Albino-Teixeira A, Azevedo I, Martel F, Osswald W
Department of Pharmacology and Therapeutics, Faculty of Medicine, Porto, Portugal.
Naunyn Schmiedebergs Arch Pharmacol. 1991 Jul;344(1):36-40. doi: 10.1007/BF00167380.
The effects of superoxide dismutase (S.O.D.) in two models of chemical denervation induced by 6-hydroxydopamine (6-OHDA) were studied. To evaluate the effects of S.O.D. on in vitro 6-OHDA-induced denervation, fragments of the lateral saphenous veins of mongrel dogs were pre-incubated in oxygenated Krebs-Henseleit solution with or without S.O.D. and then incubated under control conditions, with 6-OHDA or with 6-OHDA + S.O.D. Following the incubation period the fragments were repeatedly washed with Krebs solution and then used for determination of noradrenaline and for morphological study. 6-OHDA produced a profound depletion of noradrenaline. This depletion was significantly reduced although not prevented by S.O.D. The protective effect of S.O.D. was concentration-dependent. The ultrastructural study confirmed the 6-OHDA-induced sympathetic nerve degeneration as well as the protective effect afforded by S.O.D. In order to evaluate the effects of S.O.D. on in vivo 6-OHDA-induced denervation, male Wistar rats were anaesthetized and the tail vein cannulated. Saline or S.O.D. were intravenously delivered. 6-OHDA was injected five minutes after the beginning of infusions. Fragments of the left ventricle and vasa deferentia were used for determination of noradrenaline and for morphological study. 6-OHDA produced a significant depletion of noradrenaline in the left ventricle and vas deferens (to 8% and 18% of control values respectively). This depletion was reduced, though not prevented by S.O.D. Morphological data confirmed the neurotoxic effect of 6-OHDA and a protective role for S.O.D.(ABSTRACT TRUNCATED AT 250 WORDS)
研究了超氧化物歧化酶(S.O.D.)在两种由6-羟基多巴胺(6-OHDA)诱导的化学去神经模型中的作用。为评估S.O.D.对体外6-OHDA诱导的去神经作用,将杂种犬的隐静脉片段在含或不含S.O.D.的充氧Krebs-Henseleit溶液中预孵育,然后在对照条件下、6-OHDA或6-OHDA + S.O.D.条件下孵育。孵育期后,将片段用Krebs溶液反复冲洗,然后用于去甲肾上腺素的测定和形态学研究。6-OHDA导致去甲肾上腺素大量耗竭。尽管S.O.D.不能完全阻止这种耗竭,但可使其显著减少。S.O.D.的保护作用呈浓度依赖性。超微结构研究证实了6-OHDA诱导的交感神经变性以及S.O.D.提供的保护作用。为评估S.O.D.对体内6-OHDA诱导的去神经作用,将雄性Wistar大鼠麻醉并插入尾静脉导管。静脉注射生理盐水或S.O.D.。输注开始5分钟后注射6-OHDA。取左心室和输精管片段用于去甲肾上腺素的测定和形态学研究。6-OHDA使左心室和输精管中的去甲肾上腺素显著耗竭(分别降至对照值的8%和18%)。这种耗竭虽未被S.O.D.阻止,但有所减少。形态学数据证实了6-OHDA的神经毒性作用以及S.O.D.的保护作用。(摘要截短至250字)