dc.contributorUniversidade Estadual Paulista (UNESP)
dc.creatorOliveira Amorim, Jose Benedito
dc.creatorMusa-Aziz, Raif
dc.creatorLessa, Lucilia M. A.
dc.creatorMalnic, Gerhard
dc.creatorFonteles, Manasses Claudino
dc.date2014-05-20T15:21:05Z
dc.date2016-10-25T17:54:22Z
dc.date2014-05-20T15:21:05Z
dc.date2016-10-25T17:54:22Z
dc.date2006-10-01
dc.date.accessioned2017-04-05T23:29:19Z
dc.date.available2017-04-05T23:29:19Z
dc.identifierCanadian Journal of Physiology and Pharmacology. Ottawa: Natl Research Council Canada-n R C Research Press, v. 84, n. 10, p. 1003-1010, 2006.
dc.identifier0008-4212
dc.identifierhttp://hdl.handle.net/11449/32267
dc.identifierhttp://acervodigital.unesp.br/handle/11449/32267
dc.identifier10.1139/Y06-044
dc.identifierWOS:000243731100006
dc.identifierhttp://dx.doi.org/10.1139/Y06-044
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/876640
dc.descriptionThe effect of uroguanylin (UGN) oil K(+) and H(+) secretion in the renal tubules of the rat kidney was studied using in vivo stationary microperfusion. For the study of K(+) secretion, a tubule was Punctured to inject a column of FDC-green-colored Ringer's solution with 0.5 mmol KCI/L 10(-6)(mol UGN/L, and oil was Used to block fluid flow. K(+) activity and transepithelial potential differences (PD) were measured with double microelectrodes (K(+) ion-selective resin vs. reference) in the distal tubules of the same nephron. During perfusion, K(+) activity rose exponentially, from 0.5 mmol/L to stationary concentration, allowing for the calculation of K(+) secretion J(K)). JK increased from 0.63 +/- 0.06 nmol.cm(-2).s(-1) in the control croup to 0.85 +/- 0.06 in the UGN group (p < 0.01). PD was -51.0 +/- 5.3 mV in the control group and -50.3 +/- 4.98 mV in the UGN group. In the presence of 10(-7) mol iberiotoxin/L, the UGN effect was abolished: JK was 0.37 +/- 0.038 nmol-cm(-2).s(-1) in the absence of, and 0.38 +/- 0.025 in the presence of, UGN. indicating its action oil rnaxi-K channels. In another series of experiments, renal tubule acidification was studied, using similar method: proximal and distal tubules were perfused with solutions containing 25 mmol NaHCO(3)/L. Acidification half-time was increased both in proximal and distal segments and, as a consequence, bicarbonate reabsorption decreased in the presence of UGN (in proximal tubules, from 2.40 +/- 0.26 to 1.56 +/- 0.21 nmol-cm(-2).s(-1)). When the Na(+)/H(+) exchanger was inhibited by 10(-4) mol hexamethylene amiloride (HMA)/L, the control and UGN groups were not significantly different. In the late distal tubule, after HMA, UGN significantly reduced J(HCO3)(-). indicating all effect of UGN oil H(+)-ATPase. These data show that UGN stimulated J(K)(+) by actin, oil maxi-K channels. and decreased J(HCO3)(-) by acting on NHE3 in proximal and H(+)-ATPase in distal tubules.
dc.languageeng
dc.publisherNatl Research Council Canada-n R C Research Press
dc.relationCanadian Journal of Physiology and Pharmacology
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectrenal tubules
dc.subjectmicroperfusion
dc.subjectpH
dc.subjectmaxi K channels
dc.subjectNa(+)/H(+)
dc.subjectH-ATPase
dc.titleEffect of uroguanylin on potassium and bicarbonate transport in rat renal tubules
dc.typeOtro


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