Both T- and L-type calcium channels are expressed in bovine adrenal glomeru
losa cells and both channels are sensitive to moderate depolarizations of t
he cell membrane induced by angiotensin II (AngII) or physiological concent
rations of extracellular K+. These channels present distinct pharmacology,
L-type channels being more sensitive to dihydropyridines, whereas T channel
s are inhibited by lower concentrations of mibefradil, a new type of calciu
m antagonist currently used for treating hypertension. The activity of thes
e channels is also differently modulated by AngII, which inhibits T channel
s through activation of protein kinase C and L channels through a Pertussis
toxin-sensitive G protein. Finally, whereas the activity of L-type channel
s is directly reflected on the levels of the cytosolic calcium concentratio
n ([Ca2+](c)), T-type channels are more closely related to the control of s
teroidogenesis, possibly through a kind of "calcium pipeline" linking the p
lasma membrane to the mitochondria.
In conclusion, two types of calcium channels, with distinct functions and d
ifferential modulation by AngII, are activated by agonists of aldosterone b
iosynthesis in adrenal glomerulosa cells. Most importantly, these channels
have distinct sensitivities to currently used antihypertensive therapeutic
drugs.