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Effect of reflux‐induced inflammation on transient receptor potential vanilloid one (TRPV1) expression in primary sensory neurons innervating the oesophagus of rats
Author(s) -
Banerjee B.,
Medda B. K.,
Lazarova Z.,
Bansal N.,
Shaker R.,
Sengupta J. N.
Publication year - 2007
Publication title -
neurogastroenterology and motility
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.489
H-Index - 105
eISSN - 1365-2982
pISSN - 1350-1925
DOI - 10.1111/j.1365-2982.2007.00947.x
Subject(s) - trpv1 , colocalization , transient receptor potential channel , chemistry , medicine , immunohistochemistry , trpm8 , endocrinology , receptor , microbiology and biotechnology , biology
A possible mechanism of oesophageal hypersensitivity is the acid‐induced activation of transient receptor potential vanilloid receptor 1 (TRPV1) in the primary sensory neurons. We investigated TRPV1 expression and its colocalization with substance P (SP) and isolectin B4 (IB4)‐positive cells in the thoracic dorsal root ganglia (DRGs) and nodose ganglia (NGs) of rats with reflux‐induced oesophagitis (RO). RO was developed by fundus ligation and partial obstruction of the pylorus of Sprague‐Dawley rats. Four groups of rats were used; fundus ligated acute (RO 48 h), chronic 7 days (RO 7D), RO 7D + omeprazole (7D + Omz, 40 mg kg −1 , i.p.) and sham‐operated controls. Immunohistochemical analysis of TRPV1, SP and IB4 expression were carried out in spinal cord (SC), DRGs and NGs. RO rats exhibited significant inflammation and increase in TRPV1‐ir and SP‐ir expressions in the SC, DRGs and NGs. The maximum colocalization of TRPV1 and SP was observed in RO 7D rats, but Omz prevented inflammation and over expression of TRPV1 and SP. TRPV1‐ir significantly increased in IB4‐positive cells in DRGs and SC, but not in the NGs. Results document that acid‐induced oesophagitis increases TRPV1 expression in both SP‐ and IB4‐positive sensory neurons. The over expression of TRPV1 may contribute to oesophageal hypersensitivity observed in gastro‐oesophageal reflux disease (GORD).