Long-term treatment with paracetamol induces cell death in cerebral cortex of rat brain.
Keywords:
Long-term paracetamol treatment, neuronal cell death, cerebral cortex, caspase-3Abstract
Background : Paracetamol (APAP) is the most widely used for treatment of pain and fever. In the last decade, several studies have demonstrated the effect of the drug in several systems including the nervous system. However, the effect is still controversial.
Objective : The present study aimed to investigate the effects of APAP for shortterm (0 and 5 days) and long-term (15 and 30 days) treatment on cell death in rat’s cerebral cortex
Methods : In this study, adult male Wistar rats were divided into two groups: control and APAP-treated groups. In the APAP-treated group, the animals were singly intraperitoneally injected with APAP at the dose of 200 mg/kg in 0 - day. In the APAP-treated group and the once daily injection at the same dose was performed in 5, 15 and 30 days APAP-treated group, respectively. After completion of the treatment, all rats were humanely killed, and the fresh specimens were collected to determine the expression of caspase-3. While the 4% paraformaldehyde fixed samples were collected for Terminal deoxynucleotidyl transferase (TdT) dUTP Nick-End Labeling (TUNEL) assay and immunohistochemical study.
Results : The results obtained from this study demonstrated that short-term treatment (0 and 5 days) with APAP had no effect on the caspase-3 expression and TUNEL-immunoreactive cells in the cerebral cortex. However, the results demonstrated that the expression of caspase-3 and the TUNEL-immunoreactive cells in the long-term APAP-treated groups were significantly greater than those in the control.
Conclusion : Based on these results, it can be suggested that short-term APAP treatment had no effect on the neurons in the cerebral cortex. However, long-term treatment with the drug can induce an increment of caspase-3 expression and neuronal cell death in this brain region.
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References
Bolesta S, Haber SL. Hepatotoxicity associated with chronic acetaminophen administration in patients without risk factors. Ann Pharmacother 2002;36:331-3. https://doi.org/10.1345/aph.1A035
Kurtovic J, Riordan SM. Paracetamol-induced hepatotoxicity at recommended dosage. J Intern Med 2003;253:240-3. https://doi.org/10.1046/j.1365-2796.2003.01097.x
Larson AM. Acetaminophen hepatotoxicity. Clin Liver Dis 2007;11:525-48.
https://doi.org/10.1016/j.cld.2007.06.006
Zimatkin SM, Rout UK, Koivusalo M, Buhler R, Lindros KO. Regional distribution of low-Km mitochondrial aldehyde dehydrogenase in the rat central nervous system. Alcohol Clin Exp Res 1992;16:1162-7. https://doi.org/10.1111/j.1530-0277.1992.tb00713.x
Haorah J, Knipe B, Leibhart J, Ghorpade A, Persidsky Y. Alcohol-induced oxidative stress in brain endothelial cells causes blood-brain barrier dysfunction. J Leukoc Biol 2005;78:1223-32.
https://doi.org/10.1189/jlb.0605340
Posadas I, Santos P, Blanco A, Munoz-Fernandez M, Cena V. Acetaminophen induces apoptosis in rat cortical neurons. PLoS One 2010;5:e15360. https://doi.org/10.1371/journal.pone.0015360
Fischer LJ, Green MD, Harman AW. Levels of acetaminophen and its metabolites in mouse tissues after a toxic dose. J Pharmacol Exp Ther 1981;219:281-6.
Tripathy D, Grammas P. Acetaminophen inhibits neuronal inflammation and protects neurons from oxidative stress. J Neuroinflammation 2009;6:10. https://doi.org/10.1186/1742-2094-6-10
Tripathy D, Grammas P. Acetaminophen protects brain endothelial cells against oxidative stress. Microvasc Res 2009;77:289-96. https://doi.org/10.1016/j.mvr.2009.02.002
Maharaj H, Maharaj DS, Daya S. Acetylsalicylic acid and acetaminophen protect against oxidative neurotoxicity. Metab Brain Dis 2006; 21:189-99. https://doi.org/10.1007/s11011-006-9012-7
Supornsilpchai W, le Grand SM, Srikiatkhachorn A. Cortical hyperexcitability and mechanism of medication-overuse headache. Cephalalgia 2010;30:1101-9. https://doi.org/10.1177/0333102409355600
Reagan-Shaw S, Nihal M, Ahmad N. Dose translation from animal to human studies revisited. FASEB J 2008;22:659-61. https://doi.org/10.1096/fj.07-9574LSF
Yisarakun W, Supornsilpchai W, Chantong C, Srikiatkhachorn A, Maneesri-le Grand S. Chronic paracetamol treatment increases alterations in cerebral vessels in cortical spreading depression model. Microvasc Res 2014;94:36-46. https://doi.org/10.1016/j.mvr.2014.04.012
Kon K, Kim JS, Jaeschke H, Lemasters JJ. Mitochondrial permeability transition in acetaminophen-induced necrosis and apoptosis of cultured mouse hepatocytes. Hepatology 2004;40:1170-9.
https://doi.org/10.1002/hep.20437
Heard KJ. Acetylcysteine for acetaminophen poisoning. N Engl J Med 2008;359:285-92.
https://doi.org/10.1056/NEJMct0708278
Baliga SS, Jaques-Robinson KM, Hadzimichalis NM, Golfetti R, Merrill GF. Acetaminophen reduces mitochondrial dysfunction during early cerebral postischemic reperfusion in rats. Brain Res 2010;1319:142-54. https://doi.org/10.1016/j.brainres.2010.01.013
Fleury C, Mignotte B, Vayssiere JL. Mitochondrial reactive oxygen species in cell death signaling. Biochimie 2002;84:131-41. https://doi.org/10.1016/S0300-9084(02)01369-X
Fakunle PB. Ajibade AJ, Oyewo EB, Alamu OA, Daramola AK. Neurohistological degeneration of the hippocampal formation following chronic simultaneous administration of ethanol and acetaminophen in adult wistar rats (Rattus norvegicus). J Pharmacol Toxicol 2011;6:701-9.
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