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Migrating motor complex

The migrating motor complex (MMC) is a recurring, cyclic pattern of gastrointestinal motility that occurs during fasting in the stomach and small intestine, propagating aborally every 90–120 minutes to clear residual undigested material, debris, and bacteria, thereby preventing small intestinal bacterial overgrowth.^[1]^[2] This interdigestive motor activity is essential for maintaining intestinal hygiene and is absent or altered postprandially, resuming only after the stomach empties.^[1] The MMC is characterized by four sequential phases, each with distinct contractile patterns observed via manometry. Phase I is a quiescent period lasting 40–60% of the cycle, featuring minimal or no contractions and low electrical activity. Phase II involves irregular, low-amplitude contractions that increase in frequency and intensity toward the end, comprising about 20–30% of the cycle and initiating peristaltic activity. Phase III, the most intense phase (lasting 4–6 minutes), consists of regular, high-amplitude contractions at maximal frequency (e.g., 3 per minute in the antrum, 11–12 per minute in the duodenum), resembling fed-state motility and often associated with hunger sensations. Phase IV serves as a brief transitional period of decreasing activity before returning to Phase I.^[1]^[2] Regulation of the MMC involves hormonal and neural mechanisms, primarily driven by the peptide hormone motilin, secreted by enteroendocrine M cells in the duodenum and proximal jejunum during fasting. Motilin binds to G protein-coupled receptors on gastrointestinal smooth muscle, triggering intracellular calcium release and contractions via a positive feedback loop with serotonin (5-HT) released from enterochromaffin cells; duodenal 5-HT4 receptors initiate Phase II, while vagal 5-HT3 pathways propagate gastric Phase III. The intestinal Phase III is mediated by intrinsic enteric neurons and is vagally independent, though stress can impair vagal tone and disrupt gastric activity. Erythromycin, a motilin receptor agonist, can mimic and enhance MMC activity.^[1]^[2] Clinically, disruptions in MMC function contribute to conditions such as functional dyspepsia, gastroparesis, and small intestinal bacterial overgrowth (SIBO), leading to symptoms like bloating, nausea, and delayed gastric emptying due to retained residues. Impaired MMC is also implicated in diabetic gastroparesis and reduced motilin levels during pregnancy, which may cause constipation. Therapeutic strategies, including prokinetics like erythromycin, aim to restore MMC integrity to improve gastrointestinal transit and alleviate associated disorders.^[1]^[2]

Overview

Definition

The migrating motor complex (MMC) is a cyclic pattern of motility in the smooth muscle of the stomach and small intestine that occurs during fasting states and is interrupted by feeding.^[1] It serves as an interdigestive housekeeping mechanism, propelling residual undigested material, bacteria, and debris aborally through the gastrointestinal tract.^[3] Key characteristics of the MMC include its periodic occurrence every 90–230 minutes in humans, with propagation from the stomach to the terminal ileum at a speed of 5–10 cm/min.^[4]^[5] This process involves coordinated electrical slow-wave activity in the smooth muscle that generates mechanical contractions, ensuring efficient clearance without the continuous propulsion seen in postprandial states.^[6] The MMC was first described in 1969 by Szurszewski in canine small intestine as a migrating electric complex.^[7] It was later confirmed in humans in the 1970s using manometric techniques, demonstrating similar cyclic patterns during fasting. Unlike the irregular, nutrient-driven peristalsis of the fed state, the MMC consists of four distinct phases that collectively maintain gut sterility by preventing bacterial overgrowth.^[1]

