# Current Treatment Options and Therapeutic Insights for Gastrointestinal Dysmotility and Functional Gastrointestinal Disorders

**Authors:** Rajan Singh, Hannah Zogg, Uday C Ghoshal, Seungil Ro

PMC · DOI: 10.3389/fphar.2022.808195 · Frontiers in Pharmacology · 2022-01-25

## TL;DR

This paper reviews current treatments and challenges in managing gut-brain interaction disorders like IBS and FD, highlighting gaps in understanding and targeting underlying mechanisms.

## Contribution

The paper provides a comprehensive review of treatment options and challenges for gastrointestinal motility and functional disorders, emphasizing the need for mechanism-based therapies.

## Key findings

- Current therapies for FGIDs lack long-term effectiveness and safety.
- Microbial dysbiosis's role in gut health remains poorly defined.
- Multi-omics studies are needed to clarify gut microbial contributions to disease.

## Abstract

Functional gastrointestinal disorders (FGIDs) have been re-named as disorders of gut-brain interactions. These conditions are not only common in clinical practice, but also in the community. In reference to the Rome IV criteria, the most common FGIDs, include functional dyspepsia (FD) and irritable bowel syndrome (IBS). Additionally, there is substantial overlap of these disorders and other specific gastrointestinal motility disorders, such as gastroparesis. These disorders are heterogeneous and are intertwined with several proposed pathophysiological mechanisms, such as altered gut motility, intestinal barrier dysfunction, gut immune dysfunction, visceral hypersensitivity, altered GI secretion, presence and degree of bile acid malabsorption, microbial dysbiosis, and alterations to the gut-brain axis. The treatment options currently available include lifestyle modifications, dietary and gut microbiota manipulation interventions including fecal microbiota transplantation, prokinetics, antispasmodics, laxatives, and centrally and peripherally acting neuromodulators. However, treatment that targets the pathophysiological mechanisms underlying the symptoms are scanty. Pharmacological agents that are developed based on the cellular and molecular mechanisms underlying pathologies of these disorders might provide the best avenue for future pharmaceutical development. The currently available therapies lack long-term effectiveness and safety for their use to treat motility disorders and FGIDs. Furthermore, the fundamental challenges in treating these disorders should be defined; for instance, 1. Cause and effect cannot be disentangled between symptoms and pathophysiological mechanisms due to current therapies that entail the off-label use of medications to treat symptoms. 2. Despite the knowledge that the microbiota in our gut plays an essential part in maintaining gut health, their exact functions in gut homeostasis are still unclear. What constitutes a healthy microbiome and further, the precise definition of gut microbial dysbiosis is lacking. More comprehensive, large-scale, and longitudinal studies utilizing multi-omics data are needed to dissect the exact contribution of gut microbial alterations in disease pathogenesis. Accordingly, we review the current treatment options, clinical insight on pathophysiology, therapeutic modalities, current challenges, and therapeutic clues for the clinical care and management of functional dyspepsia, gastroparesis, irritable bowel syndrome, functional constipation, and functional diarrhea.

## Linked entities

- **Diseases:** irritable bowel syndrome (MONDO:0005052), gastroparesis (MONDO:0006769), functional diarrhea (MONDO:0001272)

