Pathological effects of pregabalin toxicity in rats

Abstract Background: Pregabalin (PGB) is one kind of gabapentinoid. The main mechanism of action is binding at the alpha-2-delta site, which inhibits calcium influx in response to depolarization at nerve terminals and, in turn, suppresses the release of glutamate, noradrenaline, and substance P. Obj...

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Main Authors: Roaa Salih Mahdi, Nawras Najah, Sura Salman Ejam
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2024-01-01
Series:Medical Journal of Babylon
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Online Access:https://doi.org/10.4103/MJBL.MJBL_1709_23
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author Roaa Salih Mahdi
Nawras Najah
Sura Salman Ejam
author_facet Roaa Salih Mahdi
Nawras Najah
Sura Salman Ejam
author_sort Roaa Salih Mahdi
collection DOAJ
description Abstract Background: Pregabalin (PGB) is one kind of gabapentinoid. The main mechanism of action is binding at the alpha-2-delta site, which inhibits calcium influx in response to depolarization at nerve terminals and, in turn, suppresses the release of glutamate, noradrenaline, and substance P. Objectives: This study aimed to study the pathological effects of PGB toxicity on brain and liver of rats. Materials and Methods: We chose 20 mature albino rats, both sexes, averaging 220 g in weight; these were divided into two groups (10 rats per group): the toxic group and the control group. Tablets of Lyrica (Pfizer) may be purchased over the counter. The 300 mg of PGB in each tablet was dissolved in 3 mL of 0.9% normal saline. The dosage was determined using the maximum lethal oral dose in rats (5000 mg/kg) (Pfizer, 2017). Based on the rats’ weights, a toxic dosage of 1000 mg of PGB was determined and reconstituted in normal saline (0.9% in 3 mL). Each animal in the acute toxicity group received a single dose of the produced medication orally. After 24 h, all of the animals in both groups were euthanized. The brain and liver were quickly dissected and removed, washed in saline solution, and then processed for histopathological study. Results: Focal regions of hemorrhage and congestion were seen in H&E-stained sections from the acute toxicity group, and most pyramidal cells were degraded, pyknotic, and exhibited karyolysis. Cerebellar cortical layers were preserved; however, Purkinje cells were destroyed in the acute toxicity group, which also exhibited an increase in pyknotic cells, hemorrhage, vascular congestion, and localized loss of tissue. Hemorrhages, congestion of portal region blood vessels, and central veins and hepatic sinusoids were some of the most notable pathological abnormalities seen in the livers of those using PGB. Hepatocytes show nuclear pyknosis and a homogeneously acidophilic cytoplasm as a result of severe degenerative alterations, such as vacuolar degeneration and severe necrotic changes. Conclusion: PGB can cause pathological lesions in the brain and liver at a single toxic dose.
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spelling doaj-art-696565b8135a448db79f224b9c6906ab2025-01-25T10:14:51ZengWolters Kluwer Medknow PublicationsMedical Journal of Babylon1812-156X2312-67602024-01-0121121922210.4103/MJBL.MJBL_1709_23Pathological effects of pregabalin toxicity in ratsRoaa Salih MahdiNawras NajahSura Salman EjamAbstract Background: Pregabalin (PGB) is one kind of gabapentinoid. The main mechanism of action is binding at the alpha-2-delta site, which inhibits calcium influx in response to depolarization at nerve terminals and, in turn, suppresses the release of glutamate, noradrenaline, and substance P. Objectives: This study aimed to study the pathological effects of PGB toxicity on brain and liver of rats. Materials and Methods: We chose 20 mature albino rats, both sexes, averaging 220 g in weight; these were divided into two groups (10 rats per group): the toxic group and the control group. Tablets of Lyrica (Pfizer) may be purchased over the counter. The 300 mg of PGB in each tablet was dissolved in 3 mL of 0.9% normal saline. The dosage was determined using the maximum lethal oral dose in rats (5000 mg/kg) (Pfizer, 2017). Based on the rats’ weights, a toxic dosage of 1000 mg of PGB was determined and reconstituted in normal saline (0.9% in 3 mL). Each animal in the acute toxicity group received a single dose of the produced medication orally. After 24 h, all of the animals in both groups were euthanized. The brain and liver were quickly dissected and removed, washed in saline solution, and then processed for histopathological study. Results: Focal regions of hemorrhage and congestion were seen in H&E-stained sections from the acute toxicity group, and most pyramidal cells were degraded, pyknotic, and exhibited karyolysis. Cerebellar cortical layers were preserved; however, Purkinje cells were destroyed in the acute toxicity group, which also exhibited an increase in pyknotic cells, hemorrhage, vascular congestion, and localized loss of tissue. Hemorrhages, congestion of portal region blood vessels, and central veins and hepatic sinusoids were some of the most notable pathological abnormalities seen in the livers of those using PGB. Hepatocytes show nuclear pyknosis and a homogeneously acidophilic cytoplasm as a result of severe degenerative alterations, such as vacuolar degeneration and severe necrotic changes. Conclusion: PGB can cause pathological lesions in the brain and liver at a single toxic dose.https://doi.org/10.4103/MJBL.MJBL_1709_23brainhistopathologyliverpregabalinrats
spellingShingle Roaa Salih Mahdi
Nawras Najah
Sura Salman Ejam
Pathological effects of pregabalin toxicity in rats
Medical Journal of Babylon
brain
histopathology
liver
pregabalin
rats
title Pathological effects of pregabalin toxicity in rats
title_full Pathological effects of pregabalin toxicity in rats
title_fullStr Pathological effects of pregabalin toxicity in rats
title_full_unstemmed Pathological effects of pregabalin toxicity in rats
title_short Pathological effects of pregabalin toxicity in rats
title_sort pathological effects of pregabalin toxicity in rats
topic brain
histopathology
liver
pregabalin
rats
url https://doi.org/10.4103/MJBL.MJBL_1709_23
work_keys_str_mv AT roaasalihmahdi pathologicaleffectsofpregabalintoxicityinrats
AT nawrasnajah pathologicaleffectsofpregabalintoxicityinrats
AT surasalmanejam pathologicaleffectsofpregabalintoxicityinrats