Functions

The migrating motor complex (MMC) primarily functions to clear residual undigested material, bacteria, and debris from the gut lumen during fasting periods, thereby preventing stagnation and maintaining gastrointestinal homeostasis.^[8] This housekeeping role ensures that the small intestine remains free of accumulated waste, which could otherwise impair digestive efficiency between meals.^[9] In terms of microbial balance, the MMC sweeps bacteria distally toward the colon, limiting proximal colonization and reducing the risk of small intestinal bacterial overgrowth (SIBO).^[10] By propelling microbial contents aborally, it helps regulate the gut microbiome, preventing excessive bacterial proliferation in the nutrient-poor environment of the upper small intestine.^[8] The MMC also contributes to gut integrity by facilitating the removal of sloughed dead epithelial cells and foreign particles, such as indigestible fiber or bone fragments, which are naturally shed into the lumen.^[11] This process supports epithelial renewal and prevents the buildup of potentially harmful particulates that could compromise the mucosal barrier.^[9] MMC activity exhibits circadian variation, with reduced frequency and duration during sleep or nighttime, aligning with lower metabolic demands and prolonged fasting states.^[12]

Phases

Phase I

Phase I represents the longest segment of the migrating motor complex (MMC) cycle, typically comprising 40-60% of the total cycle duration and lasting approximately 40-70 minutes in humans.^[13] This phase is marked by near-complete quiescence in the smooth muscle of the stomach and small bowel, with a profound absence of organized contractions and associated action potentials.^[3] It serves as a period of recovery following the intense activity of the preceding cycle, allowing the gastrointestinal tract to return to a baseline resting state during fasting.^[2] Physiologically, Phase I features minimal electrical activity, with rare action potentials and only occasional slow waves that do not culminate in spike potentials or muscle contractions.^[6] Pressure changes are negligible during this phase, reflecting the lack of phasic activity and maintaining a stable baseline intraluminal tone.^[1] This quiescent state contrasts with the continuous, irregular motility pattern observed in the fed state, effectively resetting the tract to interdigestive conditions.^[13] The phase originates in the gastric antrum and extends through the small intestine with minimal propagation of any residual activity, ensuring widespread motor silence.^[3] It concludes with the gradual emergence of sporadic contractions, marking the transition to Phase II. In clinical assessment, Phase I is identified via antroduodenal manometry as a prolonged interval of baseline pressure without spike bursts or pressure waves.^[14]

Phase II

Phase II represents a transitional period in the migrating motor complex (MMC), featuring irregular contractions that progressively increase in frequency and amplitude. This phase typically occupies 20–30% of the overall MMC cycle, lasting approximately 20–50 minutes in humans.^[11]^[15] Physiologically, Phase II is marked by intermittent action potentials occurring at rates of up to 10 per minute in the duodenum and fewer than 2 per minute in the antrum, producing pressure waves of low to moderate amplitude (generally below 20 mmHg) with variable propagation speeds over short distances.^[14]^[16] Up to 32% of these pressure waves may propagate bidirectionally.^[15] The phase is often subdivided into an early Phase II, characterized by low-amplitude, largely stationary contractions, and a late Phase II, with higher-amplitude contractions that migrate distally along the gastrointestinal tract.^[17]^[18] Regional differences are notable, with Phase II activity being more prominent in the duodenum than in the stomach, where contractions exhibit bursts approaching 50% of Phase III intensity.^[19]^[15] The duration of Phase II shows variability, tending to shorten in proximity to feeding due to nutrient-induced suppression of the MMC.^[20]^[19] This phase precedes the intense, regular activity of Phase III.^[21]

Phase III

Phase III represents the most intense and organized phase of the migrating motor complex (MMC), characterized by a short burst of regular, high-amplitude contractions that closely resemble the peristaltic activity observed during the fed state. This phase constitutes approximately 5-15% of the overall MMC cycle, typically lasting 5-10 minutes in humans.^[19]^[22] Physiologically, Phase III features maximal electrical activity, with rhythmic bursts of 10-12 action potentials per minute in the duodenum, accompanied by high-amplitude contractions generating intraluminal pressure spikes often reaching 50 mmHg or more. These contractions propagate aborally at a velocity of 6-8 cm/min, facilitating efficient propulsion of residual contents through the gastrointestinal tract.^[23]^[22]^[24] In humans, Phase III typically initiates in the gastric antrum or proximal duodenum, migrating distally for approximately 150-200 cm along the small intestine, often reaching the ileum, though some complexes may include occasional retrograde contractions within the propagated front. In contrast, Phase III in dogs more commonly originates in the duodenum.^[25]^[22]^[26] The onset of Phase III coincides with peaks in plasma motilin levels, which serve as a key trigger for this activity. Phase III terminates abruptly, either transitioning directly into the quiescent Phase I or preceded by a brief period of irregular contractions.^[19]^[1]

