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硫醇调节剂和铜/锌超氧化物歧化酶抑制对大鼠胃底一氧化氮能舒张的影响。

Effect of thiol modulators and Cu/Zn superoxide dismutase inhibition on nitrergic relaxations in the rat gastric fundus.

作者信息

De Man J G, De Winter B Y, Boeckxstaens G E, Herman A G, Pelckmans P A

机构信息

Division of Gastroenterology, Faculty of Medicine, University of Antwerp (UIA), Antwerpen-Wilrijk, Belgium.

出版信息

Br J Pharmacol. 1996 Nov;119(5):1022-8. doi: 10.1111/j.1476-5381.1996.tb15773.x.

Abstract
  1. The effects of superoxide anion generators before and after treatment with inhibitors of Cu/Zn superoxide dismutase (Cu/Zn SOD) and the effects of thiol-modulating agents were investigated on nitrergic relaxations to electrical stimulation of non-adrenergic non-cholinergic (NANC) nerves of the rat gastric fundus and on relaxations to authentic nitric oxide (NO) and nitroglycerin. 2. The superoxide anion generators, pyrogallol (30 microM) and duroquinone (30-60 microM), significantly inhibited the relaxations to NO (0.03-3 microM) but not nitrergic relaxations to NANC nerve stimulation (0.5-8 Hz) or those to ATP (10 microM). Treatment of the rat gastric fundus with the inhibitors of Cu/Zn SOD, diethyldithiocarbamate (DETC, 1 mM for 2 h) or triethylenetetramine (TETA, 100 microM for 2 h) had no effect on the relaxations to NANC nerve stimulation (1-8 Hz), NO (0.03-3 microM) or on those to ATP (10 microM). 3. After treatment of the rat gastric fundus with DETC (1 mM) but not after treatment with TETA (100 microM), pyrogallol (30 microM) and duroquinone (30-60 microM) significantly inhibited the nitrergic relaxations to electrical stimulation (0.5-8 Hz) and those to NO (0.03-3 microM). This inhibitory effect of pyrogallol and duroquinone was prevented by addition of exogenous SOD (250 units ml-1). Pyrogallol but not duroquinone also inhibited the NO-independent relaxations to ATP (10 microM). 4. The thiol modulators, buthionine sulphoximine (1 mM for 2 h) and ethacrynic acid (30 microM for 2 h), significantly inhibited the relaxations to nitroglycerin (0.03-3 microM) but had no effect on the nitrergic relaxations to electrical stimulation (0.5-8 Hz) or on those to NO (0.03-10 microM) and ATP (10 microM). The thiol modulators, sulphobromophthalein (100 microM for 2 h) and diamide (30-100 microM for 2 h) did not affect the relaxations to nitroglycerin, or those to NANC nerve stimulation and NO. 5. In summary, thiol modulators significantly inhibited the thiol-dependent relaxations to nitroglycerin but not those to NANC nerve stimulation or NO. Relaxations to nitrergic stimulation were decreased by superoxide anion generators only after inhibition of Cu/Zn SOD. These results suggest that the nitrergic NANC neurotransmitter in the rat gastric fundus is not a nitrosothiol but more likely free NO, which is protected from breakdown by tissue SOD.
摘要
  1. 研究了超氧阴离子生成剂在经铜/锌超氧化物歧化酶(Cu/Zn SOD)抑制剂处理前后的作用,以及硫醇调节剂对大鼠胃底非肾上腺素能非胆碱能(NANC)神经电刺激引起的一氧化氮能舒张、对真实一氧化氮(NO)和硝酸甘油舒张的影响。2. 超氧阴离子生成剂连苯三酚(30微摩尔)和杜醌(30 - 60微摩尔)显著抑制对NO(0.03 - 3微摩尔)的舒张,但不抑制对NANC神经刺激(0.5 - 8赫兹)或对ATP(10微摩尔)的一氧化氮能舒张。用Cu/Zn SOD抑制剂二乙基二硫代氨基甲酸盐(DETC,1毫摩尔处理2小时)或三亚乙基四胺(TETA,100微摩尔处理2小时)处理大鼠胃底,对NANC神经刺激(1 - 8赫兹)、NO(0.03 - 3微摩尔)或对ATP(10微摩尔)的舒张均无影响。3. 用DETC(1毫摩尔)处理大鼠胃底后而非用TETA(100微摩尔)处理后,连苯三酚(30微摩尔)和杜醌(30 - 60微摩尔)显著抑制对电刺激(0.5 - 8赫兹)和对NO(0.03 - 3微摩尔)的一氧化氮能舒张。加入外源性SOD(250单位/毫升)可阻止连苯三酚和杜醌的这种抑制作用。连苯三酚而非杜醌也抑制对ATP(10微摩尔)的非NO依赖性舒张。4. 硫醇调节剂丁硫氨酸亚砜胺(1毫摩尔处理2小时)和依他尼酸(30微摩尔处理2小时)显著抑制对硝酸甘油(0.03 - 3微摩尔)的舒张,但对NANC神经电刺激(0.5 - 8赫兹)、对NO(0.03 - 10微摩尔)和ATP(10微摩尔)的一氧化氮能舒张无影响。硫醇调节剂磺溴酞(100微摩尔处理2小时)和二酰胺(30 - 100微摩尔处理2小时)不影响对硝酸甘油的舒张,也不影响对NANC神经刺激和NO的舒张。5. 总之,硫醇调节剂显著抑制对硝酸甘油的硫醇依赖性舒张,但不抑制对NANC神经刺激或NO的舒张。仅在抑制Cu/Zn SOD后,超氧阴离子生成剂才会降低对一氧化氮能刺激的舒张。这些结果表明,大鼠胃底的一氧化氮能NANC神经递质不是亚硝基硫醇,而更可能是游离NO,其受到组织SOD的保护而不被分解。

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