Review article: new receptor targets for medical therapy in irritable bowel syndrome

Authors

  • M. CAMILLERI

    1. Clinical Enteric Neuroscience Translational and Epidemiological Research (C.E.N.T.E.R.), College of Medicine, Mayo Clinic, Rochester, MN, USA
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Dr M. Camilleri, Clinical Enteric Neuroscience Translational and Epidemiological Research (C.E.N.T.E.R.), College of Medicine, Mayo Clinic, Charlton 8-110, 200 First St. S.W., Rochester, MN 55905, USA.
E-mail: camilleri.michael@mayo.edu

Summary

Background  Despite setbacks to the approval of new medications for the treatment of irritable bowel syndrome, interim guidelines on endpoints for irritable bowel syndrome (IBS) trials have enhanced interest as new targets for medical therapy are proposed based on novel mechanisms or chemical entities.

Aims  To review the approved lubiprostone, two targets that are not meeting expectations (tachykinins and corticotrophin-releasing hormone), the efficacy and safety of new 5-HT4 agonists, intestinal secretagogues (chloride channel activators, and guanylate cyclase-C agonists), bile acid modulation, anti-inflammatory agents and visceral analgesics.

Methods  Review of selected articles based on PubMed search and clinically relevant information on mechanism of action, safety, pharmacodynamics and efficacy.

Results  The spectrum of peripheral targets of medical therapy addresses chiefly the bowel dysfunction of IBS and these effects are associated with pain relief. The pivotal mechanisms responsible for the abdominal pain or visceral sensation in IBS are unknown. The new 5-HT4 agonists are more specific than older agents and show cardiovascular safety to date. Secretory agents have high specificity, low bioavailability and high efficacy. The potential risks of agents ‘borrowed’ from other indications (such as hyperlipidaemia, inflammatory bowel disease or somatic pain) deserve further study.

Conclusions  There is reason for optimism in medical treatment of IBS with a spectrum of agents to treat bowel dysfunction. However, visceral analgesic treatments are still suboptimal.

Introduction

Despite claims based on meta-analyses1 that there are several treatments such as peppermint oil, antidepressants and probiotics based on Bifidobacteria, which are efficacious for the treatment of irritable bowel syndrome (IBS), patients and clinicians question their effectiveness. A recent review assessed the pipeline of medical treatments in IBS, as well as challenges in study design and regulatory guidance.2 Although the list is exhaustive, many candidate medications are still at a very early stage of development. What are realistic receptor targets of medical therapy of IBS? What targets appear to be less promising based on initial experience in humans? To appraise realistic opportunities and to assess whether there is any reason for optimism, this overview focuses on classes of medications or individual medications where there is at least mechanistic proof of concept in humans and initial evidence of efficacy in clinical trials. There are some targets of therapy that appeared to be very promising, but they have been disappointing, and they are briefly discussed. While some targets for therapy are not necessarily new, there are new approaches which promise to produce safer restoration of normal bowel function by stimulating motility and secretion. There are still no robust targets or proven therapies directed at visceral pain.

Thus, this overview will address the current state of knowledge in efficacy and safety of new 5-HT4 agonists, intestinal secretagogues [chloride channel activators, guanylate cyclase C (GC-C) agonists], bile acid modulation, anti-inflammatory approaches, κ-opioid agonist, pregabalin and gabapentin.

Medications aimed at putative targets that have not fulfilled their promise to date

There are two targets of medical therapy with potential in IBS which have been less promising in human studies than was predicted based on animal models.

Tachykinin antagonists

While NK1-antagonists such as aprepitant and casopitant are effective in chemotherapy-induced emesis or post-operative nausea or vomiting,3–5 there are no reports of pharmacodynamic6 or clinical efficacy in changing bowel sensation or motility in humans (healthy or IBS). Similarly, the NK3 antagonist class has been tested in pharmacodynamic studies in which it did not significantly alter rectal sensation in humans7 and in clinical trials.8 The NK2-receptor antagonist, nepadutant,9 reduced contraction frequency and amplitude on migrating motor complexes in the small intestine in healthy controls. It also effectively antagonized the motility-stimulating effects of infused NKA. Effects in clinical trials have not been reported.

