EPR evidence for nitric oxide production from guanidino nitrogens of L-arginine in animal tissues in vivo.
EPR evidence for nitric oxide production from guanidino nitrogens of L-arginine in animal tissues in vivo.
复制标题
动物组织体内 L-精氨酸的胍基氮产生一氧化氮的 EPR 证据。
DOI:
10.1016/0005-2728(92)90032-w
复制
发表时间:
1992
期刊:
影响因子:
--
通讯作者:
A. Vanin
中科院分区:
文献类型:
--
作者:
L. Kubrina;W. Caldwell;P. Mordvintcev;I. V. Malenkova;A. Vanin
Administration of Fe 2+-citrite complex (50 mg/kg of FeSO 4 or FeCl 2 plus 250 mg/kg of sodium citrate) subcutaneously in the thigh or Escherichia coli lipopolysaccharide (LPS, 1 mg/kg) intraperitoneally,(ip) to mice induced NO formation in the livers in vivo at the rate of 0.2–0.3 μg/g wet tissue per 0.5 h. The NO synthesized was specifically trapped with Fe 2+-diethyldithio-carbamate complex (FeDETC 2), tormed from endogenous iron and diethyldithiocarbamate (DETC) administered ip 0.5 h before decapitation of the animals. NO bound with this trap resulted in the formation of a paramagnetic mononitrosyl iron complex with DETC (NO-FeDETC 2), characterized by an EPR signal at g⊥= 2.035, g= 2.02 with triplet hyperfine structure (HFS) at g⊥. This allowed quantification of the amount of NO formed in the livers. An inhibitor of enzymatic NO synthesis from l-arginine, N G-nitro-l-arginine (NNLA, 50 mg/kg) attenuated the NO synthesis in vivo. l-Arginine (500 mg/kg) reversed this effect. Injection of l-[guanidineimino-15 N 2] arginine combined with Fe 2+-citrate or LPS led to the formation of the EPR signal of NO-FeDETC 2 characterized by a doublet HFS at g⊥, demonstrating that the NO originates from the guanidino nitrogens of l-arginine in vivo.
影响因子:
2.9
作者:
MARLETTA, MA;YOON, PS;WISHNOK, JS
通讯作者:
WISHNOK, JS