Holtug K, Shipley A, Dantzer V, Sten-Knudsen O, Skadhauge E
Department of Anatomy and Physiology, Royal Veterinary and Agricultural University, Copenhagen, Denmark.
J Membr Biol. 1991 Jun;122(3):215-29. doi: 10.1007/BF01871422.
Hen coprodeum absorbs sodium electrogenically and, when stimulated by theophylline, secretes chloride. In this study the vibrating microprobe technique was used to localize the transport of these ions to intestinal villi/folds and crypts. With the isolated, stretched epithelium, controlled by light microscopy and scanning electron microscopy, in open circuit, currents were inward, 40 +/- 7 microA/cm2, 50 microns vertically above villi, and outward, 36 +/- 7 microA/cm2 above crypts. The currents decayed exponentially to near zero at 300 microns with the same length constant. A physical model simulating the observed loci of current sources and sinks predicts potential profiles consistent with our data. Extrapolation of the currents gives a surface potential of 45 microV, negative on villi and positive above crypts. Short circuiting increased villus current to 86 +/- 27 microA/cm2 at 50 microns, and amiloride treatment reduced it to -8 microA/cm2; in both cases crypt currents were abolished. The inward currents are compatible with sodium absorption. Induction of chloride secretion after amiloride treatment, resulted in current circuits similar to those induced by sodium absorption, with villus currents of 23 +/- 7 microA/cm2. This is in accord with chloride secretion at the villi. Quantitative estimates of crypt number (860/cm2) and opening diameter (15 microns), in conjunction with isotopic measurements of active and electrical potential-driven ion fluxes demonstrate, however, that only 4% of the potential-driven co-ion transport occurs through the crypts. This indicates that nearly all chloride secretion comes from the sodium-absorbing villar area. Were the chloride secretion to occur solely from the crypts, the current should have been in the opposite direction and 10,000-fold larger.
母鸡泄殖腔以电方式吸收钠,在茶碱刺激下分泌氯。在本研究中,使用振动微探针技术来定位这些离子向肠绒毛/皱襞和隐窝的转运。在光学显微镜和扫描电子显微镜控制下,将分离的伸展上皮置于开路状态,绒毛上方50微米处电流向内,为40±7微安/平方厘米,隐窝上方电流向外,为36±7微安/平方厘米。电流以相同的长度常数呈指数衰减至300微米处接近零。模拟观察到的电流源和电流汇位置的物理模型预测的电位分布与我们的数据一致。电流外推得出表面电位为45微伏,绒毛上为负,隐窝上方为正。短路使绒毛电流在50微米处增加到86±27微安/平方厘米,氨氯吡脒处理使其降至 -8微安/平方厘米;在这两种情况下,隐窝电流均消失。内向电流与钠吸收一致。氨氯吡脒处理后诱导氯分泌,产生的电流回路与钠吸收诱导的相似,绒毛电流为23±7微安/平方厘米。这与绒毛处的氯分泌一致。然而,结合活性和电位驱动离子通量的同位素测量,对隐窝数量(860个/平方厘米)和开口直径(15微米)的定量估计表明,只有4%的电位驱动的共离子转运通过隐窝进行。这表明几乎所有的氯分泌都来自吸收钠的绒毛区域。如果氯分泌仅发生在隐窝,电流方向应该相反且大10000倍。