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遗传性代谢疾病与智力发育迟缓的发病机制。

Inherited metabolic diseases and pathogenesis of mental retardation.

作者信息

Brady R O

出版信息

Ann Biol Clin (Paris). 1978;36(2):113-9.

PMID:100026
Abstract

Continuing progress has been made in the exploration of the biochemical causes of mental illness. Recent research has indicated that selected abnormalities of specific isoenzymes play an important role in the pathogenesis of heritable metabolic disorders such as phenylketonuria and Niemann-Pick disease. The roles of "animal lectins" and glycosidic enzymes in brain development and synaptogenesis appear to have received important substantiation within the past year. In additions, it has been shown that the blood-brain barrier can be temporarily altered so that exogenous enzymes can enter the central nervous system, and imperative consideration for enzyme replacement therapy in mental disorders. Less satisfactory progress has been made concerining potential anabolic disorders of lipids affecting the nervous system. Finally, novel experimental directions concerning energy metabolism by the brain offer considerable hope for the elucidation of some of the causes of mental retardation.

摘要

在精神疾病生化病因的探索方面持续取得了进展。最近的研究表明,特定同工酶的某些异常在苯丙酮尿症和尼曼-匹克病等遗传性代谢紊乱的发病机制中起重要作用。“动物凝集素”和糖苷酶在大脑发育和突触形成中的作用在过去一年似乎得到了重要证实。此外,已表明血脑屏障可被暂时改变,以便外源性酶能够进入中枢神经系统,这是精神障碍酶替代疗法的重要考虑因素。在影响神经系统的潜在脂质合成代谢紊乱方面取得的进展不太令人满意。最后,关于大脑能量代谢的新实验方向为阐明一些智力迟钝的病因带来了很大希望。

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