Greger R, Bleich M, Warth R, Thiele I, Forrest J N
Physiologisches Institut, Albert-Ludwigs-Universität, Hermann-Herder-Strasse 7, D-79104 Freiburg, Germany.
Pflugers Arch. 1999 Jun;438(1):15-22. doi: 10.1007/s004240050874.
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.
我们研究了C型利钠肽(CNP)通过第二信使环磷酸鸟苷(cGMP)发挥作用从而增强棘鲨直肠腺中氯化钠分泌的机制。手动解剖单个直肠腺小管(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)。将浓度在1至1000 nmol / l之间的CNP添加到管腔和基底外侧灌注液中,并将其对上述参数的影响与“刺激混合物”(Stim,含有二丁酰环磷酸腺苷、腺苷和福斯高林)进行比较,后者可最大程度地增强胞质环磷酸腺苷,还与其他激动剂和激素(如鸟苷素、血管活性肠肽(VIP)和腺苷)进行比较。CNP从管腔侧给药无作用(n = 6)。其从基底外侧给药的作用包括Isc大幅增加(从-31.6±7.7至-316±82.2 μA/cm²,n = 15)。CNP使管腔膜显著去极化,从-87.4±1.0 mV变为-82.3±2.6 mV(n = 12)。Vbl未改变(n = 12),但K⁺的分数电导率增加(n = 3)。这些作用在质量上甚至数量上与通过胞质环磷酸腺苷起作用的其他激动剂相当,但不如Stim引起的作用明显(n = 64)。VIP和CNP对Isc的作用不是相加的(n = 5)。使用fura-2荧光比率(FFR 340/380 nm)监测胞质Ca²⁺浓度([Ca²⁺]i),发现CNP与通过环磷酸腺苷起作用的激动剂一样,可使FFR从1.02±0.05显著增加至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,通过第二信使cGMP起作用的CNP可诱导直肠腺中Isc显著增加。伴随的Rte下降对应于管腔膜Cl⁻电导率和基底外侧膜K⁺电导率的增加。后一种作用可能是由于[Ca²⁺]i增加所致。