Schmalzl J, Plumhoff P, Gilbert F, Gohlke F, Konrads C, Brunner U, Jakob F, Ebert R, Steinert A F
1 Department of Orthopaedic Surgery, Julius Maximilians University of Wuerzburg, Wuerzburg, Germany.
2 Department of Traumatology and Hand Surgery, St. Vincentius Clinic, Suedendstraße Karlsruhe, Germany.
J Orthop Surg (Hong Kong). 2019 Jan-Apr;27(1):2309499018820349. doi: 10.1177/2309499018820349.
The long head of the biceps (LHB) is often resected in shoulder surgery. However, its contribution to inflammatory processes in the shoulder remains unclear. In the present study, inflamed and noninflamed human LHBs were comparatively characterized for features of inflammation.
Twenty-two resected LHB tendons were classified into inflamed ( n = 11) and noninflamed ( n = 11) samples. For histological examination, samples were stained with hematoxylin eosin, Azan, van Gieson, and Masson Goldner trichrome. Neuronal tissue was immunohistochemically visualized. In addition, specific inflammatory marker gene expression of primary LHB-derived cell cultures were analyzed.
Features of tendinopathy, such as collagen disorganization, infiltration by inflammatory cells, neovascularization, and extensive neuronal innervation were found in the tendinitis group. Compared to noninflamed samples, inflamed LHBs showed a significantly increased inflammatory marker gene expression.
Structural and biomolecular differences of both groups suggest that the LHB tendon acts as an important pain generator in the shoulder joint. These findings can, on the one hand, contribute to the understanding of the biomolecular genesis of LHB tendinitis and, on the other hand, provide possibilities for new therapeutic approaches.
肱二头肌长头(LHB)在肩部手术中常被切除。然而,其在肩部炎症过程中的作用仍不清楚。在本研究中,对发炎和未发炎的人类LHB进行了炎症特征的比较。
将22条切除的LHB肌腱分为发炎样本(n = 11)和未发炎样本(n = 11)。用于组织学检查的样本用苏木精伊红、偶氮胭脂红、维多利亚蓝和马松-戈德纳三色染色法染色。通过免疫组织化学观察神经元组织。此外,还分析了原代LHB衍生细胞培养物中特定炎症标志物基因的表达。
在肌腱炎组中发现了肌腱病的特征,如胶原纤维紊乱、炎症细胞浸润、新生血管形成和广泛的神经支配。与未发炎样本相比,发炎的LHB显示出炎症标志物基因表达显著增加。
两组的结构和生物分子差异表明,LHB肌腱是肩关节中重要的疼痛产生源。这些发现一方面有助于理解LHB肌腱炎的生物分子发病机制,另一方面为新的治疗方法提供了可能性。