Phase IV

Phase IV is a brief transitional phase following Phase III, comprising about 5% of the MMC cycle and lasting 1–5 minutes. It features decreasing contractile activity and action potentials, serving as a bridge back to the quiescence of Phase I. This phase ensures a smooth return to motor silence without abrupt changes.^[1]

Regulation

Neural Mechanisms

The enteric nervous system (ENS) serves as the primary controller of the migrating motor complex (MMC), orchestrating its propagation through interconnected neural circuits within the gastrointestinal tract. The myenteric plexus, a key component of the ENS, coordinates local excitatory and inhibitory neurons to generate and sustain the aboral progression of MMC activity across intestinal segments.^[19] These circuits enable the rhythmic, migrating pattern essential for clearing residual contents during fasting.^[1] Interstitial cells of Cajal (ICCs), particularly those in the myenteric plexus layer (ICC-MY), function as pacemakers by generating electrical slow waves that underpin the cyclical nature of the MMC. These slow waves, originating in the stomach and propagating distally, drive the high-amplitude contractions characteristic of Phase III bursts, with frequencies of approximately 11–12 cycles per minute in the duodenum, decreasing distally to about 8 cycles per minute in the ileum.^[27]^[28] ICCs integrate with ENS neurons to modulate wave propagation, ensuring coordinated motility without direct neural firing.^[27] Extrinsic innervation modulates MMC initiation and regional activity. Vagal efferents, via cholinergic pathways and 5-HT3 receptors, facilitate gastric MMC onset in a vago-vagal reflex arc, influencing periodicity from the duodenum.^[19] Spinal sympathetic pathways, originating from thoracolumbar segments, exert inhibitory effects on intestinal MMC propagation, particularly in distal regions, by reducing contraction amplitude and velocity through noradrenergic transmission.^[29] Key neurotransmitters mediate the excitatory and inhibitory phases of the MMC. Acetylcholine, released from cholinergic enteric motor neurons, drives contractile activity by activating muscarinic receptors on smooth muscle, promoting the irregular contractions of Phase II and bursts of Phase III.^[30] Nitric oxide, produced by nitrergic neurons in the ENS, induces relaxation and maintains the quiescence of Phase I by hyperpolarizing smooth muscle cells via soluble guanylate cyclase.^[30] Feedback loops involving intrinsic sensory neurons, such as intrinsic primary afferent neurons (IPANs), allow dynamic adjustment of MMC timing. These neurons detect luminal distension or contents through mechanoreceptors and mucosal signals like serotonin release, triggering reflex arcs in the myenteric plexus to accelerate or delay cycles as needed.^[31] This sensory integration ensures adaptability to fasting conditions.^[19] Pharmacological interventions underscore the neural dependency of the MMC. Atropine, a muscarinic antagonist, abolishes Phase II and III contractions by blocking cholinergic excitation, while hexamethonium, a nicotinic ganglion blocker, disrupts ganglionic transmission and halts cycle propagation, confirming the essential role of ENS circuitry.^[1]

