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体内大鼠远端结肠跨上皮电势以及钠和钾转运的氨氯吡咪敏感性

Amiloride sensitivity of the transepithelial electrical potential and of sodium and potassium transport in rat distal colon in vivo.

作者信息

Edmonds C J

出版信息

J Physiol. 1981;313:547-59. doi: 10.1113/jphysiol.1981.sp013681.

DOI:10.1113/jphysiol.1981.sp013681
PMID:7277236
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1274467/
Abstract
  1. The effect of amiloride within the gut lumen on the transepithelial electrical potential difference (p.d.) and Na and K transport by the distal colon of adrenalectomized (dexamethasone-maintained), normal, aldosterone-infused and Na-depleted groups of rats was examined. 2. Amiloride had no effect in adrenalectomized rats; in normal rats, only the p.d. was significantly reduced. 3. In the group given a short (2 hr) aldosterone infusion, amiloride reduced the elevated p.d. and K secretion rate to normal levels. There was no change in apparent K permeability of the epithelium. 4. In the Na-depleted group, p.d. and Na absorption were virtually abolished by amiloride but although K secretion was reduced it still remained much above normal levels. Adrenalectomy prevented the effects of Na depletion. 5. P.d. change occurred rapidly when amiloride was added to the perfusate. Increasing the Na concentration in the perfusate reduced the sensitivity to amiloride. Apparent 'Km' values estimated from p.d. changes (luminal Na, 50 mM) were similar for aldosterone-infused (7.6 X 10(-6) M) and Na-depleted (5.4 X 10(-6) M) rats. 6. Aldosterone appears to be essential for the induction of amiloride-sensitive Na paths in the mucosal plasma membrane of rat colonic epithelial cells. Prolonged aldosterone stimulation, as in the Na-depleted rats, increases the amiloride-sensitive Na paths while largely suppressing the amiloride-insensitive Na paths; in addition, the K/Na clearance rate ratio of the epithelium is increased. AMiloride interacts only with one set of Na paths and does not interact directly with K paths.
摘要
  1. 研究了肠道腔内氨氯吡咪对肾上腺切除(地塞米松维持)、正常、输注醛固酮和缺钠组大鼠远端结肠跨上皮电位差(p.d.)以及钠和钾转运的影响。2. 氨氯吡咪对肾上腺切除的大鼠无作用;在正常大鼠中,仅电位差显著降低。3. 在短时间(2小时)输注醛固酮的组中,氨氯吡咪将升高的电位差和钾分泌率降至正常水平。上皮细胞的表观钾通透性无变化。4. 在缺钠组中,氨氯吡咪几乎消除了电位差和钠吸收,但尽管钾分泌减少,仍远高于正常水平。肾上腺切除可防止缺钠的影响。5. 当将氨氯吡咪添加到灌注液中时,电位差迅速变化。增加灌注液中的钠浓度可降低对氨氯吡咪的敏感性。从电位差变化估计的表观“Km”值(管腔钠,50 mM)在输注醛固酮(7.6×10⁻⁶ M)和缺钠(5.4×10⁻⁶ M)的大鼠中相似。6. 醛固酮似乎对于在大鼠结肠上皮细胞的粘膜质膜中诱导氨氯吡咪敏感的钠通道至关重要。如在缺钠大鼠中那样,长期的醛固酮刺激增加了氨氯吡咪敏感的钠通道,同时在很大程度上抑制了氨氯吡咪不敏感的钠通道;此外,上皮细胞的钾/钠清除率比值增加。氨氯吡咪仅与一组钠通道相互作用,不直接与钾通道相互作用。

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Transport of potassium by the colon of normal and sodium-depleted rats.正常大鼠和缺钠大鼠结肠对钾的转运
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[Effect of amiloride on electrolyte transport in the rat colon and its dependency from mineral corticoids].[氨氯吡咪对大鼠结肠电解质转运的影响及其对盐皮质激素的依赖性]
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