Yoon Young Chul, Lee Dosang, Park Jung Hyun, Choi Ho Joong, Jeon Sang-Jin, Kim Ok-Hee, Kim Say-June
Department of Surgery, Incheon St. Mary's Hospital, College of Medicine, The Catholic University of Korea Seoul 06591, Republic of Korea.
Catholic Central Laboratory of Surgery, College of Medicine, The Catholic University of Korea Seoul 06591, Republic of Korea.
Am J Transl Res. 2024 Nov 15;16(11):7054-7070. doi: 10.62347/BAMT2384. eCollection 2024.
While methyl-tertiary butyl ether (MTBE) remains the sole clinical topical agent for gallstone dissolution, its utility is limited due to side effects, largely stemming from its relatively low boiling point (55°C). In this study, we introduced 2-methoxy-6-methylpyridine (MMP), a novel gallstone-dissolving compound featuring an aromatic moiety and a substantially higher boiling point (156°C), designed to mitigate these side effects. We conducted a comprehensive evaluation of the efficacy and potential toxicities of MMP compared to MTBE using both in vitro and in vivo models. In the in vitro setting, MMP demonstrated significantly higher solubility than MTBE, achieving dissolution rates of 75% vs. 56%, 95% vs. 69%, and 100% vs. 82% at 60, 120, and 240 minutes, respectively (P < 0.05). In a porcine model with cholesterol gallstones, solubility assessments via direct injection of each solvent into the gallbladder showed that MMP exhibited approximately 1.8 times higher solubility compared to MTBE (P < 0.05). Further pharmacokinetic analysis in SD rats revealed that MMP is rapidly absorbed and efficiently cleared from the bloodstream, with dose-dependent variations in half-life, indicating favorable excretion profiles. Toxicological assessments in both rodents and pigs showed that MMP induces significantly less tissue damage than MTBE, with lower levels of apoptosis and inflammation in vital organs, as confirmed by molecular analyses including real-time PCR, Western blotting, and immunohistochemistry. Our findings indicate that MMP offers superior efficacy in cholesterol gallstone dissolution and presents a significantly lower toxicological profile, suggesting its potential as a safer and more effective alternative to MTBE.
虽然甲基叔丁基醚(MTBE)仍然是唯一用于胆结石溶解的临床外用药物,但其效用因副作用而受到限制,这些副作用主要源于其相对较低的沸点(55°C)。在本研究中,我们引入了2-甲氧基-6-甲基吡啶(MMP),这是一种新型的胆结石溶解化合物,具有芳香部分和显著更高的沸点(156°C),旨在减轻这些副作用。我们使用体外和体内模型对MMP与MTBE的疗效和潜在毒性进行了全面评估。在体外环境中,MMP表现出比MTBE显著更高的溶解度,在60、120和240分钟时的溶解率分别为75%对56%、95%对69%和100%对82%(P<0.05)。在患有胆固醇胆结石的猪模型中,通过将每种溶剂直接注入胆囊进行的溶解度评估表明,MMP的溶解度比MTBE高约1.8倍(P<0.05)。在SD大鼠中进行的进一步药代动力学分析表明,MMP能迅速被吸收并从血液中有效清除,半衰期存在剂量依赖性变化,表明其排泄情况良好。在啮齿动物和猪身上进行的毒理学评估表明,MMP诱导的组织损伤明显少于MTBE,重要器官中的凋亡和炎症水平较低,这通过实时PCR、蛋白质印迹和免疫组织化学等分子分析得到证实。我们的研究结果表明,MMP在胆固醇胆结石溶解方面具有卓越的疗效,并且呈现出显著更低的毒理学特征,表明它有潜力成为MTBE的一种更安全、更有效的替代品。