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World J Gastroenterol. May 14, 2006; 12(18): 2846-2857
Published online May 14, 2006. doi: 10.3748/wjg.v12.i18.2846
Upper gastrointestinal sensory-motor dysfunction in diabetes mellitus
Jing-Bo Zhao, Jens Brøndum Frøkjær, Asbjørn Mohr Drewes, Niels Ejskjaer
Jing-Bo Zhao, Jens Brøndum Frøkjær, Asbjørn Mohr Drewes, Center of Excellence in Visceral Biomechanics and Pain, Aalborg Hospital, Søndre Skovvej 15, DK-9000 Aalborg, Denmark & Center for Sensory-Motor Interactions, Department of Health Science, Aalborg University, Fredrik Bajers Vej 7 D-3, DK-9220 Aalborg, Denmark
Niels Ejskjaer, Department of Medicine M (Diabetes & Endocrinology), Aarhus University Hospital, Norrebrogade 44, DK 8000 Aarhus C, Denmark
Supported by the Danish Diabetes Association, the Research Council of North Jutland County, the Toyota Foundation and the SparNord Foundation
Correspondence to: Jingbo Zhao, Center of Excellence in Visceral Biomechanics and Pain, the Research Building room 404, Aalborg Hospital, Sdr. Skovvej 15, DK-9000 Aalborg, Denmark. aas.jzhao@nja.dk
Telephone: +45-99326907 Fax: +45-99326801
Received: March 25, 2006
Revised: March 28, 2006
Accepted: April 10, 2006
Published online: May 14, 2006

Abstract

Gastrointestinal (GI) sensory-motor abnormalities are common in patients with diabetes mellitus and may involve any part of the GI tract. Abnormalities are frequently sub-clinical, and fortunately only rarely do severe and life-threatening problems occur. The pathogenesis of abnormal upper GI sensory-motor function in diabetes is incompletely understood and is most likely multi-factorial of origin. Diabetic autonomic neuropathy as well as acute suboptimal control of diabetes has been shown to impair GI motor and sensory function. Morphological and biomechanical remodeling of the GI wall develops during the duration of diabetes, and may contribute to motor and sensory dysfunction. In this review sensory and motility disorders of the upper GI tract in diabetes is discussed; and the morphological changes and biomechanical remodeling related to the sensory-motor dysfunction is also addressed.

Key Words: Diabetes, Esophagus, Stomach, Intestine, Motility, Pain, Diabetic neuropathy, Hyperglycemia, Remodeling


Citation: Zhao JB, Frøkjær JB, Drewes AM, Ejskjaer N. Upper gastrointestinal sensory-motor dysfunction in diabetes mellitus. World J Gastroenterol 2006; 12(18): 2846-2857
INTRODUCTION

Diabetes mellitus (DM) is a chronic disease requiring lifelong medical attention in order to limit the development of potentially devastating late complications and to manage them if they occur. In the USA, the per capita cost of healthcare in 2002 was $13 243 for patients with diabetes and $2560 for patients without diabetes[1]. Gastrointestinal (GI) disorders are common in diabetic patients[2,3]. As many as 75% of patients attending DM clinics report significant GI symptoms[2]. The entire GI tract from the esophagus to the anorectal region may be affected. Common complaints include dysphasia, early satiety, reflux, constipation, abdominal pain, nausea, vomiting and diarrhea. The symptoms may be severe and substantially decrease quality of life. The pathogenesis of the GI abnormalities is complex of nature, multi-factorial (motor dysfunction, autonomic neuropathy, glycemic control, psychological factors, etc.) and is not well understood[4]. A number of abnormal conditions have been described in different segments of the GI tract in patients with diabetic autonomic neuropathy (DAN): esophagus (dysmotility), stomach (dysmotility, delayed emptying) and small and large bowel (dysmotility, delayed transit, bacterial overgrowth and diarrhea)[4]. Only a few studies have addressed the visceral sensory function in DM[5-7] and have demonstrated abnormalities in perception thresholds, vagal tonus and evoked brain potentials in patients with DAN. This indicates that DM related neuronal changes may be located both in the peripheral and in the central nervous system (CNS). As mentioned the entire GI tract may be involved in DM, but our review describes the upper GI tract only.

