BACKGROUND Atropine, an anticholinergic agent with central and peripheral actions, reduces gastro-oesophageal reflux (GOR) in normal subjects and patients with gastro-oesophageal reflux disease (GORD) by inhibiting the frequency of transient lower oesophageal sphincter relaxation (TLOSR).
AIMS To compare the effect of methscopolamine bromide (MSB), a peripherally acting anticholinergic agent, with atropine on the rate and mechanism of GOR in patients with GORD.
METHODS Oesophageal motility and pH were recorded for 120 minutes in 10 patients with GORD who were studied on three separate occasions. For the first two recording periods, either atropine (15 μg/kg bolus, 4 μg/kg/h infusion) or saline were infused intravenously. MSB (5 mg orally, four times daily) was given for three days prior to the third recording period.
RESULTS Atropine significantly reduced basal LOS pressure (12.6 (0.17) mm Hg to 7.9 (0.17) mm Hg), and the number of TLOSR (8.1 (0.56) to 2.8 (0.55)) and reflux episodes (7.0 (0.63) to 2.0 (0.43)) (p<0.005 for all comparisons). MSB reduced basal LOS pressure (12.6 (0.17) to 8.7 (0.15) mm Hg, p<0.005), but had no effect on the frequency of TLOSR (8.1 (0.56) to 7.5 (0.59)) and reflux episodes (7.0 (0.63) to 4.9 (0.60)) (p>0.05).
CONCLUSION In contrast to atropine, MSB has no effect on the rate of TLOSR or GOR in patients with GORD. Atropine induced inhibition of TLOSR and GOR is most likely mediated through a central cholinergic blockade.
- gastro-oesophageal reflux
- cholinergic blockade
- transient lower oesophageal sphincter relaxation
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Tonic contraction at the oesophagogastric junction is believed to be the principal mechanism preventing gastro-oesophageal reflux (GOR). The sphincter mechanism at the oesophagogastric junction is composed of the smooth muscle lower oesophageal sphincter (LOS) and the skeletal muscle crural diaphragm. Weakness of either can lead to GOR; however, the most prevalent mechanism of GOR is not due to weakness of the LOS or crural diaphragm, rather it is due to transient relaxation of the LOS (TLOSR).1 2 TLOSR is the major mechanism of GOR in normal subjects and patients with mild to moderate gastro-oesophageal reflux disease (GORD).1 3 4 It is hypothesised that TLOSR is also the predominant mechanism of GOR in patients with moderate to severe GORD.5 We have recently shown that atropine, despite causing a significant reduction in basal LOS pressure,6 7 reduces GOR in normal subjects and patients with GORD by inhibiting the frequency of TLOSR. The mechanism by which atropine reduces the frequency of TLOSR is not known.
TLOSR is a neural reflex which is mediated through the brain stem. The afferent pathways for this reflex project from receptors in the gastric fundus to the nucleus tractus solitareus and dorsal motor nucleus of the vagus in the medulla.8 The efferent pathway for TLOSR is also in the vagus nerve.9 As atropine crosses the blood−brain barrier it may exert its anticholinergic effects either peripherally at the level of the myenteric plexus or centrally, at the level of medulla and higher cerebral centres.
We hypothesised that the inhibitory effects of atropine on TLOSR may be mediated at the level of the central nervous system. Methscopolamine bromide (MSB) is a quaternary ammonium anticholinergic agent, which does not cross the blood−brain barrier.10 The aim of this study was to compare the effect of MSB, a peripherally acting anticholinergic agent, with atropine on the rate and mechanism of reflux in patients with GORD.
Studies were performed in 10 volunteers (four men, six women) with GORD. The latter was defined when classic symptoms of GORD were present and there was evidence of mucosal erosions and ulceration on endoscopy. The median age of the volunteers was 42 years (range 24–54). Volunteers with a history of upper gastrointestinal surgery, or other systemic disease known to influence reflux were excluded from the study. Volunteers with known contraindications for anticholinergic medication including asthma, cardiovascular disease, glaucoma, and prostatic hypertrophy were also excluded. None of the volunteers were taking any medication known to affect oesophageal motor function. Proton pump inhibitors were stopped at least five days and H2 antagonists were stopped at least three days prior to the study day. Each volunteer gave written informed consent and the protocol was approved by the University of Virginia Human Investigations Committee.
Oesophageal manometry was performed using a six lumen assembly. A reverse perfused sleeve sensor11 monitored LOS pressure. Side holes monitored pressure in the pharynx, at three sites in the oesophagus, 2, 7, and 12 cm above the LOS, and in the gastric fundus. The pharyngeal side hole was water filled but the remaining manometric channels were perfused at 0.5 ml/min by a low compliance pneumohydraulic capillary infusion pump. Oesophageal pH was monitored at 5 cm above the proximal margin of the LOS with an antimony electrode (Synectics Medical, AB, Stockholm, Sweden). The manometric and pH signals were recorded on a multichannel recorder (Synectics Medical).
