Hp. Schedl et al., VITAMIN-D AND ENTEROCYTE BRUSH-BORDER MEMBRANE CALCIUM-TRANSPORT AND FLUIDITY IN THE RAT, Metabolism, clinical and experimental, 43(9), 1994, pp. 1093-1103
Prior studies of vitamin D repletion showed a threefold increase in th
e maximum rate (Vmax) for calcium uptake by brush border membrane vesi
cles, but did not differentiate saturable and nonsaturable uptake comp
onents. We studied the calcium uptake and fluidity response of intesti
nal brush border vesicles to vitamin D by treatment with 1 alpha,25-di
hydroxy-24,24-difluorocholecalciferol (24,24-F-1,25-(OH)(2) D-3) Treat
ment responses were measured by effects on (1) saturable and nonsatura
ble initial uptake rates of calcium by rat proximal small intestinal b
rush border membrane vesicles; (2) transmucosal calcium transport by e
verted duodenal sac; and (3) fluorescence anisotropy. Treatment of vit
amin D-depleted weanlings increased the Vmax by 50% (P < .05) in vesic
les from the proximal 12 cm of small intestine from rats injected with
disodium ethane-1-hydroxy-1,1-diphosphonate (EHDP), but there was no
response in rats not injected with EHDP or in vesicles from the proxim
al 30 cm of small intestine. Vitamin D-depleted weanlings were D-defic
ient based on serum 25-hydroxycalciferol (25-OH-D) concentration, but
to produce 1 alpha,25-dihydroxycalciferol [1,25-(OH)(2)D] depletion, E
HDP injection was required. Treatment of vitamin D-replete adult rats
caused a 20% (P < .05) increase in Vmax. Treatment did not affect the
calcium concentration at half-Vmax (Kr), the rate constant for nonsatu
rable uptake (K-D), or vesicle fluidity measured as fluorescence aniso
tropy. Contrasting with these minimal effects of treatment on brush bo
rder Vmax, treatment increased transmucosal calcium transport by evert
ed duodenal sac almost threefold in vitamin D-depleted weanlings admin
istered EHDP. Thus, vitamin D actions on enterocyte calcium transport
(1) at the brush border increase saturable but not nonsaturable uptake
, and (2) produce the major transport response distal to the brush bor
der. Despite previously described changes in membrane lipid, brush bor
der fluidity is unaffected by vitamin D treatment. Copyright (C) 1994
by W.B. Saunders Company