Istituto di Chimica Biologica "G. Fornaini", Via A. Saffi 2, University of Urbino, 1-61029 Urbino (PS), Italy.
Restor Neurol Neurosci. 1996 Jan 1;10(2):69-75. doi: 10.3233/RNN-1996-10202.
The effects of the rat sciatic nerve crush on the activities of glucose-6-phosphate dehydrogenase (G6PD), glutathione reductase (GR), glutathione peroxidase (GPX), superoxide dismutase (SOD) and catalase (CAT) were examined in regenerating nerve and in two reinnervating muscles: the slow twitch soleus and the fast twitch extensor digitorum longus (edl). The enzyme activities in the crushed side, were compared with the contralateral homologue tissues and basal values, determined in uncrushed animals. In the crushed side, the activity of G6PD, GR, GPX and CAT of the sciatic nerve and both muscles markedly increased in comparison with the uncrushed side. In the nerve and in both muscles, SOD activity decreased at 13 days, then rose to values higher than normal, but the pattern of the crushed side was not significantly different from that of the uncrushed. In the uncrushed side, we observed a significant increase of nerve G6PD, GPX and CAT activities compared to basal values, while in both muscles, values fluctuated around the normal without any significant variation. The mechanism of these enzymatic changes is unknown, however our work suggests that: (i) during nerve regeneration, an oxidative stress occurs in nerve and muscle, which causes adaptive responses in antioxidant enzymes; (ii) the maximum antioxidant power is expressed during the period of synaptic retraction; (iii) G6PD and GR activities are synergistically modulated with GPX and CAT, while SOD activity appears independently regulated.
研究了大鼠坐骨神经挤压对葡萄糖-6-磷酸脱氢酶(G6PD)、谷胱甘肽还原酶(GR)、谷胱甘肽过氧化物酶(GPX)、超氧化物歧化酶(SOD)和过氧化氢酶(CAT)活性的影响,这些酶存在于再生神经和两个再支配肌肉中:慢收缩比目鱼肌和快收缩伸趾长肌(edl)。将挤压侧的酶活性与对侧同源组织和未挤压动物的基础值进行比较。在挤压侧,与未挤压侧相比,坐骨神经和两块肌肉的 G6PD、GR、GPX 和 CAT 活性明显增加。在神经和两块肌肉中,SOD 活性在第 13 天下降,然后升高到高于正常水平,但挤压侧的模式与未挤压侧没有显著差异。在未挤压侧,我们观察到神经 G6PD、GPX 和 CAT 活性与基础值相比显著增加,而在两块肌肉中,值在正常范围内波动,没有任何显著变化。这些酶变化的机制尚不清楚,然而,我们的工作表明:(i)在神经再生过程中,神经和肌肉中发生氧化应激,导致抗氧化酶产生适应性反应;(ii)最大的抗氧化能力在突触回缩期间表达;(iii)G6PD 和 GR 活性与 GPX 和 CAT 协同调节,而 SOD 活性似乎独立调节。