Many studies have demonstrated prominent morphological changes of the small intestine and esophagus in DM[8-11]. Lately, several studies have described biomechanical remodeling as well as morphological remodeling in experimental diabetic rats[12-18]. Recently, Frøkjær et al[19] have shown that both the neuronal function of the contractile system as well as the structural apparatus of the GI tract may be affected in patients with longstanding DM and DAN. Therefore we suggest that along with DAN and glycemic control, the structural and biomechanical changes may play important roles in the symptomatology of GI abnormalities in long-standing DM. The future management of diabetic patients with GI symptoms may develop accordingly.

SYMPTOMS FROM THE UPPER GI TRACT IN DIABETES MELLITUS

Motor and sensory abnormalities in DM may affect the entire GI tract or part hereof, and the perceived symptoms may originate from one or several parts of the gut, such as the esophagus, stomach and small intestine[20,21]. The prevalence of upper GI symptoms is high in both insulin dependent DM (IDDM) and non-insulin dependent DM (NIDDM)[22-28]. The symptoms relating to the esophagus, stomach and small intestine are as follows: (1) Esophagus: Heartburn, dysphagia and chest pain[37]; (2) Stomach: weight loss and abdominal pain[38]; (3) Small intestine: Diarrhea, discomfort, pain and pseudo-obstruction. Most symptoms are non-specific of nature and may relate to other GI disorders not necessarily related to DM. Therefore, when dealing with GI symptoms, some specific issues need to be addressed. Chest pain may relate to reflux or esophageal motor disorders, but ischemic heart disease and other causes of non-cardiac chest pain are also possible causes and must be excluded. Dysphagia, the most characteristic symptom of impaired esophageal transit, may be caused by motility disorders of the esophagus. It is very important, however, to emphasize that dysphagia is more often caused by mechanical obstruction such as tumors and peptic stenosis than by motility disorders. A number of other incidental conditions must be excluded when diabetic gastroparesis is suspected: gastric outlet obstruction caused by tumors and ulcer disease; metabolic abnormalities such as diabetic ketoacidosis or uremia and side effects of pharmacotherapy. A gastroscopy and biochemical screening followed by physical examination are obligatory requisites to reach the correct diagnosis. The symptoms of diabetic gastroparesis tend to increase in intensity and frequency over the duration of diabetes in patients affected. Most often symptoms are vague and nonspecific such as early satiety, slight abdominal discomfort and perhaps bloating, and fortunately more rarely do nausea and vomiting develop. When nausea and vomiting becomes continuous hospitalization is needed to control glucose homeostasis, electrolytes and fluid substitution is needed. This is a potential life threatening situation. In the long run diabetic gastroparesis may be accompanied by poor diabetic control, weight loss and diminished quality of life partly due to frequent hospital contacts. The symptoms may last for days to months, and do often occur in cycles with symptom free intervals[29,30]. Diabetic patients frequently report abdominal pain and this may be the only symptom of diabetic gastroparesis; however, abdominal pain can also be seen in diabetic ketoacidosis and severe metabolic acidosis[31]. These conditions are followed by other symptoms as well and therefore distinguishable from gastroparesis. Diabetic patients with thoracic polyradiculopathy, a rare condition, may also suffer from abdominal pain[32]. Diarrhea in DM patients may be induced by a number of factors. These may include food composition, abnormal intestinal motility, small intestinal bacterial overgrowth, excessive loss of bile acids, pancreatic insufficiency and more[33]. Abnormal small intestinal motility (rapid or delayed transit) is a frequent condition in the diabetic patients as described below. Rapid transit may induce an increase in intra-luminal contents that reach the caecum, whereas delayed transit may cause bacterial overgrowth, both potentially resulting in diabetic diarrhea. Bacterial overgrowth has been reported in up to 40% of diabetic patients with diarrhea[34,35]. Celiac disease is overrepresented in IDDM and a cause of severe diarrhea to be excluded when dealing with diabetic diarrhea[36]. In its most fulminate form, diabetic diarrhea is a devastating and horrible condition for the person affected, sometimes resulting in catastrophical nightly soiling in bed and an uncontrollable condition during daytime. Most often, fortunately, this condition is self limiting and symptoms are more manageable.

