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C Lippe

Publications and source records attributed to C Lippe.

28 records · Page 2Linked to original sources
PubMed1977

Noradrenaline induced secretion of nonelectrolytes through frog skin.

Addition of noradrenaline (4 x 10(-5) M) to the inner bathing fluid in the skin of the frog Rana esculenta results in increased unidirectional fluxes of urea, thiourea, N-methyl-thiourea, N-N'-dimethylthiourea and mannitol. Fluxes towards the external medium (phi o) undergo a much greater increase than those moving the opposite direction (phi i). The effect of noradrenaline on phi o is higher for urea and thiourea than mannitol, while its effect on phi o thiourea derivatives is related to lipid solubility. This phenomenon does not occur for phi i of the same molecules. FCCP (10(-6) M) pretreatment strongly inhibits the noradrenaline effect on phi o. In skin pretreated with colchicine (2 x 10(-5) M) both urea fluxes are increased to the same extent by noradrenaline. Noradrenaline is concluded to exert two separate effects: (1) a change in permeability in both directions; (2) a secretion of nonelectrolytes towards the external fluid. Such secretion is most probably associated with the hormone-induced secretion of fluid and electrolytes, perhaps mediated by an exocytotic mechanism.

Animals↗
PubMed1976

Facilitated transport of urea across the toad gallbladder.

The toad gallbladder epithelium is much more selective than that of the rabbit especially as to the permeability of two molecules like urea and thiourea. These observations can probably be attributed to different permeation mechanisms of the 2 molecules. Neither active transport nor solvent drag can explain these phenomena. 10(-4) M phloretin strongly inhibits urea movement, but does not alter either thiourea fluxes or isotonic net water transport: these results suggest that a specific mechanism is involved in urea movement. The urea transport shows saturation kinetic which is consistent with the presence of a facilitated mechanism.

Animals↗
PubMed1975

Permeability pathways for non-electrolytes through Bufo bufo gall-bladder.

Amphotericin B treatment increases the thiourea, D-xylose and mannitol fluxes and lowers those of urea, N-methyl-urea, acetamide, formamide, and N-N'-dimethyl-thiourea. The degree of flux inhibition is related to the cellular permeability of these compounds. Most probably Amphotericin B increases the permeability of all those molecules across the luminal plasma membrane, but simultaneously elicits a cellular swelling, which reduces the diffusion across the lateral plasma membranes. This effect masks the polyene effect especially for molecules showing a mainly cellular permeation pathway such as amides and lipid soluble molecules.

Acetamides↗