Hormonal Mechanisms

The migrating motor complex (MMC) is primarily initiated by motilin, a 22-amino-acid peptide hormone secreted in a pulsatile manner from enteroendocrine M cells in the duodenum and proximal jejunum every 90-120 minutes during fasting states.^[2] Motilin binds to its G-protein-coupled receptor (GPR38, also known as motilin receptor) expressed on gastrointestinal smooth muscle cells and enteric neurons, triggering the onset of phase III contractions that propagate aborally from the stomach to the terminal ileum.^[32] This binding activates phospholipase C, leading to the production of inositol trisphosphate (IP3) and subsequent intracellular calcium influx, which facilitates the strong, rhythmic contractions characteristic of phase III.^[2]^[33] Circulating motilin levels exhibit cyclic fluctuations that align closely with MMC phases, peaking at the onset of phase III and remaining elevated during fasting periods, while declining rapidly upon nutrient ingestion to suppress interdigestive motility.^[34]^[35] Ghrelin, another orexigenic hormone produced mainly in the gastric fundus, enhances motilin's effects by promoting phase II activity and amplifying overall MMC propagation in a vagus-dependent manner, though it does not directly bind the motilin receptor.^[36]^[32] In contrast, inhibitory hormones such as somatostatin, released from D cells in the gastric and duodenal mucosa, suppress MMC activity during the fed state by reducing motilin release and directly inhibiting gastrointestinal contractility.^[37] Cholecystokinin (CCK), secreted postprandially from I cells in the duodenum, further attenuates MMC cycles by inducing a fed-like motility pattern and inhibiting phase III initiation.^[38] In clinical contexts, erythromycin acts as a motilin receptor agonist, mimicking motilin's effects to induce premature phase III activity and restore disrupted MMC cycles in conditions like gastroparesis.^[39]^[40] Hormonal regulation of the MMC shows species-specific differences; while motilin is essential for initiating gastric phase III in humans, canine MMC cycles can proceed with less dependence on motilin, highlighting variations in receptor expression and potency across mammals.^[41]^[42] These endocrine signals are briefly amplified by neural pathways in the enteric nervous system to coordinate the full MMC propagation.^[36]

Pathophysiology

Impairments

Impairments in the migrating motor complex (MMC) can arise from various pharmacological agents that directly suppress its phases. Opioids, such as morphine, inhibit MMC activity by activating mu-opioid receptors in the enteric nervous system, leading to reduced frequency and amplitude of contractions across the small intestine.^[43] Similarly, anticholinergics like atropine block muscarinic receptors, abolishing phase III activity and disrupting overall propagation.^[44] Autonomic neuropathy, particularly in conditions like diabetes, impairs MMC propagation by damaging vagal and enteric nerves, resulting in uncoordinated or diminished motor patterns.^[45] This neuropathy reduces the neural coordination necessary for the aboral migration of complexes, often leading to incomplete cycles.^[46] Structural alterations also contribute to MMC dysfunction. Surgical interventions such as vagotomy disrupt initiation of gastric phase III by severing vagal innervation, preventing the complex from originating in the stomach and propagating distally.^[47] In scleroderma, progressive fibrosis of smooth muscle impairs contractility, causing abnormal MMC cycling with shortened or absent phases.^[48] Metabolic factors further compromise MMC integrity. Hypothyroidism is associated with gastrointestinal motor dysfunction, leading to slowed motility and prolonged interdigestive periods.^[49] In critical illness, such as in intensive care unit patients, MMC is frequently abolished due to systemic inflammation, sedation, and opioid use, resulting in fed-like motor patterns during fasting states.^[50] Common cycle abnormalities include the absence of phase III, which fails to generate the high-amplitude bursts essential for clearance, promoting luminal stasis.^[51] Uncoordinated propagation manifests as retrograde or stationary complexes, where motor activity does not migrate properly aborally, disrupting the sweeping mechanism.^[52] Diagnostic evaluation via antroduodenal manometry reveals these impairments through reduced MMC frequency, typically less than one cycle per hour, or absent pressure bursts during phase III.^[53] These findings indicate underlying disruptions in the cyclical pattern. The primary consequence of MMC impairments is luminal stasis in the small intestine, where residual contents accumulate due to ineffective propulsion.^[3] This stasis increases the risk of bacterial overgrowth by hindering bacterial clearance.^[49]

