The Impact of Chitosan on Oxidative Stress in Liver of Rats Loaded With Lead Acetate


Δημοσιευμένα: Jan 20, 2023
U Ozdek
https://orcid.org/0000-0002-0709-1545
H Toz
AU Kömüroğlu
L Mis
Y Değer
Περίληψη

This study was conducted to determine the impact of chitosan on lead (Pb)-induced hepatotoxicity. Thus, lead acetate was administered intraperitoneally (50 mg/kg for 5 days) and chitosan was given as 200 mg/kg via oral gavage for 28 days. When the trial was terminated, it was determined that aspartate aminotransferase (AST), alanine aminotransferase  (ALT) and alkaline phosphatase (ALP) activities in serum as well as Pb, 8-hydroxy-deoxyguanosine (8-OHdG) and malondialdehyde (MDA) levels and catalase (CAT) activity in liver tissue significantly increased, however reduced glutathione (GSH) and ceruloplasmin (Cp) levels in liver and high density lipoproteins (HDL) in serum had a significant decrease in the Pb group when compared to the control group. The administration of chitosan significantly prevented Pb-induced changes in serum liver enzyme activities, 8-OHdG and MDA levels. In addition, chitosan showed a statistically insignificant effect on reduced GSH, Cp, HDL levels and CAT activity. Accordingly, administration of chitosan can strengthen the antioxidant defence system of liver tissue and may decrease oxidative stress.

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Αναφορές
Abdel-Moneim, AE, Dkhil, MA, and Al-Quraishy, S (2011) The redox status in rats treated with flaxseed oil and lead-induced hepatotoxicity. Biological trace element research 143:1:457-467.
Ademuyiwa, O, Agarwal, R, Chandra, R, and Behari, JR (2009) Lead-induced phospholipidosis and cholesterogenesis in rat tissues. Chemico-Biological Interactions 179:2-3:314-320.
Anandan, R, Nair, PG, and Mathew, S (2004) Anti-ulcerogenic effect of chitin and chitosan on mucosal antioxidant defence system in HCl-ethanol-induced ulcer in rats. J Pharm Pharmacol 56:2:265-269.
Antonowicz, J, Andrzejak, R, Lepetow, T, Skoczynska, A, and Smolik, R (1996) Blood lipid parameters in smelters chronically exposed to heavy metals. Med Pr 47:3:207-215.
Chiang, M-T, Yao, H-T, and Chen, H-C (2000) Effect of dietary chitosans with different viscosity on plasma lipids and lipid peroxidation in rats fed on a diet enriched with cholesterol. Bioscience, biotechnology, and biochemistry 64:5:965-971.
Çaylak, E (2010) Lead toxication and oxidative stress in children and antioxidant effects of thiol compounds. The Journal of the Child 10:1:13-23.
DeLeve, LD, and Kaplowitz, N (1991) Glutathione metabolism and its role in hepatotoxicity. Pharmacology & therapeutics 52:3:287-305.
Demirdag, R, Comakli, V, Ozkaya, A, Sahin, Z, Dag, U, Yerlikaya, E, and Kuzu, M (2015) Examination of Changes in Enzyme Activities of Erythrocyte Glucose 6‐Phosphate Dehydrogenase and 6‐Phosphogluconate Dehydrogenase in Rats Given Naringenin and Lead Acetate. Journal of biochemical and molecular toxicology 29:1:43-47.
Flora, S, Flora, G, Saxena, G, and Mishra, M (2007) Arsenic and lead induced free radical generation and their reversibility following chelation. Cell Mol Biol (Noisy-le-grand) 53:1:26-47.
Flora, S, Pande, M, Kannan, G, and Mehta, A (2004) Lead induced oxidative stress and its recovery following co-administration of melatonin or N-acetylcysteine during chelation with succimer in male rats. Cellular and molecular biology (Noisy-le-Grand, France) 50:543-551.
