Differential gene expression changes in the dorsal root versus trigeminal ganglia following peripheral nerve injury in rats. (13th March 2020)

• Record Type: Journal Article
• Authors: Korczeniewska, Olga A.; Katzmann Rider, Giannina; Gajra, Sheetal; Narra, Vivek; Ramavajla, Vaishnavi; Chang, Yun‐Juan; Tao, Yuanxiang; Soteropoulos, Patricia; Husain, Seema; Khan, Junad; Eliav, Eli; Benoliel, Rafael
• Is Part Of: European journal of pain. Volume 24:Number 5(2020)
• Page Start: 967
• Page End: 982
• Publication Date: 2020-03-13
• Subjects: Pain -- Periodicals; Pain -- Treatment -- Periodicals; Pain -- Physiological aspects -- Periodicals; 616.0472
• DOI: 10.1002/ejp.1546
• Languages: English
• ISSNs: 1090-3801

Abstract

Abstract: Background: The dorsal root (DRG) and trigeminal (TG) ganglia contain cell bodies of sensory neurons of spinal and trigeminal systems, respectively. They are homologs of each other; however, differences in how the two systems respond to injury exist. Trigeminal nerve injuries rarely result in chronic neuropathic pain (NP). To date, no genes involved in the differential response to nerve injury between the two systems have been identified. We examined transcriptional changes involved in the development of trigeminal and spinal NP. Methods: Trigeminal and spinal mononueropathies were induced by chronic constriction injury to the infraorbital or sciatic nerve. Expression levels of 84 genes in the TG and DRG at 4, 8 and 21 days post‐injury were measured using real‐time PCR. Results: We found time‐dependent and ganglion‐specific transcriptional regulation that may contribute to the development of corresponding neuropathies. Among genes significantly regulated in both ganglia Cnr2, Grm5, Htr1a, Il10, Oprd1, Pdyn, Prok2 and Tacr1 were up‐regulated in the TG but down‐regulated in the DRG at 4 days post‐injury; at 21 days post‐injury, Adora1, Cd200, Comt, Maob, Mapk3, P2 rx4, Ptger1, Tnf and Slc6a2 were significantly up‐regulated in the TG but down‐regulated in the DRG. Conclusions: Our findings suggest that spinal and trigeminal neuropathies due to trauma are differentially regulated. Subtle but important differences between the two ganglia may affect NP development. Significance: We present distinct transcriptional alterations in the TG and DRG that may contribute to differences observed in the corresponding mononeuropathies. Since the trigeminal system seems more resistant to developing NP following trauma our findings lay ground for future research to detect genes and pathways that may act in a protective or facilitatory manner. These may be novel and important therapeutic targets.