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Exp Parasitol ; 91(2): 119-25, 1999 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-9990339

RESUMO

Na(+)-glucose transport and transepithelial permeability were investigated during symptomatic acute cryptosporidiosis in newborn rats. The infection resulted in a significant (P < 0.01) decrease in the ileal short-circuit current and a nonsignificant fall in the transepithelial potential difference and conductance. In glucose-stimulated conditions, the rise in ileal short-circuit current and transepithelial permeability were significantly lower in Cryptosporidium parvum-infected rats than in controls (delta Isc = 3.24 +/- 1.21 microA.cm-2 vs delta Isc = 5.09 +/- 2.23 microA.cm-2 in infected and control animals, respectively; P < 0.001; delta PD = -0.35 +/- 0.13 mV vs delta PD = -0.44 +/- 0.14 mV for infected and control animals, respectively; P < 0.01). Electrical parameters were not affected by addition of the cyclooxygenase inhibitor indomethacin in either Cryptosporidium-infected newborn rats or controls. Horseradish peroxidase and mannitol flux studies demonstrated a significant decrease (P < 0.05) in transepithelial molecular permeability in infected enterocyte rats, HRP flux = 380, range 68-5570 ng.cm-2, and mannitol flux = 1.06, range, 0.34-1.44%.cm-2.min-1, compared with controls rats, HRP flux = 4446 range, 1121-124,363 ng.cm-2, and mannitol flux = 1.99, range, 0.57-5.09%.cm-2.min-1; P < 0.05. These effects could originate from C. parvum-induced alteration of intracellular trafficking of pinocytosis vesicles and therefore account for the decrease in permeability to solute and macromolecules, together with impaired transcellular nutrient transport, in suckling rats.


Assuntos
Criptosporidiose/fisiopatologia , Cryptosporidium parvum/fisiologia , Glucose/metabolismo , Íleo/fisiopatologia , Proteínas de Transporte de Monossacarídeos/fisiologia , Sódio/metabolismo , Animais , Animais Lactentes , Colorimetria , Criptosporidiose/metabolismo , Cryptosporidium parvum/ultraestrutura , Modelos Animais de Doenças , Eletrofisiologia , Feminino , Peroxidase do Rábano Silvestre/farmacologia , Humanos , Íleo/parasitologia , Íleo/ultraestrutura , Mucosa Intestinal/parasitologia , Mucosa Intestinal/fisiopatologia , Mucosa Intestinal/ultraestrutura , Manitol/farmacologia , Camundongos , Microscopia Eletrônica , Proteínas de Transporte de Monossacarídeos/metabolismo , Proteínas de Transporte de Monossacarídeos/ultraestrutura , Permeabilidade , Ratos , Ratos Sprague-Dawley , Contagem de Cintilação , Organismos Livres de Patógenos Específicos
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