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过氧化氢参与超氧化物歧化酶诱导的兔肠系膜阻力动脉内皮依赖性舒张增强作用。

Involvement of H2O2 in superoxide-dismutase-induced enhancement of endothelium-dependent relaxation in rabbit mesenteric resistance artery.

作者信息

Itoh Takeo, Kajikuri Junko, Hattori Tomonori, Kusama Nobuyoshi, Yamamoto Tamao

机构信息

Department of Cellular and Molecular Pharmacology, Graduate School of Medical Sciences, Nagoya City University, Nagoya 467-8601, Japan.

出版信息

Br J Pharmacol. 2003 May;139(2):444-56. doi: 10.1038/sj.bjp.0705255.

Abstract

1 The mechanism underlying the enhancement by superoxide dismutase (SOD) of endothelium-dependent relaxation was investigated in rabbit mesenteric resistance arteries. 2 SOD (200 U ml(-1)) increased the production of H(2)O(2) in smooth muscle cells (as indicated by the use of an H(2)O(2)-sensitive fluorescent dye). 3 Neither SOD nor catalase (400 U ml(-1)) modified either the resting membrane potential or the hyperpolarization induced by acetylcholine (ACh, 1 micro M) in smooth muscle cells. 4 In arteries constricted with noradrenaline, the endothelium-dependent relaxation induced by ACh (0.01-1 micro M) was enhanced by SOD (200 U ml(-1)) (P<0.01). This action of SOD was inhibited by L-N(G)-nitroarginine (nitric oxide (NO)-synthase inhibitor) but not by either charybdotoxin+apamin (Ca(2+)-activated-K(+)-channel blockers) or diclofenac (cyclooxygenase inhibitor). 5 Neither ascorbate (50 micro M) nor tiron (0.3 mM), superoxide scavengers, had any effect on the ACh-induced relaxation, but each attenuated the enhancing effect of SOD on the ACh-induced relaxation. Similarly, catalase (400 U ml(-1)) inhibited the effect of SOD without changing the ACh-induced relaxation. 6 In endothelium-denuded strips constricted with noradrenaline, SOD enhanced the relaxation induced by the NO donor 1-hydroxy-2-oxo-3-(N-methyl-3-aminopropyl)-3-methyl-1-triazene (NOC-7) (P<0.05). Ascorbate and catalase each attenuated this effect of SOD. 7 H(2)O(2) (1 micro M) enhanced the relaxation on the noradrenaline contraction induced by NOC-7 and that induced by 8-bromo-cGMP, a membrane-permeable analogue of guanosine 3',5' cyclic monophosphate (cGMP). 8 SOD had no effect on cGMP production, whether measured in endothelium-intact strips following an application of ACh (0.1 micro M) or in endothelium-denuded strips following an application of NOC-7 (0.1 micro M). 9 It is suggested that in rabbit mesenteric resistance arteries, SOD increases the ACh-induced, endothelium-dependent relaxation by enhancing the action of NO in the smooth muscle via its H(2)O(2)-producing action (rather than via a superoxide-scavenging action).

摘要
  1. 我们在兔肠系膜阻力动脉中研究了超氧化物歧化酶(SOD)增强内皮依赖性舒张的机制。2. SOD(200 U ml(-1))增加了平滑肌细胞中H(2)O(2)的生成(使用对H(2)O(2)敏感的荧光染料表明)。3. SOD和过氧化氢酶(400 U ml(-1))均未改变平滑肌细胞的静息膜电位或乙酰胆碱(ACh,1 μM)诱导的超极化。4. 在去甲肾上腺素收缩的动脉中,SOD(200 U ml(-1))增强了ACh(0.01 - 1 μM)诱导的内皮依赖性舒张(P<0.01)。SOD的这种作用被L-N(G)-硝基精氨酸(一氧化氮(NO)合酶抑制剂)抑制,但未被蝎毒素 + 蜂毒明肽(Ca(2 +)激活的K(+)通道阻滞剂)或双氯芬酸(环氧化酶抑制剂)抑制。5. 超氧化物清除剂抗坏血酸(50 μM)和替诺(0.3 mM)对ACh诱导的舒张均无影响,但均减弱了SOD对ACh诱导舒张的增强作用。同样,过氧化氢酶(400 U ml(-1))在不改变ACh诱导舒张的情况下抑制了SOD的作用。6. 在去甲肾上腺素收缩的内皮剥脱条带中,SOD增强了NO供体1 - 羟基 - 2 - 氧代 - 3 -(N - 甲基 - 3 - 氨丙基)- 3 - 甲基 - 1 - 三氮烯(NOC - 7)诱导的舒张(P<0.05)。抗坏血酸和过氧化氢酶均减弱了SOD的这种作用。7. H(2)O(2)(1 μM)增强了NOC - 7诱导的去甲肾上腺素收缩的舒张以及8 - 溴 - cGMP(鸟苷3',5' - 环磷酸(cGMP)的膜通透性类似物)诱导的舒张。8. 无论在应用ACh(0.1 μM)后的内皮完整条带中还是在应用NOC - 7(0.1 μM)后的内皮剥脱条带中测量,SOD对cGMP的生成均无影响。9. 提示在兔肠系膜阻力动脉中,SOD通过其产生H(2)O(2)的作用(而非通过超氧化物清除作用)增强平滑肌中NO的作用,从而增加ACh诱导的内皮依赖性舒张。

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