N-G-METHYL-L-ARGININE, AN INHIBITOR OF NITRIC-OXIDE FORMATION, REVERSES IL-2-MEDIATED HYPOTENSION IN DOGS

被引:42
作者
KILBOURN, RG
OWENSCHAUB, LB
CROMEENS, DM
GROSS, SS
FLAHERTY, MJ
SANTEE, SM
ALAK, AM
GRIFFITH, OW
机构
[1] UNIV TEXAS,MD ANDERSON CANC CTR,DEPT IMMUNOL,HOUSTON,TX 77030
[2] UNIV TEXAS,MD ANDERSON CANC CTR,DEPT VET MED & SURG,HOUSTON,TX 77030
[3] CORNELL UNIV,COLL MED,DEPT PHARMACOL,NEW YORK,NY 10021
[4] RUSH PRESBYTERIAN ST LUKES MED CTR,CHICAGO,IL 60612
[5] MED COLL WISCONSIN,DEPT BIOCHEM,MILWAUKEE,WI 53226
关键词
LYMPHOKINE-ACTIVATED KILLER CELLS; ENDOTHELIUM-DERIVED RELAXING FACTOR; TUMOR NECROSIS FACTOR; INTERLEUKIN-1;
D O I
10.1152/jappl.1994.76.3.1130
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
N-G-methyl-L-arginine, an inhibitor of nitric oxide formation, reverses IL-2-mediated hypotension in dogs. J. Appl. Physiol. 76(3): 1130-1137, 1994. - The effects of N-G-methyl-L-arginine (L-NMA), an inhibitor of nitric oxide formation, were studied in dogs treated with interleukin-2 (IL-2). The administration of IL-2 to dogs resulted in hypotension within 3 days of treatment. The development of hypotension correlated with accumulation in the serum of nitrate, which is a stable breakdown product of nitric oxide. Administration of L-NMA decreased serum nitrate levels and increased the mean arterial pressure. The antihypotensive effect was dose dependent with a maximum effect observed at a dose of 20 mg/kg. Administration of a continuous infusion of L-NMA (5 mg.kg(-1).h(-1)) maintained the mean arterial pressure for 48 h with concurrent administration of IL-2. Evaluation of IL-2-induced lymphokine-activated killer cell proliferation and tumoricidal activity toward a canine glioblastoma target cell line was unaffected by L-NMA. These studies imply that L-NMA may effectively ameliorate the dose-limiting hypotension associated with administration of IL-2 without adversely affecting the antitumor effects.
引用
收藏
页码:1130 / 1137
页数:8
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