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1.
Biocell ; 23(3): 161-170, Dec. 1999.
Article in English | LILACS | ID: lil-340368

ABSTRACT

The luminal membrane of collecting duct cells, specially the intercalated cells, is normally exposed to active kallikrein. This is due to the specific localization of renal kallikrein in the connecting tubule cells. We have previously reported inhibition of distal bicarbonate secretion by renal kallikrein. The present study was performed to evaluate the participation of basolateral Cl-/HCO3- exchanger and luminal H(+)-ATPase activity of cortical collecting duct segments (CCD) in the mechanism involved in the inhibition of bicarbonate secretion induced by the enzyme. The effect of orthograde injections of 1 microgram/ml (250 U/6.3 mg) pig pancreatic kallikrein, in the absence and presence of 1 mM DIDS (stilbene-disulfonic acid) in the renal tubule system, was evaluated. Urine fractions were collected after two-minutes stop-flow. Changes in the urine fraction (Fr) related to those in free-flow urine samples (Ff) were related to the respective polyfructosan (Inutest) ratio. Renal kallikrein activity (Fr:Ff kallikrein/Fr:Ff polyfructosan) increased significantly in the first 120 microliters urine fraction collected after glandular 1 microgram/ml kallikrein, P < 0.05, (first stop-flow) and after glandular 1 microgram/ml kallikrein plus 1 mM. DIDS P < 0.05 (second stop flow). Bicarbonate secretion rate (Fr:Ff HCO3-/Fr:Ff polyfructosan) of collecting ducts was significantly reduced in the first 120 microliters urine fraction collected, related to control, during the first and second stop-flow periods. No difference was shown in bicarbonate excretion between the first 120 microliters urine fractions collected after administration of glandular kallikrein and glandular kallikrein plus DIDS. To measure H(+)-ATPase activity, rat microdissected cortical collector tubules (CCD) were incubated in the presence of increasing glandular kallikrein doses (A: 93, B: 187 and C: 375 mU/200 microL) in the presence of ouabain (4 microM) and omeprazole (100 microM) to inhibit Na(+)-K(+)-ATPase and H(+)-K(+)-ATPase, respectively. In CCD, bafilomycin-sensitive H(+)-ATPase activity (pmol/mm/min) after increasing kallikrein doses did not differ significantly from control...


Subject(s)
Animals , Female , Rats , Antiporters , Proton-Translocating ATPases/metabolism , Bicarbonates , Biological Transport , Kallikreins/pharmacology , Chloride-Bicarbonate Antiporters , Coagulants , Rats, Inbred WKY , Kidney Tubules, Collecting/cytology , Kidney Tubules, Collecting/enzymology
2.
In. Douglas, Carlos Roberto. Patofisiologia oral: fisiologia normal e patológica aplicada a odontologia e fonoaudiologia. Säo Paulo, Pancast, 1998. p.129-32. (BR).
Monography in Portuguese | LILACS, BBO | ID: lil-246789
3.
Ciênc. cult. (Säo Paulo) ; 42(7): 453-7, jul. 1990. ilus
Article in English | LILACS | ID: lil-96123

ABSTRACT

O extrato de Mandevilla velutina inibe as contraçöes induzidas pela bradicinina e cininogenases (calicreína, tripsina e tonina) no útero de rata. As contraçöes por angiotensina II e mesmo por cloreto de bário também foram inibidas, quando o íleo de cobaia foi usado, a contraçäo evocada pela histamina foi inibida. Esses experimentos sugerem que a inibiçäo causada pelo extrato de Mandevilla velutina näo é seletiva para bradicinina


Subject(s)
Guinea Pigs , Rats , Animals , Female , Uterine Contraction , Ileum , Plant Extracts/pharmacology , Angiotensin II/pharmacology , Barium/pharmacology , Bradykinin/pharmacology , Kallikreins/pharmacology , Histamine/pharmacology , Peptidyl-Dipeptidase A/pharmacology , Trypsin/pharmacology
4.
Arq. bras. cardiol ; 49(2): 73-78, ago. 1987. tab
Article in Portuguese | LILACS | ID: lil-42880

ABSTRACT

Avaliou-se o comportamento dos componentes do sistema renina-angiotensina-aldosterona (SRAA) e do sistema calicreína-cinina (SCC) e as conseqüências das mudanças posturais sobre a pressäo arterial (PA), diurese, natriurese e caliurese em diferentes fases da gravidez normal. Foram estudadas 15 gestantes no 1§, 2§, e 3§ trimestres da gestaçäo e 5 meses após o parto, momento em que se procedeu às determinaçöes da fase controle. Em cada fase de análise as pacientes adotavam, durante 90 minutos, o decúbito dorsal, o decúbito lateral esquerdo e a ortostasia. Verificou-se importante ativaçäo dos componentes do SRAA durante o ciclo gravídico e as mudanças posturais modificaram significativamente os valores da atividade plasmática de seus componentes. No 2§ e 3§ trimestres o decúbito lateral esquerdo, comparado com as outras posiçöes, reduziu a atividade plasmática de renina e a aldosteronemia e ocasionou, por outro lado, o aumento da diurese, natriurese e caliurese. A análise do SCC mostrou que determinados componentes desse sistema variam substancialmente durante a gravidez, observando-se reduçäo progressiva nos níveis de cininogênio e de pré-calicreína e elevaçäo da calicreína circulante. As mudanças posturais näo interferiram nos valores dos componentes plasmáticos desse sistema. Os níveis do fator potenciador de cininas näo se alteraram na gestaçäo. A excreçäo urinária de calicreína elevou-se até o 2§ trimestre e as mudanças posturais modificaram a excreçäo urinária da enzima. A PA e os níveis séricos de sódio e potássio mantiveram-se normais, sem diferenças significativas, quando foram consideradas as mudanças posturais e os periódos de gestaçäo. Conclui-se que a hiperatividade do SRAA, e o consumo significante de cininogênio e as modificaçöes na diurese, natriurese e caliurese se harmonizam de modo a manter normal a PA e o metabolismo hidrossalino


Subject(s)
Humans , Female , Adolescent , Adult , Renin-Angiotensin System , Pregnancy/drug effects , Kinins/pharmacology , Kallikreins/pharmacology , Arterial Pressure/drug effects
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