## Full-text entities

- **Genes:** OCLN (occludin) [NCBI Gene 100506658] {aka BLCPMG, PPP1R115, PTORCH1}, CNR2 (cannabinoid receptor 2) [NCBI Gene 1269] {aka CB-2, CB2, CX5}, TPH1 (tryptophan hydroxylase 1) [NCBI Gene 7166] {aka TPRH, TRPH}, NR1H4 (nuclear receptor subfamily 1 group H member 4) [NCBI Gene 9971] {aka BAR, FXR, HRR-1, HRR1, PFIC5, RIP14}, SLC6A4 (solute carrier family 6 member 4) [NCBI Gene 6532] {aka 5-HTT, 5-HTTLPR, 5HTT, HTT, OCD1, SERT}, CLCN2 (chloride voltage-gated channel 2) [NCBI Gene 1181] {aka CIC-2, CLC2, ECA2, ECA3, EGI11, EGI3}, GHSR (growth hormone secretagogue receptor) [NCBI Gene 2693] {aka GHDP, GHS-R1a, GHSR-1a}, TRPV1 (transient receptor potential cation channel subfamily V member 1) [NCBI Gene 7442] {aka VR1}, NPR3 (natriuretic peptide receptor 3) [NCBI Gene 4883] {aka ANP-C, ANPR-C, ANPRC, BOMOS, C5orf23, GUCY2B}, CLDN1 (claudin 1) [NCBI Gene 9076] {aka CLD1, ILVASC, SEMP1}, NGF (nerve growth factor) [NCBI Gene 4803] {aka Beta-NGF, HSAN5, NGFB}, CFTR (CF transmembrane conductance regulator) [NCBI Gene 1080] {aka ABC35, ABCC7, CF, CFTR/MRP, MRP7, TNR-CFTR}, HTR4 (5-hydroxytryptamine receptor 4) [NCBI Gene 3360] {aka 5-HT4, 5-HT4R}, HMOX1 (heme oxygenase 1) [NCBI Gene 3162] {aka HMOX1D, HO-1, HSP32, bK286B10}, SLC10A2 (solute carrier family 10 member 2) [NCBI Gene 6555] {aka ASBT, IBAT, ISBT, NTCP2, PBAM, PBAM1}, TACR1 (tachykinin receptor 1) [NCBI Gene 6869] {aka NK1R, NKIR, SPR, TAC1R}, TAC1 (tachykinin precursor 1) [NCBI Gene 6863] {aka Hs.2563, NK2, NKNA, NPK, TAC2}, FGF19 (fibroblast growth factor 19) [NCBI Gene 9965], HTR3A (5-hydroxytryptamine receptor 3A) [NCBI Gene 3359] {aka 5-HT-3, 5-HT3A, 5-HT3R, 5HT3R, HTR3}, ACHE (acetylcholinesterase (Yt blood group)) [NCBI Gene 43] {aka ACEE, ARACHE, N-ACHE, YT}, HTR1A (5-hydroxytryptamine receptor 1A) [NCBI Gene 3350] {aka 5-HT-1A, 5-HT1A, 5HT1a, ADRB2RL1, ADRBRL1, G-21}, TJP1 (tight junction protein 1) [NCBI Gene 7082] {aka ZO-1}, HRH1 (histamine receptor H1) [NCBI Gene 3269] {aka H1-R, H1R, HH1R, hisH1}, ARRB1 (arrestin beta 1) [NCBI Gene 408] {aka ARB1, ARR1}
- **Diseases:** cardiovascular and cerebrovascular ischaemic (MESH:D002318), PDS (MESH:D012128), -related disorders (MESH:D019973), SIBO (MESH:D001765), malabsorption (MESH:D008286), epigastric burning (MESH:C537170), emetic (MESH:D020250), neuron degeneration (MESH:D009410), Gut Immune Dysfunction (MESH:D007154), Gastroparesis (MESH:D018589), tardive dyskinesia (MESH:D004409), chronic constipation (MESH:D003248), GI symptoms (MESH:D012817), mast (MESH:D000090362), poor sleep (MESH:D012893), anxiety (MESH:D001007), Gut motility disorders (MESH:D015835), primary biliary cholangitis (MESH:D008105), depression (MESH:D003866), emesis (MESH:D014839), cardiac (MESH:D006331), IBS (MESH:D043183), bile acid malabsorption (MESH:C567652), Visceral Hypersensitivity (MESH:D004342), function (MESH:D003291), fullness (MESH:C537270), Gastroduodenal Motility Disorders (MESH:D010437), QT prolongation (MESH:D008133), EPS (MESH:C538101), dyspeptic symptoms (MESH:D012816), loss of appetite (MESH:D001068), Microbial Dysbiosis (MESH:D064806), bloating (MESH:C535647), epigastric pain (MESH:D010146), abnormal gut muscular movements (MESH:C536735), abdominal bloating (MESH:D000007), Bowel Disorders (MESH:D012778), diarrhea (MESH:D003967), Functional Gastrointestinal Disorders (MESH:D005767), disorders of gut-brain interactions (MESH:D001927), nausea (MESH:D009325), barrier dysfunction (MESH:C536830), GERD (MESH:D005764), Gastrointestinal Dysmotility (MESH:D015154), duodenal hypersensitivity (MESH:D004378), acute pain (MESH:D059787), colonic dysmotility (MESH:D003108), FD (MESH:D004415), flatulence (MESH:D005414), chronic pain syndromes (MESH:D059350), abdominal pain (MESH:D015746), colorectal distension (MESH:D015179), colitis (MESH:D003092), ventricular arrhythmia (MESH:D001145), Zollinger-Ellison syndrome (MESH:D015043), inflammatory (MESH:D007249), psychological disorders (MESH:D000067073), Intestinal Barrier Dysfunction (MESH:D007410), defecatory disorders (MESH:D009358), visceral pain (MESH:D059265)
- **Chemicals:** Tradipitant (MESH:C527551), tryptamine (MESH:C030820), prostaglandins (MESH:D011453), 5-HT (MESH:D012701), propionate (MESH:D011422), Elobixibat (MESH:C581303), Oliceridine (MESH:C586842), Pantoprazole (MESH:D000077402), Ebastine (MESH:C058249), Metoclopramide (MESH:D008787), tryptophan (MESH:D014364), Linaclotide (MESH:C523483), morphine (MESH:D009020), Rifaximin (MESH:D000078262), Mirtazapine (MESH:D000078785), water (MESH:D014867), acetylcholine (MESH:D000109), Ramosetron (MESH:C071315), TeCAs (MESH:C005084), neomycin (MESH:D009355), imipramine (MESH:D007099), Histamine (MESH:D006632), NCT01007123 (-), hemin (MESH:D006427), Tandospirone (MESH:C055267), milnacipran (MESH:D000078764), Alosetron (MESH:C090840), CH4 (MESH:D008697), Itopride (MESH:C102254), cGMP (MESH:D006152), SCFAs (MESH:D005232), bicarbonate (MESH:D001639), Ketotifen (MESH:D007665), Chloride (MESH:D002712), capsaicin (MESH:D002211), Prucalopride (MESH:C406662), NA (MESH:D009638), butyrate (MESH:D002087), omeprazole (MESH:D009853), Amitriptyline (MESH:D000639), Buspirone (MESH:D002065), Duloxetine (MESH:D000068736), rabeprazole (MESH:D064750), lansoprazole (MESH:D064747), ondansetron (MESH:D017294), Tegaserod (MESH:C105050), Relamorelin (MESH:C000593860), Acotiamide (MESH:C410959), Tropifexor (MESH:C000630573), BA (MESH:D001647), Lubiprostone (MESH:D000068238), sodium (MESH:D012964), Mesalazine (MESH:D019804), Citalopram (MESH:D015283), Domperidone (MESH:D004294), Obeticholic acid (MESH:C464660)
- **Species:** Helicobacter pylori (species) [taxon 210], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090], Lactobacillus gasseri (species) [taxon 1596], Bifidobacterium animalis subsp. lactis (subspecies) [taxon 302911]
- **Mutations:** C825T

## Full text

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## Figures

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## References

184 references — full list in the complete paper: https://tomesphere.com/paper/PMC8822166/full.md

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Source: https://tomesphere.com/paper/PMC8822166