Subjects were studied after an eight hour fast. The manometric assembly and pH electrodes were passed via the nose. A cannula was inserted into the forearm for subsequent infusion of saline or atropine for the first two study periods. The subjects were allowed to accommodate to the assembly for 15 minutes following placement. Each subject then performed four water swallows of a 5 ml bolus. The subjects then ate a standardised 3.8 MJ soft meal. Normal saline was administered intravenously following the ingestion of the meal and recordings were performed for an additional two hours with the subjects in the supine or left lateral position in the bed. On separate days after 30 minutes of control recordings, the subjects received intravenous atropine (15 μg/kg bolus, 4 μg/kg/h infusion) and recordings were performed as on day 1. For the third recording period subjects ingested MSB (5 mg orally, four times daily) for three days prior to the recording period. Recordings were obtained for a further two hour period during which the subjects lay quietly in the bed and were asked not to talk (fig 1). Either an assistant or one of the investigators observed the subjects and ensured that they did not sleep during the monitoring period. During atropine infusion the blood pressure and pulse rate were recorded every 15 minutes and the subjects were asked about symptoms such as blurred vision and dry mouth. The saline, atropine, or MSB were given on separate days at least one week apart.
Basal LOS pressure was measured at end expiration and referenced to intragastric pressure; visual mean measurements were taken at five minute intervals and an overall mean for the 120 minute recording period was calculated.
Acid reflux was defined as a drop in pH of at least two pH units. The onset of the drop in oesophageal pH was used as the reference time for analysis of the motor events associated with reflux. For each reflux episode the mechanism of reflux was determined from the pattern of LOS pressure, pharyngeal activity, oesophageal body activity, and increases in intragastric pressure (straining). TLOSRs were defined according to the previously published criteria.3 12 Figure 2 shows the various mechanisms of reflux detected in this study. Primary peristalsis in response to wet swallows was analysed for peristaltic velocity and mean amplitude of contraction at the proximal and distal ports.
Data were analysed using the paired t test and Mann-Whitney test. All data are presented as mean (SEM). A p value of less than 0.05 was judged to indicate statistical significance.
BASAL LOS PRESSURE
Atropine and MSB reduced basal LOS pressure, from 12.6 (0.17) mm Hg to 7.9 (0.17) mm Hg and from 12.6 (0.17) mm Hg to 8.7 (0.15) mm Hg respectively (p<0.001 for both comparisons). Atropine increased the proportion of time LOS pressure was less than 5 mm Hg from 9.0 (5.2)% to 41 (9.4)% (p<0.005). MSB increased the proportion of time the basal LOS pressure was less than 5 mm Hg from 9.0 (5.2)% to 28 (7.3)% (p<0.005) (fig 3). Atropine and MSB caused a concomitant reduction in the time LOS pressure was between 15 and 20 mm Hg.
TRANSIENT LOS RELAXATION
Atropine reduced the number of TLOSR episodes versus those occurring with saline (from 8.1 (0.56) to 2.8 (0.55), p<0.002) and MSB (from 7.5 (0.59) to 2.8 (0.55), p<0.005). MSB had no effect on the number of TLOSR episodes versus those occurring during saline infusion (7.5 (0.59) versus 8.1 (0.56), p=0.69) (fig 4). During saline infusion there were 81 TLOSR episodes of which 32 (39.5%) were associated with reflux. During atropine infusion there were 28 TLOSR episodes of which nine (32%) were associated with reflux. There were 75 TLOSR episodes during the MSB study periods of which 30 (40%) were associated with reflux. There was no significant difference in the percentage of TLOSRs associated with reflux during the three study periods (p>0.05 for all comparisons).
Atropine reduced the number of reflux episodes versus saline (7.0 (0.63) to 2.0 (0.43), p<0.004) and versus MSB (4.9 (0.60) to 2.0 (0.43), p<0.04). MSB had no effect on the number of reflux episodes versus saline (7.0 (0.63) versus 4.9 (0.60), p=0.26) (fig 4). Overall, the predominant mechanism of reflux was TLOSR during all three recording periods. Atropine reduced the number of reflux episodes due to TLOSR versus saline (3.2 (0.42) to 0.9 (0.30), p<0.004) and versus MSB (2.9 (0.54), p<0.05). MSB, however, had no effect on the number of reflux episodes due to TLOSR versus saline (3.2 (0.43) versus 2.9 (0.54), p=0.85). During saline infusion there were 70 episodes of reflux recorded in the 10 subjects of which 32 (46%) occurred during TLOSR (fig 5). During atropine infusion there were 20 episodes of reflux of which nine (45%) occurred during TLOSR; while on MSB 49 episodes occurred of which 29 (59%) occurred during TLOSR. There was no significant difference in the percentage of reflux occurring during TLOSR for the three study periods (p>0.05 for all comparisons).
Cholinergic blockade also reduced the number of reflux episodes due to swallow induced LOS relaxation (fig 5). During saline infusion there were 21 episodes of reflux occurring during swallow induced LOS relaxation versus three episodes each during atropine infusion and the MSB period.
