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2-巯基乙醇对小鼠和大鼠缺氧后及与年龄相关的生化和行为变化的影响。

Effect of 2-mercaptoethanol on posthypoxic and age-related biochemical and behavioural changes in mice and rats.

作者信息

Fischer H D, Wustmann C, Rudolph E, Oehler J, Jähkel M, Rostock A, Siegemund C, Pénzes L

机构信息

Institute of Pharmacology and Toxicology, Medical Academy, Carl Gustav Carus, Dresden, GDR.

出版信息

Biomed Biochim Acta. 1990;49(10):1085-90.

PMID:2080907
Abstract

2-Mercaptoethanol (2-ME) has a beneficial effect on the mean life span of laboratory rodents. This paper deals with the effects of 2-ME on changes of dopamine release from brain slices of old aged or hypoxia exposed mice and rats. The results were compared with data which reflect spontaneous peroxidation of brain lipid constituents. In addition, adequate behavioural properties were studied. Long-term 2-ME treatment for months abolishes the age-related decrease of transmitter release and prevents changes in malondialdehyde formation. If age-dependent release failure is already established, then neither single high doses of 2-ME nor repeated treatment for 3 weeks are effective. Posthypoxic release inhibition is prevented by a 2-ME pretreatment for 3 weeks but not by an acute single application even at high dosages. The preventive effect of 2-ME is a mediated one rather than an immediate direct action. Age-related behavioural deficits, such as locomotor activity, habituation performance and learning ability, do not reflect any effect of 2-ME long-term treatment.

摘要

2-巯基乙醇(2-ME)对实验啮齿动物的平均寿命具有有益影响。本文探讨了2-ME对老年或缺氧小鼠及大鼠脑片多巴胺释放变化的影响。研究结果与反映脑脂质成分自发过氧化的数据进行了比较。此外,还研究了相应的行为特性。连续数月进行2-ME长期治疗可消除与年龄相关的递质释放减少,并防止丙二醛形成的变化。如果年龄依赖性释放失败已经确立,那么单次高剂量的2-ME或连续3周的治疗均无效。2-ME预处理3周可预防缺氧后释放抑制,但即使高剂量急性单次应用也无效。2-ME的预防作用是一种介导作用,而非直接即时作用。与年龄相关的行为缺陷,如运动活动、习惯化表现和学习能力,并未显示出2-ME长期治疗的任何效果。

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