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CHRONIC ANABOLIC-ANDROGENIC STEROID TREATMENT AFFECTS BRAIN GABA(A) RECEPTOR-GATED CHLORIDE ION TRANSPORT

机译:慢性厌氧-雄激素治疗对脑GABA(A)受体控制的氯离子转运的影响

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摘要

Previous research in this laboratory has shown that chronic treatment of adult male rats with an anabolic-androgenic steroid (AAS) produced anxiolytic behavior and increased the functional response of cortical gamma-aminobutyric acid(A) (GABA(A)) receptors. The experiments reported here were aimed at further characterizing the effect of chronic AAS exposure on cerebral cortical GABA(A) receptors. Adult male rats were injected with dianabol (1,4-androstadien-17 alpha-methyl-17 beta-ol-3-one; 10 mg/kg/day, SC) for 4 weeks. A significant decrease in ventral prostate gland weight was found after 2 weeks of dianabol, and returned to control levels 3 and 10 days after steroid discontinuation. Testicular weights decreased throughout the treatment period but reached statistical significance only during the withdrawal period. Serum 3 alpha-androstanediol level was marginally increased after 2 weeks of dianabol injection, and was significantly decreased at 3 and 10 days after withdrawal. GABA-stimulated (36)chloride (Cl-) influx in cortical synaptoneurosomes was increased in animals treated with dianabol for 2 and 4 weeks, and remained elevated 3 days after dianabol withdrawal, returning to control levels at withdrawal day 10. The increase in receptor efficacy was associated with a transient increase in receptor sensitivity (inverse of EC(50)), apparent after 2 weeks of AAS treatment and at withdrawal day 3. In a follow-up experiment, metabolites of dianabol were tested for the in vitro efficacy in potentiating GABA-stimulated Cl- transport. Only 3 alpha-androstanediol and androsterone were found to have potent stimulatory effects. The 3 beta-reduced metabolites were inactive, as were metabolites that contained a methyl group at the 17 alpha position. These results point to significant facilitative effects of dianabol treatment on brain GABA(A) receptors via the metabolic formation of neuroactive steroids. [References: 39]
机译:该实验室先前的研究表明,用合成代谢雄激素类固醇(AAS)长期治疗成年雄性大鼠会产生抗焦虑行为,并增加了皮质γ-氨基丁酸(A)(GABA(A))受体的功能反应。本文报道的实验旨在进一步表征慢性AAS暴露对大脑皮层GABA(A)受体的影响。成年雄性大鼠被注射dianabol(1,4-androstadien-17 alpha-methyl-17 beta-ol-3-one; 10 mg / kg / day,SC)4周。在dianabol 2周后发现腹侧前列腺重量显着减少,在类固醇停用后3天和10天恢复到对照水平。在整个治疗期间,睾丸重量下降,但仅在停药期间才达到统计学意义。注射dianabol 2周后,血清3α-雄甾烷二醇水平略有增加,停药后3天和10天显着降低。接受dianabol处理2周和4周的动物中,GABA刺激的皮质突触神经小体中的(36)氯化物(Cl-)流入量增加,并在dianabol撤药后3天保持升高,在撤药第10天恢复到对照水平。受体的增加疗效与受体敏感性的短暂升高相关(EC(50)的倒数),在AAS治疗2周后和戒断第3天时明显可见。在后续实验中,检测了dianabol代谢物的体外功效。增强GABA刺激的Cl转运。仅发现3种α-雄甾烷二醇和雄甾酮具有有效的刺激作用。 3个减少了β的代谢物是无活性的,在17个α位上含有甲基的代谢物也没有活性。这些结果表明,大力神治疗通过神经活性类固醇的代谢形成对脑GABA(A)受体具有明显的促进作用。 [参考:39]

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