Society: AGA

Background
Electrogastrography (EGG) non-invasively evaluates gastric motility but is widely viewed as lacking clinical utility. Gastric Alimetry® is a new diagnostic test that combines high-resolution body surface gastric mapping (BSGM) with validated symptom profiling, with the goal of overcoming numerous technical limitations of the EGG. This study directly compared EGG and BSGM to define performance differences in spectral analysis.

Methods
Comparisons between Gastric Alimetry BSGM and EGG were conducted by protocolized evaluation of 178 subjects (110 controls; 68 nausea and vomiting (NVS) and/or type 1 diabetes (T1D)). Data collection was identical. Comparisons followed standard methodologies for each test, with statistical evaluations for group-level differences, symptom correlations, and patient-level classifications. Four spectral metrics were computed for BSGM tests (Gastric Alimetry Rhythm IndexTM (GA-RI), Principal Gastric Frequency (PGF), BMI-Adjusted Amplitude, and Fed:Fasted Amplitude Ratio)¹ and EGG tests (% time normal frequency, dominant frequency, amplitude, and amplitude ratio)². Patient-level classifications were determined by a blinded consensus panel reference standard³ and automatedly, using published reference values as cutoffs for EGG and BSGM metrics^2,4.

Results
Group-level: BSGM showed tighter frequency ranges vs EGG in controls (median 3.04 cpm (IQR 2.90-3.18) vs 2.88 (1.50-3.12); p<0.0001). Both tests detected rhythm instability in NVS (p<0.001) and T1D (p<0.05), but EGG showed opposite frequency effects in T1D (2.50 vs controls 2.88; p=0.28) to BSGM (3.15 vs 3.04; p=0.0004). Symptom correlations: GA-RI correlated with nausea, pain, bloating, and total symptom burden; PGF deviation with excessive fullness, pain, bloating; % time in normal frequency correlated with bloating (p<0.05). Patient-level: EGG sensitivity was 1.0, specificity 0.38; BSGM sensitivity 1.0, specificity 0.96 (Figure 1).

Conclusions and Inferences
EGG detected group-level differences in patients, but lacked symptom correlations and showed poor accuracy at patient-level classification, explaining EGG’s weak clinical utility. BSGM demonstrated substantial performance improvements over EGG across all domains.

References
1. Schamberg G et al.. Neurogastroenterol Motil. Published online November 21, 2022:e14491.
2. Yin J, Chen JDZ. Journal of Neurogastroenterology and Motility. 2013;19(1):5-17.
3. Gharibans AA et al. Sci Transl Med. 2022;14(663):eabq3544.
4. Varghese C et al. Am J Gastroenterol; In Press [doi:10.1101/2022.07.25.22278036]

Figure 1: Individual classifications using rhythmic stability metrics and reference labels. (A) Confusion matrix for GA-RI ≥ 0.25. (B) Confusion matrix for % time normal frequency ≥ 70%. (C) ROC curves with the location on the curve associated (published thresholds indicated by a dot). (D) Quantitative evaluation.

<b>Individual classifications using rhythmic stability metrics and reference labels. (A) Confusion matrix for GA-RI ≥ 0.25. (B) Confusion matrix for % time normal frequency ≥ 70%. (C) ROC curves with the location on the curve associated (published thresholds indicated by a dot). (D) Quantitative evaluation.</b>

Individual classifications using rhythmic stability metrics and reference labels. (A) Confusion matrix for GA-RI ≥ 0.25. (B) Confusion matrix for % time normal frequency ≥ 70%. (C) ROC curves with the location on the curve associated (published thresholds indicated by a dot). (D) Quantitative evaluation.

