RESUMO
The effects of deoxycholate, taurocholate and cholate on transport and mucosal ATPase activity have been investigated in the rat jejunum in vivo using closed-loop and perfusion techniques. In the closed-loops, 5 mM deoxycholate selectively inactivated (Na+ + K+)-ATPase, and net secretion of Na+ induced by 2.5 mM deoxycholate was due to reduced lumen to plasma flux of the ion; deoxycholate (2.5 mM) produced marked inhibition of 3-0-methylglucose transport. Luminal disappearance rates of deoxycholate (60.5 plus or minus 2.9% per g wet st of gut) greatly exceeded those of taurocholate (4.3 plus or minus 1.0). In the perfusion studies 1 mM deoxycholate induced net secretion of water, Na+ and C1-, and inhibited active glucose transport; concomitantly "total" ATPase, (Na+ + K+)-ATPase, and Mg-2+-ATPase were inhibited. At higher concentrations (5 mM) deoxycholate stimulated Mg-2+-ATPase activity. Taurocholate and cholate at 1mM had no effect on transport of (Na+ + K+)-ATPase. Mucosal lactase, sucrase and maltase activities were not affected by 1 mM deoxycholate, taurocholate or cholate. These results suggest that deoxycholate inhibits sodium-coupled glucose transport by inhibition of (Na+ + K+)-ATPase at the lateral and basal membranes of the epithelial cell, rather than from an effect at the brush-border membrane level.
Assuntos
Adenosina Trifosfatases/metabolismo , Ácidos e Sais Biliares/farmacologia , Metabolismo dos Carboidratos , Mucosa Intestinal/metabolismo , Jejuno/metabolismo , Animais , Transporte Biológico , Transporte Biológico Ativo , Ácidos Cólicos/farmacologia , Ácido Desoxicólico/farmacologia , Ativação Enzimática/efeitos dos fármacos , Glucose/metabolismo , Glucosidases/metabolismo , Mucosa Intestinal/efeitos dos fármacos , Jejuno/efeitos dos fármacos , Lactose , Magnésio/farmacologia , Maltose/metabolismo , Metilglucosídeos/metabolismo , Potássio/farmacologia , Ratos , Sódio/farmacologia , Sacarase/metabolismo , Ácido Taurocólico/farmacologiaRESUMO
The characteristics and kinetics of intact transmucosal transport of lactose have been studied in the rat jejunum using an everted sac preparation. Lactose transport displayed linear kinetics up to the maximum concentration (150 mM) of lactose studied. Ouabain (1 mM) when placed in the serosal solution, and phlorhizin (0.1 mM) when placed in the mucosal solution, had no significant effect on lactose transport. In contrast to glucose, transport of intact lactose did not occur against a concentration gradient. These results strongly suggest that intact transmucosal transport of lactose occurs by a process of simple passive diffusion, and that it is independent of the sodium-coupled glucose transport system.