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衰老对1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP)对大鼠纹状体和脑干神经毒性作用的影响。

Effects of ageing on 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) neurotoxic effects on striatum and brainstem in the rat.

作者信息

Desole M S, Esposito G, Enrico P, Miele M, Fresu L, De Natale G, Miele E, Grella G

机构信息

Institute of Pharmacology, University of Sassari, Italy.

出版信息

Neurosci Lett. 1993 Sep 3;159(1-2):143-6. doi: 10.1016/0304-3940(93)90819-7.

Abstract

In 3- and 18-month-old male Wistar rats, levels of dopamine (DA), dihydroxyphenylacetic acid (DOPAC), ascorbic acid (AA), dehydroascorbic acid (DHAA), noradrenaline (NA), uric acid, glutathione (GSH) and 1-methyl-4-phenylpyridinium ion (MPP+) were determined by HPLC in the striatum and/or in the brainstem 24 h after single injections of MPTP (12-35 mg/kg i.p.). Aged rats had lower baseline levels of AA and GSH, compared to young rats. In aged rats, MPTP 35 mg/kg induced a 70% death rate and a decrease in striatal DOPAC/DA ratio which was significantly correlated to MPP+ concentrations (r = -0.840, P < 0.005); in addition, MPTP did not increase AA oxidation. In the brainstem, the MPTP-induced decrease in NA levels and increase in uric acid levels were significantly correlated to the MPP+ concentrations (r = -0.709, P < 0.05, and r = +0.888, P < 0.001, respectively). In conclusion, evidence is given of a mechanism of toxicity of MPTP involving oxidative stress produced by xanthine oxidase; in addition, in aged rats the neuronal antioxidant system (levels of AA and GSH) is considerably lower than in young rats and may play an enabling role in the MPTP age-related neurotoxic effects on striatum and brainstem.

摘要

在3月龄和18月龄的雄性Wistar大鼠中,单次腹腔注射MPTP(12 - 35 mg/kg)24小时后,通过高效液相色谱法测定纹状体和/或脑干中多巴胺(DA)、二羟基苯乙酸(DOPAC)、抗坏血酸(AA)、脱氢抗坏血酸(DHAA)、去甲肾上腺素(NA)、尿酸、谷胱甘肽(GSH)和1 - 甲基 - 4 - 苯基吡啶离子(MPP+)的水平。与年轻大鼠相比,老年大鼠的AA和GSH基线水平较低。在老年大鼠中,35 mg/kg的MPTP诱导了70%的死亡率,并导致纹状体DOPAC/DA比值降低,这与MPP+浓度显著相关(r = -0.840,P < 0.005);此外,MPTP并未增加AA的氧化。在脑干中,MPTP诱导的NA水平降低和尿酸水平升高与MPP+浓度显著相关(分别为r = -0.709,P < 0.05,和r = +0.888,P < 0.001)。总之,有证据表明MPTP的毒性机制涉及黄嘌呤氧化酶产生的氧化应激;此外,在老年大鼠中,神经元抗氧化系统(AA和GSH水平)比年轻大鼠低得多,可能在MPTP对纹状体和脑干的年龄相关神经毒性作用中起促成作用。

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