Factors in the Control of Interdigestive and Postprandial Myoelectric Patterns of Canine Jejunoileum: Role of Extrinsic and Intrinsic Nerves

Our aim was to determine the roles of extrinsic and intrinsic (enteric) neural continuity to the jejunoileum in control of postprandial and fasting motility patterns. Four groups of dogs were prepared: control, neurally intact; intrinsic transection, distal duodenal transection to disrupt intrinsic myoneural continuity with jejunum; extrinsic transection, transection of all extrinsic nerves to jejunoileum; and intrinsic/extrinsic transection, disruption of both intrinsic myoneural and extrinsic neural continuity to jejunoileum. Duodenal and jejunal electrodes were placed to monitor motility. After 2 weeks, the dogs were studied while fasting, after meals, and during intravenous infusions of cholecystokinin octapeptide at 0.5μg/(kg · h) and pentagastrin at 2μg/(kg · h). During fasting, although the migrating motor complex (MMC) occurred in each region, coordination between duodenum and jejunoileum was disrupted in intrinsic/extrinsic transection dogs, but only partially in intrinsic transection dogs. Small meals (50 g of liver) interrupted the duodenal MMC in all groups and the jejunoileal MMC only in control dogs. A larger (500-g) meal disrupted the MMC in both regions for comparable durations in all groups. Cholecystokinin octapeptide and pentagastrin inhibited the MMC in duodenum and jejunoileum in all groups. Both intrinsic myoneural and extrinsic neural continuity play a role in regional coordination of interdigestive and digestive gut motility. Both hormonal and neural factors (central, enteric) participate in the regulation of onset of postprandial motor patterns.     

Role of Peptide YY in Intestinal and Gallbladder Motility in Dogs

The purpose of this study was to characterize the action of exogenous PYY, an ileocolonic peptide released by fatty meal, and that released by Heal perfusion with oleate on intestinal and gallbladder motility patterns and the posssible role of the adrenergic pathway in this action. Dogs were equipped with chronic duodenal electrodes for recording myoelectric activity and with a cannula in the gallbladder fundus for measuring the gallbladders intraluminal pressure and volume and calculating its motility index (MI) and emptying rate. After intravenous infusion of PYY, there was a dose-dependent prolongation of the migrating motor complex (MMC) interval and almost complete abolition of the contractions and emptying of gallbladder during the duodenal activity front. After meat feeding or during intravenous infusion of cerulein, 50 pmol/(kg · h), the MMC was interrupted and replaced by irregular spike activity, accompanied by a marked increase in the gallbladder MI and about 80% to 90% reduction of its volume. PYY, 200 pmol/(kg · h), reduced significantly the meal- or cerulein-induced duodenal spike activity but failed to affect the MI and volume of the gallbladder. Similar changes in fasted and fed patterns of motility were observed after Heal oleate (16 mM/h), producing plasma PYY levels in a range similar to that observed after infusion of exogenous PYY. The inhibitory effects of PYY or Heal fat on intestinal myoelectric activity were reversed in part by α-adrenergic blockade (phentolamine). We conclude that exogenous PYY or endogenous hormone released by Heal oleate inhibits the interdigestive and postprandial motility pattern of the small bowel but does not affect gallbladder motility, and that the inhibition of intestinal motility involves, at least in part, the adrenergic pathway.     

Phase III of the migrating motor complex: associated with endogenous xenin plasma peaks and induced by exogenous xenin

Xenin, a recently discovered peptide produced by specific endocrine cells of the duodenal mucosa, has shown exocrine, endocrine and motility effects in the gastroenteropancreatic system in animal experiments. The aim of the present investigation was to study the role of xenin in the regulation of duodenojejunal motility of humans. Twenty-nine healthy volunteers from the hospital staff gave informed consent to participate in this investigation. In 20 volunteers, we determined plasma concentrations of immunoreactive xenin at 15 min intervals over a mean time period of 8 h fasting and recorded the interdigestive motor activity of the duodenojejunum. In a double-blind randomized crossover study on other nine subjects, synthetic xenin in a dose of 4 pmol kg-1 min-1 or placebo was infused for 10 min intravenously in the interdigestive period and postprandially after a liquid meal. Duodenojejunal motility was recorded simultaneously. Predefined interdigestive xenin plasma peaks were found to be significantly associated with the phases III of the migrating motor complex. In the interdigestive period, xenin induced a premature phase III activity in each volunteer; this was followed by a second phase III in five out of nine subjects. In the postprandial state, xenin significantly increased contraction frequency and the percentage of aborally propagated contractions. These findings suggest a role of the peptide hormone xenin in modulating interdigestive and postprandial duodenojejunal motility in humans.     