Purpose: Enteric neuropathies result from abnormalities of the enteric nervous system (ENS). The goal of this study was to determine the feasibility of isolating, expanding, and transplanting autologous enteric neural stem cells (ENSCs) to improve colonic function in a non-lethal mouse model of colonic aganglionosis.
Methods: Wnt1::Cre;R26iDTR (Wnt1-iDTR) mice at 2-3 months of age were used. ENSCs were isolated from a short segment of small intestine resected from Wnt1-iDTR mice in which focal colonic aganglionosis was created by injection of diphtheria toxin (DT) into the wall of the mid-colon. Autologous ENSCs were expanded in culture to form neurospheres, transduced with lentiviral GFP or channelrhodopsin-2 (ChR2) vector, and transplanted into the aganglionic segment 2 weeks following the first surgery (n=12). Immunohistochemistry, organ bath studies, and optogenetics were used to determine outcomes 1 to 8 weeks following cell transplantation. Results were compared to two groups: R26iDTR mice with DT injection (Control, n=8) and DT-induced aganglionosis (DT-AG, n=8) without cell transplantation using multiple t-test analysis.
Results: ENSCs, as neurospheres, were successfully obtained from mouse small intestine (mean 477 ± 123 neurospheres per cm of small intestine, n=12). Transplanted ENSCs were identified within the aganglionic colon based on GFP fluorescence. Immunohistochemical evaluation demonstrated extensive cell migration, nerve fiber projections, and differentiation into neurons and glial cells. Organ bath studies demonstrated that the lack of contraction of DT-induced aganglionic smooth muscle was rescued by ENSC transplantation (0.10 ± 0.09 gm in DT-AG vs 1.45 ± 0.23 gm in DT-AG + Cells, n = 4, p<0.001) 3 weeks following cell transplant. Interestingly, restoration of muscle contractility progressed over time. Contractile activity of colonic smooth muscle in mice with DT-induced aganglionosis was normalized by ENSC transplantation 8 weeks after surgery (3.11 ± 0.13 gm in Control vs 2.95 ± 0.39 gm in DT-AG + Cells, n = 4, p>0.05). Optogenetic analysis in mice receiving ENSCs expressing ChR2 confirmed functional neuromuscular signalling between transplanted autologous ENSC-derived neurons and the colonic smooth muscle.
Conclusions: Autologously derived ENSCs successfully engrafted within aganglionic gut in vivo, where neuroglial differentiation and functional integration with colonic smooth muscle occurred. By 8 weeks after cell transplant, normalization of colonic smooth muscle contractility was observed. This study, using a novel and non-lethal mouse model of colonic aganglionosis, demonstrates the potential of autologous ENSCs to improve functional outcomes in neurointestinal disease and lays the groundwork for clinical application of this regenerative cell-based strategy.

[Background] Several studies have assessed the effect of cool temperature on gastrointestinal peristalsis. Transient receptor potential melastatin 8 (TRPM8) is a temperature-sensitive ion channel activated by mild cooling expressed in the gastrointestinal tract. We examined the antispasmodic effect of cool temperature on gastrointestinal peristalsis in a prospective, randomized, single-blind trial and based on the video imaging and intraluminal pressure of the proximal colon in TRPM8-deficient mice.
[Method] In the clinical trial, we randomly assigned a total of 86 patients scheduled to undergo esophagogastoroduodenoscopy to 2 groups (the mildly cool water [n=43] and room temperature (RT) [n=43] groups) and a total of 94 patients scheduled to undergo colonoscopy to 2 groups (the mildly cool water [n=47] and RT [n=47] groups). We used 20 mL of 15 °C water as mildly cool water. Both treatments were sprayed locally onto the gastric mucosa or colonic mucosa via an endoscope. The primary outcome was the proportion of subjects with improved peristalsis after treatment (Clinical trial registry website: Trial No. UMIN-CTR UMIN000030725). In the rodent colon model, we placed a 2- to 3-cm segment of the proximal colon in an organ bath (100 mL volume) and perfused the bath with Krebs solution (34-35 °C, 3.5 mL/min). We securely attached the oral and aboral ends of the proximal colon segment with string to the saline input and output ports, respectively. In the colon, we used a Mikro-Tip catheter pressure transducer (SPR-524; Millar Instruments, Houston, TX, USA) to monitor the intraluminal pressure (cmH₂O). With a data acquisition and analysis system (MP100; BIOPAC Systems, Goleta, CA, USA), we evaluated the intraluminal pressure waves. We macroscopically observed motility through video (HDC-HS 100-K; Panasonic, Osaka, Japan). In the proximal colon of TRPM8-deficient mice and wild mice, we evaluated the intraluminal pressure and performed video imaging of the TRPM8-deficient mouse colon by administering cool water into the colonic lumen.
[Results] In the randomized controlled trial, after treatment, the proportion of subjects with no colonic peristalsis was significantly higher in the cool water group than in the RT group (44.7% vs. 23.4%; P < 0.05). Regarding gastric peristalsis, there were no significant differences between the cool water group and the RT group. In the rodent colon model, cool water was associated with a significant decrease in colonic peristalsis through its suppression of the peak frequency ratio (P < 0.05). Cool water-treated TRPM8-deficient mice did not show a reduction in colonic peristalsis compared with wild-type mice.
[Conclusion] We showed for the first time that cool temperature-dependent suppression of colonic peristalsis may be associated with TRPM8 activation.