Associated Disorders

Impairments in the migrating motor complex (MMC) are strongly linked to small intestinal bacterial overgrowth (SIBO), where failure of the MMC's cleansing action allows bacterial proliferation in the small intestine, leading to symptoms such as bloating, diarrhea, and abdominal pain.^[10] This association is particularly evident in conditions disrupting intestinal motility, with MMC dysfunction contributing to the stasis that promotes overgrowth.^[54] Gastroparesis, characterized by delayed gastric emptying, often involves absent or disrupted gastric Phase III of the MMC, resulting in retained food and symptoms like nausea and vomiting.^[55] It is commonly observed in diabetic patients due to autonomic neuropathy and can also arise post-virally, highlighting the MMC's role in coordinating gastric and small bowel propulsion.^[56] Chronic intestinal pseudo-obstruction (CIPO) features disrupted MMC propagation, mimicking mechanical obstruction through uncoordinated contractions and stasis, often idiopathic or secondary to neurological disorders such as Parkinson's disease.^[57] Manometric studies reveal complex migrating motor disorders with reduced contraction frequency, exacerbating symptoms of abdominal distension and constipation.^[58] In irritable bowel syndrome (IBS), MMC cycles may be altered, with studies showing fewer phase III activities in subsets with bacterial overgrowth.^[59] Similarly, in anorexia nervosa, delayed gastric emptying can occur due to stress-related hormonal changes, leading to further nutritional compromise.^[60] Dysmotility, potentially including MMC impairments, is reported in over 50% of patients with unexplained gastrointestinal symptoms and suspected SIBO, with higher SIBO prevalence in the elderly due to age-related motility changes.^[61]^[10] Diagnostic overlap exists, as hydrogen breath tests for SIBO indirectly reflect MMC integrity through evidence of bacterial overgrowth from impaired clearance. Recent guidelines (as of 2025) emphasize prokinetics to enhance MMC function in managing SIBO related to motility disorders.^[62]^[63]

Clinical Applications

Diagnosis

The primary method for diagnosing migrating motor complex (MMC) dysfunction is antroduodenal manometry, considered the gold standard for directly measuring interdigestive motility patterns in the stomach and proximal small intestine. This invasive procedure involves the placement of a catheter with multiple pressure sensors through the nose or mouth into the antrum and duodenum, where it records intraluminal pressures over a fasting period of 4-6 hours to capture at least one full MMC cycle, including its phases and aboral propagation.^[64] In normal individuals, antroduodenal manometry reveals cyclic MMC activity with phase III occurring approximately every 90-120 minutes, resulting in 1-2 such events over a 4-hour recording, characterized by high-amplitude contractions (typically >20 mmHg) at 10-12 cycles per minute that propagate distally from the antrum through the duodenum and, in extended recordings, to the ileum.00219-4/pdf)^[64] Abnormal findings, such as absent or non-propagating cycles, indicate MMC impairment and are particularly useful for evaluating refractory gastroparesis or suspected chronic intestinal pseudo-obstruction (CIPO), where the absence of phase III suggests underlying neuromuscular dysfunction.02411-X/fulltext)^[65] Indirect assessments provide supportive evidence of MMC function without direct pressure measurement. Gastric emptying scintigraphy, using radiolabeled meals during fasting conditions, can infer phase III activity by observing periodic clearance patterns that align with MMC sweeps, though it primarily evaluates overall emptying rather than specific phases.^[66] Hydrogen breath tests, often used to detect small intestinal bacterial overgrowth (SIBO), serve as a proxy for MMC failure, as impaired motility allows bacterial proliferation leading to elevated hydrogen levels after substrate ingestion; this indirectly confirms MMC-related impairments in disorders like SIBO.00357-2/fulltext) Despite its diagnostic value, antroduodenal manometry faces challenges, including its invasive nature, which involves discomfort from intubation and limits its routine clinical use to specialized centers, as well as the need for overnight studies to account for circadian variations in MMC frequency that peak during sleep.^[67]00219-4/pdf) Emerging noninvasive alternatives, such as wireless motility capsules like the SmartPill, enable ambulatory monitoring of interdigestive pressure patterns and pH changes over 24-72 hours, detecting up to 86% of phase III events compared to manometry and allowing assessment of propagation through the small bowel without hospitalization. Additionally, as of 2025, non-invasive body surface gastric mapping has emerged as a promising alternative, demonstrating comparability to antroduodenal manometry in diagnosing neuropathic gastroduodenal disorders.^[67]^[68]^[69]

