Mechanisms of guanylin action via cyclic GMP in the kidney

被引:43
作者
Forte, LR [1 ]
London, RM
Krause, WJ
Freeman, RH
机构
[1] Harry S Truman Mem Vet Hosp, Columbia, MO 65212 USA
[2] Univ Missouri, Sch Med, Dept Pharmacol, Columbia, MO 65212 USA
[3] Univ Missouri, Sch Med, Dept Pathol, Columbia, MO 65212 USA
[4] Univ Missouri, Sch Med, Dept Anat Sci, Columbia, MO 65212 USA
[5] Univ Missouri, Sch Med, Dept Physiol, Columbia, MO 65212 USA
关键词
uroguanylin; lymphoguanylin; E. coli heat-stable enterotoxin; guanylate cyclase; intestine;
D O I
10.1146/annurev.physiol.62.1.673
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Guanylin, uroguanylin, and lymphoguanylin are small peptides that activate cell-surface guanylate cyclase receptors and influence cellular function via intracellular cGMP. Guanylins activate two receptors, GC-C and OK-GC, which are expressed in intestine and/or kidney. Elevation of cCMP in the intestine elicits an increase in electrolyte and water secretion. Activation of renal receptors by uroguanylin stimulates urine flow and excretion of sodium, chloride, and potassium. Intracellular cGMP pathways for guanylins include activation of PKG-II and/or indirect stimulation of PKA-II. The result is activation of CFTR and/or ClC-2 channel proteins to enhance the electrogenic secretion of chloride and bicarbonate. Similar cellular mechanisms may be involved in the renal responses to guanylin peptides. Uroguanylin serves as an intestinal natriuretic hormone in postprandial states, thus linking the digestive and renal organ systems in a novel endocrine axis. Therefore, uroguanylin participates in the complex physiological processes underlying the saliuresis that is elicited by a salty meal.
引用
收藏
页码:673 / 695
页数:23
相关论文
共 83 条
[21]  
Fonteles MC, 1999, FASEB J, V13, pA727
[22]   Lymphoguanylin: Cloning and characterization of a unique member of the guanylin peptide family [J].
Forte, LR ;
Eber, SL ;
Fan, XH ;
London, RM ;
Wang, Y ;
Rowland, LM ;
Chin, DT ;
Freeman, RH ;
Krause, WJ .
ENDOCRINOLOGY, 1999, 140 (04) :1800-1806
[23]   STIMULATION OF INTESTINAL CL- TRANSPORT BY HEAT-STABLE ENTEROTOXIN - ACTIVATION OF CAMP-DEPENDENT PROTEIN-KINASE BY CGMP [J].
FORTE, LR ;
THORNE, PK ;
EBER, SL ;
KRAUSE, WJ ;
FREEMAN, RH ;
FRANCIS, SH ;
CORBIN, JD .
AMERICAN JOURNAL OF PHYSIOLOGY, 1992, 263 (03) :C607-C615
[24]   Guanylin regulatory peptides: structures, biological activities mediated by cyclic GMP and pathobiology [J].
Forte, LR .
REGULATORY PEPTIDES, 1999, 81 (1-3) :25-39
[25]   RECEPTORS AND CGMP SIGNALING MECHANISM FOR ESCHERICHIA-COLI ENTERO-TOXIN IN OPOSSUM KIDNEY [J].
FORTE, LR ;
KRAUSE, WJ ;
FREEMAN, RH .
AMERICAN JOURNAL OF PHYSIOLOGY, 1988, 255 (05) :F1040-F1046
[26]   GUANYLIN STIMULATION OF CL- SECRETION IN HUMAN INTESTINAL T(84) CELLS VIA CYCLIC GUANOSINE-MONOPHOSPHATE [J].
FORTE, LR ;
EBER, SL ;
TURNER, JT ;
FREEMAN, RH ;
FOK, KF ;
CURRIE, MG .
JOURNAL OF CLINICAL INVESTIGATION, 1993, 91 (06) :2423-2428
[27]   ESCHERICHIA-COLI ENTERO-TOXIN RECEPTORS - LOCALIZATION IN OPOSSUM KIDNEY, INTESTINE, AND TESTIS [J].
FORTE, LR ;
KRAUSE, WJ ;
FREEMAN, RH .
AMERICAN JOURNAL OF PHYSIOLOGY, 1989, 257 (05) :F874-F881
[28]   ISOTYPE-SPECIFIC ACTIVATION OF CYSTIC-FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR-CHLORIDE CHANNELS BY CGMP-DEPENDENT PROTEIN-KINASE-II [J].
FRENCH, PJ ;
BIJMAN, J ;
EDIXHOVEN, M ;
VAANDRAGER, AB ;
SCHOLTE, BJ ;
LOHMANN, SM ;
NAIRN, AC ;
DEJONGE, HR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (44) :26626-26631
[29]  
FULLER F, 1988, J BIOL CHEM, V263, P9395
[30]  
Giannella RA, 1999, FASEB J, V13, pA725