Postprandial peristalsis in the human duodenum

MMC-related retroperistalsis is a cyclical phenomenon in the duodenum linked to phase III. The aim of this study was to elucidate the direction of propagation of juxtapyloric duodenal pressure waves in the postprandial state in healthy humans and to compare with the contractions in the interdigestive phase II. Antroduodenal manometry was performed in 11 healthy subjects. Individual pressure waves propagating along a 6-cm duodenal segment were analysed with respect to the proportions of antegrade and retrograde propagation in the four duodenal subsegments (D1–D2) to (D4–D5), each subsegment being 15 mm. A test meal was given 30 min after a phase III had passed and motility recording continued for 60 min after the meal. During both the first and the second 30-min period of postprandial recording the proportion of retrograde pressure waves was larger just distal to the pylorus, (D1–D2), 40% (23–68) and 50% (23–68), respectively, compared to the distal part, (D4–D5), of the duodenal segment, 29% (12–30) and 10%(10–24), respectively (P < 0.05 and 0.01). In contrast, during late phase II of the interdigestive state antegrade pressure waves predominated in all four duodenal subsegments. We conclude that in the postprandial state a high proportion of the duodenal pressure waves (40–50%) is retrograde in the immediate juxtapyloric area while antegrade contractions predominate at a distance 5–6 cm distal to the pylorus. These manometric data together with recent observations of postprandial transpyloric liquid flow, indicate that retrograde duodenogastric propelling of contents may be an important determinant for the gastric emptying rate.     

Characteristic motor patterns of phase II and behaviour of phase III in the fed state

The motor pattern of the phase II of the migration motor complex (MMC) is poorly characterized and it remains to be determined whether it differs from the fed motor-pattern. Furthermore, discrepancy exists on the disruption of ongoing MMCs by feeding, and finally, the understanding of the behaviour of phase Ills during enteral nutrition is incomplete. Therefore, canine intestinal motility was studied after meal and during enteral infusion of nutrients (elemental diet, glucose, maltose, amino acids) or of hypertonic saline (300–1520 mosmol kg^?1). Motility of the proximal, mid- and distal jejunum was recorded with strain-gauge transducers. The motor patterns of the interdigestive phase II, after feeding and during enteral nutrition were analysed by a computer. Additionally, the disruption of the MMC by food and by enteral infusion of nutrients or hypertonic saline was investigated. The inter digestive phase II consisted of three different contractile patterns, clustered contractions, a mixed contractile pattern and non-migrating bursts of propagated contractions (NBPCs). NBPCs differed significantly from the phase III activity in several motility parameters and by the lack of aboral migration. Only small differences existed between the motor patterns of phase II and of the fed state, whereas the motor pattern induced by enteral infusion of an elemental diet differed significantly from that of phase II. Ongoing MMCs of the proximal jejunum often continued to migrate to the mid- and distal jejunum. During enteral infusion of nutrients or of hypertonic saline, phase Ills recurred. The migration of ongoing phase Ills and the recurrence of subsequent phase Ills decreased with increasing caloric or osmotic loads. The following conclusions were reached, (a) The phase II of the MMC is a complex motor-pattern. NBPCs represent a new contractile pattern, (b) The MMC is a characteristic feature of the empty gut. After meal and during enteral nutrition, phase Ills are usually suppressed but they can recur during the digestive period.     

