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Comparison of the efficacy of carbamazepine, gabapentin and lamotrigine for neuropathic pain in rats

BACKGROUND: Neuropathic pain in cancer patients remain a treatment challenge. Many of the anticancer drugs have to be abandoned because patients develop neuropathic pain. Several antiepileptic drugs like carbamazepine, phenytoin, lamotrigine, felbamate are effective in neuropathic pain and trigemina...

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Autores principales: Chogtu, Bharti, Bairy, K. L., Smitha, D., Dhar, Supurna, Himabindu, P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3195135/
https://www.ncbi.nlm.nih.gov/pubmed/22022008
http://dx.doi.org/10.4103/0253-7613.84980
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author Chogtu, Bharti
Bairy, K. L.
Smitha, D.
Dhar, Supurna
Himabindu, P.
author_facet Chogtu, Bharti
Bairy, K. L.
Smitha, D.
Dhar, Supurna
Himabindu, P.
author_sort Chogtu, Bharti
collection PubMed
description BACKGROUND: Neuropathic pain in cancer patients remain a treatment challenge. Many of the anticancer drugs have to be abandoned because patients develop neuropathic pain. Several antiepileptic drugs like carbamazepine, phenytoin, lamotrigine, felbamate are effective in neuropathic pain and trigeminal neuralgia. However, their efficacy varies. AIM: The aim of this study is to compare the efficacy of antiepileptic drugs in neuropathic pain induced by anticancer drugs. MATERIALS AND METHODS: Neuropathic pain was induced in rats by injecting 4 doses of paclitaxel. The rats were divided into four groups of six animals each. Group I was treated with oral carbamazepine (cbz) 100 mg/kg, group II received oral gabapentin (gbp) 60 mg/kg, and group III was treated with oral lamotrigine (lam) 40 mg/kg and group IV was the control group. Behavioural testing for thermal hyperalgesia and mechanical hyperalgesia was assessed from 26(th) day of paclitaxel administration to next five days by hot plate method and Randall Siletto test, respectively, in all the four groups. One way analysis of variance followed by Scheffe's post hoc test was used for statistical analysis. RESULTS: In thermal hyperalgesia lam treated group was found to be significantly (P < 0.001) superior to cbz and gbp treated group. In mechanical hyperalgesia, lam group showed significant response (P < 0.05) as compared to gbp group. However, the gbp treated group showed a significant (P < 0.01) improvement after three days of treatment. CONCLUSIONS: In paclitaxel induced neuropathic pain, lamotrigine appears to be a promising drug. The difference in responses shown by different antiepileptics’ depends on the etiology of the underlying mechanisms in neuropathic pain.
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spelling pubmed-31951352011-10-21 Comparison of the efficacy of carbamazepine, gabapentin and lamotrigine for neuropathic pain in rats Chogtu, Bharti Bairy, K. L. Smitha, D. Dhar, Supurna Himabindu, P. Indian J Pharmacol Short Communication BACKGROUND: Neuropathic pain in cancer patients remain a treatment challenge. Many of the anticancer drugs have to be abandoned because patients develop neuropathic pain. Several antiepileptic drugs like carbamazepine, phenytoin, lamotrigine, felbamate are effective in neuropathic pain and trigeminal neuralgia. However, their efficacy varies. AIM: The aim of this study is to compare the efficacy of antiepileptic drugs in neuropathic pain induced by anticancer drugs. MATERIALS AND METHODS: Neuropathic pain was induced in rats by injecting 4 doses of paclitaxel. The rats were divided into four groups of six animals each. Group I was treated with oral carbamazepine (cbz) 100 mg/kg, group II received oral gabapentin (gbp) 60 mg/kg, and group III was treated with oral lamotrigine (lam) 40 mg/kg and group IV was the control group. Behavioural testing for thermal hyperalgesia and mechanical hyperalgesia was assessed from 26(th) day of paclitaxel administration to next five days by hot plate method and Randall Siletto test, respectively, in all the four groups. One way analysis of variance followed by Scheffe's post hoc test was used for statistical analysis. RESULTS: In thermal hyperalgesia lam treated group was found to be significantly (P < 0.001) superior to cbz and gbp treated group. In mechanical hyperalgesia, lam group showed significant response (P < 0.05) as compared to gbp group. However, the gbp treated group showed a significant (P < 0.01) improvement after three days of treatment. CONCLUSIONS: In paclitaxel induced neuropathic pain, lamotrigine appears to be a promising drug. The difference in responses shown by different antiepileptics’ depends on the etiology of the underlying mechanisms in neuropathic pain. Medknow Publications 2011 /pmc/articles/PMC3195135/ /pubmed/22022008 http://dx.doi.org/10.4103/0253-7613.84980 Text en Copyright: © Indian Journal of Pharmacology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Short Communication
Chogtu, Bharti
Bairy, K. L.
Smitha, D.
Dhar, Supurna
Himabindu, P.
Comparison of the efficacy of carbamazepine, gabapentin and lamotrigine for neuropathic pain in rats
title Comparison of the efficacy of carbamazepine, gabapentin and lamotrigine for neuropathic pain in rats
title_full Comparison of the efficacy of carbamazepine, gabapentin and lamotrigine for neuropathic pain in rats
title_fullStr Comparison of the efficacy of carbamazepine, gabapentin and lamotrigine for neuropathic pain in rats
title_full_unstemmed Comparison of the efficacy of carbamazepine, gabapentin and lamotrigine for neuropathic pain in rats
title_short Comparison of the efficacy of carbamazepine, gabapentin and lamotrigine for neuropathic pain in rats
title_sort comparison of the efficacy of carbamazepine, gabapentin and lamotrigine for neuropathic pain in rats
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3195135/
https://www.ncbi.nlm.nih.gov/pubmed/22022008
http://dx.doi.org/10.4103/0253-7613.84980
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