Study on the mechanism of Giardia lambdia induced diarrhoea in mice

S Gorowara, NK Ganguly, RC Mahajan… - Biochimica et Biophysica …, 1992 - Elsevier
S Gorowara, NK Ganguly, RC Mahajan, BNS Walia
Biochimica et Biophysica Acta (BBA)-Molecular Basis of Disease, 1992Elsevier
The transmucosal fluxes of Na+ and Cl− were studied in Giardia lamblia infected mice in the
presence or absence of phorbol-12-myristate-13-acetate (PMA), the activator of protein
kinase C (PKC) or 1-(5-isoquinolinylsulphonyl)-2-methylpiperazine (H-7), the inhibitor of
PKC or Ca 2+-calmodulin. There was net secretion of Na+ and Cl− in infected animals, while
in control animals there was net absorption of these ions. The addition of ionophore or PMA
resulted in net secretion of Na+ and Cl− in the control group while in the infected group there …
Abstract
The transmucosal fluxes of Na+ and Cl were studied in Giardia lamblia infected mice in the presence or absence of phorbol-12-myristate-13-acetate (PMA), the activator of protein kinase C (PKC) or 1-(5-isoquinolinylsulphonyl)-2-methylpiperazine (H-7), the inhibitor of PKC or Ca2+-calmodulin. There was net secretion of Na+ and Cl in infected animals, while in control animals there was net absorption of these ions. The addition of ionophore or PMA resulted in net secretion of Na+ and Cl in the control group while in the infected group there was no change in the fluxes of these ions. The selective potent inhibitor of protein kinase, C, H-7, reversed the secretion of Na+ and Cl in infected group to absorption. The addition of PMA and Ca2+-ionophore together in the infected group had a partial additive effect. This study suggests that G. lamblia induced fluid secretion involves protein kinase C and further protein kinase C acts in synergism with calcium.
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