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生理学和疾病中的去甲肾上腺素转运体

The norepinephrine transporter in physiology and disease.

作者信息

Bönisch H, Brüss M

机构信息

Department of Pharmacology and Toxicology, University of Bonn, Reuterstr. 2b, 53115 Bonn, Germany.

出版信息

Handb Exp Pharmacol. 2006(175):485-524. doi: 10.1007/3-540-29784-7_20.

Abstract

The norepinephrine transporter (NET) terminates noradrenergic signalling by rapid re-uptake of neuronally released norepinephrine (NE) into presynaptic terminals. NET exerts a fine regulated control over NE-mediated behavioural and physiological effects including mood, depression, feeding behaviour, cognition, regulation of blood pressure and heart rate. NET is a target of several drugs which are therapeutically used in the treatment or diagnosis of disorders among which depression, attention-deficit hyperactivity disorder and feeding disturbances are the most common. Individual genetic variations in the gene encoding the human NET (hNET), located at chromosome 16q12.2, may contribute to the pathogenesis of those diseases. An increasing number of studies concerning the identification of single nucleotide polymorphisms in the hNET gene and their potential association with disease as well as the functional investigation of naturally occurring or induced amino acid variations in hNET have contributed to a better understanding of NET function, regulation and genetic contribution to disorders. This review will reflect the current knowledge in the field of NET from its initial discovery until now.

摘要

去甲肾上腺素转运体(NET)通过将神经元释放的去甲肾上腺素(NE)快速重新摄取到突触前终末来终止去甲肾上腺素能信号传导。NET对NE介导的行为和生理效应,包括情绪、抑郁、摄食行为、认知、血压和心率调节,发挥着精细调控作用。NET是几种药物的作用靶点,这些药物在治疗或诊断疾病中具有治疗用途,其中抑郁症、注意力缺陷多动障碍和摄食障碍最为常见。位于16号染色体q12.2上的人类NET(hNET)编码基因的个体遗传变异可能与这些疾病的发病机制有关。越来越多关于hNET基因单核苷酸多态性的鉴定及其与疾病潜在关联的研究,以及对hNET中自然发生或诱导的氨基酸变异的功能研究,有助于更好地理解NET的功能、调节以及对疾病的遗传贡献。本综述将反映从NET最初发现至今该领域的现有知识。

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