Franco, R, Schoneveld, O, Pappa, A, and Panayiotidis, M (2007) The central role of glutathione in the pathophysiology of human diseases. Archives of physiology and biochemistry 113:4-5:234-258.
Heidarian, E, and Rafieian-Kopaei, M (2013) Protective effect of artichoke (Cynara scolymus) leaf extract against lead toxicity in rat. Pharmaceutical biology 51:9:1104-1109.
Hossain, S, Bhowmick, S, Islam, S, Rozario, L, Jahan, S, Hassan, M, Sarkar, M, Choudhury, BK, Ahmed, S, and Shahjalal, H (2015) Oral administration of ganoderma lucidum to lead-exposed rats protects erythrocytes against hemolysis: implicates to anti-anemia. Evidence-Based Complementary and Alternative Medicine 2015:463703.
Ichiba, M, Maeta, Y, Mukoyama, T, Saeki, T, Yasui, S, Kanbe, T, Okano, JI, Tanabe, Y, Hirooka, Y, and Yamada, S (2003) Expression of 8‐hydroxy‐2′‐deoxyguanosine in chronic liver disease and hepatocellular carcinoma. Liver international 23:5:338-345.
Jacob, RA (1995) The integrated antioxidant system. Nutrition research 15:5:755-766.
Jain, NK, and Singhai, AK (2011) Protective effects of Phyllanthus acidus (L.) Skeels leaf extracts on acetaminophen and thioacetamide induced hepatic injuries in Wistar rats. Asian Pacific Journal of Tropical Medicine 4:6:470-474.
Jeon, TI, Hwang, SG, Park, NG, Jung, YR, Im Shin, S, Choi, SD, and Park, DK (2003) Antioxidative effect of chitosan on chronic carbon tetrachloride induced hepatic injury in rats. Toxicology 187:1:67-73.
Kristal-Boneh, E, Coller, D, Froom, P, Harari, G, and Ribak, J (1999) The association between occupational lead exposure and serum cholesterol and lipoprotein levels. American journal of public health 89:7:1083-1087.
Kummrow, F, Silva, FF, Kuno, R, Souza, AL, and Oliveira, PV (2008) Biomonitoring method for the simultaneous determination of cadmium and lead in whole blood by electrothermal atomic absorption spectrometry for assessment of environmental exposure. Talanta 75:1:246-252.
Liu, C-M, Zheng, Y-L, Lu, J, Zhang, Z-F, Fan, S-H, Wu, D-M, and Ma, J-Q (2010) Quercetin protects rat liver against lead-induced oxidative stress and apoptosis. Environmental toxicology and pharmacology 29:2:158-166.
Markiewicz-Górka, I, Januszewska, L, Michalak, A, Prokopowicz, A, Januszewska, E, Pawlas, N, and Pawlas, K (2015) Effects of chronic exposure to lead, cadmium, and manganese mixtures on oxidative stress in rat liver and heart/Utjecaj kronične istodobne izloženosti olovu, kadmiju i manganu na oksidativni stres u jetri i srcu štakora. Archives of Industrial Hygiene and Toxicology 66:1:51-62.
Mehana, E, Meki, ARM, and Fazili, KM (2012) Ameliorated effects of green tea extract on lead induced liver toxicity in rats. Experimental and toxicologic pathology 64:4:291-295.
Mutlu, N, Ersan, Y, Nur, G, and Koç, E (2011) Protective effect of caffeic acid phenethyl ester against lead acetate-induced hepatotoxicity in mice. Kafkas Univ Vet Fak Derg 17:Suppl A:S1-S5.
Mylroie, AA, Collins, H, Umbles, C, and Kyle, J (1986) Erythrocyte superoxide dismutase activity and other parameters of copper status in rats ingesting lead acetate. Toxicology and applied pharmacology 82:3:512-520.
Ozcelik, E, Uslu, S, Erkasap, N, and Karimi, H (2014) Protective effect of chitosan treatment against acetaminophen-induced hepatotoxicity. The Kaohsiung journal of medical sciences 30:6:286-290.