Corticotrophin releasing hormone I antagonist

CRH stimulates colonic motility in healthy humans,10, 11 activates CRH receptor subtypes R1 and R2 on subepithelial mast cells, thereby inducing increased transcellular uptake of protein antigens in human colonic biopsies in Ussing chambers,12, 13 and the CRH 1 antagonist reduces sensation11 as well as the EEG signal in response to rectal distension.14 However, a proof of concept study with a CRF1 antagonist, pexacerafont and colonic transit and bowel function in IBS-D showed no advantage of pexacerafont over placebo.15 The selective CRF-1 receptor antagonist, GW876008, was shown to attenuate psychological stress-induced rectal hypersensitivity in nine patients with IBS.16 However, a multicentre, randomized, double blind, placebo controlled, two-period crossover clinical trial of 19-week duration with the same agent (GW876008) showed no significant difference from placebo in the global improvement scale, daily self-assessment of IBS pain/discomfort or individual lower GI symptoms.17

5-HT1A receptor antagonist

A large study of 402 patients explored the efficacy of AZD7371, a 5-HT1A receptor antagonist, which was equivalent to placebo in providing adequate relief from IBS or change in score in validated symptom and quality-of-life questionnaires. Hallucinations were reported by eight patients taking AZD7371, none on placebo.18

Cholecystokinin antagonist

Dexloxiglumide is a competitive antagonist of the CCK1 receptor. CCK is thought as a potential mediator of the colonic contraction in response to feeding that may cause symptoms such as urgency or diarrhoea. Initially, studies conducted in female patients with IBS-C provided contradictory results, with two large phase III trials showing no efficacy.19 This latter was consistent with a pharmacodynamic study in C-IBS,20 which paradoxically showed slowing of ascending colon emptying and no significant effect on overall colonic transit or satisfactory relief of IBS. In a more recent phase III randomized withdrawal study, dexloxiglumide demonstrated sustained relief of symptoms or at least a longer time to loss of therapeutic response in a randomized withdrawal trial in women (not in men) IBS patients.21 It is worth noting that among 869 IBS-C patients receiving single-blinded dexloxiglumide, there were 413 responders. The clinical benefit of this class of medication remains unclear.

Beta-3 adrenergic agonist

Solabegron was proposed after animal studies showed functional receptors on enteric neurons.22 However, a reliable pharmacodynamic assessment in humans failed to show any significant effect on gastrointestinal or colonic transit.23 A clinical trial with this medication has been completed, and a preliminary report shows that solabegron, 200 mg, b.d., led to a statistically significant increase in the proportion of women (= 0.019) and possibly both genders (= 0.06) achieving adequate relief of IBS pain and discomfort compared to placebo. There were also improvements in pain scores and number of pain-free days, but (consistent with transit results) no significant change in bowel symptoms.24

What went wrong? Was the problem in the target or the specific medication?

One feature in common with all these classes of medications is that their investigation in humans followed extensive animal toxicology and preclinical effects that appeared robust. However, application of the same principles in human proof of concept studies has been disappointing. There may be several reasons, some of which are reviewed in a scholarly treatise on the topic by Mayer et al.;25 others may be more speculative.

First, there is little evidence that CRF mechanisms are upregulated in the human condition and the degree of stress experienced by patients attending a clinic is not as severe as that of a rat avoiding water! In addition, there is no evidence that drug alteration of rectal sensory threshold predicts responsiveness in clinical trials in IBS.

Second, the efficacy of neurokinin modulators predicted from animal studies has been uniformly disappointing in larger human studies. It is conceivable that redundant mechanisms in sensation (e.g. norepinephrine, CGRP) or motor function (e.g. acetyl choline) compensate for the specific antagonism of the neurokinin receptors.

Third, the role of 5-HT1A receptors in modulating colonic motor or sensory function suspected from animal models was not confirmed in our study in healthy volunteers.26 Thus, buspirone did not significantly alter colonic compliance, tone, or sensation relative to placebo, whereas a positive control (venlafaxine) was effective.

Fourth, if CCK is associated with colonic motor response to feeding, why would it be tested in patients with IBS-C? In addition, dexloxiglumide slowed ascending colon emptying time which might be predicted to aggravate constipation or at least to cause harder stool consistency.

