Pasternak Artur, Bugajska Jolanta, Szura Mirosław, Walocha Jerzy A, Matyja Andrzej, Gajda Mariusz, Sztefko Krystyna, Gil Krzysztof
Cell Transplant. 2017 Jan 24;26(1):125-133. doi: 10.3727/096368916X692717. Epub 2016 Aug 5.
It has been reported that intake of ω-3 polyunsaturated fatty acids (PUFAs) reduces the risk of coronary heart disease. It also influences bile composition, decreasing biliary cholesterol saturation in the bile of patients with gallstones. In addition to bile composition disturbances, gallbladder hypomotility must be a cofactor in the pathogenesis of cholelithiasis, as it leads to the prolonged nucleation phase. Our current knowledge about gallbladder motility has been enhanced by the study of a population of newly described interstitial (stromal) cells-telocytes (TCs). The purpose of this study was to determine whether TC loss, reported by our team recently, might be related to bile lithogenicity, expressed as cholesterol saturation index or the difference in biliary PUFA profiles in patients who suffer from cholecystolithiasis and those not affected by this disease. We determined biliary lipid composition including the fatty acid composition of the phospholipid species in bile. Thus, we investigated whether differences in biliary fatty acid profiles (ω-3 PUFA and ω-6 PUFA) in gallbladder bile may influence its lithogenicity and the quantity of TCs within the gallbladder wall. We conclude that the altered PUFA concentrations in the gallbladder bile, with elevation of ω-6 PUFA, constitute important factors influencing TC density in the gallbladder wall, being one of the possible pathophysiological components for the gallstone disease development. This study established that altered bile composition in patients with cholelithiasis may influence TC quantity within the gallbladder muscle, and we concluded that reduction in TC number may be a consequence of the supersaturated bile toxicity, while some other bile components (ω-3 PUFA, glycocholic, and taurocholic acids) may exert protective effects on TC and thus possibly influence the mechanisms regulating gallbladder and extrahepatic bile duct motility. Thus, ω-3 PUFA may represent a possible option to prevent formation of cholesterol gallstones.
据报道,摄入ω-3多不饱和脂肪酸(PUFA)可降低冠心病风险。它还会影响胆汁成分,降低胆结石患者胆汁中的胆汁胆固醇饱和度。除了胆汁成分紊乱外,胆囊运动功能减退必定是胆石症发病机制中的一个辅助因素,因为它会导致成核期延长。对一群新描述的间质(基质)细胞——间充质细胞(TCs)的研究,增强了我们目前对胆囊运动的认识。本研究的目的是确定我们团队最近报道的TCs减少是否可能与胆石生成有关,胆石生成以胆固醇饱和指数或患胆囊结石患者与未受此病影响患者胆汁中PUFA谱的差异来表示。我们测定了胆汁脂质成分,包括胆汁中磷脂种类的脂肪酸组成。因此,我们研究了胆囊胆汁中胆汁脂肪酸谱(ω-3 PUFA和ω-6 PUFA)的差异是否会影响其成石性以及胆囊壁内TCs的数量。我们得出结论,胆囊胆汁中PUFA浓度的改变,伴随着ω-6 PUFA的升高,是影响胆囊壁TC密度的重要因素,是胆结石疾病发展的可能病理生理成分之一。本研究证实,胆石症患者胆汁成分的改变可能会影响胆囊肌层内的TC数量,我们得出结论,TC数量的减少可能是过饱和胆汁毒性的结果,而其他一些胆汁成分(ω-3 PUFA、甘氨胆酸和牛磺胆酸)可能对TC发挥保护作用,从而可能影响调节胆囊和肝外胆管运动的机制。因此,ω-3 PUFA可能是预防胆固醇胆结石形成的一种可能选择。