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首页> 外文期刊>Pfluegers Archiv: European Journal of Physiology >The cellular mechanisms of Cl- secretion induced by C-type natriuretic peptide (CNP). Experiments on isolated in vitro perfused rectal gland tubules of Squalus acanthias.
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The cellular mechanisms of Cl- secretion induced by C-type natriuretic peptide (CNP). Experiments on isolated in vitro perfused rectal gland tubules of Squalus acanthias.

机译:C型利钠肽(CNP)诱导Cl分泌的细胞机制。角鲨的体外离体灌注直肠小管的实验。

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We have examined the mechanism whereby C-type natriuretic peptide (CNP), an agonist acting through the second messenger cGMP, enhances NaCl secretion in the rectal gland of Squalus acanthias. Single rectal gland tubules (RGT) were dissected manually, perfused in vitro and equivalent short-circuit current [Isc=transepithelial voltage/transepithelial resistance (Rte)] as well as basolateral membrane voltage (Vbl) were measured. CNP was added to luminal and basolateral perfusates at concentrations between 1 and 1000 nmol/l and its effects on the above parameters were compared to those of a "stimulation cocktail" (Stim, containing dibutyryl cAMP, adenosine and forskolin) that maximally enhances cytosolic cAMP, and other agonists and hormones such as guanylin, vasoactive intestinal peptide (VIP), and adenosine. CNP had no effect from the luminal side (n=6). Its effects from the basolateral side consisted of a substantial increase in Isc (-31.6+/-7.7 to -316+/-82.2 microA/cm2, n=15). CNP significantly depolarized the luminal membrane from -87. 4+/-1.0 to -82.3+/-2.6 mV (n=12). Vbl was not changed (n=12) but the fractional conductance for K+ was increased (n=3). These effects were qualitatively and even quantitatively comparable to those of other agonists acting via cytosolic cAMP, but were less marked than those caused by Stim (n=64). The effects of VIP and CNP on Isc were not additive (n=5). The cytosolic Ca2+ concentration ([Ca2+]i) was monitored using the fura-2 fluorescence ratio (FFR 340/380 nm) and it was found that CNP, like agonists acting via cAMP, enhances FFR significantly from 1.02+/-0.05 to 1.32+/-0.05 (n=8) with a time constant in the 1-2 min in range. Our data suggest that CNP, acting via the second messenger cGMP, induces a marked increase in Isc in the rectal gland. The concomitant fall in Rte corresponds to increases in the luminal membrane Cl- conductance and in the basolateral membrane K+ conductance. The latter effect is probably due to an increase in [Ca2+]i.
机译:我们已经研究了通过第二种信使cGMP发挥作用的激动剂C型利钠肽(CNP)增强棘角棘鱼直肠腺体NaCl分泌的机制。手动解剖单个直肠小管(RGT),进行体外灌注,并测量等效短路电流[Isc =跨上皮电压/跨上皮电阻(Rte)]以及基底外侧膜电压(Vbl)。将CNP以1至1000 nmol / l的浓度添加到腔内和基底外侧灌流液中,并将其对上述参数的影响与最大程度地增强胞质cAMP的“刺激性混合物”(Stim,含有二丁酰cAMP,腺苷和福司可林)进行比较。 ,以及其他激动剂和激素,例如鸟苷,血管活性肠肽(VIP)和腺苷。 CNP从管腔侧面无影响(n = 6)。它从基底外侧的影响包括Isc的显着增加(-31.6 +/- 7.7至-316 +/- 82.2 microA / cm2,n = 15)。 CNP使-87的腔膜显着去极化。 4 +/- 1.0至-82.3 +/- 2.6 mV(n = 12)。 Vbl不变(n = 12),但K +的分数电导增加(n = 3)。这些作用在质量上和数量上都与通过细胞溶质cAMP发挥作用的其他激动剂相当,但不及Stim(n = 64)引起。 VIP和CNP对Isc的影响不是累加的(n = 5)。使用fura-2荧光比率(FFR 340/380 nm)监测胞浆中Ca2 +的浓度([Ca2 +] i),发现CNP像通过cAMP起作用的激动剂一样,将FFR从1.02 +/- 0.05显着提高到1.32 +/- 0.05(n = 8),时间常数在1-2分钟范围内。我们的数据表明,CNP通过第二个信使cGMP起作用,导致直肠中Isc明显增加。 Rte的相应下降对应于腔膜Cl-电导和基底外侧膜K +电导的增加。后一种效应可能是由于[Ca2 +] i的增加。

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