首页> 美国卫生研究院文献>The Journal of Clinical Investigation >Elevated intracellular Ca2+ acts through protein kinase C to regulate rabbit ileal NaCl absorption. Evidence for sequential control by Ca2+/calmodulin and protein kinase C.
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Elevated intracellular Ca2+ acts through protein kinase C to regulate rabbit ileal NaCl absorption. Evidence for sequential control by Ca2+/calmodulin and protein kinase C.

机译:升高的细胞内Ca2 +通过蛋白激酶C调节家兔回肠NaCl的吸收。 Ca2 + /钙调蛋白和蛋白激酶C进行顺序控制的证据。

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摘要

Calcium/calmodulin is involved in the regulation of basal rabbit ileal active Na and Cl absorption, but the mechanism by which elevated intracellular Ca2+ affects Na and Cl transport is unknown. To investigate the roles of the Ca2+/calmodulin and protein kinase C systems in ileal NaCl transport, two drugs, the isoquinolenesulfonamide, H-7, and the naphthalenesulfonamide, W13, were used in concentrations that conferred specificity in the antagonism of protein kinase C (60 microM H-7) and Ca2+/calmodulin (45 microM W13), respectively, as determined using phosphorylation assays in ileal villus cells. W13 but not H-7 stimulated basal active NaCl absorption. H-7 inhibited changes in Na and Cl absorption caused by maximal concentrations of Ca2+ ionophore A23187 and carbachol and serotonin, secretagogues that act by increasing cytosol Ca2+, while W13 had no effect. In contrast, neither H-7 nor W13 altered the change in NaCl transport caused by the cyclic nucleotides 8-Br-cAMP and 8-Br-cGMP. These data suggest that: (a) basal rabbit ileal NaCl absorption is regulated by the Ca2+/calmodulin complex and not by protein kinase C; (b) the effect of elevating intracellular Ca2+ to decrease NaCl absorption is mediated via protein kinase C but not by Ca2+/calmodulin; (c) the effects of protein kinase C are not overlapping or synergistic with those of Ca2+/calmodulin on either basal absorption or on the effects of increased Ca2+; and (d) neither Ca2+/calmodulin nor protein kinase C are involved in the effects of cAMP and cGMP on ileal active NaCl transport.
机译:钙/钙调蛋白参与基底兔回肠活性Na和Cl吸收的调节,但是细胞内Ca2 +升高影响Na和Cl转运的机制尚不清楚。为了研究Ca2 + /钙调蛋白和蛋白激酶C系统在回肠NaCl转运中的作用,使用了两种药物,即异喹啉磺酰胺H-7和萘磺酰胺W13,以一定浓度赋予了蛋白激酶C拮抗作用的特异性(如在回肠绒毛细胞中使用磷酸化测定所确定的,分别测定了60 microM H-7)和Ca2 + /钙调蛋白(45 microM W13)。 W13但不刺激H-7刺激基础活性NaCl吸收。 H-7抑制了最大浓度的Ca2 +离子载体A23187和碳酰胆碱和血清素引起的Na和Cl吸收变化,而促分泌素通过增加细胞溶质Ca2 +起作用,而W13没有作用。相反,H-7和W13均未改变由环状核苷酸8-Br-cAMP和8-Br-cGMP引起的NaCl转运的变化。这些数据表明:(a)基底兔回肠NaCl的吸收受Ca2 + /钙调蛋白复合物的调节,而不受蛋白激酶C的调节; (b)升高细胞内Ca2 +降低NaCl吸收的作用是通过蛋白激酶C介导的,而不是通过Ca2 + /钙调蛋白来介导的; (c)蛋白激酶C与Ca2 + /钙调蛋白的作用在基础吸收或Ca2 +增加的作用上没有重叠或没有协同作用; (d)Ca2 + /钙调蛋白和蛋白激酶C均不参与cAMP和cGMP对回肠活性NaCl转运的影响。

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