOTO, T., HIGUCHI, T., FUJII, S., SATO, S., TAKAMI, H., and SAITO, Y., 2000. Secondary acute nonlymphocytic leukemia following successful chemotherapy combining cisplatin, doxorubicin, and cyclophosphamide for stage IV epithelial ovarian cancer. Archives of Gynecology and Obstetrics 263, (4), 206-207. DOI https://doi.org/10.1007/s004040050285. |
[56] | HELLER, A., TRIFONOV, V., RUBTSOV, N., SAUERBREY, A., STARKE, H., LONCAREVIC, I. F., CLAUSSEN, U., and LIEHR, T., 2003. Complex chromosomal rearrangements in a secondary acute myeloblastic leukemia after chemotherapy in TRAPS. Oncology reports 10, (6), 1789-1792. DOI https://doi.org/10.3892/or.10.6.1789. |
[57] | BLOCK, G., PATTERSON, B., and SUBAR, A., 1992. Fruit, vegetables, and cancer prevention: a review of the epidemiological evidence. Nutrition and cancer 18, (1), 1-29. DOI 10.1080/01635589209514201. |
[58] | GARCı́A-ALONSO, M. A., DE PASCUAL-TERESA, S., SANTOS-BUELGA, C., and RIVAS-GONZALO, J. C., 2004. Evaluation of the antioxidant properties of fruits. Food Chemistry 84, (1), 13-18. DOI 10.1016/S0308-8146(03)00160-2. |
[59] | CAMPBELL, O. E. and PADILLA-ZAKOUR, O. I., 2013. Phenolic and carotenoid composition of canned peaches (Prunus persica) and apricots (Prunus armeniaca) as affected by variety and peeling. Food research international 54, (1), 448-455. DOI https://doi.org/10.1016/j.foodres.2013.07.016. |
[60] | EDENHARDER, R., FRANGART, J., HAGER, M., HOFMANN, P., and RAUSCHER, R., 1998. Protective Effects of Fruits and Vegetables against In Vivo Clastogenicity of Cyclophosphamide or Benzo [a] pyrene in Mice. Food and Chemical Toxicology 36, (8), 637-645. DOI https://doi.org/10.1016/S0278-6915(98)00035-0. |
[61] | GHOBADI POUR, M., MIRAZI, N., and SEIF, A., 2019. Treatment of liver and spleen illnesses by herbs: Recommendations of Avicenna's heritage "Canon of Medicine". Avicenna journal of phytomedicine 9, (2), 101-116. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6448543/. |
[62] | SAOUDI, S., KHENNOUF, S., MAYOUF, N., AMIRA, S., and DAHAMNA, S., 2019. Evaluation of the in vivo and in vitro antioxidant capacity and phytochemical Screening of phenolic compounds of Fargaria ananassa, Prunus armeniaca and Prunus persica fruits growing in Algeria. Progress in Nutrition 22, (1). DOI https://doi.org/10.23751/pn.v22i1.8011. |
[63] | NORATTO, G., PORTER, W., BYRNE, D., and CISNEROS-ZEVALLOS, L., 2014. Polyphenolics from peach (Prunus persica var. Rich Lady) inhibit tumor growth and metastasis of MDA-MB-435 breast cancer cells in vivo. The Journal of nutritional biochemistry 25, (7), 796-800. DOI https://doi.org/10.1016/j.jnutbio.2014.03.001. |
[64] | BARCELOUX, D. G., 2008. Medical toxicology of natural substances: foods, fungi, medicinal herbs, plants, and venomous animals. John Wiley & Sons. |
[65] | NORATTO, G., PORTER, W., BYRNE, D., and CISNEROS-ZEVALLOS, L., 2009. Identifying Peach and Plum Polyphenols with Chemopreventive Potential against Estrogen-Independent Breast Cancer Cells. Journal of Agricultural and Food Chemistry 57, (12), 5219-5226. DOI https://doi.org/10.1021/jf900259m. |
[66] | HEO, M. Y., KIM, S. H., YANG, H. E., LEE, S. H., JO, B. K., and KIM, H. P., 2001. Protection against ultraviolet B-and C-induced DNA damage and skin carcinogenesis by the flowers of Prunus persica extract. Mutation Research/Genetic Toxicology and Environmental Mutagenesis 496, (1-2), 47-59. DOI https://doi.org/10.1016/S1383-5718(01)0218-2. |
[67] | LEE, C. K., PARK, K.-K., HWANG, J.-K., LEE, S. K., and CHUNG, W.-Y., 2008. The pericarp extract of Prunus persica attenuates chemotherapy-induced acute nephrotoxicity and hepatotoxicity in mice. Journal of medicinal food 11, (2), 302-306. DOI https://doi.org/10.1089/jmf.2007.545. |
