4.7 Article

Inhibition of Na+/H+ exchanger isoform 3 improves gut fluidity and alkalinity in cystic fibrosis transmembrane conductance regulator-deficient and F508del mutant mice

期刊

BRITISH JOURNAL OF PHARMACOLOGY
卷 178, 期 5, 页码 1018-1036

出版社

WILEY
DOI: 10.1111/bph.15323

关键词

anion secretion; DIOS; fluid secretion; intestinal fluid absorption; mucoviscidosis; sodium hydrogen exchange

资金

  1. Cystic Fibrosis Trust [SRC011]
  2. Deutsche Forschungsgemeinschaft [SE460/19-1, SE460/21-1]
  3. Volkswagen Foundation [ZN1953]

向作者/读者索取更多资源

Linaclotide, lubiprostone and tenapanor can reduce fluid absorption and increase alkaline output in the CF gut, potentially ameliorating constipation and reducing obstructive episodes in CF patients.
Background and Purpose: Constipation and intestinal obstructive episodes are major health problems in cystic fibrosis (CF) patients. Three FDA-approved drugs against constipation-prone irritable bowel syndrome were tested for their ability to increase luminal fluidity and alkalinity in cystic fibrosis transmembrane conductance regulator (CFTR) null (cftr(-/-)) and F508del mutant (F508del(mut/mut)) murine intestine. Experimental Approach: Guanylate cyclase C agonist linaclotide, PGE(1) analogue lubiprostone and intestine-specific NHE3 inhibitor tenapanor were perfused through a similar to 3 cm jejunal, proximal or mid-distal colonic segment in anaesthetized cftr(-/-), F508del(mut/mut) and WT mice. Net fluid balance was determined gravimetrically and alkaline output by pH-stat back titration. Key Results: Basal jejunal fluid absorptive rates were significantly higher and basal HCO3- output was significantly lower in cftr(-/-) and F508del(mut/mut) compared to WT mice. In cftr(-/-) and F508del(mut/mut) mice, all three drugs significantly inhibited the fluid absorptive rate and increased alkaline output in the jejunum and tenapanor and lubiprostone, but not linaclotide, in the colon. After tenapanor pre-incubation, linaclotide elicited a robust fluid secretory response in WT jejunum, while no further change in absorptive rates was observed in cftr(-/-) and F508del(mut/mut) jejunum, suggesting that the increase in gut fluidity and alkalinity by linaclotide in CF gut is mediated via NHE3 inhibition. Lubiprostone also inhibited fluid absorption in cftr(-/-) and F508del(mut/mut) jejunum via NHE3 inhibition but had a residual NHE3-independent effect. Conclusion and Implications: Linaclotide, lubiprostone and tenapanor reduced fluid absorption and increased alkaline output in the CF gut. Their application may ameliorate constipation and reduce obstructive episodes in CF patients.

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