Department of Removable Prosthodontics, University of Zagreb School of Dental Medicine, University of Zagreb, Zagreb, 10000, Croatia.
Department of Dental Medicine, Clinical Hospital Centre Zagreb, Zagreb, 10000, Croatia.
Clin Oral Investig. 2024 Apr 9;28(5):246. doi: 10.1007/s00784-024-05653-y.
Opiorphin is an analgesic peptide released by salivary glands and capsaicin an agonist of TRPV1 receptors eliciting burning sensations. The primary objective of this study was to assess opiorphin release after stimulation of the tongue by capsaicin (STC). The secondary objectives were to compare opiorphin release after STC in 3 groups of subjects [healthy (CTRL), Burning Mouth Syndrome (BMS), painful Temporomandibular disorders (TMDp)] and pain evoked by STC in these 3 groups.
Salivary opiorphin was assessed with high-performance liquid chromatography at 3 different time points (baseline, after 5 min and 20 min of STC). Pain was self-reported on a (0-10) numeric rating scale.
Three groups (N = 16) of adults were recruited at the Clinical Hospital Centre and School of Dental Medicine in Zagreb. Opiorphin levels were higher (1) in TMDp compared to CTRL in 1st (2.23 ± 1.72 pg/ul vs. 0.67 ± 0.44 pg/ul, p = 0.002) and 3rd sampling (2.44 ± 2.01 pg/ul vs. 0.74 ± 0.52 pg/ul, p = 0.020) and (2) within BMS group at 3rd sampling vs. baseline (p < 0.025). Pain scores were higher in BMS compared to TMDp (p < 0.025) and CTRL (p < 0.025).
This study evidenced (1) a differential basal amount of opiorphin in two pain conditions and control subjects (2) a differential kinetic of release of opiorphin after STC in CTRL, BMS and TMDp (3) a differential pain perception after STC in BMS and TMDp vs. CTRL, which can provide a readout for animal models.
The specific regulation of opiorphin release in patients with orofacial painful conditions provides valuable insights for clinicians and researchers in physiology and pathology and encourages further research in this area.
ClinicalTrials.gov NCT04694274. Registered on 01/05/2021.
阿片啡肽是一种由唾液腺释放的镇痛肽,辣椒素是 TRPV1 受体的激动剂,能引起烧灼感。本研究的主要目的是评估舌部受辣椒素刺激(STC)后阿片啡肽的释放。次要目的是比较健康对照组(CTRL)、灼口综合征(BMS)和疼痛性颞下颌关节紊乱(TMDp)三组患者 STC 后阿片啡肽的释放和 STC 引起的疼痛。
采用高效液相色谱法在 3 个不同时间点(基线、STC 后 5 分钟和 20 分钟)评估唾液阿片啡肽。疼痛通过 0-10 数字评分量表自我报告。
共招募了来自萨格勒布临床医院中心和牙医学院的三组(每组 16 名)成年人。与 CTRL 相比,TMDp 组 1 次(2.23±1.72 pg/ul 比 0.67±0.44 pg/ul,p=0.002)和 3 次采样(2.44±2.01 pg/ul 比 0.74±0.52 pg/ul,p=0.020)时阿片啡肽水平更高,BMS 组 3 次采样时比基线时更高(p<0.025)。BMS 组的疼痛评分高于 TMDp 组(p<0.025)和 CTRL 组(p<0.025)。
本研究表明:(1)两种疼痛状态和对照组的基础阿片啡肽含量不同;(2)STC 后阿片啡肽在 CTRL、BMS 和 TMDp 中的释放动力学不同;(3)BMS 和 TMDp 组与 CTRL 组相比,STC 后的疼痛感知不同,这可为动物模型提供参考。
口腔颌面部疼痛性疾病患者阿片啡肽释放的特定调节为生理和病理生理学的临床医生和研究人员提供了有价值的见解,并鼓励在该领域进行进一步研究。
ClinicalTrials.gov NCT04694274。注册于 2021 年 1 月 5 日。