Tang Lieqi, Peng Minzhi, Liu Li, Chang Wenhan, Binder Henry J, Cheng Sam X
Division of Gastroenterology, Nutrition and Hepatology, Department of Pediatrics, University of Florida, Gainesville, Florida;
Department of Pediatrics, Guangzhou Women and Children's Medical Center, Guangzhou, Guangdong, People's Republic of China;
Am J Physiol Gastrointest Liver Physiol. 2015 May 15;308(10):G874-83. doi: 10.1152/ajpgi.00341.2014. Epub 2015 Mar 19.
Colonic bicarbonate (HCO3(-)) secretion is a well-established physiological process that is closely linked to overall fluid and electrolyte movement in the mammalian colon. These present studies show that extracellular calcium-sensing receptor (CaSR), a fundamental mechanism for sensing and regulating ionic and nutrient compositions of extracellular milieu in the small and large intestine, regulates HCO3(-) secretion. Basal and induced HCO3(-) secretory responses to CaSR agonists were determined by pH stat techniques used in conjunction with short-circuit current measurements in mucosa from rat distal colon mounted in Ussing chambers. R568, a specific CaSR activator, stimulated lumen Cl(-)- and short-chain fatty acid (SCFA)-dependent HCO3(-) secretion but inhibited cyclic nucleotide-activated HCO3(-) secretion. Consequently, at physiological conditions (either at basal or during lumen acid challenge) when electroneutral Cl(-)/HCO3(-) and SCFA/HCO3(-) exchangers dominate, CaSR stimulates HCO3(-) secretion; in contrast, in experimental conditions that stimulate fluid and HCO3(-) secretion, e.g., when forskolin activates electrogenic cystic fibrosis transmembrane conductance regulator-mediated HCO3(-) conductance, CaSR activation inhibits HCO3(-) secretion. Corresponding changes in JHCO3 (μeq·h(-1)·cm(-2), absence vs. presence of R568) were 0.18 ± 0.03 vs. 0.31 ± 0.08 under basal nonstimulated conditions and 1.85 ± 0.23 vs. 0.45 ± 0.06 under forskolin-stimulated conditions. Similarly, activation of CaSR by R568 stimulated Cl(-)- and SCFA-dependent HCO3(-) secretion and inhibited cAMP-dependent HCO3(-) secretion in colon mucosa of wild-type mice; such effects were abolished in CaSR-null mice. These results suggest a new paradigm for regulation of intestinal ion transport in which HCO3(-) secretion may be fine-tuned by CaSR in accordance with nutrient availability and state of digestion and absorption. The ability of CaSR agonists to inhibit secretagogue-induced intestinal HCO3(-) secretion suggests that modulation of CaSR activity may provide a new therapeutic approach to correct HCO3(-) deficit and metabolic acidosis, a primary cause of morbidity and mortality in acute infectious diarrheal illnesses.
结肠碳酸氢盐(HCO3(-))分泌是一个已被充分证实的生理过程,与哺乳动物结肠中的整体液体和电解质运动密切相关。目前的这些研究表明,细胞外钙敏感受体(CaSR)作为小肠和大肠中感知和调节细胞外环境离子及营养成分的基本机制,可调节HCO3(-)分泌。通过pH计技术结合安装在尤斯灌流小室中的大鼠远端结肠黏膜短路电流测量,来测定对CaSR激动剂的基础和诱导性HCO3(-)分泌反应。R568是一种特异性CaSR激活剂,可刺激管腔Cl(-)和短链脂肪酸(SCFA)依赖性HCO3(-)分泌,但抑制环核苷酸激活的HCO3(-)分泌。因此,在生理条件下(无论是基础状态还是管腔酸刺激期间),当电中性Cl(-)/HCO3(-)和SCFA/HCO3(-)交换体起主导作用时,CaSR会刺激HCO3(-)分泌;相反,在刺激液体和HCO3(-)分泌的实验条件下,例如当福斯可林激活电生性囊性纤维化跨膜电导调节因子介导的HCO3(-)电导时,CaSR激活会抑制HCO3(-)分泌。在基础非刺激条件下,JHCO3(μeq·h(-1)·cm(-2),无R568与有R568相比)的相应变化为0.18±0.03对0.31±0.08,在福斯可林刺激条件下为1.85±0.23对0.45±0.06。同样,R568激活CaSR可刺激野生型小鼠结肠黏膜中Cl(-)和SCFA依赖性HCO3(-)分泌,并抑制cAMP依赖性HCO3(-)分泌;在CaSR基因敲除小鼠中这种作用消失。这些结果提示了一种肠道离子转运调节的新范式,即HCO3(-)分泌可能根据营养物质可用性以及消化吸收状态由CaSR进行微调。CaSR激动剂抑制促分泌剂诱导的肠道HCO3(-)分泌的能力表明,调节CaSR活性可能为纠正HCO3(-)缺乏和代谢性酸中毒提供一种新的治疗方法,而代谢性酸中毒是急性感染性腹泻疾病发病和死亡的主要原因。