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Antinociceptive and anti-inflammatory effects of N-acetylcysteine and verapamil in Wistar rats

BACKGROUND: Antinociceptive anti-inflammatory drugs have many adverse effects. The goal of this investigation is to study the probable anti-inflammatory and analgesic effects of verapamil and N-acetylcysteine (NAC) in experimental rats. METHODS: Adult male Wistar rats were randomly divided into 4 gr...

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Autores principales: Elberry, Ahmed Abdullah, Sharkawi, Souty Mouner Zaky, Wahba, Mariam Rofaiel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Pain Society 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6813896/
https://www.ncbi.nlm.nih.gov/pubmed/31569917
http://dx.doi.org/10.3344/kjp.2019.32.4.256
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author Elberry, Ahmed Abdullah
Sharkawi, Souty Mouner Zaky
Wahba, Mariam Rofaiel
author_facet Elberry, Ahmed Abdullah
Sharkawi, Souty Mouner Zaky
Wahba, Mariam Rofaiel
author_sort Elberry, Ahmed Abdullah
collection PubMed
description BACKGROUND: Antinociceptive anti-inflammatory drugs have many adverse effects. The goal of this investigation is to study the probable anti-inflammatory and analgesic effects of verapamil and N-acetylcysteine (NAC) in experimental rats. METHODS: Adult male Wistar rats were randomly divided into 4 groups in the antinociceptive study, each containing 6 rats; the normal control group, which received saline (1 mL/kg); the diclofenac group, which received diclofenac sodium (5 mg/kg); the NAC group, which received NAC (125 mg/kg); and the verapamil group, which received verapamil (8 mg/kg). In the anti-inflammatory study, 5 groups were used, the 4 previous groups with the addition of an edema control group, received saline and were subjected to formalin test. Hot plate latency time was recorded for antinociceptive evaluation. Paw edema thickness and biochemical parameters were recorded for anti-inflammatory evaluation. RESULTS: Administration of NAC showed significant prolongation of hot plate latency time at 1 hour when compared to the control group while verapamil showed a significant prolongation of hot plate latency time at 1 and 2 hours when compared to the control group and NAC group values. Administration of NAC and verapamil significantly decreased paw edema thickness at 2, 4, and 8 hours when compared to edema control values. Regarding biochemical markers, NAC and verapamil significantly decreased serum nitric oxide synthase, C-reactive protein, and cyclooxygenase-2 levels compared to the edema control value. In accordance, a marked improvement of histopathological findings was observed with both drugs. CONCLUSIONS: NAC and verapamil have antinociceptive and anti-inflammatory effects comparable to diclofenac sodium.
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spelling pubmed-68138962019-10-30 Antinociceptive and anti-inflammatory effects of N-acetylcysteine and verapamil in Wistar rats Elberry, Ahmed Abdullah Sharkawi, Souty Mouner Zaky Wahba, Mariam Rofaiel Korean J Pain Original Article BACKGROUND: Antinociceptive anti-inflammatory drugs have many adverse effects. The goal of this investigation is to study the probable anti-inflammatory and analgesic effects of verapamil and N-acetylcysteine (NAC) in experimental rats. METHODS: Adult male Wistar rats were randomly divided into 4 groups in the antinociceptive study, each containing 6 rats; the normal control group, which received saline (1 mL/kg); the diclofenac group, which received diclofenac sodium (5 mg/kg); the NAC group, which received NAC (125 mg/kg); and the verapamil group, which received verapamil (8 mg/kg). In the anti-inflammatory study, 5 groups were used, the 4 previous groups with the addition of an edema control group, received saline and were subjected to formalin test. Hot plate latency time was recorded for antinociceptive evaluation. Paw edema thickness and biochemical parameters were recorded for anti-inflammatory evaluation. RESULTS: Administration of NAC showed significant prolongation of hot plate latency time at 1 hour when compared to the control group while verapamil showed a significant prolongation of hot plate latency time at 1 and 2 hours when compared to the control group and NAC group values. Administration of NAC and verapamil significantly decreased paw edema thickness at 2, 4, and 8 hours when compared to edema control values. Regarding biochemical markers, NAC and verapamil significantly decreased serum nitric oxide synthase, C-reactive protein, and cyclooxygenase-2 levels compared to the edema control value. In accordance, a marked improvement of histopathological findings was observed with both drugs. CONCLUSIONS: NAC and verapamil have antinociceptive and anti-inflammatory effects comparable to diclofenac sodium. The Korean Pain Society 2019-10 2019-10-01 /pmc/articles/PMC6813896/ /pubmed/31569917 http://dx.doi.org/10.3344/kjp.2019.32.4.256 Text en © The Korean Pain Society, 2019 This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Elberry, Ahmed Abdullah
Sharkawi, Souty Mouner Zaky
Wahba, Mariam Rofaiel
Antinociceptive and anti-inflammatory effects of N-acetylcysteine and verapamil in Wistar rats
title Antinociceptive and anti-inflammatory effects of N-acetylcysteine and verapamil in Wistar rats
title_full Antinociceptive and anti-inflammatory effects of N-acetylcysteine and verapamil in Wistar rats
title_fullStr Antinociceptive and anti-inflammatory effects of N-acetylcysteine and verapamil in Wistar rats
title_full_unstemmed Antinociceptive and anti-inflammatory effects of N-acetylcysteine and verapamil in Wistar rats
title_short Antinociceptive and anti-inflammatory effects of N-acetylcysteine and verapamil in Wistar rats
title_sort antinociceptive and anti-inflammatory effects of n-acetylcysteine and verapamil in wistar rats
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6813896/
https://www.ncbi.nlm.nih.gov/pubmed/31569917
http://dx.doi.org/10.3344/kjp.2019.32.4.256
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