Mechanism of regulation of rabbit intestinal villus cell brush border membrane Na/H exchange by nitric oxide

被引:9
作者
Coon, Steven
Shao, Guohong
Wisel, Sheik
Vulaupalli, Raju
Sundaram, Uma
机构
[1] W Virginia Univ, Sch Med, Sect Digest Dis, Dept Med, Morgantown, WV 26506 USA
[2] Ohio State Univ, Columbus, OH 43210 USA
[3] Univ Rochester, Rochester, NY USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY | 2007年 / 292卷 / 02期
关键词
nitro-L-arginine methyl ester; N-6-(1-imonoethyl)-L-lysine dihydrochloride; nitric oxide; NHE3; NH/E exchange; AMINO-ACID COTRANSPORT; ELECTROLYTE TRANSPORT; CHRONIC INFLAMMATION; RAT INTESTINE; ILEAL CRYPT; L-ARGININE; SECRETION; INHIBITION; STIMULATION; INVOLVEMENT;
D O I
10.1152/ajpgi.00263.2005
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
In the mammalian small intestine, coupled NaCl absorption occurs via the dual operation of Na/H and Cl/HCO3 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/HCO3 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.
引用
收藏
页码:G475 / G481
页数:7
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