Mechanisms underlying duodeno-gastric reflux in man

BACKGROUND: Recent studies suggest that duodeno-gastro-oesophageal reflux (DGER) contributes to the occurrence of reflux oesophagitis and Barrett's oesophagus. The mechanisms underlying duodeno-gastric reflux (DGR), a prerequisite for DGER, are poorly understood. AIMS: To study the occurrence of DGR in relation to interdigestive and postprandial gastroduodenal motility. SUBJECTS AND METHODS: Ten healthy subjects underwent stationary gastroduodenal manometry with simultaneous duodenal and antral Bilitec recording 4 h before and 5 h after ingestion of a liquid meal. Eight volunteers underwent the same study, with administration of erythromycin postprandially. RESULTS: During the interdigestive phase II, all volunteers had short DGR episodes. Postprandially, DGR occurred in all subjects, on average 39 +/- 28 min after the start of the meal, and was cleared from the stomach after 242 +/- 23 min. Induction of increased antral motility and of a premature phase III, by administration of erythromycin, was associated with faster gastric DGR clearance. However, there was no direct temporal relationship between erythromycin-induced gastric phase III and erythromycin-induced DGR clearance. CONCLUSION: In healthy subjects, duodenogastric reflux occurs sporadically in the interdigestive state and is a normal phenomenon in the postprandial period. Erythromycin induces faster clearance of DGR from the stomach, which depends on enhanced antral contractile activity rather than premature phase III.     

The peptide hormone xenin induces gallbladder contractions in conscious dogs

Xenin is a 25-amino acid peptide isolated from human gastric mucosa. The biological activities of xenin include modulating intestinal motility and affecting exocrine pancreatic secretion and gastric acid secretion. The physiological effect of xenin on the gastrointestinal tract, however, is incomplete. The objective of this study is to investigate the effects of xenin on the gastrointestinal tract motility of conscious dogs. Gastrointestinal tract and gallbladder contractions were monitored by chronically implanted force transducers. Synthetic xenin was injected intravenously during the interdigestive state with or without pretreatment with cholinergic blockers. The effects of xenin following cholecystectomy and truncal vagotomy were also investigated. Xenin induced gallbladder and jejunal contractions, although a dose-dependent response was shown only with gallbladder contractions. These effects were inhibited by pretreatment with cholinergic blockers, but were not enhanced by truncal vagotomy. The jejunal contractions were completely inhibited by cholecystectomy. The only direct effect of xenin in terms of gastrointestinal motility was to induce gallbladder contractions in conscious dogs. The neural pathway mediating xenin's action was cholinergic, but not the vagal. This novel finding indicates a new role of xenin.     

The Rectal Motor Complex

To identify patterns of motility in the rectum of humans during the day while awake and at night during sleep, and to correlate the patterns with interdigestive duodenal motor complexes and sleep cycles, intraluminal rectal pressure was recorded in 12 healthy subjects (five female, seven male; mean age, 28 years) using a flexible, noncompliant, silastic catheter and an Arndorfer system with a single perfused rectal port 6 cm above the anorectal junction, duodenal motility was recorded via a perfused oroduodenal tube, and sleep stages were determined electroencephalographically. Discrete bursts of rectal motor waves, called rectal motor complexes (RMCs), were identified on 72 occasions in 11 of the 12 subjects during 157 hours of recording. The RMCs were found in daytime during fasting or after feeding (0.2 ± 0.1 RMCs/hour), but were more easily and frequently identified at night during sleep (0.8 RMCs/hour, p < .01). The complexes had a distinct onset, a mean duration ± SEM of 9.5 ± 1.0 minutes, and a distinct decline. Within each complex, the waves had a mean frequency of 3.8 ± 0.3 per minute and a mean amplitude of 19 ± 2.7 mm Hg. Complex-to-complex intervals at night averaged 74 ± 15 minutes. No clear-cut temporal association was present between the complexes and phase III of interdigestive duodenal motor complex or the REM stage of sleep.     

Effect of truncal vagotomy on gallbladder bile kinetics in conscious dogs

Previous studies on the effects of vagotomy on gallbladder (GB) motility have yielded conflicting results. The aim of this study was to evaluate the effects of vagotomy on GB motility and bile kinetics using a new method. Twelve dogs were divided into two groups of six (control and pyloroplasty) and, 4 weeks later, underwent truncal vagotomy. A catheter secured in the GB fundus was used to monitor GB volume. After injecting polyethylene glycol (PEG) into the GB, combined measurements of GB volume and PEG concentration enabled GB emptying and bile kinetics to be estimated. Seven and five of the 12 vagotomized dogs were classified as having large and normal fasting GB volumes, respectively. Postprandial GB emptying was impaired when the fasting GB volume was enlarged. In the fasting state, bile kinetics of vagotomized dogs were significantly smaller than the control values. The emptying ability of the GB of vagotomized dogs with large fasting GB volumes was reduced considerably both in the postprandial and the fasting states. Such retention of bile in the GB after vagotomy may facilitate cholesterol crystal nucleation and stone growth.     

