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Hangover headache and its behavioral changes in rats
OBJECTIVE(S): The present study aims to establish and evaluate a rat model for hangover headaches caused by alcoholic drinks. MATERIALS AND METHODS: Chronic migraine (CM) model rats were divided into 3 groups, and intragastrically administered alcoholic drinks (sample A, B, or C) to simulate hangove...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Mashhad University of Medical Sciences
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9922361/ https://www.ncbi.nlm.nih.gov/pubmed/36865042 http://dx.doi.org/10.22038/IJBMS.2023.66724.14644 |
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author | Lu, Shiguang Zhang, Ying Yang, Yuejun Zhang, Yafang Qin, Guangcheng Fu, Qingqing Shi, Yingying Zhang, Fan Wang, Zhe Chen, Yanhe Liu, Yuancai Chen, Lixue |
author_facet | Lu, Shiguang Zhang, Ying Yang, Yuejun Zhang, Yafang Qin, Guangcheng Fu, Qingqing Shi, Yingying Zhang, Fan Wang, Zhe Chen, Yanhe Liu, Yuancai Chen, Lixue |
author_sort | Lu, Shiguang |
collection | PubMed |
description | OBJECTIVE(S): The present study aims to establish and evaluate a rat model for hangover headaches caused by alcoholic drinks. MATERIALS AND METHODS: Chronic migraine (CM) model rats were divided into 3 groups, and intragastrically administered alcoholic drinks (sample A, B, or C) to simulate hangover headache attacks. The withdrawal threshold for the hind paw/face and the thermal latency of hind paw withdrawal were detected after 24 hr. Serum was collected from the periorbital venous plexus of rats in each group, and enzymatic immunoassays were used to determine the serum levels of calcitonin gene-related peptide (CGRP), substance P (SP), and nitric oxide (NO). RESULTS: Compared with the control group, the mechanical hind paw pain threshold was significantly lower in rats administered Samples A and B after 24 hr; however, no significant difference was observed across groups for the thermal pain threshold. The mechanical threshold for periorbital pain was only significantly reduced in rats administered Sample A. Immunoassays further indicated that serum levels of SP in the group administered Sample A were significantly higher than those in the control group; the serum levels of NO and CGRP were significantly higher in the group of rats receiving Sample B. CONCLUSION: We successfully developed an effective and safe rat model for investigating alcohol drink induced hangover headaches. This model could be used to investigate the mechanisms associated with hangover headaches for the development of novel and promising candidates for the future treatment or prophylaxis of hangover headaches. |
format | Online Article Text |
id | pubmed-9922361 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Mashhad University of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-99223612023-03-01 Hangover headache and its behavioral changes in rats Lu, Shiguang Zhang, Ying Yang, Yuejun Zhang, Yafang Qin, Guangcheng Fu, Qingqing Shi, Yingying Zhang, Fan Wang, Zhe Chen, Yanhe Liu, Yuancai Chen, Lixue Iran J Basic Med Sci Original Article OBJECTIVE(S): The present study aims to establish and evaluate a rat model for hangover headaches caused by alcoholic drinks. MATERIALS AND METHODS: Chronic migraine (CM) model rats were divided into 3 groups, and intragastrically administered alcoholic drinks (sample A, B, or C) to simulate hangover headache attacks. The withdrawal threshold for the hind paw/face and the thermal latency of hind paw withdrawal were detected after 24 hr. Serum was collected from the periorbital venous plexus of rats in each group, and enzymatic immunoassays were used to determine the serum levels of calcitonin gene-related peptide (CGRP), substance P (SP), and nitric oxide (NO). RESULTS: Compared with the control group, the mechanical hind paw pain threshold was significantly lower in rats administered Samples A and B after 24 hr; however, no significant difference was observed across groups for the thermal pain threshold. The mechanical threshold for periorbital pain was only significantly reduced in rats administered Sample A. Immunoassays further indicated that serum levels of SP in the group administered Sample A were significantly higher than those in the control group; the serum levels of NO and CGRP were significantly higher in the group of rats receiving Sample B. CONCLUSION: We successfully developed an effective and safe rat model for investigating alcohol drink induced hangover headaches. This model could be used to investigate the mechanisms associated with hangover headaches for the development of novel and promising candidates for the future treatment or prophylaxis of hangover headaches. Mashhad University of Medical Sciences 2023-03 /pmc/articles/PMC9922361/ /pubmed/36865042 http://dx.doi.org/10.22038/IJBMS.2023.66724.14644 Text en https://creativecommons.org/licenses/by/3.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/ (https://creativecommons.org/licenses/by/3.0/) ) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Lu, Shiguang Zhang, Ying Yang, Yuejun Zhang, Yafang Qin, Guangcheng Fu, Qingqing Shi, Yingying Zhang, Fan Wang, Zhe Chen, Yanhe Liu, Yuancai Chen, Lixue Hangover headache and its behavioral changes in rats |
title | Hangover headache and its behavioral changes in rats |
title_full | Hangover headache and its behavioral changes in rats |
title_fullStr | Hangover headache and its behavioral changes in rats |
title_full_unstemmed | Hangover headache and its behavioral changes in rats |
title_short | Hangover headache and its behavioral changes in rats |
title_sort | hangover headache and its behavioral changes in rats |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9922361/ https://www.ncbi.nlm.nih.gov/pubmed/36865042 http://dx.doi.org/10.22038/IJBMS.2023.66724.14644 |
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