[68] | XI, S., SHI, M., JIANG, X., MINUK, G. Y., CHENG, Y., PENG, Y., GONG, Y., XU, Y., WANG, X., and YANG, J., 2016. The effects of Tao-Hong-Si-Wu on hepatic necroinflammatory activity and fibrosis in a murine model of chronic liver disease. Journal of ethnopharmacology 180, 28-36. DOI https://doi.org/10.1016/j.jep.2016.01.030. |
[69] | ZHANG, Y., LUO, J.-X., HU, X.-Y., YANG, F., ZHONG, S., and LIN, W., 2016. Improved prescription of taohechengqi-tang alleviates D-galactosamine acute liver failure in rats. World journal of gastroenterology 22, (8), 2558. DOI 10.3748/wjg.v22.i8.2558. |
[70] | ZHAO, X., LIAO, Z., QI, Y., SHEN, X., BI, K., and JIA, Y., 2016. Antioxidative activity of methyl amygdalinate from the seeds of Prunus persica and neuroprotective effects on Aβ 1–42-induced neurodegeneration models. RSC Advances 6, (96), 93794-93800. DOI 10.1039/C6RA18913J. |
[71] | KIM, S.-R., LEE, J.-W., LIM, S.-Y., JUNG, Y.-S., CHOI, H.-Y., and KIM, J.-D., 2012. Rat single oral dose toxicity test of Armeniacae Semen (including endocarp). The Journal of Internal Korean Medicine 33, (2), 145-159. https://www.jikm.or.kr/journal/view.php?number=1650. |
APA Style
Heba Mohamed Salah, Ezzat Ibrahim Aboul-Ela, Hamdy Hamed Swelim. (2019). Ameliorative Effect of Peach Seed Extract on Cyclophosphamide- Induced Cytogenetic and Histological Effects in Mice. International Journal of Genetics and Genomics, 7(4), 136-147. https://doi.org/10.11648/j.ijgg.20190704.19
ACS Style
Heba Mohamed Salah; Ezzat Ibrahim Aboul-Ela; Hamdy Hamed Swelim. Ameliorative Effect of Peach Seed Extract on Cyclophosphamide- Induced Cytogenetic and Histological Effects in Mice. Int. J. Genet. Genomics 2019, 7(4), 136-147. doi: 10.11648/j.ijgg.20190704.19
AMA Style
Heba Mohamed Salah, Ezzat Ibrahim Aboul-Ela, Hamdy Hamed Swelim. Ameliorative Effect of Peach Seed Extract on Cyclophosphamide- Induced Cytogenetic and Histological Effects in Mice. Int J Genet Genomics. 2019;7(4):136-147. doi: 10.11648/j.ijgg.20190704.19
@article{10.11648/j.ijgg.20190704.19, author = {Heba Mohamed Salah and Ezzat Ibrahim Aboul-Ela and Hamdy Hamed Swelim}, title = {Ameliorative Effect of Peach Seed Extract on Cyclophosphamide- Induced Cytogenetic and Histological Effects in Mice}, journal = {International Journal of Genetics and Genomics}, volume = {7}, number = {4}, pages = {136-147}, doi = {10.11648/j.ijgg.20190704.19}, url = {https://doi.org/10.11648/j.ijgg.20190704.19}, eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.ijgg.20190704.19}, abstract = {Cyclophosphamide (CP) is a frequently used drug for its anticancer and immunosuppressive potential. However metabolism of CP in the body results into toxic chemical compounds (to the liver itself and other non-target vital organs) via oxidative stress, apoptosis induction and finally necrosis. Since there is no escaping of using such medications in spite of their harms this study was designed to access the ability to alleviate the side-effects of CP by using peach seed methanolic extract, due to its nutritional value and therapeutic properties. The peach seed extract has bioactive constituents such as phenols and carotenoids. Methanoloic extract is the most widely used since it offers a high recovery of antioxidant compounds. Mice were divided into five major groups: negative control (untreated group), positive control, was injected (IP) with CP in dose 75mg/kg b. wt., Third group received peach seed extract only in a dose of 500 mg/kg b.w., and the fourth and fifth