Effect of casein and casein hydrolysate on small bowel motility and D-Xylose absorption in dogs

Abstract Food administration is followed by the appearance of a small intestinal pattern of irregular contractions. Studies on the relationship between intestinal motor activity, transit and absorption have yielded contradictory results. Since previous studies have shown that casein and casein hydrolysate led to a decrease of small intestinal motor activity and transit, the aim was to evaluate the effect of these nutrients on small intestinal motility and D-Xylose absorption. Studies were performed in five dogs with a duodenal fistula; motility was recorded by means of six infused catheters and external transducers. Three test solutions with the same osmolality, lactulose, casein and casein hydrolysate, were continuously infused through the duodenal cannula. D-Xylose was injected in the duodenum and plasma levels determined at regular intervals. Absorption of D-Xylose was greatest during the administration of casein hydrolysate, the lowest levels were seen with lactulose and intermediate levels were obtained with casein. The effect of casein hydrolysate on small intestinal motility was characterized by a decrease in the frequency of contractions. Propulsive contractions were decreased after the infusion of both casein and casein hydrolysate. Lactulose infusion was followed by the greatest motor activity of both frequency and propulsive contractions. These results suggest that the motor patterns observed with casein and casein hydrolysate lead to increased intestinal absorption of D-Xylose.     

Effects of motilin on human interdigestive gastrointestinal and gallbladder motility, and involvement of 5HT3 receptors.

A plasma motilin peak and a partial gallbladder emptying precede the antral phase III of the migrating motor complex (MMC). To clarify the causal relationship between these factors, we aimed to study the role of motilin in interdigestive gastrointestinal and gallbladder motility simultaneously. In addition, involvement of 5HT3 receptors in the action of motilin was studied. Eight fasting, healthy male volunteers received 13Leu-motilin or 0.9% NaCl i.v. for 30 min, in randomized order on two separate occasions, from 30 min after phase III. Seven of the eight subjects also received the 5HT3 receptor antagonist ondansetron in addition to motilin, on a third occasion. Antroduodenal motility, gallbladder volumes and plasma motilin were measured. The interval between the start of infusion and phase III was 95.0 (57.6-155.7) min for saline, 28.7 (21.0-33.2) min for motilin, and 39.3 (30.7-100.5) min for motilin + ondansetron (P < 0.05). Gallbladder volume decreased by one-third from 10 min after both motilin and motilin + ondansetron infusion (P < 0.05), and returned to baseline with duodenal passage of phase III. In two of the seven subjects phase III was absent after motilin + ondansetron, although gallbladder volume decreased and only refilled during a later spontaneous phase III. We conclude that motilin induces both partial gallbladder emptying and antral phase III. Indeed, although gallbladder emptying clearly precedes antral phase III, ondansetron only prevented phase III in some cases and had no effect on gallbladder emptying. Passage of phase III in the duodenum makes an important contribution to gallbladder refilling.     

Differential effects of motilin on interdigestive motility of the human gastric antrum, pylorus, small intestine and gallbladder