SENSORY DYSFUNCTION

Although both the afferent and efferent nerves are affected in DM, the data related to the sensory dysfunction of the GI tract are sparse compared with those relating to the motor dysfunction of the upper GI tract. Elevation of perception thresholds to esophageal electrical stimulation has been observed in patients with DAN and different severity of GI symptoms[7]. Increased vagal tonus and abnormal evoked brain potentials to mechanical and electrical stimulation of the esophagus has also been shown[5,6]. Rayner et al performed isovolumetric and isobaric distensions of the proximal stomach in ten randomly selected patients with IDDM[39]. They demonstrated that the perception of gastric distension during euglycemia was increased compared with healthy controls. To study mechanisms behind postprandial symptoms in patients with diabetes, the gastric accommodation of the meal was assessed by abdominal ultrasound[40]. In DM patients, a large proximal stomach was associated with perception of fullness and a large antrum was associated with perception of pain after a meal. More recently, Frøkjær et al[41] used a multimodal stimulation device (Figure 1) to investigate the visceral sensitivity to mechanical, thermal and electrical stimulation in the esophagus and duodenum in IDDM patients with DAN and GI symptoms. This study demonstrated that the patients had decreased sensitivity to the stimulations of the esophagus and duodenum. This indicates that the affection of the sensory nerves is widespread in the GI tract. As the multimodal approach is thought to stimulate the mucosa, submucosa and muscle layers differentially, the disease seems to be generalized to nerves in all layers of the gut.

Figure 1
Figure 1 Top: The probe design allowing mechanical, heat and electrical stimulation of both the oesophagus and duodenum. The centre of the bag contains the sensor of the ultrasound probe imaging the oesophagus and duodenum during mechanical distension. The thermal stimuli were given by a pump system, which re-circulates water at 60 °C through two channels in the probe. The electrodes allowed electrical stimulation delivered directly to the mucosal surface. Bottom: The somatic referred pain areas to mechanical distension of the duodenum for the controls (left) and diabetic patients (right). The areas were larger for the diabetic patients.
MOTILITY DISORDERS

Long ago, it was known that abnormal motility of the GI tract occurred during the development of DM[42]. So far many studies have demonstrated that DM patients have slow transit and abnormal motility. The most frequent motility disorders of upper GI tract are shown in Table 1.

Table 1 Motility disorders of upper GI tract in DM.
OrganMotility disorder
EsophagusAmplitude[88,89] and number[46,90] of peristaltic contractions↑
Number of spontaneous and non-propagated contractions↑[45]
Amplitude of lower esophageal sphincter pressure↓[88]
Multi-peaked contractions[78,79]
StomachAntral IMMC↓[87]
Post-prandial antral activity and the number of antral contractions↓[91]
Pyloric dysmotility[92]
Small intestineFrequency and amplitude of the antropyloroduodenal contractions↑↓[93]
Duration of MMC cycle↑[85]
Early recurrence of the MMC and clusters of contractile activity[94]
Upper GI transit disorders in DM

Esophagus: Impaired esophageal transit has been reported both in IDDM and NIDDM patients[43-47]. The esophageal transit appears to be delayed in about 50% of patients with long-standing DM[48]. The retarded esophageal transit in the DM usually reflects either peristaltic failure or focal low-amplitude pressure waves[49].

Stomach: Several animal studies reported a slowing gastric emptying in IDDM and NIDDM rats[50-55], whereas other studies on IDDM and NIDDM animals demonstrated that gastric emptying increased[56-59]. Using radionuclide measuring techniques it has been demonstrated that gastric empting of solid, or liquid meals was abnormally slow in 30%-50% of patients with long-standing IDDM and NIDDM[60,61]. The gastroparesis in DM has been known clinically for more than 50 years[29]. It is not surprising that the gastric emptying delay in DM is related to both slow transit with increased retention of food in the proximal and distal stomach[62,63], and abnormal motility of the gastric wall[64].

