Mitsuhata H, Saitoh J, Hasome N, Takeuchi H, Horiguchi Y, Shimizu R
Department of Anesthesiology, Jichi Medical School, Tochigi, Japan.
Shock. 1995 Aug;4(2):143-8. doi: 10.1097/00024382-199508000-00011.
We studied the effects of a nitric oxide synthase (NOS) inhibitor, N omega-nitro-L-arginine-methyl ester (L-NAME), on cardiac depression and bronchospasm provoked by systemic anaphylaxis in vivo in rabbits. Animals pretreated with L-NAME showed lower survival rates than control animals pretreated with normal saline. The survival rate in L-NAME-pretreated animals was increased by the administration of L-arginine after initiation of anaphylaxis. Cardiac output fell significantly in animals pretreated with L-NAME compared with controls, although venous return was increased. In animals pretreated with L-NAME, pulmonary resistance was significantly increased, and administration of arginine attenuated the bronchospasm. In conclusion, these results, along with the low survival rates in the L-NAME-treated animals, suggest that NO production may be beneficial to cardiac depression and bronchospasm in anaphylaxis in vivo.
我们研究了一氧化氮合酶(NOS)抑制剂Nω-硝基-L-精氨酸甲酯(L-NAME)对兔体内全身性过敏反应诱发的心脏抑制和支气管痉挛的影响。用L-NAME预处理的动物的存活率低于用生理盐水预处理的对照动物。过敏反应开始后给予L-精氨酸可提高L-NAME预处理动物的存活率。与对照组相比,用L-NAME预处理的动物心输出量显著下降,尽管静脉回流量增加。在用L-NAME预处理的动物中,肺阻力显著增加,给予精氨酸可减轻支气管痉挛。总之,这些结果以及L-NAME处理动物的低存活率表明,体内过敏反应中一氧化氮的产生可能对心脏抑制和支气管痉挛有益。