Db. Shennan et al., CHARACTERISTICS OF L-CARNITINE TRANSPORT BY LACTATING RAT MAMMARY TISSUE, Biochimica et biophysica acta, L. Lipids and lipid metabolism, 1393(1), 1998, pp. 49-56
The transport of L-carnitine by lactating rat mammary tissue has been
examined. L-Carnitine uptake by rat mammary tissue explants isolated f
rom lactating rats, 3-4 days post partum, was via both Na+-dependent a
nd Na+-independent pathways. The Na+-dependent pathway, the predominan
t route for L-carnitine uptake, was a saturable process: the K-m and V
-max were, respectively, 132 mu M and 201 pmol/2 h/mg of intracellular
water. The Na+-independent pathway, which was nonsaturable, had a coe
fficient of 0.26 mu l/mg of intracellular water/2 h. The Na+-dependent
component of L-carnitine uptake by mammary tissue explants was cis-in
hibited by D-carnitine and acetyl-L-carnitine, but not by choline or t
aurine. In contrast, the Na+-independent component of L-carnitine upta
ke was not affected by any of these compounds. The uptake of L-carniti
ne by mammary tissue isolated from lactating rats, 10-12 days post par
tum, was qualitatively similar to that by mammary tissue taken from ra
ts during the early stage of lactation. However, L-carnitine uptake wa
s quantitatively lower: this was attributable to a reduction in the Na
+-dependent component of L-carnitine uptake. L-Carnitine efflux from r
at mammary tissue taken from animals 3-4 days post partum, consisted o
f at least two components; a fast extracellular component and a slow m
embrane-limited component. Reversing the trans-membrane Na+-gradient d
id not stimulate L-carnitine afflux suggesting that the Na+-dependent
L-carnitine carrier operates with asymmetrical kinetics. A hyposmotic
shock, hence cell-swelling, increased L-carnitine efflux from mammary
tissue explants. (C) 1998 Elsevier Science B.V. All rights reserved.