Small intestine: Delayed and rapid transit in the small intestine was observed in animal diabetic models[65,66,67,68]. El-Salhy reported that the GI transit was rapid in non-obese diabetic mice[67] and was slower in obese diabetic mice[68]. Anjaneyulu and Ramarao[69] reported an increase in intestinal transit and a decrease in intestinal tone due to increased cholinergic and decreased beta-adrenergic receptor activities in DM rats. Slow small intestinal transit in DM patients have been documented using breath hydrogen appearance time after the ingestion of lactulose[70,71], by using radiopaque markers[72,73] and by use of metal-detector test[74]. On the other hand, Keshavarzian and Iber[75] investigated intestinal transit in IDDM patients after the ingestion of both liquid and solid meals and showed abnormal fast intestinal transit in their sample of diabetic patients. Nguyen et al[76] used intraluminal multiple impedance measurements to identify the postprandial duodenal chyme transport in patients with long standing IDDM. They demonstrated that the patients had disturbed propulsive chyme transport through the duodenum and the duodenal chyme clearance activity was decreased.

The transit disorders can occur in any region of the gut and in every stage of diabetes[74], and can affect each other. Since transit of food through the esophagus is relative fast, the gastric emptying rate is the major determinant of the food delivery to the small intestine. The relationship between esophageal transit and the rate of gastric empting appears to be poor[43] and the gastroparesis is often associated with the intestinal transit delay in DM[74,77].

Abnormal patterns of upper GI motility in DM

Esophagus: Esophageal manometric abnormalities occur in over 50% of patients with DM (see Table 1)[37]. The reduced amplitude of lower esophageal sphincter pressure is in accordance with the increased prevalence of gastroesophageal reflux disease in DM. More recently the evoked esophageal contractile activity to standardized bag distension was assessed using a specialized ultrasound-based probe by Frøkjær et al[19]. A balloon-like bag was positioned 10 cm above the lower esophageal sphincter and inflated. It was demonstrated, both at the bag and 6 cm proximally, that the distension induced hyperreactivity and impaired the coordination of the contractions in the diabetic patients.

Stomach: Motility disorders of the fundus and pylorus have been demonstrated in the diabetic animals[80-83]. In the human studies, it is recognized that disordered gastric contractile activity as assessed by manometry and gastric emptying occurs frequently in DM[84,85]. The motility disorders may include three aspects: Inter-digestive migrating motor complex (IMMC), amplitude and frequency of contractions, and pyloric dysfunction (Table 1).

Small intestine: Camilleri and Malagelada reported that small intestinal motility was abnormal in about 80% patients of long-standing DM with delayed gastric emptying[86]. Both postprandial and fasting small intestinal dysmotility in the DM was reported (Table 1). Dooley et al[87] studied fasting GI motility by manometry for a mean of 210 min in a group of 12 NIDDM patients with diarrhea and DAN. The patients showed grossly disordered motility. The migrating motor complex (MMC) disorders reflect the prolongation of phase II without change in the duration of phase I and III. The results of studies on postprandial motility at the level of the small intestine are inconsistent. However, abnormal motility patterns were observed in the diabetic subjects[85].

PATHOPHYSIOLOGY OF GI MOTILITY AND SENSORY DYSFUNCTION IN DM
Hyperglycemia

Disordered GI function in DM has been attributed to irreversible DAN but it is now clear that acute high blood glucose concentration per se have a major reversible influence on upper-GI tract motility and sensory function. An animal study demonstrated that the correction of hyperglycemia to euglycemic levels restores the delayed transit[65]. Several studies in both healthy subjects and DM patients have shown that the GI motor function is impaired during acute hyperglycemia (Table 2)[84,95-97]. Marked acute hyperglycemia affects the motility in every region of the GI tract[98]. This may indicate that cholinergic activity is affected during hyperglycemia. Hyperglycemia may also affect the perception of sensations arising from the GI tract (Table 2). However, much of the data have been observational, and there is relatively little information relating to potential mechanisms by which these effects are mediated. Because both stimulatory and inhibitory effects occur during the hyperglycemia, the effects of glucose are likely to be mediated by neural or humoral mechanisms, rather than a direct effect on the smooth muscle of the GI tract. The secretion of pancreatic polypeptide, which is under vagal cholinergic control, is diminished during acute hyperglycemia in healthy control subjects[99]. In healthy volunteers, plasma concentrations of motilin are less during hyperglycemia when compared with euglycemia[100]. Considering the effects of systemic changes in blood glucose concentrations, animal studies have revealed the presence of glucose-responsive neurons in the central nervous system, which may modify vagal efferent activity[101]. Neurons responsive to glucose have recently been identified in the rat small intestine[102], but their response to systemic rather than luminal glucose is unclear. Much work is required to elucidate the neural, humoral, and cellular mechanisms by which systemic glucose levels affects GI motility and sensation.