Motilin was infused in this study with the aim of examining refractory characteristics for motilin stimulation of antral phase III and fasting gallbladder emptying. Moreover, interdigestive pyloric and small intestinal motility from duodenum to ileum were studied, as these may be target organs for motilin. Eight fasting, healthy male volunteers received, on separate subsequent days, repeated infusions of 13leucine-motilin (8 pmol (kg min)(-1) for 5 min) or saline at 30 min after phase IIIs in the duodenum. Interdigestive motility of the antrum, pylorus, duodenum, jejunum and ileum was measured for maximum 10 h by using a 21-lumen perfused catheter. Gallbladder motility was measured by ultrasonography. Motilin infusions induced antral phase IIIs, but only after a preceding phase III of duodenal origin. Under this condition, time-interval to phase III at the duodenal recording site was 30 +/- 13 (SEM) min after motilin, compared with 79 +/- 14 min after saline (P < 0.01), and compared with 121 +/- 13 min for motilin infusion following an antral phase III (P < 0.001). Motilin did not affect small intestinal motility or isolated pyloric pressure waves (IPPWs). However, the number of IPPWs was significantly affected by the origin of the preceding phase III, irrespective of whether motilin or saline was infused. Gallbladder volume decreased significantly within 10 min after each motilin infusion. We conclude that this study clearly demonstrates differential regional effects of motilin. Motilin initiates antral phase IIIs, but stimulation is subject to a refractory period which is clearly prolonged after a preceding antral phase III. Motilin induced gallbladder emptying, however, is not subject to a refractory state. Small intestinal phase IIIs as well as pyloric IPPWs are not affected by motilin.     

Dual pulse intestinal electrical stimulation normalizes intestinal dysrhythmia and improves symptoms induced by vasopressin in fed state in dogs

To assess effects of dual pulse intestinal electrical stimulation (DPIES) on intestinal dysrhythmia and motility, and symptoms induced by vasopressin in conscious dogs. The study was performed in three postprandial sessions (control; vasopressin; DPIES) in six dogs with two pairs of electrodes chronically implanted on the serosal surface of the proximal jejunum and with a chronic duodenal fistula. A manometric catheter was advanced into the small intestine via the intestinal cannula. Motility and intestinal slow waves were recorded. Symptoms were assessed. During vasopressin infusion, the percentage of normal intestinal slow wave frequency was decreased (P < 0.01), reflected as a significant increase in the percentage of both bradygastria and tachygastria; the motility index decreased (P < 0.01) and the symptom score increased (P < 0.01). In the session of DPIES, the percentage of normal slow wave frequency was recovered (P < 0.05 vs vasopressin), attributed to a reduction in both bradyarrhythmia and tachyarrhythmia; the symptom score was reduced (P < 0.05 vs vasopressin); the motility index was not significantly increased. These results suggest that vasopressin induces intestinal dysrhythmia and emetic symptoms and inhibits intestinal motility. Dual pulse intestinal electrical stimulation is capable of improving intestinal dysrhythmia and emetic symptoms but not impaired intestinal motility induced by vasopressin.     

Sham feeding disrupts phase III of the duodenal migrating motor complex in humans

The role of the vagus nerve in the control of the intestinal migrating motor complex (MMC) is unclear. This study aimed to evaluate the effect of physiological vagal stimulation with sham feeding on phase III of the MMC. Antroduodenal motility was recorded in six healthy volunteers. The first phase III was used as a control, and sham feeding was performed during the second phase III. The MMC was disrupted within 1.5 ± 0.4 min of sham feeding and its duration was shorter than the control phase III. Phase III propagation was inhibited in all subjects, most of them exhibiting no propagation beyond the third duodenal recording site. During sham feeding, the antrum exhibited transient phasic contractions in five out of six subjects. The duodenal motility index recorded for up to 30 min after the onset of the sham feeding was unchanged in five out of six subjects. We conclude that sham feeding consistently interrupted phase III of the duodenal MMC and induced antral contractions, but failed to provoke significant motor events in the duodenum.     

Coordination of biliary and upper gastrointestinal motility in the fasted conscious pig

