Effects of Agro-based Adsorbents on the Biochemical Profiles of Wistar Rats Exposed to Cyanide

World Health Organization (WHO). Cyanide in Drinking Water. In. Background document for development of WHO Guidelines for Drinking Water quality. World Health Organization: Geneva 2018.

World Health Organization (WHO) (2020). Public health impact of chemicals, knowns and unknowns. Geneva: Geneva 2016.

Centre for Disease Control (2019). Morbidity and Mortality weekly report (MMWR). Weekly April 5, 2019/68(13); 308-311.

Zuhra, K., & Szabo, C. The two faces of cyanide: an environmental toxin and a potential novel mammalian gasotransmitter. The FEBS journal, 289(9), 2022; 2481–2515. https://doi.org/10.1111/febs.16135.

Petrikovics I, Budai M, Kovacs K & Thompson DE. Past, present and future of cyanide antagonism research: From the early remedies to the current therapies. World J Methodol 2015;5, 88–100. [PMC free article] [PubMed] [Google Scholar].

Hendry‐Hofer TB, Ng PC, Witeof AE, Mahon SB, Brenner M, Boss GR & Bebarta VS. A review on ingested cyanide: risks, clinical presentation, diagnostics, and treatment challenges. J Med Toxicol 2019; 15, 128–133. [PMC free article] [PubMed] [Google Scholar]

Singh P, Rao P, Yadav SK, Gujar NL, Satpute RM & Bhattacharya R. Time‐ and temperature‐dependent changes in cytochrome c oxidase activity and cyanide concentration in excised mice organs and mice cadavers. J Forensic Sci 2015;60, S162–170. [PubMed] [Google Scholar]

Marziaz ML, Frazier K, Guidry PB, Ruiz RA, Petrikovics I & Haines DC. Comparison of brain mitochondrial cytochrome c oxidase activity with cyanide LD50 yields insight into the efficacy of prophylactics. J Appl Toxicol 2013;33, 50–55. [PubMed] [Google Scholar]

Niknahad H & O'Brien PJ. Mechanism of sulfite cytotoxicity in isolated rat hepatocytes. Chem Biol Interact 2008;174, 147–154. [PubMed] [Google Scholar]

Idonije OB, Festus OO, Ihongbe JC, Eidangbe GO, Agbebaku SO, Nwokocha MC. Some liver function indicators in guinea pigs injected with cyanide. Scientific Journal of Pure and Applied Sciences. 2013;2(7):279-83.

Leavesley HB, Li L, Prabhakaran K, Borowitz JL & Isom GE. Interaction of cyanide and nitric oxide with cytochrome c oxidase: implications for acute cyanide toxicity. Toxicol Sci 2008;101, 101–111. [PubMed] [Google Scholar]

Hariharakrishnan J, Satpute RM, Prasad GB & Bhattacharya R. Oxidative stress mediated cytotoxicity of cyanide in LLC‐MK2 cells and its attenuation by alpha‐ketoglutarate and N‐acetyl cysteine. Toxicol Lett 2009;185, 132–141. [PubMed] [Google Scholar]

Dalal P & Romani A. Adenosine triphosphate depletion by cyanide results in a Na+ -dependent Mg2+ extrusion from liver cells. Metabolism 2010;59, 1663–1671.

Yamagiwa T, Inokuchi S, Saito T, Inoue S, Morita S & Kawaguchi AT. A stable in vitro method for assessing the toxicity of potassium cyanide and its antidote. Tokai J Exp Clin Med 2013;38, 114–122. [PubMed] [Google Scholar].

Njankouo YN, Nyegue MA, Njingou I, Moundipa PF, Mounjouenpou P. Toxic Potential of Crude Extract From Cassava Cortex Containing Scopoletin and Cyanide on Wistar Rats and Broilers. Dose Response. 2023 Sep 22;21(3):15593258231203587. doi: 10.1177/15593258231203587. PMID: 37744654; PMCID: PMC10517615.

Ferner RE. Our poisoned patients QJM 2004; 94:117-20.

Li H. Li M. J. Zheng F. Wang J. Chen L. Hu P. F. Zhen Q. Bashir S. Liu J. L. Efficient removal of water pollutants by hierarchical porous zeolite-activated carbon prepared from coal gangue and bamboo. J. Cleaner Prod. 2021;325:129322. [Google Scholar].

Ekpete O.A., Horsfall M. Kinetic sorption study of phenol onto activated carbon derived from fluted pumpkin stem waste (Telfairia occidentalis Hook. F) ARPN J. Eng. Appl. Sci. 2011;6:43–49. [Google Scholar.

Chacko B, Peter JV. Antidotes in Poisoning. Indian J Crit Care Med 2019;23(Suppl 4):S241-S249.

Neuvonen PJ, Elonen E, Mattila MJ. Oral activated charcoal and dapsone elimination. Clin Pharmacol Ther 1980; 27: 823-7.

Alaspaa O, Kvisma J, Happu K, Neurvonem P (2000). Feasibility activated charcoal given prehospital by emergency medical system in acute intoxication. J Toxicol 38: 152-156.

McGoodwin L, Schaeffer S. Availability of activated charcoal in the metropolitan area of Oklahoma City . J Toxicol. 2000;38: 401-407.

Cooper GM, Le Couteur DG, Richardson D, Buckley NA. A randomized clinical of activated charcoal for the routine management of oral drug overdose OJM 2005;98(9) 655-60.

