Glycosphingolipid Biosynthesis Pathway in the Spinal Cord and Dorsal Root Ganglia During Inflammatory Pain: Early and Late Changes in Expression Patterns of Glycosyltransferase Genes. (21st January 2020)

• Record Type: Journal Article
• Authors: Morita, Motoki; Watanabe, Shun; Oyama, Misa; Iwai, Takashi; Tanabe, Mitsuo
• Is Part Of: Neuroscience. Volume 428(2020)
• Page Start: 217
• Page End: 227
• Publication Date: 2020-01-21
• Subjects: AD Alzheimer's disease -- ALS amyotrophic lateral sclerosis -- CFA complete Freund's adjuvant -- DRG dorsal root ganglion -- GlcCer glucosylceramide -- GSLs glycosphingolipids; glycosphingolipid -- ganglioside -- glycosyltransferase -- inflammatory pain -- spinal cord -- dorsal root ganglion; Neurochemistry -- Periodicals; Neurophysiology -- Periodicals; Neurology -- Periodicals; Neurochimie -- Périodiques; Neurophysiologie -- Périodiques; Neurochemistry; Neurophysiology; Electronic journals; Periodicals; Electronic journals; 612.8
• DOI: 10.1016/j.neuroscience.2019.12.029
• Languages: English
• ISSNs: 0306-4522

Abstract

Highlights: Inflammatory pain affects glycosyltransferase gene expression involved in glycosphingolipid synthesis in spinal cord and DRG. Glycosyltransferase expression patterns differ in early versus chronic inflammatory pain. Spinal glycosyltransferase expression is decreased bilaterally in chronic inflammatory pain with bilateral allodynia. Abstract: Glycosphingolipids (GSLs) are abundant, ceramide-containing lipids in the nervous system that play key functional roles in pain and inflammation. We measured gene expression ( Ugcg, St3gal5, St8sia1, B4galNT1, Ugt8a, and Gal3st1 ) of glycosyltransferases involved in GSL synthesis in murine dorsal root ganglion (DRG) and spinal cord after complete Freund's adjuvant (CFA)-induced unilateral hind-paw inflammation (1 day vs. 15 days). Chronic inflammation (15 days) sensitized both ipsilateral and contralateral paws to pain. One day of induced unilateral hind-paw inflammation (1d-IUHI) increased Ugcg, St8sia1, B4galnt1, and Gal3st1 expression in ipsilateral cord, suggesting that sulfatide and b-series gangliosides were also elevated. In addition, 1d-IUHI increased Ugcg, st3gal5 and Gal3st1 expression in contralateral cord, suggesting that sulfatide and a-/b-series gangliosides were elevated. By contrast, 1d-IUHI decreased Ugcg, St3gal5, and St8sia1 expression bilaterally in the DRG, suggesting that b-series gangliosides were depressed. Since intrathecal injection of b-series ganglioside induced mechanical allodynia in naïve mice, it seems reasonable that b-series gangliosides synthesized from upregulated St8sia1 in the ipsilateral spinal cord are involved in mechanical allodynia. By contrast, chronic inflammation led to a decrease of Ugcg, St3gal5, B4galnt 1, and Gal3st1 expression in spinal cord bilaterally and an increase of St8sia1 expression in the ipsilateral DRG, suggesting that a-/b-series gangliosides in the spinal cord decreased and b-series gangliosides in ipsilateral DRG increased. These changes in glycosyltransferase gene expression in the DRG and the spinal cord may contribute to the modification of pain sensitivity in both inflamed and non-inflamed tissues and the transition from early to chronic inflammatory pain.