Abstract A chronic pig model was developed which permits the simultaneous measurement of integrated biliary motility as resistance to flow (CBD inflow), gallbladder, duodenal and gastric motility in addition to collection of venous blood samples for gut hormones estimations. Animals displayed a duodenal interdigestive cycle of 55.4 ± 3.4 min (mean ± SEM, n = 6), consisting of phase I, II and III (21.2 ± 2.1, 70.5 ± 2.0, 8.7 ± 0.5% of the cycle, respectively). A gastric inter-digestive cycle of 60.2 ± 6.5 min (n = 4) was similarly demonstrated consisting of three phases which corresponded to the three duodenal phases. The gastric phases I, II and III comprised 26.3 ± 3.0, 71.2 ± 2.7 and 2.5 ± 0.8% of the cycle, respectively. The gastric phase III immediately preceded the onset of the duodenal phase III. The gallbladder likewise displayed an interdigestive cycle of 54.5 ± 7.2 min (n = 6) consisting of a quiescent period (37.2 ± 3.7% of the cycle) corresponding temporally to duodenal phase III and phase I. This quiescent phase was followed by a period of rhythmic contractions (64.5 ± 4.1% of the cycle) which corresponded temporally to duodenal phase II. The onset of the gallbladder quiescent period coincided with the onset of duodenal phase III. The CBD inflow similarly demonstrated an interdigestive cycle of 53.4 ± 9.6 min (n = 4) duration, consisting of three phases. The initial phase was evident as a period of rapid inflow, the onset of which coincided with the onset of duodenal phase III and the gallbladder quies-centperiod, andoccupied 12.0 ± 0.8% of the cycle. The secondphase which occupied 18.0 ± 7.4% of the cycle, was typified as a period of declining inflow which reached a relatively stable level at a time corresponding to the end of duodenal phase I. The third phase consisted of the maintenance of the inflow rate achieved at the end of the previous phase (60% of maximum inflow), corresponding in onset and duration with duodenal phase II and occupied 70.0 ± 8.6% of the cycle. Plasma motilin levels fluctuated in relation to the duodenal interdigestive cycle, peaking during phase III relative to phase I (36.9 ± 8.5 vs 25.4 ± 7.7 pg mL^?1, respectively, n = 5, P < 0.05). Cholecystokinin levels did not fluctuate, remaining low (2.3 ± 2.1 pM cholecystokinin octapeptide equivalents, n = 5) throughout the duodenal interdigestive cycle, but increased about two fold after ingestion of solid food. Feeding disrupted the gastric, duodenal, gallbladder and CBD inflow cycles.     

Activity Fronts of Migrating Myoelectric Complex: Initiation by Luminal Bile Acids in Rat Small Intestine

The aim of the present study was to investigate the possible role of bile in regulation of fasting small intestinal motility in the rat. Myoelectric activity was recorded by bipolar electrodes implanted in the jejunum, 15, 25, and 35 cm distal to the pylorus. After recording migrating myoelectric complexes (MMCs), total biliary drainage was performed by cannulating the bile duct of 15 rats. After biliary drainage for 267 (222–312) minutes (mean and 95% confidence interval), a characteristic continuous irregular spiking activity appeared at all recording sites. When continuous irregular spiking had persisted for 2 hours, a mixture of 20 mM taurocholic and 10 mM taurochenodeoxycholic acid was infused into the duodenum (0.5 μ/mol/min for 90 min) of seven rats. Bile acid infusion induced three to six activity fronts within 25 to 47 minutes in all animals. Maximal bile acid secretion in response to bile acid infusion was obtained about 1 hour after the last induced activity front, when the motility pattern had returned to irregular spiking. In eight rats with biliary drainage but without bile acid infusion, irregular spiking activity persisted for at least 10 hours. In sham-operated rats, regular activity fronts started after 221 (146–296) minutes. Thus drainage of bile changes the motility pattern from MMC to continuous irregular spiking, while duodenal bile acid infusion after biliary drainage reinstates the MMC pattern in rat small intestine.     

Gastric myoelectrical and antroduodenal motor activity in patients with achalasia

Achalasia is a primary motor disorder of the oesophagus, in which the myenteric plexus is involved. However, abnormalities in other parts of the digestive tract have also been described in achalasia. Whether gastric myoelectrical and duodenal motor activity in these patients is also affected is unknown. Therefore, interdigestive and postprandial gastric myoelectrical and antroduodenal motor activity were studied in 11 patients with achalasia, using electrogastrography (EGG) and stationary antroduodenal manometry.
Electrogastrographically, no differences were found in the gastric frequency, incidence of dysrhythmias and postprandial/fasting power ratio. In the interdigestive state a lower propagation velocity of phase III episodes was found in the achalasia patients, but other parameters were unaltered. Postprandially, no differences were found in the number of pressure waves, in the amplitude of pressure waves or in antro-duodenal coordination.
We conclude that gastric myoelectrical activity and antral motor activity in patients with achalasia is normal, suggesting an intact extrinsic and intrinsic neural innervation of the distal stomach. Although postprandial duodenal motility is normal, a lower propagation velocity of phase III suggests involvement of the small intestine in achalasia.     