Green R, Grierson R, Sitar DS, Tenenbein M (2001). How long after drug ingestion is activated charcoal still effective? J Toxicol Clin Toxicol; 39:601-5

Christophersen AB, Levin D, Hoegberg LC, Angelo HR, Kampmann JP. Activated charcoal alone or after gastric lavage: a simulated large paracetamol intoxication. Br J Clin Pharmacol 2002; 53:312-7

Subramani T; Revathi PK. .Production of activated carbon from agricultural raw waste. J. Eng. 2015; 5(5): 54-63.

Babalola T.O., Oyawale F.E., Adejumo I.O., Bolu S.A. Effects of dietary fish oil replacement by vegetable oil on the serum biochemical and haematological parameters of African catfish (Heterobranchus longifilis) fingerlings. Iran. J. Fish. Sci 2016;15(2):775–788. [Google Scholar].

Baghshani H, Ghodsi V. Evaluation of some enzymatic changes in the liver and kidney of rats following exposure to sublethal concentration of potassium cyanide.

Kadiri HE, Asagba SO. The biochemical effects of cyanide on the activity of the transaminases and alkaline phosphatase in broilers (Gallus domesticus). American J. Biochem. 2015;5(2):23-9.

Boby R.G., Indira M. Effect of co-administration of cassava Manihot esculenta (Crantz) rich diet and alcohol in rats. Indian J. Physiol. Pharmacol 2004;48(1):41–50. [PubMed] [Google Scholar].

Soto-Blanco B, Marioka PC and Gorniak SL. Effects of long-term low-dose cyanide administration to rats. Ecotoxicology and Environmental Safety 2002, 53, 37–41.

Manzano, H., de Sousa, A.B., Soto-Blanco, B., Guerra, J.L., Maiorka, P.C., Gorniak, S.L. Effects of long-term cyanide ingestion by pigs. Veterinary Research Communications 2007; 31, 93–104. doi:10.1007/ s11259-006-3361-x

Kadiri HE, Asagba SO. The biochemical effects of cyanide on the activity of the transaminases and alkaline phosphatase in broilers (Gallus domesticus). American J. Biochem. 2015;5(2):23-9.

Tulsawani RK, Debnath M, Pant SC, Kumar O, Prakash AO, Vijayaraghavan R and Bhattacharya R. Effect of sub-acute oral cyanide administration in rats: protective efficacy of alpha-ketoglutarate and sodium thiosulfate. Chemico-Biological Interactions 2005; 156, 1–12.

Anwar MM, Mohammed NE, Rad J. Impact of flax seed and canola oil mixture supplementation in physiological and biochemical changes induced by monosodium glutamate in rats. Food science and human wellness 2010;7(2): 234-242.

Kazi MD, Mahmudul H, Nasrin TMD, Anwarul H. Biochemical and histopathological profiling of wistar rats treated with Brassica napus as a supplementary feed. Food Science and Human Wellness 2018; 7(1):77-82.

Njankouo YN, Nyegue MA, Njingou I, Moundipa PF, Mounjouenpou P. Toxic Potential of Crude Extract From Cassava Cortex Containing Scopoletin and Cyanide on Wistar Rats and Broilers. Dose Response. 2023 Sep 22;21(3):15593258231203587. doi: 10.1177/15593258231203587. PMID: 37744654; PMCID: PMC10517615.

Ihedioha T.E., Odo R.I., Onoja U.S., Chiwetalu C.E., Ihedioha J.I. Effects of methanolic tuber extract of Cyperus esculentus Linn (tiger nuts) on sub-acute liver damage in albino rats. African J. Pharm. Pharmacol 2019;13(15):236–243. [Google Scholar]

Ojeniyi FD, Ehigie AF, Ehigie OL. Evaluation of Enzymatic Changes in Sublethal Cyanide Poisoning in Wistar Rats Treated with Chromolaena odorata (Linn.) and Sodium Thiosulphate. J Plant Biochem Physiol. 2019;7:242.

Sousa AB, Soto-Blanco B, Guerra JL, Kimura ET and Gorniak SL. Does prolonged oral exposure to cyanide promote hepatotoxicity and nephrotoxicity? Toxicology 2002; 174, 87–95.

Sadati Fahimeh, Davar Shahasavani and Hasan Baghshani. Biochemical Alterations induced by sublethal cyanide exposure in common Carp. J Biol. Envirn Sci 2013;7(20):65-69).

Bhadauria M., Nirala S.K., Shukla S. Hepatoprotective efficacy of Propolis Extract: a biochemical and histopathological approach. Iran. J 2007; Pharmacol. Ther. 2007;6(2):145–154. [Google Scholar].

Okolie NP, Osagie AU. Liver and kidney lesions and associated enzyme changes induced in rabbits by chronic cyanide exposure. Food Chem Toxicol. 1999 Jul;37(7):745-50. doi: 10.1016/s0278-6915(99)00059-9. PMID: 10496376.

Oyewole O.I., Olayinka E.T. Hydroxocobalamin (Vit. B 12a) effectively reduced extent of cyanide poisoning arising from oral amygdalin ingestion in rats. J. Toxicol. Environ. Health Sci. 2009;1(1):8–11. [Google Scholar]

Khan HA, Alhomida AS, Sobki SH et al (2013). Serum markers of tissue damage and oxidative stress in patients with acute myocardial infarction. Biomed Res. 2013;24: 15-20.

留言 (0)

沒有登入
gif