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The relation between the effect of a subhypnotic dose of thiopental on claw pain threshold in rats and adrenalin, noradrenalin and dopamine levels
Thiopental sodium (TPS) needs to be applied together with adrenalin in order to establish its analgesic effect in general anesthesia. We aimed to investigate the effect of TPS on the claw pain threshold in rats and evaluated its relationship with endogenous adrenalin (ADR), noradrenalin (NDR), and d...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Japanese Association for Laboratory Animal Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4637376/ https://www.ncbi.nlm.nih.gov/pubmed/26211784 http://dx.doi.org/10.1538/expanim.15-0028 |
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author | Aksoy, Mehmet Ahiskalioglu, Ali Ince, Ilker Celik, Mine Dostbil, Aysenur Kuyrukluyildiz, Ufuk Altuner, Durdu Kurt, Nezahat Suleyman, Halis |
author_facet | Aksoy, Mehmet Ahiskalioglu, Ali Ince, Ilker Celik, Mine Dostbil, Aysenur Kuyrukluyildiz, Ufuk Altuner, Durdu Kurt, Nezahat Suleyman, Halis |
author_sort | Aksoy, Mehmet |
collection | PubMed |
description | Thiopental sodium (TPS) needs to be applied together with adrenalin in order to establish its analgesic effect in general anesthesia. We aimed to investigate the effect of TPS on the claw pain threshold in rats and evaluated its relationship with endogenous adrenalin (ADR), noradrenalin (NDR), and dopamine (DOP) levels. Intact and adrenalectomized rats were used in the experiment. Intact animals were divided into the following groups: 15 mg/kg TPS (TS), 0.3 mg/kg ADR+15 mg/kg TPS (ATS) and 0.3 mg/kg ADR alone (ADR). Adrenalectomized animals were divided into the following groups: 15 mg/kg TPS (A-TS), 0.3 mg/kg ADR+15 mg/kg TPS (A-ATS) and 0.3 mg/kg ADR alone (A-ADR). Claw pain threshold and blood ADR, NDR, and DOP levels were measured. The TS group’s claw pain threshold was found low. However, the claw pain thresholds of the ATS and ADR groups increased significantly. In the A-TS group, the pain threshold decreased compared with normal, and in the A-ATS and A-ADR groups, the pain threshold increased. TPS reduced the blood ADR levels in intact rats; however, no significant changes were observed in the NDR and DOP levels. #TPS provides hyperalgesia by reducing the production of ADR in rats. The present study shows that to achieve analgesic activity, TPS needs to be applied together with ADR. |
format | Online Article Text |
id | pubmed-4637376 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Japanese Association for Laboratory Animal Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-46373762015-11-09 The relation between the effect of a subhypnotic dose of thiopental on claw pain threshold in rats and adrenalin, noradrenalin and dopamine levels Aksoy, Mehmet Ahiskalioglu, Ali Ince, Ilker Celik, Mine Dostbil, Aysenur Kuyrukluyildiz, Ufuk Altuner, Durdu Kurt, Nezahat Suleyman, Halis Exp Anim Original Thiopental sodium (TPS) needs to be applied together with adrenalin in order to establish its analgesic effect in general anesthesia. We aimed to investigate the effect of TPS on the claw pain threshold in rats and evaluated its relationship with endogenous adrenalin (ADR), noradrenalin (NDR), and dopamine (DOP) levels. Intact and adrenalectomized rats were used in the experiment. Intact animals were divided into the following groups: 15 mg/kg TPS (TS), 0.3 mg/kg ADR+15 mg/kg TPS (ATS) and 0.3 mg/kg ADR alone (ADR). Adrenalectomized animals were divided into the following groups: 15 mg/kg TPS (A-TS), 0.3 mg/kg ADR+15 mg/kg TPS (A-ATS) and 0.3 mg/kg ADR alone (A-ADR). Claw pain threshold and blood ADR, NDR, and DOP levels were measured. The TS group’s claw pain threshold was found low. However, the claw pain thresholds of the ATS and ADR groups increased significantly. In the A-TS group, the pain threshold decreased compared with normal, and in the A-ATS and A-ADR groups, the pain threshold increased. TPS reduced the blood ADR levels in intact rats; however, no significant changes were observed in the NDR and DOP levels. #TPS provides hyperalgesia by reducing the production of ADR in rats. The present study shows that to achieve analgesic activity, TPS needs to be applied together with ADR. Japanese Association for Laboratory Animal Science 2015-07-22 2015 /pmc/articles/PMC4637376/ /pubmed/26211784 http://dx.doi.org/10.1538/expanim.15-0028 Text en ©2015 Japanese Association for Laboratory Animal Science http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License. |
spellingShingle | Original Aksoy, Mehmet Ahiskalioglu, Ali Ince, Ilker Celik, Mine Dostbil, Aysenur Kuyrukluyildiz, Ufuk Altuner, Durdu Kurt, Nezahat Suleyman, Halis The relation between the effect of a subhypnotic dose of thiopental on claw pain threshold in rats and adrenalin, noradrenalin and dopamine levels |
title | The relation between the effect of a subhypnotic dose of thiopental on claw
pain threshold in rats and adrenalin, noradrenalin and dopamine levels |
title_full | The relation between the effect of a subhypnotic dose of thiopental on claw
pain threshold in rats and adrenalin, noradrenalin and dopamine levels |
title_fullStr | The relation between the effect of a subhypnotic dose of thiopental on claw
pain threshold in rats and adrenalin, noradrenalin and dopamine levels |
title_full_unstemmed | The relation between the effect of a subhypnotic dose of thiopental on claw
pain threshold in rats and adrenalin, noradrenalin and dopamine levels |
title_short | The relation between the effect of a subhypnotic dose of thiopental on claw
pain threshold in rats and adrenalin, noradrenalin and dopamine levels |
title_sort | relation between the effect of a subhypnotic dose of thiopental on claw
pain threshold in rats and adrenalin, noradrenalin and dopamine levels |
topic | Original |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4637376/ https://www.ncbi.nlm.nih.gov/pubmed/26211784 http://dx.doi.org/10.1538/expanim.15-0028 |
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