Jeong Byeongseok, Lee Jun Hyung, Lee Jin-A, Kim Seong Jung, Lee Junhyung, So Insuk, Jun Jae Yeoul, Hong Chansik
Department of Physiology, Chosun University College of Medicine, Gwangju 61452, Republic of Korea.
Department of Physiology, Seoul National University College of Medicine, Seoul 03080, Republic of Korea.
Pharmaceuticals (Basel). 2024 Oct 4;17(10):1327. doi: 10.3390/ph17101327.
Prokinetic agents are effective in increasing gastrointestinal (GI) contractility and alleviating constipation, often caused by slow intestinal motility. Lubiprostone (LUB), known for activating CLC-2 chloride channels, increases the chloride ion concentration in the GI tract, supporting water retention and stool movement. Despite its therapeutic efficacy, the exact mechanisms underlying its pharmacological action are poorly understood. Here, we investigated whether LUB activates the canonical transient receptor potential cation channel type 4 (TRPC4) through stimulation with E-type prostaglandin receptor (EP) type 3.
Using isotonic tension recordings on mouse colon strips, we examined LUB-induced contractility in both proximal and distal colon segments. Quantitative real-time polymerase chain reaction (qRT-PCR) was conducted to determine mRNA levels of EP1-4 receptor subtypes in distal colonic muscular strips and isolated myocytes. The effects of a TRPC4 blocker and EP3 antagonist on LUB-stimulated contractions were also evaluated.
LUB showed significant contraction in the distal segment compared to the proximal segment. EP3 receptor mRNA levels were highly expressed in the distal colon tissue, which correlated with the observed enhanced contraction. Furthermore, LUB-induced spontaneous contractions in distal colon muscles were reduced by a TRPC4 blocker or EP3 antagonist, indicating that LUB-stimulated EP3 receptor activation may lead to TRPC4 activation and increased intracellular calcium in colonic smooth muscle.
These findings suggest that LUB improves mass movement through indirect activation of the TRPC4 channel in the distal colon. The segment-specific action of prokinetic agents like LUB provides compelling evidence for a personalized approach to symptom management, supporting the defecation reflex.
促动力药物在增强胃肠道(GI)收缩力和缓解通常由肠道蠕动缓慢引起的便秘方面有效。鲁比前列酮(LUB)以激活CLC-2氯离子通道而闻名,它可增加胃肠道中的氯离子浓度,促进水分潴留和粪便移动。尽管其具有治疗效果,但其药理作用的具体机制仍知之甚少。在此,我们研究了LUB是否通过E型前列腺素受体(EP)3型刺激激活典型瞬时受体电位阳离子通道4型(TRPC4)。
我们使用小鼠结肠条的等张张力记录,检查了LUB在近端和远端结肠段诱导的收缩力。进行定量实时聚合酶链反应(qRT-PCR)以确定远端结肠肌条和分离的心肌细胞中EP1-4受体亚型的mRNA水平。还评估了TRPC4阻滞剂和EP3拮抗剂对LUB刺激的收缩的影响。
与近端段相比,LUB在远端段显示出明显的收缩。EP3受体mRNA水平在远端结肠组织中高度表达,这与观察到的增强收缩相关。此外,TRPC4阻滞剂或EP3拮抗剂可减少LUB诱导的远端结肠肌肉自发性收缩,表明LUB刺激的EP3受体激活可能导致TRPC4激活并增加结肠平滑肌中的细胞内钙。
这些发现表明,LUB通过间接激活远端结肠中的TRPC4通道来改善集团蠕动。像LUB这样的促动力药物的节段特异性作用为个性化症状管理方法提供了有力证据,支持排便反射。