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新型促甲状腺激素释放激素类似物水合他替瑞林(TA - 0910)对大鼠脑内多巴胺释放及代谢周转的影响

Effects of taltirelin hydrate (TA-0910), a novel thyrotropin-releasing hormone analog, on in vivo dopamine release and turnover in rat brain.

作者信息

Fukuchi I, Asahi T, Kawashima K, Kawashima Y, Yamamura M, Matsuoka Y, Kinoshita K

机构信息

Pharmaceutical Development Research Laboratory, Tanabe Seiyaku Co., Ltd., Saitama, Japan.

出版信息

Arzneimittelforschung. 1998 Apr;48(4):353-9.

PMID:9608876
Abstract

Effects of taltirelin hydrate (CAS 103300-74-9, TA-0910), a novel thyrotropin-releasing hormone (TRH) analog, on the cerebral monoamine systems, especially the release and turnover of dopamine (DA) in rat brain were compared with those of TRH by intraperitoneal administration. Taltirelin hydrate (1-10 mg/kg) increased the extracellular levels of DA and its metabolites, 3,4-dihydroxyphenylacetic acid (DOPAC) and homovanillic acid (HVA) in the nucleus accumbens and corpus striatum for 3 h in a microdialysis study. TRH (30 mg/kg) also increased the levels of these substances, the potency of TRH being the same as that of taltirelin hydrate at doses of 1-3 mg/kg. Taltirelin hydrate (10 mg/kg) also caused an increase in 3-methoxytyramine (3-MT: DA metabolite) until 6 h after the treatment and L-3-dihydroxyphenylalanine (DOPA: precursor of DA and noradrenaline). Taltirelin hydrate also increased the 3-methoxy-4-hydroxyphenylglycol (MHPG: noradrenaline metabolite) level in the frontal cortex and hypothalamus, and 5-hydroxytryptophan (5-HTP: serotonin precursor) accumulation and 5-hydroxyindoleacetic acid (5-HIAA: serotonin metabolite) level in the nucleus accumbens or corpus striatum. These results suggest that taltirelin hydrate possesses not only an enhancing effect on DA release, but also a stimulating effect on the monoamine system. Moreover, these actions were 10-30 times stronger and also longer-lasting than those of TRH. In addition, the mechanisms of DA release induced by these drugs were different from those induced by methamphetamine.

摘要

通过腹腔注射,比较新型促甲状腺激素释放激素(TRH)类似物水合他替瑞林(CAS 103300-74-9,TA-0910)对脑单胺系统,尤其是大鼠脑内多巴胺(DA)释放和周转的影响与TRH的影响。在微透析研究中,水合他替瑞林(1-10mg/kg)使伏隔核和纹状体内DA及其代谢产物3,4-二羟基苯乙酸(DOPAC)和高香草酸(HVA)的细胞外水平在3小时内升高。TRH(30mg/kg)也使这些物质的水平升高,在1-3mg/kg剂量下,TRH的效力与水合他替瑞林相同。水合他替瑞林(10mg/kg)还使治疗后6小时内的3-甲氧基酪胺(3-MT:DA代谢产物)增加,以及左旋多巴(DOPA:DA和去甲肾上腺素的前体)增加。水合他替瑞林还使额叶皮质和下丘脑内的3-甲氧基-4-羟基苯乙二醇(MHPG:去甲肾上腺素代谢产物)水平升高,以及伏隔核或纹状体内的5-羟色氨酸(5-HTP:血清素前体)蓄积和5-羟吲哚乙酸(5-HIAA:血清素代谢产物)水平升高。这些结果表明,水合他替瑞林不仅对DA释放具有增强作用,而且对单胺系统具有刺激作用。此外,这些作用比TRH强10-30倍,且持续时间更长。此外,这些药物诱导DA释放的机制与甲基苯丙胺诱导的机制不同。

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