碳环血栓素A2抑制大鼠结肠对Cl-的吸收。

Eicosanoids Pub Date : 1991-01-01
M Diener, W Rummel
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引用次数: 0

摘要

研究了碳环血栓素A2 (CTXA2)对有和无粘膜下丛大鼠结肠降液的短路电流(Isc)的影响。在两种制剂中,CTXA2 (10(-7)-5 × 10(-6) mol.l-1)依赖性地增加Isc浓度。其作用不受神经毒素、河豚毒素或吲哚美辛的抑制,表明其直接作用于上皮。Isc的增加依赖于培养基中Cl-和HCO3-阴离子的存在,但不受Cl分泌抑制剂如速尿或Cl通道阻滞剂的影响。对Na+和Cl-单向通量的测量表明,CTXA2的主要作用是抑制粘膜对浆膜的Cl-通量。血栓素受体阻滞剂SK&F 88046预处理可阻止CTXA2的作用。它也被TMB-8抑制,TMB-8是一种阻止细胞内Ca2+释放的物质,但其作用并不依赖于细胞外Ca2+的存在。结果表明,血栓素可以通过依赖于细胞内Ca2+的机制调节cl通过结肠上皮的转运。
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Carbocyclic thromboxane A2 inhibits Cl- absorption in the rat colon.

The effect of carbocyclic thromboxane A2 (CTXA2) on short-circuit current (Isc) was studied in two preparations of the rat colon descendens, one with and one without the submucosal plexus. In both preparations, CTXA2 (10(-7)-5 x 10(-6) mol.l-1) increased Isc concentration-dependently. Its action was not inhibited by the neurotoxin, tetrodotoxin, or by indomethacin, indicating a direct action on the epithelium. The increase in Isc was dependent on the presence of Cl- and HCO3- anions in the medium, but it was not affected by inhibitors of Cl-secretion such as furosemide or a Cl- channel blocker. Measurements of the unidirectional fluxes of Na+ and Cl-revealed that the dominant action of CTXA2 was an inhibition of the mucosa to serosa flux of Cl-. The action of CTXA2 was prevented by pretreatment with the thromboxane receptor blocker, SK&F 88046. It was also inhibited by TMB-8, a substance preventing the release of Ca2+ from intracellular stores, but its effect was not dependent on the presence of extracellular Ca2+. The results indicate that thromboxanes can modulate Cl-transport through the colonic epithelium by a mechanism dependent on intracellular Ca2+.

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