Selenium reduces nociceptive response in acute 1-methyl-4-phenyl-1, 2, 3, 6-tetrahydropyridine (MPTP)-induced neurotoxicity

The potential of Se to alleviate pain associated with 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-induced neurotoxicity was investigated.Swiss mice were intraperitoneally injected with MPTP (20 mg/kg) 4 times with an interval of 2 h in 1 day. Seven days after MPTP injection, the mice (n = 5...

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Main Authors: Patrick Oluwole Abolarin, Abdulrazaq Bidemi Nafiu, Aboyeji Lukuman Oyewole, Abdulbasit Amin, Olalekan Michael Ogundele, Bamidele Victor Owoyele
Format: Article
Language:English
Published: Elsevier 2022-06-01
Series:IBRO Neuroscience Reports
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2667242121000476
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author Patrick Oluwole Abolarin
Abdulrazaq Bidemi Nafiu
Aboyeji Lukuman Oyewole
Abdulbasit Amin
Olalekan Michael Ogundele
Bamidele Victor Owoyele
author_facet Patrick Oluwole Abolarin
Abdulrazaq Bidemi Nafiu
Aboyeji Lukuman Oyewole
Abdulbasit Amin
Olalekan Michael Ogundele
Bamidele Victor Owoyele
author_sort Patrick Oluwole Abolarin
collection DOAJ
description The potential of Se to alleviate pain associated with 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-induced neurotoxicity was investigated.Swiss mice were intraperitoneally injected with MPTP (20 mg/kg) 4 times with an interval of 2 h in 1 day. Seven days after MPTP injection, the mice (n = 5 mice per group) were randomly assigned to groups: MPTP-, DOPA (50 mg/kg)-, Se4 (0.4 mg/kg)-, Se6 (0.6 mg/kg)-, DOPA+Se4-, and DOPA+Se6-treated groups were compared with controls. MPTP mice were treated for seven days; thereafter, motor-coordination and nociceptive-motor reactions were assessed. Pro-inflammatory cytokines (IL-1β, IL-6 and TNFα), and selected pain biomarkers (substance P (SP), glutamate and β-endorphin) were assessed in the serum and the substantial nigra pars compacta (SNpc).Motor activity was increased slightly by Se (0.6 or 0.4 mg/kg) vs. MPTP (10.48 ± 2.71 or 11.81 ± 1.28 s vs. 3.53 ± 0.06 s respectively) but considerably increased by DOPA (50 mg/kg) vs. MPTP (50.47 ± 3.06 s vs. 3.53 ± 0.06 s respectively). Se and DOPA increased nociceptive threshold but Se alone reduced both serum and SN pro-inflammatory cytokines. Se modulates SP while DOPA modulates SP and glutamate in the SNpc of mice treated with MPTP.Se suppressed pro-inflammatory cytokines and restored the basal pain biomarkers in the SNpc of mice treated with MPTP. Se requires further study as analgesic adjuvant.
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spelling doaj.art-158d29ff4440452191da5ae905af990f2022-12-22T00:18:49ZengElsevierIBRO Neuroscience Reports2667-24212022-06-0112111Selenium reduces nociceptive response in acute 1-methyl-4-phenyl-1, 2, 3, 6-tetrahydropyridine (MPTP)-induced neurotoxicityPatrick Oluwole Abolarin0Abdulrazaq Bidemi Nafiu1Aboyeji Lukuman Oyewole2Abdulbasit Amin3Olalekan Michael Ogundele4Bamidele Victor Owoyele5Department of Physiology, University of Ilorin, P.M.B 1515, Ilorin, NigeriaDepartment of Human Physiology, Federal University Dutse, Dutse, Jigawa State, NigeriaDepartment of Physiology, University of Ilorin, P.M.B 1515, Ilorin, NigeriaDepartment of Physiology, University of Ilorin, P.M.B 1515, Ilorin, NigeriaDepartment of Comparative Biomedical Sciences, Louisiana State University, School of Veterinary Medicine, Baton Rouge, LA, USADepartment of Physiology, University of Ilorin, P.M.B 1515, Ilorin, Nigeria; Corresponding author.The potential of Se to alleviate pain associated with 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-induced neurotoxicity was investigated.Swiss mice were intraperitoneally injected with MPTP (20 mg/kg) 4 times with an interval of 2 h in 1 day. Seven days after MPTP injection, the mice (n = 5 mice per group) were randomly assigned to groups: MPTP-, DOPA (50 mg/kg)-, Se4 (0.4 mg/kg)-, Se6 (0.6 mg/kg)-, DOPA+Se4-, and DOPA+Se6-treated groups were compared with controls. MPTP mice were treated for seven days; thereafter, motor-coordination and nociceptive-motor reactions were assessed. Pro-inflammatory cytokines (IL-1β, IL-6 and TNFα), and selected pain biomarkers (substance P (SP), glutamate and β-endorphin) were assessed in the serum and the substantial nigra pars compacta (SNpc).Motor activity was increased slightly by Se (0.6 or 0.4 mg/kg) vs. MPTP (10.48 ± 2.71 or 11.81 ± 1.28 s vs. 3.53 ± 0.06 s respectively) but considerably increased by DOPA (50 mg/kg) vs. MPTP (50.47 ± 3.06 s vs. 3.53 ± 0.06 s respectively). Se and DOPA increased nociceptive threshold but Se alone reduced both serum and SN pro-inflammatory cytokines. Se modulates SP while DOPA modulates SP and glutamate in the SNpc of mice treated with MPTP.Se suppressed pro-inflammatory cytokines and restored the basal pain biomarkers in the SNpc of mice treated with MPTP. Se requires further study as analgesic adjuvant.http://www.sciencedirect.com/science/article/pii/S2667242121000476NeurotoxicitySeleniumMotor coordinationNociceptive thresholdNeuroinflammationPain biomarkers
spellingShingle Patrick Oluwole Abolarin
Abdulrazaq Bidemi Nafiu
Aboyeji Lukuman Oyewole
Abdulbasit Amin
Olalekan Michael Ogundele
Bamidele Victor Owoyele
Selenium reduces nociceptive response in acute 1-methyl-4-phenyl-1, 2, 3, 6-tetrahydropyridine (MPTP)-induced neurotoxicity
IBRO Neuroscience Reports
Neurotoxicity
Selenium
Motor coordination
Nociceptive threshold
Neuroinflammation
Pain biomarkers
title Selenium reduces nociceptive response in acute 1-methyl-4-phenyl-1, 2, 3, 6-tetrahydropyridine (MPTP)-induced neurotoxicity
title_full Selenium reduces nociceptive response in acute 1-methyl-4-phenyl-1, 2, 3, 6-tetrahydropyridine (MPTP)-induced neurotoxicity
title_fullStr Selenium reduces nociceptive response in acute 1-methyl-4-phenyl-1, 2, 3, 6-tetrahydropyridine (MPTP)-induced neurotoxicity
title_full_unstemmed Selenium reduces nociceptive response in acute 1-methyl-4-phenyl-1, 2, 3, 6-tetrahydropyridine (MPTP)-induced neurotoxicity
title_short Selenium reduces nociceptive response in acute 1-methyl-4-phenyl-1, 2, 3, 6-tetrahydropyridine (MPTP)-induced neurotoxicity
title_sort selenium reduces nociceptive response in acute 1 methyl 4 phenyl 1 2 3 6 tetrahydropyridine mptp induced neurotoxicity
topic Neurotoxicity
Selenium
Motor coordination
Nociceptive threshold
Neuroinflammation
Pain biomarkers
url http://www.sciencedirect.com/science/article/pii/S2667242121000476
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