Corticotropin Releasing Factor (CRF) increases post-prandial duodenal motor activity in humans

The effects of peripherally administered Corticotropin Releasing Factor (CRF) on post-prandial gastrointestinal motility were studied in normal subjects. Pressure activity was monitored for 90 min pre-and 120 min post-prandially in the antrum and duodenum in 8 healthy male volunteers (mean age 45.5 years). Subjects received, on separate days, ovine CRF (0.6 nmol/kg) or vehicle, infused intravenously over 5 min, 15 min after the beginning of the meal. In all subjects, CRF infusion transiently increased the frequency of contractile events to the frequency of the duodenal slow wave (11.7 ± 0.3 cpm). The postprandial duodenal mobility index (MI) after CRF infusion was significantly greater (7.72 ± 0.29) when compared to vehicle infusion (4.34 ± 0.14) (mean ± SEM; P < 0.001). However, the fraction of propagated contractile events was not altered significantly after CRF when compared to vehicle. In contrast, the antral post-prandial MI was not affected by the CRF application. Serum cortisol levels increased significantly at 60 and 90 min post-CRF injection. These data indicate that CRF transiently switches the post-prandial duodenal motor activity to a band of non-propagated high frequency contractions, but does not affect antral contractions.     

The effect of cholecystectomy on duodenojejunal motility in humans

We hypothesized that certain gastrointestinal symptoms following cholecystectomy could be explained by motor disturbances. To test this hypothesis, we compared pre- and post-operative motor patterns between symptomatic and asymptomatic patients after surgery to evaluate whether some motor changes could be induced by gallbladder removal and associated with symptoms. Twenty-three patients were prospectively evaluated before and 3 months after cholecystectomy. After surgery, 17 patients were asymptomatic and six were symptomatic. Duodenojejunal manometric recordings were performed for 3 h during fasting, then 3 h after a 750-kcal meal. Patient motor results were compared to those obtained in the duodenojejunum of 20 healthy controls. After surgery, only a few modifications in duodenojejunal motility were observed compared to the preoperative period. Motor changes related to cholecystectomy were increase in phase III amplitude and the absence of progressive decrease of the duodenojejunal motor response after the meal. After surgery, symptomatic patients had a lower postprandial duodenal motility index after the meal than asymptomatic patients (P < 0.03) and more frequent propagated clusters of contractions (PCCs) (P < 0.02). Preoperative motor patterns associated with postoperative symptoms were postprandial only and included a low duodenal motility index (P < 0.03), and a higher number of PCCs (P < 0.02). Removal of the gallbladder has a limited effect on duodenojejunal motility. Few motor differences existed between symptomatic and asymptomatic patients after surgery. However, a low duodenal motor response to a meal and PCCs were often associated with symptoms.     

Intestinal and colonic motor alterations associated with irradiation-induced diarrhoea in rats

Localized application of ionizing radiation to the gastrointestinal tract frequently elicits responses, which include diarrhoea. The origin of this symptom is not clear but has been attributed to loss of epithelial integrity, together with alterations in motility and increased secretion. The purpose of this study was to examine whether a 10 Gy abdominal gamma irradiation leads to an inflammatory reaction, and to compare intestinal and colonic motility in controls and abdominally irradiated rats 1, 3 and 7 days after irradiation, using an electromyographic technique. The motility parameters analysed were the frequency and velocity of propagation of migrating myoelectric complexes (MMC) in the jejunum and colonic spike activity (long spike bursts; LSB) per 10 min in fasted rats. The MMC frequency was significantly reduced on days 1 and 7 after irradiation and the MMC pattern was markedly disrupted on day 3. The frequency of colonic LSB was significantly reduced on days 1, 3 and 7. Mouth to anus transit was significantly accelerated on day 3 only and diarrhoea was observed at this time. Myeloperoxidase activity in the jejunum and colon was also increased on this day only. It is concluded that irradiation-induced diarrhoea occurs contemporaneously with disruption of MMC in the small intestine.