# Changrun Formula Relieves Functional Constipation by Improving Intestinal Motility in Rats

**Authors:** Qiuping Xiao, Yanqiu Hong, Xuesi Geng

PMC · DOI: 10.1155/grp/5790162 · Gastroenterology Research and Practice · 2025-05-27

## TL;DR

This study shows that Changrun Formula improves intestinal motility in rats with functional constipation by targeting specific ion channels and signaling pathways.

## Contribution

The study identifies HCN1/HCN2 and SCF/c-kit as novel targets for CRF's therapeutic effects on functional constipation.

## Key findings

- CRF increased expressions of c-kit, SCF, HCN1, and HCN2 in rat colon tissue.
- CRF enhanced colonic smooth muscle contractility and improved muscle tension.
- HCN1 colocalized with c-kit, SP, and VIP in the model group.

## Abstract

Background and Study Aim: Changrun Formula (CRF) is a representative traditional Chinese medicine prescription for functional constipation (FC). However, the mechanism by which CRF alleviates FC remains unclear. Therefore, this study aimed to investigate the therapeutic mechanism of CRF in an FC rat model.

Material and Methods: A total of 72 healthy SD rats were selected and randomly divided into six groups: the blank group, model group, hemp seed pill (HSP) group, high-dose CRF group, medium-dose CRF group, and low-dose CRF group. Except for the blank group, all the other groups were administered compound diphenoxylate via oral gavage to establish the FC rat model with impaired intestinal motility. The expression of genes related to intestinal motility in the colon tissues of rats was analyzed using Western blotting and real-time PCR. The effect of CRF on isolated colonic smooth muscle was assessed through electrophysiological analysis.

Results: Compared with the blank group, the other groups exhibited a longer time to expel the first black stool and a reduced number of fecal particles within 6 h, confirming the successful establishment of the FC rat model. Furthermore, the expressions of HCN1, c-kit, and SP in the colon tissue of the model group were significantly decreased, while the expression level of VIP was significantly increased. HCN1 was found to colocalize with c-kit, SP, and VIP. Treatment of CRF (high and medium doses) significantly increased the expressions of c-kit, SCF, HCN1, and HCN2, enhanced the contractile movement of colonic smooth muscle, and improved muscle tension.

Conclusions: CRF likely improves intestinal motility by targeting HCN1 and HCN2 ion channels and the SCF/c-kit signaling pathway, thereby alleviating FC symptoms in rats.

## Linked entities

- **Genes:** HCN1 (hyperpolarization activated cyclic nucleotide gated potassium channel 1) [NCBI Gene 348980], KIT (KIT proto-oncogene, receptor tyrosine kinase) [NCBI Gene 3815], TFF2 (trefoil factor 2) [NCBI Gene 7032], VIP (vasoactive intestinal peptide) [NCBI Gene 7432], HCN2 (hyperpolarization activated cyclic nucleotide gated potassium and sodium channel 2) [NCBI Gene 610], KITLG (KIT ligand) [NCBI Gene 4254]
- **Species:** Rattus norvegicus (taxon 10116)

## Full-text entities

- **Genes:** Hcn2 (hyperpolarization activated cyclic nucleotide gated potassium and sodium channel 2) [NCBI Gene 114244], Tff2 (trefoil factor 2) [NCBI Gene 116592], Kitlg (KIT ligand) [NCBI Gene 60427] {aka Kitl, Mgf, SCF}, Vip (vasoactive intestinal peptide) [NCBI Gene 117064] {aka vip/phi27}, Hcn1 (hyperpolarization-activated cyclic nucleotide-gated potassium channel 1) [NCBI Gene 84390]
- **Diseases:** Constipation (MESH:D003248), impaired intestinal motility (MESH:D007410)
- **Chemicals:** diphenoxylate (MESH:D004157), HSP (-)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12133367/full.md

## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12133367/full.md

## References

27 references — full list in the complete paper: https://tomesphere.com/paper/PMC12133367/full.md

---
Source: https://tomesphere.com/paper/PMC12133367