Fifth, studies of a β3-adrenergic agonist that alters enteric cholinergic neurons may require a baseline measurement of symptoms in detail or an assessment of colonic transit to select patients more likely to respond to this form of therapy.

In summary, it appears that failures might be attributable to insufficient proof of concept in humans before embarking on costly and time-consuming phase IIb or III clinical trials.

Medications that are fulfilling their promise to date

Table 1 provides a summary of the classes of medications targeting motor, secretory or sensory mechanisms that appear to be fulfilling their promise to date.

Table 1.   Summary of mechanism of action and clinical efficacy of new or promising medications in treatment of irritable bowel syndrome
Drug classExamplesRationale or Putative ActionPharmacodynamic (intestine or colon)Clinical efficacy: phase IIB or III primary endpoints Safety issues/comments
  1. Adapted from Camilleri and Chang2.

  2. IBS, irritable bowel syndrome;

CCK1 antagonistDexloxiglumideCompetitive antagonist of the CCK1 receptorSlower ascending colon emptying with no significant effect on overall colonic transitTwo initial IIB or III trials: not efficacious in IBS-C; a randomized withdrawal design trial showed longer time to loss of therapeutic response, longer for dexloxiglumide 
NK antagonistsNK1 antagonist, ezlozipantNK1 receptors’ role in nociceptionReduce the emotional response of IBS patients to rectosigmoid distensionNone 
NK2 antagonist, nepadutantNK2 receptors’ influence on smooth muscle contractilityReduce contraction frequency and amplitude on MMC in SB in healthy menNone 
NK3 antagonist, talnetantNK3 receptors’ role in nociceptionNo effect on rectal compliance, sensory thresholds or intensity ratings in healthy controlsTwo IIB trials in 1350 IBS patients: no benefit 
5-HT4-agonistsPrucaloprideStimulate intrinsic cholinergic neurons to enhance motilityIncreases SB, colon motility and transit in healthy controls and patients with chronic constipationIIB and III in CC (thousands of pts): BM frequency and satisfaction with bowel function both improvedGreater selectivity for 5-HT4 than 5-HT1B or hERG channel
ATI-7505Stimulate intrinsic cholinergic neurons to enhance motilityIncreases colon transit in healthy controlsNone reportedGreater selectivity for 5-HT4; not metabolized by CTP 3A4
Velusetrag (TD-5108)Stimulate intrinsic cholinergic neurons to enhance motilityDose-related increase in SB and colon transit in healthy controlsIIB, dose-ranging study in 401 CC patients increased BM frequency and proportion with adequate reliefGreater selectivity for 5-HT4
5-HT3 antagonistRamosetronInhibits secretion, motility, nociceptionNone reportedIIB, dose-ranging studies document benefit on global relief and bowel function endpoints in IBS-DSafety concern regarding ischaemic colitis with same drug class
Cl–C2 channel activatorLubiprostoneIncreases intestinal water and electrolyte secretionAccelerates SB and colonic transit in healthy controlsTwo phase III in several hundred CC and IBS-C patients: efficaciousNausea that is usually mild; FDA approved
Guanylate cyclase-C agonistLinaclotideIncreases intestinal water and electrolyte secretionAccelerated ascending colonic transit and altered bowel function in 36 women with IBS-CIIA and IIB studies in CC or IBS: increased BM frequency 
κ-Opioid agonistAsimadolineκ-Opioid receptors in visceral perceptionReduce sensation in response to colon distensions in the non-noxious range; relax colon tone in healthy controls; increase sensory thresholds in patients with IBSOn-demand dosing not effective in reducing severity of abdominal pain in 100 IBS patients; IIB, dose-ranging study, 596 IBS patients: at least average moderate pain benefit in IBS-D and IBS-A 
2,3-Benzodi-azepine modulatorDextofisopamPotential to reduce stimulation-induced colonic motility and visceral sensitivityNone reportedIIB study in 140 IBS patients: increased number of months of adequate overall relief of IBS symptoms; efficacy lower over timePossibly more abdominal pain or headache vs. placebo

5-HT4 agonists

Withdrawal of cisapride and tegaserod because of cardiac or potential vascular adverse events requires that any new drugs in this class prove selectivity27 for the 5-HT4 receptor over other receptors (e.g. 5-HT2B, 5-HT7) and channels (e.g. delayed rectifier potassium channel) and safety through studies of arrhythmogenic potential and effects on QT interval.28 Three 5-HT4 agonists in development are reported to have greater selectivity for 5-HT4 over other receptors and have advanced to human trials.

