We previously reported that hypertension in stroke-prone spontaneously
hypertensive rats (SHRSP) caused renal membrane phospholipid degradat
ion. Renal phospholipase A(2) activity increased and membranous phosph
olipids decreased with age in SHRSP. Membranous abnormalities induced
by membrane fluidity and calcium permeability may contribute to the el
evation of blood pressure in SHRSP. Docosahexa-enoic acid (DHA; 22: 6n
-3) has a physiological effect on several important properties of biom
embranes. The purpose of this study is to clarify the effect of DHA on
the relationship between the renal function and the time-course of hy
pertension in SHRSP. Six week-old male SHRSP were fed a semi-purified
diet supplemented with DHA (0%, 1% and 5%) for 14 weeks. The systolic
blood pressure of control SHRSP (DHA 0%) was significantly increased f
rom 120.2 mmHg to 202.9 mmHg. This increase in systolic blood pressure
was significantly inhibited in a dose-dependent manner in SHRSP that
received DHA diet (1% and 5%) io 167.8 mmHg and to 149.8 mmHg, respect
ively. Serum creatinine concentration and blood urea nitrogen were sig
nificantly decreased in DHA (5%)-treated SHRSP as compared to those of
the control SHRSP. Renal dope decarboxylase activity of the control S
HRSP was significantly decreased as compared to that of WKY. In DHA (5
%)-treated SHRSP, dopa decarboxylase activity was increased and plasma
dopamine concentration was intended to increase. An increase in dopam
inergic tone was attributable to modulate sympathetic tone by DHA. The
se results suggest that DHA may prevent lipid alteration, renal membra
ne fluidity and prolong the time course of hypertension in SHRSP.