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Epinephrine penetrates through gingival sulcus unlike keratinized gingiva and evokes remote vasoconstriction in human
BACKGROUND: It has been demonstrated in non-oral tissues that the locally evoked vasoconstriction could elicit remote vasoconstriction. This study aimed to investigate the spreading vasoconstrictor effects of epinephrine in the gingiva. METHODS: Gingival blood flow (GBF) was measured by laser speckl...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7640651/ https://www.ncbi.nlm.nih.gov/pubmed/33148235 http://dx.doi.org/10.1186/s12903-020-01296-z |
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author | Vág, János Gánti, Bernadett Mikecs, Barbara Szabó, Enikő Molnár, Bálint Lohinai, Zsolt |
author_facet | Vág, János Gánti, Bernadett Mikecs, Barbara Szabó, Enikő Molnár, Bálint Lohinai, Zsolt |
author_sort | Vág, János |
collection | PubMed |
description | BACKGROUND: It has been demonstrated in non-oral tissues that the locally evoked vasoconstriction could elicit remote vasoconstriction. This study aimed to investigate the spreading vasoconstrictor effects of epinephrine in the gingiva. METHODS: Gingival blood flow (GBF) was measured by laser speckle contrast imager in 21 healthy volunteers. In group A, two wells were fabricated from orthodontic elastic ligature and placed 2 mm apically to the free gingival margin at the mid buccal line of 12 (test side) and 21 (control side) teeth. The GBF was measured in the wells and tightly apical, coronal, distal and mesial to the wells. In group B, the wells were made on the buccal surface of the same teeth, including the gingival sulcus. Four regions were selected for measurement from the gingival margin reaching the mucogingival line (coronal, midway1, midway2 and apical). After the baseline recording, 3 µg epinephrine was applied into the test, and physiological saline into the control well. The GBF was recorded for 14 min. The gingival thickness was measured with a PIROP Ultrasonic Biometer. RESULTS: In group A, the GBF did not increase or decrease after the application of epinephrine. In group B, the GBF significantly decreased in all regions of the test side and remained low for the observation period. The vasoconstriction appeared with delays in more apical regions (at min 1 in the coronal and the midway1, at min 2 in the midway2, at min 4 in the apical region). Similarly, the amount of the decrease at 14 min was the largest close to sulcus (− 53 ± 2.9%), followed by the midway1 (− 51 ± 2.8%) and midway2 (− 42 ± 4.2%) and was the lowest in the apical region (− 32 ± 5.8%). No correlation was found between GBF and gingival thickness. CONCLUSION: Epinephrine could evoke intense vasoconstriction propagating to the mucogingival junction, indicating the presence of spreading vasoconstriction in the human gingiva. The attached gingiva is impermeable to epinephrine, unlike the gingival sulcus. This trial was registered in ClinicalTrials.gov titled as Evidence of Spreading Vasoconstriction in Human Gingiva with the reference number of NCT04131283 on 16 October 2019. https://clinicaltrials.gov/show/NCT04131283 |
format | Online Article Text |
id | pubmed-7640651 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-76406512020-11-04 Epinephrine penetrates through gingival sulcus unlike keratinized gingiva and evokes remote vasoconstriction in human Vág, János Gánti, Bernadett Mikecs, Barbara Szabó, Enikő Molnár, Bálint Lohinai, Zsolt BMC Oral Health Research Article BACKGROUND: It has been demonstrated in non-oral tissues that the locally evoked vasoconstriction could elicit remote vasoconstriction. This study aimed to investigate the spreading vasoconstrictor effects of epinephrine in the gingiva. METHODS: Gingival blood flow (GBF) was measured by laser speckle contrast imager in 21 healthy volunteers. In group A, two wells were fabricated from orthodontic elastic ligature and placed 2 mm apically to the free gingival margin at the mid buccal line of 12 (test side) and 21 (control side) teeth. The GBF was measured in the wells and tightly apical, coronal, distal and mesial to the wells. In group B, the wells were made on the buccal surface of the same teeth, including the gingival sulcus. Four regions were selected for measurement from the gingival margin reaching the mucogingival line (coronal, midway1, midway2 and apical). After the baseline recording, 3 µg epinephrine was applied into the test, and physiological saline into the control well. The GBF was recorded for 14 min. The gingival thickness was measured with a PIROP Ultrasonic Biometer. RESULTS: In group A, the GBF did not increase or decrease after the application of epinephrine. In group B, the GBF significantly decreased in all regions of the test side and remained low for the observation period. The vasoconstriction appeared with delays in more apical regions (at min 1 in the coronal and the midway1, at min 2 in the midway2, at min 4 in the apical region). Similarly, the amount of the decrease at 14 min was the largest close to sulcus (− 53 ± 2.9%), followed by the midway1 (− 51 ± 2.8%) and midway2 (− 42 ± 4.2%) and was the lowest in the apical region (− 32 ± 5.8%). No correlation was found between GBF and gingival thickness. CONCLUSION: Epinephrine could evoke intense vasoconstriction propagating to the mucogingival junction, indicating the presence of spreading vasoconstriction in the human gingiva. The attached gingiva is impermeable to epinephrine, unlike the gingival sulcus. This trial was registered in ClinicalTrials.gov titled as Evidence of Spreading Vasoconstriction in Human Gingiva with the reference number of NCT04131283 on 16 October 2019. https://clinicaltrials.gov/show/NCT04131283 BioMed Central 2020-11-04 /pmc/articles/PMC7640651/ /pubmed/33148235 http://dx.doi.org/10.1186/s12903-020-01296-z Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article Vág, János Gánti, Bernadett Mikecs, Barbara Szabó, Enikő Molnár, Bálint Lohinai, Zsolt Epinephrine penetrates through gingival sulcus unlike keratinized gingiva and evokes remote vasoconstriction in human |
title | Epinephrine penetrates through gingival sulcus unlike keratinized gingiva and evokes remote vasoconstriction in human |
title_full | Epinephrine penetrates through gingival sulcus unlike keratinized gingiva and evokes remote vasoconstriction in human |
title_fullStr | Epinephrine penetrates through gingival sulcus unlike keratinized gingiva and evokes remote vasoconstriction in human |
title_full_unstemmed | Epinephrine penetrates through gingival sulcus unlike keratinized gingiva and evokes remote vasoconstriction in human |
title_short | Epinephrine penetrates through gingival sulcus unlike keratinized gingiva and evokes remote vasoconstriction in human |
title_sort | epinephrine penetrates through gingival sulcus unlike keratinized gingiva and evokes remote vasoconstriction in human |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7640651/ https://www.ncbi.nlm.nih.gov/pubmed/33148235 http://dx.doi.org/10.1186/s12903-020-01296-z |
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