Lubiprostone Improves Distal Segment-Specific Colonic Contractions through TRPC4 Activation Stimulated by EP3 Prostanoid Receptor.

IF 4.3 3区 医学 Q2 CHEMISTRY, MEDICINAL
Pharmaceuticals Pub Date : 2024-10-04 DOI:10.3390/ph17101327
Byeongseok Jeong, Jun Hyung Lee, Jin-A Lee, Seong Jung Kim, Junhyung Lee, Insuk So, Jae Yeoul Jun, Chansik Hong
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引用次数: 0

Abstract

Background: 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.

Methods: 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.

Results: 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.

Conclusions: 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.

通过 EP3 类前列腺素受体刺激 TRPC4 激活,路比前列酮可改善结肠远段特异性收缩。
背景:促动力药能有效增加胃肠道(GI)收缩力,缓解通常由肠道蠕动缓慢引起的便秘。鲁比前列酮(LUB)以激活 CLC-2 氯离子通道而闻名,它能增加胃肠道中的氯离子浓度,支持水分潴留和粪便移动。尽管它具有治疗功效,但人们对其药理作用的确切机制却知之甚少。在此,我们研究了 LUB 是否会通过 E 型前列腺素受体(EP)3 型的刺激激活典型瞬时受体电位阳离子通道 4 型(TRPC4):方法:通过对小鼠结肠条带进行等张力记录,我们检测了 LUB 诱导的近端和远端结肠节段的收缩力。我们进行了定量实时聚合酶链反应(qRT-PCR),以确定远端结肠肌条和离体肌细胞中 EP1-4 受体亚型的 mRNA 水平。还评估了 TRPC4 阻断剂和 EP3 拮抗剂对 LUB 刺激收缩的影响:结果:与近端相比,LUB 在远端表现出明显的收缩。远端结肠组织中 EP3 受体 mRNA 水平表达较高,这与观察到的收缩增强相关。此外,TRPC4阻断剂或EP3拮抗剂可减少LUB诱导的结肠远端肌肉自发收缩,这表明LUB刺激的EP3受体活化可能导致TRPC4活化和结肠平滑肌细胞内钙增加:这些研究结果表明,LUB 可通过间接激活远端结肠的 TRPC4 通道来改善大便质量。LUB 等促动力药剂的分段特异性作用为个性化症状管理方法提供了有力的证据,支持排便反射。
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来源期刊
Pharmaceuticals
Pharmaceuticals Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
6.10
自引率
4.30%
发文量
1332
审稿时长
6 weeks
期刊介绍: Pharmaceuticals (ISSN 1424-8247) is an international scientific journal of medicinal chemistry and related drug sciences.Our aim is to publish updated reviews as well as research articles with comprehensive theoretical and experimental details. Short communications are also accepted; therefore, there is no restriction on the maximum length of the papers.
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