Clinical Enteric Neuroscience Translational and Epidemiological Research (C.E.N.T.E.R.), Mayo Clinic, Minnesota, USA.
Clin Transl Gastroenterol. 2019 Apr;10(4):e00019. doi: 10.14309/ctg.0000000000000019.
Aquaporin (AQP) channels are involved in regulating fluid homeostasis in the colon. Several AQP channels were detected in human colon epithelial cells. In a previous study, rats fed 1% (wt/wt) sodium cholate had increased AQP3, 7, and 8 levels, suggesting AQP involvement in bile acid diarrhea (BAD). Our aim was to compare AQP expressions in rectosigmoid mucosal (RSM) biopsies from patients with irritable bowel syndrome-diarrhea (IBS-D) (divided into those with normal or high fecal BA excretion) and in patients with IBS-constipation (IBS-C) compared with healthy controls.
In RSM biopsies from 44 patients with IBS-D (with normal (<) or high (>2,337 μmol/48 hours (BAD)) fecal BA excretion), 10 patients with IBS-C, and 17 healthy controls, we measured expressions of AQP1, 3, 7, and 8, with RT-PCR (housekeeper gene GAPDH). We analyzed RNA for expression by RT-PCR assays, with expression calculated using 2-based fold-change. Comparisons of IBS groups were corrected for false detection rate (Bonferroni correction for 12 comparisons; P < 0.0042). AQP protein measurements on biopsies from 3 healthy controls, 3 patients with IBS-D, and 3 patients with BAD were performed by western blots (GAPDH housekeeping protein).
In RSM from patients with IBS-D (but not IBS-C), mRNA expression of AQP3 was decreased, and AQP7 and 8 were increased relative to controls. Fold differences were not different in IBS-D with or without BAD. Western blots confirmed increased expression of AQP7 and 8 and decreased AQP3 proteins in biopsies from patients with IBS-D compared with controls.
Increased AQP7 and 8 and decreased AQP3 expressions in RSM suggest that further studies on AQPs' potential role in the pathophysiology of diarrhea in IBS-D are warranted.
水通道蛋白(AQP)通道参与调节结肠中的液体稳态。在人结肠上皮细胞中检测到几种 AQP 通道。在之前的一项研究中,给予 1%(wt/wt)胆酸钠的大鼠增加了 AQP3、7 和 8 水平,提示 AQP 参与胆酸腹泻(BAD)。我们的目的是比较直肠乙状结肠黏膜(RSM)活检中肠易激综合征腹泻(IBS-D)患者(分为粪便胆汁酸排泄正常或高的患者)与 IBS-便秘(IBS-C)患者和健康对照者的 AQP 表达。
在 44 例 IBS-D(粪便胆汁酸排泄正常(<)或高(>2,337 μmol/48 小时(BAD))患者、10 例 IBS-C 患者和 17 例健康对照者的 RSM 活检中,我们用 RT-PCR(管家基因 GAPDH)测量了 AQP1、3、7 和 8 的表达。我们通过 RT-PCR 检测分析了 RNA 的表达,并用 2 进制倍数变化计算表达。对 IBS 组的比较进行了假阳性检测率校正(12 次比较的 Bonferroni 校正;P < 0.0042)。通过 Western 印迹(管家蛋白 GAPDH)对 3 例健康对照者、3 例 IBS-D 患者和 3 例 BAD 患者的 RSM 活检进行了 AQP 蛋白测量。
在 IBS-D 患者(而非 IBS-C 患者)的 RSM 中,与对照组相比,AQP3 的 mRNA 表达减少,AQP7 和 8 增加。在 IBS-D 有或无 BAD 的患者中,倍数差异无差异。Western 印迹证实,与对照组相比,IBS-D 患者的 RSM 中 AQP7 和 8 的表达增加,AQP3 蛋白减少。
RSM 中 AQP7 和 8 的表达增加和 AQP3 的表达减少表明,需要进一步研究 AQP 在 IBS-D 腹泻发病机制中的潜在作用。