Ursodeoxycholic acid protects interstitial Cajal-like cells in the gallbladder from undergoing apoptosis by inhibiting TNF-α expression

• Published in: Acta pharmacologica Sinica 2018-09, Vol.39 (9), p.1493-1500
• Main Authors: Wan, Jiang-fan, Chu, Shi-feng, Zhou, Xin, Li, Yue-ting, He, Wen-bin, Tan, Feng, Luo, Piao, Ai, Qi-di, Wang, Qi, Chen, Nai-hong
• Format: Article
• Language: English
• Subjects: Acetylcholine; Anesthesia; Animals; Anti-Inflammatory Agents, Non-Steroidal - therapeutic use; Apoptosis; Apoptosis - drug effects; Biomedical and Life Sciences; Biomedicine; c-Kit protein; Calculi; Cholagogues and Choleretics - therapeutic use; Cholecystectomy; Cholecystokinin; Cholesterol; Gallbladder; Gallbladder Emptying - drug effects; Gallstones; Guinea Pigs; High cholesterol diet; Immunoglobulins; Immunology; Inflammation; Internal Medicine; Localization; Male; Medical Microbiology; Muscle contraction; Muscles; Pharmacology/Toxicology; Protective Agents - therapeutic use; Signal Transduction - drug effects; Telocytes - drug effects; Tumor Necrosis Factor-alpha - antagonists & inhibitors; Tumor necrosis factor-α; Ursodeoxycholic acid; Ursodeoxycholic Acid - therapeutic use; Vaccine; Western blotting
• ISSN: 1671-4083; 1745-7254
• DOI: 10.1038/aps.2017.206

Hypomotility is a common symptom of gallstone disease, which is accompanied by a loss of interstitial Cajal-like cells (ICLCs) in the gallbladder. Ursodeoxycholic acid (UDCA) is widely used in treating gallstone disease, and has shown anti-apoptotic and anti-inflammatory effects apart from its ability to dissolve gallstones. In this study, we investigated the anti-apoptotic and anti-inflammatory effects of UDCA on ICLCs in guinea pigs with gallstones. Guinea pigs were fed a high-cholesterol diet for 8 weeks to induce the formation of gallstones. A group of animals was administered UDCA (50 mg·kg −1 ·d −1 , ig) simultaneously. At the end of 8 weeks, the animals were euthanized with anesthesia, cholecystectomy was performed immediately and gallbladder was collected for further analysis. We showed that in the model group the contractility of gallbladder muscle strips in response to both acetylcholine (ACh) and CCK-8 was severely impaired, which was significantly improved by UDCA administration. Furthermore, UDCA administration significantly reduced the apoptotic ratio of ICLCs, based on the observation of co-localization imaging of apoptotic cells and c-kit-positive cells. Western blotting analysis and real-time PCR results revealed that the TNF-α/Caspase8/Caspase3 pathway was suppressed in the UDCA-treated animals, confirming the anti-apoptotic effect of UDCA in the gallbladder. The H&E staining showed that UDCA administration significantly attenuated inflammatory cell infiltration in the gallbladder wall. In conclusion, UDCA can protect ICLCs in the gallbladder from undergoing apoptosis by inhibiting the TNF-α/Caspase8/caspase3 pathway.