Therapeutic Stimulation

Therapeutic stimulation of the migrating motor complex (MMC) primarily involves pharmacological interventions aimed at restoring or enhancing its cyclic activity in conditions where it is impaired, such as gastroparesis or small intestinal bacterial overgrowth (SIBO). Prokinetics like erythromycin, a motilin receptor agonist, effectively induce Phase III-like activity of the MMC by mimicking the hormone motilin's effects on gastrointestinal smooth muscle, with oral doses of 40-200 mg triggering premature Phase III complexes that propagate from the stomach to the small intestine.^[70] Similarly, prucalopride, a selective 5-HT4 receptor agonist, promotes MMC propagation by enhancing propulsive motor activities in the small bowel and colon, particularly through intraluminal activation that increases the occurrence and amplitude of contractions.^[71] Other pharmacological agents target neural pathways to support MMC function. Metoclopramide, a dopamine D2 receptor antagonist, enhances cholinergic drive and reverses stress-induced inhibition of MMC cycles, thereby improving interdigestive motility without disrupting the fasting pattern.^[72] Neostigmine, an acetylcholinesterase inhibitor, is used for acute reversal of MMC inhibition, such as in postoperative ileus or colonic pseudo-obstruction, by increasing antral and intestinal motor activity through parasympathetic potentiation.^[73] Non-pharmacological approaches focus on lifestyle modifications to facilitate natural MMC cycling. Intermittent fasting or spaced meal intervals (typically 4-5 hours between meals) allow the interdigestive state to predominate, enabling the MMC to occur unimpeded and clear residual contents from the gut.^[74] Timing prokinetic administration before meals can further synchronize drug-induced MMC activity with endogenous cycles, optimizing motility without constant suppression. In severe, refractory cases like diabetic gastroparesis, surgical options such as gastric electrical stimulation may be employed to improve gastric emptying and alleviate symptoms, though evidence remains limited to specialized centers.^[75] Vagal nerve stimulation, targeting neural mechanisms, has also shown potential in modulating MMC initiation and propagation in animal models, but clinical application is rare and investigational.^[21] Clinical evidence supports these interventions, particularly for conditions linked to MMC dysfunction. Low-dose erythromycin restores MMC activity and delays symptom recurrence in SIBO patients by addressing motility deficits at the root cause, potentially reducing reliance on broad-spectrum antibiotics; studies indicate efficacy in preventing relapse for up to several months post-treatment.^[76] Post-treatment antroduodenal manometry is recommended to confirm MMC cycle restoration, assessing Phase III frequency and propagation to guide ongoing management.^[77]

