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一氧化氮合酶和环氧化酶抑制剂对角叉菜胶诱导的大鼠足爪肿胀的协同作用。

Synergistic effect of nitric oxide synthase and cyclooxygenase inhibitors on carrageenan-induced paw edema in rats.

作者信息

Sakaguchi Yasue, Shirahase Hiroaki, Kunishiro Kazuyoshi, Ichikawa Atsuko, Kanda Mamoru, Uehara Yoshio

机构信息

Kobuchisawa Laboratories, Fuji Biomedix Co., Ltd., Yamanashi 408-0044, Japan.

出版信息

Arzneimittelforschung. 2006;56(10):695-9. doi: 10.1055/s-0031-1296775.

Abstract

The present study examined the effects of L-nitroarginine methylester (L-NAME, CAS 50903-99-6), a non-selective nitric oxide synthase (NOS) inhibitor, indometacin (IND, CAS 3305-29-1), a non-selective cyclooxygenase (COX) inhibitor, and a combination of these agents (L-NAME + IND) on carrageenan-induced paw edema for 4 h after the injection of carrageenan in rats. L-NAME at 10 and 30 mg/ kg but not 3 mg/kg (i.p.) decreased paw volume slightly but significantly only at 1 h after the carrageenan injection. IND reduced paw volume slightly at 1 and 3 mg/kg, and markedly at 10 mg/kg (p.o.). A combination of L-NAME and IND at a subthreshold dose (3 mg/kg, i.p. and 1 mg/kg, p.o., respectively) caused a marked reduction of paw edema, which was also confirmed by histopathological examinations. A combination of N-(3-(aminomethyl)benzyl)acetamidine (1400W, CAS 180001-34-7), a selective inhibitor of inducible NOS, and IND at 3 mg/kg, i.p., and 1 mg/kg, p.o., respectively, did not show synergistic anti-inflammatory effects. In conclusion, the combination of non-selective NOS and COX inhibitors had synergistic anti-inflammatory effects on carrageenan-induced paw edema at an early stage, suggesting negative crosstalk between the endogenous NOS-NO and COX-PG pathways in the early stages of acute inflammation.

摘要

本研究检测了非选择性一氧化氮合酶(NOS)抑制剂L-硝基精氨酸甲酯(L-NAME,CAS 50903-99-6)、非选择性环氧化酶(COX)抑制剂吲哚美辛(IND,CAS 3305-29-1)以及这两种药物的组合(L-NAME + IND)对大鼠注射角叉菜胶后4小时内角叉菜胶诱导的爪部水肿的影响。腹腔注射10和30 mg/kg而非3 mg/kg的L-NAME仅在注射角叉菜胶后1小时轻微但显著地降低了爪部体积。1和3 mg/kg的IND轻微降低了爪部体积,10 mg/kg(口服)则显著降低了爪部体积。亚阈值剂量(分别为腹腔注射3 mg/kg和口服1 mg/kg)的L-NAME和IND组合导致爪部水肿显著减轻,组织病理学检查也证实了这一点。选择性诱导型NOS抑制剂N-(3-(氨基甲基)苄基)脒(1400W,CAS 180001-34-7)与分别为腹腔注射3 mg/kg和口服1 mg/kg的IND组合未显示出协同抗炎作用。总之,非选择性NOS和COX抑制剂的组合在早期对角叉菜胶诱导的爪部水肿具有协同抗炎作用,提示在急性炎症早期内源性NOS-NO和COX-PG途径之间存在负性相互作用。

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