  • (i) Prucalopride is efficacious in accelerating colonic transit29 and in the treatment of severe chronic constipation unresponsive to laxative treatment.30–32 More recent reports document the continued efficacy in a 2-year open-label study of patients recruited from 7 previous placebo-controlled, randomized, controlled trials. Cardiovascular safety was also reported in 100 elderly constipated patients randomized (25/treatment group) to prucalopride in a dose-escalation study. Vital Signs, ECG and Holter data in these patients (∼80% of whom had history of or current cardiovascular disease) were not different from those under placebo and, importantly, no patient had QTcF >500 ms.33, 34
  • (ii) ATI-7505 is a benzamide 5-HT4 receptor agonist the chemical structure of which includes substituted piperidine-based scaffolds that are similar to cisapride. ATI-7505 is the pure (3S, 4R) isomer, whereas cisapride is a mixture of (3R, 4S) and (3S, 4R) isomers. It is a full agonist in the GI tract, but a partial agonist in the heart, devoid of other 5-HT receptor activities and negligible inhibitory activity at the hERG channel. The affinity ratio between IKr and 5-HT4 receptors is at least 1000-fold. Its primary metabolite is 100-fold less active than the parent drug at the 5-HT4 receptor and it has no detectable hERG channel inhibitory activity.35 Unlike cisapride, ATI-7505 undergoes hydrolytic esterase metabolism, but not oxidative CYP450 metabolism. Therefore, drug interactions with agents that affect or are metabolized by CYP 3A4 are unlikely. A dose–response pharmacodynamic study showed ATI-7505 accelerated colonic transit and enhanced evacuation of stool.36 A study in rodents suggests that ATI-7505 may alter visceral sensitivity.37 Results from clinical trials and dose–response clarifications are awaited.
  • (iii) Velusetrag (TD-5108) is a potent agonist at human 5-HT4 receptors with high intrinsic activity and selectivity for 5-HT4, >500-fold selective over other 5-HT receptors (including h5-HT2B and h5-HT3A). At 3 μm, TD-5108 had no effect on human ether-à-go-go-related gene encoded K+ channels.38, 39 In pharmacodynamic studies, velusetrag dose dependently accelerated colonic transit after single doses; with multiple doses, gastric and colonic transit were accelerated by 15 and 30 mg doses.40 Clinical trials demonstrate that these doses are also effective in the treatment of chronic constipation.41 To date, placebo-controlled trials in 60 healthy volunteers and >400 patients did not identify any cardiac rhythm abnormalities.

Novel 5-HT3 antagonist

Previous studies have shown that this class of drugs inhibits colonic secretion and motility, and visceral sensation through central and peripheral mechanisms. In experimental animal models, ramosetron inhibited stress or exogenous CRF-induced water secretion and acceleration of colonic transit, as well as colonic nociception in stress models.42, 43 In a double-blind, placebo-controlled, parallel-group study of 418 IBS-D patients, the 5-HT3 receptor antagonist, ramosetron, 5 and 10 μg once daily, increased monthly responder rates of ‘Patient-reported global assessment of relief of IBS symptoms’ compared to placebo; the benefit was similar in men and women.44 In a second study, ramosetron, 5 μg once daily, was effective and well tolerated in the treatment of abdominal pain, discomfort and bowel habits in IBS-D patients.45

Inhibition of serotonin synthesis

Given the concerns that 5-HT3 antagonists may be associated with ischaemic colitis and evidence that plasma serotonin or jejunal mucosal serotonin content are increased in patients with diarrhoea-predominant IBS,46, 47 there are novel approaches to reduce serotonergic stimulation by inhibition of the synthesis of the biogenic amine.

The novel oral tryptophan hydroxylase inhibitor, LX1031, resulted in significant reductions in urinary 5-HIAA and was well tolerated in total daily doses up to 4 g over 14 days. These data indicate successful pharmacological inhibition of the target enzyme in the GI tract;48 clinical trials are in progress.

