Geibel J P, Rajendran V M, Binder H J
Department of Surgery, Yale University, New Haven, Connecticut, USA.
Gastroenterology. 2001 Jan;120(1):144-50. doi: 10.1053/gast.2001.20890.
BACKGROUND & AIMS: The traditional paradigm of fluid movement in the mammalian colon is that fluid absorption and secretion are present in surface and crypt cells, respectively. We have recently demonstrated Na(+)-dependent fluid absorption in isolated crypts that are devoid of neurohumoral stimulation. We now explore the mechanism of Na(+)-dependent fluid absorption in isolated rat colonic crypts.
Net fluid absorption was determined using microperfusion techniques and methoxy[(3)H]inulin with ion substitutions and transport inhibitors.
Net fluid absorption was reduced but not abolished by substitution of either N-methyl-D-glucamine- Cl(-) or tetramethylammonium for Na(+) and by lumen addition of 5-ethylisopropyl amiloride, an amiloride analogue that selectively inhibits Na(+)-H(+) exchange. Net fluid absorption was also dependent on lumen Cl(-) because removal of lumen Cl(-) significantly (P < 0.001) reduced net fluid absorption. DIDS at 100 micromol/L, a concentration at which DIDS is an anion exchange inhibitor, minimally reduced net fluid absorption (P < 0.05). In contrast, either 500 micromol/L DIDS, a concentration at which DIDS is known to act as a Cl(-) channel blocker, or 10 micromol/L NPPB, a Cl(-) channel blocker, both substantially inhibited net fluid absorption (P < 0.001). Finally, both the removal of bath Cl(-) and addition of bath bumetanide, an inhibitor of Na-K-2Cl cotransport and Cl(-) secretion, resulted in a significant increase in net fluid absorption.
(1) Net Na(+)-dependent net fluid absorption in the isolated colonic crypt represents both a larger Na(+)-dependent absorptive process and a smaller secretory process; and (2) the absorptive process consists of a Na(+)-dependent, HCO(3)(-)-independent process and a Na(+)-independent, Cl(-)-dependent, HCO(3)(-)-dependent process. Fluid movement in situ represents these transport processes plus fluid secretion induced by neurohumoral stimulation.
哺乳动物结肠中液体流动的传统模式是,液体吸收和分泌分别发生在表面细胞和隐窝细胞中。我们最近在缺乏神经体液刺激的分离隐窝中证实了钠依赖性液体吸收。现在我们探讨分离的大鼠结肠隐窝中钠依赖性液体吸收的机制。
使用微灌注技术和甲氧基[³H]菊粉,通过离子替代和转运抑制剂来测定净液体吸收。
用N-甲基-D-葡萄糖胺-Cl⁻或四甲基铵替代钠,以及在肠腔中加入5-乙基异丙基氨氯吡咪(一种选择性抑制钠-氢交换的氨氯吡咪类似物),净液体吸收减少但未消除。净液体吸收也依赖于肠腔氯离子,因为去除肠腔氯离子会显著(P < 0.001)降低净液体吸收。100 μmol/L的二异丙基氟磷酸(DIDS),此浓度下DIDS是一种阴离子交换抑制剂,对净液体吸收的降低作用最小(P < 0.05)。相比之下,500 μmol/L的DIDS(已知此浓度下DIDS作为氯离子通道阻滞剂起作用)或10 μmol/L的NPPB(一种氯离子通道阻滞剂),两者均显著抑制净液体吸收(P < 0.001)。最后,去除浴液中的氯离子以及加入浴液中的布美他尼(一种钠-钾-2氯共转运和氯离子分泌的抑制剂),均导致净液体吸收显著增加。
(1)分离的结肠隐窝中钠依赖性净液体吸收既代表一个较大的钠依赖性吸收过程,也代表一个较小的分泌过程;(2)吸收过程包括一个钠依赖性、不依赖于碳酸氢根的过程和一个不依赖于钠、依赖于氯离子、依赖于碳酸氢根的过程。原位的液体流动代表这些转运过程加上神经体液刺激诱导的液体分泌。