EFFECT ON PRIMARY SWALLOW INDUCED OESOPHAGEAL CONTRACTIONS
MSB significantly reduced the oesophageal contraction amplitude at both the proximal and distal ports as well as increased the velocity of peristalsis compared with saline (table 1). Wet swallows were performed prior to atropine infusion; its effects on primary peristalsis were therefore not measured.
SYSTEMIC AND OESOPHAGEAL ANTICHOLINERGIC EFFECTS
There were no significant differences in the type or total number of anticholinergic side effects noted by the subjects while taking atropine or MSB. The number of subjects experiencing any anticholinergic side effect was the same during atropine infusion or while taking MSB (table 2).
Atropine has previously been shown to decrease GOR through a reduction in the TLOSR in healthy subjects and patients with GORD.6 7 However, it was unclear whether the mechanism of action was through central or peripheral cholinergic blockade. Selective peripheral cholinergic blockade with MSB did not reduce GOR, TLOSR, or GOR due to TLOSR in patients with GORD. Therefore, we may conclude that atropine induced inhibition of GOR and TLOSR is most likely mediated through a central cholinergic blockade.
Could the lack of inhibition of GOR and TLOSR by MSB be due to insufficient dosage to achieve peripheral cholinergic blockade? The dose chosen in our study was higher than initially recommended to achieve an anticholinergic effect10 and most subjects noted anticholinergic side effects while on MSB or atropine. More convincingly, MSB administration reduced the mean basal LOS pressure to almost the same degree as seen with atropine. Finally, MSB reduced the amplitude of primary peristalsis as has been shown previously with atropine.13
In a previous study of patients with GORD, the frequency of GOR was reduced by near abolition of both TLOSR induced reflux and swallow induced reflux.7 In this study we found that reflux occurring during swallow induced LOS relaxation was notably decreased with atropine which is in accordance with the previous published study. We found that in this study, similarly to atropine, MSB also reduced the swallow mediated reflux. However, while atropine significantly reduced the overall number of TLOSR episodes and GOR due to TLOSR compared with placebo and MSB, the relative frequency of GOR due to TLOSR was not significantly different. This most likely reflects the heterogeneous mechanisms of reflux in patients with GORD14and differences in the two GORD populations studied.
The central neural pathways mediating TLOSR have not been clearly defined, but are thought to reside in the brain stem. Afferent stimuli from the gastric fundus travel to the sensory nucleus in the medulla, the nucleus tractus solitareus. A programmed set of events in the brain stem occurs in the region of the dorsal vagal nucleus and the nucleus ambiguous, which then mediates the efferent signals for TLOSR.8 The central anticholinergic effect of atropine most likely occurs in this region of the brain stem. In support of this concept is the observation that atropine reduces the oral phase of swallowing in response to electrical stimulation of the superior laryngeal nerve in the opossum, suggesting that atropine acts at the level of the central nervous system to block the swallow reflex.14 Furthermore, Berger reported that cholinergic receptors are present in the swallowing centre in the brain stem and muscarinic blockade inhibits the oesophageal phase of swallowing.15
Atropine was recently reported to inhibit gastric distension induced TLOSR and pharyngeal receptor mediated LOS relaxation.17The mechanism of the effect of atropine on gastric distension induced TLOSR could be mediated through its inhibitory effect on gastric fundic tone. It was also proposed that inhibition of both gastric distension and pharyngeal receptor mediated LOS relaxation could be mediated through a central cholinergic blockade.16 The data from the current study support the existence of a central mechanism of TLOSR which is sensitive to cholinergic blockade.
Our results are in agreement with the recently reported effects of hyoscine bromide, a peripherally acting anticholinergic agent, on GOR and TLOSR in normal subjects published in abstract form.17Lidums et al also found that peripheral cholinergic blockade with hyoscine had no effect on GOR and TLOSR. Hyoscine bromide, similar to MSB and atropine, had inhibitory effects on the oesophageal contraction amplitude.17
We have previously shown that despite decreasing basal LOS pressure, non-selective cholinergic blockade with atropine actually decreases GOR by decreasing TLOSR in healthy subjects and in patients with GORD. This study further elucidates the mechanism of action of atropine by showing that it occurs through a central cholinergic blockade. Pharmacological reduction of GOR by inhibition of TLOSR with anticholinergic agents is an attractive therapeutic option to treat GORD by reversing its primary pathophysiological derangement. However, atropine and MSB reduce the salivary flow and reduce the amplitude of primary oesophageal peristalsis, both of which are important for normal oesophageal acid clearance. Therefore this class of compounds is contraindicated in reflux disease. However, whether it is possible to design a selective centrally acting anticholinergic compound that may inhibit TLOSR without any deleterious effects on saliva and oesophageal contractions remains to be seen.
This study was supported by NIH grant RO3 DK 52094–01 SRC C and by a restricted grant from Astra Merck Pharmaceuticals.
- gastro-oesophageal reflux
- gastro-oesophageal reflux disease
- lower oesophageal sphincter
- methscopolamine bromide
- transient lower oesophageal sphincter relaxation
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