Chloride secretion

Epithelial chloride transport induces fluid secretion: the main fluxes of chloride (Figure 1)49 are the basolateral Na+-K+-2Cl co-transporter, which brings chloride into the enterocytes, aided by the Na pump, and K channel which transport the cations out through the basolateral membrane. In the apical membrane, the cystic fibrosis transmembrane regulator (CFTR) and ClC-2 Cl channels in the apical membrane allow Cl exit, and this induces fluid secretion.

Figure 1.

 Chloride transport is also pivotal in the regulation of fluid secretion in the gastrointestinal tract by organs that drain into the intestine. This model of the chloride secretory mechanism in intestinal epithelial cells shows that secretion can be stimulated by increases in intracellular messengers, either cyclic nucleotides (cAMP/cGMP) or cytosolic calcium ([Ca2+]i). Major targets for regulation of secretion include channels in the apical membrane: CFTR, cystic fibrosis transmembrane conductance regulator; CaCC, calcium-activated chloride channel and ClC-2 (chloride channel type 2). Activation of these channels by the intracellular messengers is indicated with solid arrows, with additional postulated sites of action indicated with broken arrows. The identity of basolateral potassium channel(s) involved in either cyclic nucleotide- or calcium-mediated chloride secretion remains unknown. Ion channels in the basolateral membrane serve to deliver chloride into the enterocytes, while ensuring that the obligatorily co-transported cations are extruded by energy-dependent (e.g. ATP) mechanisms. These transporters are particularly needed to re-cycle potassium ions. They include: NKCC1 (sodium/potassium/2 chloride co-transporter type 1), IK, intermediate conductance potassium channel; K-cAMP channel, putative potassium channel regulated by cAMP and KCNQ1/KCNE3 heteromeric K+ channels (not shown). Adapted from Barrett and Keely49.

Currently, there are three targets of medical therapy related to chloride channels.

  • (i) Crofelemer is an antagonist at the CFTR; it may antagonize bowel dysfunction in IBS-D50 based on a single clinical trial.
  • (ii) ClC-2 and ClC-3 are expressed in most cells. Lubiprostone is a bicyclic fatty acid chloride channel activator in a drug class called prostones that induces chloride secretion by enterocytes and colonocytes;51 there are contradictory data in the literature regarding the activation of smooth muscle or activation of prostaglandin receptors by lubiprostone.52, 53
  • In humans, lubiprostone induces acceleration of colonic transit.54 Clinical trials show that lubiprostone at 24 μg b.d. is effective in the treatment of constipation;55 the dose approved for IBS-C is 8 μg b.d.,56 which is associated with lower prevalence of nausea. A human study assessed the effects of lubiprostone on colonic motility; minor changes in colonic tone and compliance were observed which are not likely to account for the clinical effects of lubiprostone; hence, the secretory effects appear to be the main mechanism responsible for the effects on constipation.57 In addition, the study showed no significant effect on colonic sensation thresholds or ratings.

  • (iii) Guanylate cyclase C is the principal receptor for heat-stable enterotoxins (STa), major causes in E. coli-induced secretory diarrhoea. GC-C is enriched in intestinal epithelium and has two endogenous ligands in the form of small cysteine-rich peptides guanylin and uroguanylin, released in an auto- or paracrine fashion into the intestinal lumen. Guanylin and uroguanylin are also endocrine hormones in gut–kidney communication, regulating ion transport in extraintestinal epithelia.58
  • Linaclotide is a synthetic GC-C agonist, which is a 14-amino acid peptide that activates the membrane GC-C on intestinal epithelial cells; highest levels of GC-C expression occur on the luminal surface of the epithelial cells. Linaclotide increases intestinal fluid secretion and increases intestinal transit. Linaclotide also decreases visceral pain in rats, and the effects are attributed to the effects of cGMP.59 In humans, there was no evidence of systemic exposure to linaclotide or its 13-amino acid active metabolite, MM-419447, after oral administration. Linaclotide accelerated colonic transit, loosened loose consistency and increased bowel frequency in patients with chronic constipation.60 Beneficial effects were replicated in a phase 2a RCT in chronic constipation61 and in a phase 2b RCT in IBS-C.62