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Top left shows phase I, phase II, and phase III of the fasting cycle. Top ... antagonist, compared to muscarinic antagonists, on the migrating motor complex in ...<|control11|><|separator|>
[54]
Antroduodenal manometry for the evaluation of patients with ...
Abnormal neural control of the antrum and small intestine is identified by the absence of a phase-3 of the migrating motor complex (MMC) or retrograde ...
[55]
Small Intestinal Bacterial Overgrowth - StatPearls - NCBI Bookshelf
So, chronic pancreatic insufficiency is associated with SIBO.[3] Migrating motor complexes are responsible for peristalsis and cleansing of the small ...
[56]
Plasma motilin concentration and interdigestive migrating ... - PubMed
We conclude that diabetic gastroparesis is associated with absence of antral interdigestive migrating motor complex and with elevated plasma motilin ...
[57]
Gastroparesis: Current Concepts and Management - PMC
In the fasting state, the proximal gastrointestinal tract displays the migrating motor complex (MMC), a cyclical motor pattern of the stomach and the small ...
[58]
Chronic Intestinal Pseudo-obstruction: Clinical and Manometric ...
The most relevant findings were the complex migrating motor disorders and decreased frequency and propagation of contractions. The 9 patients who died had a ...
[59]
Chronic Intestinal Pseudo-obstruction: Clinical and Manometric ...
Apr 30, 2017 · The most relevant findings were the complex migrating motor disorders and decreased frequency and propagation of contractions. The 9 ...
[60]
Small intestinal bacterial overgrowth in patients with irritable bowel ...
... migrating motor complex; SIBO, small intestinal bacterial overgrowth. Results from the small‐bowel manometries in patients with IBS with and without SIBO ...
[61]
Erythromycin effects on gastric emptying, antral motility and plasma ...
In primary anorexia nervosa, gastric motility is often impaired and ensuing symptoms further discourage eating. Prokinetic agents have been shown to ...
[62]
Dysmotility and ppi use are independent risk factors for small ... - NIH
Dysmotility and PPI use were independent risk factors for SIBO or SIFO and were present in over 50% of subjects with unexplained gastrointestinal symptoms.<|control11|><|separator|>
[63]
Microflora Modulation of Motility - PMC - PubMed Central - NIH
The relationship between the integrity of the migrating motor complex and the absence of small intestinal bacterial overgrowth (SIBO) was, in fact, first ...
[64]
How to Perform Antroduodenal Manometry - PMC - NIH
The contraction frequency of duodenum is between 11-12 cpm with amplitude of more than 20 mmHg during the phase III MMC. Most of the phase III contractions ...
[65]
[PDF] Patients with Specific Gastrointestinal Motility Disorders are ...
Jun 22, 2021 · Primary gastrointestinal (GI) motility disorders, such as gastroparesis and chronic intestinal pseudo-obstruction, ... absent migratory motor ...<|control11|><|separator|>
[66]
Advances in the physiology of gastric emptying - PMC
Phase I lasts approximately 45‐60 minutes, during which the peristaltic pump exhibits electrical slow waves that are not associated with muscle contractions.
[67]
Comparative analysis of phase III migrating motor complexes in ...
Comparative analysis of phase III migrating motor complexes in stomach and small bowel using wireless motility capsule and antroduodenal manometry.
[68]
A Technical Review and Clinical Assessment of the Wireless Motility ...
The WMC is a single-use, orally ingested, nondigestible capsule that is capable of measuring gastric emptying time (GET), small bowel transit time (SBTT), ...
[69]
use of erythromycin as a gastrointestinal prokinetic agent in adult ...
Feb 8, 2007 · Forty mg erythromycin A elicited a premature phase 3 complex that started in the stomach and migrated to the small intestine, while doses of 200 ...
[70]
Intraluminal prucalopride increases propulsive motor activities via ...
Intraluminal prucalopride and intraluminal exogenous 5-HT strongly evoked or enhanced the colonic motor complex at all levels of excitation.
[71]
Effects of Different Types of Stress and of "Prokinetic" Drugs on the ...
The stress-induced inhibition of migrating motor complexes was reversed by oral metoclopramide; however, the drug did not reverse the cardiovascular or ...
[72]
Effect of Neostigmine on Gastroduodenal Motility in Patients ... - NIH
The phases of migrating motor complexes (MMC) were identified and characterized based on established criteria (28). Phase 3 of the MMC was considered to have a ...
[73]
The migrating motor complex: control mechanisms and its role in ...
Mar 27, 2012 · The migrating motor complex (MMC) is a cyclic, recurring motility pattern that occurs in the stomach and small bowel during fasting; ...
[74]
Gastric electrical stimulation for gastroparesis: A goal greatly ...
Jan 21, 2011 · A: On the first day, the postprandial gastric motor activity was very low and only three activity fronts of the Migrating Motor Complex were ...
[75]
Low-Dose Nocturnal Tegaserod or Erythromycin Delays Symptom ...
Tegaserod significantly prevents the recurrence of IBS symptoms after antibiotic treatment compared to erythromycin or no prevention.
[76]
Erythromycin induces migrating motor complex in human ... - PubMed
It is concluded that erythromycin at a dose of 1-3 mg/kg/hr for 15 min during the interdigestive state, similar to motilin, has a significant influence upon the ...Missing: prokinetic | Show results with:prokinetic