Author:
Yamada Tomohiro,Horikawa Makoto,Sato Tomohito,Kahyo Tomoaki,Takanashi Yusuke,Ushirozako Hiroki,Kurosu Kenta,Al Mamun Md.,Mihara Yuki,Oe Shin,Arima Hideyuki,Banno Tomohiro,Yosida Go,Hasegawa Tomohiko,Yamato Yu,Matsuyama Yukihiro,Setou Mitsutoshi
Abstract
AbstractLigamentum flavum hypertrophy (HLF) is the most important component of lumbar spinal canal stenosis (LSCS). Analysis of hypertrophied ligamentum flavum (HLF) samples from patients with LSCS can be an important que. The current study analyzed the surgical samples of HLF samples in patients with LCSC using quantitative and qualitative high performance-liquid chromatography and mass spectrometry. We collected ligamentum flavum (LF) tissue from twelve patients with LSCS and from four patients with lumbar disk herniation (LDH). We defined LF from LSCS patients as HLF and that from LDH patients as non-hypertrophied ligamentum flavum (NHLF). Total lipids were extracted from the LF samples and evaluated for quantity and quality using liquid chromatography and mass spectrometry. The total lipid amount of the HLF group was 3.6 times higher than that of the NHLF group. Phosphatidylcholines (PCs), ceramides (Cers), O-acyl-ω-hydroxy fatty acids (OAHFAs), and triglycerides (TGs) in the HLF group were more than 32 times higher than those of the NHLF group. PC(26:0)+H+, PC(25:0)+H+, and PC(23:0)+H+ increased in all patients in the HLF group compared to the NHLF group. The thickness of the LF correlated significantly with PC(26:0)+H+ in HLF. We identified the enriched specific PCs, Cers, OAHFAs, and TGs in HLF.
Funder
Japan Society for the Promotion of Science
Imaging Platform
CREST from the Japan Agency for Medical Research and Development, AMED
Publisher
Springer Science and Business Media LLC
Cited by
19 articles.
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