Medications ‘borrowed’ from other indications

Bile acid modulation

Up to 95% of bile acids secreted into bile are actively reabsorbed in the terminal ileum. Inadequate absorption of bile in the distal small intestine increases its delivery into the caecum and colon, where bile acids may cause secretory diarrhoea.63 Previous studies have shown that both conjugated and nonconjugated bile acids induce secretion in the human colon.64, 65 There is also evidence that the di-α-hydroxy bile salt chenodeoxycholate (CDC) increases colonic motility,66, 67 although the effective dose is unclear. Ileocolonic delivery of CDC results in accelerated colonic transit and increased stool frequency and consistency in healthy volunteers.68 This ileocolonic delivery is effective at relatively low doses of 0.5–1.0 g/day, whereas effect of higher doses (2.25 g/day) of oral CDC were of variable efficacy in chronic constipation.69 There is considerable information about CDC safety from its use in the dissolution of gallstones. Thus, doses of 7–20 mg CDCA per kg body/weight/day were not hepatotoxic in humans.70

Conversely, bile acid binding with cholestyramine is effective for the treatment of diarrhoea related to bile acid malabsorption,71 but compliance with cholestyramine is poor because of unpalatability, gritty texture and gastrointestinal side effects, which limit its long-term use despite formulations sweetened with sucrose or aspartame. A newer bile acid binder, colesevelam hydrochloride, is better tolerated, has fewer gastrointestinal side effects and is easily administered.72 Initially approved as a lipid-lowering agent, colesevelam is now also approved as an adjunct therapy to improve glycaemic control in patients with type 2 diabetes mellitus.73, 74 Colesevelam slows colonic transit in a subset of patients with IBS-D (Odunsi S and Camilleri M, unpublished observations). Formal clinical trials are required to determine the role of bile acid binding in chronic diarrhoea and IBS-D especially as it has been suggested that up to 70% of patients with chronic watery diarrhoea have bile acid malabsorption,75 and 20% of unselected IBS-D patients had serological evidence of bile acid malabsorption.76

Anti-inflammatory approaches

There is evidence of a low-grade inflammation in IBS, involving mast cells in some patients, particularly in those with postinfectious aetiology.77 Three anti-inflammatory targets are being targeted in lower functional gastrointestinal disorders.

  • (i) Sodium cromoglycate: Jejunal fluid and a biopsy were obtained in health and IBS, 6 months after random allocation to no treatment (IBS, = 7) or oral DSCG, 200 mg/8 h (IBS-DSCG, = 11). BMs, stool consistency and abdominal pain were monitored. Mast cell degranulation was assessed by luminal tryptase release and transmission electron microscopy. Mast cell-mediated transcriptional restoration of relevant immunomodulatory genes in mucosal inflammation with cromoglycate results in clinical improvement of bowel function in IBS-D.78
  • (ii) Ketotifen, a mast cell stabilizer, has been shown to improve gastric emptying significantly after abdominal surgery and it may play a role in therapy for post-operative ileus, which is associated experimentally with mast cell degranulation.79 In a preliminary report of 60 IBS patients, it was claimed that ketotifen, but not placebo, increased the threshold for discomfort in visceral hypersensitive IBS patients (= 30); however, the post-treatment thresholds in the two treatment arms were not compared and do not appear to be significant. This effect on rectal sensory thresholds was not observed in normosensitive IBS patients (= 30). Importantly, the percentage of patients reporting severe abdominal pain was significantly decreased by ketotifen (30–7%, = 0.031), but not by placebo (32–29%, N.S.); similarly, severe complaints of abdominal bloating, flatulence, diarrhoea and incomplete evacuation were significantly reduced and quality of life subscales of sleep, diet and sexual functioning improved with ketotifen compared to placebo. Interestingly, spontaneous release of tryptase from IBS patients’ rectal mucosal biopsies was lower from that in healthy volunteers (in contrast to previous studies),80 and ketotifen treatment of IBS patients did not affect the release of tryptase.81 In summary, these provocative data support the need for further studies; an additional precaution to avoid unblinding of patients would be to use a control medication that induces some sedation or drowsiness.
  • (iii) Mesalazine (mesalamine) reduces total immunocytes, mast cells, as well as mucosal IL-1β (pg/mL), histamine (ng/mL) and tryptase (ng/mL) in patients with IBS. This was associated with improved well-being and satisfaction with treatment, but the study was too small to demonstrate significance in bowel and pain symptoms.82

