Modulation of Tryptophan and Serotonin Metabolism as a Biochemical Basis of the Behavioral Effects of Use and Withdrawal of Androgenic-Anabolic Steroids and Other Image- and Performance-Enhancing Agents.

IF 2.7 Q3 NEUROSCIENCES
International Journal of Tryptophan Research Pub Date : 2018-02-19 eCollection Date: 2018-01-01 DOI:10.1177/1178646917753422
Abdulla A-B Badawy
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引用次数: 20

Abstract

Modulation of tryptophan (Trp) metabolism may underpin the behavioral effects of androgenic-anabolic steroids (AAS) and associated image and performance enhancers. Euphoria, arousal, and decreased anxiety observed with moderate use and exercise may involve enhanced cerebral serotonin synthesis and function by increased release of albumin-bound Trp and estrogen-mediated liver Trp 2,3-dioxygenase (TDO) inhibition and enhancement of serotonin function. Aggression, anxiety, depression, personality disorders, and psychosis, observed on withdrawal of AAS or with use of large doses, can be caused by decreased serotonin synthesis due to TDO induction on withdrawal, excess Trp inhibiting the 2 enzymes of serotonin synthesis, and increased cerebral levels of neuroactive kynurenines. Exercise and excessive protein and branched-chain amino acid intakes may aggravate the effects of large AAS dosage. The hypothesis is testable in humans and experimental animals by measuring parameters of Trp metabolism and disposition and related metabolic processes.

Abstract Image

Abstract Image

Abstract Image

色氨酸和血清素代谢的调节是使用和停用雄激素合成代谢类固醇和其他图像和性能增强药物的行为影响的生化基础。
色氨酸(Trp)代谢的调节可能支持雄激素合成代谢类固醇(AAS)和相关图像和性能增强剂的行为影响。适度使用和运动可观察到的愉悦感、觉醒和焦虑减少,可能涉及通过增加白蛋白结合色氨酸的释放和雌激素介导的肝脏色氨酸2,3-双加氧酶(TDO)抑制和增强血清素功能来增强脑血清素合成和功能。在AAS停药或大剂量使用时观察到的攻击性、焦虑、抑郁、人格障碍和精神病,可能是由于停药时TDO诱导血清素合成减少、过量色氨酸抑制血清素合成的2种酶以及脑内神经活性犬尿氨酸水平升高引起的。运动和过量摄入蛋白质和支链氨基酸可加重大剂量AAS的影响。通过测量色氨酸代谢和处置及相关代谢过程的参数,可以在人类和实验动物中验证这一假设。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.30
自引率
4.50%
发文量
19
审稿时长
8 weeks
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