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电解产生的自由基可使离体大鼠心脏中的硝基蓝四氮唑还原。

Free radicals generated by electrolysis reduces nitro blue tetrazolium in isolated rat heart.

作者信息

Chahine R, Huet M P, Oliva L, Nadeau R

机构信息

Research Centres, Hôpital du Sacré-Coeur de Montreal, Quebec, Canada.

出版信息

Exp Toxicol Pathol. 1997 Feb;49(1-2):91-5. doi: 10.1016/S0940-2993(97)80074-7.

Abstract

Oxygen free radicals (OFR) are highly cytotoxic when produced in the myocardium under certain pathological conditions. In isolated rat hearts perfused retrogradely, OFR were generated by electrolysis of the Krebs-Henseleit buffer (two platinum electrodes, DC current, 10 mA, 1 min). In order to find evidence that OFR are produced, we used nitro blue tetrazolium (NBT) a soluble compound which yields a dark blue formazan pigment in the presence of reducing agents. Hearts were subdivided into: control, electrolysed, NBT (3.3 mg/ml) perfusion during electrolysis in the presence or absence of scavengers. The xanthine-xanthine oxidase (XXO) system known to produce superoxide radical was used as a reference. Specimens were fixed with formaldehyde and stained with eosine or Kernechtrot in preparation for light microscopical examination. Several areas of acute necrosis expressed by hyalinisation and loss of striation were observed in electrolysed hearts which present a pattern of wavy disrupted myofibers and an increase in interstitial spaces. A very faint deposition of formazan was observed in some rare areas of NBT perfused heart. Only the electrolysed group perfused with NBT and the one perfused with XXO plus NBT presented an extensive formazan deposition, mostly in the areas of fibre necrosis. Formazan was barely detectable when superoxide dismutase plus catalase were perfused in the XXO system, while it was still apparent when perfused in electrolysed hearts. These results support the hypothesis that electrolysis can be used to generate different species of OFR and to evaluate the protective action of scavenger and antioxidants against OFR-induced myocardial damage.

摘要

在某些病理条件下,心肌中产生的氧自由基(OFR)具有高度细胞毒性。在逆行灌注的离体大鼠心脏中,通过电解 Krebs-Henseleit 缓冲液(两个铂电极,直流电流,10 mA,1 分钟)产生 OFR。为了找到 OFR 产生的证据,我们使用了硝基蓝四唑(NBT),一种可溶性化合物,在还原剂存在的情况下会产生深蓝色的甲臜色素。心脏被分为:对照组、电解组、在有或没有清除剂存在的情况下电解期间用 NBT(3.3 mg/ml)灌注组。已知产生超氧阴离子自由基的黄嘌呤-黄嘌呤氧化酶(XXO)系统用作参考。标本用甲醛固定,并用伊红或苏木精染色,以准备进行光学显微镜检查。在电解的心脏中观察到几个由玻璃样变和横纹消失表示的急性坏死区域,呈现出波浪状中断的肌纤维模式和间质间隙增加。在 NBT 灌注心脏的一些罕见区域观察到非常微弱的甲臜沉积。只有用 NBT 灌注的电解组和用 XXO 加 NBT 灌注的组呈现出广泛的甲臜沉积,主要在纤维坏死区域。当在 XXO 系统中灌注超氧化物歧化酶加过氧化氢酶时,甲臜几乎检测不到,而当在电解心脏中灌注时仍然明显。这些结果支持这样的假设,即电解可用于产生不同种类的 OFR,并评估清除剂和抗氧化剂对 OFR 诱导的心肌损伤的保护作用。

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