Clinical associations between acetylcholine levels and cholinesterase activity in saliva and gingival crevicular fluid and periodontal diseases

Apatzidou, D. A., Iskas, A., Konstantinidis, A., Alghamdi, A. M., Tumelty, M., Lappin, D. F. and Nile, C. J. (2018) Clinical associations between acetylcholine levels and cholinesterase activity in saliva and gingival crevicular fluid and periodontal diseases. Journal of Clinical Periodontology, 45(10), pp. 1173-1183. (doi: 10.1111/jcpe.12989) (PMID:30022504)

[img]
Preview
Text
165781.pdf - Accepted Version

648kB

Abstract

Aim: The oral mucosa possesses a non‐neuronal cholinergic system. This study aimed to determine clinical evidence for a role of cholinergic mechanisms in the pathogenesis of periodontal diseases. Materials and Methods: Fifty healthy participants, 52 patients with gingivitis and 49 with periodontitis were recruited. Full periodontal parameters were recorded and saliva and gingival crevicular fluid (GCF) collected. Levels of acetylcholine and inflammatory mediators were quantified using commercially available assay kits. Acetylcholinesterase and butyrylcholinesterase activity were measured using a published biochemical assay. Results: Acetylcholine levels are significantly elevated in saliva and GCF, whereas GCF levels of butyrylcholinesterase activity are significantly decreased, in patients with periodontal diseases. Acetylcholine levels in saliva and GCF correlated positively with clinical markers of disease severity and with increased levels of IL‐17A and IL‐17F. In contrast, butyrylcholinesterase activity levels in GCF showed significant negative correlations with clinical markers of disease severity and IL‐17A and IL‐17F levels. None of the findings were due to smoking. Conclusions: Elevated acetylcholine levels and reduced butyrylcholinesterase activity are clinically associated with periodontal diseases and elevated levels of IL‐17A and IL‐17F. Therefore, non‐neuronal cholinergic mechanisms may influence IL‐17 biology and the aetiopathogenesis of periodontal diseases and therefore are possible therapeutic targets.

Item Type:Articles
Status:Published
Refereed:Yes
Glasgow Author(s) Enlighten ID:Alghamdi, Abeer Muhammad A and Lappin, Dr David and Tumelty, Dr Maria and Nile, Dr Christopher
Authors: Apatzidou, D. A., Iskas, A., Konstantinidis, A., Alghamdi, A. M., Tumelty, M., Lappin, D. F., and Nile, C. J.
College/School:College of Medical Veterinary and Life Sciences > School of Medicine, Dentistry & Nursing > Dental School
Journal Name:Journal of Clinical Periodontology
Publisher:Wiley
ISSN:0303-6979
ISSN (Online):1600-051X
Published Online:19 July 2018
Copyright Holders:Copyright © 2018 John Wiley and Sons A/S
First Published:First published in Journal of Clinical Periodontology 45(10): 1173-1183
Publisher Policy:Reproduced in accordance with the publisher copyright policy

University Staff: Request a correction | Enlighten Editors: Update this record