Table 2 Acute hyperglycemia and upper GI disorders.
Motility disorderSensory disorder
Peristaltic wave duration[98]↑Amplitude of the cortical evoked
Peristaltic velocity in the distalbrain potentials to moderate
part of the esophagus↓[103]esophageal distension↑[98]
Pressure of the low esophagealPerception during proximal
sphincter↓[103]gastric distension in healthy subjects
Gastric emptying of both solidsboth in the fasted state and during
and nutrient liquids↓[104]intra-duodenal lipid infusion↑[95]
Motility index and propagationInfluencing the postprandial
of duodenal and jejunal waves↓[84]fullness in IDDM patients↑[105]
Cycle length of inter-digestive
motor activity in the fasted state↓[56]
Small intestinal transit↓[71]
Proximal duodenal pressure waves↓[104]
Peripheral and central neuronal changes

DAN is seen as a major factor in the pathogenesis of disordered GI motor and sensory functions in DM[106,107]. Although GI manifestations related to DAN are diverse, many GI complications of DM seem to be related to DAN[19,48,72,108-110].

Histological findings: The best-characterized signs of damage to the autonomic nervous system during DM are morphological animal studies[111-117]. The number of myelinated axons in the vagosympathetic trunk is decreased in diabetic rats[118]. In the GI tract, many changes of nerves and ganglia were observed i.e. (1) dystrophic axonopathy[119]; (2) degeneration of mesenteric nerves and ganglia[111]; (3) number of vasoactive intestinal peptide (VIP)-IR neurons in myenteric ganglia[112]; (4) relative volume density in myenteric plexus[120]; (5) number of adrenergic and serotonergic neurons[111]. In addition, the surrounding tissue is also often disturbed. There is a thickening of the endothelium[121,122], which may sensitize axons to damage from increased pressure or decreased oxygen and glucose availability. It is thus possible that axonal damage may be secondary to disorders in tissue surrounding the neurons. Nitric oxide (NO) is a key neurotransmitter in the regulation of GI motor function[123,124]. In rodents with streptozotocin (STZ)-induced diabetes, NO synthase expression in the gastric myenteric neurons is diminished[125] and associated with delayed gastric emptying. The results of morphologic studies of the vagal nerves in diabetic patients are less consistent. One study demonstrated a decrease in unmyelinated axons in the abdominal vagus, another study found no abnormalities[126,127].

