X. Cheng et al., REVERSAL BY L-ENANTIOMER AND D-ENANTIOMER OF N-G-NITRO-ARGININE OF ENDOTOXIN-INDUCED HYPOTENSION AND VASCULAR HYPORESPONSIVENESS, Journal of cardiovascular pharmacology, 28(1), 1996, pp. 75-81
We examined the effects of D-NNA (N-G-nitro-D-arginine) and L-NNA (N-G
-nitro-L-arginine) on suppression of Escherichia coli lipopolysacchari
de (LPS)induced vascular hyporeactivity in pentobarbital-anesthetized
rats. Mean arterial pressure (MAP) and presser response to norepinephr
ine (NE) were reduced at 40 min (early phase) and 3.5-4 h (late phase)
after i.v. injection of LPS (10 mg/kg). Pretreatment with either D-NN
A (16 mg/kg) or L-NNA (8 mg/kg) abolished LPS-induced reduction in MAP
and hyporesponsiveness to NE during the early phase but not the late
phase of endotoxemia and increased mortality. In contrast, posttreatme
nt with D-NNA and L-NNA at 3 h after the injection of LPS prevented fu
rther decreases of MAP and presser response to NE during the late phas
e of endotoxemia. The restoration of vascular response by pretreatment
with either D-NNA or L-NNA during the early phases or posttreatment w
ith either of these two agents during the late phase of endotoxemia wa
s abolished by i.v. infusion (10 mg/kg/min) of L-arginine (L-Arg), but
not D-arginine (D-Arg), suggesting involvement of the L-Arg/nitric ox
ide pathway.