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Maisonneuve-Rosemont Hospital; Guy-Bernier Research Center; and University of Montreal, Montreal, Quebec, Canada H1T 2M4
In the rat and the rabbit, a number of
studies have reported the effects of angiotensin II (ANG II) on
Na+ reabsorption by the proximal (PT) and distal (DT)
convoluted tubules of the kidney. The aim of the present study was to
examine the effect of ANG II on Ca2+ uptake by the luminal
membranes of the PT and DT of the rabbit. Incubation of PT and DT with
10
12 M ANG II enhanced the initial Ca2+
uptake in the two segments. Dose-response experiments revealed, for
Ca2+ as well as for Na+ transport, a biphasic
action with a maximal effect at 10
12 M. Ca2+
transport by the DT luminal membrane presents a dual kinetic. ANG II
action influenced the high-affinity Ca2+ channel,
increasing maximal velocity from 0.72 ± 0.03 to 0.90 ± 0.05 pmol · µg
1 · 10 s
1
(P < 0.05, n = 3) and leaving the
Michaelis-Menten constant unchanged. The effect of ANG II was abolished
by losartan, suggesting that the hormone is acting through
AT1 receptors. In the PT, calphostin C inhibited the effect
of the hormone. It is therefore probable that protein kinase C is
involved as a messenger. In the DT, however, neither Rp cAMP,
calphostin C, nor econazole (a phospholipase A inhibitor) influenced
the hormone action. Therefore, the mechanisms involved in the hormone
action remain undetermined. Finally, we questioned whether ANG II acts
in the same DT segment as does parathyroid hormone on Ca2+
transport. The two hormones increased Ca2+ transport, but
their actions were not additive, suggesting that they both influence
the same channels in the same segment of the distal nephron, i.e., the
segment responsible for the high-affinity calcium channel.
renal calcium transport
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