Clinical findings: One study has shown that abnormal esophageal motility is more frequent in the diabetic patients with evidence of DAN than in those without[37]. The presence of abnormal gastroesophageal reflux in diabetic patients has also been associated with the existence of DAN[128]. Increased cholinergic tone may relate to multi-peaked waves in the diabetic esophagus in these patients[78]. Gastric emptying largely depends on vagus nerve function, which can be severely disrupted in DM[60]. Studies using cardiac autonomic nerve function tests to assess the involvement of the autonomic nerve system in diabetic patients have indicated that the prevalence and severity of dysmotility of the small intestine is substantially greater in DM patients with DAN compared to patients with normal autonomic function[129]. Diarrhea is evident in 20% of diabetic patients, particularly those with known DAN[130,131]. Altogether, abnormal upper GI motility in DM has been associated to DAN. However, the question arises as to whether neuropathic changes in the intramural GI plexuses, the extrinsic neuronal pathways or in the central nervous system are primary or secondary. In a recent study, Frøkjær et al found hyperreactivity and impaired coordination to bag distension of the esophagus in IDDM patients, which indicates that a neuronal dysfunction is responsible for the hyperreactivity[19]. This dysfunction can theoretically be addressed to the mechano-sensitive afferent fibers, inter-neurons or efferent fibers located in the esophageal wall. However, impaired extra-intestinal pathways can potentially also affect the motor response. In another study, Frøkjær et al demonstrated that IDDM patients had decreased sensitivity to the stimulations of the esophagus and duodenum[41]. This was accompanied by an increase in somatic referred pain areas to the gut stimulation (Figure 1). As the referred pain is a result of convergence between visceral and somatic afferents on central neurons, the findings are indirect evidence for central hyperexcitability and neuroplastic changes. Altogether, this indicate that the neuronal changes can be located both peripherally (receptors, nerve fibers, ganglions) and in the CNS. Sensory nerve dysfunction in the gut may explain why diabetic patients with severe GI motility disorders often do not suffer from the GI symptoms expected from the abnormal motility and motor function. On the another hand a large subgroup of patients with longstanding DM suffers from severe GI symptoms[2,26,27]. This overall hyperalgesia/hypersensitivity is in contrast to the peripheral autonomic afferent neuropathy that most likely impairs the perception from the GI tract. The mismatch between hypo-and hypersensitivity can likely be explained by an impaired balance between peripheral and central neuronal changes. Hence, the impaired function of the peripheral afferent nerves is likely counterbalanced (or even overruled) by increased central (spinal and/or brain) neuronal excitability and this balance may determine the symptoms in individual patients.

It is likely that different pathophysiological mechanisms contribute to the peripheral and central neuronal changes in DM, including metabolic alterations, microvascular changes, and inflammatory changes[132]. Hypoxia, hyperglycemia, and increased oxidative stress in DM contribute directly and indirectly to Schwann cell dysfunction[133]. This will result in impaired paranodal barrier function, damaged myelin, reduced antioxidative capacity, and decreased neurotrophic support for axons. Furthermore, the direct effects of prolonged hyperglycemia through the glycation on nervous tissue are also important in the development of DAN[134-136].

Morphological and biomechanical remodeling

Although the hyperglycemia and neuropathy seem to be the main mechanisms to the motor-sensory dysfunction in the upper GI tract in DM, the question remains whether the disordered motor and sensory functions of the GI tract are only due to the neuronal changes and dysfunction or if primary diabetes-induced structural and biomechanical changes in the GI tract also play a role Data on the biomechanical properties are crucial for the understanding of the motor function of the GI tract because, (1) peristaltic motion that propels the food through the GI tract is a result of interaction of the passive and active tissue forces and the hydrodynamic forces in the food bolus and (2) remodeling of the mechanical properties reflects the changes in the tissue structure that determine a specific motor dysfunction. Therefore, the morphological and biomechanical remodeling of the GI wall may also be an important factor in the pathogenesis to the GI motor-sensory dysfunction in the diabetic patients.

Esophageal remodeling: Many studies have shown that DM causes morphological changes and biomechanical remodeling in the esophagus. Yang et al[13] in the in vitro study on the STZ-induced diabetic rat esophagus found that the wall thickness and cross-sectional wall area increased after the induction of diabetes. Twenty-eight days after the diabetic esophagus became stiffer both in shear and in the longitudinal direction. The esophageal remodeling was also found in NIDDM rat esophagus[18]. In the diabetic rats the opening angle and residual strain distribution in the outer surface of the wall decreased, the collagen fraction in the mucosa-submucosa layer and the passive circumferential stiffness of the esophageal wall increased (Figure 2). Furthermore, the esophageal weight per length, wall thickness and cross-sectional wall area increased in the NIDDM rats. One previous human study reported that among six cases of diffuse muscular hypertrophy of the esophagus, four cases were associated with DM[137]. Recently, Frøkjær et al[19] in an human study found an increase in esophageal wall thickness and altered deformation to the distension with reduced longitudinal shortening and the radial stretch in IDDM patients (Figure 3).