Ozkaya, A, Sahin, Z, Dag, U, and Ozkaraca, M (2016) Effects of naringenin on oxidative stress and histopathological changes in the liver of lead acetate administered rats. Journal of biochemical and molecular toxicology 30:5:243-248.
Ozkaya, A, Sahin, Z, Kuzu, M, Saglam, YS, Ozkaraca, M, Uckun, M, Yologlu, E, Comakli, V, Demirdag, R, and Yologlu, S (2018) Role of geraniol against lead acetate-mediated hepatic damage and their interaction with liver carboxylesterase activity in rats. Archives of physiology and biochemistry 124:1:80-87.
Özkan-Yılmaz, F, Özlüer-Hunt, A, Gündüz, SG, Berköz, M, and Yalın, S (2014) Effects of dietary selenium of organic form against lead toxicity on the antioxidant system in Cyprinus carpio. Fish physiology and biochemistry 40:2:355-363.
Patra, R, Rautray, AK, and Swarup, D (2011) Oxidative stress in lead and cadmium toxicity and its amelioration. Veterinary medicine international 2011:Article ID 457327.
Sarkar, A, Sengupta, D, Mandal, S, Sen, G, Dutta Chowdhury, K, and Chandra Sadhukhan, G (2015) Treatment with garlic restores membrane thiol content and ameliorates lead induced early death of erythrocytes in mice. Environmental toxicology 30:4:396-410.
Saxena, G, Pathak, U, and Flora, S (2005) Beneficial role of monoesters of meso-2, 3-dimercaptosuccinic acid in the mobilization of lead and recovery of tissue oxidative injury in rats. Toxicology 214:1-2:39-56.
Seki, S, Kitada, T, Yamada, T, Sakaguchi, H, Nakatani, K, and Wakasa, K (2002) In situ detection of lipid peroxidation and oxidative DNA damage in non-alcoholic fatty liver diseases. Journal of hepatology 37:1:56-62.
Shalan, M, Mostafa, M, Hassouna, M, El-Nabi, SH, and El-Refaie, A (2005) Amelioration of lead toxicity on rat liver with vitamin C and silymarin supplements. Toxicology 206:1:1-15.
Skoczyńska, A, and Smolik, R (1994) The effect of combined exposure to lead and cadmium on serum lipids and lipid peroxides level in rats. International journal of occupational medicine and environmental health 7:3:263-271.
Skoczyńska, A, Smolik, R, and Jeleń, M (1993) Lipid abnormalities in rats given small doses of lead. Archives of toxicology 67:3:200-204.
Subramanian, KS (1996) Determination of metals in biofluids and tissues: sample preparation methods for atomic spectroscopic techniques. Spectrochimica Acta Part B: Atomic Spectroscopy 51:3:291-319.
Toz, H, and Değer, Y (2018) The effect of chitosan on the erythrocyte antioxidant potential of lead toxicity-induced rats. Biological trace element research 184:114-118.
Tsai, J-P, Liou, J-H, Yeh, K-T, Tai, H-C, Cheng, Y-W, and Chang, H-R (2011) Intensity of cytosol expression of 8-OHdG in normal renal tubules is associated with the severity of renal fibrosis. Swiss medical weekly 141:4142.
Uhlikova, E, Kupcova, V, Szantova, M, and Turecky, L (2008) Plasma copper and ceruloplasmin in patients with alcoholic liver steatosis. Bratislavske lekarske listy 109:10:431-433.
Vassiliev, V, Harris, ZL, and Zatta, P (2005) Ceruloplasmin in neurodegenerative diseases. Brain Research Reviews 49:3:633-640.
Wang, Z, Yan, Y, Yu, X, Li, W, Li, B, and Qin, C (2016) Protective effects of chitosan and its water-soluble derivatives against lead-induced oxidative stress in mice. International journal of biological macromolecules 83:442-449.