Irritable bowel syndrome (IBS) affects roughly 12% of humans and is more common in women than men. Peripheral and central neuroplasticity produce abdominal pain and altered intestinal function in IBS but the exact cause of neuroplasticity is not understood. Experiencing early life adversity increases susceptibility to developing IBS through an interplay between genes and the environment, yet how early life stress affects specific cell types and mechanisms in the enteric nervous system function remains unknown. Here, we tested the hypothesis that early life stress disrupts enteric nervous system function through genomic changes induced in enteric glia.
We used the neonatal-maternal separation (NMS) model as a psychological stressor, and studied glial-specific transcriptional signatures using Sox10^CreERT2;RiboTag mice. Distal colons were collected at 16-20 weeks of age and RNA-seq of myenteric glial mRNA was performed using STAR and DESeq2. Specific transcripts of interest were localized in situ by RNAscope with co-immunolabeling to quantify cellular expression. Integrative physiological consequences were assessed by measuring visceral hypersensitivity and in vivo motility, and cellular physiological responses were studied using calcium imaging in Wnt1^{Cre;GCaMP5g-tdT}/Gfap^hM3Dq mice, which express chemogenetic hM3Dq receptors in GFAP⁺ cells and GCaMP5g in neurons and glia.
In normal animals, more than 600 genes are differentially expressed between male and female enteric glia. Males that underwent NMS exhibited large shifts in glial genomic profiles with 469 genes upregulated, while subtler effects were observed in females with 124 genes downregulated. Interestingly, the gene expression patterns of male glia become more like those from females following NMS. In addition to the change in expression level, spatial distribution of target RNA, such as immune-related signaling gene Oasl2 (p<0.01) or Ifit1 (p<0.05), is affected by NMS. This remodeling of molecular architecture is associated with a higher excitability of enteric glia, demonstrated by an increased frequency of calcium responses after specific glial stimulation. Finally, we observed an increased visceral sensitivity in males after NMS (p<0.01), and a slower intestinal transit after glial specific activation in both sexes (p<0.05), which may be linked to the hyperexcitability of glia.
Together, these data show that early life adversity shifts the molecular architecture of enteric glia in a sex-specific manner, with a prominent effect in males where NMS promotes a ‘feminization’ of genomic signatures. This remodeling is associated with physiological consequences on intestinal motility and visceral hypersensitivity, however the mechanisms involved in these changes remain to be identified.

BACKGROUND Enteroendocrine cells (EECs) are specialized mechanoreceptors in the gastrointestinal (GI) epithelium. The mechanosensitive EEC population is characterized by expression of mechanogated ion channel Piezo2, which is required for a mechanosensitive milliseconds-long receptor current that initiates a seconds-long intracellular calcium cascade and results in neurotransmitter release. The mechanisms that amplify the initial receptor current into a coordinated calcium cascade are largely undefined. The T-type voltage gated ion channel Ca_V3.2 is expressed by skin neuronal mechanoreceptors, where, together with Piezo2 channels, it participates in mechanotransduction. We and others have found abundant Cacna1h (Ca_V3.2) expression in EECs from mouse small and large bowel.
AIM To determine the role of Ca_V3.2 in EEC mechanotransduction and GI physiology.
METHODS Ca_V3.2 expression in the epithelium was assessed via immunofluorescence in NeuroD1-Cre::GCaMP5/tdTomato tissue. Primary EECs were dissociated, mechanically stimulated and calcium dynamics measured in the context of Ca_V3.2 knockdown (KD) via GCaMP fluorescence. A pan-epithelial Ca_V3.2 conditional knockout (Ca_V-CKO) model (Vil-Cre::Ca_V3.2-flox) was used for Ussing chamber assay as well as the following in vivo assays: whole gut transit, colonic bead expulsion, and colonic sensitivity (quantified as the visceral motor response (VMR) to distension pressures of 15-60 mmHg).
RESULTS In the small bowel epithelium, Ca_V3.2 could only be detected in Neurod1+ cells (EECs), with no labeling detected in tdTomato- cells. Compared to non-target siRNA controls, Ca_V3.2 KD decreased peak calcium responses to mechanical stimulation by 69±30% (NT siRNA: peak = 3.6±0.9, n = 7; Ca_V3.2 siRNA: peak = 1.1±0.7, n = 8; p = 0.04). Compared to control mice, Ca_V3.2 KO decreased short circuit currents to mechanical stimulation by 51±12% (control: current = 26.3±1.4 µA, n = 10; Ca_V-CKO: current = 13.0±2.9 µA, n = 6; p = 0.004). Ca_V-CKO did not affect whole gut transit times in male mice (control: time = 211±40 s, n = 7; Ca_V3.2 KO: time = 231±41 s, n = 5; p = 0.74) but delayed bead expulsion times by 39±17% (control: time = 47±3 s, n = 10; Ca_V-CKO: time = 66±8 s, n = 9; p = 0.035). Male Ca_V3.2 KO mice showed increased VMR to 15 mmHg distension only (control: VMR AUC =10.7±2.1, n = 9; Ca_V3.2 KO: VMR AUC = 16.2±2.7, n = 11; p = 0.013).
CONCLUSIONS Ca_V3.2 is a necessary mechanotransducer in the mechanosensitive EEC response and impacts GI physiology. Pressure-induced secretion and colonic expulsion decreased in Ca_V3.2 KO, while mechanosensitive VMR responses increased at low pressures. These data demonstrate the important roles of T-type calcium channels in EECs. Future studies will explore the role of the epithelial T-type calcium channel in potentiating motor responses to low-threshold stimuli.

Purna Kashyap

Mayo Clinic

Appearances