Figure 2
Figure 2 Microphotos of esophageal layer thickness in GK rats (left) and normal rats (middle). The muscle layer was biggest in the GK esophagus. Correspondingly the circumferential stress-strain curves of diabetic and non-diabetic esophageal wall showed in the right. The curve in the GK rats was shifted to the left, indicating that the esophageal wall stiffness increased.
Figure 3
Figure 3 Left: Cross-sectional ultrasound image of the distended distal esophagus allows identification of the esophageal layers, i. e. mucosa-submucosa, muscle and adventitia layers. The white round shadow in the center is caused by the intraluminal ultrasound probe. Right: The distension-induced change in longitudinal stretch ratio is illustrated as function of the esophageal radius. The curves were obtained during smooth muscle relaxation with butylscopolamine. Exponential trend lines of the patients and controls are shown. The shortening during distension was clearly reduced in the diabetic patients.

Stomach remodeling: A morphological study in DM rats demonstrated that the gastric mucosa thickness increased in DM rats compared with controls[138]. Remodeling of the interstitial cells network of Cajal in the stomach were found both in animals and humans with DM[139-141]. A histopathological study of the human stomach in DM patients with severe gastroparesis showed prominent collagenization and smooth muscle atrophy of the muscle layer[142]. Regarding the biomechanical remodeling of the stomach only one report by Liao et al is available[17]. The rat stomach was distended in vitro. Gastric compliance, the surface tension, and circumferential and longitudinal deformation-pressure curves were calculated based on three-dimensional ultrasound reconstructions of non-diabetic and diabetic stomach models. In experimental DM, gastric compliance was lowered both in the non-glandular stomach (proximal part) and the whole stomach (Figure 4). Furthermore, the circumferential stiffness in the non-glandular part increased. The structural changes of the stomach due to DM may together with the sensory and motor nerve dysfunction contribute to the delayed gastric emptying and the symptoms in diabetic patients.

Figure 4
Figure 4 The micro-photographs show the normal (A) and 4 wk STZ-induced diabetic (B) duodenal histological sections. It clearly demonstrates that the muscle and submucosa layers in the diabetic duodenum became much thicker than in the normal duodenum. The bar is 100 μm. Correspondingly, the circumferential (C) and longitudinal (D) stress-strain relation curves of the duodenum in the STZ-induced diabetic rats shifted to the left indicating the wall became stiffer.

Small intestinal remodeling: Many human[2,11,143,144] and animal [2,3,10,145-148] studies have shown that DM causes morphological alterations in the small intestine (Table 3). However, only few data exist relating to biomechanical remodeling of the small intestine in DM[12]. Recently we did a series of studies on the morphological and biomechanical remodeling of small intestine in the STZ-induced diabetic rats[14-16]. The major findings in our studies are summarized in Table 3 and briefly showed that the stiffness of the diabetic intestinal wall increased in a time-dependent manner (Figure 5). The viscoelastic behavior of intestinal wall also changed during the development of diabetes (Table 3). The stress-strain distribution and viscoelastic behavior mainly reflects the elastic properties of intestine. The changes in elastic properties reflect the structural remodeling of the intestinal wall during the diabetic development.

Table 3 Morphological and biomechanical changes of small intestine in DM.
Morphological changeBiomechanical change
Intestinal weight, length, and weight per unit length↑Opening angle and residual strain in duodenum↓
Surface area of mucosa↑Opening angle and residual
Number of goblet cells per villus↑strain in jejunum and ileum↑ Circumferential stiffness of
Smooth muscle mass↑the intestinal wall↑
Different layer thickness↑Longitudinal stiffness of the
Proliferating cell nuclear antigen (PCNA) ↑intestinal wall↑ Stress relaxation of small
interstitial cells of Cajal volume↓intestine↓
Figure 5
Figure 5 The circumferential curvature at the distension pressure of 1. 0 (A,B) and 4.0 (C,D) cmH2O in the non-diabetic (A,C) and the diabetic stomach (B,D). The circumferential deformation of the stomach in the non-diabetic rats was significantly bigger than that in the diabetic Goto-Kakizaki (GK) rats, indicating the stiffness of the diabetic gastric wall increased in the diabetic GK rats.

