首页> 外文期刊>American Journal of Physiology >Mechanism of regulation of rabbit intestinal villus cell brush border membrane Na/H exchange by nitric oxide.
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Mechanism of regulation of rabbit intestinal villus cell brush border membrane Na/H exchange by nitric oxide.

机译:一氧化氮调节家兔小肠绒毛细胞刷状缘膜Na / H交换的机制。

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摘要

In the mammalian small intestine, coupled NaCl absorption occurs via the dual operation of Na/H and Cl/HCO(3) exchange on the villus cell brush border membrane (BBM). Although constitutive nitric oxide (cNO) has been demonstrated to alter gastrointestinal tract functions, how cNO may specifically alter these two transporters to regulate coupled NaCl absorption is unknown. In villus cells, inhibition of cNO synthase (cNOS) with l-N(G)-nitroarginine methylester (l-NAME) stimulated Na/H exchange whereas Cl/HCO(3) exchange was unaffected. In villus cell BBM vesicles (BBMV) prepared from rabbits treated with l-NAME, Na/H exchange was also stimulated. d-NAME, an inactive analog of l-NAME, and N(6)-(1-imonoethyl)-l-lysine dihydrochloride, a more selective inhibitor of inducible NO synthase, did not affect Na/H exchange. Kinetic studies demonstrated that the mechanism of stimulation is secondary to an increase in the maximal rate of uptake of Na, without an alteration in the affinity of the transporter for Na.Northern blot studies demonstrated an increase in the message for the BBM Na/H exchanger NHE3, and Western blot studies showed that the immunoreactive protein levels of NHE3 was increased when cNOS was inhibited. Thus these results indicate that cNO under nominal physiological states most likely maintains an inhibitory tone on small intestinal coupled NaCl absorption by specifically inhibiting BBM Na/H expression.
机译:在哺乳动物的小肠,耦合的NaCl吸收通过绒毛细胞刷状缘膜(BBM)上的Na / H和Cl / HCO(3)交换的双重操作而发生。尽管已经证明本构性一氧化氮(cNO)会改变胃肠道功能,但cNO如何特异性改变这两种转运蛋白以调节耦合的NaCl吸收尚不清楚。在绒毛细胞中,用l-N(G)-硝基精氨酸甲酯(l-NAME)抑制cNO合酶(cNOS)刺激Na / H交换,而Cl / HCO(3)交换不受影响。在用l-NAME处理的兔子制备的绒毛细胞BBM囊泡(BBMV)中,Na / H交换也被刺激。 d-NAME(l-NAME的无活性类似物)和N(6)-(1-imonoethyl)-1-赖氨酸二盐酸盐(诱导型NO合酶的选择性更高的抑制剂)不影响Na / H交换。动力学研究表明,刺激的机制是继最大的Na吸收速率增加后继发的,而转运蛋白对Na的亲和力却没有改变。Northernblot研究表明,BBM Na / H交换子的信息增加NHE3和Western blot研究表明,当cNOS被抑制时,NHE3的免疫反应蛋白水平升高。因此,这些结果表明,在正常生理状态下的cNO最有可能通过特异性抑制BBM Na / H表达来维持小肠偶联NaCl吸收的抑制音。

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