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生长抑素对大鼠远端结肠细胞体积、氯离子电流及跨上皮氯离子转运的影响

Effect of somatostatin on cell volume, Cl- currents, and transepithelial Cl- transport in rat distal colon.

作者信息

Diener M, Gartmann V

机构信息

Institut für Veterinär-Physiologie, Universität Zürich, Switzerland.

出版信息

Am J Physiol. 1994 Jun;266(6 Pt 1):G1043-52. doi: 10.1152/ajpgi.1994.266.6.G1043.

Abstract

Somatostatin (10(-10)-10(-7) mol/l) caused a concentration-dependent increase of the diameter of isolated crypts from the rat distal colon. Cell swelling was restricted to the upper one-third of the crypt and was dependent on the presence of Na+ and Cl- ions, indicating that it was caused by the stimulation of NaCl absorption by the hormone. Swelling was followed by a regulatory volume decrease, which could be inhibited by K+ and Cl- channel blockers. Also a lipoxygenase inhibitor and a leukotriene D4 receptor blocker inhibited volume regulation. Whole cell recordings performed in parallel revealed that somatostatin induced a depolarization of the cells at the upper one-third of the crypt but had no effect in the deeper parts of the crypt. This depolarization was concomitant with an increase in Cl- (and partially also HCO3-) conductance and was suppressed by a leukotriene D4 receptor blocker. In contrast, when Cl- secretion was stimulated by vasoactive intestinal peptide, a secretagogue acting on the adenosine 3',5'-cyclic monophosphate (cAMP) pathway, the effect of somatostatin was reversed from a depolarization into a hyperpolarization, an effect that was also observed in deeper parts of the crypt. Consequently, in crypts stimulated via the cAMP pathway, somatostatin inhibits the activation of apical Cl- channels. Somatostatin also partially inhibited the increase of K+ conductance induced by carbachol, a secretagogue acting on the Ca2+ pathway. Ussing chamber experiments showed that somatostatin caused a concentration-dependent decrease of short-circuit current. This decrease was dependent on the presence of Cl- and HCO3- ions. Measurements of unidirectional ion fluxes indicated that somatostatin stimulated Cl- absorption by an increase of the mucosa-to-serosa flux of this ion. The stimulation of Cl- absorption was completely suppressed by a Cl- channel blocker and by a lipoxygenase inhibitor. Consequently, the activation of a volume/leukotriene-sensitive basolateral Cl- conductance seems to be involved in the stimulation of Cl- absorption by somatostatin.

摘要

生长抑素(10⁻¹⁰ - 10⁻⁷mol/l)可使大鼠远端结肠孤立隐窝的直径呈浓度依赖性增加。细胞肿胀局限于隐窝的上三分之一部分,且依赖于Na⁺和Cl⁻离子的存在,这表明其是由该激素刺激NaCl吸收所致。肿胀之后会出现调节性容积减小,这可被K⁺和Cl⁻通道阻滞剂抑制。此外,一种脂氧合酶抑制剂和一种白三烯D4受体阻滞剂也可抑制容积调节。同时进行的全细胞记录显示,生长抑素可使隐窝上三分之一部分的细胞发生去极化,但对隐窝深部无影响。这种去极化与Cl⁻(部分还有HCO₃⁻)电导增加相伴,且被白三烯D4受体阻滞剂抑制。相反,当血管活性肠肽(一种作用于腺苷3',5'-环磷酸(cAMP)途径的促分泌素)刺激Cl⁻分泌时,生长抑素的作用从去极化转变为超极化,这种效应在隐窝深部也可观察到。因此,在通过cAMP途径刺激的隐窝中,生长抑素可抑制顶端Cl⁻通道的激活。生长抑素还可部分抑制卡巴胆碱(一种作用于Ca²⁺途径的促分泌素)诱导的K⁺电导增加。尤斯灌流小室实验表明,生长抑素可使短路电流呈浓度依赖性降低。这种降低依赖于Cl⁻和HCO₃⁻离子的存在。单向离子通量测量表明,生长抑素通过增加该离子从黏膜到浆膜的通量来刺激Cl⁻吸收。Cl⁻通道阻滞剂和脂氧合酶抑制剂可完全抑制Cl⁻吸收的刺激作用。因此,一种对容积/白三烯敏感的基底外侧Cl⁻电导的激活似乎参与了生长抑素对Cl⁻吸收的刺激过程。

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