Advanced glycation end products (AGEs) produced during the development of DM likely relate to the morphological changes and biomechanical remodeling of the GI tract in DM. AGEs are generated by the sequential non-enzymatic glycation of protein amino groups and by oxidation reaction[149]. The accumulation of AGEs in tissues will alter the structure and function of matrix proteins[150]. Studies on DM and ageing show that AGEs are causing cross-linking of collagen molecules responsible for basement membrane thickening and loss of matrix elasticity[151-153]. AGEs may contribute to the diabetic GI morphological and biomechanical remodeling by at least two major mechanisms. The first is receptor-independent alteration of the extracellular matrix architecture by non-enzymatic glycation and the formation of protein cross-links. The second mechanism is receptor-dependent and consists of modulation of cellular functions through ligation of specific cell surface receptors[154-156]. Sanchez SS and coworkers have demonstrated that the expression of small intestinal extracellular matrix proteins have changed in STZ-induced diabetic rats[152]. Therefore, the nonenzymatic glycation of the GI tissue induced by long-term hyperglycemia seems to be an important mechanism behind the GI wall remodeling in DM.

Implication of GI remodeling on mechanosensory assessments: Mechanosensation is of fundamental importance for the GI function. The mechanosensitive nerve endings exist extensively in the GI tract where they serve a critical role in homeostasis. Several mechanoreceptor-like structures have been identified such as intraganglionic laminar nerve endings (IGLE) and intramuscular arrays (IMA) in the GI tract[157-164]. The mechanosensitive afferents in the intrinsic and extrinsic pathways were described as low-, wide-dynamic- or high-threshold tension-receptors[165]. Therefore, the GI tract structure as well as the tension, stress and strain distribution in the wall is important for the GI sensory and motor function. The GI wall structure or deformation changes in the DM will alter the relative positions of the mechanosensitive afferents (zero setting of the mechanosensitive afferents)[166]. The biomechanical remodeling in the DM such as alterations of residual strain and stress distribution and increase the wall stiffness will alter the tension and stress distribution of the mechanosensitive afferents. As results, the perception and motility of the GI tract will change as well. Hence, the morphological changes and biomechanical remodeling of GI tract in the DM is likely to affect the function of mechanosensitive afferents in the GI wall and further affect the motor and sensory function. However, so far the data are sparse about the association between the morphological and biomechanical remodeling of GI tract and the motor-sensory dysfunction in the DM[19,41]. The multimodal stimulations have proven accurate and reliable in the assessment of visceral sensation in several studies[167-169]. The geometry data of GI tract can be obtained by impedance and cross-sectional imaging such as ultrasound[170-172]. Combined with pressure recordings, biomechanical parameters such as tension, stress and strain can be obtained and correlated to the symptoms and mechanosensory data in the DM subjects[41]. Therefore, combined studies the GI motor-sensory dysfunction and morphological and biomechanical remodeling in the diabetic GI tract will improve our understanding about the pathophysiology of GI disorders in the DM patients. In the future, animal studies are needed to investigate the passive and active biomechanical and mechanosensory properties of the GI tract related to DM. The experiments should simulate the physiological conditions both in vivo and in vitro in normal and diabetic animals. The identification of mechanosensitive afferents and enteric nerve responses to the different stimuli will obviously be beneficial to understand the mechanisms of GI motor-sensory dysfunction in the DM.

In conclusion, GI symptoms are frequent in the diabetic patients and are associated with sensory-motor abnormalities, such as impaired perception and motility of the GI tract. The pathogenesis of abnormal GI sensory-motor function in DM is clearly multi-factorial. DAN seems to be the major factor in the pathogenesis of disordered GI motor and sensory functions in DM. Hyperglycemia has also been shown to impair GI motor and sensory function. Furthermore, the morphological changes and biomechanical remodeling of the GI wall may compromise the GI motor function and affect the function of the mechanosensitive afferents in the GI wall. Studies of the relation between the GI motor-sensory dysfunction, morphological changes and biomechanical remodeling in the diabetic GI tract may shed of more light to understand the mechanism of GI motor-sensory dysfunction in the diabetic patients. This knowledge may prove to be valuable in the development of new treatment strategies, which can also be evaluated with the developed methods. New treatments that may be based on the present knowledge and methods are: (1) neurostimulation of afferent visceral nerves, i.e. gastric electric stimulation, (2) agents which can break down already formed glycation end product protein-protein crosslinks, and (3) modulation of the central nervous system excitability by drugs.

Footnotes

S- Editor Pan BR E- Editor Bai SH

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