groups received two doses of Peach seeds extract 500 and 250 mg/kg b.wt. after receiving a single dose of CP intraperitoneally. Assessment of the extract was performed using micronucleus test, mitotic chromosomal aberration assay using bone marrow cells, and liver samples were collected for histopathology. Our results demonstrated that CP induced highly significant e genotoxicity, which recorded 9.49% PE's with micronuclei, comparing to 1.03% as control, while the induction of chromosomal aberrations was recorded as 67.6% against 4.4% as negative control. The histological study on the liver cells recorded noticeable damage with liver cells treated with CP. After peach treatment a significant reduction in CP- induced damage was observed and those groups treated with both extract and CP became nearly similar to the untreated group in all tested parameters. peach methanolic seed extract has the potential to ameliorate the damaging effect of cyclophosphamide at both the genetic and histological levels.}, year = {2019} }
TY - JOUR T1 - Ameliorative Effect of Peach Seed Extract on Cyclophosphamide- Induced Cytogenetic and Histological Effects in Mice AU - Heba Mohamed Salah AU - Ezzat Ibrahim Aboul-Ela AU - Hamdy Hamed Swelim Y1 - 2019/12/04 PY - 2019 N1 - https://doi.org/10.11648/j.ijgg.20190704.19 DO - 10.11648/j.ijgg.20190704.19 T2 - International Journal of Genetics and Genomics JF - International Journal of Genetics and Genomics JO - International Journal of Genetics and Genomics SP - 136 EP - 147 PB - Science Publishing Group SN - 2376-7359 UR - https://doi.org/10.11648/j.ijgg.20190704.19 AB - Cyclophosphamide (CP) is a frequently used drug for its anticancer and immunosuppressive potential. However metabolism of CP in the body results into toxic chemical compounds (to the liver itself and other non-target vital organs) via oxidative stress, apoptosis induction and finally necrosis. Since there is no escaping of using such medications in spite of their harms this study was designed to access the ability to alleviate the side-effects of CP by using peach seed methanolic extract, due to its nutritional value and therapeutic properties. The peach seed extract has bioactive constituents such as phenols and carotenoids. Methanoloic extract is the most widely used since it offers a high recovery of antioxidant compounds. Mice were divided into five major groups: negative control (untreated group), positive control, was injected (IP) with CP in dose 75mg/kg b. wt., Third group received peach seed extract only in a dose of 500 mg/kg b.w., and the fourth and fifth groups received two doses of Peach seeds extract 500 and 250 mg/kg b.wt. after receiving a single dose of CP intraperitoneally. Assessment of the extract was performed using micronucleus test, mitotic chromosomal aberration assay using bone marrow cells, and liver samples were collected for histopathology. Our results demonstrated that CP induced highly significant e genotoxicity, which recorded 9.49% PE's with micronuclei, comparing to 1.03% as control, while the induction of chromosomal aberrations was recorded as 67.6% against 4.4% as negative control. The histological study on the liver cells recorded noticeable damage with liver cells treated with CP. After peach treatment a significant reduction in CP- induced damage was observed and those groups treated with both extract and CP became nearly similar to the untreated group in all tested parameters. peach methanolic seed extract has the potential to ameliorate the damaging effect of cyclophosphamide at both the genetic and histological levels. VL - 7 IS - 4 ER -