Ra. Brown et al., Increased (Na plus K plus Cl) cotransport in rat arterial smooth muscle indeoxycorticosterone (DOCA)/salt-induced hypertension, J VASC RES, 36(6), 1999, pp. 492-501
Citations number
44
Categorie Soggetti
Cardiovascular & Respiratory Systems","Cardiovascular & Hematology Research
The inhibition by loop diuretics of K efflux (tracer Rb-86) from the rat fe
moral arterial smooth muscle was measured in normotension and in DOCA-salt
hypertension. The sensitivity sequence (bumetanide > piretanide > furosemid
e) was the characteristic pharmacological profile of (Na+K+Cl) cotransport,
In hypertension, cotransport activity was 46% greater than in normotension
and the sensitivity to loop diuretics was threefold less. Intracellular [K
] and the Na, K and CI permeability ratios and electrogenic Na pump activit
y were assessed electrophysiologically in normotension and hypertension. [K
](i) was lower in hypertension (173 mM) than normotension (198 mM) but the
other parameters (P-Na/Cl = 0.14, P-Cl/P-K = 0.19 and electrogenic pump = -
8.3 mV in normotension) were not significantly different. Ionic permeabilit
ies to Ma, K and CI were significantly lower in hypertension than normotens
ion. Plasma [Na], but not [K], was higher in hypertension than normotension
. The conclusion is that increased activation of (Na+K+Cl) cotransport in h
ypertension plays a major role in the elevation of [Cl](i) and depolarisati
on of the membrane potential in vascular smooth muscle in DOCA-salt hyperte
nsion. The role of (Na+K+Cl) cotransport in vascular smooth muscle in this
model of hypertension is discussed in relation to [Cl](i), depolarisation o
f the membrane potential and contraction and in relation to cell growth, Co
pyright(C) 1999 S. Karger AG, Basel.