Visceral sensation as a target

The κ-opioid agonist, asimadoline, has been extensively studied with pharmacodynamic trials showing reduced pain sensation at relatively low levels of colonic distension,83 and clinical trials that suggest adequate relief especially in patients with IBS-D and at least moderate pain during the run-in period.84 Intermittent use of asimadoline during attacks of IBS pain was not an effective therapy.85

Gabapentin, a 3-alkylated analogue of γ-amino butyric acid (GABA), has been shown to reduce elements of central sensitization in human experimental hyperalgesia. Forty patients with IBS-D were randomized for 5 days treatment with gabapentin, 300 mg/day and then 600 mg/day, which increased rectal sensory thresholds through attenuating rectal sensitivity to distension and enhancing rectal compliance.86 Pregabalin has been tested in IBS patients in pharmacodynamic study,87 but no clinical trials are reported to date.

New centrally acting agents in IBS

Benzodiazepine receptor modulator

Dextofisopam binds to 2,3-benzodiazepine receptors located in subcortical and hypothalamic regions. In animal models, dextofisopam reduced stimulation-induced colonic motility and visceral sensitivity. A 12 week, placebo-controlled, phase II study in patients with diarrhoea-predominant or alternating-IBS showed longer duration with adequate relief in the dextofisopam compared with the placebo group.88 The most prominent effects were observed within the first 4 weeks of treatment and included an improved consistency and frequency of bowel movements. The drug was well tolerated; however, the significance of the 12% of the patients experiencing worse abdominal pain (vs. 4% with placebo) requires further study.

Anti-psychotic agent

Quetiapine is an atypical antipsychotic agent that ameliorates anxiety and sleep disturbances, augments the effect of antidepressants and provides an independent analgesic effect. In a medical records study of patients with severe refractory functional gastrointestinal disorders, Grover et al.89 reported that among the 11 of 21 patients still on the medication at follow-up, six demonstrated global relief of symptoms and nine were satisfied with treatment. The remaining 10 of 21 discontinued therapy because of somnolence and lack of GI benefits. This is a very specific group of patients with known psychiatric diagnoses, including 14 anxiety, three post-traumatic stress disorder and five depression, and other centrally acting medications. The dose escalation, unblinded treatment and adverse effects also may have influenced the reporting of benefit. This approach requires further blinded studies before it can be endorsed. In addition, physicians without experience with this class of agents should probably avoid using such medications because of significant risk of central side effects.

Conclusions

The peripheral targets of medical therapy address the bowel dysfunction of IBS and this is often associated with pain relief. There are less clear targets related to the abdominal pain or visceral sensation in IBS. In recent years, the field of IBS therapy has been characterized by initial promise and subsequent disappointment because of withdrawal or restrictive use of new medications. However, there is reason to be optimistic. Representatives of the Food and Drug Administration have proposed interim endpoints for use in trials of IBS drugs that are based on clinically valid concepts.90 This has provided much appreciated guidance. The new 5-HT4 agonists are more specific and continue to show cardiovascular safety. Secretory agents have high specificity and low bioavailability. The potential risks of agents ‘borrowed’ from other indications (like hyperlipidaemia, inflammatory bowel disease or somatic pain) are known. With the convergence of greater understanding of pathophysiological mechanisms in IBS,91 relevant targets for medical therapy, a pipeline of medications that appear safe and clarity on trial endpoints, there is reason to believe that new medications will relieve patients with IBS.

Acknowledgements

Declaration of personal interests: Mayo Clinic has filed a provisional patent application (inventors: M. Camilleri, D. Burton) related to ileocolonic delivery of chenodeoxycholic acid: No. 61/143,727.The excellent secretarial support of Mrs Cindy Stanislav is gratefully acknowledged. Declaration of funding interests: This study was funded in part by National Institutes of Health (RO1-DK-54681).

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