Abstract

BackgroundHydrochloric acid (HCl) is a potential threat to the integrity of the gastric mucosa and is known to contribute to upper abdominal pain. We have previously found that gastric mucosal challenge with excess HCl is signalled to the rat brainstem, but not spinal cord, as visualized by expression of c-fos messenger ribonucleic acid (mRNA), a surrogate marker of neuronal excitation. This study examined whether gastric mucosal exposure to capsaicin, a stimulant of nociceptive afferents that does not damage the gastric mucosa, is signalled to both brainstem and spinal cord and whether differences in the afferent signalling of gastric HCl and capsaicin challenge are related to different effects on gastric emptying.ResultsRats were treated intragastrically with vehicle, HCl or capsaicin, activation of neurons in the brainstem and spinal cord was visualized by in situ hybridization autoradiography for c-fos mRNA, and gastric emptying deduced from the retention of intragastrically administered fluid. Relative to vehicle, HCl (0.5 M) and capsaicin (3.2 mM) increased c-fos transcription in the nucleus tractus solitarii by factors of 7.0 and 2.1, respectively. Capsaicin also caused a 5.2-fold rise of c-fos mRNA expression in lamina I of the caudal thoracic spinal cord, although the number of c-fos mRNA-positive cells in this lamina was very small. Thus, on average only 0.13 and 0.68 c-fos mRNA-positive cells were counted in 0.01 mm sections of the unilateral lamina I following intragastric administration of vehicle and capsaicin, respectively. In contrast, intragastric HCl failed to induce c-fos mRNA in the spinal cord. Measurement of gastric fluid retention revealed that HCl suppressed gastric emptying while capsaicin did not.ConclusionThe findings of this study show that gastric mucosal exposure to HCl and capsaicin is differentially transmitted to the brainstem and spinal cord. Since only HCl blocks gastric emptying, it is hypothesized that the two stimuli are transduced by different afferent pathways. We infer that HCl is exclusively signalled by gastric vagal afferents whereas capsaicin is processed both by gastric vagal and intestinal spinal afferents.

Highlights

  • Hydrochloric acid (HCl) is a potential threat to the integrity of the gastric mucosa and is known to contribute to upper abdominal pain

  • This finding is consistent with our observation that IG administration of HCl is signalled to the nucleus tractus solitarii (NTS) of the rat brainstem, the central termination area of vagal afferents, as visualized by expression of messenger ribonucleic acid for the immediate early gene c-fos, whereas no induction of c-fos mRNA is seen in the spinal cord [5,6]

  • Gastric challenge with HCl and capsaicin is differentially signalled to the NTS and spinal cord, which indicates that the two stimuli are processed by disparate nociceptive afferent pathways

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Summary

Introduction

Hydrochloric acid (HCl) is a potential threat to the integrity of the gastric mucosa and is known to contribute to upper abdominal pain. Gastric chemonociception evoked by exposure of the rat stomach to excess HCl is mediated by vagal afferent neurons, given that the visceromotor pain response to intragastric (IG) administration of HCl is abolished by bilateral vagotomy, whereas the visceromotor response to distension remains unaltered [4] This finding is consistent with our observation that IG administration of HCl is signalled to the nucleus tractus solitarii (NTS) of the rat brainstem, the central termination area of vagal afferents, as visualized by expression of messenger ribonucleic acid (mRNA) for the immediate early gene c-fos, whereas no induction of c-fos mRNA is seen in the spinal cord [5,6]. This is because capsaicin stimulates afferent neurons by gating transient receptor potential ion channels of vanilloid type 1 (TRPV1), which are expressed by both vagal and spinal afferent neurons innervating the rat stomach and intestine [12,13,14,15,16]

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