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CO2 permeability and bicarbonate transport in microperfused interlobular ducts isolated from guinea-pig pancreas

机译:豚鼠胰腺微灌流小叶间导管中的二氧化碳渗透性和碳酸氢根转运

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摘要

class="enumerated" style="list-style-type:decimal">Permeabilities of the luminal and basolateral membranes of pancreatic duct cells to CO2 and HCO3 were examined in interlobular duct segments isolated from guinea-pig pancreas. Intracellular pH (pHi) was measured by microfluorometry in unstimulated, microperfused ducts loaded with the pH-sensitive fluoroprobe 2′7′-bis(2-carboxyethyl)-5(6)-carboxyfluorescein (BCECF).When HCO3/CO2 was admitted to the bath, pHi decreased transiently as a result of CO2 diffusion and then increased to a higher value as a result of HCO3 uptake across the basolateral membrane by Na+-HCO3 cotransport.When HCO3/CO2 was admitted to the lumen, pHi again decreased but no subsequent increase was observed, indicating that the luminal membrane was permeable to CO2 but did not allow HCO3 entry to the cells from the lumen. Only when the luminal HCO3 concentration was raised above 125 mm was HCO3 entry detected. The same was true of duct cells stimulated with forskolin.Recovery of pHi from an acid load, induced by exposure to an NH4+ pulse, was dependent on basolateral but not luminal Na+ and could be blocked by basolateral application of methylisobutylamiloride and H2DIDS. This indicates that the Na+-H+ exchangers and Na+-HCO3 cotransporters are located exclusively at the basolateral membrane.In the presence of HCO3/CO2, substitution of basolateral Cl with glucuronate caused larger increases in pHi than substitution of luminal Cl. This suggests that the anion exchanger activity in the basolateral membrane is greater than that in the luminal membrane.We conclude that the luminal and basolateral membranes are both freely permeable to CO2, but while the basolateral membrane has both uptake and efflux pathways for HCO3, the luminal membrane presents a significant barrier to the re-entry of secreted HCO3, largely through the inhibition of the luminal anion exchanger by high luminal HCO3 concentrations.
机译:class =“ enumerated” style =“ list-style-type:decimal”> <!-list-behavior =枚举前缀-word = mark-type = decimal max-label-size = 0-> 在从豚鼠胰腺分离的小叶间管段中,检查了胰管细胞腔壁和基底外侧膜对CO2和HCO3 -的渗透性。通过微荧光法在未刺激的微灌注导管中测量细胞内pH(pHi),该导管装有pH敏感的氟探针2'7'-双(2-羧乙基)-5(6)-羧基荧光素(BCECF)。 当HCO3 - / CO2进入水浴时,pHi由于CO2扩散而瞬时降低,然后由于HCO3 -在整个容器中的吸收而升高至更高的值。 Na + -HCO3 -共转运的基底外侧膜。 当HCO3 - / CO2进入管腔时,pHi再次降低,但未观察到随后的增加,表明腔膜可透过CO2,但不允许HCO3 -从管腔进入细胞。仅当腔内HCO3 -浓度升高到125 mm以上时,才会检测到HCO3 -进入。用福司可林刺激的导管细胞也是如此。 通过暴露于NH 4 i 中恢复> + 脉冲取决于基底外侧,但不依赖腔室Na + ,并且可以被基底外侧应用甲基异丁基阿米洛利和H 2 DIDS阻断。这表明Na + -H + 交换子和Na + -HCO 3 -共转运蛋白仅位于基底外侧膜。 在存在HCO 3 - / CO 2 的情况下,用葡萄糖醛酸替代基底外侧Cl -引起的pH i 的增加要大于内腔Cl -的改变。这表明在基底外侧膜中的阴离子交换剂活性要比在腔管膜中的阴离子交换剂活性高。 我们得出结论,腔管膜和基底外侧膜均可自由渗透CO 2 ,但是,尽管基底外侧膜同时具有HCO 3 -的摄取和流出途径,但腔膜对分泌的HCO 3 < / sub> -,主要是由于高腔内HCO 3 -浓度抑制了腔内阴离子交换剂。

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