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过氧亚硝酸盐对Oddi括约肌运动功能的影响。

The effect of peroxynitrite on sphincter of Oddi motility.

作者信息

Herrmann B W, Cullen J J, Ledlow A, Murray J A, Conklin J L

机构信息

Departments of Surgery and Internal Medicine, University of Iowa College of Medicine, Iowa City, Iowa, 52242, USA.

出版信息

J Surg Res. 1999 Jan;81(1):55-8. doi: 10.1006/jsre.1998.5436.

Abstract

BACKGROUND

Nitric oxide (NO*) is an inhibitory neurotransmitter that induces sphincter of Oddi relaxation. Superoxide (O*-2)-scavenging enzymes are present in enteric plexuses of the sphincter of Oddi and O*-2 alters sphincter of Oddi motor function. O*-2 rapidly oxidizes nitric oxide (NO*) to form peroxynitrite (ONOO-), thus terminating the biological activity of NO*. The aim of our study was to determine the effects of ONOO- on sphincter of Oddi motility in vitro.

MATERIALS AND METHODS

Adult opossums were sacrificed and the sphincter of Oddi was removed and placed in a tissue bath containing oxygenated Krebs solution at 37 degreesC. In the first series of experiments, force transducers recorded tension in a transverse orientation at two sites along the spontaneously contracting sphincter of Oddi. In a second series of experiments, circular muscle strips were precontracted with carbachol and stimulated by an electrical field.

RESULTS

ONOO-, superoxide dismutase (SOD), Nomega-nitro-l-arginine (l-NNA), or oxyhemoglobin were added to the tissue baths. ONOO- decreased the frequency of contractions in the spontaneously contracting sphincter of Oddi. Adding hemoglobin increased the frequency of contractions. ONOO- also increased the stimulation-induced relaxation compared to controls. The increase in relaxation induced by ONOO- was inhibited by oxyhemoglobin and l-NNA but not SOD. Pretreatment with oxyhemoglobin prevented the increase in the stimulation-induced relaxation caused by ONOO-.

CONCLUSION

These results suggest that hemoglobin binds ONOO- or that ONOO- generates NO.

摘要

背景

一氧化氮(NO*)是一种抑制性神经递质,可诱导奥迪括约肌松弛。超氧化物(O*-2)清除酶存在于奥迪括约肌的肠神经丛中,且O*-2会改变奥迪括约肌的运动功能。O*-2可迅速将一氧化氮(NO*)氧化形成过氧亚硝酸盐(ONOO-),从而终止NO*的生物活性。我们研究的目的是确定ONOO-对体外奥迪括约肌运动的影响。

材料与方法

处死成年负鼠,取出奥迪括约肌并置于37℃含充氧 Krebs 溶液的组织浴中。在第一组实验中,力传感器记录沿着自发收缩的奥迪括约肌两个部位横向方向的张力。在第二组实验中,环形肌条先用卡巴胆碱预收缩,然后用电场刺激。

结果

将ONOO-、超氧化物歧化酶(SOD)、Nω-硝基-L-精氨酸(L-NNA)或氧合血红蛋白加入组织浴中。ONOO-降低了自发收缩的奥迪括约肌的收缩频率。加入血红蛋白增加了收缩频率。与对照组相比,ONOO-还增加了刺激诱导的松弛。ONOO-诱导的松弛增加被氧合血红蛋白和L-NNA抑制,但未被SOD抑制。用氧合血红蛋白预处理可防止ONOO-引起的刺激诱导松弛增加。

结论

这些结果表明血红蛋白结合ONOO-或ONOO-产生NO。

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